publication venue for
- Alternatives to project-specific consent for access to personal information for health research: Canadian public opinion 2007
- What are the views of Quebec and Ontario citizens on the tiebreaker criteria for prioritizing access to adult critical care in the extreme context of a COVID-19 pandemic?. 25:31. 2024
- Preparing ethical review systems for emergencies: next steps. 24:92. 2023
- Artificial intelligence for good health: a scoping review of the ethics literature. 22:14. 2021
- The impact of reporting magnetic resonance imaging incidental findings in the Canadian alliance for healthy hearts and minds cohort. 22:145. 2021
- "It gets people through the door": a qualitative case study of the use of incentives in the care of people at risk or living with HIV in British Columbia, Canada. 21:105. 2020
- Implementation challenges for an ethical introduction of noninvasive prenatal testing: a qualitative study of healthcare professionals’ views from Lebanon and Quebec. 21:15. 2020
- Huge variation in obtaining ethical permission for a non-interventional observational study in Europe. 20:39. 2019
- Women’s perspectives on the ethical implications of non-invasive prenatal testing: a qualitative analysis to inform health policy decisions. 19:27. 2018
- Familiar ethical issues amplified: how members of research ethics committees describe ethical distinctions between disaster and non-disaster research. 18:44. 2017
- This moral coil: a cross-sectional survey of Canadian medical student attitudes toward medical assistance in dying. 18:58. 2017
- Steps toward improving ethical evaluation in health technology assessment: a proposed framework. 17:34. 2016
- Innovations in research ethics governance in humanitarian settings. 16:10. 2015
- What makes public health studies ethical? Dissolving the boundary between research and practice. 15:61. 2014
- Access and use of human tissues from the developing world: ethical challenges and a way forward using a tissue trust. 12:2. 2011
- Ethics, economics and the regulation and adoption of new medical devices: case studies in pelvic floor surgery. 11:14. 2010
- Consent for use of personal information for health research: Do people with potentially stigmatizing health conditions and the general public differ in their opinions?. 10:10. 2009
- Alternatives to project-specific consent for access to personal information for health research: Insights from a public dialogue. 9:18. 2008
- When research seems like clinical care: a qualitative study of the communication of individual cancer genetic research results. 9:4. 2008
- Who's minding the shop? The role of Canadian research ethics boards in the creation and uses of registries and biobanks. 9:17. 2008
- Taking tissue seriously means taking communities seriously. 8:11. 2007
- On pandemics and the duty to care: whose duty? who cares?. 7:E5. 2006
- Pandemic influenza preparedness: an ethical framework to guide decision-making. 7:E12. 2006
- Critical reflections on evidence, ethics and effectiveness in the management of tuberculosis: public health and global perspectives.. 5:E2. 2004
- DNA databanks and consent: A suggested policy option involving an authorization model. 4:E1. 2003
- Hepatitis B virus infected physicians and disclosure of transmission risks to patients: a critical analysis.. 2:E4. 2001