2025
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
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Rapid UPF1 depletion illuminates the temporal dynamics of the NMD-regulated human transcriptome.
Molecular Cell, 85 (18).
3524-3546.e12.
Elsevier.
ISSN 1097-2765
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
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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
2023
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
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Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions.
Genome Medicine, 15 (1).
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Springer Nature.
ISSN 1756-994X
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