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Jennifer T Loud

Biographic Data

ID6066402
NAMEJennifer T Loud
GIVEN NAMESJennifer T
FAMILY NAMELoud
SIGNATURELOUD J T
AFFILIATIONSLaura M. Koehly is with the Social and Behavioral Research Branch, National Human Genome Research Institute, National Institutes Health, Department of Health and Human Services, Bethesda, MD. June A. Peters, Lindsey M. Hoskins, Jennifer T. Loud, and Mark H. Greene are with the Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Department of Health and Human Services, Rockville, MD. Regina Kenen is with the Department of...
ORCID0000-0002-2049-5712
VERIFIEDYes
TOTAL WORKS2
TOTAL CITATIONS7
WORKS AS AUTHOR2
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2008
LATEST PUBLICATION YEAR2009
H-INDEX1
  • Characteristics of Health Information Gatherers, Disseminators, and Blockers Within Families at Risk of Hereditary Cancer

    Laura M Koehly, June A Peters et al.•ARTICLE•American Journal of Public Health•2009•Cited by: 7•References: 47

    Objectives. Given the importance of the dissemination of accurate family history to assess disease risk, we characterized the gatherers, disseminators, and blockers of health information within families at high genetic risk of cancer. Methods. A total of 5466 personal network members of 183 female participants of the Breast Imaging Study from 124 families with known mutations in the BRCA1/2 genes (associated with high risk of breast, ovarian, and…

  • BRCA mutation‐negative women from hereditary breast and ovarian cancer families

    Open Access•Alexis D Bakos, Sadie P Hutson et al.•ARTICLE•Health Expectations•2008

    Background When women from families with a known BRCA1 or BRCA2 mutation test negative for the family mutation, it is assumed that they will transition their personal cancer risk perception from high to average risk. However, there are scant data regarding the experience of mutation‐negative women after genetic testing disclosure, particularly related to the shift of risk perception from assumed mutation‐positive to actual mutation‐negative. This…

  • Characteristics of Health Information Gatherers, Disseminators, and Blockers Within Families at Risk of Hereditary Cancer

    Laura M Koehly, June A Peters et al.•ARTICLE•American Journal of Public Health•2009•Cited by: 7•References: 47

    Objectives. Given the importance of the dissemination of accurate family history to assess disease risk, we characterized the gatherers, disseminators, and blockers of health information within families at high genetic risk of cancer. Methods. A total of 5466 personal network members of 183 female participants of the Breast Imaging Study from 124 families with known mutations in the BRCA1/2 genes (associated with high risk of breast, ovarian, and…

  • BRCA mutation‐negative women from hereditary breast and ovarian cancer families

    Open Access•Alexis D Bakos, Sadie P Hutson et al.•ARTICLE•Health Expectations•2008

    Background When women from families with a known BRCA1 or BRCA2 mutation test negative for the family mutation, it is assumed that they will transition their personal cancer risk perception from high to average risk. However, there are scant data regarding the experience of mutation‐negative women after genetic testing disclosure, particularly related to the shift of risk perception from assumed mutation‐positive to actual mutation‐negative. This…

  • Characteristics of Health Information Gatherers, Disseminators, and Blockers Within Families at Risk of Hereditary Cancer

    Laura M Koehly, June A Peters et al.•ARTICLE•American Journal of Public Health•2009•Cited by: 7•References: 47

    Objectives. Given the importance of the dissemination of accurate family history to assess disease risk, we characterized the gatherers, disseminators, and blockers of health information within families at high genetic risk of cancer. Methods. A total of 5466 personal network members of 183 female participants of the Breast Imaging Study from 124 families with known mutations in the BRCA1/2 genes (associated with high risk of breast, ovarian, and…

BRCA gene mutations in cancer (2 works) · Breast cancer (2 works) · Cancer (2 works) · Internal Medicine (2 works) · Medicine (2 works) · Psychiatry (2 works) · Biology (1 work) · BRCA mutation (1 work) · Clinical Psychology (1 work) · Demography (1 work)

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