Show 20 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="Scherer, Stephen W" or (type exact bookEditor and editor="Scherer, Stephen W") Add to list Journal Article A1 De novo missense variants in RAC3 cause a novel neurodevelopmental syndrome Gregory Costain, Bert Callewaert (UGent) , Heinz Gabriel, Tiong Y Tan, Susan Walker, John Christodoulou, Tamas Lazar, Björn Menten (UGent) , Julia Orkin, Simon Sadedin, et al. (2019) GENETICS IN MEDICINE. 21(4). p.1021-1026 Add to list Journal Article A1 Analysis of shared heritability in common disorders of the brain Verneri Anttila, Brendan Bulik-Sullivan, Hilary K Finucane, Raymond K Walters, Jose Bras, Laramie Duncan, Valentina Escott-Price, Guido J Falcone, Padhraig Gormley, Rainer Malik, et al. (2018) SCIENCE. 360(6395). Add to list Journal Article A1 Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus Gea Beunders, Els Voorhoeve, Christelle Golzio, Luba M Pardo, Jill A Rosenfeld, Michael E Talkowski, Ingrid Simonic, Anath C Lionel, Sarah Vergult (UGent) , Robert E Pyatt, et al. (2013) AMERICAN JOURNAL OF HUMAN GENETICS. 92(2). p.210-220