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  1.  36
    Introduction: Sharing Data in a Medical Information Commons.Amy L. McGuire, Mary A. Majumder, Angela G. Villanueva, Jessica Bardill, Juli M. Bollinger, Eric Boerwinkle, Tania Bubela, Patricia A. Deverka, Barbara J. Evans, Nanibaa' A. Garrison, David Glazer, Melissa M. Goldstein, Henry T. Greely, Scott D. Kahn, Bartha M. Knoppers, Barbara A. Koenig, J. Mark Lambright, John E. Mattison, Christopher O'Donnell, Arti K. Rai, Laura L. Rodriguez, Tania Simoncelli, Sharon F. Terry, Adrian M. Thorogood, Michael S. Watson, John T. Wilbanks & Robert Cook-Deegan - 2019 - Journal of Law, Medicine and Ethics 47 (1):12-20.
    Drawing on a landscape analysis of existing data-sharing initiatives, in-depth interviews with expert stakeholders, and public deliberations with community advisory panels across the U.S., we describe features of the evolving medical information commons. We identify participant-centricity and trustworthiness as the most important features of an MIC and discuss the implications for those seeking to create a sustainable, useful, and widely available collection of linked resources for research and other purposes.
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  2.  16
    New Words and Old Stories: Indigenous Teachings in Health Care and Bioethics.Jessica Bardill & Nanibaa' A. Garrison - 2016 - American Journal of Bioethics 16 (5):50-52.
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  3.  2
    Naming Indigenous Concerns, Framing Considerations for Stored Biospecimens.Jessica Bardill & Nanibaa' A. Garrison - 2015 - American Journal of Bioethics 15 (9):73-75.
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  4.  3
    Parts, Transmission, and Remains: How Blood Makes and Is Made Into Life.Jessica Bardill - 2015 - American Journal of Bioethics 15 (2):1-2.
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