Publications
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In Press
Breast cancer risk counseling improves womens functioning,
, Patient Education and Counseling, (In Press)
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Case series models for BRCA 1/2 modifiers of breast cancer risk,
, ?, (In Press)
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Design issues in a multi-center study of linkage for susceptibility loci in cancer,
, (In Press)
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1999
Analysis of masked mutations in familial adenomatous polyposis,
, Proc Natl Acad Sci USA, 1999, Volume 96, Issue 5, p.2322-6, (1999)
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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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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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2000
Mammography behavior after receiving a negative BRCA1 mutation test result in the Ashkenazim: a community-based study.,
, Genet Med, 11/2000, Volume 2, Issue 6, p.307-311, (2000)
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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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2001
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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2002
Basic Concepts for Genetic Testing in Common Hereditary Colorectal Cancer Syndromes,
, Current Gastroenterology Reports, 2002, Volume 4, Issue 5, p.404-413, (2002)
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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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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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Patient preferences of decision-making in the context of genetic testing for breast cancer risk,
, Genetics in in Medicine, 2002, Volume 4, p.150-157, (2002)
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Counseling the at risk patient in the BRCA1 and BRCA2 Era.,
, Obstet Gynecol Clin North Am, 06/2002, Volume 29, Issue 2, p.341-366, (2002)
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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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2003
Achieving utility with family history: colorectal cancer risk,
, American Journal of Preventive Medicine, 2003, Volume 24, Issue 2, (2003)
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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)
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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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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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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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Analysis of association among clustered binary data in the presence of varying cluster sizes: Application to family studies,
, JRSS-C, Volume 54, Issue 5, p.847-62, (2005)
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Association between screening family medical history in general medical care and lower burden of cancer worry among women with a close family history of breast cancer,
, Genetics in Medicine, Volume 36, Issue 9, p.1-6, (2005)
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