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Plos One|August 17, 2018
The ethics conundrum in Recall by Genotype (RbG) research: Perspectives from birth cohort participantsJoel T Minion, Frances Butcher, Nicholas Timpson, et al.
Biopreservation and Biobanking|May 21, 2016
International Data Sharing in Practice: New Technologies Meet Old GovernanceMadeleine J Murtagh, Andrew Turner, Joel T Minion, et al.
Joint Commission Journal on Quality and Patient Safety|June 7, 2024
Evaluating Real-World Implementation of INFORM (Improving Nursing Home Care through Feedback on Performance Data): An Improvement Initiative in Canadian Nursing HomesSeyedehtanaz Saeidzadeh, Joel T Minion, Stirling Bryan, et al.
BMC Medical Ethics|June 25, 2021
What does engagement mean to participants in longitudinal cohort studies? A qualitative studyCynthia A Ochieng, Joel T Minion, Andrew Turner, et al.
Personalized Medicine|April 6, 2021
Views on genomic research result delivery methods and informed consent: a reviewDanya F Vears, Joel T Minion, Stephanie J Roberts, et al.
Intensive & Critical Care Nursing|August 6, 2022
The lived experience by patients and family members of extracorporeal membrane oxygenation: A qualitative studyJoel T Minion, Liza Mastikhina, Laura Dowsett, et al.
BMC Medical Ethics|April 6, 2017
The ECOUTER methodology for stakeholder engagement in translational researchMadeleine J Murtagh, Joel T Minion, Andrew Turner, et al.
BMC Health Services Research|May 30, 2026
"We feel like we don't matter": the work experience of caring for long-term care residents with suspected trauma-related responsive behaviorsJoel T Minion, Hadiya M Huijer, Tosin Y Akintunde, et al.
Plos One|November 8, 2021
Return of individual research results from genomic research: A systematic review of stakeholder perspectivesDanya F Vears, Joel T Minion, Stephanie J Roberts, et al.
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