Journal of Medical Ethics · 2011 · 50 citations · 14 references
Life SciencesGeneticsPsychiatryDementiaHuman GeneticsMedical GeneticsGenetic Research EthicsHuntington DiseaseMental IllnessPsychiatric DiagnosisPsychiatric GeneticsStigmatizationEthics Of Psychiatric DiagnosisEthics Of Psychiatric GeneticsGenetic ConfidentialityGenetic Test Result DisclosureGenetic Testing Informed ConsentGenetic Testing RightsInformed Consent In Genetic CounselingInformed Consent In Psychiatry
This paper will consider the right not to know in the context of psychiatric disorders. It will outline the arguments for and against acquiring knowledge about the results of genetic testing for conditions such as breast cancer and Huntington's disease, and examine whether similar considerations apply to disclosing to clients the results of genetic testing for psychiatric disorders such as depression and Alzheimer's disease. The right not to know will also be examined in the context of the diagnosis of psychiatric disorders that are associated with stigma or for which there is no effective treatment.
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To tell or not to tell: barriers and facilitators in family communication about genetic risk
Karen Forrest, SA Simpson, Wilson Bj et al. · Clinical Genetics · 2003 · 371 citations
Education, Counseling, Genetics +17
The right not to know: an autonomy based approach
Roberto Andorno · Journal of Medical Ethics · 2004 · 309 citations · Full text
Law, Genetics, Human Rights Law +10
Genetic testing: Psychological aspects and implications.
Caryn Lerman, Robert T. Croyle, Kenneth P. Tercyak et al. · Journal of Consulting and Clinical Psychology · 2002 · 246 citations
Life Sciences, Genetics, Psychology +14
Genetic testing: Psychological aspects and implications.
Caryn Lerman, Robert T. Croyle, Kenneth P. Tercyak et al. · Journal of Consulting and Clinical Psychology · 2002 · 222 citations
Life Sciences, Genetics, Psychology +14