Nature GeneticsGeneticsPeer-reviewed journal article
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders
iPSYCH-Broad Autism Group, Daniel J. WeineriD, Emilie M. WigdoriD, Stephan RipkeiD, Raymond Kenney WaltersiD, Jack A. KosmickiiD, Jakob GroveiD, Kaitlin E. SamochaiD, Jacqueline I. GoldsteiniD, Aysu OkbayiD, Jonas Bybjerg‐GrauholmiD, Thomas Mears WergeiD, DAVID MICHAEL HOUGAARDiD, Jacob L. TayloriD, David SkuseiD, Bernie DevliniD, Richard AnneyiD, Stephan SandersiD, Somer Bishop, Preben Bo MortenseniD, Anders Dupont BørglumiD, George Davey SmithiD, Mark J. DalyiD, Elise RobinsoniD
Abstract
Autism spectrum disorder (ASD) risk is influenced by both common polygenic and de novo variation. The purpose of this analysis was to clarify the influence of common polygenic risk for ASDs and to identify subgroups of cases, including those with strong acting de novo variants, in which different types of polygenic risk are relevant. To do so, we extend the transmission disequilibrium approach to encompass polygenic risk scores, and introduce the polygenic transmission disequilibrium test. Using data from more than 6,400 children with ASDs and 15,000 of their family members, we show that polygenic risk for ASDs, schizophrenia, and greater educational attainment is over transmitted to children with ASDs in two independent samples, but not to their unaffected siblings. These findings hold independent of proband IQ. We find that common polygenic variation contributes additively to risk in ASD cases that carry a very strong acting de novo variant. Lastly, we find evide ...
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- 516
- FWCI
- 38.43
- Field percentile
- top 1%
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