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GWAS Study

Heritability and molecular genetic basis of electrodermal activity: a genome-wide association study.

Vaidyanathan U, Isen JD, Malone SM et al.

25387706 PubMed ID
GWAS Study Type
4424 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

VU
Vaidyanathan U
IJ
Isen JD
MS
Malone SM
MM
Miller MB
MM
McGue M
IW
Iacono WG
Chapter II

Abstract

Summary of the research findings

The molecular genetic basis of electrodermal activity (EDA) was analyzed using 527,829 single nucleotide polymorphisms (SNPs) in a large population-representative sample of twins and parents (N = 4,424) in relation to various EDA indices. Biometric analyses suggested that approximately 50% or more of variance in all EDA indices was heritable. The combined effect of all SNPs together accounted for a significant amount of variance in each index, affirming their polygenic basis and heritability. However, none of the SNPs were genome-wide significant for any EDA index. Previously reported SNP associations with disorders such as substance dependence or schizophrenia, which have been linked to EDA abnormalities, were not significant; nor were associations between EDA and genes in specific neurotransmitter systems. These results suggest that EDA is influenced by multiple genes rather than by polymorphisms with large effects.

Up to 4,424 European ancestry twins and their parents

Chapter III

Study Statistics

Key metrics and study information

4424
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
U.S.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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