The role of race and trust in tissue/blood donation for genetic research

This publication has 25 references indexed in Scilit:

• Public Expectations for Return of Results from Large-Cohort Genetic Research
  American Journal of Bioethics, 2008
• Studying Genetic Research Participants: Lessons from the “Learning About Research in North Carolina” Study
  Cancer Epidemiology, Biomarkers & Prevention, 2008
• Public Willingness to Participate in and Public Opinions About Genetic Variation Research: A Review of the Literature
  American Journal of Public Health, 2006
• Genetic research and donation of tissue samples to biobanks. What do potential sample donors in the Swedish general public think?
  European Journal of Public Health, 2005
• Warranted concerns, warranted outlooks: a focus group study of public understandings of genetic research
  Social Science & Medicine, 2004
• Willingness to donate blood samples for genetic research: a survey from a community in Singapore
  Clinical Genetics, 2003
• “What Are They Going to Do With the Information?” Latino/Latina and African American Perspectives on the Human Genome Project
  Health Education & Behavior, 2003
• Perceptions of Genetics Research As Harmful to Society: Differences among Samples of African-Americans and European-Americans
  Genetic Testing, 2002
• Through the Community Looking Glass: Reevaluating the Ethical and Policy Implications of Research on Adolescent Risk and Psychopathology
  Ethics & Behavior, 2000
• The Continuing Legacy of the Tuskegee Syphilis Study: Considerations for Clinical Investigation
  The Lancet Healthy Longevity, 1999