2014

• 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.

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