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GWAS Study

Variability in the common genetic architecture of social-communication spectrum phenotypes during childhood and adolescence.

St Pourcain B, Skuse DH, Mandy WP et al.

24564958 PubMed ID
GWAS Study Type
5628 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

SP
St Pourcain B
SD
Skuse DH
MW
Mandy WP
WK
Wang K
HH
Hakonarson H
TN
Timpson NJ
ED
Evans DM
KJ
Kemp JP
RS
Ring SM
MW
McArdle WL
GJ
Golding J
SG
Smith GD
Chapter II

Abstract

Summary of the research findings

Social-communication abilities are heritable traits, and their impairments overlap with the autism continuum. To characterise the genetic architecture of social-communication difficulties developmentally and identify genetic links with the autistic dimension, we conducted a genome-wide screen of social-communication problems at multiple time-points during childhood and adolescence.

Up to 5,628 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

5628
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
U.K.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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Analysis In Progress

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