Identification of common genetic risk variants for autism spectrum disorder
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Published:2019-02-25
Issue:3
Volume:51
Page:431-444
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ISSN:1061-4036
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Container-title:Nature Genetics
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language:en
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Short-container-title:Nat Genet
Author:
Grove JakobORCID, , Ripke Stephan, Als Thomas D.ORCID, Mattheisen Manuel, Walters Raymond K.ORCID, Won HyejungORCID, Pallesen Jonatan, Agerbo EsbenORCID, Andreassen Ole A.ORCID, Anney Richard, Awashti Swapnil, Belliveau Rich, Bettella Francesco, Buxbaum Joseph D., Bybjerg-Grauholm JonasORCID, Bækvad-Hansen Marie, Cerrato Felecia, Chambert Kimberly, Christensen Jane H.ORCID, Churchhouse Claire, Dellenvall Karin, Demontis DitteORCID, De Rubeis Silvia, Devlin Bernie, Djurovic SrdjanORCID, Dumont Ashley L., Goldstein Jacqueline I., Hansen Christine S.ORCID, Hauberg Mads Engel, Hollegaard Mads V., Hope Sigrun, Howrigan Daniel P.ORCID, Huang Hailiang, Hultman Christina M., Klei Lambertus, Maller Julian, Martin Joanna, Martin Alicia R., Moran Jennifer L., Nyegaard MetteORCID, Nærland TerjeORCID, Palmer Duncan S., Palotie Aarno, Pedersen Carsten BøckerORCID, Pedersen Marianne Giørtz, dPoterba Timothy, Poulsen Jesper Buchhave, Pourcain Beate StORCID, Qvist PerORCID, Rehnström Karola, Reichenberg Abraham, Reichert Jennifer, Robinson Elise B., Roeder Kathryn, Roussos Panos, Saemundsen EvaldORCID, Sandin Sven, Satterstrom F. KyleORCID, Davey Smith GeorgeORCID, Stefansson Hreinn, Steinberg StacyORCID, Stevens Christine R., Sullivan Patrick F.ORCID, Turley Patrick, Walters G. BragiORCID, Xu Xinyi, Stefansson KariORCID, Geschwind Daniel H.ORCID, Nordentoft Merete, Hougaard David M.ORCID, Werge ThomasORCID, Mors Ole, Mortensen Preben Bo, Neale Benjamin M.ORCID, Daly Mark J.ORCID, Børglum Anders D.ORCID, , ,
Publisher
Springer Science and Business Media LLC
Reference122 articles.
1. De Rubeis, S. et al. Synaptic, transcriptional and chromatin genes disrupted in autism. Nature 515, 209–215 (2014). 2. Gaugler, T. et al. Most genetic risk for autism resides with common variation. Nat. Genet. 46, 881–885 (2014). 3. Iossifov, I. et al. The contribution of de novo coding mutations to autism spectrum disorder. Nature 515, 216–221 (2014). 4. Krumm, N. et al. Excess of rare, inherited truncating mutations in autism. Nat. Genet. 47, 582–588 (2015). 5. Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium. Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. Mol. Autism 8, 21 (2017).
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