- Human genetic biobanks in Asia: politics of trust and scientific advancement.Margaret Sleeboom-Faulkner (ed.) - 2009 - New York: Routledge.details
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Rethinking Research Ethics.Rosamond Rhodes - 2010 - American Journal of Bioethics 10 (10):19-36.details
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Why Communities and Their Goods Matter: Illustrated with the Example of Biobanks.Heather Widdows & Sean Cordell - 2011 - Public Health Ethics 4 (1):14-25.details
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Public health research ethics: A research agenda.Marcel Verweij & Angus Dawson - 2009 - Public Health Ethics 2 (1):1-6.details
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Changing Ethical Frameworks: From Individual Rights to the Common Good?Margit Sutrop - 2011 - Cambridge Quarterly of Healthcare Ethics 20 (4):533-545.details
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Health Ideologies, Objectivism, and the Common Good: On the Rights of Dissidents.Roger Strand - 2011 - Cambridge Quarterly of Healthcare Ethics 20 (4):605-611.details
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Catharsis and Moral Therapy I: A Platonic Account.Jan Helge Solbakk - 2006 - Medicine, Health Care and Philosophy 9 (1):57-67.details
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The consent problem within DNA biobanks.Darren Shickle - 2006 - Studies in History and Philosophy of Science Part C: Studies in History and Philosophy of Biological and Biomedical Sciences 37 (3):503-519.details
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The consent problem within DNA biobanks.Darren Shickle - 2004 - Studies in History and Philosophy of Science Part C: Studies in History and Philosophy of Biological and Biomedical Sciences 37 (3):503-519.details
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Expanding the Ethical Analysis of Biobanks.Mark A. Rothstein - 2005 - Journal of Law, Medicine and Ethics 33 (1):89-101.details
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Expanding the Ethical Analysis of Biobanks.Mark A. Rothstein - 2005 - Journal of Law, Medicine and Ethics 33 (1):89-101.details
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Tackling Epistemological Naivety: Large-Scale Information Systems and the Complexities of the Common Good.Kjetil Rommetveit - 2011 - Cambridge Quarterly of Healthcare Ethics 20 (4):584-595.details
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Coding and Consent: Moral Challenges of the Database Project in Iceland.VilhjÁlmur Rnason - 2004 - Bioethics 18 (1):27-49.details
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Rethinking research ethics.Rosamond Rhodes - 2005 - American Journal of Bioethics 5 (1):7 – 28.details
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Human Tissue Samples and Ethics: – Attitudes of the General Public in Sweden to Biobank Research.Tore Nilstun & Göran Hermerén - 2005 - Medicine, Health Care and Philosophy 9 (1):81-86.details
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From genomic databases to translation: a call to action.B. M. Knoppers, J. R. Harris, P. R. Burton, M. Murtagh, D. Cox, M. Deschenes, I. Fortier, T. J. Hudson, J. Kaye & K. Lindpaintner - 2011 - Journal of Medical Ethics 37 (8):515-516.details
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Ethical Endgames: Broad Consent for Narrow Interests; Open Consent for Closed Minds.Jan Reinert Karlsen, Jan Helge Solbakk & Søren Holm - 2011 - Cambridge Quarterly of Healthcare Ethics 20 (4):572-583.details
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Gene concepts and Genethics: Beyond exceptionalism.Péter Kakuk - 2008 - Science and Engineering Ethics 14 (3):357-375.details
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Broadening consent--and diluting ethics?B. Hofmann - 2009 - Journal of Medical Ethics 35 (2):125-129.details
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The consent problem within DNA biobanks.Darren Shickle - 2006 - Studies in History and Philosophy of Science Part C: Studies in History and Philosophy of Biological and Biomedical Sciences 37 (3):503-519.details
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The future of bioethics: Three dogmas and a cup of hemlock.Angus Dawson - 2010 - Bioethics 24 (5):218-225.details
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DNA databanks and consent: A suggested policy option involving an authorization model. [REVIEW]Timothy Caulfield, Ross Upshur & Abdallah Daar - 2003 - BMC Medical Ethics 4 (1):1-4.details
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Coding and Consent: Moral Challenges of the Database Project in Iceland.Vilhjálmur Árnason - 2004 - Bioethics 18 (1):27-49.details
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DNA databanks and consent: A suggested policy option involving an authorization model.Daar Abdallah, E. G. Upshur Ross & Caulfield Timothy - 2003 - BMC Medical Ethics 4 (1):1.details
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Ethical implications of the use of whole genome methods in medical research.Jane Kaye, Paula Boddington, Jantina de Vries, Naomi Hawkins & Karen Melham - unknowndetails
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