Universität zu Köln

Boehm, Volker ORCID: 0000-0001-7588-9842, Wallmeroth, Damaris ORCID: 0000-0003-3437-4070, Wulf, Paul O., Popp, Oliver, Teixeira Alves, Luiz Gustavo, Reinecke, Lucie, Riedel, Maximilian, Wyler, Emanuel, Franitza, Marek, Becker, Kerstin ORCID: 0009-0009-7897-7181, Polkovnychenko, Karina ORCID: 0009-0001-9468-3150, Del Giudice, Simone, Benlasfer, Nouhad, Mertins, Philipp, Landthaler, Markus and Gehring, Niels H. ORCID: 0000-0001-7792-1164 (2025). Rapid UPF1 depletion illuminates the temporal dynamics of the NMD-regulated human transcriptome. Molecular Cell, 85 (18). 3524-3546.e12. Elsevier. ISSN 1097-2765

Tschernoster, Nikolai ORCID: 0000-0002-6058-9342, Erger, Florian ORCID: 0000-0002-2768-1702, Kohl, Stefan, Reusch, Björn ORCID: 0000-0002-8963-6835, Wenzel, Andrea ORCID: 0009-0005-3280-0947, Walsh, Stephen, Thiele, Holger ORCID: 0000-0003-4495-4597, Becker, Christian ORCID: 0009-0002-2964-4486, Franitza, Marek, Bartram, Malte P., Kömhoff, Martin, Schumacher, Anna-Lena ORCID: 0000-0001-7739-486X, Kukat, Christian ORCID: 0000-0003-1508-0229, Borodina, Tatiana, Quedenau, Claudia, Nürnberg, Peter ORCID: 0000-0002-7228-428X, Rinschen, Markus M, Driller, Jan H., Pedersen, Bjørn P., Schlingmann, Karl P., Hüttel, Bruno ORCID: 0000-0001-7165-1714, Bockenhauer, Detlef, Beck, Bodo Bernhard ORCID: 0000-0003-0495-7670 and Altmüller, Janine ORCID: 0000-0003-4372-1521 (2023). Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions. Genome Medicine, 15 (1). p. 62. Springer Nature. ISSN 1756-994X

Wenzel, Marten C. ORCID: 0009-0009-0322-2577, Dasmeh, Pouria, Plum, Patrick S. ORCID: 0000-0002-8165-4553, Giel, Ann-Sophie, Hoppe, Sascha ORCID: 0000-0001-9246-3747, Franitza, Marek, Jonas, Christoph, Thieme, René, Zhao, Yue ORCID: 0000-0002-6790-3402, Heider, Dominik, Palles, Claire, Fitzgerald, Rebecca Claire, Bruns, Christiane J. ORCID: 0000-0001-6590-8181, Buettner, Reinhard ORCID: 0000-0001-8806-4786, Quaas, Alexander ORCID: 0000-0002-3537-6011, Gockel, Ines, Maj, Carlo, Chon, Seung-Hun ORCID: 0000-0002-8923-6428, Schumacher, Johannes and Hillmer, Axel M. ORCID: 0000-0002-3381-7266 (2025). Single-cell analysis of Barrett’s esophagus and carcinoma reveals cell types conferring risk via genetic predisposition. Cell Genomics, 5 (10). pp. 1-19. Elsevier. ISSN 2666-979X