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Times Cited: 491
Times Cited: 491
Times Cited
Times Co-cited
Similarity
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Jonathan Tyrer, Stephen W Duffy, Jack Cuzick. Stat Med 2004
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The BOADICEA model of genetic susceptibility to breast and ovarian cancer.
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The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions.
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Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2: analysis of 10,000 individuals.
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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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American Cancer Society guidelines for breast screening with MRI as an adjunct to mammography.
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Evaluation of breast cancer risk assessment packages in the family history evaluation and screening programme.
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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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Predicting the likelihood of carrying a BRCA1 or BRCA2 mutation: validation of BOADICEA, BRCAPRO, IBIS, Myriad and the Manchester scoring system using data from UK genetics clinics.
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BRCAPRO validation, sensitivity of genetic testing of BRCA1/BRCA2, and prevalence of other breast cancer susceptibility genes.
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Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers.
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Validity of models for predicting BRCA1 and BRCA2 mutations.
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Giovanni Parmigiani, Sining Chen, Edwin S Iversen, Tara M Friebel, Dianne M Finkelstein, Hoda Anton-Culver, Argyrios Ziogas, Barbara L Weber, Andrea Eisen, Kathleen E Malone,[...]. Ann Intern Med 2007
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Evaluating the performance of the breast cancer genetic risk models BOADICEA, IBIS, BRCAPRO and Claus for predicting BRCA1/2 mutation carrier probabilities: a study based on 7352 families from the German Hereditary Breast and Ovarian Cancer Consortium.
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A comprehensive model for familial breast cancer incorporating BRCA1, BRCA2 and other genes.
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Probability of carrying a mutation of breast-ovarian cancer gene BRCA1 based on family history.
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The contributions of breast density and common genetic variation to breast cancer risk.
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BayesMendel: an R environment for Mendelian risk prediction.
Sining Chen, Wenyi Wang, Karl W Broman, Hormuzd A Katki, Giovanni Parmigiani. Stat Appl Genet Mol Biol 2004
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Identification of the breast cancer susceptibility gene BRCA2.
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A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1.
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Breast cancer risk models: a comprehensive overview of existing models, validation, and clinical applications.
Jessica A Cintolo-Gonzalez, Danielle Braun, Amanda L Blackford, Emanuele Mazzola, Ahmet Acar, Jennifer K Plichta, Molly Griffin, Kevin S Hughes. Breast Cancer Res Treat 2017
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Breast cancer risk assessment across the risk continuum: genetic and nongenetic risk factors contributing to differential model performance.
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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).
Nasim Mavaddat, Daniel Barrowdale, Irene L Andrulis, Susan M Domchek, Diana Eccles, Heli Nevanlinna, Susan J Ramus, Amanda Spurdle, Mark Robson, Mark Sherman,[...]. Cancer Epidemiol Biomarkers Prev 2012
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The calculation of breast cancer risk for women with a first degree family history of ovarian cancer.
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Breast Cancer Screening for Women at Average Risk: 2015 Guideline Update From the American Cancer Society.
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Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
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Mammographic density adds accuracy to both the Tyrer-Cuzick and Gail breast cancer risk models in a prospective UK screening cohort.
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Incorporating truncating variants in PALB2, CHEK2, and ATM into the BOADICEA breast cancer risk model.
Andrew J Lee, Alex P Cunningham, Marc Tischkowitz, Jacques Simard, Paul D Pharoah, Douglas F Easton, Antonis C Antoniou. Genet Med 2016
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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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Assessment of clinical validity of a breast cancer risk model combining genetic and clinical information.
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Recent Enhancements to the Genetic Risk Prediction Model BRCAPRO.
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Breast-cancer risk in families with mutations in PALB2.
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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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The prevalence of common BRCA1 and BRCA2 mutations among Ashkenazi Jews.
P Hartge, J P Struewing, S Wacholder, L C Brody, M A Tucker. Am J Hum Genet 1999
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Recent BRCAPRO upgrades significantly improve calibration.
Emanuele Mazzola, Jonathan Chipman, Su-Chun Cheng, Giovanni Parmigiani. Cancer Epidemiol Biomarkers Prev 2014
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Performance of common genetic variants in breast-cancer risk models.
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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.