Show 15 5 10 15 20 50 100 250 Sort by year (new to old) Actions Download search results Subscribe to news feed Your filters: cql: author="Jägle, Herbert" or (type exact bookEditor and editor="Jägle, Herbert") Add to list Miscellaneous Resolving the dark matter of ABCA4 for 1,054 Stargardt disease probands through integrated genomics and transcriptomics Mubeen Khan, Stéphanie S. Cornelis, Marta del Pozo-Valero, Laura Whelan, Esmee H. Runhart, Ketan Mishra, Femke Bults, Yahya AlSwaiti, Alaa AlTabishi, Elfride De Baere (UGent) , et al. (2019) bioRxiv. Add to list Journal Article A1 Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response Bernd Wissinger, Simone Schaich, Britta Baumann, Michael Bonin, Herbert Jägle, Christoph Friedburg, Balázs Varsányi, Carel B Hoyng, Hélène Dollfus, John R Heckenliyely, et al. (2011) HUMAN MUTATION. 32(12). p.1398-1406