Identification of common genetic risk variants for autism spectrum disorder-Reference-Cited by-同舟云学术

Identification of common genetic risk variants for autism spectrum disorder

Published:2019-02-25 Issue:3 Volume:51 Page:431-444
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Grove Jakob^ORCID, ,Ripke Stephan,Als Thomas D.^ORCID,Mattheisen Manuel,Walters Raymond K.^ORCID,Won Hyejung^ORCID,Pallesen Jonatan,Agerbo Esben^ORCID,Andreassen Ole A.^ORCID,Anney Richard,Awashti Swapnil,Belliveau Rich,Bettella Francesco,Buxbaum Joseph D.,Bybjerg-Grauholm Jonas^ORCID,Bækvad-Hansen Marie,Cerrato Felecia,Chambert Kimberly,Christensen Jane H.^ORCID,Churchhouse Claire,Dellenvall Karin,Demontis Ditte^ORCID,De Rubeis Silvia,Devlin Bernie,Djurovic Srdjan^ORCID,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 Mette^ORCID,Nærland Terje^ORCID,Palmer Duncan S.,Palotie Aarno,Pedersen Carsten Bøcker^ORCID,Pedersen Marianne Giørtz,dPoterba Timothy,Poulsen Jesper Buchhave,Pourcain Beate St^ORCID,Qvist Per^ORCID,Rehnström Karola,Reichenberg Abraham,Reichert Jennifer,Robinson Elise B.,Roeder Kathryn,Roussos Panos,Saemundsen Evald^ORCID,Sandin Sven,Satterstrom F. Kyle^ORCID,Davey Smith George^ORCID,Stefansson Hreinn,Steinberg Stacy^ORCID,Stevens Christine R.,Sullivan Patrick F.^ORCID,Turley Patrick,Walters G. Bragi^ORCID,Xu Xinyi,Stefansson Kari^ORCID,Geschwind Daniel H.^ORCID,Nordentoft Merete,Hougaard David M.^ORCID,Werge Thomas^ORCID,Mors Ole,Mortensen Preben Bo,Neale Benjamin M.^ORCID,Daly Mark J.^ORCID,Børglum Anders D.^ORCID, , ,

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/s41588-019-0344-8.pdf

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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