A major cause of cancer related mortality in the United States is breast cancer. A significant portion of breast cancer cases are inherited and more is learned about the genetics of hereditary breast cancer risk each year. Screening and risk-reducing surgery recommendations can improve outcomes through early detection and disease prevention. As genetic markers for breast cancer risk are identified, it is important to update recommendations for screening and risk reducing surgery. This article aims to summarize and discuss current recommendations for non-BRCA, moderate to high risk genomic biomarkers for unaffected women
Breast cancer is the most frequent cancer and the the 2nd leading cause of cancer deaths occurring i...
The identification of women at higher risk for breast cancer is a matter of public health and anyone...
Item does not contain fulltextBACKGROUND: The currently known breast cancer-associated single nucleo...
© 2019 American Medical Association. All rights reserved. Importance: Potentially harmful mutations ...
ImportancePotentially harmful mutations of the breast cancer susceptibility 1 and 2 genes (BRCA1/2) ...
Importance: Potentially harmful mutations of the breast cancer susceptibility 1 and 2 genes (BRCA1/2...
textabstract"Women with a BRCA1 or BRCA2 mutation, who have a considerable increased risk of develop...
Force (USPSTF) recommendation on genetic risk assessment and BRCA mutation testing for breast and ov...
Background: The US Preventative Service Task Force recommends that physicians perform a genetic risk...
ABSTRACTBackgroundThe US Preventative Service Task Force recommends that physicians perform a geneti...
Breast cancer is the most common cancer in women. While advances have been made in its detection an...
Women who have inherited mutations in the BRCA1 or BRCA2 (BRCA1/2) genes have a substantially elevat...
AbstractNowadays, the major tasks of the increasing number of family cancer clinics are to provide g...
Background: There is uncertainty about the benefits of using genome-wide sequencing to implement per...
Genetics and predictive tests are changing breast cancer prevention, both in terms of subjective ex...
Breast cancer is the most frequent cancer and the the 2nd leading cause of cancer deaths occurring i...
The identification of women at higher risk for breast cancer is a matter of public health and anyone...
Item does not contain fulltextBACKGROUND: The currently known breast cancer-associated single nucleo...
© 2019 American Medical Association. All rights reserved. Importance: Potentially harmful mutations ...
ImportancePotentially harmful mutations of the breast cancer susceptibility 1 and 2 genes (BRCA1/2) ...
Importance: Potentially harmful mutations of the breast cancer susceptibility 1 and 2 genes (BRCA1/2...
textabstract"Women with a BRCA1 or BRCA2 mutation, who have a considerable increased risk of develop...
Force (USPSTF) recommendation on genetic risk assessment and BRCA mutation testing for breast and ov...
Background: The US Preventative Service Task Force recommends that physicians perform a genetic risk...
ABSTRACTBackgroundThe US Preventative Service Task Force recommends that physicians perform a geneti...
Breast cancer is the most common cancer in women. While advances have been made in its detection an...
Women who have inherited mutations in the BRCA1 or BRCA2 (BRCA1/2) genes have a substantially elevat...
AbstractNowadays, the major tasks of the increasing number of family cancer clinics are to provide g...
Background: There is uncertainty about the benefits of using genome-wide sequencing to implement per...
Genetics and predictive tests are changing breast cancer prevention, both in terms of subjective ex...
Breast cancer is the most frequent cancer and the the 2nd leading cause of cancer deaths occurring i...
The identification of women at higher risk for breast cancer is a matter of public health and anyone...
Item does not contain fulltextBACKGROUND: The currently known breast cancer-associated single nucleo...