Publications

Risk Assessment Tools in Policing Contexts: 10 Key Ethical Challenges

DOUGLAS T. et al, (2026), Policing (Oxford), 20

Justification of Deferral of Consent in the ACT-GLOBAL Adaptive Platform Trial in Stroke.

Shamy M. et al, (2026), J Clin Epidemiol

Public support for food subsidy and tax scenarios to promote healthy and sustainable diets: Evidence from deliberative forums in two UK locations

Forde H. et al, (2025), Food Policy

Environmental sustainability and the limits of healthcare resource allocation.

Hart J. et al, (2025), Bioethics, 39, 538 - 545

The role of the enrolling clinician in emergency research conducted under an exception from informed consent.

Sahan K. et al, (2025), Theor Med Bioeth, 46, 231 - 246

Protocol for an eDelphi study to identify consensus on policy metrics which should be included in future assessments of the England Rare Diseases Action Plans

Wark PA. et al, (2025)

Alterations in care for children with special healthcare needs during the early COVID-19 pandemic: ethical and policy considerations.

Jones J. et al, (2024), Monash Bioeth Rev

Towards an understanding of the ethics of electronic consent in clinical trials.

Sahan K. et al, (2024), Trials, 25

Healthcare resource allocation decisions and non-emergency treatments in the aftermath of Covid-19 pandemic. How should children with chronic illness feature in prioritisation processes?

Lignou S. et al, (2024)

‘A commitment to Equality, Diversity and Inclusion’: a conceptual framework for equality of opportunity in Patient and Public Involvement in research

Lignou S. et al, (2024), Research Ethics, 20, 288 - 303

The myth of translational bioethics.

Dunn M. and Sheehan M., (2024), Bioethics, 38, 196 - 203

Getting rights right: Implementing 'Martha's Rule'

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

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

Graham M. et al, (2023), J Med Ethics, 49, 670 - 673

Reasons for Not Participating in PCTs: The Comparative Case of Emergency Research under an Exception from Informed Consent (EFIC).

Sahan K. et al, (2023), Am J Bioeth, 23, 70 - 72

TREs are still not about trust

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

Healthcare resource allocation decisions and non-emergency treatments in the aftermath of Covid-19 pandemic. How should children with chronic illness feature in prioritisation processes?

Lignou S. et al, (2023), Wellcome Open Res, 8

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

Resource allocation in genetic and genomic medicine.

Buchanan J. et al, (2022), Journal of community genetics, 13, 463 - 466

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

Lignou S. et al, (2022), Inquiry, 59

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), Front Big Data, 5

Decisions on Innovation or Research for Devastating Disease.

Andreae MH. et al, (2021), Am J Bioeth, 21, 28 - 31

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

Thomas O. et al, (2021), Am J Bioeth, 21, 51 - 53

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

Friesen P. et al, (2021), Health Expect, 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 Med Ethics, 22

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 Med Inform Decis Mak, 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), 20, 308 - 325

Ethical Issues in Consent for the Re-use of Data in Health Data Platforms

MCKEOWN A. et al, (2020), Science and Engineering Ethics

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

Newdick C. et al, (2020), J Med Ethics, 46, 646 - 651

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

Shepherd V. et al, (2020), J Med Ethics

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

Erikainen S. et al, (2020), Journal of Medical Ethics

Trust, trustworthiness and sharing patient data for research.

Sheehan M. et al, (2020), J Med 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

Misuse of "Usual Care" in Emergency Care Research: A Call for Adapting Rules Governing Exception from Informed Consent (EFIC) Studies.

Cowan E. et al, (2020), The American journal of bioethics : AJOB, 20, 59 - 61

Learning by Doing: The Challenge of Aligning Theory and Practice in School-Based, Post-graduate, Teacher Education Programmes

Sheehan M., (2020), 261 - 272

Experimental philosophical bioethics

Earp BD. et al, (2019), Ajob Empirical Bioethics

'It's a tough decision': a qualitative study of proxy decision-making for research involving adults who lack capacity to consent in UK.

Shepherd V. et al, (2019), Age Ageing, 48, 903 - 909

Structural Transformation to Attain Responsible BIOSciences (STARBIOS2): Protocol for a Horizon 2020 Funded European Multicenter Project to Promote Responsible Research and Innovation (Preprint)

Colizzi V. et al, (2019), Preprint

Authority and the Future of Consent in Population-level Biomedical Research

Sheehan M. et al, (2019), Public Health Ethics

Should the Decisions of Institutional Review Boards Be Consistent?

(2019), Ethics and Human Research

Protection by exclusion? The (lack of) inclusion of adults who lack capacity to consent to research in clinical trials in the UK.

Shepherd V. et al, (2019), Trials, 20

Research involving adults lacking capacity to consent: a content analysis of participant information sheets for consultees and legal representatives in England and Wales.

Shepherd V. et al, (2019), Trials, 20, 233 - 233

Patient and public involvement: Two sides of the same coin or different coins altogether?

McCoy MS. et al, (2019), Bioethics

Structural Transformation to Attain Responsible BIOSciences (STARBIOS2): Protocol for a Horizon 2020 Funded European Multicenter Project to Promote Responsible Research and Innovation

BUCHAN ALASTAIR., (2019), JMIR Research Protocols

Understanding and using patient experiences as evidence in healthcare priority setting.

Rand L. et al, (2019), Cost Eff Resour Alloc, 17

New Zealand

Sheehan M., (2019), 403 - 412

Exploring the ethics of global health research priority-setting.

Pratt B. et al, (2018), BMC medical ethics, 19, 94 - 94

National Standards for Public Involvement in Research: missing the forest for the trees.

McCoy MS. et al, (2018), Journal of medical ethics

In defence of governance: ethics review and social research.

Sheehan M. et al, (2018), Journal of medical ethics, 44, 710 - 716

Reasonable disagreement and the justification of pre-emptive ethics governance in social research: a response to Hammersley.

Sheehan M. et al, (2018), J Med Ethics, 44, 719 - 720

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