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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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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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Screening for large rearrangements of the BRCA2 gene in Spanish families with breast/ovarian cancer

Breast cancer research and treatment, 2007-05, Vol.103 (1), p.103-107

2007

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Pathology of Breast and Ovarian Cancers among BRCA1 and BRCA2 Mutation Carriers: Results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)

Cancer epidemiology, biomarkers & prevention, 2012-01, Vol.21 (1), p.134-147

2012

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Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk

PLoS genetics, 2013, Vol.9 (3), p.e1003212-e1003212

2013

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BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers

JNCI : Journal of the National Cancer Institute, 2016-02, Vol.108 (2), p.djv315

2016

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Predominance of pathogenic missense variants in the RAD51C gene occurring in breast and ovarian cancer families

Human molecular genetics, 2012-07, Vol.21 (13), p.2889-2898

2012

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Transcriptome‐wide association study of breast cancer risk by estrogen‐receptor status

Genetic epidemiology, 2020-07, Vol.44 (5), p.442-468

2020

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Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women

Breast cancer research : BCR, 2016-11, Vol.18 (1), p.112-112, Article 112

2016

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Associations of height, body mass index, and weight gain with breast cancer risk in carriers of a pathogenic variant in BRCA1 or BRCA2: the BRCA1 and BRCA2 Cohort Consortium

Breast cancer research : BCR, 2023-06, Vol.25 (1), p.72-72, Article 72

2023

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Breast cancer risks associated with missense variants in breast cancer susceptibility genes

Genome medicine, 2022-05, Vol.14 (1), p.51-17, Article 51

2022

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About 1% of the breast and ovarian Spanish families testing negative for BRCA1 and BRCA2 are carriers of RAD51D pathogenic variants

International journal of cancer, 2014-05, Vol.134 (9), p.2088-2097

2014

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Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers

Human molecular genetics, 2009-11, Vol.18 (22), p.4442-4456

2009

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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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DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers

PLoS genetics, 2014-04, Vol.10 (4), p.e1004256

2014

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BRCA2 gene mutations and coagulation-associated biomarkers

Thrombosis and haemostasis, 2016, Vol.115 (2), p.415-423

2016

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A HRM-based screening method detects RAD51C germ-line deleterious mutations in Spanish breast and ovarian cancer families

Breast cancer research and treatment, 2011-10, Vol.129 (3), p.939-946

2011

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Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers

Communications biology, 2022-10, Vol.5 (1), p.1061-1061, Article 1061

2022

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Breast Cancer Risk Genes — Association Analysis in More than 113,000 Women

The New England journal of medicine, 2021-02, Vol.384 (5), p.428-439

2021

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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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Ovarian and Breast Cancer Risks Associated With Pathogenic Variants in RAD51C and RAD51D

JNCI : Journal of the National Cancer Institute, 2020-12, Vol.112 (12), p.1242-1250

2020

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Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer

JAMA : the journal of the American Medical Association, 2015-04, Vol.313 (13), p.1347

2015

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BRCA Challenge: BRCA Exchange as a global resource for variants in BRCA1 and BRCA2

PLoS genetics, 2018-12, Vol.14 (12), p.e1007752-e1007752

2018

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

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

Screening for large rearrangements of the BRCA2 gene in Spanish families with breast/ovarian cancer

Pathology of Breast and Ovarian Cancers among BRCA1 and BRCA2 Mutation Carriers: Results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)

Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk

BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers

Predominance of pathogenic missense variants in the RAD51C gene occurring in breast and ovarian cancer families

Transcriptome‐wide association study of breast cancer risk by estrogen‐receptor status

Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women

Associations of height, body mass index, and weight gain with breast cancer risk in carriers of a pathogenic variant in BRCA1 or BRCA2: the BRCA1 and BRCA2 Cohort Consortium

Breast cancer risks associated with missense variants in breast cancer susceptibility genes

About 1% of the breast and ovarian Spanish families testing negative for BRCA1 and BRCA2 are carriers of RAD51D pathogenic variants

Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers

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

DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers

Analysis of PALB2 gene in BRCA1/BRCA2 negative Spanish hereditary breast/ovarian cancer families with pancreatic cancer cases

BRCA2 gene mutations and coagulation-associated biomarkers

A HRM-based screening method detects RAD51C germ-line deleterious mutations in Spanish breast and ovarian cancer families

Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers

Analysis of BRCA1 and BRCA2 genes in Spanish breast/ovarian cancer patients: A high proportion of mutations unique to Spain and evidence of founder effects

Breast Cancer Risk Genes — Association Analysis in More than 113,000 Women

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

Ovarian and Breast Cancer Risks Associated With Pathogenic Variants in RAD51C and RAD51D

Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer

BRCA Challenge: BRCA Exchange as a global resource for variants in BRCA1 and BRCA2

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