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Rare variants in the ATM gene and risk of breast cancer

Breast cancer research : BCR, 2011-07, Vol.13 (4), p.R73-R73

2011

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Age-specific breast cancer risk by body mass index and familial risk: prospective family study cohort (ProF-SC)

Breast cancer research : BCR, 2018-11, Vol.20 (1), p.132-132, Article 132

2018

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Breast Cancer Prognosis in BRCA1 and BRCA2 Mutation Carriers: An International Prospective Breast Cancer Family Registry Population-Based Cohort Study

Journal of clinical oncology, 2012-01, Vol.30 (1), p.19-26

2012

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Alcohol consumption, cigarette smoking, and familial breast cancer risk: findings from the Prospective Family Study Cohort (ProF-SC)

Breast cancer research : BCR, 2019-11, Vol.21 (1), p.128-128, Article 128

2019

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Regular use of aspirin and other non-steroidal anti-inflammatory drugs and breast cancer risk for women at familial or genetic risk: a cohort study

Breast cancer research : BCR, 2019-04, Vol.21 (1), p.52-52, Article 52

2019

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Risk-Reducing Oophorectomy and Breast Cancer Risk Across the Spectrum of Familial Risk

JNCI : Journal of the National Cancer Institute, 2019-03, Vol.111 (3), p.331-334

2019

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Rare, Evolutionarily Unlikely Missense Substitutions in ATM Confer Increased Risk of Breast Cancer

American journal of human genetics, 2009-10, Vol.85 (4), p.427-446

2009

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RAD51 and breast cancer susceptibility: no evidence for rare variant association in the Breast Cancer Family Registry study

PloS one, 2012-12, Vol.7 (12), p.e52374-e52374

2012

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Breast Cancer Risk for Noncarriers of Family-Specific BRCA1 and BRCA2 Mutations: Findings From the Breast Cancer Family Registry

Journal of clinical oncology, 2011-12, Vol.29 (34), p.4505-4509

2011

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Benign breast disease increases breast cancer risk independent of underlying familial risk profile: Findings from a Prospective Family Study Cohort

International journal of cancer, 2019-07, Vol.145 (2), p.370-379

2019

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Rare, evolutionarily unlikely missense substitutions in CHEK2 contribute to breast cancer susceptibility: results from a breast cancer family registry case-control mutation-screening study

Breast cancer research : BCR, 2011-01, Vol.13 (1), p.R6-R6

2011

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BRCA2 mutation-associated breast cancers exhibit a distinguishing phenotype based on morphology and molecular profiles from tissue microarrays

The American journal of surgical pathology, 2007, Vol.31 (1), p.121-128

2007

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Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent

PLoS medicine, 2016-08, Vol.13 (8), p.e1002105

2016

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Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants

Genetics in medicine, 2022-01, Vol.24 (1), p.119-129

2022

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Diagnostic Chest X-Rays and Breast Cancer Risk before Age 50 Years for BRCA1 and BRCA2 Mutation Carriers

Cancer epidemiology, biomarkers & prevention, 2013-09, Vol.22 (9), p.1547-1556

2013

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Second primary breast cancer in BRCA1 and BRCA2 mutation carriers: 10-year cumulative incidence in the Breast Cancer Family Registry

Breast cancer research and treatment, 2015-06, Vol.151 (3), p.653-660

2015

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Prediagnosis Reproductive Factors and All-Cause Mortality for Women with Breast Cancer in the Breast Cancer Family Registry

Cancer epidemiology, biomarkers & prevention, 2009-06, Vol.18 (6), p.1792-1797

2009

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BRCA1 and BRCA2 Mutation Carriers, Oral Contraceptive Use, and Breast Cancer Before Age 50

Cancer epidemiology, biomarkers & prevention, 2006-10, Vol.15 (10), p.1863-1870

2006

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The potential value of sibling controls compared with population controls for association studies of lifestyle-related risk factors: an example from the Breast Cancer Family Registry

International journal of epidemiology, 2011-10, Vol.40 (5), p.1342-1354

2011

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Medical radiation exposure and breast cancer risk: Findings from the Breast Cancer Family Registry

International journal of cancer, 2007-07, Vol.121 (2), p.386-394

2007

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A genome-wide linkage study of mammographic density, a risk factor for breast cancer

Breast cancer research : BCR, 2011-01, Vol.13 (6), p.R132-R132, Article R132

2011

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Rare variants in the ATM gene and risk of breast cancer

Age-specific breast cancer risk by body mass index and familial risk: prospective family study cohort (ProF-SC)

Breast Cancer Prognosis in BRCA1 and BRCA2 Mutation Carriers: An International Prospective Breast Cancer Family Registry Population-Based Cohort Study

Alcohol consumption, cigarette smoking, and familial breast cancer risk: findings from the Prospective Family Study Cohort (ProF-SC)

Breast cancer risk prediction using a polygenic risk score in the familial setting: a prospective study from the Breast Cancer Family Registry and kConFab

Tamoxifen and Risk of Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers

Regular use of aspirin and other non-steroidal anti-inflammatory drugs and breast cancer risk for women at familial or genetic risk: a cohort study

Risk-Reducing Oophorectomy and Breast Cancer Risk Across the Spectrum of Familial Risk

Rare key functional domain missense substitutions in MRE11A, RAD50, and NBN contribute to breast cancer susceptibility: results from a Breast Cancer Family Registry case-control mutation-screening study

Rare, Evolutionarily Unlikely Missense Substitutions in ATM Confer Increased Risk of Breast Cancer

RAD51 and breast cancer susceptibility: no evidence for rare variant association in the Breast Cancer Family Registry study

Breast Cancer Risk for Noncarriers of Family-Specific BRCA1 and BRCA2 Mutations: Findings From the Breast Cancer Family Registry

Benign breast disease increases breast cancer risk independent of underlying familial risk profile: Findings from a Prospective Family Study Cohort

Rare, evolutionarily unlikely missense substitutions in CHEK2 contribute to breast cancer susceptibility: results from a breast cancer family registry case-control mutation-screening study

BRCA2 mutation-associated breast cancers exhibit a distinguishing phenotype based on morphology and molecular profiles from tissue microarrays

Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent

Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants

Diagnostic Chest X-Rays and Breast Cancer Risk before Age 50 Years for BRCA1 and BRCA2 Mutation Carriers

Second primary breast cancer in BRCA1 and BRCA2 mutation carriers: 10-year cumulative incidence in the Breast Cancer Family Registry

Prediagnosis Reproductive Factors and All-Cause Mortality for Women with Breast Cancer in the Breast Cancer Family Registry

Recreational Physical Activity and Outcomes After Breast Cancer in Women at High Familial Risk

BRCA1 and BRCA2 Mutation Carriers, Oral Contraceptive Use, and Breast Cancer Before Age 50

The potential value of sibling controls compared with population controls for association studies of lifestyle-related risk factors: an example from the Breast Cancer Family Registry

Medical radiation exposure and breast cancer risk: Findings from the Breast Cancer Family Registry

A genome-wide linkage study of mammographic density, a risk factor for breast cancer

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