- Individual human rights in genetic research : blurring the line between collective and individual interests.Hélène Boussard - 2009 - In Thérèse Murphy (ed.), New technologies and human rights. New York: Oxford University Press.details
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The connected self: the ethics and governance of the genetic individual.Heather Widdows - 2013 - New York: Cambridge University Press.details
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Managing Incidental Findings in Human Subjects Research: Analysis and Recommendations.Susan M. Wolf, Frances P. Lawrenz, Charles A. Nelson, Jeffrey P. Kahn, Mildred K. Cho, Ellen Wright Clayton, Joel G. Fletcher, Michael K. Georgieff, Dale Hammerschmidt, Kathy Hudson, Judy Illes, Vivek Kapur, Moira A. Keane, Barbara A. Koenig, Bonnie S. LeRoy, Elizabeth G. McFarland, Jordan Paradise, Lisa S. Parker, Sharon F. Terry, Brian Van Ness & Benjamin S. Wilfond - 2008 - Journal of Law, Medicine and Ethics 36 (2):219-248.details
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To know or not to know? Genetic ignorance, autonomy and paternalism.Jane Wilson - 2005 - Bioethics 19 (5-6):492-504.details
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Privacy and disclosure in medical genetics examined in an ethics of care.Dorothy C. Wertz & John C. Fletcher - 1991 - Bioethics 5 (3):212–232.details
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A Theory of Freedom.Richard Warner - 1992 - Philosophical Review 101 (2):468.details
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The right not to know: an autonomy based approach.R. Andorno - 2004 - Journal of Medical Ethics 30 (5):435-439.details
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Solidarity in contemporary bioethics – towards a new approach.Barbara Prainsack & Alena Buyx - 2012 - Bioethics 26 (7):343-350.details
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Rethinking the ‘right not to know’.Rosalind McDougall - 2004 - Monash Bioethics Review 23 (1):22-36.details
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Ignorance, information and autonomy.John Harris & Kirsty Keywood - 2001 - Theoretical Medicine and Bioethics 22 (5):415-436.details
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Duty to disclose what? Querying the putative obligation to return research results to participants.F. A. Miller, R. Christensen, M. Giacomini & J. S. Robert - 2008 - Journal of Medical Ethics 34 (3):210-213.details
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Review of Ruth R. Faden and Tom L. Beauchamp: A History and Theory of Informed Consent. [REVIEW]William G. Bartholome - 1988 - Ethics 98 (3):605-606.details
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Privacy and Disclosure in Medical Genetics Examined in an Ethics of Care.John C. Fletcher Dorothy C. Wertz - 2007 - Bioethics 5 (3):212-232.details
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Communication of genetic information within families: The case for familial comity. [REVIEW]Angela Davey, Ainsley Newson & Peter O’Leary - 2006 - Journal of Bioethical Inquiry 3 (3):161-166.details
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The relative importance of undesirable truths.Lisa Bortolotti - 2012 - Medicine Healthcare and Philosophy (4):683-690.details
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The relative importance of undesirable truths.Lisa Bortolotti - 2013 - Medicine, Health Care and Philosophy 16 (4):683-690.details
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The right not to know: the case of psychiatric disorders.Lisa Bortolotti & Heather Widdows - 2011 - Journal of Medical Ethics 37 (11):673-676.details
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Autonomy and Trust in Bioethics.Onora O'Neill - 2002 - New York: Cambridge University Press.details
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Genetic Privacy: A Challenge to Medico-Legal Norms.Graeme Laurie - 2002 - New York: Cambridge University Press.details
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A Theory of Freedom.Stanley I. Benn - 1988 - Cambridge University Press.details
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Human genetic research: emerging trends in ethics.Ruth Chadwick & Bartha Maria Knoppers - 2005 - .details
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Privacy, morality, and the law.W. A. Parent - 1983 - Philosophy and Public Affairs 12 (4):269-288.details
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