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BRCA1 and BRCA2 pathogenic sequence variants in women of African origin or ancestry

Human mutation, 2019-10, Vol.40 (10), p.1781-1796

2019

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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, 2012-01, Vol.14 (1), p.R33-R33

2012

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Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

Breast cancer research : BCR, 2016-06, Vol.18 (1), p.64, Article 64

2016

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Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations

Human mutation, 2018-05, Vol.39 (5), p.593-620

2018

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Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses

Nature genetics, 2020-06, Vol.52 (6), p.572-581

2020

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Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers

Cancer epidemiology, biomarkers & prevention, 2015-01, Vol.24 (1), p.308-316

2015

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Prediction of Breast and Prostate Cancer Risks in Male BRCA1 and BRCA2 Mutation Carriers Using Polygenic Risk Scores

Journal of clinical oncology, 2017-07, Vol.35 (20), p.2240-2250

2017

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Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170

Nature genetics, 2016-04, Vol.48 (4), p.374-386

2016

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Height and Body Mass Index as Modifiers of Breast Cancer Risk in BRCA1/2 Mutation Carriers: A Mendelian Randomization Study

JNCI : Journal of the National Cancer Institute, 2019-04, Vol.111 (4), p.350-364

2019

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Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

Nature genetics, 2017-12, Vol.49 (12), p.1767-1778

2017

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Common Genetic Variation at BARD1 Is Not Associated with Breast Cancer Risk in BRCA1 or BRCA2 Mutation Carriers

Cancer epidemiology, biomarkers & prevention, 2011, Vol.20 (5), p.1032-1038

2011

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A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers (vol 12, 1078, 2021)

NATURE COMMUNICATIONS, 2021-05, Vol.12 (1)

2021

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Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

Nature genetics, 2020-01, Vol.52 (1), p.56-73

2020

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A Nonsynonymous Polymorphism in IRS1 Modifies Risk of Developing Breast and Ovarian Cancers in BRCA1 and Ovarian Cancer in BRCA2 Mutation Carriers

Cancer epidemiology, biomarkers & prevention, 2012-08, Vol.21 (8), p.1362-1370

2012

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Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

Nature communications, 2019-04, Vol.10 (1), p.1741-18, Article 1741

2019

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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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GEMO, a National Resource to Study Genetic Modifiers of Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Pathogenic Variant Carriers

Frontiers in oncology, 2018-10, Vol.8, p.490-490

2018

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Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

Nature genetics, 2017-05, Vol.49 (5), p.680-691

2017

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A new hybrid record linkage process to make epidemiological databases interoperable: application to the GEMO and GENEPSO studies involving BRCA1 and BRCA2 mutation carriers

BMC medical research methodology, 2021-07, Vol.21 (1), p.1-155, Article 155

2021

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The rs2910164:G>C SNP in the MIR146A gene is not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers

Human mutation, 2011-09, Vol.32 (9), p.1004-1007

2011

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A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population

Nature genetics, 2010-10, Vol.42 (10), p.885-892

2010

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A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers

Nature communications, 2021-02, Vol.12 (1), p.1078-22, Article 1078

2021

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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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The predictive ability of the 313 variant–based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant

Genetics in medicine, 2021-09, Vol.23 (9), p.1726-1737

2021

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Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

Genetics in medicine, 2020-10, Vol.22 (10), p.1653-1666

2020

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BRCA1 and BRCA2 pathogenic sequence variants in women of African origin or ancestry

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

Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations

Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses

Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers

Prediction of Breast and Prostate Cancer Risks in Male BRCA1 and BRCA2 Mutation Carriers Using Polygenic Risk Scores

Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170

Height and Body Mass Index as Modifiers of Breast Cancer Risk in BRCA1/2 Mutation Carriers: A Mendelian Randomization Study

Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

Common Genetic Variation at BARD1 Is Not Associated with Breast Cancer Risk in BRCA1 or BRCA2 Mutation Carriers

A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers (vol 12, 1078, 2021)

Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

A Nonsynonymous Polymorphism in IRS1 Modifies Risk of Developing Breast and Ovarian Cancers in BRCA1 and Ovarian Cancer in BRCA2 Mutation Carriers

Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

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

GEMO, a National Resource to Study Genetic Modifiers of Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Pathogenic Variant Carriers

Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

A new hybrid record linkage process to make epidemiological databases interoperable: application to the GEMO and GENEPSO studies involving BRCA1 and BRCA2 mutation carriers

The rs2910164:G>C SNP in the MIR146A gene is not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers

A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population

A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers

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

The predictive ability of the 313 variant–based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant

Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

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