Common genetic risk variants identified in the SPARK cohort support DDHD2 as a candidate risk gene for autism

Autism spectrum disorder (ASD) is a highly heritable neurodevelopmental disorder. Large genetically informative cohorts of individuals with ASD have led to the identification of a limited number of common genome-wide significant (GWS) risk loci to date. However, many more common genetic variants are...

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Vydáno v:	Translational psychiatry Ročník 10; číslo 1; s. 265
Hlavní autoři:	Matoba, Nana, Liang, Dan, Sun, Huaigu, Aygün, Nil, McAfee, Jessica C., Davis, Jessica E., Raffield, Laura M., Qian, Huijun, Piven, Joseph, Li, Yun, Kosuri, Sriam, Won, Hyejung, Stein, Jason L.
Médium:	Journal Article
Jazyk:	angličtina
Vydáno:	London Nature Publishing Group UK 03.08.2020 Nature Publishing Group
Témata:	631/208 692/699/476/1373 Autism Autism Spectrum Disorder - genetics Autistic Disorder Behavioral Sciences Biological Psychology Genome-Wide Association Study Genomes Humans Medicine Medicine & Public Health Neurodevelopmental disorders Neurosciences Pharmacotherapy Phospholipases Polymorphism, Single Nucleotide Psychiatry Quantitative Trait Loci Risk Factors
ISSN:	2158-3188, 2158-3188
On-line přístup:	Získat plný text
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