•  727
    Comparing the Understanding of Subjects receiving a Candidate Malaria Vaccine in the United States and Mali
    with R. D. Ellis, I. Sagara, A. Durbin, A. Dicko, D. Shaffer, L. Miller, M. H. Assadou, M. Kone, B. Kamate, O. Guindo, M. P. Fay, D. A. Diallo, O. K. Doumbo, and J. Millum
    American Journal of Tropical Medicine and Hygiene 83 (4): 868-72. 2010.
    Initial responses to questionnaires used to assess participants' understanding of informed consent for malaria vaccine trials conducted in the United States and Mali were tallied. Total scores were analyzed by age, sex, literacy (if known), and location. Ninety-two percent (92%) of answers by United States participants and 85% of answers by Malian participants were correct. Questions more likely to be answered incorrectly in Mali related to risk, and to the type of vaccine. For adult participant…Read more
  •  42
    Although for the last 50 years, ethicists dealing with human experimentation have focused primarily on the need to protect individual research subjects and vulnerable groups, biomedical research, especially in genetics, now requires the establishment of standards for the protection of communities. We have developed such a strategy, based on five steps. (i) Identification of community characteristics relevant to the biomedical research setting, (ii) delineation of a typology of different types of…Read more
  •  33
    “Physician-Assisted Suicide among Oregon Cancer Patients”: A Fading Issue
    with C. C. Denny
    Journal of Clinical Ethics 17 (1): 39-42. 2006.
  •  4
    Philosophical justifications of informed consent in research
    with D. Brock, C. Grady, R. Lie, F. Miller, and D. Wendler
    In Ezekiel J. Emanuel (ed.), The Oxford textbook of clinical research ethics, Oxford University Press. 2008.
  • Assessing the effect of a shorter consent form on comprehension in healthy volunteers
    with L. Stunkel, M. Benson, L. McLellan, N. Sinaii, and G. Bedarida
    IRB: Ethics & Human Research 32 (4): 1-9. 2010.