Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Continue' we'll assume that you are happy to receive all cookies and you won't see this message again. Click 'Find out more' for information on how to change your cookie settings.

Continue

Publications

The NeuroDev Study: Phenotypic and Genetic Characterization of Neurodevelopmental Disorders in Kenya and South Africa.

de Menil V. et al, (2019), Neuron, 101, 15 - 19

Exploring the ethics of global health research priority-setting.

Pratt B. et al, (2018), BMC Med Ethics, 19

Medical Ethics: A very short introduction

DUNN MC. and Hope T., (2018)

Ethical considerations in Controlled Human Malaria Infection studies in low resource settings: Experiences and perceptions of study participants in a malaria Challenge study in Kenya

Njue M. et al, (2018), Wellcome Open Research

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

McCoy MS. et al, (2018), J Med Ethics

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

Health professionals’ and researchers’ perspectives on prenatal whole genome and exome sequencing: ‘We can’t shut the door now, the genie’s out, we need to refine it’

HORN R. and PARKER M., (2018), PLoS ONE

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), J Med Ethics, 44, 632 - 637

Good Care at Home for Older People in Singapore

Chin J. et al, (2018)

Lay perspectives on receiving different types of genomic secondary findings: a qualitative vignette study

Vornanen M. et al, (2018), Journal of Genetic Counseling

High-Risk Women’s Risk Perception After Receiving Personalized Polygenic Breast Cancer Risk Information

Forrest L. et al, (2018), Journal of Community Genetics

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

Ives J. et al, (2018), BMC Med Ethics, 19

"I would like to discuss it further with an expert": a focus group study of Finnish adults' perspectives on genetic secondary findings.

Vornanen M. et al, (2018), J Community Genet, 9, 305 - 314

Between the Reasonable and the Particular: Deflating Autonomy in the Legal Regulation of Informed Consent to Medical Treatment.

Dunn M. et al, (2018), Health care analysis : HCA : journal of health philosophy and policy

A mobile revolution for healthcare? Setting the agenda for bioethics.

Lucivero F. and Jongsma KR., (2018), J Med Ethics

Research or clinical care: what's the difference?

Hallowell N., (2018), J Med Ethics, 44, 359 - 360

Patients' Views of Treatment-Focused Genetic Testing (TFGT): Some Lessons for the Mainstreaming of BRCA1 and BRCA2 Testing.

Wright S. et al, (2018), J Genet Couns

Book Review - Social Services Disrupted: Changes, Challenges and Policy Implications for Europe in Times of Austerity

Dunn MC., (2018), Ethics and Social Welfare, 12, 90 - 93

Ethical considerations in Controlled Human Malaria Infection studies in low resource settings: Experiences and perceptions of study participants in a malaria Challenge study in Kenya.

Njue M. et al, (2018), Wellcome Open Res, 3

Elbow Room for Best Practice? Montgomery, Patients' values, and Balanced Decision-Making in Person-Centred Clinical Care.

Herring J. et al, (2017), Medical law review, 25, 582 - 603

Load More

Include forthcoming?