All Publications

Kaye, J and Gibbons, S (2008). Mapping the Regulatory Space for Genetic Databases and Biobanks in England and Wales Medical Law International, 9(2):111-130.

Gibbons, S and Kaye, J (2007). Governing Genetic Databases: Collection, Storage and Use King’s Law Journal , 18(2).

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.

Kaye, J (2006). Police access to DNA samples and information Genomics, Society and Policy, 2(1).

Lucassen, A and Kaye, J (2006). Genetic testing without consent: the implications of the new Human Tissue Act 2004 Journal of Medical Ethics, 32(12).

Gibbons, S, Helgason, H, Kaye, J, Nomper, A, and Wendel, L (2005). Lessons from European Population Genetic Databases: Comparing the law in Iceland, Sweden, Estonia and the UK European Journal of Health Law, 12:103-133.

Kaye, J (2005). Do we need a uniform regulatory system for biobanks across Europe? European Journal of Human Genetics, 14:245-248.

Kaye, J and Martin, P (2000). Safeguards for research using large scale DNA collections British Medical Journal, 32(1):1146-1149.