학술논문

Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals
Document Type
Journal
Author
Feng, Yen-Chen AnneHowrigan, Daniel P.Abbott, Liam E.Tashman, KatherineCerrato, FeleciaSingh, TarjinderHeyne, HenrikeByrnes, AndreaChurchhouse, ClaireWatts, NickSolomonson, MatthewLal, DennisHeinzen, Erin L.Dhindsa, Ryan S.Stanley, Kate E.Cavalleri, Gianpiero L.Hakonarson, HakonHelbig, IngoKrause, RolandMay, PatrickWeckhuysen, SarahPetrovski, SlaveKamalakaran, SitharthanSisodiya, Sanjay M.Cossette, PatrickCotsapas, ChrisDe Jonghe, PeterDixon-Salazar, TracyGuerrini, RenzoKwan, PatrickMarson, Anthony G.Stewart, RandyDepondt, ChantalDlugos, Dennis J.Scheffer, Ingrid E.Striano, PasqualeFreyer, CatharineMcKenna, KevinRegan, Brigid M.Bellows, Susannah T.Leu, CostinBennett, Caitlin A.Johns, Esther M. C.Macdonald, AlexandraShilling, HannahBurgess, RosemaryWeckhuysen, DorienBahlo, MelanieO'Brien, Terence J.Todaro, MarianStamberger, HannahAndrade, Danielle M.Sadoway, Tara R.Mo, KellyKrestel, HeinzGallati, SabinaPapacostas, Savvas S.Kousiappa, IoannaTanteles, George A.Sterbova, KatalinVlckova, MarketaSedlackova, LucieLassuthova, PetraKlein, Karl MartinRosenow, FelixReif, Philipp S.Knake, SusanneKunz, Wolfram S.Zsurka, GaborElger, Christian E.Bauer, JurgenRademacher, MichaelPendziwiat, ManuelaMuhle, HiltrudRademacher, Annikavan Baalen, Andreasvon Spiczak, SarahStephani, UlrichAfawi, ZaidKorczyn, Amos D.Kanaan, MoienCanavati, ChristinaKurlemann, GerhardMueller-Schlueter, KarenKluger, GerhardHausler, MartinBlatt, IlanLemke, Johannes R.Krey, IlonaWeber, Yvonne G.Wolking, StefanBecker, FelicitasHengsbach, ChristianRau, SarahMaisch, Ana F.Steinhoff, Bernhard J.Schulze-Bonhage, AndreasSchubert-Bast, SusanneSchreiber, HerbertBorggrafe, IngoSchankin, Christoph J.Mayer, ThomasKorinthenberg, RudolfBrockmann, KnutDennig, DieterMadeleyn, ReneKalviainen, ReettaAuvinen, PiaSaarela, AnniLinnankivi, TarjaLehesjoki, Anna-ElinaRees, Mark, IChung, Seo-KyungPickrell, William O.Powell, RobertSchneider, NataschaBalestrini, SimonaZagaglia, SaraBraatz, VeraJohnson, Michael R.Auce, PaulsSills, Graeme J.Baum, Larry W.Sham, Pak C.Cherny, Stacey S.Lui, Colin H. T.Barisic, NinaDelanty, NormanDoherty, Colin P.Shukralla, ArifMcCormack, MarkEl-Naggar, HanyCanafoglia, LauraFranceschetti, SilvanaCastellotti, BarbaraGranata, TizianaZara, FedericoIacomino, MicheleMadia, FrancescaVari, Maria StellaMancardi, Maria MargheritaSalpietro, VincenzoBisulli, FrancescaTinuper, PaoloLicchetta, LauraPippucci, TommasoStipa, CarlottaMinardi, RaffaellaGambardella, AntonioLabate, AngeloAnnesi, GraziaManna, LorellaGagliardi, MonicaParrini, ElenaMei, DavideVetro, AnnalisaBianchini, ClaudiaMontomoli, MartinoDoccini, ViolaMarini, CarlaSuzuki, ToshimitsuInoue, YushiYamakawa, KazuhiroTumiene, BiruteSadleir, Lynette G.King, ChontelleMountier, EmilyCaglayan, S. HandeArslan, MutluayYapici, ZuhalYis, UlucTopaloglu, PinarKara, BulentTurkdogan, DilsadGundogdu-Eken, AsliBebek, NersesUgur-Iseri, SibelBaykan, BetulSalman, BarisHaryanyan, GarenYucesan, EmrahKesim, YesimOzkara, CigdemPoduri, AnnapurnaShiedley, Beth R.Shain, CatherineBuono, Russell J.Ferraro, Thomas N.Sperling, Michael R.Lo, WarrenPrivitera, MichaelFrench, Jacqueline A.Schachter, StevenKuzniecky, Ruben, IDevinsky, OrrinHegde, ManuKhankhanian, PouyaHelbig, Katherine L.Ellis, Colin A.Spalletta, GianfrancoPiras, FabrizioPiras, FedericaGili, TommasoCiullo, ValentinaReif, AndreasMcQuillin, AndrewBass, NickMcIntosh, AndrewBlackwood, DouglasJohnstone, MandyPalotie, AarnoPato, Michele T.Pato, Carlos N.Bromet, Evelyn J.Carvalho, Celia BarretoAchtyes, Eric D.Azevedo, Maria HelenaKotov, RomanLehrer, Douglas S.Malaspina, DoloresMarder, Stephen R.Medeiros, HelenaMorley, Christopher P.Perkins, Diana O.Sobell, Janet L.Buckley, Peter F.Macciardi, FabioRapaport, Mark H.Knowles, James A.Fanous, Ayman H.McCarroll, Steven A.Gupta, NamrataGabriel, Stacey B.Daly, Mark J.Lander, Eric S.Lowenstein, Daniel H.Goldstein, David B.Lerche, HolgerBerkovic, Samuel F.Neale, Benjamin M.Epi25 CollaborativeGenomic Psychiat Cohort GPC Consor
Source
AMERICAN JOURNAL OF HUMAN GENETICS; AUG 2019, 105 2, p267-p282, 16p.
Subject
Language
English
ISSN
15376605