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authFullName_s : John Hopper
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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.
Breast Cancer Research, 2012, 14 (1), pp.R33. ⟨10.1186/bcr3121⟩
Journal articles inserm-00681614v1

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.
Nature Communications, 2020, 11 (1), ⟨10.1038/s41467-020-14389-8⟩
Journal articles hal-02872359v1

Discovery of common and rare genetic risk variants for colorectal cancer

Jeroen Huyghe , Stephanie Bien , Tabitha Harrison , Hyun Min Kang , Sai Chen et al.
Nature Genetics, 2019, 51 (1), pp.76-87. ⟨10.1038/s41588-018-0286-6⟩
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.
Nature Communications, 2021, 12 (1), pp.1078. ⟨10.1038/s41467-020-20496-3⟩
Journal articles hal-03660355v1

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.
npj Breast Cancer, 2019, 5 (1), ⟨10.1038/s41523-019-0127-5⟩
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.
Breast Cancer Research, 2011, 13 (6), pp.R110. ⟨10.1186/bcr3052⟩
Journal articles inserm-00670601v1