- HIV and the right not to know: a reply to replies.Jonathan Youngs & Joshua Simmonds - 2016 - Journal of Medical Ethics 42 (2):108-110.details
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HIV and the right not to know.Jonathan Youngs & Joshua Simmonds - 2016 - Journal of Medical Ethics 42 (2):95-99.details
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The “We” in the “Me”: Solidarity and Health Care in the Era of Personalized Medicine.Barbara Prainsack - 2018 - Science, Technology, and Human Values 43 (1):21-44.details
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The Ethics of General Population Preventive Genomic Sequencing: Rights and Social Justice.Clair Morrissey & Rebecca L. Walker - 2018 - Journal of Medicine and Philosophy 43 (1):22-43.details
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From Genetics to Genomics: Facing the Liability Implications in Clinical Care.Gary Marchant, Mark Barnes, James P. Evans, Bonnie LeRoy & Susan M. Wolf - 2020 - Journal of Law, Medicine and Ethics 48 (1):11-43.details
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Looking for Trouble: Preventive Genomic Sequencing in the General Population and the Role of Patient Choice.Gabriel Lázaro-Muñoz, John M. Conley, Arlene M. Davis, Marcia Van Riper, Rebecca L. Walker & Eric T. Juengst - 2015 - American Journal of Bioethics 15 (7):3-14.details
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Ethical Design of Intelligent Assistive Technologies for Dementia: A Descriptive Review.Marcello Ienca, Tenzin Wangmo, Fabrice Jotterand, Reto W. Kressig & Bernice Elger - 2018 - Science and Engineering Ethics 24 (4):1035-1055.details
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Contacting gamete donors to facilitate diagnostic genetic testing for the donor-conceived child: what are the rights and obligations of gamete donors in these cases? A response to Horton et al.Lucy Frith - 2020 - Journal of Medical Ethics 46 (3):220-222.details
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How do healthcare professionals respond to ethical challenges regarding information management? A review of empirical studies.Cornelius Ewuoso, Susan Hall & Kris Dierickx - 2021 - Global Bioethics 32 (1):67-84.details
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Familial genetic risks: how can we better navigate patient confidentiality and appropriate risk disclosure to relatives?Edward S. Dove, Vicky Chico, Michael Fay, Graeme Laurie, Anneke M. Lucassen & Emily Postan - 2019 - Journal of Medical Ethics 45 (8):504-507.details
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The right not to know and the obligation to know.Ben Davies - 2020 - Journal of Medical Ethics 46 (5):300-303.details
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The Right Not to Know: some Steps towards a Compromise.Ben Davies & Julian Savulescu - 2020 - Ethical Theory and Moral Practice 24 (1):137-150.details
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Preserving children’s fertility: two tales about children’s right to an open future and the margins of parental obligations.Daniela Cutas & Kristien Hens - 2015 - Medicine, Health Care and Philosophy 18 (2):253-260.details
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Online consent: how much do we need to know?Bartlomiej Chomanski & Lode Lauwaert - forthcoming - AI and Society:1-11.details
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Mandatory Disclosure and Medical Paternalism.Emma C. Bullock - 2016 - Ethical Theory and Moral Practice 19 (2):409-424.details
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Aid-in-dying laws and the physician's duty to inform.Mara Buchbinder - 2017 - Journal of Medical Ethics 43 (10):666-669.details
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