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Publications

The ethics of instantaneous contact tracing using mobile phone apps in the control of the COVID-19 pandemic

PARKER M. et al, (2020), Journal of Medical Ethics

Quantifying SARS-CoV-2 transmission suggests epidemic control with digital contact tracing

PARKER M. et al, (2020), Science

Fair Allocation of Scarce Medical Resources in the Time of Covid-19.

Emanuel EJ. et al, (2020), N Engl J Med

Publisher Correction: In emergencies, health research must go beyond public engagement toward a true partnership with those affected.

Wright K. et al, (2020), Nat Med, 26

Stakeholder views on the acceptability of human infection studies in Malawi.

Kapumba BM. et al, (2020), BMC Med Ethics, 21

In emergencies, health research must go beyond public engagement toward a true partnership with those affected.

Wright K. et al, (2020), Nat Med

Informed Consent in Genomic research and Biobanking: Taking feedback of findings seriously

PARKER M., (2020), Global Bioethics

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

Engaging research ethics committees to develop an ethics and governance framework for best practices in genomic research and biobanking in Africa: the H3Africa model.

Tindana P. et al, (2019), BMC Med Ethics, 20

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

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

Ethical considerations and call to action for achieving equitable access to human milk for vulnerable infants

PARKER M. and KELLEY M., (2019), Lancet Global Health

The ethics of sequencing infectious disease pathogens for clinical and public health.

Johnson SB. and Parker M., (2019), Nat Rev Genet, 20, 313 - 315

Health-emergency disaster risk management and research ethics.

Chan EYY. et al, (2019), Lancet, 393, 112 - 113

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

Ethical considerations in global HIV phylogenetic research.

Coltart CEM. et al, (2018), Lancet HIV

Six dimensions of research trial acceptability: how much, what, when, in what circumstances, to whom and why?

Gooding K. et al, (2018), Soc Sci Med, 213, 190 - 198

Big data phenotyping in rare diseases: some ethical issues.

Hallowell N. et al, (2018), Genet Med

Views of rare disease participants in a UK whole-genome sequencing study towards secondary findings: a qualitative study.

Mackley MP. et al, (2018), Eur J Hum Genet, 26, 652 - 659

Using a genetic test result in the care of family members: How does the duty of confidentiality apply?

Parker M., (2018), European Journal of Human Genetics, 26, 955 - 959

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, 13

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