- The complexities of ethical evaluation of genomics research.R. Hoedemaekers, B. Gordijn, Y. Hekster & F. Van Agt - 2006 - HEC Forum 18 (1):18-36.details
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Equitable Access to Human Biological Resources in Developing Countries: Benefit Sharing Without Undue Inducement.Roger Scarlin Chennells - 2015 - Cham: Imprint: Springer.details
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Biobanks--When is Re-consent Necessary?K. S. Steinsbekk & B. Solberg - 2011 - Public Health Ethics 4 (3):236-250.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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Biobanking and the Abandonment of Informed Consent: An Ethical Imperative.Stephanie Solomon Cargill - 2016 - Public Health Ethics 9 (3):255-263.details
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Challenges in biobank governance in Sub-Saharan Africa.Ciara Staunton & Keymanthri Moodley - 2013 - BMC Medical Ethics 14 (1):35.details
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In Defence of informed consent for health record research - why arguments from ‘easy rescue’, ‘no harm’ and ‘consent bias’ fail.Thomas Ploug - 2020 - BMC Medical Ethics 21 (1):1-13.details
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Breite Einwilligung (broad consent) zur Biobank-Forschung – die ethische Debatte.Gesine Richter & Alena Buyx - 2016 - Ethik in der Medizin 28 (4):311-325.details
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Eliciting meta consent for future secondary research use of health data using a smartphone application - a proof of concept study in the Danish population.Thomas Ploug & Søren Holm - 2017 - BMC Medical Ethics 18 (1):51.details
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Evaluating models of consent in changing health research environments.Svenja Wiertz & Joachim Boldt - 2022 - Medicine, Health Care and Philosophy 25 (2):269-280.details
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Health Research with Big Data: Time for Systemic Oversight.Effy Vayena & Alessandro Blasimme - 2018 - Journal of Law, Medicine and Ethics 46 (1):119-129.details
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"It's for a good cause, isn't it?" - Exploring views of South African TB research participants on sample storage and re-use.Gerrit van Schalkwyk, Jantina de Vries & Keymanthri Moodley - 2012 - BMC Medical Ethics 13 (1):19-.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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Sharing the benefits of genetic research.Doris Schroeder - 2005 - British Medical Journal 331 (7529):1351-1352.details
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Database Research: Public and Private Interests.Vilhjálmur Árnason - 2011 - Cambridge Quarterly of Healthcare Ethics 20 (4):563-571.details
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Informed consent in biobanking and genetic research.Antonio Casado da Rocha & Arantza Etxeberria Agiriano - 2008 - Arbor 184 (730).details
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Ethical considerations of research policy for personal genome analysis: the approach of the Genome Science Project in Japan.Kazuto Kato, Tetsuya Shirai & Jusaku Minari - 2014 - Life Sciences, Society and Policy 10 (1):1-11.details
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Biobanking: International Norms.Bartha Maria Knoppers - 2005 - Journal of Law, Medicine and Ethics 33 (1):7-14.details
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Digital pills: a scoping review of the empirical literature and analysis of the ethical aspects.Andrea Martani, Lester Darryl Geneviève, Christopher Poppe, Carlo Casonato & Tenzin Wangmo - 2020 - BMC Medical Ethics 21 (1):1-13.details
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Biobanking: International Norms.Bartha Maria Knoppers - 2005 - Journal of Law, Medicine and Ethics 33 (1):7-14.details
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Motivating Donors to Genetic Research? Anthropological Reasons to Rethink the Role of Informed Consent.Klaus Hoeyer & Niels Lynöe - 2005 - Medicine, Health Care and Philosophy 9 (1):13-23.details
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CQ Sources/Bibliography.Bette Anton - 2008 - Cambridge Quarterly of Healthcare Ethics 17 (4):465-467.details
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In Defense of Broad Consent.Gert Helgesson - 2012 - Cambridge Quarterly of Healthcare Ethics 21 (1):40-50.details
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Four Themes in Recent Swedish Bioethics Debates.Gert Helgesson & Stefan Eriksson - 2011 - Cambridge Quarterly of Healthcare Ethics 20 (3):409-417.details
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Public Health Genomics (PHG): From Scientific Considerations to Ethical Integration.Yanick Farmer & BÉatrice Godard - 2007 - Genomics, Society and Policy 3 (3):1-14.details
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Biobancos, cultura científica y ética de la investiación.Antonio Casado Da Rocha - 2010 - Dilemata 4.details
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CQ Sources/Bibliography.Bette Anton - 1999 - Cambridge Quarterly of Healthcare Ethics 8 (4):348-350.details
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The informed consent aftermath of the genetic revolution. An Italian example of implementation.Federica Artizzu - 2008 - Medicine, Health Care and Philosophy 11 (2):181-190.details
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CQ Sources/Bibliography.Bette Anton - 2008 - Cambridge Quarterly of Healthcare Ethics 17 (2).details
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