Show 10 5 10 15 20 50 100 250 Sort by year (new to old) Actions Save this search Download search results Subscribe to news feed Your filters: cql: author="Crosiers, David" or (type any "bookEditor journalEditor issueEditor" and editor="Crosiers... Add to list Journal Article A1 open access Exome sequencing and multigene panel testing in 1,411 patients with adult-onset neurologic disorders Nika Schuermans (UGent) , Hannah Verdin (UGent) , Jody Ghijsels (UGent) , Madeleine Hellemans (UGent) , Elke Debackere (UGent) , Elke Bogaert (UGent) , Sofie Symoens (UGent) , Leslie Naesens (UGent) , Elien Lecomte, David Crosiers, et al. (2023) NEUROLOGY-GENETICS. 9(3). Add to list Miscellaneous open access Homozygous and compound heterozygous rare variants in VPS13C contribute to Lewy body diseases Stefanie Smolders, Stéphanie Philtjens, David Crosiers, Anne Sieben (UGent) , Elisabeth Hens, Bavo Heeman, Sara Van Mossevelde, Philippe Pals, Bob Asselbergh, Roberto Dos Santos Dias, et al. (2020) Research Square. Add to list Journal Article A1 open access Mutated ATP10B increases Parkinson's disease risk by compromising lysosomal glucosylceramide export Shaun Martin, Stefanie Smolders, Chris Van den Haute, Bavo Heeman, Sarah van Veen, David Crosiers, Igor Beletchi, Aline Verstraeten, Helena Gossye, Geraldine Gelders, et al. (2020) ACTA NEUROPATHOLOGICA. 139(6). p.1001-1024