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Genome-wide association study of germline variants and breast cancer-specific mortality

British journal of cancer, 2019, Vol.120 (6), p.647-657

2019

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Common variants in breast cancer risk loci predispose to distinct tumor subtypes

Breast cancer research : BCR, 2022-01, Vol.24 (1), p.2-13, Article 2

2022

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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

Breast cancer research : BCR, 2012-02, Vol.14 (1), p.R33-R33

2012

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Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers

Breast cancer research : BCR, 2014-12, Vol.16 (6), p.3416-3416, Article 3416

2014

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Spectrum and Frequency of Germline FANCM Protein-Truncating Variants in 44,803 European Female Breast Cancer Cases

Cancers, 2023, Vol.15 (13), p.3313

2023

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The Spectrum of FANCM Protein Truncating Variants in European Breast Cancer Cases

Cancers, 2020-01, Vol.12 (2), p.292

2020

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Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3

Breast cancer research and treatment, 2017-01, Vol.161 (1), p.117-134

2017

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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

Breast cancer research : BCR, 2011-01, Vol.13 (6), p.R110-R110, Article R110

2011

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Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study

Breast cancer research : BCR, 2014-01, Vol.16 (3), p.R51-R51, Article R51

2014

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Evaluation of variation in the phosphoinositide-3-kinase catalytic subunit alpha oncogene and breast cancer risk

British journal of cancer, 2011-12, Vol.105 (12), p.1934-1939, Article 1934

2011

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Evaluation of the XRCC1 gene as a phenotypic modifier in BRCA1/2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2

British journal of cancer, 2011-04, Vol.104 (8), p.1356-1361

2011

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Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers

JNCI : Journal of the National Cancer Institute, 2017-07, Vol.109 (7)

2017

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Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

Cancer research (Chicago, Ill.), 2020-02, Vol.80 (3), p.624-638

2020

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Associations of a Breast Cancer Polygenic Risk Score With Tumor Characteristics and Survival

Journal of clinical oncology, 2023-04, Vol.41 (10), p.1849-1863

2023

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An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers

Breast cancer research : BCR, 2015-04, Vol.17 (1), p.61, Article 61

2015

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No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer

Gynecologic oncology, 2016-05, Vol.141 (2), p.386-401

2016

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The FANCM :p.Arg658 truncating variant is associated with risk of triple-negative breast cancer

NPJ breast cancer, 2019, Vol.5 (1), p.38-14, Article 38

2019

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Genome-wide association study of germline variants and breast cancer-specific mortality

Common variants in breast cancer risk loci predispose to distinct tumor subtypes

Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers

Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers

Spectrum and Frequency of Germline FANCM Protein-Truncating Variants in 44,803 European Female Breast Cancer Cases

The Spectrum of FANCM Protein Truncating Variants in European Breast Cancer Cases

Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3

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

Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study

Evaluation of variation in the phosphoinositide-3-kinase catalytic subunit alpha oncogene and breast cancer risk

Evaluation of the XRCC1 gene as a phenotypic modifier in BRCA1/2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2

Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers

Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

Associations of a Breast Cancer Polygenic Risk Score With Tumor Characteristics and Survival

An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers

No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer

The FANCM :p.Arg658 truncating variant is associated with risk of triple-negative breast cancer

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