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Health Research Policy and Systems|July 10, 2020
Developing pathways for community-led research with big data: a content analysis of stakeholder interviewsShira Grayson, Megan Doerr, Joon-Ho YuEthics & Human Research|October 1, 2023
Translational Research and CommunitiesMegan Doerr, Joon-Ho YuPacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|April 10, 2019
Implementing a universal informed consent process for the All of Us Research ProgramMegan Doerr, Shira Grayson, Sarah Moore, et al.Health Expectations : an International Journal of Public Participation in Health Care and Health Policy|March 18, 2026
Cultivating Authentic Partnership: Cooperative Development of a Toolkit to Mitigate Group Harm in Biorepository-Enabled ResearchShauntey Kalweit, Carly Marten, Odia Kane, et al.The Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics|April 29, 2020
Who Are the People in Your Neighborhood? Personas Populating Unregulated mHealth ResearchMegan Doerr, Christi GuerriniCleveland Clinic Journal of Medicine|May 3, 2012
Family history: still relevant in the genomics eraMegan Doerr, Kathryn TengEthics & Human Research|July 8, 2022
Big Health Data Research and Group Harm: The Scope of IRB ReviewMegan Doerr, Sara MeederJournal of Law and the Biosciences|August 1, 2020
Research ethics in a pandemic: considerations for the use of research infrastructure and resources for public health activitiesMegan Doerr, Jennifer K WagnerAmerican Journal of Medical Genetics. Part C, Seminars in Medical Genetics|March 8, 2018
Engaging populations underrepresented in research through novel approaches to consentStephanie A Kraft, Megan DoerrPageof 9