Identification of common genetic risk variants for autism spectrum disorder
scientific article published on 25 February 2019
Author/s
author: Jakob Grove, Thomas D. Als, Raymond K Walters, Hyejung Won, Esben Agerbo, Ole A. Andreassen, Joseph Buxbaum, Jonas Bybjerg-Grauholm, Jane H Christensen, Ditte Demontis, Srdjan Djurovic, Christine Søholm Hansen, Daniel P Howrigan, Mette Nyegaard, Mette Nyegaard, Terje Nærland, Carsten Bøcker Pedersen, Beate St Pourcain, Per Qvist, Evald Saemundsen, Sven Sandin, F. Kyle Satterstrom, George Davey Smith, Stacy Steinberg, Patrick F Sullivan, G. Bragi Walters, Kári Stefánsson, Daniel Geschwind, Merete Nordentoft, David M Hougaard, Thomas Werge, Preben Bo Mortensen, Benjamin M. Neale, Mark Joseph Daly, Anders D. Børglum, Stephan Ripke, 23andMe Research Team, Jacqueline I Goldstein, Alicia R Martin, Duncan S Palmer, Elise B Robinson, Christina M. Hultman, Jennifer L. Moran, Marie Bækvad-Hansen, Ole Mors, Manuel Mattheisen, Marianne Giørtz Pedersen, Hreinn Stefansson, Jesper Buchhave Poulsen, Rich Belliveau, Claire Churchhouse, Karin Dellenvall, Sigrun Hope, Julian Maller, Karola Rehnström, Joanna Martin, Felecia Cerrato, Kimberly Chambert, Ashley Dumont, Christine Stevens, Panos Roussos, Richard Anney, Mads Vilhelm Hollegaard, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium (PGC), Kathryn Roeder, Aarno Palotie, Abraham Reichenberg, Silvia De Rubeis, Jennifer Reichert, Francesco Bettella
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