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Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers.
Antonis Antoniou
,
Karoline Kuchenbaecker
,
Penny Soucy
,
Jonathan Beesley
,
Xiaoqing Chen
et al.
Journal articles
inserm-00681614v1
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Physical activity and risks of breast and colorectal cancer: a Mendelian randomisation analysis
Nikos Papadimitriou
,
Niki Dimou
,
Konstantinos Tsilidis
,
Barbara Banbury
,
Richard Martin
et al.
Journal articles
hal-02872359v1
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Discovery of common and rare genetic risk variants for colorectal cancer
Jeroen Huyghe
,
Stephanie Bien
,
Tabitha Harrison
,
Hyun Min Kang
,
Sai Chen
et al.
Journal articles
hal-02153497v1
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A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
Juliette Coignard
,
Michael Lush
,
Jonathan Beesley
,
Tracy O'Mara
,
Joe Dennis
et al.
Journal articles
hal-03660355v1
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The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer
Gisella Figlioli
,
Massimo Bogliolo
,
Irene Catucci
,
Laura Caleca
,
Sandra Viz Lasheras
et al.
Journal articles
hal-02463255v1
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Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2.
Anna Marie Mulligan
,
Fergus Couch
,
Daniel Barrowdale
,
Susan Domchek
,
Diana Eccles
et al.
Journal articles
inserm-00670601v1
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