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Genetic variation in <i>TERT</i> modifies the risk of hepatocellular carcinoma in alcohol-related cirrhosis: results from a genome-wide case-control study.

Buch S, Innes H, Lutz PL et al.

35788059 PubMed ID
GWAS Study Type
3080 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

BS
Buch S
IH
Innes H
LP
Lutz PL
NH
Nischalke HD
MJ
Marquardt JU
FJ
Fischer J
WK
Weiss KH
RJ
Rosendahl J
MA
Marot A
KM
Krawczyk M
CM
Casper M
LF
Lammert F
EF
Eyer F
VA
Vogel A
MS
Marhenke S
VF
von Felden J
SR
Sharma R
AS
Atkinson SR
MA
McQuillin A
NJ
Nattermann J
SC
Schafmayer C
FA
Franke A
SC
Strassburg C
RM
Rietschel M
AH
Altmann H
SS
Sulk S
TV
Thangapandi VR
BM
Brosch M
LC
Lackner C
SR
Stauber RE
CA
Canbay A
LA
Link A
RT
Reiberger T
MM
Mandorfer M
SG
Semmler G
SB
Scheiner B
DC
Datz C
RS
Romeo S
GC
Ginanni Corradini S
IW
Irving WL
MJ
Morling JR
GI
Guha IN
BE
Barnes E
AM
Ansari MA
QJ
Quistrebert J
VL
Valenti L
MS
Müller SA
MM
Morgan MY
DJ
Dufour JF
TJ
Trebicka J
BT
Berg T
DP
Deltenre P
MS
Mueller S
HJ
Hampe J
SF
Stickel F
Chapter II

Abstract

Summary of the research findings

Objective: Hepatocellular carcinoma (HCC) often develops in patients with alcohol-related cirrhosis at an annual risk of up to 2.5%. Some host genetic risk factors have been identified but do not account for the majority of the variance in occurrence. This study aimed to identify novel susceptibility loci for the development of HCC in people with alcohol related cirrhosis.

1,066 European ancestry cases, 844 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

3080
Total Participants
GWAS
Study Type
Yes
Replicated
148 European ancestry cases, 1,022 European ancestry controls
Replication Participants
European
Ancestry
Austria, Switzerland, Germany, Italy, U.K.
Recruitment Country
Chapter IV

AI-Generated Summary

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