Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes
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Chen, Siwei | Abou-Khalil, Bassel | Afawi, Zaid | Ali, Quratulain Zulfiqar | Amadori, Elisabetta | Anderson, Alison | Anderson, Joe | Andrade, Danielle | Annesi, Grazia | Arslan, Mutluay | Auce, Pauls | Bahlo, Melanie | Baker, Mark | Balagura, Ganna | Balestrini, Simona | Banks, Eric | Barba, Carmen | Barboza, Karen | Bartolomei, Fabrice | Bass, Nick | Baum, Larry | Baumgartner, Tobias | Baykan, Betül | Bebek, Nerses | Becker, Felicitas | Bennett, Caitlin | Beydoun, Ahmad | Bianchini, Claudia | Bisulli, Francesca | Blackwood, Douglas | Blatt, Ilan | Borggräfe, Ingo | Bosselmann, Christian | Braatz, Vera | Brand, Harrison | Brockmann, Knut | Buono, Russell | Busch, Robyn | Caglayan, S. 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