Publications
Filters: author is C [Clear All Filters]
A
Breast cancer worry and mammography use by women with and without a family history in a population based sample,
, Cancer Epidemiology Biomarkers, and Prevention, Volume 12, p.314-320, (2003)
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Cancer Genetics Network: Recruitment results and pilot studies,
, Community Genetics, Volume 6, Issue 3, p.171-177, (2003)
Abstract
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B
Assessing BRCA carrier probabilities in extended families,
, Journal of Clinical Oncology, Volume 24, p.354-60, (2006)
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BRCAPRO validation, sensitivity of genetic testing of BRCA1/BRCA2, and prevalence of other breast cancer susceptibility genes,
, Journal of Clinical Oncology, 2002, Volume 20, p.2701-12, (2002)
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Cancer genetics network education tools: Development of an internet-based resource for health professionals,
, National Society of Genetic Counselors, (2000)
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Attitudes, knowledge and risk perceptions of women with breast and/or ovarian cancer considering testing for BRCA1 and BRCA2,
, Journal of Clinical Oncology, 1999, Volume 17, p.1040-1046, (1999)
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Breast cancer risk counseling improves womens functioning,
, Patient Education and Counseling, (In Press)
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C
Use of total abdominal hysterectomy and hormone replacement therapy in BRCA1 and BRCA2 mutation carriers undergoing risk-reducing salpingo-oophorectomy,
, Familial Cancer, (2008)
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Characterization of BRCA1 and BRCA2 mutations in a large United States sample,
, Journal of Clinical Oncology, Volume 24, p.863-871, (2006)
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D
Attitudes about genetic testing in a diverse sample of Washington State women,
, Cancer Epidemiology, Biomarkers, and Prevention, 1999, Volume 8, p.369-375, (1999)
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F
Active recruitment increased enrollment in a hereditary cancer registry,
, J Clin Epidemiol, Volume 57, Issue 11, p.1172-6, (2004)
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Primary care physicians' attitudes and practices regarding cancer genetics: a comparison of 2001 with 1996 survey results.,
, J Cancer Educ, Volume 18, Issue 2, p.91-94, (2003)
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H
Assay validation for identification of hereditary nonpolyposis colon cancer-causing mutations in mismatch repair genes MLH1, MSH2, and MSH6.,
, J Mol Diagn, 10/2005, Volume 7, Issue 4, p.525-534, (2005)
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I
Breast and ovarian cancer screening practices in healthy women with a strong family history of breast or ovarian cancer,
, Breast Cancer Res and Treat, 2002, Volume 71, p.103-112, (2002)
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Population-Calibrated Gene Characterization: Cancer Penetrance Among BRCA 1/2 Mutation Carriers,
, (In Press)
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J
The impact of direct-to-consumer marketing of cancer genetic testing on women according to their genetic risk,
, Genetics in Medicine, 12/2008, Volume 10, Issue 12, p.888-894, (2008)
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Reduced Physical Functional Performance in Older Cancer Survivors,
, Gerontological Society of America, November, (2007)
Abstract
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K
Age at first birth and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers,
, Breast Cancer Res Treat, (2007)
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CGH-targeted linkage analysis reveals a possible BRCA1 modifier locus on chromosome 5q,
, Human Molecular Genetics, Volume 11, Issue 11, p.1327-1332, (2002)
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Design issues in a multi-center study of linkage for susceptibility loci in cancer,
, (In Press)
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L
Cancer yield of mammography, MR, and US in high-risk women: prospective multi-institution breast cancer screening study,
, Radiology, Volume 244, p.381-8, (2007)
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Case series models for BRCA 1/2 modifiers of breast cancer risk,
, ?, (In Press)
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M
Analysis of co-aggregation of cancer based on registry data,
, Community Genetics, Volume 9, Issue 2, p.87-92, (2006)
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Awareness of genetic testing for breast cancer risk among women with a family history of breast cancer: effect of women's information sources on their awareness,
, Cancer Detection and Prevention, 2001, Volume 25, Issue 4, p.319-327, (2001)
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P
Successful Strategies for Increasing African American Participation in Cancer Genetic Studies: Hopeful Signs for Equalizing the Benefits of Genetic Medicine,
, Community Genetics, Volume 11, p.208-214, (2008)
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