Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals

Author:

Feng Yen-Chen Anne,Howrigan Daniel P.,Abbott Liam E.,Tashman Katherine,Cerrato Felecia,Singh Tarjinder,Heyne Henrike,Byrnes Andrea,Churchhouse Claire,Watts Nick,Solomonson Matthew,Lal Dennis,Heinzen Erin L.,Dhindsa Ryan S.,Stanley Kate E.,Cavalleri Gianpiero L.,Hakonarson Hakon,Helbig Ingo,Krause Roland,May Patrick,Weckhuysen Sarah,Petrovski Slavé,Kamalakaran Sitharthan,Sisodiya Sanjay M.,Cossette Patrick,Cotsapas Chris,De Jonghe Peter,Dixon-Salazar Tracy,Guerrini Renzo,Kwan Patrick,Marson Anthony G.,Stewart Randy,Depondt Chantal,Dlugos Dennis J.,Scheffer Ingrid E.,Striano Pasquale,Freyer Catharine,McKenna Kevin,Regan Brigid M.,Bellows Susannah T.,Leu Costin,Bennett Caitlin A.,Johns Esther M.C.,Macdonald Alexandra,Shilling Hannah,Burgess Rosemary,Weckhuysen Dorien,Bahlo Melanie,O’Brien Terence J.,Todaro Marian,Stamberger Hannah,Andrade Danielle M.,Sadoway Tara R.,Mo Kelly,Krestel Heinz,Gallati Sabina,Papacostas Savvas S.,Kousiappa Ioanna,Tanteles George A.,Štěrbová Katalin,Vlčková Markéta,Sedláčková Lucie,Laššuthová Petra,Klein Karl Martin,Rosenow Felix,Reif Philipp S.,Knake Susanne,Kunz Wolfram S.,Zsurka Gábor,Elger Christian E.,Bauer Jürgen,Rademacher Michael,Pendziwiat Manuela,Muhle Hiltrud,Rademacher Annika,van Baalen Andreas,von Spiczak Sarah,Stephani Ulrich,Afawi Zaid,Korczyn Amos D.,Kanaan Moien,Canavati Christina,Kurlemann Gerhard,Müller-Schlüter Karen,Kluger Gerhard,Häusler Martin,Blatt Ilan,Lemke Johannes R.,Krey Ilona,Weber Yvonne G.,Wolking Stefan,Becker Felicitas,Hengsbach Christian,Rau Sarah,Maisch Ana F.,Steinhoff Bernhard J.,Schulze-Bonhage Andreas,Schubert-Bast Susanne,Schreiber Herbert,Borggräfe Ingo,Schankin Christoph J.,Mayer Thomas,Korinthenberg Rudolf,Brockmann Knut,Kurlemann Gerhard,Dennig Dieter,Madeleyn Rene,Kälviäinen Reetta,Auvinen Pia,Saarela Anni,Linnankivi Tarja,Lehesjoki Anna-Elina,Rees Mark I.,Chung Seo-Kyung,Pickrell William O.,Powell Robert,Schneider Natascha,Balestrini Simona,Zagaglia Sara,Braatz Vera,Johnson Michael R.,Auce Pauls,Sills Graeme J.,Baum Larry W.,Sham Pak C.,Cherny Stacey S.,Lui Colin H.T.,Barišić Nina,Delanty Norman,Doherty Colin P.,Shukralla Arif,McCormack Mark,El-Naggar Hany,Canafoglia Laura,Franceschetti Silvana,Castellotti Barbara,Granata Tiziana,Zara Federico,Iacomino Michele,Madia Francesca,Vari Maria Stella,Mancardi Maria Margherita,Salpietro Vincenzo,Bisulli Francesca,Tinuper Paolo,Licchetta Laura,Pippucci Tommaso,Stipa Carlotta,Minardi Raffaella,Gambardella Antonio,Labate Angelo,Annesi Grazia,Manna Lorella,Gagliardi Monica,Parrini Elena,Mei Davide,Vetro Annalisa,Bianchini Claudia,Montomoli Martino,Doccini Viola,Marini Carla,Suzuki Toshimitsu,Inoue Yushi,Yamakawa Kazuhiro,Tumiene Birute,Sadleir Lynette G.,King Chontelle,Mountier Emily,Caglayan S. Hande,Arslan Mutluay,Yapıcı Zuhal,Yis Uluc,Topaloglu Pınar,Kara Bulent,Turkdogan Dilsad,Gundogdu-Eken Aslı,Bebek Nerses,Uğur-İşeri Sibel,Baykan Betül,Salman Barış,Haryanyan Garen,Yücesan Emrah,Kesim Yeşim,Özkara Çiğdem,Poduri Annapurna,Shiedley Beth R.,Shain Catherine,Buono Russell J.,Ferraro Thomas N.,Sperling Michael R.,Lo Warren,Privitera Michael,French Jacqueline A.,Schachter Steven,Kuzniecky Ruben I.,Devinsky Orrin,Hegde Manu,Khankhanian Pouya,Helbig Katherine L.,Ellis Colin A.,Spalletta Gianfranco,Piras Fabrizio,Piras Federica,Gili Tommaso,Ciullo Valentina,Reif Andreas,McQuillin Andrew,Bass Nick,McIntosh Andrew,Blackwood Douglas,Johnstone Mandy,Palotie Aarno,Pato Michele T.,Pato Carlos N.,Bromet Evelyn J.,Carvalho Celia Barreto,Achtyes Eric D.,Azevedo Maria Helena,Kotov Roman,Lehrer Douglas S.,Malaspina Dolores,Marder Stephen R.,Medeiros Helena,Morley Christopher P.,Perkins Diana O.,Sobell Janet L.,Buckley Peter F.,Macciardi Fabio,Rapaport Mark H.,Knowles James A.,Fanous Ayman H.,McCarroll Steven A.,Gupta Namrata,Gabriel Stacey B.,Daly Mark J.,Lander Eric S.,Lowenstein Daniel H.,Goldstein David B.,Lerche Holger,Berkovic Samuel F.,Neale Benjamin M.

Funder

National Human Genome Research Institute

NHGRI

National Heart, Lung, and Blood Institute

NHLBI

“Epi25 Clinical Phenotyping R03,”

National Institutes of Health

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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