Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders-Reference-Cited by-同舟云学术

Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

Published:2017-05-15 Issue:7 Volume:49 Page:978-985
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Weiner Daniel J, ,Wigdor Emilie M,Ripke Stephan,Walters Raymond K,Kosmicki Jack A,Grove Jakob^ORCID,Samocha Kaitlin E,Goldstein Jacqueline I,Okbay Aysu,Bybjerg-Grauholm Jonas,Werge Thomas,Hougaard David M^ORCID,Taylor Jacob,Skuse David,Devlin Bernie,Anney Richard,Sanders Stephan J,Bishop Somer,Mortensen Preben Bo,Børglum Anders D,Smith George Davey,Daly Mark J^ORCID,Robinson Elise B,

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.3863.pdf

Reference35 articles.

1. Sanders, S.J. et al. Insights into autism spectrum disorder genomic architecture and biology from 71 risk loci. Neuron 87, 1215–1233 (2015).

2. Gaugler, T. et al. Most genetic risk for autism resides with common variation. Nat. Genet. 46, 881–885 (2014).

3. De Rubeis, S. et al. Synaptic, transcriptional and chromatin genes disrupted in autism. Nature 515, 209–215 (2014).

4. Iossifov, I. et al. The contribution of de novo coding mutations to autism spectrum disorder. Nature 515, 216–221 (2014).

5. Bulik-Sullivan, B.K. et al. LD Score regression distinguishes confounding from polygenicity in genome-wide association studies. Nat. Genet. 47, 291–295 (2015).

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