[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 …
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 …
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 …
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 …
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
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 …
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 …
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
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 …
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 …
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 …
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 …
Mutations in the BRCA1 and BRCA2 genes account for the majority of high risk families with …