Gene family information facilitates variant interpretation and identification of disease-associated genes in neurodevelopmental disorders
Authors: Dennis Lal; Patrick May; Eduardo Perez-Palma; Kaitlin Samocha; Jack A. Kosmicki; Elsie Robinson; Rikke Moller; Roland Krause; Peter Nurnberg; Sarah Weckhuysen; Peter De Jonghe; Renzo Guerrini; Lisa Niestroj; Juliana Du; Carla Marini; James S Ware; Mitja Kurki; Padhraig Gormley; Sha Tang; Sitao Wu; Saskia Biskup; Annapurna Poduri; Bernd A. Neubauer; Bobby P.C. Koeleman; Katherine L. Helbig; Yvonne G. Weber; Ingo Helbig; Amit Majithia; Aarno Palotie; Mark J. Daly
Collaborators: Antwerp University Hospital; Boston Children's Hospital; Broad Institute of MIT and Harvard; Center for Molecular Neurology, VIB; Children's Hospital of Philadelphia; Cleveland Clinic; Harvard T.H. Chan School of Public Health; Massachusetts General Hospital; National Heart and Lung Institute & MRC London Institute of Medical Sciences, Imperial College London; The Danish Epilepsy Centre; University Medical Center Utrecht; University of Aachen; University of California, San Diego; University of Cologne; University of Florence; University of Giessen; University of Helsinki; University of Pennsylvania; University of Southern Denmark; University of Tübingen; Wellcome Trust Sanger Institute