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Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies

dc.contributor.authorNalls, MAen_US
dc.contributor.authorBlauwendraat, Cen_US
dc.contributor.authorVallerga, CLen_US
dc.contributor.authorHeilbron, Ken_US
dc.contributor.authorBandres-Ciga, Sen_US
dc.contributor.authorChang, Den_US
dc.contributor.authorTan, Men_US
dc.contributor.authorKia, DAen_US
dc.contributor.authorNoyce, AJen_US
dc.contributor.authorXue, Aen_US
dc.contributor.authorBras, Jen_US
dc.contributor.authorYoung, Een_US
dc.contributor.authorvon Coelln, Ren_US
dc.contributor.authorSimon-Sanchez, Jen_US
dc.contributor.authorSchulte, Cen_US
dc.contributor.authorSharma, Men_US
dc.contributor.authorKrohn, Len_US
dc.contributor.authorPihlstrom, Len_US
dc.contributor.authorSiitonen, Aen_US
dc.contributor.authorIwaki, Hen_US
dc.contributor.authorLeonard, Hen_US
dc.contributor.authorFaghri, Fen_US
dc.contributor.authorGibbs, JRen_US
dc.contributor.authorHernandez, DGen_US
dc.contributor.authorScholz, SWen_US
dc.contributor.authorBotia, JAen_US
dc.contributor.authorMartinez, Men_US
dc.contributor.authorCorvol, J-Cen_US
dc.contributor.authorLesage, Sen_US
dc.contributor.authorJankovic, Jen_US
dc.contributor.authorShulman, LMen_US
dc.contributor.authorSutherland, Men_US
dc.contributor.authorTienari, Pen_US
dc.contributor.authorMajamaa, Ken_US
dc.contributor.authorToft, Men_US
dc.contributor.authorAndreassen, OAen_US
dc.contributor.authorBangale, Ten_US
dc.contributor.authorBrice, Aen_US
dc.contributor.authorYang, Jen_US
dc.contributor.authorGan-Or, Zen_US
dc.contributor.authorGasser, Ten_US
dc.contributor.authorHeutink, Pen_US
dc.contributor.authorShulman, JMen_US
dc.contributor.authorWood, NWen_US
dc.contributor.authorHinds, DAen_US
dc.contributor.authorHardy, JAen_US
dc.contributor.authorMorris, HRen_US
dc.contributor.authorGratten, Jen_US
dc.contributor.authorVisscher, PMen_US
dc.contributor.authorGraham, RRen_US
dc.contributor.authorSingleton, ABen_US
dc.contributor.authorTeam, MRen_US
dc.contributor.authorDis, SGPen_US
dc.contributor.authorGenomics, IPDen_US
dc.date.accessioned2020-01-14T15:44:44Z
dc.date.available2019-07-16en_US
dc.date.issued2019-12en_US
dc.identifier.issn1474-4422en_US
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/62389
dc.format.extent1091 - 1102en_US
dc.language.isoenen_US
dc.relation.ispartofLANCET NEUROLOGYen_US
dc.rights© 2019. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/
dc.titleIdentification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studiesen_US
dc.typeArticle
pubs.author-urlhttp://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000495892200015&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=612ae0d773dcbdba3046f6df545e9f6aen_US
pubs.issue12en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume18en_US
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US


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