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GWAS Study

Association of CD247 with systemic lupus erythematosus in Asian populations.

Li R, Yang W, Zhang J et al.

22004975 PubMed ID
GWAS Study Type
11922 Participants
27 Views
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

LR
Li R
YW
Yang W
ZJ
Zhang J
HN
Hirankarn N
PH
Pan HF
MC
Mok CC
CT
Chan TM
WR
Wong RW
MM
Mok MY
LK
Lee KW
WS
Wong SN
LA
Leung AM
LX
Li XP
AY
Avihingsanon Y
LT
Lee TL
HM
Ho MH
LP
Lee PP
WW
Wong WH
WC
Wong CM
NI
Ng IO
YJ
Yang J
LP
Li PH
ZY
Zhang Y
ZL
Zhang L
LW
Li W
BL
Baum L
KP
Kwan P
RP
Rianthavorn P
DT
Deekajorndej T
SK
Suphapeetiporn K
SV
Shotelersuk V
GM
Garcia-Barceló MM
CS
Cherny SS
TP
Tam PK
SP
Sham PC
LC
Lau CS
SN
Shen N
LY
Lau Yl
YD
Ye DQ
Chapter II

Abstract

Summary of the research findings

Objective: Systemic lupus erythematosus (SLE) is a prototypic autoimmune disease with complex genetic inheritance. CD247 (CD3Z, TCRZ) plays a vital role in antigen recognition and signal transduction in antigen-specific immune responses, and is known to be involved in SLE pathogenesis. Weak disease association was reported for genetic variants in this gene in Caucasian studies for SLE, Crohn's disease and systemic sclerosis, but its role as a genetic risk factor was never firmly established.

612 Chinese ancestry cases, 2,193 Chinese ancestry controls

Chapter III

Study Statistics

Key metrics and study information

11922
Total Participants
GWAS
Study Type
Yes
Replicated
2,866 East Asian ancestry cases, up to 4,808 East Asian ancestry controls, 473 Thai ancestry cases, up to 970 Thai ancestry controls
Replication Participants
South East Asian, East Asian
Ancestry
Thailand, China, Hong Kong SAR
Recruitment Country
Chapter IV

AI-Generated Summary

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