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BRCA1 and BRCA2 genetic testing—pitfalls and recommendations for managing variants of uncertain clinical significance

Annals of oncology, 2015-10, Vol.26 (10), p.2057-2065

2015

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PREDICT Plus: development and validation of a prognostic model for early breast cancer that includes HER2

British journal of cancer, 2012-08, Vol.107 (5), p.800-807

2012

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Mutant K-Ras increases GSK-3β gene expression via an ETS-p300 transcriptional complex in pancreatic cancer

Oncogene, 2011-08, Vol.30 (34), p.3705-3715

2011

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Efficacy of Bilateral Prophylactic Mastectomy in BRCA1 and BRCA2 Gene Mutation Carriers

JNCI : Journal of the National Cancer Institute, 2001-11, Vol.93 (21), p.1633-1637

2001

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Genetic counselors' practices and confidence regarding variant of uncertain significance results and reclassification from BRCA testing

Clinical genetics, 2015-12, Vol.88 (6), p.523-529

2015

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Association of Childhood and Adolescent Anthropometric Factors, Physical Activity, and Diet with Adult Mammographic Breast Density

American journal of epidemiology, 2007-08, Vol.166 (4), p.456-464

2007

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Gene‐panel testing of breast and ovarian cancer patients identifies a recurrent RAD51C duplication

Clinical genetics, 2018-03, Vol.93 (3), p.595-602

2018

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Integrated Evaluation of DNA Sequence Variants of Unknown Clinical Significance: Application to BRCA1 and BRCA2

American journal of human genetics, 2004-10, Vol.75 (4), p.535-544

2004

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Centrosome-related genes, genetic variation, and risk of breast cancer

Breast cancer research and treatment, 2011-01, Vol.125 (1), p.221-228

2011

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BRCA1 Mutations in Women Attending Clinics That Evaluate the Risk of Breast Cancer

The New England journal of medicine, 1997-05, Vol.336 (20), p.1409-1415

1997

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Variation in genes required for normal mitosis and risk of breast cancer

Breast cancer research and treatment, 2010-01, Vol.119 (2), p.423-430

2010

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Rapid progression of prostate cancer in men with a BRCA2 mutation

British journal of cancer, 2008-07, Vol.99 (2), p.371-374

2008

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Cell cycle genes and ovarian cancer susceptibility: a tagSNP analysis

British journal of cancer, 2009-10, Vol.101 (8), p.1461-1468

2009

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CBP truncating mutations in ovarian cancer

Journal of medical genetics, 2005-06, Vol.42 (6), p.514-518

2005

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Risk of breast cancer with oral contraceptive use in women with a family history of breast cancer

JAMA : the journal of the American Medical Association, 2000-10, Vol.284 (14), p.1791

2000

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The Structure and Function of Folliculo-Stellate Cells in the Anterior Pituitary Gland

Archives of Histology and Cytology, 1999, Vol.62(3), pp.205-218

1999

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Stable Interaction between the Products of the BRCA1 and BRCA2 Tumor Suppressor Genes in Mitotic and Meiotic Cells

Molecular cell, 1998-09, Vol.2 (3), p.317-328

1998

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Mutations in the BRCA1 gene in families with early-onset breast and ovarian cancer

Nature genetics, 1994-12, Vol.8 (4), p.387-391

1994

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ATR phosphorylates SMARCAL1 to prevent replication fork collapse

Genes & development, 2013-07, Vol.27 (14), p.1610-1623

2013

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A candidate tumor suppressor HtrA1 is downregulated in ovarian cancer

Oncogene, 2004-02, Vol.23 (8), p.1636-1644

2004

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BRCA2 germline mutations in male breast cancer cases and breast cancer families

Nature genetics, 1996-05, Vol.13 (1), p.123-125

1996

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Mutations in the ryanodine receptor gene in central core disease and malignant hyperthermia

Nature genetics, 1993-09, Vol.5 (1), p.51-55

1993

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The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds

Nature genetics, 1996-03, Vol.12 (3), p.333-337

1996

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Genetic, functional, and histopathological evaluation of two C-terminal BRCA1 missense variants

Journal of medical genetics, 2006-01, Vol.43 (1), p.74-83

2006

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A Systematic Genetic Assessment of 1,433 Sequence Variants of Unknown Clinical Significance in the BRCA1 and BRCA2 Breast Cancer–Predisposition Genes

American journal of human genetics, 2007-11, Vol.81 (5), p.873-883

2007

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BRCA1 and BRCA2 genetic testing—pitfalls and recommendations for managing variants of uncertain clinical significance

PREDICT Plus: development and validation of a prognostic model for early breast cancer that includes HER2

Mutant K-Ras increases GSK-3β gene expression via an ETS-p300 transcriptional complex in pancreatic cancer

Efficacy of Bilateral Prophylactic Mastectomy in BRCA1 and BRCA2 Gene Mutation Carriers

Genetic counselors' practices and confidence regarding variant of uncertain significance results and reclassification from BRCA testing

Association of Childhood and Adolescent Anthropometric Factors, Physical Activity, and Diet with Adult Mammographic Breast Density

Gene‐panel testing of breast and ovarian cancer patients identifies a recurrent RAD51C duplication

Integrated Evaluation of DNA Sequence Variants of Unknown Clinical Significance: Application to BRCA1 and BRCA2

Centrosome-related genes, genetic variation, and risk of breast cancer

BRCA1 Mutations in Women Attending Clinics That Evaluate the Risk of Breast Cancer

Variation in genes required for normal mitosis and risk of breast cancer

Rapid progression of prostate cancer in men with a BRCA2 mutation

Cell cycle genes and ovarian cancer susceptibility: a tagSNP analysis

CBP truncating mutations in ovarian cancer

Risk of breast cancer with oral contraceptive use in women with a family history of breast cancer

The Structure and Function of Folliculo-Stellate Cells in the Anterior Pituitary Gland

Stable Interaction between the Products of the BRCA1 and BRCA2 Tumor Suppressor Genes in Mitotic and Meiotic Cells

Mutations in the BRCA1 gene in families with early-onset breast and ovarian cancer

ATR phosphorylates SMARCAL1 to prevent replication fork collapse

A candidate tumor suppressor HtrA1 is downregulated in ovarian cancer

BRCA2 germline mutations in male breast cancer cases and breast cancer families

Mutations in the ryanodine receptor gene in central core disease and malignant hyperthermia

The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds

Genetic, functional, and histopathological evaluation of two C-terminal BRCA1 missense variants

A Systematic Genetic Assessment of 1,433 Sequence Variants of Unknown Clinical Significance in the BRCA1 and BRCA2 Breast Cancer–Predisposition Genes

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