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GWAS Study

A genome-wide search for determinants of survival in 1926 patients with advanced colorectal cancer with follow-up in over 22,000 patients.

Wills C, He Y, Summers MG et al.

34794066 PubMed ID
GWAS Study Type
24565 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

WC
Wills C
HY
He Y
SM
Summers MG
LY
Lin Y
PA
Phipps AI
WK
Watts K
LP
Law PJ
AN
Al-Tassan NA
MT
Maughan TS
KR
Kaplan R
HR
Houlston RS
PU
Peters U
NP
Newcomb PA
CA
Chan AT
BD
Buchanan DD
GS
Gallinger S
ML
Marchand LL
PR
Pai RK
SQ
Shi Q
AS
Alberts SR
GV
Gray V
WH
West HD
EV
Escott-Price V
DM
Dunlop MG
CJ
Cheadle JP
Chapter II

Abstract

Summary of the research findings

While genome-wide association studies (GWAS) have identified germline variants influencing the risk of developing colorectal cancer (CRC), there has been limited examination of the possible role of inherited variation as a determinant of patient outcome.

1,926 unknown and European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

24565
Total Participants
GWAS
Study Type
Yes
Replicated
22,639 unknown and European ancestry individuals
Replication Participants
NR, European
Ancestry
U.K.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

Important Disclaimer: This review has been performed semi-automatically and is provided for informational purposes only. While we strive for accuracy, this analysis may contain errors, omissions, or misinterpretations of the original research. DNA Genics disclaims all liability for any inaccuracies, errors, or consequences arising from the use of this information. Users should independently verify all information and consult original research publications before making any decisions based on this content. This analysis is not intended as a substitute for professional scientific review or medical advice.

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.