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Times Cited: 523
Times Cited: 523
Times Cited
Times Co-cited
Similarity
Determining carrier probabilities for breast cancer-susceptibility genes BRCA1 and BRCA2.
G Parmigiani, D Berry, O Aguilar. Am J Hum Genet 1998
G Parmigiani, D Berry, O Aguilar. Am J Hum Genet 1998
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Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2: analysis of 10,000 individuals.
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A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1.
Y Miki, J Swensen, D Shattuck-Eidens, P A Futreal, K Harshman, S Tavtigian, Q Liu, C Cochran, L M Bennett, W Ding. Science 1994
Y Miki, J Swensen, D Shattuck-Eidens, P A Futreal, K Harshman, S Tavtigian, Q Liu, C Cochran, L M Bennett, W Ding. Science 1994
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BRCAPRO validation, sensitivity of genetic testing of BRCA1/BRCA2, and prevalence of other breast cancer susceptibility genes.
Donald A Berry, Edwin S Iversen, Daniel F Gudbjartsson, Elaine H Hiller, Judy E Garber, Beth N Peshkin, Caryn Lerman, Patrice Watson, Henry T Lynch, Susan G Hilsenbeck,[...]. J Clin Oncol 2002
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BRCA1 sequence analysis in women at high risk for susceptibility mutations. Risk factor analysis and implications for genetic testing.
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Sequence analysis of BRCA1 and BRCA2: correlation of mutations with family history and ovarian cancer risk.
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The BOADICEA model of genetic susceptibility to breast and ovarian cancer.
A C Antoniou, P P D Pharoah, P Smith, D F Easton. Br J Cancer 2004
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A new scoring system for the chances of identifying a BRCA1/2 mutation outperforms existing models including BRCAPRO.
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A breast cancer prediction model incorporating familial and personal risk factors.
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Identification of the breast cancer susceptibility gene BRCA2.
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Probability of carrying a mutation of breast-ovarian cancer gene BRCA1 based on family history.
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Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2.
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The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions.
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Linkage of early-onset familial breast cancer to chromosome 17q21.
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Assessing BRCA carrier probabilities in extended families.
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Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13.
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Evaluation of models to predict BRCA germline mutations.
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Limited family structure and BRCA gene mutation status in single cases of breast cancer.
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Bilateral prophylactic mastectomy reduces breast cancer risk in BRCA1 and BRCA2 mutation carriers: the PROSE Study Group.
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A comprehensive model for familial breast cancer incorporating BRCA1, BRCA2 and other genes.
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10
American Society of Clinical Oncology policy statement update: genetic testing for cancer susceptibility.
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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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The pathology of familial breast cancer: predictive value of immunohistochemical markers estrogen receptor, progesterone receptor, HER-2, and p53 in patients with mutations in BRCA1 and BRCA2.
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American Cancer Society guidelines for breast screening with MRI as an adjunct to mammography.
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American Society of Clinical Oncology policy statement update: genetic and genomic testing for cancer susceptibility.
Mark E Robson, Courtney D Storm, Jeffrey Weitzel, Dana S Wollins, Kenneth Offit. J Clin Oncol 2010
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A probability model for predicting BRCA1 and BRCA2 mutations in breast and breast-ovarian cancer families.
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Pretest prediction of BRCA1 or BRCA2 mutation by risk counselors and the computer model BRCAPRO.
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Risks of cancer in BRCA1-mutation carriers. Breast Cancer Linkage Consortium.
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Genetic risk assessment and BRCA mutation testing for breast and ovarian cancer susceptibility: systematic evidence review for the U.S. Preventive Services Task Force.
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BRCA1 and BRCA2 mutation predictions using the BOADICEA and BRCAPRO models and penetrance estimation in high-risk French-Canadian families.
Antonis C Antoniou, Francine Durocher, Paula Smith, Jacques Simard, Douglas F Easton. Breast Cancer Res 2006
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Update on the Manchester Scoring System for BRCA1 and BRCA2 testing.
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The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews.
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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 and penetrance of germline BRCA1 and BRCA2 mutations in a population series of 649 women with ovarian cancer.
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A single BRCA2 mutation in male and female breast cancer families from Iceland with varied cancer phenotypes.
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Prevalence of BRCA1 and BRCA2 gene mutations in patients with early-onset breast cancer.
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Cancer Incidence in BRCA1 mutation carriers.
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Genome-wide association study identifies novel breast cancer susceptibility loci.
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26
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.