Publikationen

• Al-Achkar W, As’sad M, Liehr T, Ikhtiar A, Wafa A. A de novo childhood case of T-cell lymphoblastic leukemia with high hyperdiploid karyotype carrying an unreported balanced translocation t(X;5)(q26;q31.3~32) in a male patient. OBM Genetics 2019; 3; doi:10.21926/obm.genet.1902081

• Ammer-Herrmenau C, Kulkarni U, Andreas N, Ungelenk M, Ravens S, Hübner C, Kather A, Kurth I, Bauer M, Kamradt T. Sepsis induces long-lasting impairments in CD4+ T-cell responses despite rapid numerical recovery of T-lymphocyte populations. PLoS One. 2019;14:e0211716.

• Barby FF, Bertollo LAC, de Oliveira EA, Yano CF, Hatanaka T, Ráb P, Sember A, Ezaz T, Ferreira Artoni R, Liehr T, Al-Rikabi ABH, Trifonov V, de Oliveira EHC, Molina WF, Jegede OI, Tanomtong A, de Bello Cioffi M. Emerging patterns of genome organization in Notopteridae species (Teleostei, Osteoglossiformes) as revealed by Zoo-FISH and Comparative Genomic Hybridization (CGH). Scient Rep 2019; 9:1112.
• Borges MLRDR, Soares-Ventura EM, Liehr T, Marques-Salles TJ. Minimally differentiated acute myeloid leukemia wth ring/marker derived chromosome 7 in a child with Down syndrome. Hematol Transfus Cell Ther 2019; 41:84-87.
• Chaudhuri JP, Karamanov S, Scott L, Liehr T, Walther JU. Leukocyte nucleus reveals a linear order of chromosomes separated in two parental genomes that favors the process of gene activation. J Histochem Cytochem 2019; 67:151-158.
• de Oliveira ES, Bertollo LAC , Rab P, Ezaz T, Yano CF, Hatanaka T, Jegede OI, Tanomtong A, Liehr T, Sember A, Maruyama SR, Feldberg E, Viana PF. Cytogenetics, genomics and biodiversity of the South American and African Arapaimidae fish family (Teleostei, Osteoglossiformes). PLoS One 2019; 14: e0214225.
• De Matos R, Ney Garcia D, Othman M, Ferreira G, Melo J, Carreira I, Meyer C, Marschalek R, Costa E, Land M, Liehr T, Ribeiro R, Macedo Silva M. A new complex karyotype involving a KMT2A-r variant three-way translocation, in a rare clinical presentation of a pediatric patient with acute myeloid leukemia. Cytogenet Genome Res 2019; 157:213-219.
• de Moraes RLR, Sember A, Bertollo LAC, de Oliveira EA, Rab P, Hatanaka T, Marinho MMF, Liehr T, Al-Rikabi ABH, Feldberg E, Viana PF, de Bello Cioffi M. Comparative cytogenetics and neo-Y formation in small-sized fish species of the genus Pyrrhulina (Characiformes, Lebiasinidae). Front Genet 2019; 10: 678.
• Ditcharoen S, Bertollo LAC, Rab P, Hnátková E, Molina WF, Liehr T, Tanomtong A, Triantaphyllidis C, Ozouf-Costaz C, Tongnunui S, Pengseng P, Supiwong W, Aroutiounian R, Cioffi M. Genomic organization of repetitive DNA elements and extensive karyotype diversity of Silurid catfishes (Teleostei: Siluriformes): A comparative cytogenetic approach. Int J Mol Sci 2019; 20:3545.
• Garcia-Angulo A, Merlo MA, Rodriguez ME, Portela-Bens S, Liehr T, Rebordinos L. Genome and phylogenetic analysis of genes involved in the immune system of Solea senegalensis - potential applications in aquaculture. Front Genet 2019; 10:529.
• Harutyunyan T, Hovhannisyan G, Sargsyan A, Grigoryan B, Al-Rikabi AH, Weise A, Liehr T, Aroutiounian R. Analysis of copy number variations induced by ultrashort electron beam radiation in human leukocytes in vitro. Mol Cytogenet 2019; 12:18.
• Hennings C, Hübner CA. Disorders of renal NaCl transprot and implications for blood pressure regulation. Med Gen 2019; 31: 1-7.

• Huebner AK, Maier H, Maul A, Nietzsche S, Herrmann T, Praetorius J, Hübner CA. Early hearing loss upon disruption of Slc4a10 in C57BL/6 mice. J Assoc Res Otolaryngol 2019; 20:233-245.

• Krumbholz A, Roempke J, Liehr T, Groth M, Meerbach A, Schacke M, Maschkowitz G, Fickenscher H, Klapper W, Sauerbrei A, Wutzler P, Zell R. Macaca arctoides gammaherpesvirus 1 (strain herpesvirus Macaca arctoides): virus sequence, phylogeny and characterisation of virus-transformed macaque and rabbit cell lines. Medic Microbiol Immunol 2019; 208:109-129.
• Khundadze M, Ribaudo F, Hussain A, Rosentreter J, Nietzsche S, Thelen M, Winter D, Hoffmann B, Afzal MA, Hermann T, de Heus C, Piskor EM, Kosan C, Franzka P, von Kleist L, Stauber T, Klumperman J, Damme M, Proikas-Cezanne T, Hübner CA. A mouse model for SPG48 reveals a block of autophagic flux upon disruption of adaptor protein complex five. Neurobiol Dis. 2019;127:419-431.
• Kurtas NE, Xumerle L, Leonardelli L, Delledonne M, Brusco A, Chrzanowska K, Schinzel A, Larizza D, Guerneri S, Natacci F, Bonaglia MC, Reho P, Manolakos E, Mattina T, Soli F, Provenzano A, Al-Rikabi AH, Errichiello E, Nazaryan-Petersen L, Giglio S, Tommerup N, Liehr T, Zuffardi O. Small supernumerary marker chromosomes: a legacy of trisomy rescue. Hum Mutat 2019; 40:193-200.
• Kurtas NE, Xumerle L, Giussani U, Pansa A, Cardarelli L, Bertini V, Valetto A, Liehr T, Bonaglia C, Erichiello E, Delledonne M, Zuffardi O. Insertional translocation involving an additional non-chromothriptic chromosome in constitutional chromothripsis: rule or exception? Mol Genet Genomic Med 2019; 7:e496.

• Lakshmana G, Baniahmad A. Interference with the androgen receptor protein stability in therapy-resistant prostate cancer. Int J Cancer 2019; 144:1775-1779.

• Liehr T. From human cytogenetics to human chromosomics. Int J Mol Sci 2019; 20:826.

• Liehr T. Non-invasive prenatal testing – safer or simply more profitable? https://atlasofscience.org/non-invasive-prenatal-testing-safer-or-simply-more-profitable
• Liehr T, Liehr LB. An update on small supernumerary marker chromosomes (sSMC). Res Results Biomed 2019; 5:4-6
• Liehr T, Carreira IM, Balogh Z, Garrido ED,  Verdorfer I, Coviello DA, Florentin L, Scheffer H, Rincic M, Williams HE. Regarding the rights and duties of Clinical Laboratory Geneticists in genetic healthcare systems; results of a survey in over 50 countries. Eur J Hum Genet 2019; 27:1168-1174.
• Merhni H, Zerkaoui M, Natiq A, Sbiti A, Liehr T, Sefiani A. Constitutional partial proximal trisomy 14q11.2 to 14q21: two new Moroccan cases and review of the literature. OBM Genetics 2019; 3:doi:10.21926/obm.genet.1903085.
• Moysés-Oliveira M, Di-Battista A, Zamariolli M, Meloni VA, Bragagnolo S, Christofolini DM, Steiner CE, Kosyakova N, Liehr T, Reymond A, Melaragno MI. Breakpoint mapping at nucleotide resolution in X-autosome balanced translocations associated with clinical phenotypes. Eur J Hum Genet 2019; 27:760-771.
• Padutsch N, Liehr T. First report on a 20qh+ heteromorphism characterized by molecular cytogenetics as amplification of D20Z1 sequences. Research Results in Biomedicine 2019, 5:22-24.
• Pessôa AI, Amorim KC, Ferreira WAS, Sagica F, Brito JR, Othman M, Meyer B, Liehr T, de Oliveira EHC. Detection and correlation of single and concomitant TP53, PTEN and CDKN2A alterations in gliomas. Int J Mol Sci 2019; 20:2658.

• Roell D, Rösler TW, Hessenkemper W, Kraft F, Hauschild M, Bartsch S, Abraham TE, Houtsmuller AB, Matusch R, van Royen ME, Baniahmad A. Halogen-substituted anthranilic acid derivatives provide a novel chemical platform for androgen receptor antagonists. J Steroid Biochem Mol Biol. 2019;188:59-70.

• Sassi FMC, Oliveira EA, Bertollo LAC, Nirchio M, Hatanaka T, Marinho MMF, Moreira-Filho O, Aroutiounian R, Liehr T, Al-Rikabi ABH, Cioffi MB. Chromosomal evolution and evolutionary relationships of Lebiasina species (Characiformes, Lebiasinidae). Int J Mol Sci 2019; 20. pii: E2944.

• Shmukler BE, Rivera A, Bhargava P, Nishimura K, Hsu A, Kim EH, Trudel M, Rust MB, Huebner CA, Brugnara C, Alper SL. Combined genetic disruption of K-Cl cotransporters and Gardos channel KCNN4 rescues erythrocyte dehydration in the SAD mouse model of sickle cell disease. Blood Cells Mol Dis 2019; 79:102346.

• Steinacker R, Liehr T, Kosyakova N, Rincic M, Hussein Azawi SS. Molecular cytogenetic characterization of two murine cancer cell lines derived from salivary gland. Biol Commun 2019; 63: 243-255.

• Supiwong W, Pinthong K, Seetapan K, Sanjundaeng P, Bertollo LAC, Aguiar de Oliveira E, Yano CF , Liehr T, Phimphan S, Tanomtong A, de Bello Cioffi M. Karyotype diversity and evolutionary trends in the Asian swamp eel Monopterus albus (Synbranchiformes, Synbranchidae). A case of chromosomal speciation? BMC Evolutionary Biology 2019; 19:73.

• Symmank J, Gölling V, Gerstmann K, Zimmer G. The Transcription Factor LHX1 Regulates the Survival and Directed Migration of POA-derived Cortical Interneurons. Cereb Cortex. 2019; 29:1644-1658.

• Teichert M, Isstas M, Liebmann L, Hübner CA, Wieske F, Winter C, Lehmann K, Bolz J. Visual deprivation independent shift of ocular dominance induced by cross-modal plasticity. PLoS One. 2019;14:e0213616.

• Warren AY, Massie CE, Watt K, Luko K, Orafidiya F, Selth LA, Mohammed H, Chohan BS, Menon S, Baridi A, Zhao W, Escriu C, Pungsrinont T, D'Santos C, Yang X, Taylor C, Qureshi A, Zecchini VR, Shaw GL, Dehm SM, Mills IG, Carroll JS, Tilley WD, McEwan IJ, Baniahmad A, Neal DE, Asim M. A reciprocal feedback between the PDZ binding kinase and androgen receptor drives prostate cancer. Oncogene 2019; 38:1136-1150.

• Weise A, Liehr T. Rapid prenatal aneuploidy screening by fluorescence in situ hybridization (FISH). Methods Mol Biol 2019; 1885:129-137.

• Weise A, Mrasek K, Pentzold C, Liehr T. Chromosomes in the DNA era: Perspectives in diagnostics and research. Med Gen 2019; 31: 8-19.
• Xu D, Sember A, Zhu Q, de Oliveira EA, Liehr T, Al-Rikabi ABH, Xiao Z, Song H, Cioffi M. Deciphering the origin and evolution of a unique X1X2Y system in two closely related Oplegnathus species (Oplegnathidae, Centrarchiformes). Int J Mol Sci 2019; 20:3570.

Bücher/ Books

• Akbaroghli S, Tonekaboni SH, Kariminejad R, Liehr T, Coci EG. De novo interstitial 2.33 Mb Deletion in 8q24.3: New insights on a very rare partial monosomy syndrome. Clin Dysmorphol 2018; 27:97-100.
• Al-Rikabi ABH, Pekova S, Fan X, Jančušková T, Liehr T. Small supernumerary marker chromosome may provide information on dosage-insensitive pericentric regions in human. Curr Genomics 2018; 19:192-199.
• Araújo T, Khayat A, Quintana L, Calcagno D, Mourão R, Modesto A, Paiva J, Lima A, Moreira F, Oliveira E, Souza M, Othman M, Liehr T, Abdelhay E, Gomes R, Santos S, Assumpção P. Piwi like RNA-mediated gene silencing 1 gene as a possible major player in gastric cancer. World J Gastroenterol 2018; 24:5338-5350.
• Barby FF, Ráb P, Lavoué S, Ezaz T, Bertollo LAC, Kilian A, Maruyama SR, de Oliveira EA, Artoni RF, Santos MH, Jegede OI, Hatanaka T, Tanomtong A, Liehr T, de Bello Cioffi M. From chromosomes to genome: Insights into the evolutionary relationships and biogeography of old world knifefishes (Notopteridae; Osteoglossiformes). Genes 2018, 9:306.
• Beetz C, Khundadze M, Goldberg LV, Hübner CA. Erbliche spastische Spinalparalysen: aktuelle Erkenntnisse und Entwicklungen. Med Genetik 2018; 30:238-245
• Benítez EO, Morales JJ, Muñoz LA, Hübner CA, Mutchinick OM. A novel GMPPA mutation in two adult sisters with achalasia, alacrima, short stature, dysmorphism, and intellectual disability. Mol Syndromol 2018; 9:110-114.
• Bock AS, Günther S, Mohr J, Goldberg LV, Jahic A, Klisch C, Hübner CA, Biskup S, Beetz C. A nonstop variant in REEP1 causes peripheral neuropathy by unmasking a 3'UTR-encoded, aggregation-inducing motif. Hum Mutat 2018; 39:193-196.
• Capela de Matos RR, Othman MAK, Ferreira GM, Costa ES, Melo JB, Carreira IM, de Souza MT, Lopes BA, Emerenciano M, Land MGP, Liehr T, Ribeiro RC, Silva MLM. Molecular approaches identify a cryptic MECOM rearrangement in a child with a rapidly progressive myeloid neoplasm. Cancer Genet 2018; 221:25-30.
• Castiglia L, Husain R, Marquardt I, Fink C, Liehr T, Serino D, Elia M, Coci E. 7q11.23 micro-duplication syndrome: neuro-physiological and neuro-radiological insights into a rare chromosomal disorder. J Intellect Disab Res 2018; 62:359-370.

• Cross I, Portela-Bens S, García-Angulo A, Merlo MA, Rodríguez ME, Liehr T, Rebordinos L. A preliminary integrated genetic map distinguishes every chromosome pair and locates essential genes related to abiotic adaptation of Crassostrea angulata/gigas. BMC Genet. 2018, 19:104.

• Čulić V, Lasan-Trcić R, Liehr T, Lebedev IN, Pivić M, Pavelic J, Vulić R. A familial small supernumerary marker chromosome 15 associated with cryptic mosaicism with two different additional marker chromosomes derived de novo from chromosome 9: Detailed case study and implications for recurrent pregnancy loss. Cytogenet Genome Res. 2018;156(4):179-184.

• Darr-Foit S, Schliemann S, Schulz S, Elsner P. Buschke-Ollendorff syndrome due to a novel LEMD3 mutation - an unusual case of alopecia. J Dtsch Dermatol Ges 2018, 16:348-349.

• de Oliveira EA, Sember A, Bertollo LAC, Yano CF, Ezaz T, Moreira-Filho O, Hatanaka T, Trifonov V, Liehr T, Hamid Al-Rikabi AB, Ráb P, Pains H, de Bello Cioffi M. Tracking the evolutionary pathway of sex chromosomes among fishes: characterizing the unique XX/XY1Y2 system in Hoplias malabaricus (Teleostei, Characiformes). Chromosoma 2018; 127:115-128
• De Souza MT, Vera-Lozada G, Othman M, Marques-Salles TJ, Pinto LW, da Rocha MM, Rouxinol S, Liehr T, Ribeiro RC, Hassan R, Silva MLM. Molecular and cytogenetic studies in a child with Burkitt lymphoma and ataxia-telangiectasia syndrome harboring MYC overexpression and partial trisomy 8. Ann Lab Med 2018; 38:63-66.
• Deutsche Gesellschaft für Humangenetik e.V. (GfH), Berufsverband Deutscher Humangenetiker e.V (T Liehr and A Weise included in commission). S2k-Leitlinie Humangenetische Diagnostik und Genetische Beratung. Med Gen 2018; 30:469-522.
• Dimaisip-Nabuab J, Duijster D, Benzian H, Heinrich-Weltzien R, Homsavath A, Monse B, Sithan H, Stauf N, Susilawati S, Kromeyer-Hauschild K. Nutritional status, dental caries and tooth eruption in children: a longitudinal study in Cambodia, Indonesia and Lao PDR. BMC Pediatr. 2018;18:300
• García-Angulo A, Merlo MA, Portela-Bens S, Rodríguez ME, García E, Al-Rikabi A, Liehr T, Rebordinos L. Evidence for a Robertsonian fusion in Solea senegalensis (Kaup, 1858) revealed by zoo-FISH and comparative genome analysis. BMC Genomics 2018, 19:818.

• Gillessen-Kaesbach G, Albrecht B, Eggermann T, Elbracht M, Mitter D, Morlot S, van Ravenswaaij-Arts CMA, Schulz S, Strobl-Wildemann G, Buiting K, Beygo J. Molecular and clinical studies in 8 patients with Temple syndrome. Clin Genet 2018; 93:1179-1188.

• Girdauskas E., Petersen J., Neumann N., Ungelenk M., Kurth I., Reichenspurner H., Zeller T. MiR-145 expression and rare NOTCH1 variants in bicuspid aortic valve-associated aortopathy. PLoS One. 2018; 13:e0200205.

• Grigoryan A, Guidi N, Senger K, Liehr T, Soller K, Marka G, Vollmer A, Markaki Y, Leonhardt H, Buske C, Lipka D, Plass C, Zheng Y, Mulaw MA, Geiger H, Florian MC. LaminA/C regulates epigenetic and chromatin architecture changes upon aging of hematopoietic stem cells. Genome Biology 2018, 19:189.

• Haag N, Schüler S, Nietzsche S, Hübner CA, Strenzke N, Qualmann B, Kessels MM. The actin nucleator cobl is critical for centriolar positioning, postnatal planar cell polarity refinement, and function of the cochlea. Cell Rep. 2018;24:2418-2431.e6.

• Hatanaka T, de Oliveira EA, Ráb P, Yano CF, Bertollo LAC, Ezaz T, Jegede OOI, LiehrT, Olaleye VF, de Bello Cioffi M. First Chromosomal Analysis in Gymnarchus niloticus (Gymnarchidae, Osteoglossiformes): Insights into the Karyotype Evolution of this ancient fish order. Biol J Linn Soc 2018; 125:83-92.
• Kirmse K, Hübner CA, Isbrandt D, Witte OW, Holthoff K. GABAergic transmission during brain development: multiple effects at multiple stages. Neuroscientist 2018; 24:36-53.
• Komatsuzaki S, Ediga RD, Okun JG, Kölker S, Sauer SW. Impairment of astrocytic glutaminolysis in glutaric aciduria type I. J Inherit Metab Dis. 2018; 41:91-99.
• Liehr T. Importance of databases for human genetic diagnostics. J Genet Genom 2018, 2:e105.
• Liehr T, Hamid Al-Rikabi AB. Impaired spermatogenesis due to small supernumerary marker chromosomes: The reason for infertility is only reliably ascertainable by cytogenetics. Sex Dev 2018; 12:281-287.
• Liehr T, Schreyer I, Kuechler A, Manolakos E, Singer S, Dufke A, Wilhelm K, Jančušková T, Čmejla R, Othman MAK, Al-Rikabi AH, Mrasek K, Ziegler M, Kankel S, Kreskowski K, Weise A. Parental origin of deletions and duplications about the necessity to check for cryptic inversions. Mol Cytogenet 2018; 11:20.
• Liehr T, Acquarola N, Pyle K, St-Pierre S, Rinholm M, Bar O, Wilhelm K, Schreyer I. Next generation phenotyping in Emanuel and Pallister Killian Syndrome using computer-aided facial dysmorphology analysis of 2D photos. Clin Genet 2018; 93:378-381.
• Liehr T, Ziegler M, Kosyakova N, Al-Rikabi ABH. Easy approach to gain interphase cells for fluorescence in situ hybridization. OBM Genetics 2018; 2:021
• LiehrT, Schreyer I, Mrasek K, Weise A. Neue Entwicklungen in der humangenetischen pränatalen Diagnostik. Ärzteblatt Thüringen 2018; 12: 689-691.
• Maass PG, Weise A, Rittscher K, Lichtenwald J, Barutcu AR, Liehr T, Aydin A, WefeldNeuenfeld Y, Pölsler L, Tinschert S, Rinn JL, Luft FC, Bähring S. Reorganization of interchromosomal interactions in the 2q37deletion syndrome. EMBO J 2018; 37:e96257
• Moassass F, Wafa A, Liehr T, Al-Ablog A, AL Achkar W. Down syndrome associated childhood myeloid leukemia with yet unreported acquired chromosomal abnormalities and a new potential adverse marker: dup(1)(q25q44). Mol Cytogenet 2018; 11:22.
• Moysés-Oliveira M, Giannuzzi G, Fish RJ, Rosenfeld JA, Petit F, de Fatima Soares M, Domenici Kulikowski L, Di Battista A, Zamariolli M, Xia F, Liehr T, Kosyakova N, Carvalheira G, Parker M, Seaby EG, Ennis S, Gilbert RD, Hagelstrom T, Basel DG, Andrieux J, Stumpp T, Antunes F, Pereira GJ, Neerman-Arbez M, Meloni VA, Drummond-Borg M, Melaragno MI, Reymond A. Inactivation of AMMECR1 is associated with growth, bone and heart alterations. Hum Mut 2018; 39:281-291.
• Münch J, Billig G, Hübner CA, Leinders-Zufall T, Zufall F, Jentsch TJ. Ca2+-activated Cl- currents in the murine vomeronasal organ enhance neuronal spiking but are dispensable for male-male aggression. J Biol Chem 2018; 293:10392-10403.
• Ornellas MH, Maioli MC, Lucena S, Bastos E, Chaves TS, Vieira de Melo K, Carvalho M, Liehr T. Complex karyotype including ring 11 chromosome in woman with acute myeloid leukemia. São Paulo Medical Journal 2018; 136:361-367.
• Othman MAK , Grygalewicz , Kołkowska-Leśniak A, Melo JB, Carreira IM, Liehr T. Cryptic NUP214-ABL1 fusion with complex karyotype, episomes and intra-tumor genetic heterogeneity in a T-cell lymphoblastic lymphoma. J Cancer Metastasis Treat 2018; 4:50.
• Papoulidis I, Vetro A, Paspaliaris V, Ziegler M, Kreskowski K, Daskalakis G, Papadopoulos V, Dagklis T, Liehr T, Thomaidis L, Manolakos E. A girl with 10 Mb distal Xp deletion arising from maternal pericentric inversion: Clinical data and molecular characterization. Curr Genomics 2018; 19:240-246.

• Pensold D, Zimmer G. Single-cell transcriptomics reveals regulators of neuronal migration and maturation during brain development. J Exp Neurosci. 2018;12:1179069518760783.

• Priya PK, Mishra VV, Liehr T, Ziegler M, Tiwari S, Patel A, Chettiar SS, Patel H. Characterization of a complex chromosomal rearrangement involving chromosomes 1, 3 and 4 in a slightly affected male partner with unsuccessful obstetric history. J Assist Reprod Genet 2018; 35:721-725.

• Rhode H, Liehr T, Kosyakova N, Rinčic M, Azawi SSH. Molecular cytogenetic characterization of two murine colorectal cancer cell lines. OBM Genetics 2018; 2(3) doi:10.21926/obm.genet.1803037.
• Ribeiro IP, Rodrigues JM, Mascarenhas A, Kosyakova N, Caramelo F, Liehr T, Melo JB, Carreira IM. Cytogenetic, genomic, and epigenetic characterization of the HSC-3 tongue cell line with lymph node metastasis. J Oral Sci 2018; 60:70-81.
• Saenjundaeng P, de Bello Cioffi M, Aguiar de Oliveira E, Tanomtong A, Supiwong W, Phimphan S, Collares-Pereira M, Sember A, Bertollo LAC, Liehr T, Yano CF, Hatanaka T, Rab P. Chromosomes of Asian cyprinid fishes: Cytogenetic analysis of two representatives of small paleotetraploid tribe Probarbini. Molecular Cytogenetics 2018; 11:51.
• Sangpakdee W, Tanomtong A, Chaveerach A, Pinthong K, Trifonov V, Loth K, Hensel C, Liehr T, Weise A, Fan X. Molecular cytogenetic analysis of one African and five Asian macaque species reveals identical karyotypes as in mandrill. Curr Genomics 2018; 19:207-215.

• Schulz S, Mensah MA, de Vries H, Fröber R, Romeike B, Schneider U, Borte S, Schindler D, Kentouche K.Microcephaly, short stature, and limb abnormality disorder due to novel autosomal biallelic DONSON mutations in two German siblings. Eur J Hum Genet 2018, 26:1282-1287.

• Sheth F, Liehr T, Mrasek K, Andrieux J, Tewari S, Lubna N, Sheth J. sSMC characterization in a male with Turner syndrome stigmata. OBM Genetics 2018; 2(3) doi:10.21926/obm.genet.1803033.
• Sheth F, Liehr T, Shah V, Sheth H, Tewari S, Solanki D, Trivedi S, Sheth J. A child with intellectual disability and dysmorphism due to complex ring chromosome 6: Identification of molecular mechanism with review of literature. Ital J Pediatr 2018; 44:114
• Wafa A, Ali B, Aljapawe A, Liehr T, ALmedani S, Al Achkar W. Unreported combination of rearrangements in a childhood B-cell acute lymphoblastic leukemia case: Coexistence of translocation t(8;14) and monoallelic loss of tumor suppressor gene TP53. Gene Reports 2018; 10:66-70.
• Wafa A, ALmedania S, Aljapawe A, Liehr T, Soulaiman SE, Mouna R, Othman MAK, ALachkar W. A new adult AML case with an extremely complex karyotype, remission and relapse combined with high hyperdiploidy of a normal chromosome set in secondary AML. BMC Hematology 2018; 18:21.
• Weihrauch-Blüher S, Kromeyer-Hauschild K, Graf C, Widhalm K, Korsten-Reck U, Jödicke B, Markert J, Müller MJ, Moss A, Wabitsch M, Wiegand S. Current guidelines for obesity prevention in childhood and adolescence. Obes Facts. 2018; 11:263-276.
• Wilhelm K, Pentzold C, Schoener S, Arakelyan A, Hakobyan A, Mrasek K, Weise A. Fragile sites as drivers of gene and genome evolution. Curr Genet Med Rep 2018, 6:136-143.
  
  

Number of publications per year (1994-2016)

• Ahmad A, Dad R, Ullah MI, Baig TA, Ahmad IN, Nasir A, Hübner CA, Hassan MJ. Clinical and genetic studies in patients with Lafora disease from Pakistan. J Neurol Sci 2017; 373:263-267.
• Ahmad A, Dad R, Ullah MI, Baig TA, Ahmad IN, Nasir A, Hübner CA, Hassan MJ. Corrigendum to "Clinical and genetic studies in patients with Lafora disease from Pakistan" [J. Neurol. Sci. 373 (2017) 263-267]. J Neurol Sci. 2017 Apr 15;375:281.
• Al-Achkar W, Moassass F, Aroutiounian R, Harutyunyan T, Liehr T, Wafa A. Effect of Glutathione S-transferase mu 1 (GSTM1) gene polymorphism on chronic myeloid leukemia risk and Imatinib treatment response. Metagene 2017, 12:113-117.
• Asim M, Tarish F, Zecchini HI, Sanjiv K, Gelali E, Massie CE, Baridi A, Warren AY, Zhao W, Ogris C, McDuffus LA, Mascalchi P, Shaw G, Dev H, Wadhwa K, Wijnhoven P, Forment JV, Lyons SR, Lynch AG, O'Neill C, Zecchini VR, Rennie PS, Baniahmad A, Tavaré S, Mills IG, Galanty Y, Crosetto N, Schultz N, Neal D, Helleday T. Synthetic lethality between androgen receptor signalling and the PARP pathway in prostate cancer. Nat Commun 2017, 8:374.
• Blanquie O, Liebmann L, Hübner CA, Luhmann HJ, Sinning A. NKCC1-mediated GABAergic signaling promotes postnatal cell death in neocortical cajal-retzius cells. Cereb Cortex. 2017, 27:1644-1659.
• Borges ML, Capela de Matos RR, Amaral BD, Soares-Ventura EM, Leite EP, Silva MO, Cornélio MT, Silva ML, Liehr T, Marques-Salles T. Molecular cytogenetic approach to characterize novel and cryptic chromosome abnormalities in childhood myeloid malignances of Fanconi anemia. J Ped Hematol Oncol 2017, 39:e85-e91.
• Busch A, Žarković M, Lowe C, Jankofsky M, Ganschow R, Buers I, Kurth I, Reutter H, Rutsch F, Hübner CA. Mutations in CRLF1 cause familial achalasia. Clin Genet. 2017, 92:104-108.
• Capela de Matos RR, Ney Garcia DR, Cifoni E, Othman MAK, Tavares de Souza M, Carboni EK, Ferreira GM, Liehr T, Ribeiro RC, M Silva MLGAS6 oncogene and reverse MLLT3-KMT2A duplications in an infant with acute myeloid leukemia and a novel complex hyperdiploid karyotype: detailed high-resolution molecular cytogenetic studies. Cytogenet Genome Res 2017, 152:33-37.
• Carvalho PC, Aguiar de Oliveira E, Bertollo ALC, Yano CF, Oliveira C, Decru E, Jegede OI, Hatanaka T, Liehr T, Al-Rikabi ABH, de Bello Cioffi M. Insights into relationship between African and Neotropical fish groups: First chromosomal analysis in Hepsetidae (Actinopterygii, Characiformes). Frontiers in Genetics, section Evolutionary and Population Genetics 2017; 8:203.
• Castori M, Morlino S, Ungelenk M, Pareyson D, Salsano E, Grammatico P, Tolosano E, Kurth I, Chiabrando D. Posterior column ataxia with retinitis pigmentosa coexisting with sensory-autonomic neuropathy and leukemia due to the homozygous p.Pro221Ser FLVCR1 mutation. Am J Med Genet B Neuropsychiatr Genet. 2017 Oct;174:732-739.
• Coci EG, Codutti L, Fink C, Bartsch S, Grüning G, Lücke T, Kurth I, Riedel J. Novel homozygous missense mutation in ALDH7A1 causes neonatal pyridoxine dependent epilepsy. Mol Cell Probes. 2017 Apr;32:18-23.
• Coci EG, Auhuber A, Langenbach A, Mrasek K, Riedel J, Leenen A, Lücke T, LiehrT. Novel unbalanced translocations affecting the long arms of chromosomes 10 and 22 cause complex syndromes with very severe neurodevelopmental delay, speech impairment, autistic behavior, and epilepsy. Cytogenet Genome Res 2017, 151:171-178.
• de Souza DC, de Figueiredo AF, Ney Garcia DR, da Costa ES, Othman MAK, Liehr T, Abdelhay E, Silva MLM, de Souza Fernandez T. A unique set of complex chromosomal abnormalities in an infant with myeloid leukemia associated with Down syndrome. Mol Cytogenet. 2017, 10:35.
• Disha K, Schulz S, Kuntze T, Girdauskas E. Transforming growth factor beta-2 mutations in Barlow's disease and aortic dilatation. Ann Thorac Surg. 2017, 104:e19-e21.
• Donat M, Louis A, Kreskowski K, Ziegler M, Weise A, Schreyer I, Liehr T. X-autosome and X-Y translocations in female carriers: X-chromosome inactivation easily detectable by 5-ethynyl-2-deoxyuridine (EdU). Balk J Med Genet 2017; 20:87-90.
• Duijster D, Monse B, Dimaisip-Nabuab J, Djuharnoko P, Heinrich-Weltzien R, Hobdell M, Kromeyer-Hauschild K, Kunthearith Y, Mijares-Majini MC, Siegmund N, Soukhanouvong P, Benzian H. 'Fit for school' - a school-based water, sanitation and hygiene programme to improve child health: Results from a longitudinal study in Cambodia, Indonesia and Lao PDR. BMC Public Health. 2017, 17:302.
• Fischer M, Kosyakova N, Liehr T, Dobrowolski P. Large deletion on the Y-chromosome long arm (Yq) of C57BL/6JBomTac inbred mice. Mamm Genome 2017, 28:31-37.
• Girdauskas E, Geist L, Disha K, Kazakbaev I, Groß T, Schulz S, Ungelenk M, Kuntze T, Reichenspurner H, Kurth I. Genetic abnormalities in bicuspid aortic valve root phenotype: preliminary results. Eur J Cardiothorac Surg. 2017; 52:156-162.
• Gold WA, Sobreira N, Wiame E, Marbaix A, Van Schaftingen E, Franzka P, Riley LG, Worgan L, Hübner CA, Christodoulou J, Adès LC. A novel mutation in GMPPA in siblings with apparent intellectual disability, epilepsy, dysmorphism, and autonomic dysfunction. Am J Med Genet A. 2017 173:2246-2250.
• Guja K, Liehr T, Rincic M, Kosyakova N, Hussein Azawi SS. Molecular cytogenetic characterization identified the murine B-Cell lymphoma cell line A-20 as a model for sporadic Burkitt's lymphoma. J Histochem Cytochem 2017, 65:669-677.
• Heimrich KG, Gühne F, Schulz S, Mutschke S, Stallmach A, Rüddel J. [Gastroparesis in Noonan syndrome]. Z Gastroenterol. 2017, 55:145-148.
• Hennings JC, Andrini O, Picard N, Paulais M, Huebner AK, Cayuqueo IK, Bignon Y, Keck M, Cornière N, Böhm D, Jentsch TJ, Chambrey R, Teulon J, Hübner CA, Eladari D. The ClC-K2 chloride channel is critical for salt handling in the distal nephron. J Am Soc Nephrol 2017;28:209-217.
• Hochstenbach R, Poot M, Liehr T. Mechanisms of origin and clinical effects of multiple small supernumerary marker chromosomes, each derived from a different chromosome. OBM Genetics 2017; 1:002.
• Karamysheva TV, Torgasheva AA, Yefremov YR, Bogomolov AG, Liehr T, Borodin PM, Rubtsov NB. Spatial organization of fibroblast and spermatocyte nuclei with different B chromosome content in Korean field mouse Apodemus peninsulae (Rodentia, Muridae). Genome 2017; 60:815-824.
• Karimzad Hagh J, Liehr T, Ghaedi H, Mossalaeie MM, Alimohammadi S, Inanloo Hajiloo F, Moeini Z, Sarabi S, Zare-Abdollahi D. Prenatal diagnosis of mosaic tetrasomy 18p in a case without sonographic abnormalities. Int J Mol Cell Med (IJMCM) 2017; 6:61-65.
• Kubicova E, Trifonov V, Borovecki F, Liehr T, Rincic M, Kosyakova N, Hussein SS. First molecular cytogenetic characterization of murine malignant mesothelioma cell line AE17 and in silico translation to the human genome. Curr Bioinform 2017, 12:11-18.
• Kurtovic-Kozaric A, Mehinovic L, Komic H, Kozaric M, Husic-Selimovic A, Ziegler M, LiehrT. Human cytogenetics case report: Yet unreported heteromorphic variant in chromosome 17. J Genetics Genomes 2017; 1:101.
• Liehr T. “Classical cytogenetics” is not equal to “banding cytogenetics”. Mol Cytogenet 2017; 10:3
• Liehr T. Chronic lymphocytic leukemia (CLL) diagnostics better to do in cultivated than native cells. (http://atlasofscience.org/chronic-lymphocytic-leukemia-cll-diagnostics-better-to-do-in-cultivated-than-native-cells/)
• Liehr T. How to characterize best the genetic content of small supernumerary marker chromosomes. (http://atlasofscience.org/how-to-characterize-best-the-genetic-content-of-small-supernumerary-marker-chromosomes/
• Liehr T. Human cells can count their chromosomes but how do they do? (http://atlasofscience.org/human-cells-can-count-their-chromosomes-but-how-do-they-do/)
• Liehr T. What about noninvasive prenatal testing (NIPT) from ‘cell-free fetal DNA’ (cffDNA)? http://atlasofscience.org/what-about-noninvasive-prenatal-testing-nipt-from-cell-free-fetal-dna-cffdna/)
• Liehr T. Thorough discussion of cancer research thoughts against the main stream. Europ J Hum Genet 2017, 25: 902-903.
• Liehr T. The first internet page on chromosomal heteromorphisms (HMs). ECA newsletter 2017, 40:32-33.
• Liehr T. What about the real costs of next generation sequencing (NGS) in human genetic diagnostics? (http://atlasofscience.org/what-about-the-real-costs-of-next-generation-sequencing-ngs-in-human-genetic-diagnostics/)
• Liehr T. Expert knowledge on human genetic counselling and chromosomics are necessary for sound genetic laboratory diagnostics. Mol Exp Biol Med 2017, 1:1-3
• Liehr T, Mrasek K, Klein E, Weise A. Modern high throughput approaches are not meant to replace ‘old fashioned’ but robust techniques. J Genet Genomes 2017, 1:e101.
• Liehr T, Lauten A, Schneider U, Schleussner E, Weise A. Noninvasive prenatal testing (NIPT) when is it advantageous to apply? Biomed Hub 2017; 2:458432.
• Liehr T, Carreira IM, Aktas D, Bakker E, Rodríguez de Alba M, Coviello DA, Florentin L, Scheffer H, Rincic M; the Clinical Laboratory Geneticists Professional Branch Board, European Board of Medical Genetics, Vienna, Austria. European registration process for Clinical Laboratory Geneticists in genetic healthcare. Europ J Hum Genet 2017, 25:515-519
• Liehr T, Weise A, Schreyer I. Humangenetische Diagnostik muss es immer NGS sein? BIOspektrum 2017, 03/17:350-351.
• Liehr T,  Buleu O, Karamysheva T, Bugrov A, Rubtsov N. New insights into Phasmatodea chromosomes. Genes (Basel) 2017; 8:E327.
• Mendez-Rosado LA, Lantigua A, Galarza J, Al-Rikabi ABH, Ziegler M, Liehr T. Unusual de novo partial trisomy 17p12p11.2 due to unbalanced insertion into 5p13.1 in a severely affected boy. J Pediatr Genet 2017, 6:165-168
• Merlo MA, Iziga R, Portela S, Cross I, Kosyakova N, Liehr T, Manchado M, Rebordinos L. Analysis of the histone cluster in Senegalese sole (Solea senegalensis): evidence for a divergent evolution of two canonical histone clusters. Genome 2017, 60:441-453.
• Mumtaz R, Trepiccione F, Hennings JC, Huebner AK, Serbin B, Picard N, Ullah AKMS, Păunescu TG, Capen DE, Lashhab RM, Mouro-Chanteloup I, Alper SL, Wagner CA, Cordat E, Brown D, Eladari D, Hübner CA. Intercalated cell depletion and vacuolar H+-ATPase mistargeting in an Ae1 R607H knockin model. J Am Soc Nephrol 2017, 28:1507-1520.
• Ney Garcia DR, de Souza MT, de Figueiredo AF, Othman MAK, Rittscher K, Abdelhay E, Capela de Matos RR, Meyer C, Marschalek R, Land MGP, Liehr T, Ribeiro RC, Silva MLM. Molecular characterization of KMT2A fusion in 13 cases of pediatric leukemia with a complex or cryptic karyotype. Hem Oncol 2017; 35:760-768.
• Papadopoulou Z, Papoulidis I, Sifaki S, Markopoulos G, Vetro A, Vlaikou A-M, Ziegler M, Liehr T, Thomaidis L, Zuffardi O, Syrrou M, George K, Manolakos E. Partial monosomy 8p and trisomy 16q in two children with developmental delay detected with aCGH. Mol Med Rep 2017;16:8808-8818.
• Pensold D, Symmank J, Hahn A, Lingner T, Salinas-Riester G, Downie BR, Ludewig F, Rotzsch A, Haag N, Andreas N, Schubert K, Hübner CA, Pieler T, Zimmer G. The DNA methyltransferase 1 (DNMT1) controls the shape and dynamics of migrating POA-derived interneurons fated for the murine cerebral cortex. Cereb Cortex 2017, 27:5696-5714.
• Portela-Bens S, Merlo MA, Rodríguez ME, Cross I, Manchado M, Kosyakova N, LiehrT, Rebordinos L. Integrated gene mapping and synteny studies give insights into the evolution of a sex proto-chromosome in Solea senegalensis. Chromosoma 2017; 126:261-277.
• Saini AG, Padmanabh H, Sahu JK, Kurth I, Voigt M, Singhi P. Hereditary sensory polyneuropathy, pain insensitivity and global developmental delay due to novel mutation in PRDM12 gene. Indian J Pediatr. 2017, 84:332-333.
• Salameh AI, Hübner CA, Boron WF. Role of Cl- -HCO3- exchanger AE3 in intracellular pH homeostasis in cultured murine hippocampal neurons, and in crosstalk to adjacent astrocytes. J Physiol 2017;595:93-124.
• Santiago F, Lima S, Pinheiro T, Silvestre RT, Otero UB, Tabalipa MM, Kosyakova N, Ornellas MH, Liehr T, Alves G. Benzene poisoning, clinical and blood abnormalities in two Brazilian female gas station attendants: two case reports. BMC Res Notes. 2017,10:52.

• Seemann E, Sun M, Krueger S, Tröger J, Hou W, Haag N, Schüler S, Westermann M, Huebner CA, Romeike B, Kessels MM, Qualmann B. Deciphering caveolar functions by syndapinIII KO-mediatedimpairment of caveolar invagination. Elife. 2017 Dec 5;6. pii: e29854.

• Sheth H, Tewari S, Shah K, Liehr T, Trivedi J, Pandya M, Sheth JJ, Sheth F. Prenatal detection of cryptic genomic rearrangement: role of detailed family history, pedigree analysis and advanced genomic technologies. Int J Preg Child Birth 2017; 3:00071.
• Sinning A, Radionov N, Trepiccione F, López-Cayuqueo KI, Jayat M, Baron S, Cornière N, Alexander RT, Hadchouel J, Eladari D, Hübner CA, Chambrey R. Double Knockout of the Na+-Driven Cl-/HCO3-exchanger and Na+/Cl- cotransporter induces hypokalemia and volume depletion. J Am Soc Nephrol 2017;28:130-139.

• Symmank J, Zimmer G. Regulation of neuronal survival by DNA methyltransferases. Neural Regen Res. 2017;12:1768-1775.

• Teichert M, Liebmann L, Hübner CA, Bolz J. Homeostatic plasticity and synaptic scaling in the adult mouse auditory cortex. Sci Rep. 2017; 7:17423.
• Tewari S, Lubna N, Shah R, Al-Rikabi ABH, Shah K, Sheth J, Sheth F. Molecular characterization and evaluation of complex rearrangements in a case of ring chromosome 15. Mol Cytogenet 2017; 10:38.
• Thooptianrat T, Chaveerach A, Sudmoon R, Tanee T, Liehr T, Babayan N. Screening of phytochemicals and toxicity of medicinal plants, Dillenia species, reveals potential natural product resources. J Food Biochem. 2017;e12363.
• Tkach IR, Huleyuk NL, Zastavna DV, Weise A, Liehr T, E Ciszkowicz, M Tyrka. Chromosomal aberrations in spontaneously aborted products of conception from Ukraine. Biopolymers Cell 2017; 33:424-433.
• Trepiccione F, Prosperi F, de la Motte LR, Hübner CA, Chambrey R, Eladari D, Capasso G. New findings on the pathogenesis of distal renal tubular acidosis. Kidney Dis (Basel). 2017;3:98-105.
• Ullah MI, Ahmad A, Zarkovic M, Shah SS, Nasir A, Mahmood S, Ahmad W, Hübner CA, Hassan MJ. Novel duplication mutation of the DYSF gene in a Pakistani family with Miyoshi Myopathy. Saudi Med J. 2017; 38:1190-1195.
• Valkova C, Liebmann L, Krämer A, Hübner CA, Kaether C. The sorting receptor Rer1 controls Purkinje cell function via voltage gated sodium channels. Sci Rep 2017;7:41248.
• Volleth M, Truong Son N, Wu Y, Li Y, Yu W, Lin L-K, Arai S, Trifonov V, Liehr T, Harada M. Comparative chromosomal studies in Rhinolophus formosae and R. luctus from China and Vietnam: elevation of R. l. lanosus to species rank. Acta Chiropt 2017, 19: 41-50.
• Wafa A, As’sad M, Liehr T, Aljapawe A, Al-Achkar W. Childhood pre-B-acute lymphoblastic leukemia with translocation t(1;19)(q21.1;p13.3) and two additional chromosomal aberrations involving chromosomes 1, 6 and 13. J Med Case Rep 2017, 11:94.
• Wafa A, Almedani S, Liehr T, Ziegler M, Aljapawe A, Al Achkar W. Complex karyotype involving six chromosomes, with one dicentric and three yet unreported acquired chromosomal aberrations in a case of splenic marginal zone lymphoma. Gene Rep 2017; 8:79-83
• Wafa A, ALmedani S, Liehr T, Moassass F, Al-Achkar W. Successful management of three pregnancies under Imatinib treatment in a chronic myeloid leukemia patient: a case report and review of the literature. J Genetics Genomes 2017, 1: 111.
• Yano CF, Bertollo LAC, Ezaz T, Trifonov V, Sember A, Liehr T, Cioffi MB. Highly conserved Z and molecularly diverged W chromosomes in the fish genus Triportheus (Characiformes, Triportheidae). Heredity 2017; 118:276-283.
• Yano CF, Bertollo LA, Rebordinos L, Merlo MA, Liehr T, Portela-Bens S, Cioffi MB. Evolutionary dynamics of rDNAs and U2 small nuclear DNAs in Triportheus (Characiformes, Triportheidae): High variability and particular syntenic organization. Zebrafish 2017, 14:146-154

Bücher/ Books

FISH-Book
Year     Chapterdownloads

2018                 20020
2017                 36152
2016                10230

• Alhourani E, Othman MAK, Melo JB, Carreira IM, Grygalewicz B, Vujić D, Zecević Z, Joksić G, Glaser A, Pohle B, Schlie C, Hauke S, Liehr T. BIRC3 alterations in chronic and B-cell acute lymphocytic leukemia patients. Oncol Lett 2016, 11:3240-3246
• Alhourani E, Aroutiounian R, Harutyunyan T, Glaser A, Schlie C, Pohle B, Liehr T. Interphase molecular cytogenetic detection rates of chronic lymphocytic leukemia specific aberrations are higher in cultivated cells than in blood or bone marrow smears. J Histochem Cytochem 2016, 64:495-501
• Amasdl S, Natiq A, Sbiti A, Zerkaoui M, Lyahyai J, Liehr T, Amzazi S, Sefiani A. 20p12.3 deletion is rare cause of syndromic cleft palate: case report and review of literature. BMC Research Notes 2016, 9:5
• Amasdl S, Natiq A, Elalaoui SC, Sbiti A, Liehr T, Sefiani A. Insulin-like growth factor type 1 deficiency in a Moroccan patient with de novo inverted duplication 9p24p12 and developmental delay: a case report. J Med Case Rep 2016 10:122
• Asim M, Massie CE, Orafidiya F, Pértega-Gomes N, Warren AY, Esmaeili M, Selth LA, Zecchini HI, Luko K, Qureshi A, Baridi A, Menon S, Madhu B, Escriu C, Lyons S, Vowler SL, Zecchini VR, Shaw G, Hessenkemper W, Russell R, Mohammed H, Stefanos N, Lynch AG, Grigorenko E, D'Santos C, Taylor C, Lamb A, Sriranjan R, Yang J, Stark R, Dehm SM, Rennie PS, Carroll JS, Griffiths JR, Tavaré S, Mills IG, McEwan IJ, Baniahmad A, Tilley WD, Neal DE. Choline kinase alpha as an androgen receptor chaperone and prostate cancer therapeutic target. J Natl Cancer Inst. 2016, 1085:djv371.
• Baniahmad A. Inhibition of the androgen receptor by antiandrogens in spinobulbar muscle atrophy. J Mol Neurosci 2016, 58:343-347.
• Barth E, Hübler R, Baniahmad A, Marz M. The evolution of COP9 signalosome in unicellular and multicellular organisms. Genome Biol Evol. 2016, 8:1279-1289
• Blüher S, Kromeyer-Hauschild K, Graf C, Grünewald-Funk D, Widhalm K, Korsten-Reck U, Markert J, Güssfeld C, Müller MJ, Moss A, Wabitsch M, Wiegand S. [Current guidelines to prevent obesity in childhood and adolescence]. Klin Padiatr 2016, 228:1-10
• Bugarski Stanojević V, Stamenković G, Blagojević J, Liehr T, Kosyakova N, Rajičić M, Vujošević M. Exploring supernumeraries - a new marker for screening of B-chromosomes presence in the yellow necked mouse Apodemus flavicollis. PLoS One 2016, 11:e0160946.
• Chiabrando D, Castori M, di Rocco M, Ungelenk M, Gießelmann S, Di Capua M, Madeo A, Grammatico P, Bartsch S, Hübner CA, Altruda F, Silengo L, Tolosano E, Kurth I. Mutations in the heme exporter FLVCR1 cause sensory neurodegeneration with loss of pain perception. PLoS Genet 2016, 12:e1006461
• Coci EG, Koehler U, Liehr T, Stelzner A, Fink C, Langen H, Riedel J. CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NIFA genes. Mol Cytogenet 2016, 9:10.
• Colditz J, Rupf B, Maiwald C, Baniahmad A. Androgens induce a distinct response of epithelial-mesenchymal transition factors in human prostate cancer cells. Mol Cell Biochem. 2016;421:139-147.
• Esmaeili M, Jennek S, Ludwig S, Klitzsch A, Kraft F, Melle C, Baniahmad A. The tumor suppressor ING1b is a novel corepressor for the androgen receptor and induces cellular senescence in prostate cancer cells. J Mol Cell Biol 2016; 8:207-220.
• Esmaeili M, Pungsrinont T, Schaefer A, Baniahmad A. A novel crosstalk between the tumor suppressors ING1 and ING2 regulates androgen receptor signaling. J Mol Med (Berl). 2016; 94:1167-1179.
• Filipović J, Joksić G, Vujić D, Joksić I, Mrasek K, Weise A, Liehr T. First molecular-cytogenetic characterization of Fanconi anemia fragile sites in primary lymphocytes of FA-D2 patients in different stages of the disease. Mol Cytogenet 2016, 9:70.
• Fischer M, Spies-Weisshart B, Schrenk K, Gruhn B, Wittig S, Glaser A, Hochhaus A, Scholl S, Schnetzke U. Polymorphisms of dectin-1 and TLR2 predispose to invasive fungal disease in patients with acute myeloid leukemia. PLoS One 2016, 11:e0150632.
• Foertsch F, Szambowska A, Weise A, Zielinski A, Schlott B, Kraft F, Mrasek K, Borgmann K, Pospiech H, Grosse F, Melle C. S100A11 plays a role in homologous recombination and genome maintenance by influencing the persistence of RAD51 in DNA repair foci. Cell Cycle 2016;15:2766-2779.
• Franke M, Ibrahim DM, Andrey G, Schwarzer W, Heinrich V, Schöpflin R, Kraft K, Kempfer R, Jerković I, Chan WL, Spielmann M, Timmermann B, Wittler L, Kurth I, Cambiaso P, Zuffardi O, Houge G, Lambie L, Brancati F, Pombo A, Vingron M, Spitz F, Mundlos S. Formation of new chromatin domains determines pathogenicity of genomic duplications. Nature 2016, 538:265-269.
• Fryssira H, Tsoutsou E, Psoni S, Amenta S, Liehr T, Anastasakis E, Skentou Ch, Ntouflia A, Papoulidis I, Manolakos E, Chaliasos N. Partial monosomy14q involving FOXG1 and NOVA1 in an infant with microcephaly, seizures and severe developmental delay. Mol Cytogenet. 2016;9:55.
• Grigaravicius P, Kaminska E, Hübner CA, McKinnon PJ, von Deimling A, Frappart PO. Rint1 inactivation triggers genomic instability, ER stress and autophagy inhibition in the brain. Cell Death Differ 2016;23:454-468.
• Günther S, Elert-Dobkowska E, Soehn AS, Hinreiner S, Yoon G, Heller R, Hellenbroich Y, Hübner CA, Ray PN, Hehr U, Bauer P, Sulek A, Beetz C. High frequency of pathogenic rearrangements in SPG11 and extensive contribution of mutational hotspots and founder alleles. Hum Mutat 2016 37:703-709.
• Hentschel J, Tatun D, Parkhomchuk D, Kurth I, Schimmel B, Heinrich-Weltzien R, Bertzbach S, Peters H, Beetz C. Identification of the first multi-exonic WDR72 deletion in isolated amelogenesis imperfecta, and generation of a WDR72-specific copy number screening tool. Gene 2016;590:1-4.
• Hovhannisyan G, Aroutiounian R, Babayan N, Harutyunyan T, Liehr T. Comparative analysis of individual chromosome involvement in micronuclei induced by mitomycin C and bleomycin in human leukocytes. Mol Cytogenet 2016, 9:49
• Hunstig F, Schulz S, Nieten I, Froster U, Boltze C, Schliemann S, Hochhaus A, La Rosée P. A case of Brooke-Spiegler syndrome with a novel mutation in the CYLD gene in a patient with aggressive non-Hodgkin's lymphoma. J Cancer Res Clin Oncol 2016, 142:845-848
• Jaenisch N, Liebmann L, Guenther M, Hübner CA, Frahm C, Witte OW. Reduced tonic inhibition after stroke promotes motor performance and epileptic seizures. Sci Rep 2016, 6:26173.
• Joshi RS, Garg P, Zaitlen N, Lappalainen T, Watson CT, Azam N, Ho D, Li X, Antonarakis SE, Brunner HG, Buiting K, Cheung SW, Coffee B, Eggermann T, Francis D, Geraedts JP, Gimelli G, Jacobson SG, Le Caignec C, de Leeuw N, Liehr T, Mackay DJ, Montgomery SB, Pagnamenta AT, Papenhausen P, Robinson DO, Ruivenkamp C, Schwartz C, Steiner B, Stevenson DA, Surti U, Wassink T, Sharp AJ. DNA methylation profiling of uniparental disomy subjects provides a map of parental epigenetic bias in the human genome. Am J Hum Genet 2016; 99:555-566.
• Kadioglu O, Cao J, Kosyakova N, Mrasek K, Liehr T, Efferth T. Genomic and transcriptomic profiling of resistant CEM/ADR-5000 and sensitive CCRF-CEM leukaemia cells for unraveling the full complexity of multifactorial multidrug resistance. Sci Rep 2016, 6:36754.
• Kurth I, Baumgartner M, Schabhüttl M, Tomni C, Windhager R, Strom TM, Wieland T, Gremel K, Auer-Grumbach M. Whole exome sequencing in congenital pain insensitivity identifies a novel causative intronic NTRK1-mutation due to uniparental disomy. Am J Med Genet B Neuropsychiatr Genet 2016, 171:875-878.
• Lang J, Birkenbeil S, Bock S, Heinrich-Weltzien R, Kromeyer-Hauschild K. Dental enamel defects in German medieval and early-modern-age populations. Anthropol Anz 2016, 73:343-354.
• Liehr T. Cytogenetically visible copy number variations (CG-CNVs) in banding and molecular cytogenetics of human; about heteromorphisms and euchromatic variants. Mol Cytogenet 2016, 9:5.
• Liehr T. Benign and pathological gain or loss of genetic material - about microscopic and submicroscopic copy number variations (CNVs) in human genetics. Tsitologiya 2016, 58:476-477
• Liehr T. BIRC3 as a yet underestimated prognostic marker of malignancies? Transl Cancer Res 2016. doi: 10.21037/tcr.2016.09.29.
• Liehr T, Heng H, Yurov Y, Meloni-Ehrig A, Iourov I. Reviewer acknowledgement 2016. Mol Cytogenet 2015, 9:24.
• Malinverni AC, Colovati ME, Perez AB, Caneloi TP, Oliveira Jr HR, Kosyakova N, Liehr T, Hamid AB, Melaragnom MI. Unusual duplication in the pericentric region of chromosome 9 in a patient with phenotypic alterations. Cytogenet Genome Res 2016, 150:100-105.
• Maßberg D, Jovancevic N, Offermann A, Simon A, Baniahmad A, Perner S, Pungsrinont T, Luko K, Philippou S, Ubrig B, Heiland M, Weber L, Altmüller J, Becker C, Gisselmann G, Gelis L, Hatt H. The activation of OR51E1 causes growth suppression of human prostate cancer cells. Oncotarget. 2016, 7:48231-48249.
• Ornellas MH, Silva MdF, Solza C, Goncalves SBSdL, Silva de Almeida L, Ayres-Silva JdP,  Seixa TL, Bastos EF, Liehr T, Alves G. Myelodysplastic syndrome without ring sideroblasts and with Janus kinase 2 gene mutation: An unusual case report. Mol Clin Oncol 2016, 5: 227-230.
• Othman MAK, Grygalewicz B, Pienkowska-Grela B, Rygier J, Ejduk A, Rincic M, Melo JB, Carreira IM, Meyer B, Liehr T. A new IGH@ gene rearrangement associated with CDKN2A/B deletion in a young adult B-cell acute lymphoblastic leukemia (B-ALL). Oncol Lett 2016, 11:2117-2122.
• Pungsrinont T, Baniahmad A. Cellular Senescence by the Epigenetic Regulators Inhibitor of Growth.  Aging Sci 2016, 4:1.
• Rincic M, Rados M, Krsnik Z, Gotovac K, Borovecki F, Liehr T, Brecevic L. Complex intrachromosomal rearrangement in 1q leading to 1q32.2 microdeletion: a potential role of SRGAP2 in the gyrification of cerebral cortex. Mol Cytogenet 2016, 9:19.
• Rinčić M, Iourov IY, Liehr T. Thoughts about SLC16A2, TSIX and XIST gene like sites in the human genome and a potential role in cellular chromosome counting. Mol Cytogenet 2016, 9:56.
• Sangpakdee W, Tanomtong A, Fan X, Pinthong K, Weise A, Liehr T. Application of multicolor banding combined with heterochromatic and locus-specific probes identify evolutionary conserved breakpoints in Hylobates pileatus. Mol Cytogenet 2016, 9:17.
• Sangpakdee W, Phimphan S, Liehr T, Fan X, Pinthong K, Patawang I, Tanomtong A. Characterization of chromosomal rearrangements in pileated gibbon (Hylobates pileatus) using multiplex-FISH technique. The Nucleus 2016, 59:131-135.
• Schulz A, Wagner F, Ungelenk M, Kurth I, Redecker C. Stroke-like onset of brain stem degeneration presents with unique MRI sign and heterozygous NMNAT2 variant: a case report. Transl Neurodegener 2016;5:23.
• Sheth FJ, Naznin L, Liehr T, Sheth JJ. FISH – The best technique in characterization of prenatally detected small supernumerary marker chromosomes (sSMC). Int J Pregn & Chi Birth 2016, 1:00005.
• Van Rheenen W, Shatunov A, Dekker AM, McLaughlin RL, Diekstra FP, Pulit SL, van der Spek RA, Võsa U, de Jong S, Robinson MR, Yang J, Fogh I, van Doormaal PT, Tazelaar GH, Koppers M, Blokhuis AM, Sproviero W, Jones AR, Kenna KP, van Eijk KR, Harschnitz O, Schellevis RD, Brands WJ, Medic J, Menelaou A, Vajda A, Ticozzi N, Lin K, Rogelj B, Vrabec K, Ravnik-Glavač M, Koritnik B, Zidar J, Leonardis L, Grošelj LD, Millecamps S, Salachas F, Meininger V, de Carvalho M, Pinto S, Mora JS, Rojas-García R, Polak M, Chandran S, Colville S, Swingler R, Morrison KE, Shaw PJ, Hardy J, Orrell RW, Pittman A, Sidle K, Fratta P, Malaspina A, Topp S, Petri S, Abdulla S, Drepper C, Sendtner M, Meyer T, Ophoff RA, Staats KA, Wiedau-Pazos M, Lomen-Hoerth C, Van Deerlin VM, Trojanowski JQ, Elman L, McCluskey L, Basak AN, Tunca C, Hamzeiy H, Parman Y, Meitinger T, Lichtner P, Radivojkov-Blagojevic M, Andres CR, Maurel C, Bensimon G, Landwehrmeyer B, Brice A, Payan CA, Saker-Delye S, Dürr A, Wood NW, Tittmann L, Lieb W, Franke A, Rietschel M, Cichon S, Nöthen MM, Amouyel P, Tzourio C, Dartigues JF, Uitterlinden AG, Rivadeneira F, Estrada K, Hofman A, Curtis C, Blauw HM, van der Kooi AJ, de Visser M, Goris A, Weber M, Shaw CE, Smith BN, Pansarasa O, Cereda C, Del Bo R, Comi GP, D'Alfonso S, Bertolin C, Sorarù G, Mazzini L, Pensato V, Gellera C, Tiloca C, Ratti A, Calvo A, Moglia C, Brunetti M, Arcuti S, Capozzo R, Zecca C, Lunetta C, Penco S, Riva N, Padovani A, Filosto M, Muller B, Stuit RJ; PARALS Registry; SLALOM Group; SLAP Registry; FALS Sequencing Consortium; SLAGEN Consortium; NNIPPS Study Group, Blair I, Zhang K, McCann EP, Fifita JA, Nicholson GA, Rowe DB, Pamphlett R, Kiernan MC, Grosskreutz J, Witte OW, Ringer T, Prell T, Stubendorff B, Kurth I, Hübner CA, Leigh PN, Casale F, Chio A, Beghi E, Pupillo E, Tortelli R, Logroscino G, Powell J, Ludolph AC, Weishaupt JH, Robberecht W, Van Damme P, Franke L, Pers TH, Brown RH, Glass JD, Landers JE, Hardiman O, Andersen PM, Corcia P, Vourc'h P, Silani V, Wray NR, Visscher PM, de Bakker PI, van Es MA, Pasterkamp RJ, Lewis CM, Breen G, Al-Chalabi A, van den Berg LH, Veldink JH. Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis. Nat Genet 2016; 48:1043-1048.
• Wafa A, Assad M, Liehr T, Aljapawe A, Al Achkar W. A new complex karyotype in a unique de novo myelodysplastic syndrome case involving ten chromosomes and monoallelic loss of TP53. Gene Rep 2016, 4:208-212.
• Wafa A, Moassass F, Liehr T, Al-Ablog A, Al-Achkar W. Acute promyelocytic leukemia with the translocation t(15;17)(q22;q21) associated with t(1;2)(q42~43;q11.2~12): a case report. J Med Case Rep 2016, 10:203.
• Wafa A, Moassass F, Liehr T, Aljapawe A, Al Achkar W. Partial trisomy 1q21-qter and partial monosomy 7q21-qter due to a derivative chromosome 7 in myelodysplastic syndrome associated with squamous cell carcinoma: Case report. Case Rep Clin Med 2016, 5:518-527.
• Wafa A, Moassass F, Liehr  T, Bhatt S, Aljapawe A, Al Achkar W. A high complex karyotype involving eleven chromosomes including three novel chromosomal aberrations and monoallelic loss of TP53 in case of follicular lymphoma transformed into B-cell lymphoblastic leukemia. Mol Cytogenet 2016, 9:91.
• Wannenmacher B, Mitter D, Kießling F, Liehr T, Weise A, Siekmeyer M, Kiess W. A 33-year-old male patient with paternal derived duplication of 14q11.2-14q22.1~22.3: clinical course, phenotypic and genotypic findings. J Pediatr Endocrinol Metab 2016, 29:611-616.
• Weise A, Bhatt S, Piaszinski K, Kosyakova N, Fan X, Altendorf-Hofmann A, Tanomtong A, Chaveerach A, Bello de Cioffi M, de Oliveira E, Walther J-U, Liehr T, Chaudhuri JP. Chromosomes in a genome-wise order: evidence for metaphase architecture. Mol Cytogenet 2016, 9:36.
• Yano CF, Bertollo LA, Liehr T, Troy WP, Cioffi MB. W chromosome dynamics in Triportheus species (Characiformes, Triportheidae) - an ongoing process narrated by repetitive sequences. J Hered 2016, 2016:342-348.
• Zlotina A, Kulikova T, Kosyakova N, Liehr T, Krasikova A. Microdissection of lampbrush chromosomes as an approach for generation of locus-specific FISH-probes and samples for high-throughput sequencing. BMC Genomics 2016, 17:126.

• Abo-Zeid MAM, Liehr T, Gamal-Eldeen AM, Zawrah M, Ali M, Othman MAK. Potential of rod, sphere and semi-cube shaped gold nanoparticles to induce cytotoxicity and genotoxicity in human blood lymphocytes in vitro. Eur J Nanomed 2015, 7: 63-75.
• Abo-Zeid MAM, Liehr T, Glei M, Gamal-Eldeen AM, Zawrah M, Ali M. Detection of cyto- and genotoxicity of rod-shaped gold nanoparticles in human blood lymphocytes using comet-FISH. Cytologia 2015, 80:173-181.
• Aguiar de Oliveira E, Bertollo LAC, Yano CF, Liehr T, de Bello Cioffi M. Comparative cytogenetics in the genus Hoplias (Characiformes, Erythrinidae) highlights contrasting karyotype evolution among congeneric species Mol Cytogenet 2015, 8:56.
• Al-Achkar W, Moassass F, Al-Ablog A, Liehr T, Fan X, Wafa A. A Syrian couple with chromosomal aberration and MTHFR polymorphism leads to recurrent pregnancy loss and partial trisomy of 5p12-15.3 in the offspring: Case report and review to the literature. Zhonghua Nan Ke Xue = Nat J Androl 2015; 21:219-224.
• Alhourani E, Rincic M, Melo JB, Carreira IM, Glaser A, Pohle B, Schlie C, Liehr T. Isochromosome 17q in chronic lymphocytic leukemia. Leuk Res Treatment 2015, 2015:489592
• Armanet N, Tosca L, Brisset S, Liehr T, Tachdjian G. Small supernumerary marker chromosomes in human infertility. Cytogenet Genome Res 2015, 146:100-108.
• Baranov VS, Ivaschenko TE, Liehr T, Yarmolinskaya MI. Systems genetics view of endometriosis – a common complex disorder. Eur J Obstet Gynecol Reprod Biol 2015 185:59-65.
• Brečević L, Rinčić M, Krsnik Ž, Sedmak G, Hamid AB, Kosyakova N, Galić I, Liehr T, Borovečki F. Association of new deletion/duplication region at chromosome 1p21 with intellectual disability, severe speech deficit and autism spectrum disorder-like behavior: an all-in approach to solving the DPYD enigma. Translat Neuroscience 2015, 6:59-86.
• Capela de Matos RR, De Figueiredo AF, Liehr T, Alhourani E, De Souza MT, Abdelhay, E Ribeiro RC, Silva MLM. A novel three-way variant t(8;13;21)(q22;q33;q22) in a child with acute myeloid leukemia FAB AML-M2: contribution of molecular approaches to reveal t(8;21) variants. Acta Hematol 2015;134:243-245.
• Chen YC, Auer-Grumbach M, Matsukawa S, Zitzelsberger M, Themistocleous AC, Strom TM, Samara C, Moore AW, Cho LT, Young GT, Weiss C, Schabhüttl M, Stucka R, Schmid AB, Parman Y, Graul-Neumann L, Heinritz W, Passarge E, Watson RM, Hertz JM, Moog U, Baumgartner M, Valente EM, Pereira D, Restrepo CM, Katona I, Dusl M, Stendel C, Wieland T, Stafford F, Reimann F, von Au K, Finke C, Willems PJ, Nahorski MS, Shaikh SS, Carvalho OP, Nicholas AK, Karbani G, McAleer MA, Cilio MR, McHugh JC, Murphy SM, Irvine AD, Jensen UB, Windhager R, Weis J, Bergmann C, Rautenstrauss B, Baets J, De Jonghe P, Reilly MM, Kropatsch R, Kurth I, Chrast R, Michiue T, Bennett DL, Woods CG, Senderek J. Transcriptional regulator PRDM12 is essential for human pain perception. Nat Genet 2015, 47:803-808.
• Chen YC, Auer-Grumbach M, Matsukawa S, Zitzelsberger M, Themistocleous AC, Strom TM, Samara C, Moore AW, Cho LT, Young GT, Weiss C, Schabhüttl M, Stucka R, Schmid AB, Parman Y, Graul-Neumann L, Heinritz W, Passarge E, Watson RM, Hertz JM, Moog U, Baumgartner M, Valente EM, Pereira D, Restrepo CM, Katona I, Dusl M, Stendel C, Wieland T, Stafford F, Reimann F, von Au K, Finke C, Willems PJ, Nahorski MS, Shaikh SS, Carvalho OP, Nicholas AK, Karbani G, McAleer MA, Cilio MR, McHugh JC, Murphy SM, Irvine AD, Jensen UB, Windhager R, Weis J, Bergmann C, Rautenstrauss B, Baets J, De Jonghe P, Reilly MM, Kropatsch R, Kurth I, Chrast R, Michiue T, Bennett DL, Woods CG, Senderek J. Corrigendum: Transcriptional regulator PRDM12 is essential for human pain perception. Nat Genet 2015, 47:962.
• Darouich AA, Liehr T, Weise A, Schlembach D, Schleußner E, Kiehntopf M, Schreyer I. Alpha-fetoprotein and its value for predicting pregnancy outcomes – a re-evaluation. J Prenat Med 2015;9:18-23.
• de Figueiredo AF, Capela de Matos RR, Othman MA, Liehr T, da Costa ES, Land MG, Ribeiro RC, Abdelhay E, Silva ML. Molecular cytogenetic studies characterizing a novel complex karyotype with an uncommon 5q22 deletion in childhood acute myeloid leukemia. Mol Cytogenet 2015, 8:62.
• Elert-Dobkowska E, Hennings JC, Hübner CA, Beetz C. Multiplex ligation-dependent probe amplification for identification of correctly targeted murine embryonic stem cell clones. Anal Biochem 2015, 474C:35-37.
• Fan X , Supiwong W, Weise A, Mrasek K, Kosyakova N, Tanomtong A, Pinthong K, Trifonov VA, de Bello Cioffi M, Grothmann P, Liehr T, de Oliveira EHC. Comprehensive characterization of evolutionary conserved breakpoints in four New World Monkey karyotypes compared to Chlorocebus aethiops and Homo sapiens. Helyion 1:e00042
• Gerstmann K, Zimmer G. Fine-tuning of cortical progenitor proliferation by thalamic afferents. Neural Regen Res 2015, 10:887-888.
• Gerstmann K, Pensold D, Symmank J, Khundadze M, Hübner CA, Bolz J, Zimmer G. Thalamic afferents influence cortical progenitors via ephrin A5-EphA4 interactions. Development 2015;142:140-150.
• Gomaa IE, Abdel Gaber SA, Bhatt S, Liehr T, Glei M, El-Tayeb TA, Abdel-Kader MH. In vitro cytotoxicity and genotoxicity studies of gold nanoparticles-mediated photo-thermal therapy versus 5-fluorouracil. J Nanopart Res 2015, 17:102.
• Gooma IE, Bhatt S, Liehr T, Glei M, El-Tayeb TA. Comparative study of Ag and Co / Ag nanoparticles mediated by photothermal therapy of cancer. Egypt J Zool 2015, 63: 99-117.
• Hamid AB, Fan X, Kosyakova N, Radhakrishnan G, Liehr T, Karamysheva T. New BAC probe set to narrow down chromosomal breakpoints in small and large derivative chromosomes, especially suited for mosaic conditions. Methods Mol Biol 2015, 1227:279-287.
• Harutyunyan T, Hovhannisyan G, Babayan N, Othman M, Liehr T, Aroutiounian R. Influence of aflatoxin B1 on copy number variants in human leukocytes in vitro. Mol Cytogenet 2015, 8:25.
• Hochstenbach R, Nowakowska B, Volleth M, Ummels A, Kutkowska-Kamierczak A, Obersztyn E, Ziemkiewicz K, Gerloff C, Schanze D, Zenker M, Muschke P, Schanze I, Poot M, Liehr T. Multiple small supernumerary marker chromosomes resulting from maternal meiosis I or II errors. Mol Syndromol 2015, 6:210-221.
• Hu Z, Qi H, Zhang R, Zhang K, Shi Z, Chang Y, Chen L, Esmaeili M, Baniahmad A, Hong W. Docosahexaenoic acid inhibits the growth of hormone-dependent prostate cancer cells by promoting the degradation of the androgen receptor. Mol Med Rep 2015, 12:3769-3774.
• Hübner CA, Schroeder BC, Ehmke H. Regulation of vascular tone and arterial blood pressure: role of chloride transport in vascular smooth muscle. Pflugers Arch. 2015, 467:605-614.
• Karamysheva T, Kosyakova N, Guediche N, Liehr. T Small supernumerary marker chromosomes and the nuclear architecture of sperm – a study in a fertile and an infertile brother. Syst Biol Reprod Med 2015, 61:32-36.
• Kehrer M, Liehr T, Benkert T, Singer S, Grasshoff U, Schaeferhoff K, Bonin M, Weichselbaum A, Tzschach A. Interstitial duplication of chromosome region 1q25.1q25.3: Report of a patient with mild cognitive deficits, tall stature and facial dysmorphisms. Am J Med Genet A 2015, 167:653-656.
• Khaminets A, Heinrich T, Mari M, Grumati P, Huebner AK, Akutsu M, Liebmann L, Stolz A, Nietzsche S, Koch N, Mauthe M, Katona I, Qualmann B, Weis J, Reggiori F, Kurth I, Hübner CA, Dikic I. Regulation of endoplasmic reticulum turnover by selective autophagy. Nature 2015, 522:354-358.
• Kirkpatrick G, Ren H, Liehr T, Chow V, Ma S. Meiotic and sperm aneuploidy studies in three carriers of Robertsonian translocations and small supernumerary marker chromosomes. Fertil Steril 2015, 103:1162–1169.e7.
• Kontodiou M, Daskalakis G, Vetro A, Paspaliaris V, Papaioannou G, Dagklis T, Tsakiridis I, Ziegler M, Liehr T, Thomaidis L, Papoulidis I, Manolakos E. Complex rearrangement involving three chromosomes, four breakpoints and a 2.7-Mb deletion in the 18q segment observed in a girl with mild learning difficulties. Cytogenet Genome Res 2015;147:118-123.
• Kurth I. [Sensory and autonomic neuropathies and pain-related channelopathies]. Schmerz 2015, 29:445-457.
• Jafari-Ghahfarokhi H, Moradi-Chaleshtori M, Liehr T, Hashemzadeh-Chaleshtori M, Teimori H, Ghasemi-Dehkordi P. Small supernumerary marker chromosomes and their correlation with specific syndromes. Adv Biomed Res 2015, 4:140.
• Jahic A, Khundadze M, Jaenisch N, Schüle R, Klimpe S, Klebe S, Frahm C, Kassubek J, Stevanin G, Schöls L, Brice A, Hübner CA, Beetz C. The spectrum of KIAA0196 variants, and characterization of a murine knockout: implications for the mutational mechanism in hereditary spastic paraplegia type SPG8. Orphanet J Rare Dis. 2015 Nov 16;10(1):147.
• Lange M, Kasper B, Bohring A, Rutsch F, Kluger G, Hoffjan S, Spranger S, Behnecke A, Ferbert A, Hahn A, Oehl-Jaschkowitz B, Graul-Neumann L, Diepold K, Schreyer I, Bernhard MK, Mueller F, Siebers-Renelt U, Beleza-Meireles A, Uyanik G, Janssens S, Boltshauser E, Winkler J, Schuierer G, Hehr U. 47 patients with FLNA associated periventricular nodular heterotopia. Orphanet J Rare Dis 2015;10:134.
• Ledig S, Preisler-Adams S, Morlot S, Liehr T, Wieacker P. Premature ovarian failure caused by a heterozygous missense mutation in POF1B and a reciprocal translocation 46,X,t(X;3)(q21.1;q21.3). Sex Dev 2015, 9:86-90.
• Leipold E, Hanson-Kahn A, Frick M, Gong P, Bernstein JA, Voigt M, Katona I, Oliver Goral R, Altmüller J, Nürnberg P, Weis J, Hübner CA, Heinemann SH, Kurth I. Cold-aggravated pain in humans caused by a hyperactive NaV1.9 channel mutant. Nat Commun 2015, 6:10049.
• Liehr T, Heng H, Yurov Y, Meloni-Ehrig A, Iourov I. Reviewer acknowledgement 2015. Mol Cytogenet 2015, 8:23.
• Liehr T, Othman MA, Rittscher K, Alhourani E. The current state of molecular cytogenetics in cancer diagnosis. Expert Rev Mol Diagn 2015, 15:517-526.
• Maass PG, Aydin A, Luft FC, Schächterle C, Weise A, Stricker S, Lindschau C, Vaegler M, Qadri F, Toka HR, Schulz H, Krawitz PM, Parkhomchuk D, Hecht J, Hollfinger I, Wefeld-Neuenfeld Y, Bartels-Klein E, Mühl A, Kann M, Schuster H, Chitayat D, Bialer MG, Wienker TF, Ott J, Rittscher K, Liehr T, Jordan J, Plessis G, Tank J, Mai K, Naraghi R, Hodge R, Hopp M, Hattenbach LO, Busjahn A, Rauch A, Vandeput F, Gong M, Rüschendorf F, Hübner N, Haller H, Mundlos S, Bilginturan N, Movsesian MA, Klussmann E, Toka O, Bähring S. PDE3A mutations cause autosomal-dominant hypertension with brachydactyly. Nat Genet 2015, 46:647-653.
• Manvelyan M, Simonyan I, Hovhannisyan G, Aroutiounian R, Hamid AB, Liehr T. A new case of a complex small supernumerary marker chromosome, a der(9)t(7;9)(p22;q22) due to a maternal balanced rearrangement. J Ped Genet 2015, 4:199-200.
• Maslova A, Zlotina A, Kosyakova N, Sidorova M, Krasikova A. Three-dimensional architecture of tandem repeats in chicken interphase nucleus. Chromosome Res. 2015, 23:625-639.
• Moysés-Oliveira , Guilherme RS, Dantas AG, Ueta R, Perez AB, Haidar M, Canonaco R, Meloni VA, Kosyakova N, Liehr T, Carvalheira GM, Melaragno MI. Genetic mechanisms leading to primary amenorrhea in balanced X-autosome translocations. Fertil Steril 2015, 103:1289-1296.
• Moysés-Oliveira M, Guilherme RS, Meloni VA, Di Battista A, de Mello CB, Bragagnolo S, Moretti-Ferreira D, Kosyakova N, Liehr T, Carvalheira GM, Melaragno MI. X-linked intellectual disability related genes disrupted by balanced X-autosome translocations. Am J Med Genet B Neuropsychiatr Genet 2015, 168:669-677.
• Mrasek K, Wilhelm K, Quintana LG, Theuss L, Liehr T, Leskovac A, Filipovic J, Joksic G, Joksic I, Weise A. BAC-probes applied for characterization of fragile sites (FS). Methods Mol Biol 2015, 1227:289-298.
• Ney Garcia DR, Liehr T, Emerenciano M, Meyer C, Marschalek R, Pombo-de-Oliveira Mdo S, Ribeiro RC, Poirot Land MG, Macedo Silva ML. Molecular studies reveal MLL-MLLT3 gene fusion displaced in a case of childhood acute lymphoblastic leukemia with complex karyotype. Cancer Genet 2015, 208:143-147.
• Othman MAK, Melo JB, Carreira IM, Rincic M, Alhourani E, Wilhelm K, Gruhn B, Glaser A, Liehr T. MLLT10 and IL3 rearrangement together with a complex four-way-translocation and trisomy 4 in a patient with early T-cell precursor acute lymphoblastic leukemia. Oncol Rep 2015, 33: 625-630.
• Othman MAK, Vujić D, Zecević , Đurišić M, Slavković B, Meyer B, Liehr T. A cryptic three-way translocation t(10;19;11)(p12.31;q13.31;q23.3) with a derivative Y-chromosome in an infant with acute myeloblastic leukemia (M5b). Gene 2015, 563:115-119.
• Othman MAK, Grygalewicz B, Pienkowska-Grela B, Rincic M, Rittscher K, Melo JB, Carreira IM, Meyer B, Marzena W, Liehr T. Novel cryptic rearrangements in adult B cell precursor acute lymphoblastic leukemia involving MLL gene. J Histochem Cytochem 2015, 63:384-390.
• Othman MAK, Melo JB, Carreira IM, Rincic M, Glaser A, Grygalewicz B, Gruhn B, Wilhelm K, Rittscher K, Meyer B, Silva MLM, de Jesus Marques Salles T, Liehr T. High rates of submicroscopic aberrations in karyotypically normal acute lymphoblastic leukemia. Mol Cytogenet 2015, 8:45.
• Perner S, Cronauer MV, Schrader AJ, Klocker H, Culig Z, Baniahmad A. Adaptive responses of androgen receptor signaling in castration-resistant prostate cancer. Oncotarget 2015, 6:35542-35555.
• Petroff D, Kromeyer-Hauschild K, Wiegand S, l'Allemand-Jander D, Binder G, Schwab KO, Stachow R, Kiess W, Hammer E, Sturm S, Holl RW, Blüher S. Introducing excess body weight in childhood and adolescence and comparison with body mass index and waist-to-height ratio. Int J Obes (Lond) 2015, 39:52-60.
• Rath M, Najm J, Sirb H, Kentouche K, Dufke A, Pauli S, Hackmann K, Liehr T, Hübner CA, Felbor U, Kompetenznetzwerk Hämorrhagische Diathesen Ost (KHDO). Large deletions play a minor but essential role in congenital coagulation factor VII and X deficiencies. Hämostaseologie 2015, 35:S36-42.
• Reichwald K, Petzold A, Koch P, Downie BR, Hartmann N, Pietsch S, Baumgart M, Chalopin D, Felder M, Bens M, Sahm A, Szafranski K, Taudien S, Groth M, Arisi I, Weise A, Bhatt SS, Sharma V, Kraus JM, Schmid F, Priebe S, Liehr T, Görlach M, Than ME, Hiller M, Kestler HA, Volff J-N, Schartl M, Cellerino A, Englert C, Platzer M. Insights into sex chromosome evolution and aging from the genome of a short-lived fish. Cell 2015, 163:1527-1538
• Romanenko SA, Perelman PL, Trifonov VA, Serdyukova NA, Li T, Fu B, O'Brien PC, Ng BL, Nie W, Liehr T, Stanyon R, Graphodatsky AS, Yang F. A First generation comparative chromosome map between guinea pig (Cavia porcellus) and humans. PLoS One 2015,10:e0127937
• Sahoo T, Wang J-C, Elnaggar MM, Sanchez-Lara P, Ross LP, Mahon LW, Hafezi K, Deming A, Hinman L, Bruno Y, Bartley JA, Liehr T, Anguiano A, Jones M. Concurrent interstitial triplication and segmental uniparental disomy: Providing evidence for microhomology-mediated break-induced replication model for complex genomic rearrangements in humans. Europ J Hum Genet 2015, 23:61-66.
• Schaefer N, Kluck CJ, Price KL, Meiselbach H, Vornberger N, Schwarzinger S, Hartmann S, Langlhofer G, Schulz S, Schlegel N, Brockmann K, Lynch B, Becker CM, Lummis SC, Villmann C. Disturbed neuronal ER-Golgi sorting of unassembled glycine receptors suggests altered subcellular processing is a cause of human hyperekplexia. J Neurosci. 2015 Jan 7;35(1):422-37.
• Schnetzke U, Spies-Weisshart B, Yomade O, Fischer M, Rachow T, Schrenk K, Glaser A, von Lilienfeld-Toal M, Hochhaus A, Scholl S. Polymorphisms of Toll-like receptors (TLR2 and TLR4) are associated with the risk of infectious complications in acute myeloid leukemia. Genes Immun 2015, 16:83-88.
• Scholten M, Vilser C, Weise A, Baniahmad A. Atypical polycystic ovary syndrome - a genetic analysis. Exp Clin Endocrinol Diabetes 2015, 123:55-60.
• Sheth F, Rahman M, Liehr T, Desai M, Patel B, Modi C, Trivedi S, Sheth J. Prenatal screening of cytogenetic anomalies – a Western Indian experience. BMC Preg Childbirth 2015, 15:90.
• Sheth F, Liehr T, Shah K, Sheth J. Prader-Willi syndrome - type 1 deletion, a consequence of an unbalanced translocation of chromosomes 13 and 15, easily to be mixed up with a Robertsonian translocation. Mol Cytogenetics 2015, 8:52.
• Sinning A, Liebmann L, Hübner CA. Disruption of Slc4a10 augments neuronal excitability and modulates synaptic short-term plasticity. Front Cell Neurosci 2015, 9:223.
• Tzschach A, Grasshoff U, Beck-Woedl S, Dufke C, Bauer C, Kehrer M, Evers C, Moog U, Oehl-Jaschkowitz B, Di Donato N, Maiwald R, Jung C, Kuechler A, Schulz S, Meinecke P, Spranger S, Kohlhase J, Seidel J, Reif S, Rieger M, Riess A, Sturm M, Bickmann J, Schroeder C, Dufke A, Riess O, Bauer P. Next-generation sequencing in X-linked intellectual disability. Eur J Hum Genet. 2015, 23:1513-1518.
• Tkach IR, Sosnina KO, Huleyuk NL, Terpylyak OI, Zastavna DV, Weise A, Kosyakova N, Liehr T. Contribution of chromosomal abnormalities and genes of the major histocompatibility complex to early pregnancy losses. Biopolymers and Cell 2015, 31:38-45.
• Varga RE, Khundadze M, Damme M, Nietzsche S, Hoffmann B, Stauber T, Koch N, Hennings JC, Franzka P, Huebner AK, Kessels MM, Biskup C, Jentsch TJ, Qualmann B, Braulke T, Kurth I, Beetz C, Hübner CA. In vivo evidence for lysosome depletion and impaired autophagic clearance in hereditary spastic paraplegia type SPG11. PLoS Genet 2015, 11:e1005454.
• Wafa A, Asa'ad M, Ikhtiar A, Liehr T, Al-Achkar W. Deletion 9p23 to 9p11.1 as sole additional abnormality in a Philadelphia positive chronic myeloid leukemia in blast crisis: a rare event. Mol Cytogenet 2015, 8:59.
• Wafa A, Almedani A, Liehr T, Al-Achkar W. Masked inv dup(22)(q11.23), tetrasomy 8 and trisomy 19 in a blast crisis-chronic myeloid leukemia after interrupted Imatinib-treatment. Mol Cytogenet 2015, 8:98.
• Weise A, Othman MA, Bhatt S, Löhmer S, Liehr T. Application of BAC-probes to visualize copy number variants (CNVs). Methods Mol Biol 2015, 1227:299-307.
• Weise A, Kosyakova N, Voigt M, Aust N, Mrasek K, Löhmer S, Rubtsov N, Karamysheva T, Trifonov V, Hardekopf D, Jancuková , Pekova S, Wilhelm K, Liehr T, Fan X. Comprehensive analyses of white handed gibbon chromosomes enables access to 92 evolutionary conserved breakpoints compared to the human genome. Cytogenet Genome Res 2015,145:42-49.
• Winkler S, Hempel M, Brückner S, Mallek F, Weise A, Liehr T, Tautenhahn HM, Bartels M, Christ B. Mouse white adipose tissue-derived mesenchymal stem cells gain pericentral and periportal hepatocyte features after differentiation in vitro, which are preserved in vivo after hepatic transplantation. Acta Physiol 2015, 215:89-104
• Woods CG, Babiker MO, Horrocks I, Tolmie J, Kurth I. The phenotype of congenital insensitivity to pain due to the NaV1.9 variant p.L811P. Eur J Hum Genet 2015, 23:561-563.
• Woods CG, Babiker MO, Horrocks I, Tolmie J, Kurth I. The phenotype of congenital insensitivity to pain due to the NaV1.9 variant p.L811P. Eur J Hum Genet 2015, 23:1434.
• Zonouzi M, Scafidi J, Li P, McEllin B, Edwards J, Dupree JL, Harvey L, Sun D, Hübner CA, Cull-Candy SG, Farrant M, Gallo V. GABAergic regulation of cerebellar NG2 cell development is altered in perinatal white matter injury. Nat Neurosci 2015, 18:674-682.

• Al Achkar W, Aljapawe A, Liehr T, Wafa A. De novo acute myeloid leukemia subtype-M4 with initial trisomy 8 and later acquired t(3;12)(q26;p12) leading to ETV6/MDS1/EVI1 fusion transcript expression: A case report. Onc Lett 2014, 7:787-790.
• Al-Achkar W, Wafa A, Othman MAK, Moassass F, Aljapawe A, Liehr T. An adult B-cell precursor acute lymphoblastic leukemia with multiple secondary cytogenetic aberrations. Mol Cytogenet 2014, 7:60.
• Al-Achkar W, Moassass F, Ikhtiar A, TLiehr T, Othman MAK, Wafa A. Hyperdiploidy associated with T315I mutation in BCR-ABL kinase domain in an accelerated phase-chronic myeloid leukemia case. Mol Cytogenet 2014, 7:89.
• Alhourani E, Rincic M, Othman MAK, Pohle B, Schlie C, Glaser A, Liehr T. Comprehensive chronic lymphocytic leukemia diagnostics by combined multiplex ligation dependent probe amplification (MLPA) and interphase fluorescence in situ hybridization (iFISH). Mol Cytogenet 2014, 7:79.
• Asiedu MN, Mejia GL, Hübner CA, Kaila K, Price TJ. Inhibition of carbonic anhydrase augments GABAA receptor-mediated analgesia via a spinal mechanism of action. J Pain 2014;15:395-406.
• Barvencik F, Kurth I, Koehne T, Stauber T, Zustin J, Tsiakas K, Ludwig CF, Beil FT, Pestka JM, Hahn M, Santer R, Supanchart C, Kornak U, Fattore AD, Jentsch TJ, Teti A, Schulz A, Schinke T, Amling M. CLCN7 and TCIRG1 mutations differentially affect bone matrix mineralization in osteopetrotic individuals. J Bone Miner Res 2014, 29:982-991.
• Bhatt SS, Manvelyan M, Moradkhani K, Hunstig F, Mrasek K, Puechberty J, Lefort G, Sarda P, Weise A, Liehr T, Pellestor F. Inverted segment size and the presence of recombination hot spot clusters matter in sperm segregation analysis. Cytogenet Genome Res 2014,142:145-149.
• Bispo AV, Burégio-Frota P, Oliveira Dos Santos L, Leal GF, Duarte AR, Araújo J, Cavalcante da Silva V, Muniz MT, Liehr T, Santos N. Y-chromosome in Turner syndrome: detection of hidden mosaicism and the report of a rare X;Y translocation case. Reprod Fert Develop 2014, 26:1176-1182.
• de Souza DC, de Figueiredo AF, Mkrtchyan H, Othman MA, Liehr T, Dobbin J, Silva ML, Abdelhay E, Fernandez Tde S. A yet unreported der(11)t(6;11)(p21;q21) included in a complex karyotype of a refractory anemia with ring sideroblasts and poor prognosis. Blood Cells Mol Dis 2014, 53:91-93.
• de Souza M, Hassan R, Liehr T, Marques-Salles T, Boulhosa AM, Abdelhay E, Ribeiro R, Silva MLM. Conventional and molecular cytogenetic characterization of Burkitt lymphoma with bone marrow involvement in Brazilian children and adolescents. Ped Blood Cancer 2014, 61:1422-1426.
• Falk J, Rohde M, Bekhite MM, Neugebauer S, Hemmerich P, Kiehntopf M, Deufel T, Hübner CA, Beetz C. Functional utation analysis provides evidence for a role of REEP1 in lipid droplet biology. Hum Mutat 2014, 35:497-504.
• Fan X, Sangpakdee W, Tanomtong A, Chaveerach A, Pinthong K, Pornnarong S, Supiwong W, Trifonov VA, Hovhannisyan GG, Aroutouinian RM, Liehr T, Weise A. Molecular cytogenetic analysis of Thai southern pig-tailed macaque (Macaca nemestrina) by multicolor banding. Proceedings of Yerevan State University 2014, 2014:46-50.
• Fan X, Sangpakdee W, Tanomtong A, Chaveerach A, Pinthong K, Pornnarong S, Supiwong W, Trifonov V, Hovhannisyan G, Loth K, Hensel C, Liehr T, Weise A. Comprehensive molecular cytogenetic analysis of Barbary macaque (Macaca sylvanus). Biol J Arm 2014, 66:98-102.
• Fan X, Tanomtong A, Chaveerach A, Pinthong K, Pornnarong S, Supiwong W, Liehr T, Weise A. High resolution karyotype of Thai crab-eating macaque (Macaca fascicularis). Genetika 2014, 46:877-882.
• Fortugno P, Josselin E, Tsiakas K, Agolini E, Cestra G, Teson M, Santer R, Castiglia D, Novelli G, Dallapiccola B, Kurth I, Lopez M, Zambruno G, Brancati F. Nectin-4 mutations causing ectodermal dysplasia with syndactyly perturb the rac1 pathway and the kinetics of adherens junction formation. J Invest Dermatol 2014,134:2146-2153.
• Heinze C, Seniuk A, Sokolov MV, Huebner AK, Klementowicz AE, Szijártó IA, Schleifenbaum J, Vitzthum H, Gollasch M, Ehmke H, Schroeder BC, Hübner CA. Disruption of vascular Ca2+-activated chloride currents lowers blood pressure. J Clin Invest. 2014, 124:675-686.
• Hessenkemper W, Roediger J, Bartsch S, Houtsmuller AB, van Royen ME, Petersen I, Grimm MO, Baniahmad A. A natural androgen receptor antagonist induces cellular senescence in prostate cancer cells. Mol Endocrinol 2014, 28:1831-1840.
• Hübner CA. The KCl-cotransporter KCC2 linked to epilepsy. EMBO Rep 2014; 15:732-733.
• Hübner CA, Kurth I. Membrane-shaping disorders: a common pathway in axon degeneration. Brain 2014, 137:3109-3121.
• Hussein SS, Kreskowski K, Ziegler M, Klein E, Hamid AB, Kosyakova N, Volleth M, Liehr T, Fan X, Piaszinski K. Mitotic stability of small supernumerary marker chromosomes depends on their shape and telomeres - a long term in vitro study. Gene 2014, 552:246-248
• Iourov I, Yurov Y, Heng H, Liehr T. In memoriam of Anna D Polityko (17.12.1959 — 20.04.2013). Mol Cytogenet 2014, 7:2.
• Iourov IY, Vorsanova SG, Liehr T, Yurov YB. Mosaike im Gehirn des Menschen. Medgen 2014, 26:242-345.
• Kampik NB, Gehring N, Schnitzbauer U, Hennings JC, Hübner CA, Wagner CA. The Murine Cl/HCO3(-) exchanger Ae3 (Slc4a3) is not required for acid-base balance but is involved in magnesium handling by the kidney. Cell Physiol Biochem 2014, 34:1566-1577.
• Kornak U, Mademan I, Schinke M, Voigt M, Krawitz P, Hecht J, Barvencik F, Schinke T, Gießelmann S, Beil FT, Pou-Serradell A, Vílchez JJ, Beetz C, Deconinck T, Timmerman V, Kaether C, De Jonghe P, Hübner CA, Gal A, Amling M, Mundlos S, Baets J, Kurth I. Sensory neuropathy with bone destruction due to a mutation in the membrane-shaping atlastin GTPase 3. Brain 2014;137:683-692.
• Kurth I, Grimm T. Mosaike bei monogenen Erkrankungen. Med Gen 2014, 26: 336-341.
• Jancuskova T, Plachy R, Zemankova L, Hardekopf DW, Stika J, Zejskova L, Praulich I, Kreuzer K-A, Rothe A, Othman MAK, Kosyakova N, Pekova S. Molecular characterization of the rare translocation t(3;10)(q26;q21) in an acute myeloid leukemia patient. Mol Cytogenet 2014;7:47.
• Liehr T. Small supernumerary marker chromosomes detected in connection with infertility. Zhonghua Nan Ke Xue 2014, 20:771-780.
• Liehr T. Bedeutung von Zellmosaiken in der genetischen Diagnostik. Medgen 2014, 26:297.
• Liehr T. Entstehungsmechanismen von Zellmosaiken in der genetischen Diagnostik. Medgen 2014, 26:298-301.
• Liehr T, Heng H, Yurov Y. Reviewer acknowledgement 2014. Mol Cytogenet 7:11.
• Manolakos E, Vetro A, Garas A, Thomaidis L, Kefalas K, Kitsos G, Ziegler M, Liehr T, Zuffardi O, Papoulidis I. A new case of proximal 10q duplication in a child with severe central hypotonia characterized by array CGH and review. Exp Therap Med 2014, 7:953-957.
• Natiq A, Elalauoi SC, Liehr T, Amzazi S, Sefiani A. Characterization of a rare short arm heteromorphism of chromosome 22 in a girl with down-syndrome like facies. Ind J Hum Genet 2014, 20:89-91.
• Natiq A, Amsdel S, Liehr T, Kreskowski K, Meyer B, Ratbi I, Amzazi S, Sefiani A. 11p13 deletion syndrome: first case in Morocco detected by FISH. J Pediatr Neonatal Care 2014, 1: 00048
• Nazaryan L, Stefanou EG, Hansen C, Kosyakova N, Bak M, Sharkey FH, Mantziou T, Papanastasiou AD, Velissariou V, Liehr T, Syrrou M, Tommerup N. The strength of combined cytogenetic and mate-pair sequencing techniques illustrated by a germline chromothripsis rearrangement involving FOXP2. Europ J Hum Genet 2014, 22:338-343.
• Ney Garcia DR, Vieira TP, Liehr T, Abdelhay E, Binato R, Neves F, de Souza MT, Ribeiro RC, Silva MLM. Cryptic t(19;19)(p13.3;q13.2), involving the TCF3/E2A gene, detected and described by molecular cytogenetics in a patient with childhood B-cell progenitor acute lymphoblastic leukemia. Atlas Genet Cytogenet Oncol Haematol 2014, 18:217-221.
• Othman MAK, Rincic M, Melo JB, Carreira IM, Alhourani E, Hunstig, Glaser A, Liehr T. A novel cryptic three-way translocation t(2;9;18)(p23.2;p21.3;q21.33) with deletion of tumor suppressor genes in 9p21.3 and 13q14 in a T-cell acute lymphoblastic leukemia. Leuk Res Treatment 2014, 2014:357123
• Pappoulidis I, Papageorgiou E, Siomou E, Oikonomidou E, Thomaidou L, Vetro A, Zuffardi O, Liehr T, Manolakos E. A patient with partial trisomy 21 and 7p deletion expresses mild Down syndrome phenotype. Gene 2014, 536:441-443.
• Poltronieri J, Marquioni V, Bertollo LAC, Kejnovsky E, Molina WF, Liehr T, Cioffi MB. Comparative chromosomal mapping of microsatellites in Leporinus species (Characiformes, Anostomidae): Unequal accumulation on the W chromosomes. Cytogenet Genome Res 2014, 142: 40-45.
• Rodríguez L, Bhatt SS, García-Castro M, Plasencia A, Fernández-Toral J, Abarca E, de Bello Cioffi M, Liehr T. A unique case of a discontinuous duplication 3q26.1-3q28 resulting from a segregation error of a maternal complex chromosomal rearrangement involving an insertion and an inversion. Gene 2014, 535:165-169.
• Roediger J, Hessenkemper W, Bartsch S, Manvelyan M, Huettner SS, Liehr T, Esmaeili M, Foller S, Petersen I, Grimm M-O, Baniahmad A. Supraphysiological androgen levels induce cellular senescence in human prostate cancer cells through the Src-Akt pathway. Mol Cancer 2014, 13:214
• Şahina S, Kiper PÖ, Alanay Y, Liehr T, Utine GE, Boduroğlu K. Partial monosomy 3q26.33-q27.3 presenting with intellectual disability, facial dysmorphism, and diaphragm eventration: a case report. Clin Dysmorphol 2014, 23:147-151.
• Santiago F, Alves G, Otero UB, Tabalipa MM, Scherrer LR, Kosyakova N, Ornellas MH, Liehr T. Monitoring of gas station attendants exposure to benzene, toluene, xylene (BTX) using three-color chromosome painting. Mol Cytogenet 2014, 7:15.
• Sanubol A, Chaveerach A, Sudmoon R, Tanee T, Liehr T. Verification of selected piper species (Piperaceae) using morphological characters, molecular data, and chemical constituents. Malay Nat J 2014, 66, 60-81.
• Schmidt T, Bierhals T, Kortüm F, Bartels I, Liehr T, Burfeind P, Shoukier M, Frank V, Bergmann C, Kutsche K. Branchio-Otic syndrome caused by a genomic rearrangement: clinical findings and molecular cytogenetic studies in a patient with a pericentric inversion of chromosome 8. Cytogenet Genome Res 2014;142:1-6.
• Schneider K, Seemann E, Liebmann L, Ahuja R, Koch D, Westermann M, Hübner CA, Kessels MM, Qualmann B. ProSAP1 and membrane nanodomain-associated syndapin I promote postsynapse formation and function. J Cell Biol. 2014, 205:197-215.
• Schnetzke U, Fix P, Spies-Weisshart B, Schrenk K, Glaser A, Fricke HJ, La Rosée P, Hochhaus A, Scholl S. Efficacy and feasibility of cyclophosphamide combined with intermediate- dose or high-dose cytarabine for relapsed and refractory acute myeloid leukemia (AML). J Cancer Res Clin Oncol 2014, 140:1391-1397.
• Sifakis S, Eleftheriades M, Kappou D, Murru R, Konstantinidou A, Orru S, Ziegler M, Liehr T, Manolakos E, Papoulidis I. Prenatal diagnosis of proximal partial trisomy 1q confirmed by Comparative Genomic Hybridization array: molecular cytogenetic analysis, fetal pathology and review of the literature. Birth Defects Research Part A: Clinical and Molecular Teratology 2014, 100:284-293.
• Spittel H, Kubek F, Kreskowski K, Ziegler M, KleinE, Hamid AB, Kosyakova N, Radhakrishnan G, Junge A, Kozlowski P, Schulze B, Martin T, Huhle D, Mehnert K, Rodríguez L, Ergun MA, Sarri C, Militaru M, Stipoljev F, Tittelbach H, Fan X, Vasheghani F, Hussein SS, Volleth M, Liehr T. Mitotic stability of small supernumerary marker chromosomes – a study based on 93 immortalized cell lines. Cytogenet Genome Res 2014, 142:151-160.
• Supiwong W, Liehr T, Cioffi M, Chaveerach A, Kosyakova N, Pinthong K, TaneeT, Tanomtong A. Genomic organization of repetitive DNAs in naked catfishes (Bagridae, Siluriformes): Insights into the evolutionary dynamics of heterochromatin. Zool Anzeiger 2014, 253:316-320.
• Supiwong W, Liehr T, Cioffi MB, Chaveerach A, Kosyakova N, Fan X, Tanee T, Tanomtong A. Comparative cytogenetic mapping of rRNA genes among naked catfishes: Implications for genomic evolution in the Bagridae family. Genet Mol Res 2014, 13:9533-9542.
• Varvagiannis K, Papoulidis I, Koromila T, Kefalas K, Ziegler M, Liehr T, Petersen MB, Gyftodimou Y, Manolakos E. De novo 393kb microdeletion of 7p11.2 characterized by aCGH in a boy with psychomotor retardation and dysmorphic features. Meta Gene 2014, 2:274-282.
• Vlaikou AM, Manolakos E, Noutsopoulos D, Markopoulos G, Liehr T, Vetro A, Ziegler M, Weise A, Kreskowski K, Papoulidis I, Thomaidis L, Syrrou M. An interstitial 4q31.21q31.22 microdeletion associated with developmental delay: Case report and literature review. Cytogenet Genome Res 2014;142:227-238.
• Vorsanova SG, Iourov IY, Demidova IA, Kolotii AD, Liehr T, Yurov YB. Microdeletion 1p36 syndrome: diagnostic problems and the use of molecular cytogenetics for the solution.//Yakut Medical Journal 2014, 2:47-48.
• Wabitsch M, Moss A, Kromeyer-Hauschild K. Unexpected plateauing of childhood obesity rates in developed countries. BMC Med 2014; 12:17.
• Wafa A, Aljapawe A, Othman MAK, Liehr T, Alhourani E, Al Achkar W. Do novo del(9)(p13) in a childhood T-cell prolymphocytic leukemia as sole abnormality. Exp Hematol Oncol 2014, 3:28.
• Weise A, Klein E, Mrasek K. Chromosomale Mosaike in der klinischen Zytogenetik. Med Gen 2014, 26: 302-308.
• A Weise, K Mrasek, T Liehr. Zytogenetische und molekularzytogenetische Methoden in der Pränataldiagnostik. Medgen 2014, 26:391-397.
• Yano CF, Poltronieri J, Bertollo LA, Artoni RF, Liehr T, de Bello Cioffi M. Chromosomal mapping of repetitive DNAs in Triportheus trifurcatus (Characidae, Characiformes): Insights into the differentiation of the Z and W chromosomes. PLoS One 2014, 9:e90946.
• Yano CF, Bertollo LAC, Molina WF, Liehr T, de Bello Cioffi M. Genomic organization of repetitive DNAs and its implications for male karyotype and the neo-Y chromosome differentiation in Erythrinus erythrinus (Characiformes, Erythrinidae). Comp Cytogen 2014, 8: 139-151
• Yurov YB, Vorsanova SG, Liehr T, Kolotii AD and Iourov IY. X chromosome aneuploidy in the Alzheimer's disease brain. Mol Cytogenet 2014, 7:20.

Bücher/ Books

UPD-Book
Year     Chapterdownloads
2018                 569
2017                  921
2016                 1211
2015                1063
2014                   877

• AbdElmontalab FY, Fadl IE, Abushama HM, Kreskowski K, Liehr T. Molecular cytogenetic study of the NF2 gene deletion in meningioma in Sudanese patients. Balk J Med Genet 2013, 16:29-32
• Abo-Zeid MA, Liehr T, El-Daly SM, Gamal-Eldeen AM, Glei M, Shabaka A, Bhatt S, Hamid A. Molecular cytogenetic evaluation of the efficacy of photodynamic therapy by Indocyanine Green in breast adenocarcinoma MCF-7 cells. Photodiagn Photodynam Therapy 2013, 10:194-202.
• Al-Achkar W, Aljapawe A, Almedani S, Liehr T, Wafa A. A novel cytogenetic abnormality t(7;8)(p11.2:q11.2) and a four-way Philadelphia translocation in an imatinib mesylate-resistant chronic myeloid leukemia patient. Oncol Lett 2013, 5: 617-620.
• Al-Achkar W, Wafa A, Liehr T. A new t(9;11;20;22)(q34;p11.2;q11.21;q11) in a Philadelphia-positive chronic myeloid leukemia case. Oncol Lett 2013, 5: 605-608.
• Al-Achkar W, Wafa A, Moassass F, Klein E, Liehr T. Multiple copies of BCR-ABL fusion gene on two isodicentric Philadelphia chromosomes in an imatinib mesylate-resistant chronic myeloid leukemia patient. Oncol Lett 2013, 5: 1579-1582.
• Al-Achkar W, Wafa A, Ikhtiar A, Liehr T. Three-way Philadelphia translocation t(9;10;22)(q34;p11.2;q11.2) as a secondary abnormality in an imatinib mesylate resistant chronic myeloid leukemia patient. Oncol Lett 2013, 5: 1656-1658.
• Al-Achkar W, Wafa A, Assaad M, Ehlers C, Liehr T. A unique case of female pseudohermaphroditism with 21-hydroxylase deficiency and small supernumerary marker chromosome 7. Mol Med Rep 2013, 7: 1545-1548.
• Al Achkar W, Wafa A, Aljapawe A, Liehr T. A de novo del(9)(p22.3) in a primary plasma cell leukemia case. Mol Cytogenet 2013, 6:33.
• Al-achkar W, Aljapawe A, Othman MA, Wafa A. A de novo acute myeloid leukemia (AML-M4) case with a complex karyotype and yet unreported breakpoints. Molecular Cytogenetics 2013, 6:18.
• Al-Achkar W, Moassass F, Ikhtiar A, Othman MAK, Liehr T, Wafa A. Cytogenetic evolution in a patient with chronic developing a secondary acute myelogenous leukemia subtype M5 resistant to Imatinib mesylate therapy. J Leuk 2013, 1: 118.
• Al Achkar W, Wafa A, Aljapawe A, Othman MAK, Liehr T. A novel cytogenetic abnormality r(7)(::p11.2->q36.3::) in a Philadelphia-positive chronic myeloid leukemia case. Case Rep Clin Med 2013, 2: 517-520.
• Al-Achkar , Wafa A, Al-Ablog A, Moassas F, Liehr T. Molecular cytogenetic characterization on an inv(Y)(p11.2q11.221q11.222) in a Syrian family. Balk J Med Genet 2013, 16:73-76
• Alexandrov T, Becker M, Guntinas-Lichius O, Ernst G, von Eggeling F. MALDI-imaging segmentation is a powerful tool for spatial functional proteomic analysis of human larynx carcinoma. J Cancer Res Clin Oncol 2013, 139:85-95.
• Alves G, Pereira DA, Sandim V, Ornellas AA, Escher N, Melle C, von Eggeling F. Urine screening by Seldi-Tof, followed by biomarker identification, in a Brazilian cohort of patients with Renal Cell Carcinoma (RCC). Int Braz J Urol 2013, 39:228-239.
• Antoine MW, Hübner CA, Arezzo JC, Hébert JM. A causative link between inner ear defects and long-term striatal dysfunction. Science 2013, 341:1120-1123.
• Aust N, Schüle S, Altendorf-Hofmann AK, Chen Y, Knösel T, Dirsch O, Settmacher U, Weise A, Mrasek K, Liehr T. Loss of chromosome 4 correlates with better long-term survival and lower relapse rate after R0-resection of colorectal liver metastases. J Cancer Res Clin Oncol 2013, 139:1861-1867.
• Baniahmad A. Why do we need to age? Horm Mol Biol Clin Invest 2013, 16:3-5
• Baniahmad A, Tresguerres JA, Zouboulis CC. Special issue on hormones and ageing. Horm Mol Biol Clin Investig 2013, 16:1-2.
• Barber JC, Hall V, Maloney VK, Huang S, Roberts AM, Brady AF, Foulds N, Bewes B, Volleth M, Liehr T, Mehnert K, Bateman M, White H. 16p11.2-p12.2 duplication syndrome; a genomic condition differentiated from euchromatic variation of 16p11.2. Eur J Hum Genet 2013, 21:182-189.
• Beetz C, Koch N, Khundadze M, Zimmer G, Nietzsche S, Hertel N, Huebner AK, Mumtaz R, Schweizer M, Dirren E, Karle KN, Irintchev A, Alvarez V, Redies C, Westermann M, Kurth I, Deufel T, Kessels MM, Qualmann B, Hübner CA. A spastic paraplegia mouse model reveals REEP1-dependent ER shaping. J Clin Invest 2013, 123:4273-4282 - see also J Clin Invest 2014,124:2809.
• Bhatt AD, Liehr T, Bakshi SR. Phenotypic spectrum in uniparental disomy: low incidence or lack of study? Indian J Hum Genet 2013, 19: 311-314.
• Bocklitz TW, Crecelius AC, Matthäus C, Tarcea N, von Eggeling F, Schmitt M, Schubert US, Popp J. Deeper understanding of biological tissue: quantitative correlation of maldi-tof and Raman imaging. Anal Chem 2013; 85:10829-10834.
• Cavdarli B, Ozgen G, Kaymak AO, Göker B, Liehr T, Ergun MA, Percin EF. A case with double translocation and Sjögren syndrome. Turkiye Klinikleri J Med Sci 2013, 33:263-236.
• Chambrey R, Kurth I, Peti-Peterdi J, Houillier P, Purkerson JM, Leviel F, Hentschke M, Zdebik AA, Schwartz GJ, Hübner CA, Eladari D. Renal intercalated cells are rather energized by a proton than a sodium pump. Proc Natl Acad Sci U S A 2013, 110:7928-7933.
• Cioffi MB, Liehr T, Trifonov V, Molina WF, Bertollo LAC. Independent sex chromosome evolution in lower vertebrates: A molecular cytogenetic overview in the Erythrinidae fish family. Cytogenet Genome Res 2013, 141:186-194.
• Eckey M, Kraft F, Kob R, Escher N, Asim M, Fischer H, Fritsche MK, Melle C, Baniahmad A. The corepressor activity of Alien is controlled by CREB-binding protein/p300. FEBS J 2013, 280:1861-1868.
• Fan X, Pinthong K, Mkrtchyan H, Siripiyasing P, Kosyakova N, Supiwong W, Tanomtong A, Chaveerach A, Liehr T, de Bello Cioffi M, Weise A. First detailed reconstruction of the karyotype of Trachypithecus cristatus (Mammalia: Cercopithecidae). Mol Cytogenet 2013, 6:58.
• Foertsch F, Teichmann N, Kob R, Hentschel J, Laubscher U, Melle C. S100A11 is involved in the regulation of the stability of cell cycle regulator p21(CIP1/WAF1) in human keratinocyte HaCaT cells. FEBS J 2013, 280:3840-3853.
• Guilherme RS, Dutra ARN, Perez AB, Takeno SS, Oliveira MM, Kulikowski D, Klein E, Hamid AB, Liehr T, Melaragno MI. First report of a small supernumerary der(8;14) marker chromosome. Cytogenet Genome Res 2013, 139:284-288.
• Guilherme RS, Klein E, Hamid AB, Bhatt S, Volleth M, Polityko A, Kulpanovich A, Dufke A, Albrecht B, Morlot S, Brecevic L, Petersen MB, Manolakos E, Kosyakova N, Liehr T. Human ring chromosomes - new insights for their clinical significance. Balk J Med Genet 2013, 16:13-19.
• Guilherme RS, Cernach MC, Sfakianakis TE, Takeno SS, Nardozza LM, Rossi C, Bhatt SS, Liehr T, Melaragno MI. A complex chromosome rearrangement involving four chromosomes, nine breakpoints and a cryptic 0.6-mb deletion in a boy with cerebellar hypoplasia and defects in skull ossification. Cytogenet Genome Res 2013, 141:317-323.
• Heinrich-Weltzien R, Monse B, Benzian H, Heinrich J, Kromeyer-Hauschild K. Association of dental caries and weight status in 6- to 7-year-old Filipino children. Clin Oral Investig 2013, 17:1515-1523.
• Heinrich-Weltzien R, Zorn C, Monse B, Kromeyer-Hauschild K. Relationship between malnutrition and the number of permanent teeth in Filipino 10- to 13-year-olds. Biomed Res Int 2013, 2013:205950.
• Hessenkemper W, Baniahmad A. Targeting heat shock proteins in prostate cancer. Curr Med Chem 2013, 20:2731-2740.
• Hoelscher M, Richter N, Melle C, von Eggeling F, Schaenzer A, Nestler U. SELDI-TOF analysis of glioblastoma cyst fluid is an approach for assessing cellular protein expression. Neurol Res 2013, 35:993-1001.
• Huebner AK, Hübner CA. Ionentransport und Taubheit. Medgen. 2013, 25:475-479.
• Hübner CA, Holthoff K. Anion transport and GABA signaling.Front Cell Neurosci 2013, 7:177.
• Hunstig F, Hammersen J, Kunert C, Petersen I, Merz H, Glaser A, Teichgräber U, Hochhaus A, Rosée PL. Complete remission after treatment with single-agent ofatumumab in a patient with high-risk leukemic mantle-cell lymphoma. J Clin Oncol 2013, 31:e312-315.
• Jacques T, Picard N, Miller RL, Riemondy KA, Houillier P, Sohet F, Ramakrishnan SK, Büsst CJ, Jayat M, Cornière N, Hassan H, Aronson PS, Hennings JC, Hübner CA, Nelson RD, Chambrey R, Eladari D. Overexpression of pendrin in intercalated cells produces chloride-sensitive hypertension. J Am Soc Nephrol 2013, 24:1104-1113.
• Jancuskova T, Plachy R, Stika J, Zemankova L, Hardekopf DW, Liehr T, Kosyakova N, Cmejla R, Zejskova L, Kozak T, Zak P, Zavrelova A, Havlikova P, Karas M, Junge A, Ramel C, Pekova S. A method to identify new molecular markers for assessing minimal residual disease in acute leukemia patients. Leuk Res 2013, 37:1363-1373.
• Jančušková T, Plachý R, Štika J, Krutílková L, Hardekopf DW, Liehr T, Kosyakova N, Čmejla R, Žejšková L, Kozák T, Žák P, Karas M, Peková S. Identifikace novych molekularnich “marker pro sledovani minimalni rezidualni nemoci u akutnich leumkemii. Transfuze a Hematologie Dnes 2013, 19:8-21.
• Kalkunte SS, Neubeck S, Norris WE, Cheng SB, Kostadinov S, Vu Hoang D, Ahmed A, von Eggeling F, Shaikh Z, Padbury J, Berg G, Olofsson A, Markert UR, Sharma S. Transthyretin is dysregulated in preeclampsia, and its native form prevents the onset of disease in a preclinical mouse model. Am J Pathol 2013, 183:1425-1436.
• Karadeniz N, Liehr T, Mrasek K, Aşık I, Aşık Z, Kosyakova N, Mkrtchyan H. C-type lectins and human epithelial membrane protein1: Are they new proteins in keratin disorders? Open J Genet 2013, 3:262-269
• Karamysheva TV, Prokhorovich MA, Lagarkova MA, Kiselev SL, Liehr T, Rubtsov NB. Chromosome rearrangements in sublines of human embryonic stem cell lines hESM01 and hESM03. BioDiscovery 2013, 7:1.
• Koehler K, Malik M, Mahmood S, Gießelmann S, Beetz C, Hennings JC, Huebner AK, Grahn A, Reunert J, Nürnberg G, Thiele H, Altmüller J, Nürnberg P, Mumtaz R, Babovic-Vuksanovic D, Basel-Vanagaite L, Borck G, Brämswig J, Mühlenberg R, Sarda P, Sikiric A, Anyane-Yeboa K, Zeharia A, Ahmad A, Coubes C, Wada Y, Marquardt T, Vanderschaeghe D, Van Schaftingen E, Kurth I, Huebner A, Hübner CA. Mutations in GMPPA cause a glycosylation disorder characterized by intellectual disability and autonomic dysfunction. Am J Hum Genet 2013, 93:727-734.
• Kosyakova N, Hamid AB, Chaveerach A, Pinthong K, Siripiyasing P, Supiwong W, Romanenko S, Trifonov V, Fan X. Generation of multicolor banding probes for chromosomes of different species. Molecular Cytogenetics 2013, 6:6.
• Kosyakova N, Trifonov V, Romanenko S, Mkrtchyan H, Graphodatsky A, Liehr T. Murine multicolor banding. Tsitologiya 2013, 55:259-260.
• Kosyakova N, Grigorian A, Liehr T, Manvelyan M, Simonyan I, Mkrtchyan H, Aroutiounian R, Polityko AD, Kulpanovich AI, Egorova T, Jaroshevich E, Frolova A, Shorokh N, Naumchik IV, Volleth M, Schreyer I, Nelle H, Stumm M, Wegner R, Reising-Ackermann G, Merkas M, Brecevic L, Martin T, Rodríguez L, Bhatt S, Ziegler M, Kreskowski K, Weise A, Sazci A, Vorsanova S, Cioffi Md, Ergul E. Heteromorphic variants of chromosome 9. Molecular Cytogenetics 2013, 6:14.
• Kreuser F, Kromeyer-Hauschild K, Gollhofer A, Korsten-Reck U, Röttger K. "Obese equals lazy?" analysis of the association between weight status and physical activity in children. J Obes 2013, 2013:437017.
• Kromeyer-Hauschild K, Neuhauser H, Schaffrath Rosario A, Schienkiewitz A. Abdominal obesity in German adolescents defined by waist-to-height ratio and its association to elevated blood pressure: The KiGGS study. Obes Facts. 2013, 6:165-175.
• Khundadze M, Kollmann K, Koch N, Biskup C, Nietzsche S, Zimmer G, Hennings JC, Huebner AK, Symmank J, Jahic A, Ilina EI, Karle K, Schöls L, Kessels M, Braulke T, Qualmann B, Kurth I, Beetz C, Hübner CA. A hereditary spastic paraplegia mouse model supports a role of ZFYVE26/SPASTIZIN for the endolysosomal system. PLoS Genet 2013, 9:e1003988.
• Leibiger C, Kosyakova N, Mkrtchyan H, Glei M, Trifonov V, Liehr T. First molecular cytogenetic high resolution characterization of the NIH 3T3 cell line by murine multicolor banding. J Histochem Cytochem 2013, 61: 306-312.
• Leipold E, Liebmann L, Korenke GC, Heinrich T, Gießelmann S, Baets J, Ebbinghaus M, Goral RO, Stödberg T, Hennings JC, Bergmann M, Altmüller J, Thiele H, Wetzel A, Nürnberg P, Timmerman V, De Jonghe P, Blum R, Schaible HG, Weis J, Heinemann SH, Hübner CA, Kurth I. A de novo gain-of-function mutation in SCN11A causes loss of pain perception. Nat Genet 2013, 45:1399-1404.
• Liehr T. Copy number variations - is there a biological difference between submicroscopic and microscopically visible ones? OA Genetics 2013, 1:2.
• Liehr T, Kosyakova N. Small supernumerary marker chromosomes (sSMC) - what about the genotype-phenotype correlation? Tsitologiya 2013, 55: 165-166.
• Liehr T, Weise A, Hamid AB, Fan X, Klein E, Aust N, Othman MA, Mrasek K, Kosyakova N. Multicolor fluorescence in situ hybridization methods in nowadays clinical diagnostics. Exp Rev Mol Diag 2013, 13: 251-255.
• Liehr T, Heng H, Yurov Y. Reviewer acknowledgement 2013. Molecular Cytogenetics 2013, 6:9.
• Liehr T, Klein E, Mrasek K, Kosyakova N, Guilherme RS, Aust N, Venner C, Weise A, Hamid AB. Clinical impact of somatic mosaicism in cases with small supernumerary marker chromosomes. Cytogenet Genome Res 2013, 139: 158-163.
• Liehr T, Heng H, Yurov Y, Meloni-Ehrig A, Iourov I. Molecular Cytogenetics: the first impact factor (2.36) journal: Molecular Cytogenetics. Mol Cytogenet 2013, 6:28.
• Liehr T, Cirkovic S, Lalic T, Guc-Scekic M, de Almeida C, Weimer J, Iourov I, Melaragno MI, Guilherme RS, Stefanou EG, Aktas D, Kreskowski K, Klein E, Ziegler M, Kosyakova N, Volleth M, Hamid AB. Complex small supernumerary marker chromosomes - an update. Mol Cytogenet 2013, 6:46.
• Manolakos M, Vetro A, Papadopoulou E, Kefalas K, Lagou M, Thomaidis L, Peitsidis P, Sifakis S, Divane A, Ziegler M, Liehr T, Zuffardi O, Papoulidis I. Partial trisomy 2p and partial monosomy 2q arising from a paternal intrachromosomal 2q-into-2p between-arm insertion and paracentric inversion: molecular cytogenetic characterization of a four break rearrangement. Cytogenet Genome Res 2013, 140: 12-20.
• Matos RRC, Mkrchyan H, Amaral BA, Liehr T, de Souza MT, Ney-Garcia DR, Santos N, Marques-Salles TJ, Ribeiro RC, Figueiredo AF, Silva MLM. An unusual cytogenetic rearrangement originating from two different abnormalities in chromosome 6 in a child with acute promyelocytic leukemia. Acta Hematologica 2013, 130:23-26.
• Matoso E, Melo JB, Ferreira SI, Jardim A, Castelo TM, Weise A, Carreira IM. Insertional translocation leading to a 4q13 duplication including the EPHA5 gene in two siblings with attention-deficit hyperactivity disorder. Am J Med Genet A 2013, 161A:1923-1928.
• Meyer T, Guntinas-Lichius O, von Eggeling F, Ernst G, Akimov D, Schmitt M, Dietzek B, Popp J. Multimodal nonlinear microscopic investigations on head and neck squamous cell carcinoma: toward intraoperative imaging. Head Neck 2013; 35:E280-E287.
• Ney-Garcia DR, Vieira TP, Liehr T, Bhatt S, de Souza MT, de Figueiredo AF, Ribeiro RC, Silva MLM. A case of childhood T cell acute lymphoblastic leukemia with a complex t(9;9) and homozygous deletion of CDKN2A gene associated with a Philadelphia-positive minor subclone. Blood Cells Mol Dis 2013, 50:131-133.
• Ney Garcia DR, Vieira TP, Liehr T, Abdelhay E, Binato R, Neves F, de Souza MT, Ribeiro RC, Silva MLM . Cryptic t(19;19)(p13.3;q13.2), involving the TCF3/E2A gene, detected and described by molecular cytogenetics in a patient with childhood B-cell progenitor acute lymphoblastic leukemia. Atlas Genet Cytogenet Oncol Haematol. July 2013. URL : http://AtlasGeneticsOncology.org/Reports/t1919p13q13NeyGarciaID100072.html
• Nolan LS, Maier H, Hermans-Borgmeyer I, Girotto G, Ecob R, Pirastu N, Cadge BA, Hübner C, Gasparini P, Strachan DP, Davis A, Dawson SJ. Estrogen-related receptor gamma and hearing function: evidence of a role in humans and mice. Neurobiol Aging 2013, 34:2077.e1-9.
• Ou J, Wang W, Liehr T, Klein E, Hamid AB, Wang F, Duan C, Li H. Characterization of three small supernumerary marker chromosomes (sSMC) in humans. J Matern Fetal Neonatal Med 2013, 26:106-108.
• Papaioannou M, Söderholm AA, Hong W, Dai Y, Roediger J, Roell D, Thiele M, Nyrönen TH, Baniahmad A. Computational and functional analysis of the androgen receptor antagonist atraric acid and its derivatives. Anticancer Agents Med Chem. 2013, 13:801-810.
• Plachta-Danielzik S, Bosy-Westphal A, Kehden B, Gehrke MI, Kromeyer-Hauschild K, Grillenberger M, Willhöft C, Heymsfield SB, Müller MJ. Adiposity rebound is misclassified by BMI rebound. Eur J Clin Nutr 2013, 67:984-989.
• Roos A, von Kaisenberg CS, Eggermann T, Schwanitz G, Löffler C, Weise A, Mrasek K, Junge A, Caliebe A, Belitz B, Kautza M, Schüler H, Zerres K, Heidemann S. Analysis of SYCP3 encoding synaptonemal complex protein 3 in human aneuploidies. Arch Gynecol Obstet 2013, 288:1153-1158.
• Ruusuvuori E, Huebner AK, Kirilkin I, Yukin AY, Blaesse P, Helmy M, Kang HJ, El Muayed M, Hennings JC, Voipio J, Sestan N, Hübner CA, Kaila K. Neuronal carbonic anhydrase VII provides GABAergic excitatory drive to exacerbate febrile seizures. EMBO J 2013 ,32:2275-2286.
• Schmidt T, Bartels I, Liehr T, Burfeind P, Zoll B, Shoukiera M. A family with an inverted tandem duplication 5q22.1-q23.2. Cytogenet Genome Res 2013,139:65-70.
• Sheth FJ, Liehr T, Kumari P, Akinde R, Sheth HJ, Sheth JJ. Chromosomal abnormalities in couples with repeated fetal loss: an Indian retrospective study. Indian J Hum Genet 2013, 19: 415-422.
• Shmukler BE, Hsu A, Alves J, Trudel M, Rust MB, Hubner CA, Rivera A, Alper SL. N-ethylmaleimide activates a Cl(-)-independent component of K(+) flux in mouse erythrocytes. Blood Cells Mol Dis 2013, 51:9-16.
• Sinning A, Hübner CA. Minireview: pH and synaptic transmission. FEBS Lett 2013, 587:1923-1928.
• Supiwong W, Liehr T, Cioffi MB, Chaveerach A, Kosyakova N, Pinthong K, Tanee T and Tanomtong A. Karyotype and cytogenetic mapping of 9 classes of repetitive DNAs in the genome of the naked catfish Mystus bocourti (Siluriformes, Bagridae). Mol Cytogenet 2013, 6:51.
• Vasconcelos DS, da Silva FPE, Quintana LG, Anselmo NP, Othman MAK, Liehr T, de Oliveira EHC. Numerical aberrations of chromosome 17 and TP53 in brain metastases derived from breast cancer. Genet Mol Res 2013, 12:2594-2600.
• Vičić A, Zudenigo D, Korać P, Liehr T, Stipoljev F. Prenatally detected interstitial deletion 13q12.3-q22 in a fetus with a cystic hygroma. Gene 2013, 531: 90-91.
• Yomade O, Spies-Weisshart B, Glaser A, Schnetzke U, Hochhaus A, Scholl S. Impact of NOD2 polymorphisms on infectious complications following chemotherapy in patients with acute myeloid leukaemia. Ann Hematol 2013, 92:1071-1077.

• Al-Achkar W, Wafa A, Moassass F, Liehr T. A chronic myeloid leukemia case with a unique variant Philadelphia translocation: t(9;22;21)(q34;q11;p12). Oncol Lett 2012, 3: 1027-1029.
• Al-Achkar W, Wafa A, Moassass F, Liehr T. A unique cytogenetic abnormality, t(2;7)(p13.1;p21.3), in a Philadelphia-positive chronic myeloid leukemia. Onc Letters 2012, 4: 209-212.
• Al-Achkar W, Wafa A, Liehr T, Klein E, Moassass F. Detailed analysis of an idic(Y)(q11.21) in a mosaic karyotype. Mol Med Report 2012, 6: 293-296.
• Al-Achkar W, Wafa A, Moassass F, Othman MAK. A novel dic (17;18) (p13.1;q11.2) with loss of TP53 and BCR/ABL rearrangement in an Imatinib resistant chronic myeloid leukemia. Mol Cytogenet 2012, 5:36.
• Baniahmad A. Benign prostate hyperplasia meets liver x receptor. Endocrinology 2012, 153:3558-3560.
• Beetz C, Pieber TR, Hertel N, Schabhüttl M, Fischer C, Trajanoski S, Graf E, Keiner S, Kurth I, Wieland T, Varga RE, Timmerman V, Reilly MM, Strom TM, Auer-Grumbach M. Exome sequencing identifies a REEP1 mutation involved in distal hereditary motor neuropathy type V. Am J Hum Genet 2012, 91:139-145.
• Briest F, Berndt A, Clement J, Junker K, von Eggeling F, Grimm S, Friedrich K. Tumor-stroma interactions in tumorigenesis: lessons from stem cell biology. Front Biosci (Elite Ed) 2012, 4:1871-1887.
• Bünger S, Haug U, Kelly M, Posorski N, Klempt-Giessing K, Cartwright A, Fitzgerald SP, Toner V, McAleer D, Gemoll T, Laubert T, Büning J, Fellermann K, Bruch HP, Roblick UJ, Brenner H, von Eggeling F, Habermann JK. A novel multiplex-protein array for serum diagnostics of colon cancer: a case-control study. BMC Cancer 2012, 12:393.
• Bucksch M, Ziegler M, Kosayakova N, Mulhatino MV, Llerena JC Jr, Morlot S, Fischer W, Polityko AD, Kulpanovich AI, Petersen MB, Belitz B, Trifonov V, Weise A, Liehr T, Hamid AB. A New Multicolor Fluorescence In Situ Hybridization Probe Set Directed Against Human Heterochromatin: HCM-FISH. J Histochem Cytochem. 2012, 60:530-536.
• Corrales NLL, Mrasek K, Voigt M, Liehr T, Kosyakova N. Copy number variations (CNVs) in human pluripotent cell-derived neuroprogenitors. Gene 2012, 506:377-379.
• Corrales NLL, Mrasek K, Voigt M, Liehr T, Kosyakova N. Comprehensive characterization of genomic instability in pluripotent stem cells and their derived neuroprogenitor cell lines. Applied & Translational Genomics 2012, 1:21-24.
• Elsing C, Georgiev T, Hübner CA, Boger R, Stremmel W, Schlenker T. Extracellular ATP induces cytoplasmic and nuclear Ca2+ transients via P2Y2 receptor in human biliary epithelial cancer cells (Mz-Cha-1). Anticancer Res 2012, 32:3759-3767.
• Faria de Figueiredo A, Vieira TP, Liehr T, Bhatt S, Binato R, de Jesus Marques Salles T, Carboni E, Ribeiro RC, Macedo Silva ML, Abdelhay E. A rare cryptic and complex rearrangement leading to MLL-MLLT10 gene fusion masked by del(10)(p12) in a child with acute monoblastic leukemia (AML-M5). Leuk Res 2012, 36: e74-e77.
• Eckmann-Scholz C, Tönnies H, Liehr T, Gesk S, Jonat W, Caliebe A. Normal prenatal ultrasound findings in a case with de novo mosaic small supernumerary marker chromosome 18 - how to counsel? J Mat-Fet Neonat Med 2012, 25:200-202.
• Fonzar Hernandes MA, de Jesus Marques-Salles T, Mkrtchyan H, Soares-Ventura EM, Pereira Leite E, Cartaxo Muniz MT, Marquim Nogueira Cornélio MT, Liehr T, Santos N, Macedo Silva ML. Extra copies of der(21)t(12;21) plus deletion of ETV6 gene due to dic(12;18) in B-cell precursor ALL with poor outcome. Case Reports Genet, 2012, doi: 10.1155/2012/186532.
• Galler K, Junker K, Franz M, Hentschel J, Richter P, Gajda M, Göhlert A, von Eggeling F, Heller R, Giavazzi R, Neri D, Kosmehl H, Wunderlich H, Berndt A. Differential vascular expression and regulation of oncofetal tenascin-C and fibronectin variants in renal cell carcinoma (RCC): implications for an individualized angiogenesis-related targeted drug delivery. Histochem Cell Biol 2012, 137:195-204.
• Grosse A, Bartsch S, Baniahmad A. Androgen receptor-mediated gene repression. Mol Cell Endocrinol 2012, 352:46-56.
• Guilherme RS, Klein E, Venner C, Hamid AB, Bhatt S, Melaragno MI, Volleth M, Polityko A, Kulpanovich A, Kosyakova N, Liehr T. Human ring chromosomes and small supernumerary marker chromosomes - do they have telomeres? Chromosome Res 2012, 20:825-835.
• Hamid AB, Kreskowski K, Weise A, Kosayakova N, Mrasek K, Voigt M, Guilherme RS, Wagner R, Hardekopf D, Pekova S, Karamysheva T, Liehr T, Klein E. How to narrow down chromosomal breakpoints in small and large derivative chromosomes - a new probe set. J Appl Genet 2012, 53:259-269.
• Hamid AB, Weise A, Voigt M, Bucksch M, Kosyakova N, Liehr T, Klein E. Clinical impact of proximal autosomal imbalances. Balk J Med Genet 2012, 15:15-21.
• Hentschel J, Riesener G, Nelle H, Stuhrmann M, Schöner A, Sommerburg O, Fritzsching E, Mall MA, von Eggeling, Mainz JG. Homozygous CFTR mutation M348K in a boy with respiratory symptoms and failure to thrive. Disease-causing mutation or benign alteration? Eur J Pediatr 2012, 171:1039.
• Hennings JC, Picard N, Huebner AK, Stauber T, Maier H, Brown D, Jentsch TJ, Vargas-Poussou R, Eladari D, Hübner CA. A mouse model for distal renal tubular acidosis reveals a previously unrecognized role of the V-ATPase a4 subunit in the proximal tubule. EMBO Mol Med 2012, 4:1057-1071.
• Hessenkemper W, Baniahmad A. Chaperones for proper androgen action - a plethora of assistance to androgen receptor function. Horm Mol Biol Clin Invest 2012, 11: 321-328.
• Hilgen G, Huebner AK, Tanimoto N, Sothilingam V, Seide C, Garrido MG, Schmidt KF, Seeliger MW, Löwel S, Weiler R, Hübner CA, Dedek K. Lack of the sodium-driven chloride bicarbonate exchanger NCBE impairs visual function in the mouse retina. PLoS One 2012, 7:e46155.
• Hovhannisyan G, Aroutiounian R, Liehr T. Chromosomal composition of micronuclei in human leukocytes exposed to mitomycin C. J Histochem Cytochem 2012, 60:316-322
• Kim HG, Kim HT, Leach NT, Lan F, Ullmann R, Silahtaroglu A, Kurth I, Nowka A, Seong IS, Shen Y, Talkowski ME, Ruderfer D, Lee JH, Glotzbach C, Ha K, Kjaergaard S, Levin AV, Romeike BF, Kleefstra T, Bartsch O, Elsea SH, Jabs EW, Macdonald ME, Harris DJ, Quade BJ, Ropers HH, Shaffer LG, Kutsche K, Layman LC, Tommerup N, Kalscheuer VM, Shi Y, Morton CC, Kim CH, Gusella JF. Translocations disrupting PHF21A in the Potocki-Shaffer-Syndrome region are associated with intellectual disability and craniofacial anomalies. Am J Hum Genet 2012, 91:56-72.
• Klag T, Schnetzke U, Benz R, Zanow J, Glaser A, Pörner TC, Scholl S, Reiter A, Hochhaus A, La Rosée P. Leriche's syndrome and Löffler endocarditis in a 30-year-old patient presenting with hypereosinophilic syndrome. Ann Hematol 2012, 91:139-141.
• Klein E, Manvelyan M, Simonyan I, Hamid AB, Santos Guilherme R, Liehr T, Karamysheva T. Centromeric association of small supernumerary marker chromosomes with their sister-chromosomes detected by three dimensional molecular cytogenetics. Mol Cytogenet 2012, 5:15.
• Klein E, Rocchi M, Ovens-Raeder A, Kosyakova N, Weise A, Ziegler M, Meins M, Morlot S, Fischer W, Volleth M, Polityko A, Mackie Ogilvie C, Kraus C, Liehr T. Five novel locations of neocentromeres in human: 18q22.1, Xq27.1~27.2, acro p13, acro p12, and heterochromatin of unknown origin. Cytogenet Genome Res 2012, 136:163-166.
• Klopocki E, Lohan S, Doelken SC, Stricker S, Ockeloen CW, Soares Thiele de Aguiar R, Lezirovitz K, Mingroni Netto RC, Jamsheer A, Shah H, Kurth I, Habenicht R, Warman M, Devriendt K, Kordaß U, Hempel M, Rajab A, Mäkitie O, Naveed M, Radhakrishna U, Antonarakis SE, Horn D, Mundlos S. Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion. J Med Genet, 49:119-125.
• Klopocki E, Kähler C, Foulds N, Shah H, Joseph B, Vogel H, Lüttgen S, Bald R, Besoke R, Held K, Mundlos S, Kurth I. Deletions in PITX1 cause a spectrum of lower-limb malformations including mirror-image polydactyly. Eur J Hum Genet 2012, 20:705-708.
• Kromeyer-Hauschild K, Gläßer N, Zellner K. Percentile curves for skinfold thickness in 7- to 14-year-old children and adolescents from Jena, Germany. Eur J Clin Nutr 2012, 66:613-621.
• Kuechler A, Hentschel J, Kurth I, Stephan B, Prott EC, Schweiger B, Schuster A, Wieczorek D, Lüdecke HJ. A novel homozygous WDR72 mutation in two siblings with amelogenesis imperfecta and mild short stature. Mol Syndromol 2012, 3:223-229.
• Liebmann L, Beetz C, Thorwarth M, Deufel T, Hübner CA. Morphological and electrophysiological features of mature neurons in differentiated skin-derived precursor cells. J Stem Cell Regenerat Med 2012, 8:35.
• Ma K, Qiu L, Mrasek K, Zhang J, Liehr T, Quintana LG, Li Z. Common fragile sites: genomic hotspots of DNA damage and carcinogenesis. Int J Mol Sci 2012, 13:11974-11999.
• Mahmood S, Beetz C, Tahir MM, Imran M, Mumtaz R, Bassmann I, Jahic A, Malik M, Nürnberg G, Hassan SA, Rana S, Nürnberg P, Hübner CA. First HPSE2 missense mutation in urofacial syndrome. Clin Genet 2012, 81:88-92.
• Manolakos E, Sifakis S, Sotiriou S, Peitsidis P, Eleftheriades M, Mersinias V, Liehr T, Thomaidis L, Kitsos G, Papoulidis I, Petersen MB, Orru S. Prenatal detection of an inverted duplication deletion in the long arm of chromosome 1 in a fetus with increased nuchal translucency. Molecular cytogenetic analysis and review of the literature. Clin Dysmorphol 2012, 21:101-105.
• Mulatinho MV, Luiz de Carvalho Serao C, Scalco F, Hardekopf D, Pekova S, Mrasek K, Liehr T, Weise A, Rao N, Llerena JC Jr. Severe intellectual disability, omphalocele, hypospadia and high blood pressure associated to a deletion at 2q22.1q22.3: Case report. Mol Cytogenet 2012, 5:30.
• Ney-Garcia DR, Liehr T, Bhatt S, de Souza MT, Capela de Matos RR, Binato R, Jordy FC, Abdelhay E, Ribeiro RC, Silva MLM. Molecular cytogenetic studies reveal an unexpected chromosomal inversion as a variant of t(12;21)(p13;q22) in a child with B-cell precursor acute lymphoblastic leukemia. Leuk Lymphoma 2012, 53:342-344.
• Ney-Garcia DR, Liehr T, Bhatt S, de Souza MT, de Matos RR, Pimenta G, Pulcheri W, Ribeiro RC, Abdelhay E, Silva MLM. Childhood B-cell progenitor acute lymphoblastic leukemia presenting a three-way t(11;12;21)(q14;p13;q22) with a RUNX1 gene signal on chromosome 11. Int J Hematol 2012, 95:112-114.
• Othman MAK, Lier A, Junker S, Kempf P, Dorka F, Gebhart E, Sheth FJ, Grygalewicz B, Bhatt S, Weise A, Mrasek K, Liehr T, Manvelyan M. Does positioning of chromosomes 8 and 21 in interphase drive t(8;21) in acute myelogenous leukemia? BioDiscovery 2012, 4:4.
• Papoulidis I, Kontodiou M, Tzimina M, Saitis I, Hamid AB, Klein E, Kosyakova N, Kordaß U, Kunz J, Siomou E, Nicolaides P, Orru S, Thomaidis L, Liehr T, Petersen MB, Manolakos E. Tetrasomy 9p mosaicism associated with a normal phenotype in two cases. Cytogenet Genome Res 2012, 136:237-241.
• Plachta-Danielzik S, Gehrke MI Kehden B, Kromeyer-Hauschild K, Grillenberger M, Willhöft C, Bosy-Westphal A, Müller MJ. Body fat percentiles for german children and adolescents. Obes Facts 2012, 5:77.
• Redies C, Hertel N, Hübner CA. Cadherins and neuropsychiatric disorders. Brain Res 2012, 1470:130-144.
• Schulz S, Fröber R, Kraus C, Schneider U. Prenatal diagnosis of hypoplastic left heart syndrome associated with Noonan Syndrome and de novo RAF1 mutation. Prenat Diagn 2012, 32:1016-1018.
• Seja P, Schonewille M, Spitzmaul G, Badura A, Klein I, Rudhard Y, Wisden W, Hübner CA, De Zeeuw CI, Jentsch TJ. Raising cytosolic Cl- in cerebellar granule cells affects their excitability and vestibulo-ocular learning. EMBO J 2012, 31:1217-1230.
• Serra A, Eirich K, Winkler AK, Mrasek K, Göhring G, Barbi G, Cario H, Schlegelberger B, Royer-Pokora B, Liehr T, Leriche C, Henne-Bruns D, Barth TF, Schindler D. Shared copy number variation in simultaneous nephroblastoma and neuroblastoma due to fanconi anemia. Mol Syndromol 2012, 3:120-130.
• Sheth F, Gohel N, Liehr T, Akinde O, Desai M, Adeteye O, Sheth J. Gain of chromosome 4qter and loss of 5pter - an unusual case with features of Cri du chat syndrome (CdCS). Case Reports Genet 2012, Article ID 153405. doi:10.1155/2012/153405
• Skeik N, Rooke TW, Davis MD, Davis DM, Kalsi H, Kurth I, Richardson RC. Severe case and literature review of primary erythromelalgia: novel SCN9A gene mutation. Vasc Med 2012, 17:44-49.
• Varga RE, Mumtaz R, Jahic A, Rudenskaya GE, Sánchez-Ferrero E, Auer-Grumbach M, Hübner CA, Beetz C. MLPA-based evidence for sequence gain: pitfalls in confirmation and necessity for exclusion of false positives. Anal Biochem 2012, 421:799-801.
• Vetro A, Manolakos E, Petersen MB, Thomaidis L, Liehr T, Croci G, Franchi F, Marinelli M, Meneghelli E, Dal Bello B, Cesari S, Iasci A, Arrigo G, Zuffardi O. Unexpected results in the constitution of small supernumerary marker chromosomes. Europ J Med Genet 2012, 55:185-190.
• von Eggeling F, Crecelius AC, Schubert US, Guntinas-Lichius O, Ernst G. MALDI-Imaging: What can be expected? Eur J Radiol. 2012, 81 Suppl 1:S183-184
• Walter J, Handel LL, Brodhun M, van Rossum D, Hanisch UK, Liebmann L, Heppner F, Goldbrunner R, Koch A, Kuhn SA. Expression of coagulation factors and their receptors in tumor tissue and coagulation factor upregulation in peripheral blood of patients with cerebral carcinoma metastases. J Cancer Res Clin Oncol 2012, 138:141-151.
• Weise A, Mrasek K, Klein E, Mulatinho M, Llerena Jr. JC, Hardekopf D, Pekova S, Bhatt S, Kosyakova N, Liehr T. Microdeletion and microduplication syndromes. J Histochem Cytochem 2012, 60:346-358.

• Al-Achkar W, Wafa A, Liehr T. Complex translocation involving four chromosomes in a novel Philadelphia-positive chronic myeloid leukemia case. Onc Lett 2011, 2:273-276.
• Al-Achkar W, Wafa A, Klein E, Aljapawe A. Biclonal myelodysplastic syndrome involving six chromosomes and monoallelic loss of RB1 - A rare case. Molecular Cytogenetics 2011, 4:16.
• Asim M, Hafeez BB, Siddiqui IA, Gerlach C, Patz M, Mukhtar H, Baniahmad A. Ligand-dependent corepressor acts as a novel androgen receptor corepressor, inhibits prostate cancer growth and is functionally inactivated by the Src kinase. J Biol Chem 2011, 286:37108-37117.
• Backsch C, Pauly B, Liesenfeld M, Scheungraber C, Gajda M, Mrasek K, Liehr T, Clad A, Schröck E, Runnebaum IB, Dürst M. Two novel unbalanced whole arm translocations are frequently detected in cervical squamous cell carcinoma. Cancer Genetics 2011, 204:646-653.
• Baniahmad A. The corepressor Alien as a novel tumor suppressor? Horm Mol Biol Clin Invest 2011, 5:11-15.
• Braulke F, Schanz J, Steffens R, Liehr T, Manvelyan M, Chudoba I, Haase D. Two different del(5q) clones in a patient with myelodysplastic syndrome. Leuk Lymph 2011, 52:1811-1844.
• Bünger S, Haug U, Kelly FM, Klempt-Giessing K, Cartwright A, Posorski N, Dibbelt L, Fitzgerald SP, Bruch HP, Roblick UJ, von Eggeling F, Brenner H, Habermann JK. Toward standardized high-throughput serum diagnostics: multiplex-protein array identifies IL-8 and VEGF as serum markers for colon cancer. J Biomol Screen 2011, 16:10180.
• Cioffi MB, Sánchez A, Marchal JA, Kosyakova N, Liehr T, Trifonov V, Bertollo LAC. Cross-species chromosome painting tracks the independent origin of multiple sex chromosomes in two cofamiliar Erythrinidae fishes. BMC Evolutionary Biology 2011, 11:186.
• Cioffi MB, Sánchez A, Marchal JA, Kosyakova N, Liehr T, Trifonov V, Bertollo LAC. Correction to: Whole chromosome painting reveals independent origin of sex chromosomes in closely related forms of a fish species. Genetica 2018; 146:123
• de Bello Cioffi M, Sánchez A, Marchal JA, Kosyakova N, Liehr T, Trifonov V, Bertollo LA. Whole chromosome painting reveals independent origin of sex chromosomes in closely related forms of a fish species. Genetica 2011, 139:1065-1072.
• Delaney JT, Urbanek A, Wehder L, Perelaer J, Crecelius AC, von Eggeling F, Schubert US. Combinatorial optimization of multiple MALDI matrices on a single tissue sample using inkjet printing. ACS Comb Sci 2011, 13:218-222.
• de Souza MT, Mkrtchyan H, Hassan R, Ney-Garcia DR, de Azevedo AM, da Costa ES, de Figueiredo AF, Liehr T, Abdelhay E, Silva ML. Secondary abnormalities involving 1q or 13q and poor outcome in high stage Burkitt leukemia/lymphoma cases with 8q24 rearrangement at diagnosis. Int J Hematol 2011; 93:232-236.
• Dobbernack G, Meinl W, Schade N, Florian S, Wend K, Voigt I, Himmelbauer H, Gross M, Liehr T, Glatt H. Altered tissue distribution of 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine-DNA adducts in mice transgenic for human sulfotransferases 1A1 and 1A2. Carcinogenesis 2011, 32:1734-1740.
• Eladari D, Hübner CA. Novel mechanisms for NaCl reabsorption in the collecting duct. Curr Opin Nephrol Hypertens 2011 , 20:506-511.
• Elsing C, Voss A, Herrmann T, Kaiser I, Huebner CA, Schlenker T. Oxidative Stress Reduces Na+/H+ Exchange (NHE) Activity in a Biliary Epithelial Cancer Cell Line (Mz-Cha-1) Anticancer Res 2011, 31:459-456.
• Enkelmann A, Heinzelmann J, von Eggeling F, Walter M, Berndt A, Wunderlich H, Junker K. Specific protein and miRNA patterns characterise tumour-associated fibroblasts in bladder cancer. J Cancer Res Clin Oncol 2011, 137:751-759.
• Escher N, Kob R, Kaatz M, Melle C, Hipler C, von Eggeling F. Confirmation of the biological significance of transthyretin as a biomarker for cutaneous T-cell lymphoma by its protein interaction partners. Mol Med Report 2011, 4:157-161.
• Faria de Figueiredo A, Liehr T, Bhatt S, Binato R, Tavares de Souza M, Rodrigues Capela de Matos R, de Jesus Marques Salles T, Jordy FC, Ribeiro RC, Abdelhay E, Macedo Silva ML. A complex karyotype masked a cryptic variant t(8;21)(q22;q22) in a child with acute myeloid leukemia. Leuk Lymph 2011, 52:1593-1596.
• Garcia DRN, Bhatt S, Manvelyan M, de Souza MT, Binato R, Aguiar TF, Abdelhay E and Silva MLM. An unusual T-cell childhood acute lymphoblastic leukemia harboring a yet unreported near-tetraploid karyotype. Mol Cytogenet 2011, 4:20. Gerlach C, Roell D, Baniahmad A. Analysis of Ligand-Specific Co-repressor Binding to the Androgen Receptor. Methods Mol Biol 2011; 776:199-223.
• Gerlach C, Roell D, Baniahmad A. Analysis of Ligand-Specific Co-repressor Binding to the Androgen Receptor. Methods Mol Biol 2011, 776:199-223
• Gläßer N, Zellner K, Kromeyer-Hauschild K. Validity of body mass index and waist circumference to detect excess fat mass in children aged 7-14 years. Eur J Clin Nutr 2011, 65:151-159.
• Hentschel J, Rubio I, Eberhart M, Hipler C, Schiefner J, Schubert K, Loncarevic IF, Wittig U, Baniahmad A, von Eggeling F. BCR-ABL- and Ras-independent activation of Raf as a novel mechanism of Imatinib resistance in CML. Int J Oncol 2011; 39:585-591.
• Holl RW, Kersting M, Kromeyer-Hauschild K, Reinehr T, Schäfer A, Tiedjen U, Widhalm K. [Certification of therapy institutions, obesity trainers, and obesity trainer academies by the German Working Group on Obesity in Children and Adolescents (AGA).] Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz 2011, 54:598-602. German.
• Hong W, Li J, Wang B, Chen L, Niu W, Yao Z, Baniahmad A. Epigenetic involvement of Alien/ESET complex in thyroid hormone-mediated repression of E2F1 gene expression and cell proliferation. Biochem Biophys Res Commun, 2011 415:650-655.
• Horsthemke B, Wawrzik M, Groß S, Lich C, Sauer B, Rost I, Krasemann E, Kosyakova N, Liehr T, Weise A, Dybowski JN, Hoffmann D, Wieczorek D. Parental origin and functional relevance of a de novo UBE3A variant. Eur J Med Genet 20111, 54:19-24.
• Huebner AK, Gandia M, Frommolt P, Maak A, Wicklein EM, Thiele H, Altmüller J, Wagner F, Viñuela A, Aguirre LA, Moreno F, Maier H, Rau I, Gießelmann S, Nürnberg G, Gal A, Nürnberg P, Hübner CA, Del Castillo I, Kurth I. Nonsense mutations in SMPX, encoding a protein responsive to physical force, result in X-chromosomal hearing loss. Am J Hum Genet 2011, 88:621-627.
• Jain S, Kim HG, Lacbawan F, Meliciani I, Wenzel W, Kurth I, Sharma J, Schoeneman M, Ten S, Layman LC, Jacobson-Dickman E. Unique phenotype in a patient with CHARGE syndrome. Int J Pediatr Endocrinol 2011, 2011:11.
• Khalilov I, Chazal G, Chudotvorova I, Pellegrino C, Corby S, Ferrand N, Gubkina O, Nardou R, Tyzio R, Yamamoto S, Jentsch TJ, Hübner CA, Gaiarsa JL, Ben-Ari Y, Medina I. Enhanced Synaptic Activity and Epileptiform Events in the Embryonic KCC2 Deficient Hippocampus. Front Cell Neurosci 2011, 5:23.
• Klag T, Schnetzke U, Benz R, Zanow J, Glaser A, Pörner TC, Scholl S, Reiter A, Hochhaus A, La Rosée P. Leriche's syndrome and Löffler endocarditis in a 30-year-old patient presenting with hypereosinophilic syndrome. Ann Hematol. 2012, 91:139-141.
• Koch D, Spiwoks-Becker I, Sabanov V, Sinning A, Dugladze T, Stellmacher A, Ahuja R, Grimm J, Schüler S, Müller A, Angenstein F, Ahmed T, Diesler A, Moser M, Tom Dieck S, Spessert R, Boeckers TM, Fässler R, Hübner CA, Balschun D, Gloveli T, Kessels MM, Qualmann B. Proper synaptic vesicle formation and neuronal network activity critically rely on syndapin I, EMBO J 2011, 30:4955-4969.
• Kraoua L, Chaabouni M, Ewers E, Chelly I, Ouertani I, Jemaa LB, Maazoul F, Liehr T, Chaabouni H. Hexasomy of the Prader-Willi/Angelman critical region, including the OCA2 gene in a patient with pigmentary dysplasia: case report. Europ J Med Genet 2011, 54:e446-450.
• Kromeyer-Hauschild K, Dortschy R, Stolzenberg H, Neuhauser H, Rosario AS. Nationally representative waist circumference percentiles in German adolescents aged 11.0-18.0 years. Int J Pediatr Obes 2011; 6:e129-137.
• Lausch E, Janecke A, Bros M, Trojandt S, Alanay Y, De Laet C, Hübner CA, Meinecke P, Nishimura G, Matsuo M, Hirano Y, Tenoutasse S, Kiss A, Rosa RF, Unger SL, Renella R, Bonafé L, Spranger J, Unger S, Zabel B, Superti-Furga A. Genetic deficiency of tartrate-resistant acid phosphatase associated with skeletal dysplasia, cerebral calcifications and autoimmunity. Nat Genet 2011, 43:132-137.
• Liehr T. What is uniparental disomy (UPD)? [online] Oxford Gene Technology. Available at: http://www.ogt.co.uk/cytosure_whatisUPD.html
• Liehr T, Bartels I, Zoll B, Ewers E, Mrasek K, Kosyakova N, Merkas M, Hamid AB, von Eggeling F, Posorski N, Weise A. Is there a yet unreported unbalanced chromosomal abnormalities without phenotypic consequences in proximal 4p? Cytogenet Genome Res 2011, 132:121-123.
• Liehr T, Ewers E, Hamid AB, Kosyakova N, Voigt M, Weise A, Manvelyan M. Small supernumerary marker chromosomes and uniparental disomy have a story to tell. J Histochem Cytochem 2011; 59:842-848.
• Liehr T, Kosayakova N, Schröder J, Ziegler M, Kreskowski K, Pohle B, Bhatt S, Theuss L, Wilhelm K, Weise A, Mrasek K. Evidence for correlation of fragile sites and chromosomal breakpoints in carriers of constitutional balanced chromosomal rearrangements. Balk J Med Genet 2011, 14:13-16.
• Linke T, Scholten M, Baniahmad A. Detection of Ligand-Selective Interactions of the Human Androgen Receptor by SELDI-MS-TOF. Methods Mol Biol 2011; 776:225-251.
• Lorenz V, Hessenkemper W, Rödiger J, Kyrylenko S, Kraft F, Baniahmad A. Sodium butyrate induces cellular senescence in neuroblastoma and prostate cancer cells. Horm Mol Biol Clin Invest 2011, 7:265-272.
• Manolakos E, Vetro A, Kefalas K, Thomaidis L, Aperis G, Sotiriou S, Kitsos G, Merkas M, Sifakis S, Papoulidis I, Liehr T, Zuffardi O, Petersen MB. Deletion 2q31.2-q31.3 in a 4-year-old girl with microcephaly and severe mental retardation. Am J Med Genet A. 2011,155:1476-1482.
• Manvelyan M, Cremer FW, Lancé J, Kläs R, Kelbova C, Ramel C, Reichenbach H, Schmidt C, Ewers E, Kreskowski K, Ziegler M, Kosyakova N, Liehr T. New cytogenetically visible copy number variant in region 8q21.2. Mol Cytogenet 2011, 4:1.
• Melo JB, Backx L, Vermeesch JR, Santos HG, Duarte AC, Kosyakova N, Weise A, von Eggeling F, Liehr T, Carreira IM. Chromosome 5 derived small supernumerary marker: towards a genotype/phenotype correlation of proximal chromosome 5 imbalances. J Appl Genet 2011, 52:193-200.
• Miene C, Weise A, Glei M. Impact of polyphenol metabolites produced by colonic microbiota on expression of COX-2 and GSTT2 in human colon cells (LT97). Nutr Cancer 2011, 63:653-662.
• Milenkovic T, Guc-Scekic M, Zdravkovic D, Topic V, Liehr T, Joksic G, Radivojevic D, Lakic N. Molecular analysis of ring Y chromosome in a 10-year-old boy with mixed gonadal dysgenesis and growth hormone deficiency. Balk J Med Genet 2011, 14:71-75.
• Pan D, Kalfa TA, Wang D, Risinger M, Crable S, Ottlinger A, Chandra S, Mount DB, Hübner CA, Franco RS, Joiner CH. K-Cl cotransporter gene expression during human and murine erythroid differentiation. J Biol Chem 2011 , 286:30492-30503.
• Pellestor F, Puechberty J, Weise A, Lefort G, Anahory T, Liehr T, Sarda P. Meiotic segregation of complex reciprocal translocations: direct analysis of the spermatozoa of a t(5;13;14) carrier. Fertil Steril 2011, 95:2433.e17-2433.e22.
• Pellestor F, Anahory T, Lefort G, Puechberty J, Liehr T, Hédon B, Sarda P. Complex chromosomal rearrangements: origin and meiotic behavior. Hum Reprod Update 2011, 17:476-494.
• Pilchowski R, Stöhr R, von Eggeling F, Hartmann A, Wunderlich H, Junker K. Specific protein patterns characterize metastatic potential of advanced bladder cancer. J Urol 2001; 186:713-720.
• Posorski N, Kaemmerer D, Ernst G, Grabowski P, Hoersch D, Hommann M, von Eggeling F. Localization of sporadic neuroendocrine tumors by gene expression analysis of their metastases. Clin Exp Metastasis 2011, 28:637-647.
• Reeb CA, Gerlach C, Heinssmann M, Prade I, Ceraline J, Roediger J, Roell D, Baniahmad A. A designed cell-permeable aptamer-based corepressor Peptide is highly specific for the androgen receptor and inhibits prostate cancer cell growth in a vector-free mode. Endocrinology 2011, 152:2174-2183.
• Roell D, Baniahmad A. The natural compounds atraric acid and N-butylbenzene-sulfonamide as antagonists of the human androgen receptor and inhibitors of prostate cancer cell growth. Mol Cell Endocrinol 2011, 332:1-8.
• Roell D, Rösler TW, Degen S, Matusch R, Baniahmad A. Antiandrogenic activity of anthranilic acid ester derivatives as novel lead structures to inhibit prostate cancer cell proliferation. Chem Biol Drug Des 2011, 77:450-459.
• Sheth F, Andrieux J, Ewers E, Kosyakova N, Weise A, Sheth H, Romana SP, Lelorc'h M, Delobel B, Theisen O, Liehr T, Nampoothiri S, Sheth J. Characterization of sSMC by FISH and molecular techniques Europ J Med Genet 2011, 54:247-255.
• Sinning A, Liebmann L, Kougioumtzes A, Westermann M, Bruehl C, Hübner CA. Synaptic glutamate release is modulated by the Na+-driven Cl-/HCO formula exchanger Slc4a8. J Neurosci 2011, 31:7300-7311.
• Soares-Ventura EM, Mkrtchyan H, de Jesus Marques-Salles T, Silva M, Santos N, de Araujo Silva Amaral B, Liehr T, Abdelhay E, Macedo Silva ML, Cartaxo Muniz MT. Molecular cytogenetics reveals complex karyotype in apparent t(8;13) therapy-related acute myeloid leukemia M2 after fibrosarcoma. Leuk Res 2011, 35:e27-e29.
• Stuhrmann-Spangenberg M, Engels H, Fritz B, Gabriel H, Gläser D, Henn W, Liehr T, Miller K, Rieder H. S2-Leitlinie Humangenetische Diagnostik. medgen 2011 23:281-323
• Villa O, Mallo M, Kosyakova N, Salido M, Liehr T, Martínez-Avilés L, Pedro C, García-Aragonés M, Espinet B, Florensa L, Arenillas L, Cuscó I, Pérez Jurado LA, Solé F. Deletion of TET2 gene in an acute myeloid leukemia case with a t(4;15)(q24;q26) characterized by glass needle based chromosome microdissection and oligonucleotide array. Leuk Res 2011,35: e161- e163.
• Westrich V, Liehr T. Molecular cytogenetic approaches and array-diagnostics in prenatal medicine. MedGen 2011, 22:463-468.
• Woelfel C, Liehr T, Weise A, Langrehr J, Amin Kotb W, Pacyna-Gengelbach M, Katenkamp D, Petersen I. Molecular cytogenetic characterization of epithelioid hemangioendothelioma. Cancer Genetics 2011, 204:671-676.

Bücher/ Books

Book performance report

• Aktas D, Utine EG, Mrasek K, Weise A, von Eggeling F, Yalaz K, Posorski N, Akarsu N, Alikasifoglu M, Liehr T, Tuncbilek E. Derivative chromosome 1 and GLUT1 deficiency syndrome in a sibling pair Mol Cytogenetics 2010, 3:10.
• Al Achkar W, Wafa A, Mkrtchyan H, Moassas F, Liehr T. A rare case of chronic myeloid leukemia with secondary chromosomal changes including partial trisomy 17q21 to 17qter and partial monosomy of 16p13.3. Mol Cytogenet 2010, 3:6.
• Al Achkar W, Wafa A, Mkrtchyan H, Moassass F, Liehr T. A rare case of Philadelphia chromosome-positive chronic myelogenous leukemia with inversion in chromosome 9 and t(10;17). Oncol Lett 2010, 1:793-795.
• Al Achkar W, Wafa A, Ali BY, Manvelyan M, Liehr T. A rare chronic myeloid leukemia case with Philadelphia chromosome, BCR-ABL e13a3 transcript and complex translocation involving four different chromosomes. Oncol Lett 2010, 1:797-800.
• Al Achkar W, Wafa A, Mkrtchyan H, Moassass F, Liehr T. A unique complex translocation involving six different chromosomes in a case of childhood acute lymphoblastic leukemia with the Philadelphia chromosome and adverse prognosis. Oncol Lett 2010, 1:801-804.
• Al-Achkar W, Liehr T, Wafa A. Insertion of the 3' ABL region into the long arm of chromosome 1 in a Philadelphia chromosome-negativechronic myeloid leukemia case. Oncol Lett 2010, 1:951-954.
• Al Achkar W, Wafa A, Moassass F, Liehr T. Partial trisomy 9p22 to 9p24.2 in combination with partial monosomy 9pter in a Syrian girl. Mol Cytogenet 2010, 3:18.
• Al-Achkar W, Wafa A, Manvelyan M, Ikhtiar A, Liehr T. De novo translocation involving two chromosomes in adult prolymphocytic leukemia-A rare case. Leuk Res 2010, 34:e345-347
• Alexandrov T, Becker M, Deininger SO, Ernst G, Wehder L, Grasmair M, von EF, Thiele H, Maass P. Spatial Segmentation of Imaging Mass Spectrometry Data with Edge-Preserving Image Denoising and Clustering. J Proteome Res 2010, 9:6535-6546.
• Auber B, Burfeind P, Thiels C, Alsat EA, Shoukier M, Liehr T, Nelle H, Bartels I, Salinas-Riester G, Laccone F. An unbalanced translocation resulting in a duplication of Xq28 causes a Rett syndrome-like phenotype in a female patient. Clin Genet 2010, 77:593-597.
• Balci S, Yuksel Konuk B, Atik F, Oguz AK, Ergun MA, Baltaci V, Kosyakova N, Liehr T. Partial deletion of the long arm of chromosome 13 (q32q33.2) associated with mental retardation, choanal atresia and fish mouth. Genetic Counselling 2010, 21:317-324.
• Barber JC, Bunyan D, Curtis M, Robinson D, Morlot S, Dermitzel A, Liehr T, Alves C, Trindade J, Paramos AI, Cooper C, Ocraft K, Taylor E, Maloney VK. 8p23.1 duplication syndrome differentiated from copy number variation of the defensin cluster at prenatal diagnosis in four new families. Mol Cytogenet 2010, 3:3.
• Burégio-Frota P, Valença L, Leal GF, Duarte AR, Bispo-Brito AV, Soares-Ventura EM, Marques-Salles TJ, Nogueira MT, Muniz MT, Silva ML, Hunstig F, Liehr T, Santos N. Identification of a de novo inv dup(X)(pter->q22) by multicolor banding in a girl with Turner syndrome. Genet Mol Res 2010, 9:780-784.
• da Silva FE, Cordeiro AB, Nagamachi CY, Pieczarka JC, Rens W, Weise A, Liehr T, Mkrtchyan H, Anselmo NP, de Oliveira EHC. A case of aggressive medulloblastoma with multiple recurrent chromosomal alterations. Cancer Genet Cytogenet 2010, 196:198-200.
• de Figueiredo AF, Liehr T, Bhatt S, Binato R, Soares Ventura EM, de Souza MT, Rodrigues Capela de Matos R, Correa Ribeiro R, Abdelhay E, Macedo Silva ML. A new cryptic ins(11;1)(q23;q21q31) detected in a t(1;8;11)(q21;p21;q23) in a baby with acute myeloid leukemia FAB AML-M5. Blood Cells Mol Dis 2010, 45:197-198
• de Jesus Marques-Salles T, da Silva Barros JEX, Soares-Ventura EM, Cartaxo-Muniz MT, Santos N, Ferreira E, Macedo Silva ML, Liehr T, Mkrtchyan H. Unusual childhood biphenotypic acute leukemia with a yet unreported t(3;13)(p25.1;q13). Leuk Res 2010, 34: e206-e207.
• de Jesus Marques-Salles T, Mkrtchyan H, Pereira Leite E, Soares-Ventura EM, Cartaxo-Muniz MT, Ferreira E, Liehr T, Macedo Silva ML, Santos N. Complex karyotype defined by FISH and M-FISH studies in an infant with acute megakarioblastic leukemia and neurofibromatosis. Cancer Genet Cytogenet 2010, 200: 167-169.
• Dittmar Y, Posorski N, Rauchfuss F, Voigt R, Heise M, Jandt K, Gajda M, Settmacher U. Relationship between degree of chromosomal aberration and survival in intestinal-type gastric cancer - a preliminary report based on three cases of hepatic metastasized gastric cancer with long-time survival. Onkologie 2010, 33:591-596.
• Egritas O, Cavdarli B, Dalgic B, Ergun MA, Percin F, Ziegler M, Pohle B, Liehr T. Duplication 4q associated with chronic cholestatic changes in liver biopsy. Eur J Med Genet 2010, 53:411-414.
• Escher N, Ernst G, Melle C, Berndt A, Clement JH, Junker K, Friedrich K, Guntinas-Lichius O, von Eggeling F. Comparative proteomic analysis of normal and tumor stromal cells by tissue on chip based mass spectrometry (toc-MS). Diagn Pathol 2010, 5:10.
• Ewers E, Yoda K, Hamid AB, Weise A, Manvelyan M, Liehr T. Centromere activity in dicentric small supernumerary marker chromosomes. Chromosome Research 2010; 18:555-562.
• Fernández-Toral J, Rodríguez L, Plasencia A, Martínez-Frías ML, Ewers E, Hamid AB, Ziegler M, Liehr T. Four small supernumerary marker chromosomes derived from chromosomes 6, 8, 11 and 12 in a patient with minimal clinical abnormalities - a case report. J Med Case Reports 2010, 4:239.
• Ferreira SI, Matoso E, Pinto M, Almeida J, Liehr T, Melo JB, Carreira IM. X-chromosome terminal deletion in a female with premature ovarian failure: Haploinsufficiency of X-linked genes as a possible explanation. Mol Cytogenet 2010, 3:14.
• Fousteris MA, Schubert U, Roell D, Roediger J, Bailis N, Nikolaropoulos SS, Baniahmad A, Giannis A. 20-Aminosteroids as a novel class of selective and complete androgen receptor antagonists and inhibitors of prostate cancer cell growth. Bioorg Med Chem 2010, 18:6960-6969.
• Gersak K, Writzl K, Veble A, Liehr T. Primary amenorrhoea in a patient with mosaicism for monosomy X and a derivative X-chromosome. Genet Couns 2010, 21:335-342.
• Gorsler T, Murzik U, Ulbricht T, Hentschel J, Hemmerich P, Melle C. DNA damage-induced translocation of S100A11 into the nucleus regulates cell proliferation. BMC Cell Biol 2010, 11:100.
• Jung MJ, Murzik U, Wehder L, Hemmerich P, Melle C. Regulation of cellular actin architecture by S100A10. Exp Cell Res 2010, 316:1234-1240.
• Karaer K, Ergun MA, Weise A, Ewers E, Liehr T, Kosyakova N, Mkrtchyan H. The case of an infertile male with an uncommon reciprocal X-autosomal translocation: how does this affect male fertility? Genet Couns 2010, 21:397-404
• Kim HG, Ahn JW, Kurth I, Ullmann R, Kim HT, Kulharya A, Ha KS, Itokawa Y, Meliciani I, Wenzel W, Lee D, Rosenberger G, Ozata M, Bick DP, Sherins RJ, Nagase T, Tekin M, Kim SH, Kim CH, Ropers HH, Gusella JF, Kalscheuer V, Choi CY, Layman LC. WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome. Am J Hum Genet 2010, 87:465-479.
• Ktistaki E, Garefalaki A, Williams A, Andrews SR, Bell DM, Foster KE, Spilianakis CG, Flavell RA, Kosyakova N, Trifonov V, Liehr T, Kioussis D. CD8 locus nuclear dynamics during thymocyte development. J Immunol 2010, 184:5686-5695.
• Kyrylenko S, Baniahmad A. Sirtuin family: a link to metabolic signaling and senescence. Curr Med Chem 2010, 17:2921-2932.
• Li Z, Zhang Q, Mao J-H, Weise A, Mrasek K, Fan X, Zhang X, Liehr T, Lu KH, Balmain A, Cai W-W. A HDAC1-binding domain within FATS bridges p21 turnover to radiation-induced tumorigenesis. Oncogene 2010, 29:2659-2671.
• Liehr T. Cytogenetic contribution to uniparental disomy (UPD). Mol Cytogenet 2010, 3:8.
• Liehr T. A new internet page on uniparental disomy. ECA-newsletter 2010, 26:22-24
• Liehr T, Kosyakova N, Weise A, Ziegler M, Raabe-Meyer G. First case of a neocentromere formation in an otherwise normal chromosome 7. Cytogenet Genome Res 2010, 218: 189-191.
• Liehr T, Wegner R-D, Stumm M, Martin T, Gillessen-Kaesbach G, Kosyakova N, Ewers E, Hamid AB, von Eggeling F, Hentschel J, Ziegler M, Weise A. Three new cases with small supernumerary marker chromosomes 1 and normal phenotype. J Chin Med Assoc 2010, 73: 205-207.
• Liehr T, Karamysheva T, Merkas M, Brecevic L, Hamid AB, Ewers E, Mrasek K, Kosyakova N, Weise A. Somatic mosaicism in cases with small supernumerary marker chromosomes. Curr Genomics 2010, 11:432-439
• Manolakis E, Peitsidis P, Elefteriades M, Dedoulis E, Ziegler M, Orru S, Liehr T, Petersen MB. Prenatal detection of full monosomy 21 in a fetus with an increased nuchal translucency. Molecular cytogenetic analysis and review of the literature. J Obstet Gynaecol Res 2010, 36: 435-440.
• Manolakos E, Kefalas K, Neroutsou R, Lagou M, Kosyakova N, Ewers E, Ziegler M, Weise A, Tsoplou P, Rapti S-M, Papoulidis I, Anastasakis E, Garas A, Sotiriou S, Eleftheriades M, Peitsidis P, Μalathrakis D, Thomaidis L, Kitsos G, Orru S,Liehr T, Petersen MB, Kitsiou-Tzeli S. Characterization of 23 small supernumerary marker chromosomes detected at pre-natal diagnosis: The value of fluorescence in situ hybridization Mol Med Rep 2010, 3:1015-1022.
• Manolakos E, Vetro A, Kefalas K, Rapti SM, Louizou E, Garas A, Kitsos G, Vasileiadis L, Tsoplou P, Eleftheriades M, Peitsidis P, Orru S, Liehr T, Petersen MB, Thomaidis L. The use of array-CGH in a cohort of Greek children with developmental delay. Mol Cytogenet 2010, 3:22.
• Mkrtchyan H, Garcia Ney DR, de Ventura ES, Liehr T, Felix GR, de Jesus Marques-Salles T, Abdelhay E, Macedo Silva ML. Molecular cytogenetic studies characterize near-triploid complex karyotype in a child with acute lymphoblastic leukemia. Cancer Genet 2010, 197:71-74.
• Mkrtchyan H, Gross M, Hinreiner S, Polytiko A, Manvelyan M, Mrasek K, Kosyakova N, Ewers E, Nelle H, Liehr T, Volleth M, Weise A. Early embryonic chromosome instability results in stable mosaic pattern in human tissues. PLoS ONE 2010, 5: e9591.
• Mkrtchyan H, Gross M, Hinreiner S, Polytiko A, Manvelyan M, Mrasek K, Kosyakova N, Ewers E, Nelle H, Liehr T, Bhatt S, Thoma K, Gebhart E, Wilhelm S, Fahsold R, Volleth M, Weise A. The human genome puzzle - the role of copy number variation in somatic mosaicism. Curr Genomics 2010, 11:426-431.
• Mrasek K, Schoder C, Teichmann AC, Behr K, Franze B, Wilhelm K, Blaurock N, Claussen U, Liehr T, Weise A. Global screening and extended nomenclature for 230 aphidicolin-inducible fragile sites, including 61 yet unreported ones. Int J Oncol 2010,36:929-40.
• Nelle H, Schreyer I, Ewers E, Mrasek K, Kosyakova N, Merkas M, Hamid AB, Weise A, Liehr T. Harmless familial small supernumerary marker chromosome 22 hampers diagnosis of fragile X-syndrome. Molecular Medicine Reports 2010, 3:571-574.
• Niksic SB, Deretic VI, Pilic GR, Ewers E, Merkas M, Ziegler M, Liehr T. Trisomy 21 with a small supernumerary marker chromosome derived from chromosomes 13/21 and 18. Balk J Med Genet 2010, 13:55-58.
• Papaioannou M, Schleich S, Roell D, Schubert U, Tanner T, Claessens F, Matusch R, Baniahmad A. NBBS isolated from Pygeum africanum bark exhibits androgen antagonistic activity, inhibits AR nuclear translocation and prostate cancer cell growth. Invest New Drugs, 28:729-743.
• Papoulidis I, Manolakos E, Siomou E, Kefalas K, Thomaidis L, Liehr T, Vetro A, Athanasiadis A, Zuffardi O, Petersen MB. A fetus with ring chromosome 21 characterized by aCGH shows no clinical findings after birth. Prenat Diag 2010, 30:586-588.
• Polityko A, Khurs O, Rumyantseva N, Naumchik I, Kosyakova N, Tönnies H, Sperling K, Neitzel H, Weise A, Liehr T. Two siblings with immunodeficiency, facial abnormalities and chromosomal instability without mutation in DNMT3B gene but liability towards malignancy; a new chromatin disorder delineation? Mol Cytogenet 2010, 3:5
• Santos M, Mrasek K, Madrigal I, Martorell MR, González-Meneses A, Rodríguez-Criado G, Milŕ M, Liehr T, Fuster C. Characterisation of a complex cryptic mosaicism for an sSMC derived from the X chromosome present in a boy with congenital malformations. Am J Med Genet 2010, 152A:2161-2163.
• Schaffrath Rosario A, Kurth BM, Stolzenberg H, Ellert U, Neuhauser H. Body mass index percentiles for children and adolescents in Germany based on a nationally representative sample (KiGGS 2003-2006). Eur J Clin Nutr 2010, 64:341-349.
• Schoder C, Liehr T, Velleuer E, Wilhelm K, Blaurock N, Weise A, Mrasek K. New aspects on chromosomal instability: chromosomal break-points in Fanconi anemia patients co-localize on the molecular level with fragile sites. Int J Oncol 2010, 36:307-312
• Soehn AS, Franck T, Biskup S, Giaime E, Melle C, Rott R, Cebo D, Kalbacher H, Ott E, Pahnke J, Meitinger T, Krüger R, Gasser T, Berg D, von Eggeling F, Engelender S, da Costa CA, Riess O. Periphilin is a novel interactor of synphilin-1, a protein implicated in Parkinson's disease. Neurogenetics 2010, 11:203-215.
• Trifonov VA, Kosyakova N, Romanenko SA, Graphodatsky AS, Liehr T. New insights into the karyotypic evolution in muroid rodents revealed by multicolor banding applying murine probes. Chr Res 2010, 18:265-275.
• Uz E, Alanay Y, Aktas D, Vargel I, Gucer S, Tuncbilek G, von Eggeling F, Yilmaz E, Deren O, Posorski N, Ozdag H, Liehr T, Balci S, Alikasifoglu M, Wollnik B, Akarsu NK. Disruption of paired-tail homeobox gene ALX1 (Cart1) causes Extreme microphthalmia and severe facial clefting: expanding the spectrum of autosomal recessive ALX-related frontonasal dysplasia. Am J Hum Genet 2010, 86:789-796.
• Walter M, Heinze C, Steiner T, Pilchowski R, von Eggeling F, Wunderlich H, Junker K. Immunochemotherapy-associated protein patterns in tumour tissue and serum of patients with metastatic renal cell carcinoma. Arch Physiol Biochem 2010, 116:197-207.
• Wehder L, Ernst G, Crecelius AC, Guntinas-Lichius O, Melle C, Schubert US, von Eggeling F. Depicting the spatial distribution of proteins in human tumor tissue combining SELDI and MALDI imaging and immunohistochemistry. J Histochem Cytochem 2010, 58:929-937.
• Weise A, Timmermann B, Grabherr M, Werber M, Heyn P, Kosyakova N, Liehr T, Neitzel H, Konrat K, Bommer C, Dietrich C, Rajab A, Reinhardt R, Mundlos S, Lindner TH, Hoffmann K. High-throughput sequencing of microdissected chromosomal regions. Eur J Hum Genet 2010, 18:457-462.

• Al Achkar W, Wafa A, Mkrtchyan H, Moassass F, Liehr T. Novel complex translocation involving 5 different chromosomes in a chronic myeloid leukemia with Philadelphia chromosome: a case report. Mol Cytogenet 2009, 2:21
• Aktas D, Weise A, Utine E, Alehan D, Mrasek K, Eggeling FV, Thieme H, Tuncbilek E, Liehr T. Clinically abnormal case with paternally derived partial trisomy 8p23.3 to 8p12 including maternal isodisomy of 8p23.3: a case report. Mol Cytogenet 2009, 2:14.
• Auber B, Bruemmer V, Zoll B, Burfeind P, Boehm D, Liehr T, Brockmann K, Willichowski E, Argyriou L, Bartels I. Identification of subtelomeric genomic imbalances and breakpoint mapping with quantitative PCR in 296 individuals with congenital defects and/or mental retardation. Mol Cytogenet 2009, 2:10.
• Aurich H, Sgodda M, Kaltwaßer P, Vetter M, Weise A, Liehr T, Brulport M, Hengstler JG, Dollinger MM, Fleig WE, Christ B. Hepatocyte differentiation of mesenchymal stem cells from human adipose tissue in vitro promotes hepatic integration in vivo. Gut 2009; 58:570-581.
• Barros Cordeiro AP, da Silva FPE, Pieczarka JC, Nagamachi CY, Anselmo NP, Brito JR, Vasconcelos DS, Liehr T, Weise A, de Oliveira EHC. Comparative analysis of proliferative and genetic alterations in a primary chordoid meningioma and its recurrent case using locus-specific probes and AgNOR. Mol Med Rep 2009, 2:449-454.
• Bhatt S, Moradkhani K, Mrasek K, Puechberty J, Manvelyan M, Hunstig F, Lefort G, Weise A, Lespinasse J, Sarda P, Liehr T, Hamamah S, Pellestor F. Breakpoint mapping and complete analysis of meiotic segregation patterns in three men heterozygous for paracentric inversions. Eur J Hum Genet 2009, 17:44-50.
• Bindl R, Bruchhaus H. Untersuchungen zur histologischen Sterbealterschätzung. Beiträge zur Archäozoologie und Prähistorischen
  Anthropologie, 2009, VII:107-12.
• Carreira IM, Melo JB, Rodrigues C, Backx L, Vermeesch J, Weise A, Kosyakova N, Oliveira G, Matoso E. Molecular cytogenetic characterisation of a mosaic add(12)(p13.3) with an inv dup(3)(q26.31->qter) detected in an autistic boy. Molecular Cytogenetics 2009, 2:16.
• Dahse R, Driemel O, Schwarz S, Dahse J, Kromeyer-Hauschild K, Berndt A, Kosmehl H. Epidermal growth factor receptor kinase domain mutations are rare in salivary gland carcinomas. Br J Cancer 2009, 100:623-625.
• Dahse R, Driemel O, Schwarz S, Kromeyer-Hauschild K, Berndt A, Kosmehl H. KRAS status and epidermal growth factor receptor expression as determinants for anti-EGFR therapies in salivary gland carcinomas. Oral Oncol. 2009;45:826-829.
• Dahse R, Kromeyer-Hauschild K, Berndt A, Kosmehl H. No incidence of BRAF mutations in salivary gland carcinomas--implications for anti-EGFR therapies. J Biomed Biotechnol. 2009, 2009:501736.
• de Figueiredo AF, Mkrtchyan H, Liehr T, Soares Ventura EM, de Jesus Marques-Salles T, Santos N, Ribeiro RC, Abdelhay E, Macedo Silva ML. A case of childhood acute myeloid leukemia AML (M5) with a neocentric chromosome neo(1)(qter-->q23 approximately 24::q23 approximately 24-->q43-->neo-->q43-->qter) and tetrasomy of chromosomes 8 and 21. Cancer Genet Cytogenet 2009, 193:123-126.
• de Jesus Marques-Salles T, Liehr T, Mkrtchyan H, Raimondi SC, Tavares de Souza M, Faria de Figueiredo A, Rouxinol S, Jordy Macedo FC, Abdelhay E, Santos N, Macedo Silva ML. A new chromosomal three-way rearrangement involving MLL masked by a t(9;19)(p11;p13) in an infant with acute myeloid leukemia. Cancer Genet Cytogenet. 2009, 189:59-62.
• Eisold M, Asim M, Eskelinen H, Linke T, Baniahmad A. Inhibition of MAPK-signaling pathway promotes the interaction of the corepressor SMRT with the human androgen receptor and mediates repression of prostate cancer cell growth in the presence of antiandrogens. J Mol Endocrinol 2009, 42:429-435.
• Ergul E, Liehr T, Mrasek K, Sazci A. A de novo complex chromosome rearrangement involving three chromosomes (2, 13, and 18) in an oligospermic male. Fertil Steril 2009, 92:391.e9-391.e12.
• Erlecke J, Hartmann I, Hoffmann M, Kroll T, Starke H, Heller A, Gloria A, Sayer HG, Johannes T, Claussen U, Liehr T, Loncarevic IF. Automated detection of residual cells after sex-mismatched stem-cell transplantation - evidence for presence of disease-marker negative residual cells. Mol Cytogenet 2009, 2:12.
• Gallagher A, Gunther MM, Bruchhaus H. Population continuity, demic diffusion and Neolithic origins in central-southern Germany: the evidence from body proportions. Homo. 2009;60:95-126.
• Gross M, Mkrtchyan H, Glaser M, Fricke HJ, Höffken K, Heller A, Weise A, Liehr T. Delineation of yet unknown cryptic subtelomere aberrations in 50% of acute myeloid leukemia with normal GTG-banding karyotype. Int J Oncol 2009, 34:417-423.
• Hong W, Baniahmad A, Li J, Chang C, Gao W, Liu Y. Bag-1M inhibits the transactivation of the glucocorticoid receptor via recruitment of corepressors. FEBS Lett. 2009,583:2451-2456.
• Iourov IY, Vorsanova SG, Liehr T, Yurov YB. Aneuploidy in the normal, Alzheimer's disease and ataxia-telangiectasia brain: differential expression and pathological meaning. Neurobiol Dis 2009, 34:212-220.
• Iourov IY, Vorsanova SG, Liehr T, Kolotii AD, Yurov YB. Increased chromosome instability dramatically disrupts neural genome integrity and mediates cerebellar degeneration in the ataxia-telangiectasia brain. Hum Mol Genet. 2009;18:2656-2669.
• Kitsiou-Tzeli S, Manolakos E, Lagou M, Anagnostopoulou K, Kontodiou M, Kosyakova N, Ewers E, Weise A, Garas A, Orru S, Liehr T, Metaxotou A. Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male. Mol Cytogenet 2009, 2:1/ 2:8.
• Kob R, Kelm J, Posorski N, Baniahmad A, von Eggeling F, Melle C. Regulation of the anaphase-promoting complex by the COP9 signalosome. Cell Cycle 2009; 8:2041-2049.
• Korsten-Reck U, Korsten K, Kreuser F, Wölker U, Etzold D, Berg A, Dickhuth HH, Kromeyer-Hauschild K. Das Freiburger Interventionsprogramm FITOC. Adipositas 2009, 3:11-16.
• Korsten-Reck U, Korsten K, Haeberle K, Kromeyer-Hauschild K, Dickhuth HH, Schulz E. The psychosocial situation of obese children: Psychological factors and quality of life. Psychology Research and Behavior Managment 2009, 2:23-29.
• Kosyakova N, Weise A, Mrasek K, Claussen U, Liehr T, Nelle H. The hierarchically organized splitting of chromosomal bands for all human chromosomes. Mol Cytogenet 2009, 2:4.
• Korsten-Reck U, Korsten K, Haeberle K, Kromeyer-Hauschild K, Dickhuth HH, Schulz E. The psychosocial situation of obese children: Psychological factors and quality of life. Psychology Research and Behavior Managment 2009, 2:23-29.
• Liehr T. The internet page on small supernumerary marker chromosomes (sSMC). ECA Newsletter 2009, 23:10-14.
• Liehr T. Small supernumerary marker chromosomes (sSMC) - a spotlight on some nomenclature problems. J Histochem Cytochem 2009, 57:991-993.
• Liehr T, Stumm M, Wegner R-D, Bhatt S, Hickmann P, Patsalis PC, Meins M, Morlot S, Klaschka V, Ewers E, Hinreiner S, Mrasek K, Kosyakova N, Cai WW, Cheung SW, Weise A. 10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences. Cytogenet Genome Res 2009, 24:102-105.
• Liehr T, Ewers E, Kosyakova N, Klaschka V, Rietz F, Wagner R, Weise A. Handling small supernumerary marker chromosomes in prenatal diagnostics. Expert Rev Mol Diagn. 2009, 9:317-324.
• Macedo Silva ML, do Socorro Pombo-de-Oliveira M, Raimondi SC, Liehr T, Abdelhay E, Faria de Figueiredo A, Tavares de Souza M, Ribeiro Ney Garcia D, Maria Soares de Ventura E, Martins de Sousa A, Mkrtchyan H. Unbalanced chromosome 1 abnormalities in four infants with Down syndrome and acute megakaryocytic leukemia. Mol Cytogenet 2009, 2:7.
• Manolakos E, Vetro A, Kitmirides S, Papoulidis I, Kosyakova N, Mrasek K, Weise A, Agapitos E, Orru S, Peitsidis P, Liehr T, Petersen MB. Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array-CGH. Prenat Diagn. 2009, 29:884-888.
• Manvelyan M, Kempf P, Weise A, Mrasek K, Heller A, Lier A, Höffken K, Fricke H-J, Sayer HG, Liehr T, Mkrtchyan H. Preferred co-localization of chromosome 8 and 21 in myeloid bone marrow cells detected by three dimensional molecular cytogenetics. Int J Mol Med 2009, 24:335-341.
• Melle C, Ernst G, Winkler R, Schimmel B, Klussmann JP, Wittekindt C, Guntinas-Lichius O, von Eggeling F. Proteomic analysis of human papillomavirus-related oral squamous cell carcinoma: Identification of thioredoxin and epidermal-fatty acid binding protein as upregulated protein markers in microdissected tumor tissue. Proteomics 2009, 9:2193-2201.
• Melle C, Ernst G, Grosheva M, Angelov DN, Irintchev A, Guntinas-Lichius O, von Eggeling F. Proteomic analysis of microdissected facial nuclei of the rat following facial nerve injury. J Neurosc Meth 2009, 185:23-28.
• Melo JB, Matoso E, Polityko A, Saraiva J, Backx L, Vermeesch JR, Kosyakova N, Ewers E, Liehr T, Carreira IM. Molecular cytogenetic characterization of two cases with de novo small mosaic supernumerary marker chromosomes derived from chromosome 16: towards a genotype/phenotype correlation. Cytogenet Genome Res 2009, 125:109-114.
• Mkrtchyan H, Scheler S, Klein I, Fahr A, Couraud P-O, Romero IA, Weksler B, Liehr T. Molecular cytogenetic characterization of the human cerebral microvessel endothelial cell line hCMEC/D3. Cytogenet Genome Res 2009; 126:313-317.
• Polityko AD, Khurs OM, Kulpanovich AI, Mosse KA, Solntsava AV, Rumyantseva NV, Naumchik IV, Liehr T, Weise, Mkrtchyan H. Paternally derived der(7)t(Y;7)(p11.1~11.2;p22.3)dn in a mosaic case with Turner syndrome. Europ J Med Gen 2009,52:207-210.
• Polityko A, Khurs O, Liehr T. Human genomic disorders. Analysis of 22q11. Proceedings of the Institute of Genetics and Cytology of National Academy of Sciences Belarus, Minsk, Special issue "Molecular and applied genetics" 2009; 10:80-88 (Russian).
• Sheth F, Ewers E, Kosyakova N, Weise A, Sheth J, Patil S, Ziegler M, Liehr T. A neocentric isochromosome Yp present as additional small supernumerary marker chromosome--evidence against U-type exchange mechanism? Cytogenet Genome Res. 2009, 125:115-116.
• Schreyer I, Hampel P. [ADHD among boys in childhood: quality of life and parenting behavior] Z Kinder Jugendpsychiatr Psychother. 2009, 37:69-75.
• Sheth F, Ewers E, Kosyakova N, Weise A, Sheth J, Desai M, Andrieux J, Vermeesch J, Hamid AB, Ziegler M, Liehr T. A small supernumerary marker chromosome present in a Turner syndrome patient not derived from X- or Y-chromosome. Mol Cytogenet 2009, 2:22.
• Soysal Y, Balci S, Hekimler K, Liehr T, Ewers E, Schoumans J, Bui TH, Içduygu FM, Kosyakova N, Imirzalıoğlu N. Characterization of double ring chromosome 4 mosaicism associated with bilateral hip dislocation, cortical dysgenesis, and epilepsy. Am J Med Gen A 2009, 149A:2782-2787.
• Tzschach A, Ramel C, Kron A, Seipel B, Wüster C, Cordes U, Liehr T, Hoeltzenbein M, Menzel C, Ropers HH, Ullmann R, Kalscheuer V, Decker J, Steinberger D. Hypergonadotropic hypogonadism in a patient with inv ins (2;4). Int J Androl 2009, 32:226-230.
• Uroz L, Liehr T, Mrasek K, Templado C. CenM-FISH on human spermatocyte I and II metaphases. Hum Reprod 2009, 24:2029-2033.
• Wehder L, Arndt S, Murzik U, Bosserhoff AK, Kob R, von Eggeling F, Melle C. Annexin A5 is involved in migration and invasion of oral carcinoma. Cell Cycle 2009, 8:1-7.
• Weise A, Mrasek K, Ewers E, Mkrtchyan H, Kosyakova N, Liehr T. Diagnostic applications of fluorescence in situ hybridization. Expert Opin Med Diagn 2009, 3:453-460.
• Winklmeier A, Contreras-Shannon V, Arndt S, Melle C, Bosserhoff AK. Cadherin-7 interacts with melanoma inhibitory activity protein and negatively modulates melanoma cell migration. Cancer Sci 2009, 100:261-268.
• Würbach A, Zellner K, Kromeyer-Hauschild K. Meal patterns among children and adolescents and their associations with weight status and parental characteristics. Public Health Nutr 2009, 26:1-7.
• Zellner K, Ulbricht G, Kromeyer-Hauschild K. Langzeittendenzen des Body Mass Index und der Energieaufnahme bei Jenaer Schulkindern. Ernährungsumschau 2009; 56: 667ff.

Bücher/ Books

note added in June 2013

Since its online publication on Nov 18, 2008, there has been a total of 16397 chapter downloads for this book on SpringerLink. Over the last year(s) the download figures have been as follows:

Chapter Downloads

2012: 2863

2011: 3949

2010: 4652

2009: 4281

This means this book was one of the top 25% most downloaded eBooks in the relevant Springer eBook Collection in 2012. This book has also been made available as an Amazon Kindle eBook version. To make it findable by search engines, the book has its own homepage.

• Asim M, Siddiqui IA, Hafeez BB, Baniahmad A, Mukhtar H. Src kinase potentiates androgen receptor transactivation function and invasion of androgen-independent prostate cancer C4-2 cells. Oncogene 2008, 27:3596-3604.
• Balikova I, Martens K, Melotte C, Amyere M, Van Vooren S, Moreau Y, Vetrie D, Fiegler H, Carter NP, Liehr T, Vikkula M, Matthijs G, Fryns JP, Casteels I, Devriendt K, Vermeesch JR. Autosomal-dominant microtia linked to five tandem copies of a copy-number-variable region at chromosome 4p16. Am J Hum Genet 2008, 82:181-187.
• Ebert B, Melle C, Lieckfeldt E, Zöller D, von Eggeling F, Fisahn J. Protein profiling of single epidermal cell types from Arabidopsis thaliana using surface-enhanced laser desorption and ionization technology. J Plant Physiol 2008, 165:1227-1237.
• Garwe F, Bauerschäfer U, Csaki A, Steinbrück A, Ritter K, Bochmann A, Bergmann J, Weise A, Akimov D, Maubach G, König K, Hüttmann G, Paa W, Popp J, Fritzsche W. Optically controlled thermal management on the nanometer length scale. Nanotechnology 2008, 19: 055207 (12pp)
• Goeman F, Otto K, Kyrylenko S, Schmidt O, Baniahmad A. ING2 recruits histone methyltransferase activity with methylation site specificity distinct from histone H3 lysines 4 and 9. Biochim Biophys Acta 2008, 1783:1673-1680.
• Hermanussen M, Tutkuviene J, Cesnys G, Lindeberg S, Kromeyer-Hauschild K, Stanley G, Godina E, Bogin B, Varela-Silva MI, Finlayson G, Rühli F, Woitek U, Tresguerres JA, Lieberman LS, Detel W. The role of taste and appetite regulation in the understanding of overweight and obesity. Georgian Med News 2008, 159:34-39.
• Hong W, Baniahmad A, Liu Y, Li H. Bag-1M is a component of the in vivo DNA-glucocorticoid receptor complex at hormone-regulated promoter. J Mol Biol 2008, 384:22-30.
• Hovhannisyan GG, Mkrtchyan H, Liehr T, Aroutiounian R. Distribution of the chromosomes X, 7 and 18 in mitomycin C induced micronuclei. Balk J Med Gen 2008:45-49.
• Iourov IY, Vorsanova SG, Liehr T, Monakhov VV, Soloviev IV, Yurov YB Dynamic mosaicism manifesting as loss, gain and rearrangement of an isodicentric Y chromosome in a male child with growth retardation and abnormal external genitalia. Cytogenet Genome Res 2008, 121:302-306.
• Karadeniz N, Mrasek K, Weise A. Further delineation of complex chromosomal rearrangements in fertile male using multicolor banding. Mol Cytogenet 2008, 7;1:17.
• Kilian O, Dahse R, Alt V, Zardi L, Hentschel J, Schnettler R, Kosmehl H. mRNA Expression and Protein Distribution of Fibronectin Splice Variants and High-Molecular Weight Tenascin-C in Different Phases of Human Fracture Healing. Calcif Tissue Int. 2008 Jul 29. [Epub ahead of print]
• Koç A, Kan D, Karaer K, Ergün MA, Karaoğuz MY, Gücüyener K, Hinreiner S, Liehr T, Perçin EF. An unexpected finding in a child with neurological problems: mosaic ring chromosome 18. Eur J Pediatr 2008, 167:655-659.
• Korsten-Reck U, Kromeyer-Hauschild K, Korsten K, Baumstark MW, Dickhuth HH, Berg A. Frequency of secondary dyslipidemia in obese children. Vasc Health Risk Manag 2008; 4:1089-1094.
• Kromeyer-Hauschild K, Gläßer N, Zellner K. Perzentile für den Taillenumfang von Jenaer Kindern im Alter von 6 bis 18 Jahren. Aktuelle Ernährungsmedizin 2008, 33:116-122.
• Lian J, Yin Y, Oliver-Bonet M, Liehr T, Ko E, Turek P, Sun F, Martin RH. Variation in crossover interference levels on individual chromosomes from human males. Hum Mol Genet 2008, 17:2583-2594.
• Liehr T. Characterization of prenatally assessed de novo small supernumerary marker chromosomes by molecular cytogenetics. Methods Mol Biol 2008, 444:27-38.
• Liehr T. The multicolor fluorescence in situ hybridization (mFISH) homepage. Balk J Med Gen 2008; 11:27-31.
• Liehr T. Multicolor-fluorescence in situ hybridization - Molecular cytogenetics in nowadays diagnostics and research. Med Gen 2008, 20:374-378 (German)
• Liehr T, Mrasek K, Kosyakova N, Ogilvie CM, Vermeesch J, Trifonov V, Rubtsov N. Small supernumerary marker chromosomes (sSMC) in humans; are there B chromosomes hidden among them. Mol Cytogenet 2008, 4;1:12.
• Liehr T, Wegner R-D, Stumm M, Joksi G, Polityko A, Kosyakova N, Ewers E, Reich D, Wagner R, Weise A. Pallister-Killian syndrome. Rare phenotypic features and variable karyotypes. Balk J Med Gen 2009:65-67
• Loncarevic IF, Hering A, Posorski N, Linden T, Hoyer H, Bucsky P. Number of genomic imbalances correlates with the overall survival for adrenocortical cancer in childhood. Pediatr Blood Cancer 2008, 51:356-362.
• Macedo Silva ML, Raimondi SC, Abdelhay E, Gross M, Mkrtchyan H, de Figueiredo AF, Ribeiro RC, de Jesus Marques-Salles T, Sobral ES, Gerardin Land MP, Liehr T. Banding and molecular cytogenetic studies detected a CBFB-MYH11 fusion gene that appeared as abnormal chromosomes 1 and 16 in a baby with acute myeloid leukemia FAB M4-Eo. Cancer Genet Cytogenet 2008, 182:56-60.
• Manolakos E, Kosyakova N, Thomaidis L, Neroutsou R, Weise A, Mihalatos M, Orru S, Kokotas H, Kitsos G, Liehr T, Petersen M. Complex chromosome rearrangement in a child with microcephaly, dysmorphic facial features and mosaicism for a terminal deletion del(18)(q21.32-qter) investigated by FISH and array-CGH. Mol Cytogenet 2008 1:24.
• Manvelyan M, Riegel M, Santos M, Fuster C, Pellestor F, Mazauric ML, Schulze B, Polityko A, Tittelbach H, Reising-Ackermann G, Belitz B, Hehr U, Kelbova C, Volleth M, Gödde E, Anderson J, Küpferling P, Köhler S, Duba HC, Dufke A, Aktas D, Martin T, Schreyer I, Ewers E, Reich D, Mrasek K, Weise A, Liehr T. 32 new cases with small supernumerary marker chromosomes (sSMC) detected in connection with fertility problems - detailed molecular cytogenetic characterization and review of the literature. Int J Mol Med 2008, 21:705-714.
• Manvelyan M, Hunstig F, Mrasek K, Bhatt S, Pellestor F, Weise A, Liehr T. Position of chromosomes 18, 19, 21 and 22 in 3D-preserved interphase nuclei of human and gorilla and white hand gibbon. Mol Cytogenet 2008, 1:9.
• Manvelyan M, Hunstig F, Bhatt S, Mrasek K, Pellestor F, Weise A, Simonyan I, Aroutiounian R, Liehr T. Chromosome distribution in human sperm - a 3D multicolor banding-study. Mol Cytogenet. 2008, 1:25.
• Meigen C, Keller A, Gausche R, Kromeyer-Hauschild K, Blüher S, Kiess W, Keller E. Secular trends in body mass index in German children and adolescents: a cross-sectional data analysis via CrescNet between 1999 and 2006. Metabolism 2008, 57:934-993.
• Melle C, Ernst G, Schimmel B, Bleul A, von Eggeling F. Colon-Derived Liver Metastasis, Colorectal Carcinoma, and Hepatocellular Carcinoma Can Be Discriminated by the Ca2+-Binding Proteins S100A6 and S100A11. PLoS ONE 2008; 3:e3767.
• Mkrtchyan H, Ghazaryan S, Avetisyan G, Hovhannisyan H, Muradyan L, Daghbashyan S, Karst C, Gross M, Hinreiner S, Aroutiounian R, Liehr T. Novel complex t(V;9;22) rearrangements in three cases with chronic myeloid leukemia and a rare translocation in a case with classical Philadelphia chromosome. Oncol Reports 2008, 20:99-104.
• Moehren U, Papaioannou M, Reeb CA, Grasselli A, Nanni S, Asim M, Roell D, Prade I, Farsetti A, Baniahmad A. Wild-type but not mutant androgen receptor inhibits expression of the hTERT telomerase subunit: a novel role of AR mutation for prostate cancer development. FASEB J 2008, 22:1258-67.
• Moehren U, Papaioannou M, Reeb CA, Grasselli A, Nanni S, Asim M, Roell D, Prade I, Farsetti A, Baniahmad A,Dehm SM. Wild-type but not mutant androgen receptor inhibits expression of the hTERT telomerase subunit: A novel role of AR mutation for prostate cancer development. Urol Oncol 2008, 26:690-691.
• Mothes H, Melle C, Ernst G, Kaufmann R, von Eggeling F, Settmacher U. Human Neutrophil Peptides 1-3--early markers in development of colorectal adenomas and carcinomas. Dis Markers 2008; 25:123-129.
• Mrasek K, Krüger G, Bauer I, Müller-Navia J, Liehr T, Weise A. A new unbalanced chromosomal abnormality in 1q31.1 to 1q32 without phenotypic consequences. Cytogenet Genome Res 2008, 121:286-287.
• Murzik U, Hemmerich P, Weidtkamp-Peters S, Ulbricht T, Bussen W, Hentschel J, von Eggeling F, Melle C. Rad54B Targeting to DNA Double-Strand Break Repair Sites Requires Complex Formation with S100A11. Mol Biol Cell 2008, 1:2926-2935.
• Papaioannou M, Reeb CA, Grasselli A, Nanni S, Asim M, Roell D, Prade I, Farsetti A, Baniahmad A, Moehren U Dehm SM. Wild-type but not mutant androgen receptor inhibits expression of the hTERT telomerase subunit: A novel role of AR mutation for prostate cancer development. Urol Oncol 2008, 26:690-691.
• Polityko AD, Lazjuk GI, Liehr T. High resolution molecular cytogenetic approaches and study of marker chromsomes. Medica Genetics 2008, 7:34-40. (in Russian)
• Pramparo T, de Gregori M, Gimelli S, Ciccone R, Frondizi D, Liehr T, Pellacani S, Masi G, Brovedani P, Zuffardi O, Guerrini R. A 7 Mb duplication at 22q13 in a girl with bipolar disorder and hippocampal malformation. Am J Med Genet A. 2008, 146A:1754-1760.
• Rodriguez L, Liehr T, Martinez-Fernandez ML, Lara A, Torres A, Martinez-Frias ML. A new small supernumerary marker chromosome, generating mosaic pure trisomy 16q11.1-q12.1 in a healthy man. Molecular Cytogenetics 2008, 1:4
• Scholl S, Theuer C, Scheble V, Kunert C, Heller A, Mügge LO, Fricke HJ, Höffken K, Wedding U. Clinical impact of nucleophosmin mutations and Flt3 internal tandem duplications in patients older than 60 yr with acute myeloid leukaemia. Eur J Haematol 2008, 80:208-215.
• Shoukier M, Teske U, Weise A, Engel W, Argyriou L. Characterization of five novel large deletions causing hereditary haemorrhagic telangiectasia. Clin Genet 2008, 73:320-330.
• Söderholm AA, Viiliäinen J, Lehtovuori PT, Eskelinen H, Roell D, Baniahmad A, Nyrönen TH. Computationally identified novel diphenyl- and phenylpyridine androgen receptor antagonist structures. J Chem Inf Model 2008, 48:1882-1890.
• Trifonov V, Fluri S, Binkert F, Nandini A, Anderson J, Rodriguez L, Gross M, Kosyakova N, Mkrtchyan H, Ewers E, Reich D, Weise A, Liehr T. Three new cases of complex rearranged small supernumerary marker chromosomes. Evidence for an underestimated entity? Mol Cytogenet 2008, 1:6.
• Von Eggeling F, Bleul A, Loncarevic IF, Michel S, Heller A, Melle C. Tapping an unexploited repository: Carnoy's fixed cell pellets for proteomic biomarker research in leukemia Mol Medicine Rep 2008, 1:585-558.
• Vorsanova SG, Iourov IY, Voinova-Ulas VY, Weise A, Monakhov VV, Kolotii AD, Soloviev IV, Novikov PV, Liehr T, Yurov YB. Partial monosomy 7q34-qter and 21pter-q22.13 due to cryptic unbalanced translocation t(7;21) but not monosomy of the whole chromosome 21: a case report plus review of the literature. Mol Cytogenet 2008, 1:13
• Weise A, Liehr T. Fluorescence in situ hybridization for prenatal screening of chromosomal aneuploidies. Expert Rev Mol Diagn 2008, 8:355-357.
• Weise A, Liehr T. Rapid prenatal aneuploidy screening by fluorescence in situ hybridization (FISH). Methods Mol Biol 2008, 444:39-48.
• Weise A, Gross M, Mrasek K, Mkrtchyan H, Horsthemke B, Jonsrud C, von Eggeling F, Hinreiner S, Witthuhn V, Claussen U, Liehr T. Parental-origin-determination FISH (pod-FISH) distinguishes homologues human chromosomes on a single cell level. Int J Mol Med 2008, 21:189-200.
• Weise A, Mrasek K, Fickelscher I, Claussen U, Cheung SW, Cai WW, Liehr T, Kosyakova N. Molecular Definition of High-resolution Multicolor Banding Probes: First Within the Human DNA Sequence Anchored FISH Banding Probe Set. J Histochem Cytochem 2008, 56:487-493.
• Yurov YB, Iourov IY, Vorsanova SG, Demidova IA, Kravetz VS, Beresheva AK, Kolotii AD, Monakhov VV, Uranova NA, Vostrikov VM, Soloviev IV, Liehr T. The schizophrenia brain exhibits low-level mosaic aneuploidy involving chromosome 1. Schizophr Res 2008, 98:139-147.
• Yurov YB, Liehr T, Shaffer LG , Iourov IY, Vorsanova SG. A new open access journal for a rapidly evolving biomedical field: introducing Molecular Cytogenetics. Mol Cytogenet 2008, 1:1

• Arndt S, Melle C, Mondal K, Klein G, von Eggeling F, Bosserhoff AK. Interactions of TANGO and leukocyte integrin CD11c/CD18 regulate the migration of human monocytes. J Leukoc Biol 2007, 82:1466-1472.
• Backx L, Van Esch H, Melotte C, Kosyakova N, Starke H, Frijns JP, Liehr T, Vermeesch JR.Array painting using microdissected chromosomes to map chromosomal breakpoints. Cytogenet Genome Res 2007, 11:158-166.
• Balci S, Unal A, Engiz O, Aktas D, Liehr T, Gross M, Mrasek K, Saygi S. Bilateral periventricular nodular heterotopia (PNH), severe mental retardation and epilepsy in a male patient with 46,XY,der(19) t(X;19)(q11.1-11.2;p13.3) due to maternal balanced translocation) Develop Med Child Neurol 2007, 49:219-224.
• Bartels I, Starke H, Argyriou L, Sauter SM, Zoll B, Liehr T. An exceptional complex chromosomal rearrangement (CCR) with eight breakpoints involving four chromosomes (1;3;9;14) in an azoospermic male with normal phenotype. Eur J Med Genet Gen 2007,50:133-138.
• Bhatt S, Moradkhani K, Mrasek K, Puechberty J, Lefort G, Lespinasse J, Sarda P, Liehr T, Hamamah S, Pellestor F. Breakpoint characterization: a new approach for segregation analysis of paracentric inversion in human sperm. Mol Hum Reprod. 2007, 13:751-756.
• Bindl R, Braun S, Bruchhaus H. Altersschätzung anhand des Os coxae - ein Beitrag zur Individualanalyse. Beiträge zur Archäozoologie und Prä-historischen Anthropologie, 2007, VI:157-165
• Bindl R, Herrmann E, Bruchhaus H. "Individualanalyse anhand des Os sacrum - ein Beitrag zur Altersschätzung". Beiträge zur Archäozoologie und Prähistorischen Anthropologie, 2007, VI:166-173
• Bochkov NP, Voronina ES, Kosyakova NV, Liehr T, Rzhaninova AA, Katosova LD, Platonova VI, Gol'dshtein DV. Chromosome variability of human multipotent mesenchymal stromal cells. Bull Exp Biol Med 2007, 143:122-126.
• Bornhöft B, Gottschaldt U, Bindl R, Bruchhaus H: "Untersuchungen zur Geschlechtsbestimmung anhand der Mandibula". Beiträge zur Archäozoologie und Prähistorischen Anthropologie, 2007, VI:189-181
• Carreira IM, Mascarenhas A, Matoso E, Couceiro AB, Ramos L, Dufke A, Mazauric M, Stressig R, Kosyakova N, Melo JB, Liehr T. Three Unusual but Cytogenetically Similar Cases With up to Five Different Cell Lines Involving Structural and Numerical Abnormalities of Chromosome 18. J Histochem Cytochem 2007, 55:1123-1128.
• Csaki A, Garwe F, Steinbruck A, Maubach G, Festag G, Weise A, Riemann I, Konig K, Fritzsche W. A parallel approach for subwavelength molecular surgery using gene-specific positioned metal nanoparticles as laser light antennas. Nano Lett 2007, 7:247-253.
• Driemel O, Kosmehl H, Rosenhahn J, Berndt A, Reichert TE, Zardi L, Dahse R. Expression analysis of extracellular matrix components in brush biopsies of oral lesions. Anticancer Res 2007, 27:1565-1570.
• Driemel O, Murzik U, Escher N, Melle C, Bleul A, Dahse R, Reichert TE, Ernst G, von Eggeling F. Protein profiling of oral brush biopsies: S100A8 and S100A9 can differentiate between normal, premalignant and tumor cells., Proteomics - Clinical Applications 2007, 1:486-493
• Escher N, Kob R, Tenbaum SP, Eisold M, Baniahmad A, von Eggeling F, Melle C.Various members of the E2F transcription factor family interact in vivo with the corepressor alien. J Proteome Res 2007, 6:1158-1164.
• Escher N, Kaatz M, Melle C, Hipler C, Ziemer M, Driesch D, Wollina U, von Eggeling F. Posttranslational modifications of transthyretin are serum markers in patients with mycosis fungoides. Neoplasia 2007, 9:254-259.
• Eckey M, Hong W, Papaioannou M, Baniahmad A. The nucleosome assembly activity of NAP1 is enhanced by Alien. Mol Cell Biol 2007, 27:3557-3568.
• Fegers I, Kob R, Eckey M, Schmidt O, Goeman F, Papaioannou M, Escher N, von Eggeling F, Melle C, Baniahmad A. The tumor suppressors p33ING1 and p33ING2 interact with alien in vivo and enhance alien-mediated gene silencing. J Proteome Res 2007, 6:4182-4188.
• Felka T, Lemke J, Lemke C, Michel S, Liehr T, Claussen U. DNA degradation during maturation of erythrocytes-molecular cytogenetic characterization of Howell-Jolly bodies. Cytogenet Genome Res 2007, 119:2-8.
• Fickelscher I, Starke H, Schulze E, Ernst G, Kosyakova N, Mkrtchyan H, Mac Dermont K, Sebire N, Liehr T. A further case with a small supernumerary marker chromosome (sSMC) derived from chromosome 1-evidence for high variability in mosaicism in different tissues of sSMC carriers. Prenat Diagn 2007, 27:783-785.
• Fickelscher I, Liehr T, Watts K, Bryant V, Barber JCK, Siebert R, Heidemann S, Hertz JM, Tumer Z, Thomas NS. The variant inv(2)(p11.2q13) is a genuinely recurrent rearrangement but displays some breakpoint heterogeneity, Am J Hum Gen 2007, 81:847-856.
• Glei M, Schaeferhenrich A, Claussen U, Kuechler A, Liehr T, Weise A, Marian B, Sendt W, Pool-Zobel BL. Comet Fluorescence in situ Hybridization Analysis for Oxidative Stress-Induced DNA Damage in Colon Cancer Relevant Genes. Toxicol Sci 2007, 96:279-284.
• Häckel M, Uerlings H, Bruchhaus H. "Geschlechtsbestimmung am Pars petrosa - eine universell anwendbare Methode ?", Beiträge zur Archäozoologie und Prähistorischen Anthropologie, 2007, VI:181-188
• Hullmann M, Reichert TE, Dahse R, von Eggeling F, Pistner H, Kosmehl H, Driemel O. [Oral cytology : Historical development, current status, and perspectives.] Mund Kiefer Gesichtschir 2007, 11:1-9.
• Iourov IY, Liehr T, Vorsanova SG, Yurov YB. Interphase chromosome-specific multicolor banding (ICS-MCB): A new tool for analysis of interphase chromosomes in their integrity. Biomol Eng 2007; 24: 415-417.
• Kaiser M, Volkmann A, Bruchhaus H: "Eine neue Methode zur Berechnung des Erhaltungszustandes subadulter Gebissindividuen am Beispiel der Gräberfelder Melchendorf (Bronzezeit) und Briesnitz (Mittelalter)", Beiträge zur Archäozoologie und Prähistorischen Anthropologie, 2007, VI:151-156
• Knöbel Y, Weise A, Glei M, Sendt W, Claussen U, Pool-Zobel BL. Ferric iron is genotoxic in non-transformed and preneoplastic human colon cells. Food Chem Toxicol 2007,45:804-811.
• Kob R, Baniahmad A, Escher N, von Eggeling F, Melle C. Detection and identification of transcription factors as interaction partners of alien in vivo. Cell Cycle 2007, 6:993-996.
• Koppe T, Schöbel S, Bärenklau M., Bruchhaus H., Jankauskas R., Kaduk W: Factors affecting the variation in the adult tempopromandibular joint of archaeological human populations Annals of anatomy, 2007, 189, p 320-325.
• Korsten-Reck U, Kaspar T, Korsten K, Kromeyer-Hauschild K, Bös K, Berg A, Dickhuth H-H. Motor abilities and aerobic fitness of obese children Int J Sports Med 2007, 28:762-767.
• Koscielny S, Dahse R, Ernst G, von Eggeling F. The Prognostic Relevance of p16 Inactivation in Head and Neck Cancer. ORL J Otorhinolaryngol Relat Spec 2007, 69:30-36.
• Kromeyer-Hauschild K, Zellner K. Trends in overweight and obesity and changes in the distribution of body mass index in schoolchildren of Jena, East Germany. Eur J Clin Nutr 2007, 61:404-411.
• Krumbholz A, Seidel J, Mentzel H-J, Kauf E, Kromeyer-Hauschild K. Diagnostik der Neurofibromatose Typ 1 im Kindesalter - Anthropometrische Merkmale als zusätzliche Kriterien. Monatsschr Kinderheilkd 2007 (DOI 10.1007/s00112-007-1639-x)
• Liehr T, Weise A. Frequency of small supernumerary marker chromosomes in prenatal, newborn, developmentally retarded and infertility diagnostics. Int J Mol Med 2007, 19:719-731.
• Liehr T, Trifonov V, Polityko A, Brecevic A, Mrasek K, Weise A, Ewers E, Reich D, Iourov I, Mkrtchyan H, Manvelyan M, Kosyakova N. Characterization of small supernumerary marker chromosomes (sSMC) by a simple molecular and molecular cytogenetics approach. Balkan J Med Gen 2007, 10:33-37.
• Liehr T, Utine GE, Trautmann U, Rauch A, Kuechler A, Pietracz J, Bocian E, Kosyakova N, Mrasek K, Boduroglu K, Weise A, Aktas D. Neocentric small supernumerary marker chromosomes (sSMC) - three more cases plus review of the literature. Cytogenet Genome Res 2007, 118:31-37.
• Manvelyan M, Schreyer I, Hols-Herpertz I, Kahler S, Niemann R, Hehr U, Belitz B, Bartels I, Gotz J, Huhle D, Kossakiewicz M, Tittelbach H, Neubauer S, Polityko A, Mazauric M-L, Wegner R, Stumm M, Kupferling P, Suss F, Kunze H, Weise A, Liehr T, Mrasek K. 48 new cases with infertility due to balanced chromosomal rearrangements - detailed molecular cytogenetic analysis of the 90 involved breakpoints. Int J Mol Med 2007, 19:855-864.
• Marx FP, Soehn AS, Berg D, Melle C, Schiesling C, Lang M, Kautzmann S, Strauss KM, Franck T, Engelender S, Pahnke J, Dawson S, von Eggeling F, Schulz JB, Riess O, Krüger R. The proteasomal subunit S6 ATPase is a novel synphilin-1 interacting protein--implications for Parkinson's disease. FASEB J 2007, 21:1759-1767.
• Mattes J, Whitehead B, Liehr T, Wilkinson I, Bear J, Fagan K, Craven P, Bennett B, Edwards M. Paternal uniparental isodisomy for chromosome 14 with a mosaicism for a supernumerary marker chromosome 14. Am J Med Gen A, 2007, 143A:2165-2171.
• Melle C, Ernst G, Scheibner O, Kaufmann R, Schimmel B, Bleul A, Settmacher U, Hommann M, Claussen U, von Eggeling F. Identification of specific protein markers in microdissected hepatocellular carcinoma. J Proteome Res 2007, 6:306-315.
• Melle C, Ernst G, Escher N, Hartmann D, Schimmel B, Bleul A, Thieme H, Kaufmann R, Felix K, Friess HM, Settmacher U, Hommann M, Richter KK, Daffner W, Taubig H, Manger T, Claussen U, von Eggeling F. Protein profiling of microdissected pancreas carcinoma and identification of HSP27 as a potential serum marker. Clin Chem 2007, 53:629-635.
• Moehren U, Papaioannou M, Reeb CA, Hong W, Baniahmad A. Alien interacts with the human androgen receptor and inhibits prostate cancer cell growth. Mol Endocrinol 2007, 21:1039-4108.
• Moss A, M. Wabitsch, K. Kromeyer-Hauschild, T. Reinehr, B.M. Kurth: Prävalenz von Übergewicht und Adipositas bei deutschen Einschulkindern
  Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz 2007, 50: 1424-1431
• Müller C, Bauer A, Bindl R Bruchhaus H."Beitrag der Wirbelsäule für die Individualanalyse", Beiträge zur Archäozoologie und Prähistorischen Anthropologie, 2007; Band VI, S.174 - 180
• Müller C, Wiederanders B, Fuhrmann R, Venbrocks RA, Mollenhauer J, Claussen U, Ruttger A. [Intra-articular pain during gonarthrosis: a case report about an extremely increased cathepsin expression in chondrocytes] Z Orthop Unfall 2007, 145:313-316. (German)
• Neubert A, Bruchhaus H. "Mehrfachbestattungen des Spätneolithikums und der Frühbronzezeit in Mitteldeutschland - komplexer Gegenstand archäoanthro-pologischer Forschung". Beiträge zur Archäozoologie und Prähistorischen Anthropologie 2007, VI:16-20
• Papaioannou M, Melle C, Baniahmad A. The coregulator Alien. Nucl Recept Signal 2007, 5:e008.
• Pietrzak J, Mrasek K, Obersztyn E, Stankiewicz P, Kosyakova N, Weise A, Cheung S Wai, Cai W Wen, Eggeling F von, Mazurczak T, Bocian E, Liehr T. Molecular cytogenetic characterization of eight small supernumerary marker chromosomes originating from chromosomes 2, 4, 8, 18, and 21 in three patients. J Appl Genet 2007, 48:167-175.
• Rodriguez L, Liehr T, Mrasek K, Mansilla E, Martinez-Fernandez ML, Garcia A, Martinez-Frias ML. Small supernumerary chromosome marker generating complete and pure trisomy 18p, characterized by molecular cytogenetic techniques and review. Am J Med Genet A 2007, 143A:2727-2732
• Rosenhahn J, Weise A, Michel S, Hennig K, Hartmann I, Schiefner J, Schubert K, Liehr T, Von Eggeling F, Loncarevic IF. Cytogenetic characterisation and proteomic profiling of the Imatinib-resistant cell line KCL22-R. Int J Oncol 2007, 31:121-128.
• Santos M, Mrasek K, Rigola MA, Starke H, Liehr T, Fuster C. Identification of a "cryptic mosaicism" involving at least four different small supernumerary marker chromosomes derived from chromosome 9 in a woman without reproductive success. Fertil Steril 2007, 88:969.e11-969-e17.
• Sauter SM, Bohm D, Bartels I, Burfeind P, Laccone FA, Neesen J, Wilken B, Liehr T, Zoll B. Partial trisomy of distal 19q detected by quantitative real-time PCR and FISH in a girl with mild facial dysmorphism, hypotonia and developmental delay. Am J Med Genet A 2007, 143:1091-1099.
• Schmidt K, Bindl R, Bruchhaus H. "Möglichkeiten der Körperhöhenschätzung am Beispiel ausgewählter schnurkeramischer Skelette". Beiträge zur Archäozoologie und Prähistorischen Anthropologie 2007, VI:194-204
• Schmidt K, Bindl R, Bruchhaus H. "Möglichkeiten der Körperhöhenschätzung an ausgewählten neolethischen und bronzezeitlichen Skeletten". Archäologische Informationen 2007, 30:51-69 und Bulletin der Schweizerischen Gesellschaft für Anthropologie 13:51-69
• Scholl S, Melle C, Bleul A, Spies-Weisshart B, Kunert C, Höffken K, von Eggeling F. Specific pattern of protein expression in acute myeloid leukemia harboring FLT3-ITD mutations. Leuk Lymphoma 2007, 48:2418-2423.
• Schröder S, Kromeyer-Hauschild K. Bedeutung der Eltern-Kind-Beziehung bei adipösen Kindern und Jugendlichen Ernährungs-Umschau. 2007; 54:64-69
• Seidel J, Hübler A, Schlenvoigt D, Hilliges P, Harbich M, Kuechler A, Liehr T, Claussen U, Kauf E. Schwere Wachstumsretardierung bei Deletion des IGF1-Rezeptor-Gens. Praktische Pädiatrische 2007, 13: 1-5.
• Serra A, Schackert HK, Mohr B, Weise A, Liehr T, Fitze G. t(11;19)(q21;p12 approximately p13.11) and MECT1-MAML2 fusion transcript expression as a prognostic marker in infantile lung mucoepidermoid carcinoma. J Pediatr Surg 2007, 42:e23-29.
• Sun F, Oliver-Bonet M, Liehr T, Starke H, Ko E, Rademaker A, Martin RH. Discontinuities and unsynapsed regions in meiotic chromosomes have a trans effect on meiotic recombination of some chromosomes in human males. Cytogenet Genome Res 2007, 119:27-32
• Tenbaum SP, Papaioannou M, Reeb CA, Goeman F, Escher N, Kob R, von Eggeling F, Melle C, Baniahmad A. Alien inhibits E2F1 gene expression and cell proliferation. Biochim Biophys Acta 2007, 1773:1447-1454.
• Thiele K, Uerlings H, Lessig R, Edelmann J, Braun S, Bindl R, Bornhöft B, Neubert A, Bruchhaus H. "Morphologische und molekulargenetische Untersuchungen zur Identifizierung einer skelettierten Leiche", Beiträge zur Archäozoologie und Prähistorischen Anthropologie 2007, VI:205-210
• Tönnies H, Pietrzak J, Bocian E, Macdermont K, Kuechler A, Belitz B, Trautmann U, Schmidt A, Schulze B, Rodriguez L, Binkert F, Yardin C, Kosyakova N, Volleth M, Mkrtchyan H, Schreyer I, von Eggeling F, Weise A, Mrasek K, Liehr T. New immortalized cell lines of patients with small supernumerary marker chromosome: towards the establishment of a cell bank. J Histochem Cytochem. 2007, 55:651-660.
• Utine GE, Aktas D, Alanay Y, Gücer S, Tuncbilek E, Mrasek K, Liehr T. Distal partial trisomy 1q: report of two cases and a review of the literature. Prenat Diagn 2007, 27:865-871.
• Uyanik G, Morris-Rosendahl DJ, Stiegler J, Klapecki J, Gross C, Berman Y, Martin P, Dey L, Spranger S, Korenke GC, Schreyer I, Hertzberg C, Neumann TE, Burkart P, Spaich C, Meng M, Holthausen H, Adčs L, Seidel J, Mangold E, Buyse G, Meinecke P, Schara U, Zeschnigk C, Muller D, Helland G, Schulze B, Wright ML, Kortge-Jung S, Hehr A, Bogdahn U, Schuierer G, Kohlhase J, Aigner L, Wolff G, Hehr U, Winkler J. Location and type of mutation in the LIS1 gene do not predict phenotypic severity. Neurology 2007, 69:442-447.
• von Eggeling F, Melle C, Ernst G. Microdissecting the proteome. Proteomics. 2007, 7:2729-2737.
• von Eggeling F, Ernst G. Microdissected tissue: an underestimated source for biomarker discovery? Biomark Med. 2007, 1:217-219.
• Weise A, Gross M, Schmidt S, Claussen U, Liehr T. New aspects of chromosomal evolution in the gorilla and the orangutan. Int J Mol Med. 2007, 19:437-443.
• Zellner K, Ulbricht U, Kromeyer-Hauschild K. Long-term trends in body mass index of children in Jena, East Germany. Econ Hum Biol 2007, 5:426-434.
• Zoll B, Böhm D, Sauter SM, Liehr T, Funke R, Auber B, Bartels I, Burfeind P. Subtelomere Rerrangements. Eine Ursache für geistige Behinderung? Kinder und Jugendarzt 2007, 38:236-243.

• Balci S, Engiz O, Aktas D, Vargel I, Beksac MS, Mrasek K, Vermeesch J, Liehr T. Ring chromosome 4 and Wolf-Hirschhorn syndrome (WHS) in a child with multiple anomalies. Am J Med Genet A 2006, 140A:628-632
• Barber JCK, Zhang S, Friend N, Collins AL, Maloney VK, Hastings R, Farren B, Barnicoat A, Polityko AD, Rumyantseva NK, Starke H, Ye S. Duplications of proximal 16q flanked by heterochromatin are not euchromatic variants and show no evidence of heterochromatic position effect. Cytogenet Genome Res. 2006, 114:351-358.
• Bindl R, Bornhöft B, Müller C, Bruchhaus H.: Eine besondere mittelalterliche Bestattung aus der Marienkirche zu Mühlhausen/Thür.
  Mühlhäuser Beiträge 2006, 29:22-34
• Bindl R, Braun S, Uerlings H, Koppe T, Bruchhaus H: . Methoden der Altersschätzung anhand des Os coxae. Bulletin der Schweizerischen Gesellschaft für Anthropologie 2006, 12:1-12.
• Bosy-Westphal A, Kromeyer-Hauschild K, Pirlich M, Schlattmann A, Scholz GH, Müller MJ. Körperzusammensetzung . Was kann man wie und mit welchem Wert in der Praxis messen? Aktuel Ernaehr Med 2006, 31:189-195
• Brecevic L, Michel S, Starke H, Müller K, Kosyakova N, Mrasek K, Weise A, Liehr T. Multicolor FISH used for the characterization of small supernumerary marker chromosomes (sSMC) in commercially available immortalized cell lines. Cytogenet Genome Res 2006, 114:270-273.
• Bruchhaus H, Birkenbeil S, Neumann R, Neubert A, Northe A, Schleier P, Thiele K, Uerlings H. "Löcher im Schädel" - Überlegungen zu einem altbekannten Phänomen (Archäologie und Anthropologie), In: Frühe Spuren der Gewalt - Schädelverletzungen und Wundversorgung an prähistorischen Menschenresten aus interdisziplinärer Sicht ,Hrsg.: Jürgen Piek und Thomas Terberger, Beiträge zur Ur- und Frühgeschichte Mecklenburg-Vorpommerns 2006, 41:115-122
• Diegmann J, Tomiuk S, Sanjmyatav J, Junker K, Hindermann W, von Eggeling F. Comparative transcriptional and functional profiling of clear cell and papillary renal cell carcinoma. Int J Mol Med 2006, 18:395-403.
• Diegmann J, Junker K, Loncarevic IF, Michel S, Schimmel B, von Eggeling F. Immune escape for renal cell carcinoma: CD70 mediates apoptosis in lymphocytes. Neoplasia 2006, 8:933-938.
• Dufke A, Singer S, Borell-Kost S, Stötter M, Pflumm DA, Mau-Holzmann UA, Starke H, Mrasek K, Enders H. De novo structural chromosomal imbalances: molecular cytogenetic characterization of partial trisomies. Cytogenet Genome Res 2006, 114:342-350.
• Ernst G, Melle C, Schimmel B, Bleul A, von Eggeling F. Proteohistography--Direct Analysis of Tissue with High Sensitivity and High Spatial Resolution Using ProteinChip Technology. J Histochem Cytochem 2006, 54:13-17.
• Escher N, Spies-Weisshart B, Kaatz M, Melle C, Bleul A, Driesch D, Wollina U, von Eggeling F. Identification of HNP3 as a tumour marker in CD4+ and CD4- lymphocytes of patients with cutaneous T-cell lymphoma. Eur J Cancer 2006,42:249-255.
• Gross M , Starke M, Trifonov V, Claussen U, Liehr T, Weise A. A molecular cytogenetic study of chromosome evolution in chimpanzee. Cytogenet Genome Res 2006, 112:67-75.
• Hering A, Guratowska M, Bucsky P, Claussen U, Decker J, Ernst G, Hoeppner W, Michel S, Neumann H, Parlowsky T, Loncarevic I. Characteristic genomic imbalances in pediatric pheochromocytoma. Genes Chromosomes Cancer 2006, 45:602-607.
• Iourov IY, Liehr T, Vorsanova SG, Kolotii AD, Yurov YB. Visualization of interphase chromosomes in postmitotic cells of the human brain by multicolour banding (MCB). Chromosome Res 2006,14:223-229.
• Karst C, Trifonov V, Romanenko SA, Claussen U, Mrasek K, Michel S, Avner P, Liehr T. Molecular cytogenetic characterization of the mouse cell line WMP2 by spectral karyotyping and multicolor banding applying murine probes. Int J Mol Med 2006, 17:209-213.
• Karst C, Gross M, Haase D, Wedding U, Höffken K, Liehr T, Mkrtchyan H. Novel cryptic chromosomal rearrangements detected in acute lymphoblastic leukemia detected by application of new multicolor fluorescent in situ hybridization approaches. Int J Oncol 2006, 28:891-897.
• Knoll N, Weise A, Claussen U, Sendt W, Marian B, Glei M, Pool-Zobel BL. 2-Dodecylcyclobutanone, a radiolytic product of palmitic acid, is genotoxic in primary human colon cells and in cells from preneoplastic lesions. Mutat Res 2006, 594:10-19.
• Knöbel Y, Glei M, Weise A, Osswald K, Schäferhenrich A, Richter KK, Claussen U, Pool-Zobel BL. Uranyl Nitrilotriacetate, a Stabilized Salt of Uranium, is Genotoxic in Nontransformed Human Colon Cells and in the Human Colon Adenoma Cell Line LT97. Toxicol Sci 2006, 93:286-297.
• Korsten-Reck U, Kromeyer-Hauschild K, Korsten K, Rücker G, Dickhuth HH, Berg A. Freiburg Intervention Trial for Obese Children (FITOC) - Ergebnisse einer Beobachtungsstudie. Deutsche Zeitschrift für Sportmedizin 2006, 2:36-41
• Kriegova E, Melle C, Kolek V, Hutyrova B, Mrazek F, Bleul A, du Bois RM, von Eggeling F, Petrek M. Protein profiles of bronchoalveolar lavage fluid from patients with pulmonary sarcoidosis. Am J Respir Crit Care Med 2006, 173:1145-1154.
• Junker K, von Eggeling F, Müller J, Steiner T, Schubert J. [Identification of biomarkers and therapeutic targets for renal cell cancer using ProteinChip technology.] Urologe A 2006, 45:305-315. (German)
• Liehr T. Familial small supernumerary marker chromosomes are predominantly inherited via the maternal line. Genet Med 2006, 8:459-462.
• Liehr T. Preface to the special issue Multicolor FISH in Human Cytogenetics. Cytogenet Genome Res 2006, 114:187-188.
• Liehr T, Gross M, Karst C, Glaser M, Mrasek K, Starke H, Weise A, Mkrtchyan H, Kuechler A. FISH banding in tumor cytogenetics. Cancer Genet Cytogenet 2006, 164:88-89.
• Liehr T, Mrasek K, Weise A, Dufke A, Rodríguez L, Martínez Guardia N, Sanchís A, Vermeesch JR, Ramel C, Polityko A, Haas O, Anderson J, Claussen U, von Eggeling F, Starke H. Small supernumerary marker chromosomes - progress towards a genotype-phenotype correlation. Cytogenet Genome Res 2006, 112:23-34.
• Liehr T, Starke H, Senger G, Melotte C, Weise A, Vermeesch JR. Overrepresentation of small supernumerary marker chromosomes (sSMC) from chromosome 6 origin in cases with multiple sSMC. Am J Med Genet A 2006, 140A:46-51.
• Liehr T, Starke H, Heller a, Kosyakova n, Mrasek k, Gross m, Karst c, Glaser m, Fickelscher i, Kuechler a, Trifonov v, Romanenko sa, Weise a. Multicolor fluorescence in situ hybridization (FISH) applied for FISH-banding. Cytogenet Genome Res 2006, 114:240-244.
• Melle C, Bogumil R, Ernst G, Schimmel B, Bleul A, von Eggeling F. Detection and identification of heat shock protein 10 as a biomarker in colorectal cancer by protein profiling. Proteomics 2006, 6:2600-2608.
• Melle C, Camacho JA, Surber R, Betge S, Von Eggeling F, Zimmer T. Region-specific alterations of global protein expression in the remodelled rat myocardium. Int J Mol Med 2006, 18:1207-1215.
• Melle C, Ernst G, Schimmel B, Bleul A, Mothes H, Kaufmann R, Settmacher U, Von Eggeling F. Different expression of calgizzarin (S100A11) in normal colonic epithelium, adenoma and colorectal carcinoma. Int J Oncol 2006, 28:195-200.
• Mitter D, Buiting K, von Eggeling F, Kuechler A, Liehr T, Mau-Holzmann UA, Prott EC, Wieczorek D, Gillessen-Kaesbach G. Is there a higher incidence of maternal uniparental disomy 14 [upd(14)mat]? Detection of 10 new patients by methylation-specific PCR. Am J Med Genet A 2006, 140A:2039-2049.
• Mkrtchyan H, Glaser M, Gross M, Wedding U, Höffken K, Liehr T, Karst C, Aroutiounian R. Multicolor-FISH applied to resolve complex chromosomal changes in a case of T-ALL (FAB L2). Cytogenet Genome Res 2006, 114:270-273.
• Müller U, Ernst G, Melle C, Guthke R, von Eggeling F. Convergence of the proteomic pattern in cancer. Bioinformatics 2006, 22:1293-1296.
• Papadopoulou E, Sifakis S, Sarri C, Gyftodimou J, Liehr T, Mrasek K, Kalmanti M, Petersen MB. A report of pure 7p duplication syndrome and review of the literature. Am J Med Genet A 2006, 140A:2802-2806.
• Reichelt O, Müller J, von Eggeling F, Driesch D, Wunderlich H, Schubert J, Grone HJ, Stein G, Ott U, Junker K. Prediction of renal allograft rejection by urinary protein analysis using ProteinChip Arrays (surface-enhanced laser desorption/ionization time-of-flight mass spectrometry). Urology 2006, 67:472-475.
• Rudolph C, Liehr T, Steinemann D, Emura M, Daibata M, Matsuo Y, Emi N, Abe M, Lai R, Mrasek K, Claussen U, Schlegelberger B. Different breakage-prone regions on chromosome 1 detected in t(11;14)-positive mantle cell lymphoma cell lines and multiple myeloma cell lines are associated with different tumor progression-related mechanisms. Cytogenet Genome Res 2006, 112:213-221.
• Sarri C, Gyftodimou Y, Grigoriadou M, Pandelia E, Kalogirou S, Kokotas H, Mrasek K, Weise A, Petersen MB. Supernumerary marker chromosome 5 diagnosed by M-FISH in a child with congenital heart defect and unusual face Cytogenet Genome Res 2006, 114:330-337.
• Schilling S, Keller U, Sprung CN, Weise A, Grabenbauer GG, Sauer R, Distel L. Breakpoint locations within chromosomes 1, 2, and 4 of patients with increased radiosensitivity. Cancer Genet Cytogenet 2006, 168:1-10.
• Scholl S, Muller R, Clement JH, Loncarevic IF, Bohmer FD, Höffken K. ATRA can enhance apoptosis that is induced by Flt3 tyrosine kinase inhibition in Flt3-ITD positive cells. Leuk Res 2006, 30:633-642.
• Siegfried W, Kromeyer-Hauschild K, Zabel G, Siegfried A, Wabitsch M, Holl RW. Stationäre Langzeittherapie der extremen junvenilen Adipositas MMW Fortschr Med 2006, 148:147-151.
• Siegfried W, Kromeyer-Hauschild K, Zabel G, Siegfried A, Wabitsch M, Holl MW. Studie zur stationären Langzeittherapie der extremen juvenilen Adipositas- Jeder Zweite nimmt langfristig ab. MMW Fortschr Med 2006, 35-36:39-41.
• Stankiewicz P, Kuechler A, Eller CD, Sahoo T, Baldermann C, Lieser U, Hesse M, Glaser C, Hagemann M, Yatsenko SA, Liehr T, Horsthemke B, Claussen U, Marahrens Y, Lupski JR, Hansmann I. Minimal phenotype in a girl with trisomy 15q due to t(X;15)(q22.3;q11.2) translocation. Am J Med Genet A 2006, 140A:442-452
• Strehl S, König M, Meyer C, Schneider B, Harbott J, Jager U, von Bergh AR, Loncarevic IF, Jarosova M, Schmidt HH, Moore SD, Marschalek R, Haas OA. Molecular dissection of t(11;17) in acute myeloid leukemia reveals a variety of gene fusions with heterogeneous fusion transcripts and multiple splice variants. Genes Chromosomes Cancer 2006, 45:1041-1049.
• Sun F, Oliver-Bonet M, Liehr T, Starke H, Turek P, Ko E, Rademaker A, Martin RH. Variation in MLH1 distribution in recombination maps for individual chromosomes from human males. Hum Mol Genet 2006, 15:2376-2391.
• Sun F, Oliver-Bonet M, Liehr T, Starke H, Turek P, Ko E, Rademaker A, Martin RH. Analysis of non-crossover bivalents in pachytene cells from 10 normal men. Hum Reprod 2006, 21:2335-2339.
• Tönnies H, Gerlach A, Heineking B, Starke H, Neitzel H, Neumann LM. Molecular cytogenetic identification and characterization of a de novo supernumerary neocentromeric derivative chromosome 13 Cytogenet Genome Res 2006, 114:325-329.

Bücher/ Books

• Baniahmad A. Nuclear hormone receptor co-repressors. J Steroid Biochem Mol Biol 2005, 93:89-97.
• Barber JCK, Thomas NS, Collinson MN, Dennis NR, Liehr T, Weise A, Belitz B, Pfeiffer L, Kirchhoff M, Krag-Olsen B, Lundsteen C. Segmental haplosufficiency: transmitted deletions of 2p12 include a pancreatic regeneration gene cluster and have no apparent phenotypic consequences. Europ J Hum Gen 2005, 13:283-291.
• Barber JC, Maloney V, Hollox EJ, Stuke-Sontheimer A, du Bois G, Daumiller E, Klein-Vogler U, Dufke A, Armour JA, Liehr T. Duplications and copy number variants of 8p23.1 are cytogenetically indistinguishable but distinct at the molecular level. Eur J Hum Genet 2005, 13:1131-1136.
• Busch A, Michel S, Hoppe C, Driesch D, Claussen U, von Eggeling F. Proteome Analysis of Maternal Serum Samples for Trisomy 21 Pregnancies Using ProteinChip Arrays and Bioinformatics. J Histochem Cytochem 2005, 53:341-343.
• Diegmann J, Junker K, Gerstmayer B, Bosio A, Hindermann W, Rosenhahn J, von Eggeling F.,Identification of CD70 as a diagnostic biomarker for clear cell renal cell carcinoma by gene expression profiling, real-time RT-PCR and immunohistochemistry. Eur J Cancer 2005, 41:1794-801.
• Finke L, Nöther S. A palato-nasal cyst assiciated with mesiodens and possible fibro-osseous dysplasia in a male of the migrations period. Paleopathology Newsletter 2005, 131:19-24
• Gessner G, Schonherr K, Soom M, Hansel A, Asim M, Baniahmad A, Derst C, Hoshi T, Heinemann SH. BKCa channels activating at resting potential without calcium in LNCaP prostate cancer cells. J Membr Biol 2005, 208:229-240.
• Glaser M, Karst C, Gross M, Mkrtchyan H, Liehr T. Chromosome torsions in cytogenetic preparations of bone-marrow - artifacts or leukemia-specific? Balk J Med Gen 2005, 8:27-31.
• Goeman F, Thormeyer D, Abad M, Serrano M, Schmidt O, Palmero I, Baniahmad A. Growth inhibition by the tumor suppressor p33ING1 in immortalized and primary cells: involvement of two silencing domains and effect of Ras. Mol Cell Biol 2005, 25:422-431.
• Gutiérrez-Mateo C, Benet J, Starke H, Oliver-Bonet M, Munné S, Liehr T, Navarro J. Karyotyping of human oocytes by cenM-FISH, a new 24-colour centromere-specific technique. Hum Reprod 2005, 20:3395-3401.
• Herbert Z, Gothe S, Caldwell JD, Bernstein HG, Melle C, von Eggeling F, Lewis J, Jirikowski GF. Identification of sex hormone-binding globulin in the human hypothalamus. Neuroendocrinology 2005, 81:287-293.
• Junker K, Gneist J, Melle C, Driesch D, Schubert J, Claussen U, Von Eggeling F. Identification of protein pattern in kidney cancer using ProteinChip arrays and bioinformatics. Int J Mol Med 2005, 15:285-90.
• Junker K, Hindermann W, von Eggeling F, Diegmann J, Haessler K, Schubert J.CD70: a new tumor specific biomarker for renal cell carcinoma. J Urol 2005, 173:2150-2153.
• Karst C, Heller A, Claussen U, Gebhart E, Liehr T. Abstract Detection of cryptic chromosomal aberrations in the in vitro non-proliferating cells of acute myeloid leukemia. Int J Oncol 2005, 27:355-359.
• Keller U, Grabenbauer G, Kuechler A, Sprung CN, Müller E, Sauer R, Distel L. Cytogenetic instability in young patients with multiple primary cancers. Cancer Genet Cytogenet 2005, 157:25-32.
• Korsten-Reck U, Kromeyer-Hauschild K, Wolfarth B, Dickhuth HH, Berg A. Freiburg Intervention Trial for Obese Children (FITOC): results of a clinical observation study. Int J Obes Relat Metab Disord 2005, 29:356-361.
• Kuechler A, Ziegler M, Blank C, Rommel B, Bullerdiek J, Ahrens J, Claussen U, Liehr T. A highly complex chromosomal rearrangement between five chromosomes in a healthy female diagnosed in preparation for ICSI. J Histochem Cytochem 2005, 53:355-357.
• Kautenburger T, Beyer-Sehlmeyer G, Festag G, Haag N, Kuhler S, Kuchler A, Weise A, Marian B, Peters WH, Liehr T, Claussen U, Pool-Zobel BL: The gut fermentation product butyrate, a chemopreventive agent, suppresses glutathione S-transferase theta (hGSTT1) and cell growth more in human colon adenoma (LT97) than tumor (HT29) cells. J Cancer Res Clin Oncol 2005, 131:692-700
• Lehmann R, Melle C, Escher N, von Eggeling F. Detection and identification of protein interactions of S100 proteins by ProteinChip technology. J Proteome Res 2005, 4:1717-1721.
• Liehr T. Eine erste Genotyp-Phänotyp-Korrelation bei kleinen überzähligen Marker-Chromosomen (small supernumerary marker chromosomes = sSMC) des Menschen. Medgen 2005, 17:454-456.
• Liehr T, Weier H-UG. 14th Workshop on Fetal Cells and Fetal DNA. J Histochem Cytochem 2005, 53:253-254.
• Liehr T, Ziegler M. Rapid prenatal diagnostics in the interphase nucleus - procedure and cut-off rates. J Histochem Cytochem 2005; 53:289-291.
• Liehr T, Brude E, Gillessen-Kaesbach G, König R, Mrasek K, von Eggeling F, Starke H. Prader-Willi syndrome with a karyotype 47,XY,+min(15)(pter->q11.1:) and maternal UPD 15 - case report plus review of similar cases. Europ J Gen 2005, 48:175-181.
• Liehr T, Mrasek K, Starke H, Claussen U, Schreiber G. Unusual small supernumerary marker chromosome (sSMC) 9 in a Klinefelter patient. Cytogenet Genome Res 2005, 111:179-181.
• Melle C, Ernst G, Schimmel B, Bleul A, Kaufmann R, Hommann M, Richter KK, Daffner W, Settmacher U, Claussen U, von Eggeling F. Characterization of pepsinogen C as a potential biomarker for gastric cancer using a histo-proteomic approach. J Proteome Res 2005, 4:1799-1804.
• Melle C, Ernst G, Schimmel B, Bleul A, Thieme H, Kaufmann R, Mothes H, Settmacher U, Claussen U, Halbhuber KJ, Von Eggeling F. Discovery and identification of alpha-defensins as low abundant, tumor-derived serum markers in colorectal cancer. Gastroenterology 2005 Jul;129:66-73.
• Melle C, Osterloh D, Ernst G, Schimmel B, Bleul A, von Eggeling F. Identification of proteins from colorectal cancer tissue by two-dimensional gel electrophoresis and SELDI mass spectrometry. Int J Mol Med 2005, 16:11-17.
• Macedo Silva ML, Land M, Heller A, Abdelhay E, do Socorro Pombo-de-Oliveira M, Ribeiro R, Alves G, Lerner D, Liehr T. New rearrangement t(3;17)(q26.3;q12) in an AML patient with a poor outcome. Oncol Rep 2005, 14:663-666.
• Mrasek K, Starke H, Liehr t. Another small supernumerary marker chromosome (sSMC) derived from chromosome 2 - towards a genotype/ phenotype correlation. J Histochem Cytochem 2005, 53:367-370.
• Mueller J, von Eggeling F, Driesch D, Schubert J, Melle C, Junker K. ProteinChip technology reveals distinctive protein expression profiles in the urine of bladder cancer patients. Eur Urol 2005, 47:885-893
• Oliver-Bonet M, Benet J, Sun F, Navarro J, Abad C, Liehr T, Starke H, Greene C, Ko E, Martin RH. Meiotic studies in two human reciprocal translocations and their association with spermatogenic failure. Human Reproduction 2005, 20:683-688.
• Papaioannou M, Reeb C, Asim M, Dotzlaw H, Baniahmad A. Co-activator and co-repressor interplay on the human androgen receptor. Andrologia 2005, 37:211-212.
• Polityko A, Starke H, Rumyantseva N, Claussen U, Liehr T, Raskin S. Three cases with rare interstitial rearrangements of chromosome 1 characterized by multicolor banding. Cytogenet Genome Res 2005, 111:171-174.
• Pramparo T, Mattina T, Gimelli S, Liehr T, Zuffardi O. Narrowing the deleted region associated with the 15q21 syndrome. Eur J Med Genet 2005, 48:346-352.
• Rodriguez L, Starke H, Guardia NM, Tonnies H, Neitzel H, Kozlowski P, Mazauric ML, Heller A, Grondona FL, Mansilla E, Santos Munoz MJ, Liehr T, Martinez-Frias ML. Three new cases with a supernumerary ring chromosome 1. Clin Dysmorphol 2005, 14:169-175.
• Schierl T, Häckel M, Bruchhaus H: Anthropologischer Befund zu den Körpergräbern der jüngeren Römischen Kaiser- und der Völkerwanderungszeit. In:Liebersee - Ein polykultureller Bestattungsplatz an der sächsischen Elbe von Jan Bemman und Esther M.Wesely-Arents Band 5, Veröffentlichungen des Landesamtes für Archäologie mit Landesmuseum für Vorgeschichte. 2005, 48:264-270
• Schmidt S, Claussen U, Liehr T, Weise A. Evolution versus constitution: differences in chromosomal inversion. Hum Genet 2005, 117:213-219.
• Scholl S, Loncarevic IF, Krause C, Clement JH, Hoffken K, Sayer HG. Analyses of minimal residual disease based on Flt3 mutations in allogeneic peripheral blood stem cell transplantation. J Cancer Res Clin Oncol 2005, 131:279-283.
• Scholl S, Krause C, Loncarevic IF, Muller R, Kunert C, Wedding U, Sayer HG, Clement JH, Hoffken K. Specific detection of Flt3 point mutations by highly sensitive real-time polymerase chain reaction in acute myeloid leukemia. J Lab Clin Med 2005, 145:295-304.
• Scholl S, Loncarevic IF, Krause C, Kunert C, Clement JH, Hoffken K. Minimal residual disease based on patient specific Flt3-ITD and -ITT mutations in acute myeloid leukemia. Leuk Res 2005, 29:849-853.
• Schreyer I, Neumann A, Beensen V, Eichhorn K-H, Heller A, Claussen U, Liehr T. dup(13)(q14.2-q14.3) - yet another new differential diagnostic aspect for short stature like phenotype. J Histochem Cytochem 2005, 53 :365-366.
• Starke H, Mrasek K, Liehr T. 3 cases with enlarged acrocentric p-arms - 2 cases with cryptic partial trisomies. J Histochem Cytochem 2005, 53:359-360.
• Sun F, Oliver-Bonet M, Liehr T, Starke H, Trpkov K, Ko E, Rademaker A, Martin RH. Discontinuities and unsynapsed regions in meiotic chromosomes have a cis effect on meiotic recombination patterns in normal human males. Hum Mol Gen 2005, 14:3013-3018
• Trifonov V, Karst C, Claussen U, Mrasek K, Michel S, Avner P, Liehr T. Microdissection-derived Murine Mcb Probes from Somatic Cell Hybrids. J Histochem Cytochem 2005, 53:791-792.
• Trimborn M, Liehr T, Belitz b, Pfeiffer L, Varon R, Neitzel H, Tönnies H. Prenatal diagnosis and molecular cytogenetic characterisation of a complex structural rearrangement in a pregnancy following intracytoplasmic sperm injection (ICSI). J Histochem Cytochem 2005, 53:351-354.
• Vermeesch JR, Melotte C, Salden I, Riegel M, Trifnov V, Polityko A, Rumyantseva N, Naumchik I, Starke H, Matthijs G, Schinzel A, Fryns JP, Liehr T. Tetrasomy 12pter-12p13.31 in a girl with partial Pallister-Killian syndrome phenotype. Eur J Med Genet 2005, 48:319-327.
• von Beust G, Sauter SM, Liehr T, Burfeind P, Bartels I, Starke H, von Eggeling F, Zoll B. Molecular cytogenetic characterization of a de novo supernumerary ring chromosome 7 resulting in partial trisomy, tetrasomy, and hexasomy in a child with dysmorphic signs, congenital heart defect, and developmental delay. Am J Med Genet A 2005, 137:59-64.
• Weise A, Starke H, Mrasek K, Claussen U, Liehr T. New insights into the evolution of chromosome 1. Cytogenet Genome Res 2005, 108:217-222.
• Weise A, Liehr T, Claussen U, Halbhuber K-J. Increased efficiency of fluorescence in situ hybridization (FISH) using the microwave. J Histochem Cytochem 2005, 53:1301-1303.
• Xiao F, Mirwald A, Papaioannou M, Baniahmad A, Klug J. Secretoglobin 2A1 is under selective androgen control mediated by a peculiar binding site for Sp family transcription factors.Mol Endocrinol 2005, 19:2964-2978.

• Boehm D, Herold S, Kuechler A, Liehr T, Laccone F. Rapid detection of subtelomeric deletion/duplication by novel real-time quantitative PCR using SYBR-green dye. Hum Mutat 2004, 23:368-378.
• Camps J, Mrasek K, Prat E, Weise A, Starke H, Egozcue J, Miro R, Liehr T. Molecular cytogenetic characterisation of the colorectal cancer cell line SW480. Oncol Rep 2004, 11:1215-1218.
• Codina-Pascual M, Oliver-Bonet M, Navarro J, Starke H, Liehr T, Gutierrez-Mateo C, Sanchez-Garcia JF, Arango O, Egozcue J, Benet J. FISH characterization of a dicentric Yq (p11.32) isochromosome in an azoospermic male. Am J Med Genet 2004, 127A:302-306.
• Gebhart E, Ries J, Wiltfang J, Liehr T, Efferth T. Genomic gain of the epidermal growth factor receptor harboring band 7p12 is part of a complex pattern of genomic imbalances in oral squamous cell carcinomas. Arch Med Res 2004, 35:385-394.
• Heller A, Loncarevic IF, G laser M, Gebhart E, Trautmann U, Claussen U, Liehr T. Breakpoint differentiation in chromosomal aberrations of hematological malignancies: Identification of 33 previously unrecorded breakpoints.Int J Oncol 2004, 24:127-136.
• Heller A, Fricke HJ, Starke H, Loncarevic IF, Claussen U, Liehr T. Characterization of a highly aberrant plasma cell leukemia karyotype: A case report. Oncol Rep 2004, 11:89-92.
• Jaeger U, Zellner K, Kromeyer-Hauschild K. Body composition and type of body shape in schoolchildren from Jena/Germany. In: Bodzsár, Č. B., and Susanne, C.: Physique and body composition. Variability and sources of variations. Biennial Books of EAA, Vol. 3. Eötvös Loránd Univ. Press, Budapest 2004:53-64.
• Jaeger U, Finke L, Zellner K. Säkulare Trends bei demographischen Parametern. Anthrop Anz 2004, 62:347-362.
• Keller U, Kuechler A, Liehr T, Muller E, Grabenbauer G, Sauer R, Distel L. Impact of Various Parameters in Detecting Chromosomal Aberrations by FISH to Describe Radiosensitivity. Strahlenther Onkol 2004, 180:289-296.
• Korsten-Reck U, Kromeyer-Hauschild K, Korsten K, Bjarnason-Wehrens B, Dickhuth HH, Berg A. Bedeutung des Freizeit- und Ernährungsverhaltens und der Sozialanamnese in der Therapie der Adipositas bei Kindern. Perfusion 2004, 17:458-464.
• Kromeyer-Hauschild K. Aktuelle Aspekte der Gewichtsentwicklung bei Kindern und Jugendlichen. Pädiatrische Praxis 2004, 64:371-378.
• Kuechler A, Liehr T. FISH - Detection of individual radiosensitivity. In: Encyclopedia of Diagnostic Genomics and Proteomics. Eds: J Fuchs; M Podda. ISBN: 0824747941 and 0824755642:474-477.
• Keller U, Grabenbauer G, Kuechler A, Sauer R, Distel L. Technical report. Radiation sensitivity testing by fluorescence in-situ hybridization: how many metaphases have to be analysed? Int J Radiat Biol 2004, 80:615-620.
• Lehrer H, Weise A, Michel S, Starke H, Mrasek K, Heller A, Kuechler A, Claussen U, Liehr T. The hierarchically organized splitting of chromosomal bands into sub-bands analyzed by multicolor banding (MCB). Cytogenet Genome Res 2004, 105:25-28.
• Liehr T. FISH-Banding Methods and their Clinical Applications. In: Encyclopedia of Diagnostic Genomics and Proteomics. Eds: J Fuchs; M Podda. pp 457- 460ISBN: 0824747941 and 0824755642:457-460.
• Liehr T. FISH - Centromere specific multicolor FISH (CenM-FISH) - a versatile tool for characterization of small supernumerary
  marker chromosomes. In: Encyclopedia of Diagnostic Genomics and Proteomics. Eds: J Fuchs; M Podda. ISBN: 0824747941 and 0824755642:468-470.
• Liehr T, Hickmann G, Kozlowski P, Claussen U, Starke U. Molecular-cytogenetic characterization of the origin andpresence of pericentromeric euchromatin on minute supernumerary marker chromosomes (SMCs). Chromosome Res 2004, 12:239-244.
• Liehr T, Starke H, Weise A, Lehrer H, Claussen U. Multicolor FISH probe sets and their applications. Histol Histopathol 2004, 19:229-237.
• Liehr T, Mrasek K, Weise A, Kuechler A, von Eggeling F, Claussen U, Starke H. Characterization of small supernumerary marker chromosomes (sSMC) in human. Current Genomics 2004, 5:279-286.
• Liehr T, Claussen U, Starke H. Small supernumerary marker chromosomes (sSMC) in humans. Cytogenet Genome Res 2004, 107:55-67.
• Liehr T, Heller A, Eichhorn KH, Beensen V, Schulze E, Starke H, Claussen U, Schreyer I. Inherited cryptic chromosomal aberrations may be more easily detected in their balanced forms: a case report with hidden der(1)t(1;17)(q44;p13.2). Prenat Diagn 2004, 24:1022-1024.
• Melle C, Kaufmann R, Hommann M, Bleul A, Driesch D, Ernst G, von Eggeling F. Proteomic profiling in microdissected hepatocellular carcinoma tissue using ProteinChip technology. Int J Oncol 2004, 24:885-891.
• Melle C, Ernst G, Schimmel B, Bleul A, Koscielny S, Wiesner A, Bogumil R, Moller U, Osterloh D, Halbhuber KJ, von Eggeling F. A technical triade for proteomic identification and characterization of cancer biomarkers. Cancer Res 2004, 64:4099-4104.
• Nazlican H, Zeschnigk M, Claussen U, Michel S, Boehringer S, Gillessen-Kaesbach G, Buiting K, Horsthemke B. Somatic mosaicism in patients with Angelman syndrome and an imprinting defect. Hum Mol Genet. 2004, 13:2547-2555.
• Opitz F, Melle C, Schenke-Layland K, Degenkolbe I, Martin DP, Von Eggeling F, Wahlers T, Stock UA. ProteinChip system technology: a powerful tool to analyze expression differences in tissue-engineered blood vessels. Tissue Eng 2004, 10:611-620.
• Polityko A, Maltseva O, Rumyantseva N, Khurs O, Seidel J, Claussen U, Weise A, Liehr T, Starke H. Two further AHO-like syndrome patients with deletion of glypican 1 gene region in 2q37.2-q37.3. Int J Mol Med 2004, 14:977-979.
• Rudolph C, Steinemann D, Von Neuhoff N, Gadzicki D, Ripperger T, Drexler HG, Mrasek K, Liehr T, Claussen U, Emura M, Schröck E, Schlegelberger B. Molecular cytogenetic characterization of the mantle cell lymphoma cell line GRANTA-519. Cancer Genet Cytogenet 2004, 153:144-150.
• Sun F, Oliver-Bonet M, Liehr T, Starke H, Ko E, Rademaker A, Navarro J, Benet J, Martin RH. Human male recombination maps for individual chromosomes. Am J Hum Genet 2004, 74:521-531.
• Taudien S, Galgoczy P, Huse K, Reichwald K, Schilhabel M, Szafranski K, Shimizu A, Asakawa S, Frankish A, Loncarevic IF, Shimizu N, Siddiqui R, Platzer M. Polymorphic segmental duplications at 8p23.1 challenge the determination of individual defensin gene repertoires and the assembly of a contiguous human reference sequence. BMC Genomics 2004, 5:92.
• Weise A, Starke H, Mrasek K, Claussen U, Liehr T. New insights into the evolution of chromosome 1. Cytogenet Genome Res 2005, 108:217-222.
• Zellner K, Jaeger U, Kromeyer-HauschildK. Height, weight and BMI of schoolchildren in Jena, Germany - are the secular changes levelling off? Economics and Hum Biol 2004, 2:281-294.
• Zumkeller W, Volleth M, Muschke P, Tönnies H, Heller A, Liehr T, Wieacker P, Stumm M. Genotype/phenotype analysis in a patient with pure and complete trisomy 12p. Am J Med Genet 2004, 129A:261-264.

• Bartels I, Schlueter G, Liehr T, Von Eggeling F, Starke H, Glaubitz R, Burfeind P.: Supernumerary small marker chromosome (SMC) and uniparental disomy 22 in a child with confined placental mosaicism of trisomy 22: Trisomy rescue due to marker chromosome formation. Cytogenet Genome Res 2003, 101:103-105.
• Bock S, Bruchhaus H: Karies in ausgewählten prähistorischen und historischen Populationen des Mittelelbe-Saale-Gebietes - Gab es Geschlechtsunterschiede Bulletin der Schweizerischen Gesellschaft für Anthropologie 2003, 1:7-22
• Bruchhaus H, Hübschmann J, Northe A, Thiele K: Zu Möglichkeiten und Grenzen der Geschlechtsbestimmung anhand morphometrischer Untersuchungen von Skelettserien - methodische Aspekte Beiträge zur Archäozoologie und Prähistorischen Anthropologie; Herausg.: Eberhard May und Norbert Benecke; 2003 IV:156-160
• Bruchhaus H, Ludwig M, Müller C, Uerlings H: Altersschätzung am Os pubis - rezentes Material - neue Ergebnisse Beiträge zur Archäozoologie und Prähistorischen Anthropologie; Herausg.: Eberhard May und Norbert Benecke; 2003, IV:133-139
• Eiholzer U, Nordmann Y, L'Allemand D, Schlumpf M, Schmid S, Kromeyer-Hauschild K. Improving body composition and physical activity in Prader-Willi Syndrome. J Pediatr 2003, 142:73-78.
• Funke K, Bruchhaus H: Anthropologische Untersuchungen an Skelettmaterial aus der Baalberger Kultur (Baalberger Gruppe der Trichterbecherkultur) Beiträge zur Archäozoologie und Prähistorischen Anthropologie; Herausg.: Eberhard May und Norbert Benecke; 2003, IV:40-45
• Gebhart E, Liehr T, Wolff E, Wiltfang J, Koscielny S, Ries J. Loss of 9p21 is embedded in a complex but consistent pattern of genomic imbalances in oral squamous cell carcinomas. Cytogenet Genome Res 2003,101:106-112.
• Gottschaldt U, Biedermann U, Bruchhaus H: Altersschätzung subadulter Individuen - Untersuchungen an einzelnen Knochen des Viscerocraniums, Beiträge zur Archäozoologie und Prähistorischen Anthropologie; Herausg.: Eberhard May und Norbert Benecke; 2003, IV:127-132
• Grasshoff U, Singer S, Liehr T, Starke H, Fode B, Schoning M, Dufke A. A complex chromosomal rearrangement with a translocation 4;10;14 in a fertile male carrier: ascertainment through an offspring with partial trisomy 14q24-->1q22 and partial monosomy 4q27-->q28. Cytogenet Genome Res 2003, 103:17-23.
• Häckel M, Uerlings H, Bruchhaus H: Zur Anwendbarkeit der metrischen Untersuchungen des Felsenbeines für die Geschlechtsbestimmung, Beiträge zur Archäozoologie und Prähistorischen Anthropologie; Herausg.: Eberhard May und Norbert Benecke; 2003, IV:161-172.
• Heller A, Brecevic L, Glaser M, Loncarevic IF, Gebhart E, Claussen U, Liehr T. Trisomy 8 as the sole chromosomal aberration in myelocytic malignacies: a comprehensive molecular cytogenetic analysis reveals no cryptic aberrations. Cancer Genet Cytogenet 2003, 146:81-83.
• Heller A, Rubtsov N, Kytöla S, Karamysheva TV, Sablina OV, Degtyareva MM, Starke H, Metzke H, Claussen U, Liehr T. Highly complex karyotypic changes in acute myelogenous leukemia: a case report. Int J Onc 2003, 23:139-143.
• Heller A, Trifonov V, Rubtsov N, Sauerbrey A, Starke H, Loncarevic IF, Claussen U, Liehr T. Complex chromosomal rearrangements in a secondary acute myeloblastic leukemia after chemotherapy in TRAPS. Oncol Rep 2003, 10:1789-1792.
• Horsthemke B, Nazlican H, Husing J, Klein-Hitpass L, Claussen U, Michel S, Lich C, Gillessen-Kaesbach G, Buiting K. Somatic mosaicism for maternal uniparental disomy 15 in a girl with Prader-Willi syndrome: confirmation by cell cloning and identification of candidate downstream genes. Hum Mol Genet 2003, 12:2723-2732.
• Houge G, Liehr T, Schoumans J, Ness GO, Solland K, Starke H, Claussen U, Stromme P, Akre B, Vermeulen S. Ten years follow up of a boy with a complex chromosomal rearrangement: Going from a > 5 to 15-breakpoint CCR. Am J Med Genet 2003, 118A:235-240.
• Kinne RW, Kunisch E, Beensen V, Zimmermann T, Emmerich F, Petrow P, Lungershausen W, Hein G, Braun RK, Foerster M, Kroegel C, Winter R, Liesaus E, Fuhrmann RA, Roth A, Claussen U, Liehr T. Parallel occurence of (mosaic) chromosomal aberrations in synovial fibroblasts and synovial macrophages from patients with rheumatoid arthritis and other inflammatory joint diseases. Genes Chromosomes Cancer 2003, 38:53-67.
• Korsten-Reck U, Kromeyer-Hauschild K, Rücker G, Baumstark M, Dickhuth HH, Berg A. Sekundäre Fettstoffwechselstörungen im Kindesalter. Zur Häufigkeit der Dyslipoproteinämien bei übergewichtigen Kindern. Z. Dt. Ges. zur Bekämpfung von Fettstoffwechselstörungen u. ihren Folgeerkrankungen DGFF (Lipid-Liga) e.V. 2003, 12:6-14.
• Kuechler A, Weise A, Michel S, Schaeferhenrich A, Pool-Zobel BL, Claussen U, Liehr T. Precise breakpoint characterization of the colon adenocarcinoma cell line HT-29 clone 19A by means of 24-color fluorescence in situ hybridization and multicolor banding. Genes Chr Cancer 2003, 36:207-210.
• Kuechler A, Dreidax M, Piegorsch SU, Liehr T, Claussen U, Wendt TG, Dunst J.: Residual chromosomal damage after radiochemotherapy with and without amifostine detected by 24-color FISH. Strahlenther Onkol 2003, 179:493-498.
• Liehr T, Ziegler M, Starke H, Heller A, Kuechler A, Kittner G, Beensen V, Seidel J, Häßler H, Müsebeck J, Claussen U. Conspicuous GTG banding results of the centromere near region can be caused by alphoid DNA heteromorphism. Clin Genet 2003, 64:166-167.
• Liehr T, Starke H, Heller A, Weise A, Beensen V, Senger G, Kittner G, Prechtel M, Claussen U, Seidel J. Evidence for a new microdeletion syndrome in 15q21. Int J Mol Med 2003, 11:575-578.
• Liehr T, Nietzel A, Starke H, Heller A, Weise A, Kuechler A, Senger G, Ebener S, Martin T, Stumm M, Wegener R, Tönnies H, Hoppe C, Claussen U, Von Eggeling F. Characterization of small marker chromosomes (SMC) by recently developed molecular cytogenetic approaches. J Ass Genet Techn 2003, 29:5-10.
• Liehr T, Nietzel A, Weise A, Mrasek K, von Eggeling F, Claussen U, Starke H. A strategy for the characterization of small supernumerary marker chromosomes (SMC). Balk J Med Gen 2003, 6:69-72.
• Ludwig M, Müller C, Bruchhaus H. Vergleich der Altersschätzung anhand des Os pubis von drei Gräberfeldern aus der Zeit des Neolithikum, der Bronzezeit und des Mittelalters, Beiträge zur Archäozoologie und Prähistorischen Anthropologie; Herausg.: Eberhard May und Norbert Benecke; 2003, IV:140-145
• Melle C, Ernst G, Schimmel B, Bleul A, Koscielny S, Wiesner A, Bogumil R, Moller U, Osterloh D, Halbhuber KJ, Von Eggeling F. Biomarker Discovery and Identification in Laser Microdissected Head and Neck Squamous Cell Carcinoma with ProteinChip(R) Technology, Two-dimensional Gel Electrophoresis, Tandem Mass Spectrometry, and Immunohistochemistry. Mol Cell Proteomics 2003, 2:443-452.
• Mrasek K, Heller A, Rubtsov N, Trifonov V, Starke H, Claussen U, Liehr T. Detailed Hylobates lar karyotype defined by 25-color FISH and multicolor banding. Int J Mol Med, Int J Mol Med 2003, 12:139-146.
• Müller C, Bock S, Wagner K, Bruchhaus H. Dentalanthropologische Untersuchungen an historischem Skelettmaterial
  Beiträge zur Archäozoologie und Prähistorischen Anthropologie; Herausg.: Eberhard May und Norbert Benecke; 2003, IV:110-117
• Nietzel A, Albrecht B, Starke H, Heller A, Gillessen-Kaesbach G, Claussen U, Liehr T. Partial hexasomy 15pter-->15q13 including SNRPN and D15S10: first molecular cytogenetically proven case report. J Med Genet 2003, 40:e28.
• Northe A, Neubert A, Bruchhaus H. Endneolithikum/Frühbronzezeit - Trennung der Geschlechter im Tod In: Archäologie in Deutschland 2003, 5:28-29
• Oliver-Bonet M, Liehr T, Nietzel A, Heller A, Starke h, Claussen u, Codina-Pascual M, Pujol A, Abad C, Egozcue J, Navarro J, Benet J. Karyotyping of human synaptonemal complexes by cenM-FISH. Europ J Hum Genet 2003, 11:879-883.
• Reichelt E, Häckel M, Bruchhaus H: Zur Schätzung der Körperhöhe am Beispiel eines mittelalterlichen Gräberfeldes, Beiträge zur Archäozoologie und Prähistorischen Anthropologie; Herausg.: Eberhard May und Norbert Benecke; 2003, IV:178-181
• Sauter S, Von Beust G, Burfeind P, Weise A, Starke H, Liehr T, Zoll B. Autistic disorder and chromosomal mosaicism 46,XY[123]/46,XY,del(20)(pter --> p12.2)[10]. Am J Med Genet. 2003, 120A:533-536.
• Schaeferhenrich A, Sendt W, Scheele J, Kuechler A, Liehr T, Claussen U, Rapp A, Greulich KO, Pool-Zobel BL. Putative colon cancer risk factors damage global DNA and TP53 in primary human colon cells isolated from surgical samples. Food Chem Toxicol 2003, 41:655-664.
• Schaeferhenrich A, Beyer-Sehlmeyer G, Festag G, Kuechler A, Haag N, Weise A, Liehr T, Claussen U, Marian B, Sendt W, Scheele J, Pool-Zobel BL.Human adenoma cells are highly susceptible to the genotoxic action of 4-hydroxy-2-nonenal. Mutat Res 2003, 526:19-32.
• Schierl T, Bruchhaus H. Anthropologischer Befund zu den Körpergräbern der jüngeren Römischen Kaiser- und der Völkerwanderungszeit. In:Liebersee - Ein polykultureller Bestattungsplatz an der sächsischen Elbe von Jan Bemman, Band 3 Veröffent-lichungen des Landesamtes für Archäologie mit Landesmuseum für Vorgeschichte. 2003, 39:33-38
• Seidel J, Heller A, Senger G, Starke H, Chudoba I, Kelbova C, Tönnies H, Neitzel H, Haase C, Beensen V, Zintl F, Claussen U, Liehr T. A multiple translocation event in a patient with hexadactyly, facial dysmorphism, mental retardation and behavior disorder characterized comprehensively by molecular cytogenetics-Case report and review of the literature.Europ J Pedriat 2003, 162:582-588.
• Spiegel M, Hickmann G, Senger G, Kozlowski P, Bartsch O. Two new cases of analphoid marker chromosomes. Am J Med Genet 2003, 116A:284-289.
• Stachow R, Wolf J, Kromeyer-Hauschild K, Dost A, Wabitsch M, Grabert M, Holl R. Übergewicht und Adipositas bei Kindern und Jugendlichen mit Diabetes mellitus Typ 1. Prävalenz und Einflussfaktoren. Monatsschr. Kinderheilkd 2003), 151:194-201.
• Starke H, Mitulla B, Nietzel A, Heller A, Beensen V, Grosswendt G, Claussen U, von Eggeling F, Liehr T. First patient with trisomy 21 accompanied by an additional der(4)(:p11->q11:) plus partial uniparental disomy 4p15-16. Am J Med Genet 2003, 116A:26-30
• Starke H, Mitulla B, Beensen V, Trifonov V, Rubtsov N, Heller A, Ziegler M, Neumann A, Claussen U, Liehr T. First postnatal case of mosaic del(22)/r(22). Prenat Diagn 2003, 23:765-767.
• Starke H, Nietzel A, Weise A, Heller A, Mrasek K, Belitz B, Kelbova C, Volleth M, Albrecht B, Mitulla B, Trappe R, Bartels I, Adolph S, Dufke A, Singer S, Stumm M, Wegner RD, Seidel J, Schmidt A, Kuechler A, Schreyer I, Claussen U, Von Eggeling F, Liehr T. Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification. Hum Genet 2003, 114:51-67.
• Thiele K, Birkenbeil S, Huck T, Bruchhaus H. DNA-Analyse an einer Körperbestattung aus der Kultur der Schnurkeramik, Beiträge zur Archäozoologie und Prähistorischen Anthropologie; Herausg.: Eberhard May und Norbert Benecke; 2003, IV:218-222
• Trifonov V, Seidel J, Starke H, Martina P, Beensen V, Ziegler M, Hartmann I, Heller A, Nietzel A, Claussen U, Liehr T. Enlarged chromosome 13 p-arm hiding a cryptic partial trisomy 6p22.2-pter. Prenat Diagn 2003, 23:427-430.
• Volleth M, Stumm M, Kalscheuer VM, Reschke K, Liehr T, Wieacker P. Premature ovarian failure in a woman with an unusual pseudoisodicenric X chromosome. Ger J Obstet Gynecol 2003, 63:1054-1057.
• von Eggeling F, Langer S, Hoppe C, Liehr T, Weise A, Lederer G, Kotzot D. Presumed mutation in a microsatellite marker mimicking segmental uniparental disomy (UPD) in a case of a small supernumerary marker chromosome (SMC) detected at prenatal diagnosis Clin Genet 2003, 64:168-171.
• Weise A, Harbarth P, Claussen U, Liehr T. Fluorescence in situ hybridization (FISH) on human chromosomes using photoprobe biotin-labeled probes. J Histochem Cytochem 2003, 51:549-551.
• Weise A, Rittinger O, Starke H, Ziegler M, Claussen U, Liehr T. De novo 9-break-event in one chromosome 21 combined with a microdeletion in 21q22.11 in a mentally retarded boy with short stature. Cytogenet Genome Res 2003, 103:14-16.
• Weise A, Heller A, Starke H, Mrasek K, Kuechler A, Pool-Zobel BL, Claussen U, Liehr T. Multitude multicolor chromosome banding (mMCB)- a comprehensive one-step multicolor FISH banding method. Cytogenet Genome Res 2003, 103:34-39.

• Bruchhaus H, Neubert A. Zur Rekonstruktion der Bevölkerungen des Spätneolithikums und der Frühbronzezeit im Mittelelbe-Saale-Gebiet. Archäologisch-anthropologische Grundlagen In: Mensch und Umwelt während des Neolithikums und der Frühbronzezeit in Mitteleuropa. Ergebnisse interdisziplinärer Zusammenarbeit zwischen Archäologie, Klimatologie, Biologie und Medizin. Herausg. von Andreas Lippert, Michael Schultz, Stephan Shennan und Maria Teschler-Nicola, Rahden/Westf.: Leidorf; 2001, 2:191-201.
• Claussen U, Michel S, Mühlig P, Westermann M, Grummt UW, Kromeyer-Hauschild K, Liehr T. Demystifying chromosome preparation and the implications for the concept of chromosome condensation during mitosis. Cytogenet Genome Res 2002, 98:136-146.
• Dahse R, Utting M, Werner W, Schimmel B, Claussen U, Junker K. TP53 alterations as a potential diagnostic marker in superficial bladder carcinoma and in patients serum, plasma and urine samples. Int J Oncol 2002, 20:107-115.
• Fiedler W, Hoppe C, Schimmel B, Koscielny S, Dahse R, Bereczki Z, Claussen U, Ernst G, von Eggeling F. Molecular characterization of head and neck tumors by analysis of telomerase activity and a panel of microsatellite markers. Int J Mol Med 2002, 9:417-423.
• Finke L, Bruchhaus H, Jaeger U: Dental anthropological investigations of neolithic skeletal material in the area of the Middle Elbe and Saale River, Germany. In: Bennike,P., Bodzsár, Č. B., and Susanne, C.: Ecological aspects of past human settlements in Europe. Biennial Books of EAA. Eötvös Loránd Univ. Press, Budapest 2002, 2:223-232.
• Heller A, Starke H, Trifonov V, Rubtsov N, Wedding U, Loncarevic I, Bleck C, Claussen U, Liehr T. A complex translocation event between the two homologues of chromosomes 5 leading to a del(5)(q21q33) as a sole aberration in a case clinically diagnosed as CML: characterization of the aberration by multicolor banding. Int J Oncol 2002, 20:1179-1181.
• Hermanussen H, Grasedyck L, Kromeyer-Hauschild K, Prokopec M, Chrzastek-Spruch M. Growth tracks in pre-puberal children. Ann. Hum. Biol 2002, 29:667-676.
• Hohmann H, Michel S, Reiber W, Kahler C, Claussen U, Von Eggeling F.: Cultivation of fetal erythroid precursors from maternal blood: isolation and characterization by PCR and FISH. Int J Mol Med 2002, 10:257-261.
• Kauf E, Jaeger U. Adipositas im Kindesalter - Epidemiologie, Erfassung, Risiken, Therapie. Ärzteblatt Thüringen 2002, 13:555-558.
• Korsten-Reck U, Rudloff C, Kayser R, Eßer J-J, Gruppe M, Emunds U, Kromeyer-Hauschild K, Rücker G, Wohlfahrt B, Berg A. Freiburger Interventionsprogramm zur ambulanten Therapie der Adipositas im Kindesalter (FITOC). Versicherungsmedizin 2002, 54:21-25.
• Kuechler A, Neubauer S, Grabenbauer GG, Claussen U, Liehr T, Sauer R, Wendt TG. Is 24-color FISH detection of in-vitro radiation-induced chromosomal aberrations suited to determine individual intrinsic radiosensitivity? Strahlenther Onkol 2002, 178:209-215.
• Lemke J, Chudoba I, Senger G, Stumm M, Loncarevic IF, Henry C, Zabel B, Claussen U. Improved definition of chromosomal breakpoints using high- resolution multicolour banding. Human Genetics 2002, 108:478-483
• Lemke J, Claussen J, Michel S, Chudoba I, Muhlig P, Westermann M, Sperling K, Rubtsov N, Grummt UW, Ullmann P, Kromeyer-Hauschild K, Liehr T, Claussen U. The DNA-based structure of human chromosome 5 in interphase. Am J Hum Genet 2002, 71:1051-1059.
• Liehr T, Claussen U. Current developments in human molecular cytogenetic techniques. Curr Mol Med 2002, 2:283-297.
• Liehr T, Claussen U. Review: Multicolor-FISH approaches for the characterization of human chromosomes in clinical genetics and tumor cytogenetics. Current Genomics 2002, 3:213-235
• Liehr T, Heller A, Starke H, Rubtsov N, Trifonov V, Mrasek K, Weise A, Kuechler A, Claussen U. Microdissection based high resolution multicolor banding for all 24 human chromosomes. Int J Mol Med 2002, 9:335-339.
• Liehr T, Schmidt M, Starke H, Ziegler M, Kittner G, Heller A, Rubtsov N, Trifonov V, Claussen U. First case of trisomy 13 plus mosaic trisomy 1q. Fetal Diagn Ther 2002, 17:133-136.
• Liehr T, Heller A, Starke H, Claussen U. FISH banding methods: applications in research and diagnostics. Expert Rev Mol Diagn 2002, 2:217-225.
• Liehr T, Schreyer I, Neumann A, Beensen V, Ziegler M, Hartmann I, Starke H, Heller A, Nietzel A, Claussen U. Two more possible pitfalls of rapid prenatal diagnostics using interphase nuclei. Prenat Diagn 2002, 22:497-499.
• Liehr T, Weise A, Heller A, Starke H, Mrasek K, Kuechler A, Weier HU, Claussen U. Multicolor chromosome banding (MCB) with YAC/BAC-based probes and region-specific microdissection DNA libraries. Cytogenet Genome Res 2002, 97:43-50.
• Liehr T, Nietzel A, Starke H, Heller A, Weise A, Mrasek K, Claussen U.: Characterization of small human marker chromosomes by centromere-specific multicolor-FISH (cenM-FISH) and high resolution multicolor banding (MCB). ECA-newsletter 2002, 10:3-8.
• Loncarevic IF, Römer J, Starke H, Heller A, Bleck C, Ziegler M, Fiedler W, Liehr T, Clement HJ, Claussen U. Heterogenic molecular basis for loss of ABL1-BCR transcription: deletions in der(9)t(9;22) and variants of standard t(9;22) in BCR-ABL1 positive Chronic Myeloid Leukemia. Genes Chr Cancer 2002, 34:193-200.
• Mueller C, Riese U, Kosmehl H, Dahse R, Claussen U, Ernst G. Telomerase activity in microdissected human breast cancer tissues: association with p53, p21 and outcome. Int J Oncol 2002, 20:385-390.
• Seidel J, Mentzel HJ, Vogt S, Beensen V, Kauf E, Kaiser W, Claussen U, Zintl F. X-linked forms of chondrodysplasia punctata- re-description of two cases originally reported by professor Erich Häßler in 1940 and the knowledge six decades later. Pediat Rel Topics 2002, 41:343-353
• Starke H, Seidel J, Henn W, Reichardt S, Volleth M, Stumm M, Behrend C, Sandig KR, Kelbova C, Senger G, Albrecht B, Hansmann I, Heller A, Claussen U, Liehr T. Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangements. Eur J Hum Genet 2002, 10:790-800.
• Steinhaeuser U, Starke H, Nietzel A, Lindenau J, Ullmann P, Claussen U, Liehr T.: Suspension (S)-FISH, a new technique for interphase nuclei. J Histochem Cytochem 2002, 50:1697-1698.
• Trappe R, Böhm D, Kohlhase J, Weise A, Liehr T, Essers G, Meins M, Zoll B, Bartels I, Burfeind P.: A novel family-specific translocation t(2;20)(p24.1;q13.1) associated with recurrent abortions: molecular characterization and segregation analysis in male meiosis. Cytogenet Genome Res 2002, 98:1-8.
• Wabitsch M, Kunze D, Keller W, Kiess K, Kromeyer-Hauschild K. Adipositas bei Kindern und Jugendlichen in Deutschland. Deutliche Zunahme der Prävalenz - Aufruf zum Handeln. Fortschr Med Orig 2002, 120:99-106.
• Wabitsch M, Kunze D, Keller W, Kiess K, Kromeyer-Hauschild K. Immer mehr Kinder und Jugendliche zu dick. Wie lässt sich die Adipositas-Epidemie stoppen? MMW Fortschr Med 2002, 144:30-34.
• Weise A, Starke H, Heller A, Tonnies H, Volleth M, Stumm M, Gabriele S, Nietzel A, Claussen U, Liehr T. Chromosome 2 aberrations in clinical cases characterised by high resolution multicolour banding and region specific FISH probes. J Med Genet 2002, 39:434-439.
• Weise A, Liehr T, Efferth T, Kuechler A, Gebhart E. Comparative M-FISH and CGH analyses in sensitive and drug-resistant human T-cell acute leukemia cell lines. Cytogenet Genome Res 2002, 98:118-125.

Bücher / Books:

T Liehr. FISH-Technology, Springer-labmanual, Springer, Berlin, pp 90-96, ISBN: 3-540-67276-1.

• Alves G, Heller A, Fiedler W, Campos MM, Claussen U, Ornellas AA, Liehr T. Genetic imbalances in 26 cases of penile squamous cell carcinoma. Genes Chr Cancer 2001, 31:48-53.
• Birkenbeil S, Bruchhaus H. Das Gräberfeld der jüngeren Bronzezeit von Gräfentonna - anthropologischer Befund Alt-Thüringen; Jahresschrift des Thüringischen Landesamtes für Archäologische Denkmalpflege; 2001, 34:123-134
• Bleichert A, Fiedler W, Claussen U, Ernst G, Loncarevic IF, Heller A, Liehr T, Kunert C, von Eggeling F.: A long distance-PCR derived FISH probe detects a deletion between p15 and p16 in CML and T-ALL patients. Int J Mol Med 2001, 7:591-595.
• Bruchhaus H, Neubert A. Zur Rekonstruktion der Bevölkerungen des Spätneolithikums und der Frühbronzezeit im Mittelelbe-Saale-Gebiet Archäologisch-anthropologische Grundlagen
  In: Mensch und Umwelt während des Neolithikums und der Frühbronzezeit in Mitteleuropa - Ergebnisse interdisziplinärer Zusammenarbeit zwischen Archäologie, Klimatologie, Biologie und Medizin, Hrsg.: Andreas Lippert, Michael Schultz, Stephen Shennan und Maria Teschler-Nicola, (Internationale Archäologie) Rahden/Westf.: Leidorf, 2001, 2:191-201.
• Dahse R, Mey J. Telomerase in human tumors - molecular diagnosis and clinical significance. Expert Rev Mol Diagn 2001, 1:89-98.
• Von Eggeling F, Junker K, Fiedle W, Wollscheid V, Durst M, Claussen U, Ernst GL. Mass spectrometry meets chip technology: a new proteomic tool in cancer research? Electrophoresis 2001, 22:2898-2902.
• Von Eggeling F, Gawriljuk A, Fiedler W, Ernst G, Claussen U, Klose J, Romer I. Fluorescent dual colour 2D-protein gel electrophoresis for rapid detection of differences in protein pattern with standard image analysis software. Int J Mol Med 2001, 8:373-377.
• Fröber R, Kohoutek T, Kähler C, Beensen V, Hauschild R, Schulze E, Linß W. Pulmonary atresia with hypoplastic right ventricle - a clinical embryological study. Fetal Diagn Ther 2001, 16:274-279
• Gottschaldt U, Bruchhaus H. Zur Rekonstruktion der Altersstruktur subadulter Individuen anhand von Einzelknochen des Neurocraniums Beiträge zur Archäozoologie und Prähistorischen Anthropologie; Herausg.: Eberhard May und Norbert Benecke; 2001, III:61-65.
• Häckel M, Wagner K, Bruchhaus H: Anthropologische Untersuchungen am mittelalterlichen Gräberfeld von Dresden-Briesnitz Beiträge zur Archäozoologie und Prähistorischen Anthropologie; Herausg.: Eberhard May und Norbert Benecke; 2001, III:106-111.
• Hohmann H, Michel S, Reiber W, Gunther M, Claussen U, von Eggeling F. Applicability of four new antibodies for the detection of fetal nucleated cells out of maternal blood by FISH analysis. Fetal Diagn Ther 2001, 16:52-56.
• Jaeger U, Zellner K, Kromeyer-Hauschild K, Lüdde R, Eisele R, Hebebrand J. Körperhöhe, Körpergewicht und BMI bei deutschen Wehrpflichtigen. Historische Rückblick und aktueller Stand. Anthrop Anz 2001, 59:251-273.
• Kinne RW, Liehr T, Beensen V, Kuhnisch E, Zimmermann T, Holland H, Pfeiffer R, Stahl HD, Lungershausen W, Hein G, Roth A, Emmerich F, Claussen U, Froster UG. Mosaic chromosomal perrations in synovial fibroblasts of patients with rheumatoid arthritis, osteoarthritis, and other inflammatory joint diseases Arthritis Res 2001, 3:319-330.
• Kromeyer-Hauschild K, Wabitsch M, Geller F, Ziegler A, Geiß H, Hesse V, v. Hippel U, Jaeger U, Johnsen D, Kiess W, Korte W, Kunze D, Menner K, Müller M, Niemann-Pilatus A, Remer T, Schaefer F, Wittchen H, Zabransky S, Zellner K, Hebebrand J: Perzentile für den Body Mass Index für das Kindes- und Jugendalter unter Heranziehung verschiedener deutscher Stichproben. Monatsschr. Kinderheilkd 2001, 194:807-818.
• Kuechler A, Mueller CR, Liehr T, Claussen U. Detection of microdeletions in the short arm of the X chromosome by chromosome stretching. Cytogenet Cell Genet 2001, 95:12-16.
• Lemke J, Chudoba I, Senger G, Stumm M, Loncarevic IF, Henry C, Zabel B, Claussen U. Improved definition of chromosomal breakpoints using high-resolution multicolour banding. Hum Genet 2001, 108:478-483.
• Liehr T, Beensen V, Starke H, Hauschild R, Hempell E, Fritsche V, Hoppe C, Grosswendt G, Prechtel M, Ziegler M, Claussen U, von Eggeling F. Tetrasomy 21 due to a de novo Robertsonian translocation t(14;21) and an additional free trisomy 21. Clin Genet 2001, 60:83-85.
• Liehr T, Beensen V, Hauschild R, Ziegler M, Hartmann I, Starke H, Heller A, Kähler C, Schmidt M, Reiber W, Hesse M, Claussen U. Pitfalls of rapid prenatal diagnosis using the interphase nucleus. Prenat Diagn 2001, 21:419-421.
• Liehr T, Beensen V, Starke H, Hauschild R, Hempel E, Fritsche V, Hoppe C, Grosswendt G, Prechtel M, Ziegler M, Claussen U, Von Eggeling F. Tetrasomy 21 due to de novo robertsonian translocation t(14;21) and an additional free trisomy 21. Clin Genet 2001, 60:83-85
• Liehr T, Reiter LT, Lupski JR, Murakami T, Claussen U, Rautenstrauss B. Regional localization of 10 mariner transposon-like ESTs by means of FISH--evidence for a correlation with fragile sites. Mamm Genome 2001, 12:326-328.
• Liss M, Bruchhaus H. Zur Rekonstruktion der Altersstruktur subadulter Individuen eines mittelalterlichen Gräberfeldes anhand von Langknochen- und Hüftbeinfragmenten In: Beiträge zur Archäozoologie und Prähistorischen Anthropologie; Herausg.: Eberhard May und Norbert Benecke; 2001, III:154-156
• Ludecke HJ, Schaper J, Meinecke P, Momeni P, Gross S, von Holtum D, Hirche H, Abramowicz MJ, Albrecht B, Apacik C, Christen HJ, Claussen U, Devriendt K, Fastnacht E, Forderer A, Friedrich U, Goodship TH, Greiwe M, Hamm H, Hennekam RC, Hinkel GK, Hoeltzenbein M, Kayserili H, Majewski F, Mathieu M, McLeod R, Midro AT, Moog U, Nagai T, Niikawa N, Orstavik KH, Plochl E, Seitz C, Schmidtke J, Tranebjaerg L, Tsukahara M, Wittwer B, Zabel B, Gillessen-Kaesbach G, Horsthemke B. Genotypic and phenotypic spectrum in tricho-rhino-phalangeal syndrome types I and III. Am J Hum Genet 2001, 68:81-91.
• Mrasek K, Heller A, Rubtsov N, Trifonov V, Starke H, Rocchi M, Claussen U, Liehr T.: Reconstruction of the female Gorilla gorilla karyotype using 25-color FISH and multicolor banding (MCB). Cytogenet Cell Genet. 2001, 93:242-248.
• Neubert A, Bruchhaus A: Zur Rekonstruktion der Bevölkerung Mitteldeutschlands im zweiten und dritten vorchristlichen Jahrtausend - Perspektiven der weiteren Forschung In: Beiträge zur Archäozoologie und Prähistorischen Anthropologie; Herausg.: Eberhard May und Norbert Benecke; 2001, III:50-54
• Nietzel A, Rocchi MA, Starke H, Heller A, Fiedler W, Wlodarska I, Loncarevic IF, Beensen V, Claussen U, Liehr T. A new multicolor-FISH approach for the characterization of marker chromosomes: centromere-specific multicolor FISH (cenM-FISH) Hum Genet 2001, 108:199-204.
• Northe A, Walter D, Bruchhaus H. Das spätneolithisch-frühbronzezeitliche Gräberfeld bei Haindorf - Vorbericht zu den archäologischen und anthropologischen Untersuchungen
  Beiträge zur Archäozoologie und Prähistorischen Anthropologie; Herausg.: Eberhard May und Norbert Benecke; 2001, III:55-60
• Salafsky IS, Mac Gregor SN, Claussen U, von Eggeling F.: Maternal UPD 20 in an infant from a pregnancy with mosaic trisomy 20. Prenat Diagn 2001, 21:860-863.
• Seidel J, Schiller S, Kelbova C, Beensen V, Orth U, Vogt S, Claussen U, Zintl F, Rappold GA. Brachytelephalangic dwarfism due to the loss of ARSE and SHOX genes resulting from an X;Y translocation. Clin Genet 2001, 59:115-121
• Schleier P, Berndt A, Berndt A, Dahse R, Zenk W, Hyckel P, Kosmehl H. Experimentelle 5-Aminolävulinsäure-induzierte Photodynamische Therapie (ALA-PDT) oraler Karzinome: Ein Verfahren zur Therapie solider Tumoren und Aufklärung des Zelltodes Mund Kiefer Gesichtschir 2001, 5:98-104
• Starke H, Raida M, Trifonov V, Clement JH, Loncarevic IF, Heller A, Bleck C, Nietzel A, Rubtsov N, Claussen U, Liehr T. Molecular cytogenetic characterization of an acquired minute supernumerary marker chromosome as the sole abnormality in a case clinically diagnosed as atypical Philadelphia-negative chronic myelogenous leukaemia. Br J Haem 2001, 113:435-438
• Starke H, Senger G, Kossakiewicz M, Tittelbach H, Rau D, Rubtsov N, Trifonov V, Heller A, Hartmann I, Claussen U, Liehr T.: Maternal insertion of 18q11.2-q12.2 in 18p11.3 of the same chromosome analysed by microdissection and multicolour banding (MCB). Prenat Diagn 2001, 21:1049-1052.
• Vollandt K, Vollandt R, Bruchhaus H. Zahnmedizinische Untersuchungen an Skelettmaterial aus dem Mittelalter Beiträge zur Archäozoologie und Prähistorischen Anthropologie; Herausg.: Eberhard May und Norbert Benecke; 2001, III:117-127
• Wicke J, Kultus M, Bruchhaus H. Skelettfunde aus Karasura, Kreis Cirpan, Zentralbulgarien - degenerative und pathologische Veränderungen an 18 spätantiken und mittelalterlichen Skeletten, Beiträge zur Archäozoologie und Prähistorischen Anthropologie; Herausg.: Eberhard May und Norbert Benecke; 2001, III:88-93

• Beensen V, Liehr T, Heller A, Starke H, Wiederhold M, Mühlig P, Ullmann P. New ways in cancer research. Three dimensional analysis of cell constituents (Confocal laser scanning microscopy with the LSM 510) Innovation Lambda. 2000, 4:18-19; Supplementary information: micro info 40-529 e/1-8.
• Borkhardt A, Bojesen S, Haas OA, Fuchs U, Bartelheimer D, Loncarevic IF, Bohle RM, Harbott J, Repp R, Jaeger U, Viehmann S, Henn T, Korth P, Scharr D, Lampert F. The human GRAF gene is fused to MLL in a unique t(5;11)(q31;q23) and both alleles are disrupted in three cases of myelodysplastic syndrome/acute myeloid leukemia with a deletion 5q. PNAS 2000, 97:9168-9173.
• Bruchhaus H, Neubert A. "Hocker" - Streitäxte - Becher. Schnurkeramische Gräber als interdisziplinärer Forschungsgegenstand von Archäologie und Anthropologie. Archäologie in Sachsen. Anhalt 2000, 9:16-25.
• Bruchhaus H, Csáki A, Neubert A. Probleme und Möglichkeiten bei der Auswertung schnurkeramischer Grabfunde. Beiträge zur Ur- und Frühgeschichte Mitteleuropas. Varia Neolithica I. 2000, 22:163-175.
• Bruchhaus H, Neubert A: Zur Rekonstruktion der Glockenbecherbevölkerung im Mittelelbe-Saale-Gebiet. Ergebnisse einer ersten Bestandsaufnahme. Beiträge zur Ur- und Frühgeschichte Mitteleuropas Varia Neolithica I. 2000, 22:177-193
• Bruchhaus H, Neubert A: Zur Anthropologie der Aunjetitzer Bevölkerung im Mittelelbe-Saale-Gebiet. Überblick nach einer ersten Bestandsaufnahme. Beiträge zur Ur- und Frühgeschichte Mitteleuropas. Varia Neolithica I. 2000, 22:195-203.
• Dahse R, Utting M, Werner W, Schubert J, Claussen U, Junker K. Prognostic significance of mutations in the p53 gene in superficial bladder cancer. Oncol Rep 2000, 7:931-936.
• Dufke A, Seidel J, Schöning M, Döbler-Neumann M, Kelbova C, Liehr T, Beensen V, Baksch C, Klein-Vogler U, Enders H. Microdeletion 4p16.3 in three unrelated patients with Wolf-Hirschhorn syndrome. Cytogenet Cell Genet 2000, 91:81-84
• von Eggeling F, Davies H, Lomas L, Fiedler W, Junker K, Claussen U, Ernst G. Tissue-specific microdissection coupled with ProteinChip array technologies: applications in cancer research. Biotechniques 2000, 29:1066-1070.
• Gebhardt M, Fischer T, Claussen U, Wollina U, Elsner P. Monilethrix--improvement by hormonal influences? Pediatr Dermatol 1999, 16:297-300.
• Heller A, Chudoba I, Bleck C, Senger G, Claussen U, Liehr T. Microdissection based comparative genomic hybridization analysis (micro-CGH) of secondary acute myelogenous leukemias. Int J Oncol 2000, 16:461-468.
• Heller A, Seidel J, Starke H, Beensen V, Senger G, Rocchi M, Wirth J, Chudoba I, Claussen U, Liehr T. Molecular cytogenetic characterization of a new case with partial trisomy 9q and pyloric stenosis and a review of the literature. J Med Genet 2000, 37:529-532
• Hübler A, Seidel J, Kauf E, Schramm D, Beenssen V, Heller A, Liehr T, Zintl F. Insulin-like growth factor serum concentrations reflect insufficient growth in a hypoplastic infant with partial trisomy 9q in the 12th week of life. Eur J Ped Endocrinol Metabolism 2000, 13:445-450
• Jaeger U, Zellner K, Voigt M, Kromeyer-Hauschild K. Veränderungen von Körperhöhe, Körpergewicht und BMI bei Kindern und jungen Erwachsenen aus Ostdeutschland nach der deutschen Wiedervereinigung. Anthrop Közl 2000, 41:155-164.
• Koscielny S, Dahse R, Sonntag J, Riese U, Theuer C, Hofmann ME, von Eggeling F, Claussen U, Beleites E, Ernst G, Fiedler W. Clinical implications of telomerase activity and inactivation of the tumor suppressor gene p16 (CDKN2A) in head and neck cancer. Otolaryngol Pol 2000, 54:291-295.
• Koscielny S, Fiedler W, Dahse R, Beleites E. Reaktivierung der Telomerase in Plattenepithelkarzinomen des Kopf-Hals-Bereiches
  Laryngorhinootologie 2000, 79:551-556
• König K, Göhlert A, Liehr T, Loncarevic IF, Riemann I. Two-photon multicolor FISH: A verstile techniqe to detect specific sequneces within singe DNA molecules in cells and tissues. Single Molecules 2000, 1:41-51
• Kromeyer-Hauschild K, Jaeger U. Growth Studies in Jena, Germany: Changes in Sitting Height, Biacromial and Bicristal Breadth in the Past Decenniums. Am J Hum Biol 2000, 12:646-654.
• Liehr T, Beensen V, Hauschild R, Ziegler M, Hartmann I, Starke H, Heller A, Kähler C, Schmidt M, Reiber W, Hesse M, Claussen U. Pitfalls of rapid prenatal diagnosis using the interphase nucleus. Prenat Diagn 2001, 21:419-421.
• Liehr T, Beensen V, Starke H, Hauschild R, Hempel E, Fritsche V, Hoppe C, Grosswendt G, Prechtel M, Ziegler M, Claussen U, v Eggeling F. Tetrasomy 21 due to de novo robertsonian translocation t(14;21) and an additional free trisomy 21 Clin Genet 2001, 60:83-85
• Liehr T, Reiter LT, Lupski JR, Murakami T, Claussen U, Rautenstrauss B. Regional localization of 10 mariner transposon-like ESTs by means of FISH--evidence for a correlation with fragile sites. Mamm Genome 2001, 12:326-328.
• Meyer E, Wiese M, Bruchhaus H, Claussen U, Klein A. Extraction and amplification of authentic DNA from ancient humen remains. Forensic Science International 2000 113:87-90
• Mrasek K, Heller A, Rubtsov N, Trifonov V, Starke H, Rocchi M, Claussen U, Liehr T. Reconstruction of the female Gorilla gorilla karyotype using 25-color FISH and multicolor banding (MCB). Cytogenet Cell Genet 2001, 93:242-248.
• Rubtsov NB, Karamisheva TV, Astakhova NM, Liehr T, Claussen U, Zhdanova NS. Zoo-FISH with region-specific paints for mink chromosome 5q: delineation of inter- and intrachromosomal rearrangements in human, pig, and fox. Cytogenet Cell Genet 2000, 90:268-270.
• Zellner K, Kromeyer-Hauschild K: Somatische Entwicklung von sehr untergewichtig (<1500 g) bzw. sehr unreif (<32 SSW) geborenen Kindern. Monatsschr. Kinderheilkd 2000, 148:131-137.

• Bruchhaus H, Csáki A, Neubert A. Probleme bei der Auswertung prähistorischer Grabfunde (Anthropologie und Archäologie). Archäologisches Nachrichtenblatt 1999, 4:89-100.
• Bruchhaus H, Neubert A. Zur Rekonstruktion endneolithischer und frühbronzezeitlicher Bevölkerungen im Mittelelbe-Saale-Gebiet. Ergebnisse einer ersten Bestandsaufnahme. Ber d Röm Germ Komm 1999-2001, 80:122-161
• Bruchhaus H, Hübschmann J, Thiele K, Uerlings H. Geschlechtsspezifische Unterschiede am menschlichen Skelett und ihre Bedeutung für die Geschlechtsbestimmung. Beiträge zur Archäozoologie und Prähistorische Anthropologie 1999, 2:219-237.
• Chudoba I, G Senger G, Plesch A, Claussen U. New developments in clinical cytogenetics. ECA Newsletter 1999, 3:3-6.
• Chudoba I, Plesch A, Lörch T, Lemke J, Claussen U, Senger G. High resolution multicolor-banding: a new technique for refined FISH analysis of human chromosomes. Cytogenet Cell Genet 1999, 84:156-60.
• Chudoba I, Franke Y, Senger G, Sauerbrei G, Demuth S, Beensen V, Neumann A, Hansmann I, Claussen U. Maternal UPD 20 in a hyperactive child with severe growth retardation Eur J Hum Genet 1999, 7:533-540
• Dahse R, Fiedler W, Junker K, Schlichter A, Schubert J, Claussen U. Telomerase activity and telomere lengths: alterations in renal cell carcinomas. Kidney Int 1999, 56:1289-1290.
• Dahse R, Fiedler W, von Eggeling F, Schimmel B, Koscielny S, Beleites E, Claussen U, Ernst G. P53 genotyping - an effective concept for molecular testing of head and neck cancer? Int J Mol Med 1999, 4:279-283.
• Fiedler W, Junker K, Schlichter A, Schubert J, Ernst G, Dahse R, Claussen U. Determination of telomerase activity for differential analysis of multifocal renal cell carcinomas. Kidney Int 1999, 56:1286-1288.
• Fröber R, Kohoutek T, Schulze E, Jagemann J, Beensen V, Hauschild R, Linss W. Eine seltene Herzmißbildung bei einem menschlichen Feten Plzen lek Sborn, Suppl. 1999, 71:201-204
• Hesse V, Bartezky R, Jaeger U, Kromeyer-Hauschild K, Zellner K, Vogel H, Bernhardt I, Hofmann A. Körper-Masse-Index: Perzentilen deutscher Kinder im Alter von 0-18 Jahren. Kinderärztl Prax 1999, 8:542-553.
• Jaeger U, Kromeyer-Hauschild K. Growth Studies in Jena, Germany: Changes in Thoracic Measurements Between 1975 and 1995. Am J Hum Biol 1999, 11:784-792.
• Jaeger U, Kromeyer-Hauschild K, Zellner K, Eisele R, Lüdde R, Hebebrand J. Veränderungen von Körpergewicht und Body-Mass-Index (BMI) bei deutschen Gemusterten (erstuntersuchten Wehrpflichtigen). Akt Ernähr-Med1999, 24:249-255.
• Junker K, Werner W, Mueller C, Ebert W, Schubert J, Claussen U. Interphase cytogenetic diagnosis of bladder cancer on cells from urine and bladder washing. Int J Oncol 1999, 14:309-313.
• Kromeyer-Hauschild K, Zellner K, Jaeger U, Hoyer H. Prevalence of overweight and obesity among school children in Jena (Germany). Int J Obes1999, 23:1143-1150.
• Liehr T, Starke H, Beensen V, Kähler CH, Harbich M, Brude E, Ziegler M, Claussen U. Translocation trisomy dup (21q) and free trisomy 21 can be distinguished by interphase-FISH. Int J Mol Med 1999, 3:11-14
• Loncarevic IF, Roitzheim B, Ritterbach J, Viehmann S, Borkhardt A, Lampert F, Harbott L. Trisomy 21 is a recurrent secondary aberration in childhood acute lymphoblastic leukemia with TEL/AMLI gene fusion. Genes Chr Cancer 1999, 24:272-277
• Reichenbach H, Holland H, Dalitz E, Demandt C, Meiner A, Chudoba I, Lemke J, Claussen U, Froster UG. De novo complete trisomy 5p: clinical report and FISH studies. Am J Med Genet 1999, 85:447-451.
• Riese U, Dahse R, Fiedler W, Theuer C, Koscielny S, Ernst G, Beleites E, Claussen U, von Eggeling F. Tumor suppressor gene p16 (CDKN2A) mutation status and promoter inactivation in head and neck cancer. Int J Mol Med 1999, 4:61-65.
• Schlichter U, Fiedler W, Junker K, Dahse R, Claussen U, Schubert J. Determination of telomerase activity in multifocal renal cell carcinoma Int J Onc 1999, 15:577-581.
• Seidel J, Vogt S, Kirchner M, Kauf E, Beensen V, Zintl F. Zur wissenschaftlichen Auseinandersetzung mit Erkrankungen des Skelettsystems in der Universitäts-Kinderklinik Jena - Ein historischer Überblick. Pädiatr Grenzgeb 1999, 38:51-63
• Seidel J, Kauf E, Zintl F, Mentzel H-J, Vogt S, Beensen V. Professor Häßlers Beitrag zur Erforschung der Erkrankungen des kindlichen Skeletts - Weiterführung unter Berücksichtigung molekulargenetischer Erkenntnisse. Ärztebl Thüring 1999, 10:204-212
• Starke H, Schreyer I, Kähler CH, Fiedler W, Beensen V, Heller A, Nietzel A, Claussen U, Liehr T. Molecular cytogenetic characterization of a prenatally detected supernumerary minute marker Chromosome 8. Prenat Diagn 1999, 19:1169-1174
• Stonane E, Fiedler W, Stonans I, von Eggeling F. Identification of differenttially expressed genes in T-lymphocyte subsets of discordant monozygotic rheumatoid arthritis twins Allergologie 1999, 22:119-126
• Uerlings H, Thiele K, Bruchhaus H. Beitrag der Osteologie bei der Identifizierung auf dem Gebiet der Forensik (Falldemonstration). Beiträge zur Archäozoologie und Prähistorische Anthropologie 1999, 2:238-242.
• von Eggeling F, Werner G, Theuer C, Riese U, Dahse R, Fiedler W, Schimmel B, Ernst G, Karte K, Claussen U, Wollina U. Analysis of the tumor suppressor gene p16(INK4A) in microdissected melanoma metastases by sequencing, and microsatellite and methylation screening. Arch Dermatol Res 1999, 291:474-477
• Zellner K, Kromeyer-Hauschild K, Stadler J, Jaeger U. Ergebnisse der Untersuchung ausgewählter Kopfmaße bei Jenaer Kindern. Anthrop Anz 1999, 57:147-163.

• Chudoba I, Plesch A, Lörch T, Lemke J, Claussen U, Senger G. High resolution multicolor-banding: a new technique for refined FISH analysis of human chromosomes. Cytogenet Cell Genet 1999, 84:156-160.
• Dahse R, Fiedler W, Riese U; v. Eggeling F, Ernst G. A semi-automated highly sensitive approach for mutation detection Trends in Genetics-Technical Tips Online (1998) Elsevier Trends Journals http://www.elsevier.nl/locate/tto (t01542)
• Edelhoff S, GrondGinsbach C, von Eggeling F, Korholz D, Gobel U, Senger G. Complex chromosomal rearrangements associated with congenital erythrophagocytotic histiocytosis Clin Gen 1998, 53:298-302
• Gebhart E, Liehr T, Wolff E, Ries J, Fiedler W, Steininger H, Koscielny S, Girod S. Pattern of genomic imbalances in oral squamous cell carcinomas with and without an increased copy number of 11q13. Int. J of Oncol 1998, 12:1151-1155.
• Jaeger U, Bruchhaus H, Finke L, Kromeyer-Hauschild K, Zellner K. Säkularer Trend bei der Körperhöhe seit dem Neolithikum. Anthrop Anz 1998, 56:117-130.
• Jaeger U, Zellner K, Kromeyer-Hauschild K, Finke L, Bruchhaus H. Werden Kopfmaße von Umweltfaktoren beeinflußt? Z Morph Anthrop 1998, 82:59-66.
• Jaeger U. Secular trend in Germany. In: Bodzsár, B.É. and C. Susanne (eds.): Secular Growth Changes in Europe. Eötvös Loránd Univ. Press, Budapest 1998, 135-160.
• Kromeyer-Hauschild K, Jaeger U. Growth Studies in Jena, Germany: Changes in Body Size and Subcutaneous Fat Distribution Between 1975 and 1995. Am J Hum Biol 1998, 10:579-587.
• Kromeyer-Hauschild K, Jaeger U. Zunahme der Häufigkeit von Übergewicht und Adipositas bei Jenaer Kindern. Monatsschr Kinderheilk 1998, 146:1192-1196.
• Liehr T, Ries J, Wolff E, Fiedler W, Dahse R, Ernst G, Steininger H, Koscielny S, Girod S, Gebhart E. Gain of DNA copy number on chromosome 3q26-qter and 5p14-pter is a frequent finding in head and neck squamous cell carcinomas. Int J Mol Med 1998, 2:173-179
• Zellner K, Jaeger U, Kromeyer-Hauschild K. Das Phänomen der Debrachykephalisation bei Jenaer Schulkindern. Anthrop Anz 1998, 4: 301-312.

• Behrens F, Claussen U, Iyer LM, Green ED, Horsthemke B, Williamson R, Huxley C, Coutelle C. Isolation of DNA from the centromere of human chromosome 7 by microdissection. Chromosome Res 1997, 5:215-220.
• von Eggeling, F, Michel S, Günther M, Schimmel B, Claussen U: The origin of nucleated cells in maternal circulation can be exactly determined with the help of random PCR and a set of length polymorphisms. Hum Gen 1997, 99:266-270
• Hesse V, Jaeger U, Vogel H, Kromeyer-Hauschild K, Zellner K, Bernhardt I, Hofmann A, Deichl A. Wachstumsdaten deutscher Kinder von Geburt bis zu 18 Jahren. Sozialpädiatrie 1997, 19:20-22.
• Hliscs R, Mühlig P, Claussen U. The nature of G-bands analyzed by chromosome stretching.Cytogenet Cell Genet. 1997, 79:162-166.
• Hliscs R, Mühlig P, Claussen U. The spreading of metaphases is a slow process which leads to a stretching of chromosomes. Cytogenet Cell Genet 1997, 76:167-171.
• Junker K, Schlichter A, Junker U, Knofel B, Kosmehl H, Schubert J, Claussen U. Cytogenetic, histopathologic, and immunologic studies of multifocal renal cell carcinoma. Cancer 1997, 79:975-981.
• Kromeyer-Hauschild K, Jaeger U. Social factors and physical growth of school children in Jena. Acta Biol Szeged 1997, 42:235-240.
• Kromeyer K, Hauspie RC, Susanne C. Socioeconomic factors and growth during childhood and early adolescence in Jena children. Annals Hum Biol 1997, 24:343-353.
• Senger G, Chudoba I, Friedrich U, Tommerup N, Claussen U, Brondum-Nielsen K. Prenatal diagnosis of a half-cryptic translocation using chromosome microdissection. Prenat Diagn 1997, 17:369-374.
• Zellner K, Keller E, Kromeyer K, Jaeger U. Acromegaloidal changes in Ullrich-Turner syndrome after treatment with growth hormone. Acta Med Auxol 1997, 29:125-133.

• Beensen V, Ernst G, Wollina U. Bedeutung genetischer Faktoren für die Entstehung maligner Melanome und dysplastischer Naevi Ärzteblatt Thüringen 1996, 12:618 - 621
• Dahse R, Fiedler W, Kosmehl H, Schlichter A, Ernst G, Schubert J, Claussen U. Changes in telomere length in Renal Cell Carcinomas. Cellular and Molecular Biology 1996, 42:477-485
• Fiedler W, Dahse R, Junker K, Schlichter A, Janitzky V, Ernst G, Schubert J, Claussen U. Telomerase activity and telomere length in different areas of renal cell carcinoma. Int J Onc 1996, 6:1227-1232
• Kelbova C, Beensen V, Senger G, Claussen U, Seidel J. Mit FISH genetisch bedingten Krankheiten auf der Spur. Zeiss Information mit Jenaer Rundschau 1996, 5:10-12.
• Kromeyer K, Wurschi F. Untersuchungen über den Zusammenhang zwischen körperlicher Entwicklung und Dentition anhand der Jenaer Längsschnittstudie. Anthrop Anz 1996, 54:255-266.
• Kromeyer K, Wurschi F. Zahneruption bei Jenaer Kindern in der ersten Phase des Wechselgebisses. Anthrop Anz 1996, 54:57-70.
• Kromeyer K, Zellner K, Jaeger U. Socio-economic factors and growth of schoolchildren in Jena. In: Bodzsár, B.É. and C. Susanne (eds.): Studies in Human Biology. Eötvös Univ. Press, Budapest 1996:131-137.
• Rubtsov N, Senger G, Kuzcera H, Neumann A, Kelbova C, Junker K, Beensen V, Claussen U. Interstitial deletion of chromosome 6q: precise definition of the breakpoints by microdissection, DNA amplification, and reverse painting. Hum Genet 1996, 97:705-709.
• Schlichter A, Junker K, Kosmehl H, Katenkamp D, Claussen U, Schubert J. Cyto- and molecular genetic studies of renal cell carcinoma with special reference to multifocal carcinoma lesions. Urologe A. 1996, 35:305-309. (German)
• Zellner K, Kromeyer K, Jaeger U. Growth studies in Jena, Germany: Historical background and secular changes in stature and weight in children 7 - 14 years. Am J Hum Biol 1996, 8:371-382.

• Claussen U, Voigt HJ, Ulmer R, Beinder E. [Rapid karyotyping in the 2nd and 3rd trimester: results and experiences] Geburtshilfe Frauenheilkd. 1995, 55:41-48. Review. (German)
• Beensen V, Gross W, Hauschild R, Kelbova C, Eichhorn K-H. Pränataldiagnostik genetisch bedingter Erkrankungen Ärzteblatt Thüringen 1995, 1:43-51
• Klink A, Schiebel K, Winkelmann M, Rao E, Horsthemke B, Ludecke HJ, Claussen U, Scherer G, Rappold G. The human protein kinase gene PKX1 on Xp22.3 displays Xp/Yp homology and is a site of chromosomal instability. Hum Mol Genet 1995, 4:869-878.
• Kromeyer K, Zellner K, Jaeger U. Zur Dynamik der Wachstumsintensität bei Jenaer Schulkindern. Anthrop Anz 1995, 53:349-357.
• Kromeyer K, Jaeger U. Auswirkungen veränderter Lebensbedingungen auf Körperhöhe und Körpergewicht bei Jenaer Vorschulkindern.
  Z Morph Anthrop 1995, 81:91-110.

• Jaeger U, Kromeyer K, Zellner K. Preliminary results of a longitudinal study of Jena preschoolers and schoolchildren. In: Hajnis, K. /Ed./: Growth and Ontogenentic Development in Man IV. Charles University, Prague 1994: 35-38.
• Kromeyer K. Die Entwicklung der Körperhöhe bei Kindern zwischen 4 und 12 Jahren - Ergebnisse der Jenaer Längsschnittuntersuchung. Anthrop Anz 1994, 52:327-340.
• Wienberg J, Jauch A, Lüdecke HJ, Senger G, Horsthemke B, Claussen U, Cremer T, Arnold N, Lengauer C. The origin of human chromosome 2 analyzed by comparative chromosome mapping with a DNA microlibrary. Chromosome Res 1994, 2:405-410.
• Voigt HJ, Beinder U, Claussen U. [Ultrasound detection of suspected chromosome abnormalities in the 1st and 2nd trimester. Results of a prospective study] Geburtshilfe Frauenheilkd 1994, 54:460-467. (German)
• Stosiek N, Ulmer R, von den Driesch P, Claussen U, Hornstein OP, Rott HD. Chromosomal mosaicism in two patients with epidermal verrucous nevus. Demonstration of chromosomal breakpoint. J Am Acad Dermatol 1994, 30:622-625