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GWAS Study

Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study.

Shatunov A, Mok K, Newhouse S et al.

20801717 PubMed ID
GWAS Study Type
13844 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

SA
Shatunov A
MK
Mok K
NS
Newhouse S
WM
Weale ME
SB
Smith B
VC
Vance C
JL
Johnson L
VJ
Veldink JH
VE
van Es MA
VD
van den Berg LH
RW
Robberecht W
VD
Van Damme P
HO
Hardiman O
FA
Farmer AE
LC
Lewis CM
BA
Butler AW
AO
Abel O
AP
Andersen PM
FI
Fogh I
SV
Silani V
CA
Chiò A
TB
Traynor BJ
MJ
Melki J
MV
Meininger V
LJ
Landers JE
MP
McGuffin P
GJ
Glass JD
PH
Pall H
LP
Leigh PN
HJ
Hardy J
BR
Brown RH
PJ
Powell JF
OR
Orrell RW
MK
Morrison KE
SP
Shaw PJ
SC
Shaw CE
AA
Al-Chalabi A
Chapter II

Abstract

Summary of the research findings

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease of motor neurons that results in progressive weakness and death from respiratory failure, commonly within about 3 years. Previous studies have shown association of a locus on chromosome 9p with ALS and linkage with ALS-frontotemporal dementia. We aimed to test whether this genomic region is also associated with ALS in an independent set of UK samples, and to identify risk factors associated with ALS in a further genome-wide association study that combined data from the independent analysis with those from other countries.

4,857 European ancestry cases, 8,987 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

13844
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Sweden, U.S., Italy, Netherlands, Belgium, U.K., France, Republic of Ireland
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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Analysis In Progress

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