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Publication
PropertyValue
Working Groups Müller-Myhsok
SubprojectNone
Open AccessOpen Access Yes
Publication TypeJournal Article
Peer ReviewedYes
PMIDPubMed ID 30804558
DOIDOI 10.1038/s41588-019-0344-8
Publication Year2019
TitleIdentification of common genetic risk variants for autism spectrum disorder. Wikidata
JournalNature genetics
ISSN1061-4036
ESSN1546-1718
URL https://www.ncbi.nlm.nih.gov/pubmed/?term=30804558%5Buid%5D
Pages431-444
Issue3
Volume51
Journal AbbreviationNat Genet
AuthorsGrove J, Ripke S, Als TD, Mattheisen M, Walters RK, Won H, Pallesen J, Agerbo E, Andreassen OA, Anney R, Awashti S, Belliveau R, Bettella F, Buxbaum JD, Bybjerg-Grauholm J, Bækvad-Hansen M, Cerrato F, Chambert K, Christensen JH, Churchhouse C, Dellenvall K, Demontis D, De Rubeis S, Devlin B, Djurovic S, Dumont AL, Goldstein JI, Hansen CS, Hauberg ME, Hollegaard MV, Hope S, Howrigan DP, Huang H, Hultman CM, Klei L, Maller J, Martin J, Martin AR, Moran JL, Nyegaard M, Nærland T, Palmer DS, Palotie A, Pedersen CB, Pedersen MG, dPoterba T, Poulsen JB, Pourcain BS, Qvist P, Rehnström K, Reichenberg A, Reichert J, Robinson EB, Roeder K, Roussos P, Saemundsen E, Sandin S, Satterstrom FK, Davey Smith G, Stefansson H, Steinberg S, Stevens CR, Sullivan PF, Turley P, Walters GB, Xu X, Stefansson K, Geschwind DH, Nordentoft M, Hougaard DM, Werge T, Mors O, Mortensen PB, Neale BM, Daly MJ, Børglum AD
First AuthorGrove J
Last AuthorBørglum AD
ScholiaScholia Wikidata-based representation at Scholia

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 Q62737119  Wikidata ID