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GWAS Study

Genetic variation in cervical preinvasive and invasive disease: a genome-wide association study.

Bowden SJ, Bodinier B, Kalliala I et al.

33794208 PubMed ID
GWAS Study Type
149550 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

BS
Bowden SJ
BB
Bodinier B
KI
Kalliala I
ZV
Zuber V
VD
Vuckovic D
DT
Doulgeraki T
WM
Whitaker MD
WM
Wielscher M
CR
Cartwright R
TK
Tsilidis KK
BP
Bennett P
JM
Jarvelin MR
FJ
Flanagan JM
CM
Chadeau-Hyam M
KM
Kyrgiou M
Chapter II

Abstract

Summary of the research findings

Most uterine cervical high-risk human papillomavirus (HPV) infections are transient, with only a small fraction developing into cervical cancer. Family aggregation studies and heritability estimates suggest a significant inherited genetic component. Candidate gene studies and previous genome-wide association studies (GWASs) report associations between the HLA region and cervical cancer. Adopting a genome-wide approach, we aimed to compare genetic variation in women with invasive cervical cancer and cervical intraepithelial neoplasia (CIN) grade 3 with that in healthy controls.

4,005 European ancestry cases, 145,545 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

149550
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
U.K.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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Analysis In Progress

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