2026

Arlt E, Bley N, Rausch A, Hauser S, Pietzsch J, Misiak D, Liehr T, Kankel S, Dautz T, Dreher L, Kǒng X, Kielstein H, Bazwinsky-Wutschke I. Sex determines the natural killer cell-mediated immunity against pancreatic cancer. Oncoimmunology 2026, 15: 2645298
Atri Roozbahani G, Heidari Horestani M, Schindler K, Kallenbach J, Baniahmad A. Induction of cellular senescence by androgen receptor agonist or antagonist is mediated via two novel common DYRK1A-DREAM and cyclin G2 signaling pathways in castration-resistant prostate cancer. J Adv Res 2026, 80: 371-392.
Asar DY, Kankel S, Keller DT, Hardt KS, Buhl EM, Liehr T, Weiskirchen R. Comprehensive cytogenetic and genomic profiling of the murine AML12 (Alpha Mouse Liver 12) hepatocyte cell line. Cells 2026, 15: 390.
Batalli A, Liehr T, Temaj G. Behçet's disease: A comprehensive overview of symptoms, pathology, genetics, and treatment. J Mother Child 2026, 30: 1-10.
Bisba M, Louizou E, Tzanakis K, Liehr T, Vittas S. Prenatal diagnosis of a low-level mosaic small supernumerary marker chromosome (sSMC): Early postnatal clinical follow-up. OBM Genetics 2026, 10: 353.
Bock A, Schurig M, Willoughby M, Mirecki A, Seemann E, Lohachova K, Katona I, Mittag S, Liebmann L, Franzka P, Heidari Horestani M, Khundadze M, Mosler T, Louie T, de Visser M, Weterman MAJ, Kiehntopf M, Beetz C, Nietzsche S, Huber O, Weis J, Kessels MM, Bhaskara RM, Qualmann B, Đikić I, Hübner CA. REEP1 accumulation disrupts ER integrity and drives spinal motoneuron degeneration in distal hereditary motor neuropathy. Adv Sci (Weinh) 2026, 13: e11483.
Bouchahta H, Benyahya N, EL Amrani Z, Ouboukss F, Liehr T, Elalaoui SC, Carreira IM, Doubaj Y, Natiq A, Sbabou L. Clinical and molecular cytogenetic characterization of a de novo 3q26.33-q28 duplication: Case report and literature review. OBM Genetics 2026, 10: 341.
Chong ML, Burssed B, Chen Z, Wen J, Ng E, Szewczyk B, Wang G, Chua KP, Liehr T, Zou Y, Murry JB, Sheth F, Li P, Melaragno MI. Unravelling ring chromosome structures and formation mechanisms by short read and long-read genomic sequencing. Genet Med Open 2026, 4: 103475.
Cornejo Müller A, Liehr T, Balakrishnan P, Keller DT, Hardt KS, Schröder-Lange SK, Kankel S, Buhl EM, Liedtke C, Weiskirchen R. Establishment and characterization of the murine liver tumor cell line ∆CN60 with conditional caspase-8 and IKKγ/NEMO inactivation and a hepatocyte-biliary, progenitor-like phenotype. Cells 2026, 15: 1325.
dos Santos N, Sassi FdMC, dos Santos RZ, Goes CAG, de Moraes RLR, Porto-Foresti F, Liehr T, Cioffi MdB, Utsunomia R. Molecular divergence and genomic composition of B chromosomes in the fish Cyphocharax modestus (Characiformes, Curimatidae). Sci Rep 2026, 16: 28198.
El Amrani Z, Ouboukss F, Lyahyai J, Padutsch N, Natiq A, Sefiani A. 14q32.31-qter duplication due to a de novo unbalanced translocation: Case report and literature review. ChrSomics 2026, 1: 5.
Erdmann H, Schaub A, Lucas MC, Scholz V, Benet-Pagès A, Becker K, Dineiger C, Mayer V, van Buren I, Breithausen E, Akbari K, Cordts I, Sauer M, Schneider C, Krakowsky R, Schnabel F, Dunker K, Fabritius L, Gerb J, Grabova D, Möhwald K, Näher M, Steinmetz K, Thiessen F, Jäck A, Schneider-Gold C, Zittel S, Petersen C, Schreyer I, Mämecke L, Wilfling S, Wunderlich G, Brenner D, Hellenbroich Y, Muhle K, Huchtemann T, Claus I, Klopstock T, Strupp M, Levin J, Höglinger GU, Huppert D, Becker-Bense S, Filippopulos F, Kilpert F, Leitão E, Kaya S, Depienne C, Schöberl F, Neuhann T, Holinski-Feder E, Zwergal A, Abicht A. Repeat-associated ataxias in a German patient cohort analysed by targeted parallel long-read sequencing. Brain 2026, 149: 993-1006.
Hahn A, Hentschel J, Saleem S, Becker S, Liehr T, Schober A, Krämer OH, Sonnemann J, Marx C. Evaluation of novel targeted small-molecule therapeutics in desmoplastic small round cell tumor (DSRCT) cells. J Cancer Res Clinical Oncol 2026; 152:192.
Hennings JC, Murthy KS, Picard N, Cabrita I, Böhm D, Huebner AK, Krause ME, Gentsch GJ, Shah V, Baraka-Vidot J, Khundadze M, Schmerler D, Kiehntopf M, Stauber T, Böckenhauer D, Jentsch TJ, Bachmann S, Franke C, Schermer B, Eladari D, Chambrey R, Hübner CA. Metabolic acidosis causes a Fanconi-like syndrome with intracellular trafficking defects and proximal tubule dysfunction. Sci Transl Med 2026, 18: eads6299.
Kavaja F, Liehr T, Temaj G. MedicalGenetic architecture of obesity and advances in precision pharmacotherapy: A comprehensive review. Acta Biochim Pol 73: 15484.
Liehr T. Challenges and ethical issues related to non-invasive prenatal testing (NIPT). OBM Genetics 2026; 10: 2601332.
Liehr T. Inclusion of human centromeres in genomic browsers – will it finally come? J Transl Genet Genom 2026; 10: 156-159.
Liehr T. Cancer type specific copy number variants are identical over species borders. Reports of NAS Ra 2026; 126: 4.
Liehr T, Rinčić M. ChromoSomics: A new home for chromosomic-related research. ChrSomics 2026, 1: 1.
Liehr T, Fuchs S. Unanswered questions when human karyotyping shows a supernumerary chromosome. Heredity (Edinb) 2026, 135:633-637.
Liehr T, Weise A. Comment on insurance information for non-invasive prenatal testing (NIPT) in Germany [Kommentar zur Versicherteninformation „Bluttest auf Trisomien. Der nicht invasive Pränataltest (NIPT) auf Trisomie 13, 18 und 21“] ChrSomics. 2026; 1(1): 46-56.
Müller-Schiffmann A, Torres F, Kitaygorodskyy A, Ramani A, Alatza A, Tschirner SK, Orts J, Haltrich A, Prikulis I, Yu S, Dey D, Mallesh S, Prasad D, Solas D, Bader V, Rozemuller A, Wray S, Gopalakrishnan J, Riek R, Lingappa VR, Korth C. Oxidized MIF is an Alzheimer's disease drug target relaying external risk factors to tau pathology. Cell Rep Med. 2026, 7: 102520.
Pires S, França I, Oliveira P, Jorge P, Liehr T, Oliva-Teles N. The role of satellite DNA-enriched heterochromatic variants in reproductive disorders: Insights from standardized cytogenetic analysis. Chromosome Res 2026, 34: 9.
Rincic M, Kopic J, Klein V, Krsnik Z, Liehr T, Giesselmann S, Kurth I, Kraft F. Structural variations in evolutionary novel genomic regions: New insights into neurodevelopmental disorders by long-read DNA sequencing. Mol Med 2026, 32: 17.
Rodríguez Martínez L, Campos-Galindo I, Padutsch N. Almost complete whole-arm reciprocal translocation t(14;21) in an infertile male: A hidden diagnostic challenge that highlights the need for cytogenetic expertise. ChrSomics 2026, 1: 4.
Setti PG, Moura de Oliveira A, Ferguson Motheo S, Gonçalves de Almeida OG, Liehr T, de Bello Cioffi M. Concanavalin A protocol for felid lymphocyte culture and chromosome preparation. Int J Mol Sci 2026, 27: 6662
Sheth F, Shah J, Muranjan M, Liehr T, Padutsch N, Mane S, Ng SME, Li P, Desai M, Kansara H, Sheth JJ, Sheth H. Genotype-phenotype correlation through breakpoint characterization of a genomically balanced complex chromosomal rearrangement using long read sequencing. Am J Med Genet 2026; 200: 1673-1681.
Silva Veiga PR, Dziechciarz Vidal JA, Liehr T, Cioffi MdB. Comparative repeatomics uncovers genome diversification in Gasteropelecidae fishes. Int J Mol Sci 2026; 27:8720.
Stallhofer J, Leonhardt J, Semmler J, Neugebauer S, Kiehntopf M, Löhden W, Homeister L, Ungelenk M, Hübner CA, Steube A, Waschina S, Stallmach A. Loss of TGR5-activating bile acids is associated with disease activity in inflammatory bowel disease. Sci Rep 2026, 16: 22812.
Taheri M, Baniahmad A. Response to letter to the editor. Int J Surg. 2026, 112: 2199.
Toma GA, de Oliveira EHC, Maurício KD, Carneiro LA, Liehr T, Cioffi MdB. The role of satellite DNAs in repeatome organization and sex chromosome evolution in the owl monkey Aotus infulatus and congeneric species. Biol Direct 2026, 21: 156.
Trifonov V, Johnson Pokorná M, Giovannotti M, de Oliveira E, Griffin DK, Parise‑Maltempi PP, Heslop‑Harrison P, Kasai F, Balmus G, Kratochvíl L, Pereira J, O’Brien P, Liehr T. A Darwinian journey into chromosomics: Comparative cytogenetics and genome evolution in the laboratory of Professor Malcolm Ferguson‑Smith. Chromosome Res 2026, 34:23.

Books

Liehr T. Fluorescence in situ Hybridization (FISH) – Application Guide, 3nd Ed., Springer, Berlin, 2026

ISBN: 978 1071651490

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