Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes

Epi25 Collaborative, Siwei Chen, Bassel Abou‐Khalil, Zaid Afawi, Quratulain Zulfiqar Ali, Elisabetta Amadori, Alison Anderson, Joe Anderson, Danielle M. Andrade, Grazia Annesi, Mutluay Arslan, Pauls Auce, Melanie Bahlo, Mark D. Baker, Ganna Balagura, Simona Balestrini, Eric Banks, Carmen Barba, Karen Barboza, Fabrice Bartoloméi, Nick Bass, Larry Baum, Tobias H. Baumgartner, Betül Baykan, Nerses Bebek, Felicitas Becker, Caitlin A. Bennett, Ahmad Beydoun, Claudia Bianchini, Francesca Bisulli, Douglas Blackwood, Ilan Blatt, Ingo Borggräfe, Christian M. Boßelmann, Vera Braatz, Harrison Brand, Knut Brockmann, Russell J. Buono, Robyn M. Busch, S. Hande Çağlayan, Laura Canafoglia, Christina Canavati, Barbara Castellotti, Gianpiero L. Cavalleri, Felecia Cerrato, Francine Chassoux, Christina Cherian, Stacey S. Cherny, Ching‐Lung Cheung, I‐Jun Chou, Seo‐Kyung Chung, Claire Churchhouse, Valentina Ciullo, Peggy O. Clark, Andrew J. Cole, Mahgenn Cosico, Patrick Cossette, Chris Cotsapas, Caroline Cusick, Mark J. Daly, Lea K. Davis, Peter De Jonghe, Norman Delanty, Dieter Dennig, Chantal Depondt, Philippe Derambure, Orrin Devinsky, Lidia Di Vito, Faith Dickerson, Dennis Dlugos, Viola Doccini, Colin P. Doherty, Hany El-Naggar, Colin A. Ellis, Leon G. Epstein, Meghan Evans, Annika Faucon, Yen‐Chen Anne Feng, Lisa Ferguson, Thomas N. Ferraro, Izabela Ferreira Da Silva, Lorenzo Ferri, Martha Feucht, Madeline Fields, Mark P. Fitzgerald, Beata Fonferko‐Shadrach, Francesco Fortunato, Silvana Franceschetti, Jacqueline A. French, Elena Freri, Jack Fu, Stacey Gabriel, Monica Gagliardi, Antonio Gambardella, Laura D. Gauthier, Tania Giangregorio, Tommaso Gili, Tracy A. Glauser, Ethan M. Goldberg, Alica M. Goldman