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GWAS Study

Female-specific Association Between Variants on Chromosome 9 and Self-reported Diagnosis of Irritable Bowel Syndrome.

Bonfiglio F, Zheng T, Garcia-Etxebarria K et al.

29626450 PubMed ID
GWAS Study Type
346075 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

BF
Bonfiglio F
ZT
Zheng T
GK
Garcia-Etxebarria K
HF
Hadizadeh F
BL
Bujanda L
BF
Bresso F
AL
Agreus L
AA
Andreasson A
DA
Dlugosz A
LG
Lindberg G
SP
Schmidt PT
KP
Karling P
OB
Ohlsson B
SM
Simren M
WS
Walter S
NG
Nardone G
CR
Cuomo R
UP
Usai-Satta P
GF
Galeazzi F
NM
Neri M
PP
Portincasa P
BM
Bellini M
BG
Barbara G
LA
Latiano A
HM
Hübenthal M
TV
Thijs V
NM
Netea MG
JD
Jonkers D
CL
Chang L
ME
Mayer EA
WM
Wouters MM
BG
Boeckxstaens G
CM
Camilleri M
FA
Franke A
ZA
Zhernakova A
DM
D'Amato M
Chapter II

Abstract

Summary of the research findings

Background & aims: Genetic factors are believed to affect risk for irritable bowel syndrome (IBS), but there have been no sufficiently powered and adequately sized studies. To identify DNA variants associated with IBS risk, we performed a genome-wide association study (GWAS) of the large UK Biobank population-based cohort, which includes genotype and health data from 500,000 participants.

7,130 British ancestry women cases, 2,446 British ancestry men cases, 178,076 British ancestry women controls, 158,423 British ancestry men controls

Chapter III

Study Statistics

Key metrics and study information

346075
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
U.K.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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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.