共 46 条
- [1] Aitken M(2016)Moving from trust to trustworthiness: Experiences of public engagement in the Scottish Health Informatics Programme Science and Public Policy 43 713-723
- [2] Appelbaum PS(1987)False hopes and best data: Consent to research and the therapeutic misconception The Hastings Center report 17 20-24
- [3] Baier A(1986)Trust and antitrust Ethics 96 231-260
- [4] Busby H(2006)Consent, trust and ethics: Reflections on the findings of an interview based study with people donating blood for genetic research for research within the NHS Clinical Ethics 1 211-215
- [5] Bussey-Jones J(2010)The role of race and trust in tissue/blood donation for genetic research Genetics in Medicine 12 116-121
- [6] Critchley C(2015)The impact of commercialisation and genetic data sharing arrangements on public trust and the intention to participate in biobank research Public Health Genomics 18 160-172
- [7] Nicol D(2006)Public knowledge and public trust Community Genetics 9 204-210
- [8] Otlowski M(2008)Bioethics and the sociology of trust: Introduction to the theme Medicine Health Care and Philosophy 11 377-379
- [9] Cunningham-Burley S(2011)Ethical issues in human genomics research in developing countries BMC Medical Ethics 12 1-5
- [10] De Vries R(2011)Access and use of human tissues from the developing world: Ethical challenges and a way forward using a tissue trust BMC Medical Ethics 12 1-5