All Publications

Boddington, P and Parker, M (2008). Preimplantation Genetic Diagnosis for Familial Hypercholesterolaemia: a Commentaty on the Recent HFEA Decision Clinical Ethics, 3:145-148.

Brown, L, Dixon-Woods, M, and Parker, M (2008). Whose Interest? UK Newspaper Reporting of Use of Medical Records for Research Journal of Health Services Research, 13(3):140-145.

Hallowell, N, Cooke, S, Crawford, G, Parker, M, and Lucassen, A (2008). Ethics and Research Governance: the Views of Researchers, Health Professionals and Other Stakeholders Clinical Ethics, 3:85-90.

April, C and Parker, M (2007). End of Life Decision-Making in Neonatal Care Journal of Medical Ethics, 33:126-127.

Boulton, M and Parker, M (2007). Informed Consent in a Changing Environment Social Science and Medicine, 65:2187-2198.

Chokshi, D, Thera, M, Parker, M, Diakite, M, Makani, J, Kwiatkowski, D, and Duombo, O (2007). Valid Consent for Genomic Epidemiology in Developing Countries PLOS Medicine, 4(4):636-641.

Gibbons, S, Kaye, J, Smart, A, Heeney, C, and Parker, M (2007). Governing Genetic Databases: Challenges Facing Research Regulation and Practice Journal of Law and Society, 34(2):163-189.

Parker, M (2007). Ethnography/Ethics Social Science and Medicine, 65:2248-2259.

Parker, M (2007). Deliberative Bioethics In: Principles of Health Care Ethics, ed. by Ashcroft, R. Dawson, A. Drawper, H. McMillan, J.. John Wiley and Sons, Chichester, chap. 24, pp. 185-191.

Parker, M (2007). The Best Possible Child Journal of Medical Ethics, 33:279-283.

Lucassen, A, Parker, M, and Wheeler, R (2006). Implications of data protection legislation for family history. BMJ, 332(7536):299-301.

Parker, M and Lucassen, A (2004). Genetic Information: A Joint Account? British Medical Journal, 329:165-167.

Parker, M, Ashcroft, R, Wilkie, A, and Kent, A (2004). Ethical Review of Research into Rare Genetic Disorders British Medical Journal, 329:288-289.