2016

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.