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  1. Social contract theory and just decision making: Lessons from genetic testing for the BRCA mutations.Bryn Williams-Jones & Michael M. Burgess - 2004 - Kennedy Institute of Ethics Journal 14 (2):115-142.
    : Decisions about funding health services are crucial to controlling costs in health care insurance plans, yet they encounter serious challenges from intellectual property protection—e.g., patents—of health care services. Using Myriad Genetics' commercial genetic susceptibility test for hereditary breast cancer (BRCA testing) in the context of the Canadian health insurance system as a case study, this paper applies concepts from social contract theory to help develop more just and rational approaches to health care decision making. Specifically, Daniels's and Sabin's "accountability (...)
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  • Ethics and genetics: Susceptibility testing in the workplace.Chris MacDonald & Bryn Williams-Jones - 2002 - Journal of Business Ethics 35 (3):235-241.
    Genetic testing in the workplace is a technology both full of promise and fraught with ethical peril. Though not yet common, it is likely to become increasingly so. We survey the key arguments in favour of such testing, along with the most significant ethical worries. We further propose a set of pragmatic criteria, which, if met, would make it permissible for employers to offer (but not to require) workplace genetic testing.
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  • The Natural Father: Genetic Paternity Testing, Marriage, and Fatherhood.Gregory E. Kaebnick - 2004 - Cambridge Quarterly of Healthcare Ethics 13 (1):49-60.
    The emerging phenomenon of genetic paternity testing shows how good science and useful social reform can run off the rails. Genetic paternity testing enables us to sort out, in a transparent and decisive way, the age-old but traditionally never-quite-answerable question of whether a child is genetically related to the husband of the child's mother. Given the impossibility of settling this question for certain, British and American law has long held that a biological relationship must almost always be assumed to exist. (...)
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  • Prenatal diagnosis and discrimination against the disabled.L. Gillam - 1999 - Journal of Medical Ethics 25 (2):163-171.
    Two versions of the argument that prenatal diagnosis discriminates against the disabled are distinguished and analysed. Both are shown to be inadequate, but some valid concerns about the social effects of prenatal diagnosis are highlighted.
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  • Bioindustry Ethics.David Finegold (ed.) - 2005 - Elsevier Academic Press.
    This book is the first systematic, detailed treatment of the approaches to ethical issues taken by biotech and pharmaceutical companies. The application of genetic/genomic technologies raises a whole spectrum of ethical questions affecting global health that must be addressed. Topics covered in this comprehensive survey include considerations for bioprospecting in transgenics, genomics, drug discovery, and nutrigenomics, as well as how to improve stakeholder relations, design ethical clinical trials, avoid conflicts of interest, and establish ethics advisory boards. The expert authors represent (...)
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  • Commercialisation of genetic services: the role of genetic counsellors.Chris MacDonald - 2002 - Human Reproduction and Genetic Ethics 8 (1):1.
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