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GWAS Study

Brugada syndrome in Japan and Europe: a genome-wide association study reveals shared genetic architecture and new risk loci.

Ishikawa T, Masuda T, Hachiya T et al.

38747976 PubMed ID
GWAS Study Type
2574 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

IT
Ishikawa T
MT
Masuda T
HT
Hachiya T
DC
Dina C
SF
Simonet F
NY
Nagata Y
TM
Tanck MWT
SK
Sonehara K
GC
Glinge C
TR
Tadros R
KA
Khongphatthanayothin A
LT
Lu TP
HC
Higuchi C
NT
Nakajima T
HK
Hayashi K
AY
Aizawa Y
NY
Nakano Y
NA
Nogami A
MH
Morita H
OS
Ohno S
AT
Aiba T
KJ
Krijger Juárez C
MJ
Mauleekoonphairoj J
PY
Poovorawan Y
GJ
Gourraud JB
SW
Shimizu W
PV
Probst V
HM
Horie M
WA
Wilde AAM
RR
Redon R
JJ
Juang JJ
NK
Nademanee K
BC
Bezzina CR
BJ
Barc J
TT
Tanaka T
OY
Okada Y
SJ
Schott JJ
MN
Makita N
Chapter II

Abstract

Summary of the research findings

Background and aims: Brugada syndrome (BrS) is an inherited arrhythmia with a higher disease prevalence and more lethal arrhythmic events in Asians than in Europeans. Genome-wide association studies (GWAS) have revealed its polygenic architecture mainly in European populations. The aim of this study was to identify novel BrS-associated loci and to compare allelic effects across ancestries.

940 East Asian ancestry cases, 1,634 East Asian ancestry controls

Chapter III

Study Statistics

Key metrics and study information

2574
Total Participants
GWAS
Study Type
No
Replicated
East Asian, European
Ancestry
Japan, Netherlands, Turkey, U.S., Belgium, Denmark, Italy, U.K., France, Germany, 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.