• 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, 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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.
• 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 MAK, 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.
• 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.
• 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.
• 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.
• 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.

Zahl der Publikation pro Jahr (1994-2012)