[HTML][HTML] Multi-gene panel testing for hereditary cancer predisposition in unsolved high-risk breast and ovarian cancer patients

B Crawford, SB Adams, T Sittler… - Breast cancer research …, 2017 - Springer
Purpose Many women with an elevated risk of hereditary breast and ovarian cancer have
previously tested negative for pathogenic mutations in BRCA1 and BRCA2. Among them, a …

Germline Mutations in BRCA1 and BRCA2 in Breast-Ovarian Families From a Breast Cancer Risk Evaluation Clinic

AM Martin, MA Blackwood, D Antin-Ozerkis… - Journal of clinical …, 2001 - ascopubs.org
PURPOSE: Data from the Breast Cancer Linkage Consortium suggest that the proportion of
familial breast and ovarian cancers linked to BRCA1 or BRCA2 may be as high as 98 …

BRCA1 and BRCA2 mutations in women of different ethnicities undergoing testing for hereditary breast‐ovarian cancer

MJ Hall, JE Reid, LA Burbidge, D Pruss… - Cancer, 2009 - Wiley Online Library
BACKGROUND: In women at increased risk for breast and ovarian cancer, the identification
of a mutation in breast cancer gene 1 (BRCA1) and BRCA2 has important implications for …

Benchmarking of a checklist for the identification of familial risk for breast and ovarian cancers in a prospective cohort

K Rhiem, HJ Bücker‐Nott, M Hellmich… - The Breast …, 2019 - Wiley Online Library
The detection of deleterious germline mutations in BRCA1 and BRCA2 considerably
influences the clinical management of healthy and diseased carriers. Therefore, the …

Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer

FJ Couch, SN Hart, P Sharma, AE Toland… - Journal of clinical …, 2015 - ascopubs.org
Purpose Recent advances in DNA sequencing have led to the development of breast cancer
susceptibility gene panels for germline genetic testing of patients. We assessed the …

Hereditary susceptibility to breast cancer: significance of age of onset in family history and contribution of BRCA1 and BRCA2

TS Frank, AM Deffenbaugh, M Hulick… - Disease …, 1999 - Wiley Online Library
OBJECTIVE: To correlate mutations in BRCA1 and BRCA2 with family history of breast
cancer in a first‐degree relative for women diagnosed with breast cancer before age 45 who …

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

AW Kurian, GD Gong, EM John… - Journal of Clinical …, 2011 - ascopubs.org
Purpose Women with germline BRCA1 and BRCA2 mutations have five-to 20-fold increased
risks of developing breast and ovarian cancer. A recent study claimed that women testing …

Influence of race/ethnicity on genetic counseling and testing for hereditary breast and ovarian cancer

AD Forman, MJ Hall - The breast journal, 2009 - Wiley Online Library
Risk assessment coupled with genetic counseling and testing for the cancer predisposition
genes BRCA1 and BRCA2 (BRCA1/2) has become an integral element of comprehensive …

[HTML][HTML] Screen-positive rates and agreement among six family history screening protocols for breast/ovarian cancer in a population-based cohort of 21-to 55-year-old …

GE Palomaki, MR McClain, K Steinort, R Sifri… - Genetics in …, 2006 - Elsevier
Purpose Mutations in the BRCA1 and BRCA2 genes are responsible for approximately 2%
of breast cancers by age 70 years. Professional and governmental groups recommend …

Etiology of familial breast cancer with undetected BRCA1 and BRCA2 mutations: clinical implications

E Yiannakopoulou - Cellular oncology, 2014 - Springer
Background Familial breast cancer accounts for 20–30% of all breast cancer cases.
Mutations in the BRCA1 and BRCA2 genes account for the majority of high risk families with …