Books
Liehr T. Fluorescence in situ Hybridization (FISH) – Application Guide, 3nd Ed., Springer, Berlin, 2026
ISBN: 978 1071651490
chek out here
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.
- 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.
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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.
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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.
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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 Mar 5;149(3):993-1006.
- 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.
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Liehr T. Challenges and ethical issues related to non-invasive prenatal testing (NIPT). OBM Genetics 2026; 10: 2601332.
- 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.
- Taheri M, Baniahmad A. Response to letter to the editor. Int J Surg. 2026, 112:2199.
