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GWAS Study

Identification of Novel Loci Shared by Juvenile Idiopathic Arthritis Subtypes through Integrative Genetic Analysis.

Li J, Li YR, Glessner JT et al.

35347896 PubMed ID
GWAS Study Type
10495 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

LJ
Li J
LY
Li YR
GJ
Glessner JT
YJ
Yang J
MM
March ME
KC
Kao C
VC
Vaccaro CN
BJ
Bradfield JP
LJ
Li J
MF
Mentch FD
QH
Qu HQ
QX
Qi X
CX
Chang X
HC
Hou C
AD
Abrams DJ
QH
Qiu H
WZ
Wei Z
CJ
Connolly JJ
WF
Wang F
SJ
Snyder J
FB
Flatø B
TS
Thompson SD
LC
Langefeld CD
LB
Lie BA
MJ
Munro JE
WC
Wise C
SP
Sleiman PMA
HH
Hakonarson H
Chapter II

Abstract

Summary of the research findings

Objective: Juvenile idiopathic arthritis (JIA) is the most common chronic immune-mediated joint disease among children and encompasses a heterogeneous group of immune-mediated joint disorders classified into 7 subtypes according to clinical presentation. However, phenotype overlap and biologic evidence suggest a shared mechanistic basis between subtypes. This study was undertaken to systematically investigate shared genetic underpinnings of JIA subtypes.

1,245 European ancestry cases, 9,250 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

10495
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
U.S., Norway, Australia
Recruitment Country
Chapter IV

AI-Generated Summary

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