Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals
Epi Collaborative, Tara Sadoway(University Health Network), Anthony G Marson(University of Liverpool), Hannah Shilling, Daniel P. Howrigan(Broad Institute), Felecia Cerrato(Broad Institute), Sarah Weckhuysen(University of Antwerp), Liam Abbott, Renzo Guerrini(Meyer Children's Hospital), Dennis Lal(Broad Institute), Tracy Dixon‐Salazar(Lennox-Gastaut Syndrome Foundation), Terence J. O’Brien(The Royal Melbourne Hospital), Andrea Byrnes(Broad Institute), Katherine Tashman(Broad Institute), Catharine Freyer, Erin L. Heinzen(University of North Carolina at Chapel Hill), Caitlin A. Bennett, Henrike Heyne(Hasso Plattner Institute), Dennis Dlugos(School of the Art Institute of Chicago), Danielle M. Andrade(University Health Network), Ingrid E. Scheffer(The University of Melbourne), Gianpiero L. Cavalleri(Royal College of Surgeons in Ireland), Costin Leu(Broad Institute), Tarjinder Singh(Wellcome Sanger Institute), Chantal Depondt(Université Libre de Bruxelles), Patrick Cossette(Centre Hospitalier de l’Université de Montréal), Kevin E. McKenna(Queen's University Belfast), Patrick May(University of Luxembourg), Claire Churchhouse, Brigid M. Regan(University of Toronto), Roland Krause(University of Luxembourg), Melanie Bahlo(Walter and Eliza Hall Institute of Medical Research), Rosemary Burgess, Randy Stewart, Susannah T. Bellows, Patrick Kwan(Boston University), Esther M.C. Johns, Sanjay M. Sisodiya(University of California San Diego), Hannah Stamberger, Håkon Håkonarson(Children's Hospital of Philadelphia), Pasquale Striano(Great Ormond Street Hospital), Alexandra MacDonald, Marian Todaro, Chris Cotsapas(Yale University), Ingo Helbig(Schneider Electric (France)), Slavé Petrovski(AstraZeneca (United Kingdom)), Peter De Jonghe(University of Antwerp), Yen‐Chen Anne Feng(National Taipei University of Nursing and Health Science), Dorien Weckhuysen, Sitharthan Kamalakaran(Columbia University Irving Medical Center)
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