Family communication regarding inherited high cholesterol: Why and how do patients disclose genetic risk?
- 30 September 2007
- journal article
- Published by Elsevier in Social Science & Medicine
- Vol. 65 (5) , 1025-1037
- https://doi.org/10.1016/j.socscimed.2007.04.008
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- 'Coming Down the Line'-- Patients' Understanding of Their Family History of Common Chronic DiseaseAnnals of Family Medicine, 2005
- Informing one’s family about genetic testing for hereditary non-polyposis colorectal cancer (HNPCC): a retrospective exploratory studyFamilial Cancer, 2005
- Family Communication about Genetic Risk: The Little That Is KnownPublic Health Genomics, 2004
- Nomogram to Diagnose Familial Combined Hyperlipidemia on the Basis of Results of a 5-Year Follow-Up StudyCirculation, 2004
- To tell or not to tell: barriers and facilitators in family communication about genetic riskClinical Genetics, 2003
- A review on the diagnosis, natural history, and treatment of familial hypercholesterolaemiaAtherosclerosis, 2003
- Communication with close and distant relatives in the context of genetic testing for hereditary breast and ovarian cancer in cancer patientsAmerican Journal of Medical Genetics Part A, 2002
- An Ecological Perspective on Health Promotion ProgramsHealth Education Quarterly, 1988
- The illusion of control.Journal of Personality and Social Psychology, 1975
- Judgment under Uncertainty: Heuristics and BiasesScience, 1974