Publications

TREs are still not about trust

GRAHAM M. et al, (2023), Journal of Medical Ethics

Children with medical complexities: their distinct vulnerability in health systems' Covid-19 response and their claims of justice in the recovery phase.

Lignou S. and Sheehan M., (2022), Medicine, health care, and philosophy

Trust and the Goldacre Review: why trusted research environments are not about trust.

Graham M. et al, (2022), Journal of medical ethics

A concentric circles view of health data relations facilitates understanding of sociotechnical challenges for learning health systems and the role of federated data networks.

Milne R. et al, (2022), Frontiers in big data, 5

Changes in Healthcare Provision During Covid-19 and Their Impact on Children With Chronic Illness: A Scoping Review.

Lignou S. et al, (2022), Inquiry : a journal of medical care organization, provision and financing, 59

Bans, Taxes or Product Placement? Applying the Liberal Perfectionist Proviso to Public Health Food Policy.

Thomas O. et al, (2021), The American journal of bioethics : AJOB, 21, 51 - 53

Transformative disciplinary learning in history and social studies: Lessons from a high autonomy curriculum in New Zealand

Wood BE. and Sheehan M., (2021), Curriculum Journal, 32, 495 - 509

Measuring the impact of participatory research in psychiatry: How the search for epistemic justifications obscures ethical considerations.

Friesen P. et al, (2021), Health expectations : an international journal of public participation in health care and health policy, 24 Suppl 1, 54 - 61

Ethics review of big data research: What should stay and what should be reformed?

Ferretti A. et al, (2021), BMC medical ethics, 22

Ethical Issues in Consent for the Reuse of Data in Health Data Platforms.

McKeown A. et al, (2021), Science and engineering ethics, 27

The ethics of grandfather clauses in healthcare resource allocation.

Wester G. et al, (2021), Bioethics, 35, 151 - 160

Development of a decision support intervention for family members of adults who lack capacity to consent to trials.

Shepherd V. et al, (2021), BMC medical informatics and decision making, 21

'There's more to life than money and health': Family caregivers' views on the role of Power of Attorney in proxy decisions about research participation for people living with dementia.

Shepherd V. et al, (2021), Dementia (London, England), 20, 308 - 325

Decisions on Innovation or Research for Devastating Disease

Andreae MH. et al, (2021), American Journal of Bioethics, 21, 28 - 31

Public involvement in the governance of population-level biomedical research: unresolved questions and future directions.

Erikainen S. et al, (2020), Journal of medical ethics

Tragic choices in intensive care during the COVID-19 pandemic: on fairness, consistency and community.

Newdick C. et al, (2020), Journal of medical ethics, 46, 646 - 651

Constructing authentic decisions: proxy decision making for research involving adults who lack capacity to consent.

Shepherd V. et al, (2020), Journal of medical ethics

'Your country needs you': the ethics of allocating staff to high-risk clinical roles in the management of patients with COVID-19.

Dunn M. et al, (2020), Journal of medical ethics, 46, 436 - 440

Trust, trustworthiness and sharing patient data for research.

Sheehan M. et al, (2020), Journal of medical ethics

Experimental Philosophical Bioethics.

Earp BD. et al, (2020), AJOB empirical bioethics, 11, 30 - 33

Cookies on this website

Publications