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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
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March 8, 2018
Engaging populations underrepresented in research through novel approaches to consent
Stephanie A Kraft, Megan Doerr
Health Research Policy and Systems
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July 10, 2020
Developing pathways for community-led research with big data: a content analysis of stakeholder interviews
Shira Grayson, Megan Doerr, Joon-Ho Yu
Journal of Medical Internet Research
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April 1, 2020
Connected Medical Technology and Cybersecurity Informed Consent: A New Paradigm
Jeffrey Tully, Andrea Coravos, Megan Doerr, et al.
JMIR Public Health and Surveillance
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September 30, 2024
AI Governance: A Challenge for Public Health
Jennifer K Wagner, Megan Doerr, Cason D Schmit
Journal of Personalized Medicine
|
January 8, 2015
Formative evaluation of clinician experience with integrating family history-based clinical decision support into clinical practice
Megan Doerr, Emily Edelman, Emily Gabitzsch, et al.
Journal of Medical Internet Research
|
June 17, 2020
Bringing Code to Data: Do Not Forget Governance
Christine Suver, Adrian Thorogood, Megan Doerr, et al.
Interactive Journal of Medical Research
|
March 19, 2025
Long-Term Engagement of Diverse Study Cohorts in Decentralized Research: Longitudinal Analysis of "All of Us" Research Program Data
Vijay Yadav, Elias Chaibub Neto, Megan Doerr, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing
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April 10, 2019
Implementing a universal informed consent process for the <i>All of Us</i> Research Program
Megan Doerr, Shira Grayson, Sarah Moore, et al.
JMIR Mhealth and Uhealth
|
September 1, 2017
Consent Processes for Mobile App Mediated Research: Systematic Review
Sarah Moore, Anne-Marie Tassé, Adrian Thorogood, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing
|
December 5, 2019
Navigating ethical quandaries with the privacy dilemma of biomedical datasets
Gamze Gürsoy, Megan Doerr, John Wilbanks, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 49) with videos related to
Sort By:
Page
of 5
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
March 8, 2018
Engaging populations underrepresented in research through novel approaches to consent
Stephanie A Kraft, Megan Doerr
Health Research Policy and Systems
|
July 10, 2020
Developing pathways for community-led research with big data: a content analysis of stakeholder interviews
Shira Grayson, Megan Doerr, Joon-Ho Yu
Journal of Medical Internet Research
|
April 1, 2020
Connected Medical Technology and Cybersecurity Informed Consent: A New Paradigm
Jeffrey Tully, Andrea Coravos, Megan Doerr, et al.
JMIR Public Health and Surveillance
|
September 30, 2024
AI Governance: A Challenge for Public Health
Jennifer K Wagner, Megan Doerr, Cason D Schmit
Journal of Personalized Medicine
|
January 8, 2015
Formative evaluation of clinician experience with integrating family history-based clinical decision support into clinical practice
Megan Doerr, Emily Edelman, Emily Gabitzsch, et al.
Journal of Medical Internet Research
|
June 17, 2020
Bringing Code to Data: Do Not Forget Governance
Christine Suver, Adrian Thorogood, Megan Doerr, et al.
Interactive Journal of Medical Research
|
March 19, 2025
Long-Term Engagement of Diverse Study Cohorts in Decentralized Research: Longitudinal Analysis of "All of Us" Research Program Data
Vijay Yadav, Elias Chaibub Neto, Megan Doerr, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing
|
April 10, 2019
Implementing a universal informed consent process for the <i>All of Us</i> Research Program
Megan Doerr, Shira Grayson, Sarah Moore, et al.
JMIR Mhealth and Uhealth
|
September 1, 2017
Consent Processes for Mobile App Mediated Research: Systematic Review
Sarah Moore, Anne-Marie Tassé, Adrian Thorogood, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing
|
December 5, 2019
Navigating ethical quandaries with the privacy dilemma of biomedical datasets
Gamze Gürsoy, Megan Doerr, John Wilbanks, et al.
Page
of 5