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Jessica L. Roberts [7]Jessica Roberts [2]
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  1.  22
    Who Owns the Data in a Medical Information Commons?Amy L. McGuire, Jessica Roberts, Sean Aas & Barbara J. Evans - 2019 - Journal of Law, Medicine and Ethics 47 (1):62-69.
    In this paper, we explore the perspectives of expert stakeholders about who owns data in a medical information commons and what rights and interests ought to be recognized when developing a governance structure for an MIC. We then examine the legitimacy of these claims based on legal and ethical analysis and explore an alternative framework for thinking about participants' rights and interests in an MIC.
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  2.  21
    A Nudge Toward Meaningful Choice.Leah R. Fowler & Jessica L. Roberts - 2019 - American Journal of Bioethics 19 (5):76-78.
    Volume 19, Issue 5, May 2019, Page 76-78.
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  3.  36
    The Erosion of Ethics: From Citizen Journalism to Social Media.Jessica Roberts - 2019 - Journal of Information, Communication and Ethics in Society 17 (4):409-421.
    Purpose The purpose of this paper is to consider the implications of the shift from citizen journalist to social media user by examining how ethics are addressed on social media sites compared to citizen journalism sites. Design/methodology/approach This paper applies the framework of a 2012 study of ethics on citizen journalism sites to social media sites’ guiding documents to compare how they discuss ethics and what they ask of the users, offering suggestions for how social media sites might imbue users (...)
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  4. Anti-Selection is Only the Beginning.Valarie K. Blake & Jessica L. Roberts - 2022 - Journal of Law, Medicine and Ethics 50 (1):155-156.
    This commentary proposes the need for greater normative debate about when, if ever, it is appropriate for insurers to access genetic information of insureds to combat anti-selection.
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  5.  18
    Stigmatizing the Unhealthy.Jessica L. Roberts & Elizabeth Weeks - 2017 - Journal of Law, Medicine and Ethics 45 (4):484-491.
    Stigma can lead to poor health outcomes. At the same time, people who are perceived as unhealthy may experience stigma as the result of that perception. As part of a larger project examining discrimination on the basis of health status or “healthism,” we explore the role of stigma in producing disadvantage based on health status. Specifically, we look to the principles of health equality and health justice. An intervention violates health equality when it is driven by animus, which can be (...)
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  6.  15
    The Legality of Biometric Screening of Professional Athletes.Jessica L. Roberts, I. Glenn Cohen, Christopher R. Deubert & Holly Fernandez Lynch - 2017 - American Journal of Bioethics 17 (1):65-67.
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  7.  9
    Negotiating Commercial Interests in Biospecimens.Jessica L. Roberts - 2017 - Journal of Law, Medicine and Ethics 45 (1):138-141.
    Proposed changes to the Common Rule would require publicly funded researchers to disclose whether a subject's biospecimens could be used for commercial profit and whether the subject will share in those proceeds. Disclosing commercial interests will inform research participants that their tissue may have commercial value, a possibility that those individuals might not have previously considered. The proposed changes may then provide people with an opportunity to negotiate commercial rights in their biospecimens despite the well-accepted legal precedent that individuals maintain (...)
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  8.  8
    Review of Isabel Karpin and Kristin Savell, Perfecting Pregnancy: Law, Disability, and the Future of Reproduction. [REVIEW]Jessica L. Roberts - 2013 - American Journal of Bioethics 13 (5):70-71.
  9.  6
    GINA's Limits or Something More? The Need for Greater Protection of Employee Health-Related Information.Jessica L. Roberts - 2014 - American Journal of Bioethics 14 (11):45-48.
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