Хайлтын үр дүнгүүд - Eric T. Juengst

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  1. 1
    Why Does the Shift from “Personalized Medicine” to “Precision Health” and “Wellness Genomics” Matter?

    Why Does the Shift from “Personalized Medicine” to “Precision Health” and “Wellness Genomics” Matter? -н Eric T. Juengst, Michelle L. McGowan

    Хэвлэсэн 2018
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    Artigo
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  2. 2
    Personalized Genomic Medicine and the Rhetoric of Empowerment

    Personalized Genomic Medicine and the Rhetoric of Empowerment -н Eric T. Juengst, Michael A. Flatt, Richard A. Settersten

    Хэвлэсэн 2012
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    Artigo
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  3. 3
    Big data, open science and the brain: lessons learned from genomics

    Big data, open science and the brain: lessons learned from genomics -н Suparna Choudhury, Jennifer R. Fishman, Michelle L. McGowan, Eric T. Juengst

    Хэвлэсэн 2014
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    Revisão
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  4. 4
    Integrating genomics into clinical oncology: Ethical and social challenges from proponents of personalized medicine

    Integrating genomics into clinical oncology: Ethical and social challenges from proponents of personalized medicine -н Michelle L. McGowan, Richard A. Settersten, Eric T. Juengst, Jennifer R. Fishman

    Хэвлэсэн 2014
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    Artigo
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  5. 5
    After the revolution? Ethical and social challenges in ‘personalized genomic medicine’

    After the revolution? Ethical and social challenges in ‘personalized genomic medicine’ -н Eric T. Juengst, Richard A. Settersten, Jennifer R. Fishman, Michelle L. McGowan

    Хэвлэсэн 2012
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    Artigo
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  6. 6
    From “Personalized” to “Precision” Medicine: The Ethical and Social Implications of Rhetorical Reform in Genomic Medicine

    From “Personalized” to “Precision” Medicine: The Ethical and Social Implications of Rhetorical Reform in Genomic Medicine -н Eric T. Juengst, Michelle L. McGowan, Jennifer R. Fishman, Richard A. Settersten

    Хэвлэсэн 2016
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    Artigo
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  7. 7
    Guidelines for return of research results from pediatric genomic studies: deliberations of the Boston Children’s Hospital Gene Partnership Informed Cohort Oversight Board

    Guidelines for return of research results from pediatric genomic studies: deliberations of the Boston Children’s Hospital Gene Partnership Informed Cohort Oversight Board -н Ingrid A. Holm, Sarah Savage, Robert C. Green, Eric T. Juengst, Amy L. McGuire, Susan Kornetsky, Stephanie J. Brewster, Steven Joffe, Patrick Taylor

    Хэвлэсэн 2014
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    Artigo
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  8. 8
    Citizen science or scientific citizenship? Disentangling the uses of public engagement rhetoric in national research initiatives

    Citizen science or scientific citizenship? Disentangling the uses of public engagement rhetoric in national research initiatives -н J. Patrick Woolley, Michelle L. McGowan, Harriet Teare, Victoria Coathup, Jennifer R. Fishman, Richard A. Settersten, Sigrid Sterckx, Jane Kaye, Eric T. Juengst

    Хэвлэсэн 2016
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    Artigo
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  9. 9
    IRB perspectives on the return of individual results from genomic research

    IRB perspectives on the return of individual results from genomic research -н Lynn G. Dressler, Sondra J. Smolek, Roselle Ponsaran, Janell M. Markey, Helene Starks, Nancy Gerson, Susan Lewis, Nancy Press, Eric T. Juengst, Georgia L. Wiesner

    Хэвлэсэн 2012
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    Artigo
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  10. 10
    A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing

    A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing -н Jonathan S. Berg, Ann Katherine M. Foreman, Julianne O’Daniel, Jessica K. Booker, Lacey Boshe, Timothy S. Carey, Kristy Crooks, Brian C. Jensen, Eric T. Juengst, Kristy Lee, Daniel K. Nelson, Bradford C. Powell, Cynthia M. Powell, Myra I. Roche, Cécile Skrzynia, Natasha T. Strande, Karen E. Weck, Kirk C. Wilhelmsen, James P. Evans

    Хэвлэсэн 2015
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    Artigo
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  11. 11
    Including all voices in international data-sharing governance

    Including all voices in international data-sharing governance -н Jane Kaye, Sharon F. Terry, Eric T. Juengst, Sarah Coy, Jennifer R. Harris, Drc Chalmers, Edward S. Dove, Isabelle Budin‐Ljøsne, Clement Adebamowo, Emilomo Ogbe, Louise Bezuidenhout, Michael Morrison, Joel T. Minion, Madeleine J. Murtagh, Jusaku Minari, Harriet Teare, Rosario Isasi, Yoshihiro Kato, Emmanuelle Rial‐Sebbag, Patricia A. Marshall, Barbara A. Koenig, Anne Cambon‐Thomsen

    Хэвлэсэн 2018
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    Artigo
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  12. 12
    Research Ethics Recommendations for Whole-Genome Research: Consensus Statement

    Research Ethics Recommendations for Whole-Genome Research: Consensus Statement -н Timothy Caulfield, Amy L. McGuire, Mildred K. Cho, Janet A. Buchanan, Michael Burgess, Ursula Danilczyk, Christina M. Diaz, Kelly Fryer‐Edwards, Shane K Green, Marc A Hodosh, Eric T. Juengst, Jane Kaye, Laurence H. Kedes, Bartha Maria Knoppers, Trudo Lemmens, Eric M. Meslin, Juli Murphy, Robert L. Nussbaum, Margaret Otlowski, Daryl Pullman, Peter N. Ray, Jeremy Sugarman, Michael Timmons

    Хэвлэсэн 2008
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    Artigo
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  13. 13
    Toward better governance of human genomic data

    Toward better governance of human genomic data -н Kieran C. O’Doherty, Mahsa Shabani, Edward S. Dove, Heidi Beate Bentzen, Pascal Borry, Michael Burgess, Drc Chalmers, Jantina de Vries, Lisa Eckstein, Stephanie M. Fullerton, Eric T. Juengst, Yoshihiro Kato, Jane Kaye, Bartha Maria Knoppers, Barbara A. Koenig, Spero M. Manson, Kimberlyn McGrail, Amy L. McGuire, Eric M. Meslin, Dianne Nicol, Barbara Prainsack, Sharon F. Terry, Adrian Thorogood, Wylie Burke

    Хэвлэсэн 2021
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    Artigo
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