학술논문

Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
Document Type
Journal
Author
van Rheenen, WouterShatunov, AlekseyDekker, Annelot M.McLaughlin, Russell L.Diekstra, Frank P.Pulit, Sara L.van der Spek, Rick A. A.Vosa, Urmode Jong, SimoneRobinson, Matthew R.Yang, JianFogh, Isabellavan Doormaal, Perry T. C.Tazelaar, Gijs H. P.Koppers, MaxBlokhuis, Anna M.Sproviero, WilliamJones, Ashley R.Kenna, Kevin P.van Eijk, Kristel R.Harschnitz, OliverSchellevis, Raymond D.Brands, William J.Medic, JelenaMenelaou, AndronikiVajda, AliceTicozzi, NicolaLin, KuangRogelj, BorisVrabec, KatarinaRavnik-Glavac, MetkaKoritnik, BlaziZidar, JanezLeonardis, LeaGroselj, Leja DolencMillecamps, StephanieSalachas, FrancoisMeininger, Vincentde Carvalho, MamedePinto, SusanaMora, Jesus S.Rojas-Garcia, RicardoPolak, MeraidaChandran, SiddharthanColville, ShunaSwingler, RobertMorrison, Karen E.Shaw, Pamela J.Hardy, JohnOrrell, Richard W.Pittman, AlanSidle, KatieFratta, PietroMalaspina, AndreaTopp, SimonPetri, SusanneAbdulla, SusanneDrepper, CarstenSendtner, MichaelMeyer, ThomasOphoff, Roel A.Staats, Kim A.Wiedau-Pazos, MartinaLomen-Hoerth, CatherineVan Deerlin, Vivianna M.Trojanowski, John Q.Elman, LaurenMcCluskey, LeoBasak, A. NazliTunca, CerenHamzeiy, HamidParman, YesimMeitinger, ThomasLichtner, PeterRadivojkov-Blagojevic, MilenaAndres, Christian R.Maurel, CindyBensimon, GilbertLandwehrmeyer, BernhardBrice, AlexisPayan, Christine A. M.Saker-Delye, SafaaDuerr, AlexandraWood, Nicholas W.Tittmann, LukasLieb, WolfgangFranke, AndreRietschel, MarcellaCichon, SvenNoethen, Markus M.Amouyel, PhilippeTzourio, ChristopheDartigues, Jean-FrancoisUitterlinden, Andre G.Rivadeneira, FernandoEstrada, KarolHofman, AlbertCurtis, CharlesBlauw, Hylke M.van der Kooi, Anneke J.de Visser, MarianneGoris, AnWeber, MarkusShaw, Christopher E.Smith, Bradley N.Pansarasa, OriettaCereda, CristinaDel Bo, RobertoComi, Giacomo P.D'Alfonso, SandraBertolin, CinziaSoraru, GianniMazzini, LetiziaPensato, VivianaGellera, CinziaTiloca, CinziaRatti, AntoniaCalvo, AndreaMoglia, CristinaBrunetti, MauraArcuti, SimonaCapozzo, RosaZecca, ChiaraLunetta, ChristianPenco, SilvanaRiva, NiloPadovani, AlessandroFilosto, MassimilianoMuller, BernardStuit, Robbert JanBlair, IanZhang, KatharineMcCann, Emily P.Fifita, Jennifer A.Nicholson, Garth A.Rowe, Dominic B.Pamphlett, RogerKiernan, Matthew C.Grosskreutz, JulianWitte, Otto W.Ringer, ThomasPrell, TinoStubendorff, BeatriceKurth, IngoHuebner, Christian A.Leigh, P. NigelCasale, FedericoChio, AdrianBeghi, EttorePupillo, ElisabettaTortelli, RosannaLogroscino, GiancarloPowell, JohnLudolph, Albert C.Weishaupt, Jochen H.Robberecht, WimVan Damme, PhilipFranke, LudePers, Tune H.Brown, Robert H.Glass, Jonathan D.Landers, John E.Hardiman, OrlaAndersen, Peter M.Corcia, PhilippeVourc'h, PatrickSilani, VincenzoWray, Naomi R.Visscher, Peter M.de Bakker, Paul I. W.van Es, Michael A.Pasterkamp, R. JeroenLewis, Cathryn M.Breen, GeromeAl-Chalabi, Ammarvan den Berg, Leonard H.Veldink, Jan H.PARALS RegistrySLALOM GrpSLAP RegistryFALS Sequencing ConsortiumSLAGEN ConsortiumNNIPPS Study Grp
Source
NATURE GENETICS; SEP 2016, 48 9, p1043-p+, 8p.
Subject
Language
English
ISSN
15461718