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Publications

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

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.

Colizzi V. et al, (2019), JMIR research protocols, 8

Exploring the ethics of global health research priority-setting.

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

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

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

Ethical understandings of proxy decision making for research involving adults lacking capacity: A systematic review (framework synthesis) of empirical research.

Shepherd V. et al, (2018), AJOB empirical bioethics, 9, 267 - 286

Healthcare professionals' understanding of the legislation governing research involving adults lacking mental capacity in England and Wales: a national survey.

Shepherd V. et al, (2018), Journal of medical ethics, 44, 632 - 637

Standards of practice in empirical bioethics research: towards a consensus.

Ives J. et al, (2018), BMC medical ethics, 19

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

Sheehan M. et al, (2018), Journal of medical ethics

The Family Context of Assent: Comparison of Child and Parent Perspectives on Familial Decision-Making

Sibley A. et al, (2017), Children & Society

In defence of governance: ethics review and social research.

Sheehan M. et al, (2017), Journal of medical ethics

The new Health Research Authority framework: still work to do to facilitate high-quality public health research in English local authorities.

Phipps E. et al, (2017), Perspectives in public health, 137, 262 - 265

Maximising value from a United Kingdom Biomedical Research Centre: study protocol.

Greenhalgh T. et al, (2017), Health research policy and systems, 15

Metaethics, relativism and empirical bioethics

Sheehan M., (2016), Empirical Bioethics: Theoretical and Practical Perspectives, 33 - 50

Gene editing of human embryos and designing descendants

Sheehan M., (2016), Maturitas, 94, 20 - 21

Just Wars and doctors' strikes

Sheehan M., (2016), Journal of Medical Ethics, 42, 693 - 694

Variation in university research ethics review: Reflections following an inter-university study in England

Vadeboncoeur C. et al, (2016), Research Ethics, 12, 217 - 233

Expertise, Ethics Expertise, and Clinical Ethics Consultation: Achieving Terminological Clarity.

Iltis AS. and Sheehan M., (2016), The Journal of medicine and philosophy, 41, 416 - 433

Placebo-controlled study in neuromyelitis optica-Ethical and design considerations.

Cree BA. et al, (2016), Multiple sclerosis (Houndmills, Basingstoke, England), 22, 862 - 872

Research led by participants: a new social contract for a new kind of research.

Vayena E. et al, (2016), Journal of medical ethics, 42, 216 - 219

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