Publications
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2009
Meta-analysis of Risk Reduction Estimates Associated With Risk-Reducing Salpingooophorectomy in BRCA1 or BRCA2 Mutation Carriers,
, JNCI, Volume 101, Issue 2, p.80-87, (2009)
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2008
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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Design considerations in a sib-pair study of linkage for susceptibility loci in cancer,
, BMC Medical Genetics, 07/2008, Volume 10, Issue 9, p.64, (2008)
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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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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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2007
Reduced Physical Functional Performance in Older Cancer Survivors,
, Gerontological Society of America, November, (2007)
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Breast Cancer Risk Among Male BRCA1 and BRCA2 Mutation Carriers,
, JNCI, 12/2007, Volume 99, p.1811-1814, (2007)
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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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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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Quality of life after contralateral prophylactic mastectomy in newly diagnosed high-risk breast cancer patients who underwent BRCA1/2 gene testing,
, J Clin Oncol, Volume 25, p.285-91, (2007)
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The Effect of Incentives on Recruitment into the Cancer Genetics Network: A Randomized Trial,
, Cancer Epidemiology, Biomarkers and Prevention, (2007)
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Validity of models for prediction of BRCA1 and BRCA2 mutations,
, Annals of Internal Medicine (IN PRESS), (2007)
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2006
Assessing BRCA carrier probabilities in extended families,
, Journal of Clinical Oncology, Volume 24, p.354-60, (2006)
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Analysis of co-aggregation of cancer based on registry data,
, Community Genetics, Volume 9, Issue 2, p.87-92, (2006)
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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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2005
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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What do cancer survivors believe causes cancer?,
, Cancer Causes Control, Volume 16, Issue 2, p.115-23, (2005)
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2004
Racial Differences in Enrolment in a Cancer Genetics Registry ,
, Cancer Epidemiol Biomarkers Prev , 08/2004, Volume 13, Issue 8, p.1349-1354 , (2004)
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Active recruitment increased enrollment in a hereditary cancer registry,
, J Clin Epidemiol, Volume 57, Issue 11, p.1172-6, (2004)
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2003
Attenuated familial adenomatous polyposis presenting as ampullary adenocarcinoma,
, Gut, 2003, Volume 52, Issue 6, p.903-4, (2003)
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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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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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2002
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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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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