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GWAS Study

Whole genome association scan for genetic polymorphisms influencing information processing speed.

Luciano M, Hansell NK, Lahti J et al.

21130836 PubMed ID
GWAS Study Type
4039 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

LM
Luciano M
HN
Hansell NK
LJ
Lahti J
DG
Davies G
MS
Medland SE
RK
Räikkönen K
TA
Tenesa A
WE
Widen E
MK
McGhee KA
PA
Palotie A
LD
Liewald D
PD
Porteous DJ
SJ
Starr JM
MG
Montgomery GW
MN
Martin NG
EJ
Eriksson JG
WM
Wright MJ
DI
Deary IJ
Chapter II

Abstract

Summary of the research findings

Processing speed is an important cognitive function that is compromised in psychiatric illness (e.g., schizophrenia, depression) and old age; it shares genetic background with complex cognition (e.g., working memory, reasoning). To find genes influencing speed we performed a genome-wide association scan in up to three cohorts: Brisbane (mean age 16 years; N = 1659); LBC1936 (mean age 70 years, N = 992); LBC1921 (mean age 82 years, N = 307), and; HBCS (mean age 64 years, N =1080). Meta-analysis of the common measures highlighted various suggestively significant (p < 1.21 × 10⁻⁵) SNPs and plausible candidate genes (e.g., TRIB3). A biological pathways analysis of the speed factor identified two common pathways from the KEGG database (cell junction, focal adhesion) in two cohorts, while a pathway analysis linked to the GO database revealed common pathways across pairs of speed measures (e.g., receptor binding, cellular metabolic process). These highlighted genes and pathways will be able to inform future research, including results for psychiatric disease.

Up to 4,039 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

4039
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Finland, Australia, 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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