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The incidence of pancreatic cancer in BRCA1 and BRCA2 mutation carriers

British journal of cancer, 2012-12, Vol.107 (12), p.2005-2009

2012

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Rare Mutations in XRCC2 Increase the Risk of Breast Cancer

American journal of human genetics, 2012-04, Vol.90 (4), p.734-739

2012

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Incidence of colorectal cancer in BRCA1 and BRCA2 mutation carriers: results from a follow-up study

British journal of cancer, 2014-01, Vol.110 (2), p.530-534

2014

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Genomic analyses of germline and somatic variation in high-grade serous ovarian cancer

Journal of ovarian research, 2023-07, Vol.16 (1), p.141-141, Article 141

2023

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Breast Cancer Risk After Bilateral Prophylactic Oophorectomy in BRCA1 Mutation Carriers

JNCI : Journal of the National Cancer Institute, 1999-09, Vol.91 (17), p.1475-1479

1999

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Replication of celiac disease UK genome-wide association study results in a US population

Human molecular genetics, 2009-11, Vol.18 (21), p.4219-4225

2009

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Cancer risks in two large breast cancer families linked to BRCA2 on chromosome 13q12-13

American journal of human genetics, 1997-07, Vol.61 (1), p.120-128

1997

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Compromised BRCA1–PALB2 interaction is associated with breast cancer risk

Oncogene, 2017-07, Vol.36 (29), p.4161-4170

2017

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Reproductive Factors, Exogenous Hormones, and Pancreatic Cancer Risk in the CTS

American journal of epidemiology, 2013-11, Vol.178 (9), p.1403-1413

2013

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Hormone Therapy and the Risk of Breast Cancer in BRCA1 Mutation Carriers

JNCI : Journal of the National Cancer Institute, 2008-10, Vol.100 (19), p.1361-1367

2008

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Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families : Results of an international study

American journal of human genetics, 1996-02, Vol.58 (2), p.271-280

1996

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Haplotype and Phenotype Analysis of Nine Recurrent BRCA2 Mutations in 111 Families: Results of an International Study

American journal of human genetics, 1998-06, Vol.62 (6), p.1381-1388

1998

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Family history of haematopoietic malignancies and non-Hodgkin's lymphoma risk in the California Teachers Study

British journal of cancer, 2009-02, Vol.100 (3), p.524-526

2009

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The risk of breast cancer in BRCA1 and BRCA2 mutation carriers without a first‐degree relative with breast cancer

Clinical genetics, 2018-05, Vol.93 (5), p.1063-1068

2018

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Prostate Cancer Susceptibility Locus HPC1 in Utah High-Risk Pedigrees

Human molecular genetics, 1999-12, Vol.8 (13), p.2437-2442

1999

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Founder populations and their uses for breast cancer genetics

Breast cancer research : BCR, 2000-01, Vol.2 (2), p.77-81, Article 77

Neuhausen, S L

2000

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Menopausal Hormone Therapy Use and Risk of Invasive Colon Cancer: The California Teachers Study

American journal of epidemiology, 2010-02, Vol.171 (4), p.415-425

2010

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Identification of a 14 kb Deletion Involving the Promoter Region of BRCA1 in a Breast Cancer Family

Human molecular genetics, 1997-09, Vol.6 (9), p.1513-1517

1997

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Evaluation of restriction fragment length polymorphism in Cucumis melo

Theoretical and applied genetics, 1992, Vol.83 (3), p.379-384

NEUHAUSEN, S. L

1992

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A P1-based physical map of the region from D17S776 to D17S78 containing the breast cancer susceptibility gene BRCA1

Human molecular genetics, 1994-11, Vol.3 (11), p.1919-1926

1994

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Pathobiologic characteristics of hereditary breast cancer

Human pathology, 1998-10, Vol.29 (10), p.1140-1144

1998

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Haplotype and cancer risk analysis of two common mutations, BRCA1 4184del4 and BRCA2 2157delG, in high risk northwest England breast/ovarian families

Journal of medical genetics, 2004-02, Vol.41 (2), p.e21-21

2004

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Tubal ligation and risk of ovarian cancer in carriers of BRCA1 or BRCA2 mutations: a case-control study

Lancet (British edition), 2001-05, Vol.357 (9267), p.1467-1470

2001

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A prior diagnosis of breast cancer is a risk factor for breast cancer in BRCA1 and BRCA2 carriers

Current oncology (Toronto), 2014-04, Vol.21 (2), p.64-68

2014

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Ethnic differences in cancer risk resulting from genetic variation

Cancer, 1999-12, Vol.86 (S11), p.2575-2582

Neuhausen, Susan L.

1999

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The incidence of pancreatic cancer in BRCA1 and BRCA2 mutation carriers

Rare Mutations in XRCC2 Increase the Risk of Breast Cancer

Incidence of colorectal cancer in BRCA1 and BRCA2 mutation carriers: results from a follow-up study

Genomic analyses of germline and somatic variation in high-grade serous ovarian cancer

Breast Cancer Risk After Bilateral Prophylactic Oophorectomy in BRCA1 Mutation Carriers

Replication of celiac disease UK genome-wide association study results in a US population

Cancer risks in two large breast cancer families linked to BRCA2 on chromosome 13q12-13

Compromised BRCA1–PALB2 interaction is associated with breast cancer risk

Reproductive Factors, Exogenous Hormones, and Pancreatic Cancer Risk in the CTS

Hormone Therapy and the Risk of Breast Cancer in BRCA1 Mutation Carriers

Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families : Results of an international study

Haplotype and Phenotype Analysis of Nine Recurrent BRCA2 Mutations in 111 Families: Results of an International Study

Family history of haematopoietic malignancies and non-Hodgkin's lymphoma risk in the California Teachers Study

The risk of breast cancer in BRCA1 and BRCA2 mutation carriers without a first‐degree relative with breast cancer

Prostate Cancer Susceptibility Locus HPC1 in Utah High-Risk Pedigrees

Founder populations and their uses for breast cancer genetics

Menopausal Hormone Therapy Use and Risk of Invasive Colon Cancer: The California Teachers Study

Identification of a 14 kb Deletion Involving the Promoter Region of BRCA1 in a Breast Cancer Family

Evaluation of restriction fragment length polymorphism in Cucumis melo

A P1-based physical map of the region from D17S776 to D17S78 containing the breast cancer susceptibility gene BRCA1

Pathobiologic characteristics of hereditary breast cancer

Haplotype and cancer risk analysis of two common mutations, BRCA1 4184del4 and BRCA2 2157delG, in high risk northwest England breast/ovarian families

Tubal ligation and risk of ovarian cancer in carriers of BRCA1 or BRCA2 mutations: a case-control study

A prior diagnosis of breast cancer is a risk factor for breast cancer in BRCA1 and BRCA2 carriers

Ethnic differences in cancer risk resulting from genetic variation

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