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GWAS Study

A genome-wide association study in multiple system atrophy.

Sailer A, Scholz SW, Nalls MA et al.

27629089 PubMed ID
GWAS Study Type
4159 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

SA
Sailer A
SS
Scholz SW
NM
Nalls MA
SC
Schulte C
FM
Federoff M
PT
Price TR
LA
Lees A
RO
Ross OA
DD
Dickson DW
MK
Mok K
MN
Mencacci NE
SL
Schottlaender L
CV
Chelban V
LH
Ling H
OS
O'Sullivan SS
WN
Wood NW
TB
Traynor BJ
FL
Ferrucci L
FH
Federoff HJ
MT
Mhyre TR
MH
Morris HR
DG
Deuschl G
QN
Quinn N
WH
Widner H
AA
Albanese A
IJ
Infante J
BK
Bhatia KP
PW
Poewe W
OW
Oertel W
HG
Höglinger GU
WU
Wüllner U
GS
Goldwurm S
PM
Pellecchia MT
FJ
Ferreira J
TE
Tolosa E
BB
Bloem BR
RO
Rascol O
MW
Meissner WG
HJ
Hardy JA
RT
Revesz T
HJ
Holton JL
GT
Gasser T
WG
Wenning GK
SA
Singleton AB
HH
Houlden H
Chapter II

Abstract

Summary of the research findings

Objective: To identify genetic variants that play a role in the pathogenesis of multiple system atrophy (MSA), we undertook a genome-wide association study (GWAS).

295 European ancestry cases, 3,864 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

4159
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
U.S., Italy, Netherlands, Portugal, Germany, U.K., Spain, Austria, Denmark
Recruitment Country
Chapter IV

AI-Generated Summary

AI-generated by DNAGENICS

Independent AI summary of health and genetic findings from the published study

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