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Publications

“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

Community, Ethics, and Homelessness

Parker M., (2020), ETHICS OF HOMELESSNESS: PHILOSOPHICAL PERSPECTIVES, 2ND EDITION, 343, 141 - 152

Ethical challenges in pathogen sequencing: a systematic scoping review.

Johnson S. and Parker M., (2020), Wellcome Open Res, 5

Medical ethics

PARKER M. et al, (2020), Oxford Textbook of Medicine

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

Ferretti L. et al, (2020)

Authority and the Future of Consent in Population-Level Biomedical Research.

Sheehan M. et al, (2019), Public Health Ethics, 12, 225 - 236

Call to action for equitable access to human milk for vulnerable infants.

Israel-Ballard K. et al, (2019), Lancet Glob Health, 7, e1484 - e1486

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

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

Strengthening ethical community engagement in contemporary Malawi

Nyirenda D. et al, (2019)

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

Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders.

Faundes V. et al, (2018), Am J Hum Genet, 102, 175 - 187

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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