1. Bell, J. 1993. Public interest: Policy or principle? In Law and the public interest, ed. R. Brownsword. Stuttgart: Franz Steiner Verlag.
2. Beskow, L.M., E.E. Namey, R.J. Cadigan, T. Brazg, J. Crouch, G.E. Henderson, et al. 2011. Research Participants’ perspectives on genotype-driven research recruitment. Journal of Empirical Research on Human Research Ethics 6(4): 3–20.
3. Beyleveld, D. 2006. Conceptualising privacy in relation to medical research values. In First do no harm, ed. S.A.M. McLean, 151–163. Aldershot: Ashgate.
4. Beyleveld, D., and R. Brownsword. 2007. Consent in the law. Oxford: Hart.
5. Beyleveld, D., and R. Brownsword. 2015. Research participants and the right to be informed. In Inspiring a medico-legal revolution: Essays in honour of Sheila McLean, ed. P. Ferguson and G. Laurie. Aldershot: Ashgate.