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Literature DB >> 11657815

In defence of ignorance: genetic information and the right not to know.

Graeme T Laurie.

Abstract

Keywords: Genetics and Reproduction; Professional Patient Relationship

Mesh：

Year: 1999 PMID： 11657815 DOI： 10.1163/15718099920522730

Source DB: PubMed Journal: Eur J Health Law ISSN： 0929-0273

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Cited

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18 in total

Review 1. Genetic information, rights, and autonomy.

Authors: M Häyry; T Takala
Journal: Theor Med Bioeth Date: 2001-09

2. Balancing autonomy and responsibility: the ethics of generating and disclosing genetic information.

Authors: N Hallowell; C Foster; R Eeles; A Ardern-Jones; V Murday; M Watson
Journal: J Med Ethics Date: 2003-04 Impact factor: 2.903

3. Questioning the consensus: managing carrier status results generated by newborn screening.

Authors: Fiona Alice Miller; Jason Scott Robert; Robin Z Hayeems
Journal: Am J Public Health Date: 2008-12-04 Impact factor: 9.308

4. Decision-making about inherited cancer risk: exploring dimensions of genetic responsibility.

Authors: Holly Etchegary; Fiona Miller; Sonya deLaat; Brenda Wilson; June Carroll; Mario Cappelli
Journal: J Genet Couns Date: 2009-03-18 Impact factor: 2.537

5. Consent to epistemic interventions: a contribution to the debate on the right (not) to know.

Authors: Niels Nijsingh
Journal: Med Health Care Philos Date: 2016-03

6. Recommendations for ethical approaches to genotype-driven research recruitment.

Authors: Laura M Beskow; Stephanie M Fullerton; Emily E Namey; Daniel K Nelson; Arlene M Davis; Benjamin S Wilfond
Journal: Hum Genet Date: 2012-05-24 Impact factor: 4.132

7. Preserving children's fertility: two tales about children's right to an open future and the margins of parental obligations.

Authors: Daniela Cutas; Kristien Hens
Journal: Med Health Care Philos Date: 2015-05