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Publications

Equitable Design and Use of Digital Surveillance Technologies During COVID-19: Norms and Concerns.

Pratt B. et al, (2022), J Empir Res Hum Res Ethics

Towards A new model of global health justice: the case of COVID-19 vaccines.

Jecker NS. et al, (2022), J Med Ethics

Respecting values and perspectives in biobanking and genetic research governance: Outcomes of a qualitative study in Bengaluru, India

Vaz M. et al, (2022), Wellcome Open Research, 7, 78 - 78

Equitable data sharing in epidemics and pandemics

Pratt B. and Bull S., (2021), BMC Medical Ethics, 22

Engaging publics in biobanking and genetic research governance - a literature review towards informing practice in India

Warrier P. et al, (2021), Wellcome Open Research, 6, 5 - 5

Key criteria for the ethical acceptability of COVID-19 human challenge studies: Report of a WHO Working Group.

Jamrozik E. et al, (2021), Vaccine, 39, 633 - 640

Engaging publics in biobanking and genetic research governance - a literature review towards informing practice in India

Warrier P. et al, (2021), Wellcome Open Research, 6, 5 - 5

Vaccine-enhanced disease: case studies and ethical implications for research and public health.

Jamrozik E. et al, (2021), Wellcome Open Res, 6

SARS-CoV-2 challenge studies: ethics and risk minimisation.

Bull S. et al, (2020), J Med Ethics

Third human challenge trial conference, Oxford, United Kingdom, February 6-7, 2020, a meeting report.

Pollard AJ. et al, (2020), Biologicals

Researcher and study participants' perspectives of consent in clinical studies in four referral hospitals in Vietnam.

Van Nuil JI. et al, (2020), BMC Med Ethics, 21

“Are we getting the biometric bioethics right?”–the use of biometrics within the healthcare system in Malawi

Mwapasa M. et al, (2020), Global Bioethics, 31, 67 - 80

The ethics of data sharing and biobanking in health research.

Bull S. and Bhagwandin N., (2020), Wellcome Open Res, 5

How should assent to research be sought in low income settings? Perspectives from parents and children in Southern Malawi.

Mangochi H. et al, (2019), BMC Med Ethics, 20

Challenges arising when seeking broad consent for health research data sharing: a qualitative study of perspectives in Thailand.

Cheah PY. et al, (2018), BMC Med Ethics, 19

Human candidate gene polymorphisms and risk of severe malaria in children in Kilifi, Kenya: a case-control association study.

Ndila CM. et al, (2018), Lancet Haematol, 5, e333 - e345

‘It is an entrustment’: Broad consent for genomic research and biobanks in sub-Saharan Africa

Tindana P. et al, (2017), Developing World Bioethics

Sharing Individual-Level Health Research Data: Experiences, Challenges and a Research Agenda.

Cheah PY. et al, (2017), Asian bioethics review, 9, 393 - 400

Admixture into and within sub-Saharan Africa

Busby GBJ. et al, (2016), eLife, 5

Best Practices for Ethical Sharing of Individual-Level Health Research Data From Low- and Middle-Income Settings.

Bull S. et al, (2015), J Empir Res Hum Res Ethics, 10, 302 - 313

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