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| 37166283 | Slowing the Slide Down the Slippery Slope of Medical Assistance in Dying: Mutual Learnings for Canada and the US. | Am J Bioeth | 2023 |
| 37805493 | Public attitudes towards genomic data sharing: results from a provincial online survey in Canada. | BMC Med Ethics | 2023 |
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| 34500452 | Psychological Distress and Quality of Life in Participants Undergoing Genetic Testing for Arrhythmogenic Right Ventricular Cardiomyopathy Caused by TMEM43 p.S358L: Is It Time to Offer Population-Based Genetic Screening? | Public Health Genomics | 2021 |
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| 30465127 | Universal tumor screening for Lynch syndrome: perspectives of Canadian pathologists and genetic counselors. | J Community Genet | 2019 |
| 31384304 | What is in a Name? Parent, Professional and Policy-Maker Conceptions of Consent-Related Language in the Context of Newborn Screening. | Public Health Ethics | 2019 |
| 31102338 | Universal tumor screening for Lynch syndrome: Perceptions of Canadian pathologists and genetic counselors of barriers and facilitators. | Cancer Med | 2019 |
| 28949838 | The interactions of Canadian ethics consultants with health care managers and governing boards during times of crisis. | AJOB Empir Bioeth | 2017 |
| 27111369 | Acknowledging Diversity of Meaning: A Reflection on American Bioethics. | Am J Bioeth | 2016 |
| 29062523 | Giving voice to older adults living with frailty and their family caregivers: engagement of older adults living with frailty in research, health care decision making, and in health policy. | Res Involv Engagem | 2016 |
| 26513349 | Perceived economic burden associated with an inherited cardiac condition: a qualitative inquiry with families affected by arrhythmogenic right ventricular cardiomyopathy. | Genet Med | 2016 |
| 27302842 | Consent for newborn screening: parents' and health-care professionals' experiences of consent in practice. | Eur J Hum Genet | 2016 |
| 27471946 | On the Curious Range of Responses to Our Curious Case: Response to Open Peer Commentaries on "The Curious Case of the De-ICD: Negotiating the Dynamics of Autonomy and Paternalism in Complex Clinical Relationships". | Am J Bioeth | 2016 |
| 27366835 | The Curious Case of the De-ICD: Negotiating the Dynamics of Autonomy and Paternalism in Complex Clinical Relationships. | Am J Bioeth | 2016 |
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| 26135297 | Triage in times of drug shortage. | Healthc Manage Forum | 2015 |
| 25694322 | Clinical genetic research 3: Genetics ELSI (Ethical, Legal, and Social Issues) research. | Methods Mol Biol | 2015 |
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| 25421341 | Stakeholder attitudes towards the role and application of informed consent for newborn bloodspot screening: a study protocol. | BMJ Open | 2014 |
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| 27774156 | A review of the key issues associated with the commercialization of biobanks. | J Law Biosci | 2014 |
| 22859644 | Privacy protection and public goods: building a genetic database for health research in Newfoundland and Labrador. | J Am Med Inform Assoc | 2013 |
| 24223516 | Reflections on the cost of "low-cost" whole genome sequencing: framing the health policy debate. | PLoS Biol | 2013 |
| 23798257 | From framework to the frontline: designing a structure and process for drug supply shortage planning. | Healthc Manage Forum | 2013 |
| 23402260 | "Media, politics and science policy: MS and evidence from the CCSVI Trenches". | BMC Med Ethics | 2013 |
| 23591403 | Consulting the community: public expectations and attitudes about genetics research. | Eur J Hum Genet | 2013 |
| 22103558 | Interest in newborn genetic testing: a survey of prospective parents and the general public. | Genet Test Mol Biomarkers | 2012 |
| 22834846 | Public attitudes about genetic testing in the newborn period. | J Obstet Gynecol Neonatal Nurs | 2012 |
| 22670101 | Specialists' perceptions of hereditary colorectal cancer screening in Newfoundland and Labrador. | Curr Oncol | 2012 |
| 22261752 | Personal privacy, public benefits, and biobanks: a conjoint analysis of policy priorities and public perceptions. | Genet Med | 2012 |
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| 20301857 | Duty to warn and genetic disease. | Can J Cardiovasc Nurs | 2010 |
| 21686303 | Keeping the GINA in the bottle: assessing the current need for genetic non-discrimination legislation in Canada. | Open Med | 2010 |
| 21212811 | Human Non-persons, Feticide, and the Erosion of Dignity. | J Bioeth Inq | 2010 |
| 20357547 | Adapting the Hamilton Health Sciences critical care pandemic triage protocol. | Healthc Q | 2010 |
| 20010364 | Translation of research discoveries to clinical care in arrhythmogenic right ventricular cardiomyopathy in Newfoundland and Labrador: lessons for health policy in genetic disease. | Genet Med | 2009 |
| 20436810 | Sorry, You Can't Have That Information: Data Holder Confusion Regarding Privacy Requirements for Personal Health Information and the Potential Chilling Effect on Health Research. | Healthc Policy | 2009 |
| 18366258 | Research ethics recommendations for whole-genome research: consensus statement. | PLoS Biol | 2008 |
| 18496224 | Is gene discovery research or diagnosis? | Genet Med | 2008 |
| 16542381 | Genetic knowledge and moral responsibility: ambiguity at the interface of genetic research and clinical practice. | Clin Genet | 2006 |
| 16042526 | Narrative means to humanistic ends. | Teach Learn Med | 2005 |
| 16459418 | Research governance, bio-politics and political will: recent lessons from Newfoundland and Labrador. | Health Law Rev | 2005 |
| 16302547 | Ethics first aid: reframing the role of "principlism" in clinical ethics education and practice. | J Clin Ethics | 2005 |
| 15909482 | T-shirts, tennis shoes, and teleradiology: technological efficiency and the end of medicine. | Clin Invest Med | 2005 |
| 15511036 | Death, dignity, and moral nonsense. | J Palliat Care | 2004 |
| 15672700 | Doing more with less: organizational ethics in a rural Canadian setting. | HEC Forum | 2004 |
| 14534126 | Memorial University of Newfoundland Faculty of Medicine, the Medical Humanities in the clinical skills course. | Acad Med | 2003 |