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GWAS Study

Large-Scale Cognitive GWAS Meta-Analysis Reveals Tissue-Specific Neural Expression and Potential Nootropic Drug Targets.

Lam M, Trampush JW, Yu J et al.

29186694 PubMed ID
GWAS Study Type
107207 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

LM
Lam M
TJ
Trampush JW
YJ
Yu J
KE
Knowles E
DG
Davies G
LD
Liewald DC
SJ
Starr JM
DS
Djurovic S
MI
Melle I
SK
Sundet K
CA
Christoforou A
RI
Reinvang I
DP
DeRosse P
LA
Lundervold AJ
SV
Steen VM
ET
Espeseth T
RK
Räikkönen K
WE
Widen E
PA
Palotie A
EJ
Eriksson JG
GI
Giegling I
KB
Konte B
RP
Roussos P
GS
Giakoumaki S
BK
Burdick KE
PA
Payton A
OW
Ollier W
CO
Chiba-Falek O
AD
Attix DK
NA
Need AC
CE
Cirulli ET
VA
Voineskos AN
SN
Stefanis NC
AD
Avramopoulos D
HA
Hatzimanolis A
AD
Arking DE
SN
Smyrnis N
BR
Bilder RM
FN
Freimer NA
CT
Cannon TD
LE
London E
PR
Poldrack RA
SF
Sabb FW
CE
Congdon E
CE
Conley ED
SM
Scult MA
DD
Dickinson D
SR
Straub RE
DG
Donohoe G
MD
Morris D
CA
Corvin A
GM
Gill M
HA
Hariri AR
WD
Weinberger DR
PN
Pendleton N
BP
Bitsios P
RD
Rujescu D
LJ
Lahti J
LH
Le Hellard S
KM
Keller MC
AO
Andreassen OA
DI
Deary IJ
GD
Glahn DC
MA
Malhotra AK
LT
Lencz T
Chapter II

Abstract

Summary of the research findings

Here, we present a large (n = 107,207) genome-wide association study (GWAS) of general cognitive ability ("g"), further enhanced by combining results with a large-scale GWAS of educational attainment. We identified 70 independent genomic loci associated with general cognitive ability. Results showed significant enrichment for genes causing Mendelian disorders with an intellectual disability phenotype. Competitive pathway analysis implicated the biological processes of neurogenesis and synaptic regulation, as well as the gene targets of two pharmacologic agents: cinnarizine, a T-type calcium channel blocker, and LY97241, a potassium channel inhibitor. Transcriptome-wide and epigenome-wide analysis revealed that the implicated loci were enriched for genes expressed across all brain regions (most strongly in the cerebellum). Enrichment was exclusive to genes expressed in neurons but not oligodendrocytes or astrocytes. Finally, we report genetic correlations between cognitive ability and disparate phenotypes including psychiatric disorders, several autoimmune disorders, longevity, and maternal age at first birth.

107,207 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

107207
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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