학술논문

Identification of common genetic risk variants for autism spectrum disorder
Document Type
Artikel
Author
Grove, JRipke, SAls, TDMattheisen, MWalters, RKWon, HPallesen, JAgerbo, EAndreassen, OAAnney, RAwashti, SBelliveau, RBettella, FBuxbaum, JDBybjerg-Grauholm, JBaekvad-Hansen, MCerrato, FChambert, KChristensen, JHChurchhouse, CDellenvall, KDemontis, DDe Rubeis, SDevlin, BDjurovic, SDumont, ALGoldstein, JHansen, CSHauberg, MEHollegaard, MHope, SHowrigan, DPHuang, HHultman, CMKlei, LMaller, JMartin, JMartin, ARMoran, JLNyegaard, MNaeland, TPalmer, DSPalotie, APedersen, CBPedersen, MGdPoterba, TPoulsen, JBSt Pourcain, BQvist, PRehnstrom, KReichenberg, AReichert, JRobinson, EBRoeder, KRoussos, PSaemundsen, ESandin, SSatterstrom, FKSmith, GDStefansson, HSteinberg, SStevens, CRSullivan, PFTurley, PWalters, GBXu, XYStefansson, KGeschwind, DHNordentoft, MHougaard, DMWerge, TMors, OMortensen, PBNeale, BMDaly, MJBorglum, ADWray, NRTrzaskowski, MByrne, EMAbdellaoui, AAdams, MJAir, TMAndlauer, TFMBacanu, SABeekman, ATFBigdeli, TBBinder, EBBlackwood, DHRBryois, JButtenschon, HNCai, NCastelao, EClarke, TKColeman, JRColodro-Conde, LCouvy-Duchesne, BCraddock, NCrawford, GEDavies, GDeary, IJDegenhardt, FDerks, EMDirek, NDolan, CDunn, ECEley, TCEscott-Price, VKiadeh, FFHFinucane, HKForstner, AJFrank, JGaspar, HAGill, MGoes, FSGordon, SDHall, LSHansen, TFHerms, SHickie, IBHoffmann, PHomuth, GHorn, CHottenga, JJIsing, MJansen, RJorgenson, EKnowles, JAKohane, ISKraft, JKretzschmar, WWKrogh, JKutalik, ZLi, YLind, PAMacIntyre, DJMacKinnon, DFMaier, RMMaier, WMarchini, JMbarek, HMcGrath, PMcGuffin, PMedland, SEMehta, DMiddeldorp, CMMihailov, EMilaneschi, YMilani, LMondimore, FMMontgomery, GWMostafavi, SMullins, NNauck, MNg, BNivard, MGNyholt, DRO'Reilly, PFOskarsson, HOwen, MJPainter, JNPeterson, REPettersson, EPeyrot, WJPistis, GPosthuma, DQuiroz, JARice, JPRiley, BPRivera, MMirza, SSSchoevers, RSchulte, ECShen, LShi, JXShyn, SSigurdsson, ESinnamon, GCBSmit, JHSmith, DJStreit, FStrohmaier, JTansey, KETeismann, HTeumer, AThompson, WThomson, PAThorgeirsson, TETraylor, MTreutlein, JTrubetskoy, VUitterlinden, AGUmbricht, DVan Der Auwera, Svan Hemert, AMViktorin, AVisscher, PMWang, YPWebb, BTWeinsheimer, SMWellmann, JWillemsen, GWitt, SHWu, YXi, HSYang, JZhang, FTArolt, VBaune, BTBerger, KBoomsma, DCichon, SDannlowski, Ude Geus, EJCDePaulo, JRDomenici, EDomschke, KEsko, TGrabe, HJHamilton, SPHayward, CHeath, ACKendler, KSKloiber, SLewis, GLi, QSLucae, SMadden, PAFMagnusson, PKMartin, NGMcIntosh, AMMetspalu, AMuller-Myhsok, BNothen, MMO'Donovan, MCPaciga, SAPedersen, NLPenninx, BWJHPerlis, RHPorteous, DJPotash, JBPreisig, MRietschel, MSchaefer, CSchulze, TGSmoller, JWTiemeier, HUher, RVolzke, HWeissman, MMLewis, CMLevinson, DFBreen, GAgee, MAlipanahi, BAuton, ABell, RKBryc, KElson, SLFontanillas, PFurlotte, NAHromatka, BSHuber, KEKleinman, ALitterman, NKMcIntyre, MHMountain, JLNoblin, ESNorthover, CAMPitts, SJSathirapongsasuti, JFSazonova, OShelton, JFShringarpure, STung, JYVacic, VWilson, CH
Source
Nature genetics. 51(3):431
Subject
Medicin och hälsovetenskap
Language
English
English
ISSN
1546-1718