Universität zu Köln

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

van Eerde, Albertien M., Teixeira, Ana, Galletti, Flavia, Maternik, Michal, Capone, Valentina, Westland, Rik, Mulder, Jaap, Halbritter, Jan, Osterholt, Thomas ORCID: 0000-0001-5047-0252, Neukel, Valentina, Weber, Lutz T. ORCID: 0000-0003-4116-598X, Liebau, Max C. ORCID: 0000-0003-0494-9080, Schaefer, Franz and Kohl, Stefan ORCID: 0000-0001-9600-8231 (2025). Risks and benefits of ChatGPT in informing patients and families with rare kidney diseases: an explorative assessment by the European Rare Kidney Disease Reference Network (ERKNet). Pediatric Nephrology, 40 (9). pp. 2899-2905. Springer Nature. ISSN 0931-041X