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GWAS Study

Genetic insight into sick sinus syndrome.

Thorolfsdottir RB, Sveinbjornsson G, Aegisdottir HM et al.

36282123 PubMed ID
GWAS Study Type
1006656 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

TR
Thorolfsdottir RB
SG
Sveinbjornsson G
AH
Aegisdottir HM
BS
Benonisdottir S
SL
Stefansdottir L
IE
Ivarsdottir EV
HG
Halldorsson GH
SJ
Sigurdsson JK
TC
Torp-Pedersen C
WP
Weeke PE
BS
Brunak S
WD
Westergaard D
PO
Pedersen OB
SE
Sorensen E
NK
Nielsen KR
BK
Burgdorf KS
BK
Banasik K
BB
Brumpton B
ZW
Zhou W
OA
Oddsson A
TV
Tragante V
HK
Hjorleifsson KE
DO
Davidsson OB
RS
Rajamani S
JS
Jonsson S
TB
Torfason B
VA
Valgardsson AS
TG
Thorgeirsson G
FM
Frigge ML
TG
Thorleifsson G
NG
Norddahl GL
HA
Helgadottir A
GS
Gretarsdottir S
SP
Sulem P
JI
Jonsdottir I
WC
Willer CJ
HK
Hveem K
BH
Bundgaard H
UH
Ullum H
AD
Arnar DO
TU
Thorsteinsdottir U
GD
Gudbjartsson DF
HH
Holm H
SK
Stefansson K
Chapter II

Abstract

Summary of the research findings

Aims: The aim of this study was to use human genetics to investigate the pathogenesis of sick sinus syndrome (SSS) and the role of risk factors in its development.

6,189 European ancestry cases, 931,046 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

1006656
Total Participants
GWAS
Study Type
Yes
Replicated
280 European ancestry cases, 69,141 European ancestry controls
Replication Participants
European
Ancestry
Denmark, U.K., Iceland, Norway
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.