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GWAS Study

Genome-wide association meta-analysis of functional outcome after ischemic stroke.

Söderholm M, Pedersen A, Lorentzen E et al.

30796134 PubMed ID
GWAS Study Type
4452 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

SM
Söderholm M
PA
Pedersen A
LE
Lorentzen E
ST
Stanne TM
BS
Bevan S
OM
Olsson M
CJ
Cole JW
FI
Fernandez-Cadenas I
HG
Hankey GJ
JJ
Jimenez-Conde J
JK
Jood K
LJ
Lee JM
LR
Lemmens R
LC
Levi C
MB
Mitchell BD
NB
Norrving B
RK
Rannikmäe K
RN
Rost NS
RJ
Rosand J
RP
Rothwell PM
SR
Scott R
SD
Strbian D
SJ
Sturm JW
SC
Sudlow C
TM
Traylor M
TV
Thijs V
TT
Tatlisumak T
WD
Woo D
WB
Worrall BB
MJ
Maguire JM
LA
Lindgren A
JC
Jern C
Chapter II

Abstract

Summary of the research findings

Objective: To discover common genetic variants associated with poststroke outcomes using a genome-wide association (GWA) study.

1,832 European and unknown ancestry modified Rankin score 0-1 cases, 2,620 European and unknown ancestry modified Rankin score 2-6 cases

Chapter III

Study Statistics

Key metrics and study information

4452
Total Participants
GWAS
Study Type
No
Replicated
European, NR
Ancestry
U.S., Australia, Belgium, Finland, Sweden, U.K., Spain
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

Important Disclaimer: This review has been performed semi-automatically and is provided for informational purposes only. While we strive for accuracy, this analysis may contain errors, omissions, or misinterpretations of the original research. DNA Genics disclaims all liability for any inaccuracies, errors, or consequences arising from the use of this information. Users should independently verify all information and consult original research publications before making any decisions based on this content. This analysis is not intended as a substitute for professional scientific review or medical advice.

Analysis In Progress

Our analysis of this publication is currently being prepared. Please check back soon for comprehensive insights into the health and genetic findings discussed in this research.