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GWAS Study

THBS2 Is a Candidate Modifier of Liver Disease Severity in Alagille Syndrome.

Tsai EA, Gilbert MA, Grochowski CM et al.

28090565 PubMed ID
GWAS Study Type
161 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

TE
Tsai EA
GM
Gilbert MA
GC
Grochowski CM
UL
Underkoffler LA
MH
Meng H
ZX
Zhang X
WM
Wang MM
SH
Shitaye H
HK
Hankenson KD
PD
Piccoli D
LH
Lin H
KB
Kamath BM
DM
Devoto M
SN
Spinner NB
LK
Loomes KM
Chapter II

Abstract

Summary of the research findings

Background & aims: Alagille syndrome is an autosomal-dominant, multisystem disorder caused primarily by mutations in JAG1, resulting in bile duct paucity, cholestasis, cardiac disease, and other features. Liver disease severity in Alagille syndrome is highly variable, however, factors influencing the hepatic phenotype are unknown. We hypothesized that genetic modifiers may contribute to the variable expressivity of this disorder.

97 European ancestry mild cases, 64 European ancestry severe cases

Chapter III

Study Statistics

Key metrics and study information

161
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
U.S.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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