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GWAS Study

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.

Anney RJL

28540026 PubMed ID
GWAS Study Type
15954 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

AR
Anney RJL
Chapter II

Abstract

Summary of the research findings

Over the past decade genome-wide association studies (GWAS) have been applied to aid in the understanding of the biology of traits. The success of this approach is governed by the underlying effect sizes carried by the true risk variants and the corresponding statistical power to observe such effects given the study design and sample size under investigation. Previous ASD GWAS have identified genome-wide significant (GWS) risk loci; however, these studies were of only of low statistical power to identify GWS loci at the lower effect sizes (odds ratio (OR) <1.15).

schizophrenia cases and controls (see Ripke, 2014), up to 6,197 European ancestry ASD cases, up to 7,377 European ancestry controls, up to 1,190 ASD cases, up to 1,190 controls

Chapter III

Study Statistics

Key metrics and study information

15954
Total Participants
GWAS
Study Type
Yes
Replicated
8,266 European ancestry cases, 147,562 European ancestry controls, 886 cases, 1,105 controls
Replication Participants
European, Other, NR
Ancestry
Canada, U.S., Germany, Iran (Islamic Republic of), Finland, U.K., Sweden, Georgia, Ukraine, Serbia, Denmark, Iceland
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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Analysis In Progress

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