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Times Co-cited
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BRCA1 and BRCA2 mutations in women of different ethnicities undergoing testing for hereditary breast-ovarian cancer.
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Prevalence and type of BRCA mutations in Hispanics undergoing genetic cancer risk assessment in the southwestern United States: a report from the Clinical Cancer Genetics Community Research Network.
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Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies.
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Genetic testing in an ethnically diverse cohort of high-risk women: a comparative analysis of BRCA1 and BRCA2 mutations in American families of European and African ancestry.
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Inherited predisposition to breast cancer among African American women.
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Association of risk-reducing surgery in BRCA1 or BRCA2 mutation carriers with cancer risk and mortality.
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Prevalence of BRCA mutations and founder effect in high-risk Hispanic families.
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Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer.
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Pathology of breast and ovarian cancers among BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA).
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High prevalence of BRCA1 and BRCA2 mutations in unselected Nigerian breast cancer patients.
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Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2.
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The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews.
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Racial differences in the use of BRCA1/2 testing among women with a family history of breast or ovarian cancer.
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A high frequency of BRCA mutations in young black women with breast cancer residing in Florida.
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A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1.
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Clinical significance of large rearrangements in BRCA1 and BRCA2.
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High proportion of BRCA1/2 founder mutations in Hispanic breast/ovarian cancer families from Colombia.
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A high prevalence of BRCA1 mutations among breast cancer patients from the Bahamas.
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Frequency of mutations in individuals with breast cancer referred for BRCA1 and BRCA2 testing using next-generation sequencing with a 25-gene panel.
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Spectrum of mutations in BRCA1, BRCA2, CHEK2, and TP53 in families at high risk of breast cancer.
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Evidence for common ancestral origin of a recurring BRCA1 genomic rearrangement identified in high-risk Hispanic families.
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Identification of the breast cancer susceptibility gene BRCA2.
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Differences in breast cancer stage at diagnosis and cancer-specific survival by race and ethnicity in the United States.
Javaid Iqbal, Ophira Ginsburg, Paula A Rochon, Ping Sun, Steven A Narod. JAMA 2015
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Gene-panel sequencing and the prediction of breast-cancer risk.
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Prevalence and penetrance of BRCA1 and BRCA2 mutations in a population-based series of breast cancer cases. Anglian Breast Cancer Study Group.
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Significant clinical impact of recurrent BRCA1 and BRCA2 mutations in Mexico.
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Concerns about cancer risk and experiences with genetic testing in a diverse population of patients with breast cancer.
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Prevalence of BRCA mutations among women with triple-negative breast cancer (TNBC) in a genetic counseling cohort.
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Impact of oophorectomy on cancer incidence and mortality in women with a BRCA1 or BRCA2 mutation.
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Prevalence of BRCA1 and BRCA2 mutations in breast cancer patients from Brazil.
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Inhibition of poly(ADP-ribose) polymerase in tumors from BRCA mutation carriers.
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Beyond Li Fraumeni Syndrome: clinical characteristics of families with p53 germline mutations.
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Prevalence of BRCA1 mutation carriers among U.S. non-Hispanic Whites.
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US incidence of breast cancer subtypes defined by joint hormone receptor and HER2 status.
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Recurrent BRCA1 and BRCA2 mutations in breast cancer patients of African ancestry.
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Frequency of breast cancer attributable to BRCA1 in a population-based series of American women.
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Large-scale genotyping identifies 41 new loci associated with breast cancer risk.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.