“It’s my blood”: ethical complexities in the use, storage and export of biological samples: perspectives from South African research participants

Qualitative study of knowledge and attitudes to biobanking among lay persons in Nigeria

(2012) Michael A Igbe et al.   BMC Medical Ethics

Seeking consent to genetic and genomic research in a rural Ghanaian setting: A qualitative study of the MalariaGEN experience

(2012) Paulina Tindana et al.   BMC Medical Ethics

"It's for a good cause, isn't it?" - Exploring views of South African TB research participants on sample storage and re-use

(2012) Gerrit van Schalkwyk et al.   BMC Medical Ethics

Attitudes towards transfers of human tissue samples across borders: An international survey of researchers and policy makers in five countries

(2010) Xinqing Zhang et al.   BMC Medical Ethics

The use of diagnostic collections of DNA for research: Interviews at the eight Belgian centers for human genetics

(2010) Kristien Hens et al.   European Journal of Medical Genetics

Collection, storage and use of blood samples for future research: views of Egyptian patients expressed in a cross-sectional survey

(2010) A. Abou-Zeid et al.   JOURNAL OF MEDICAL ETHICS

Examining the public refusal to consent to DNA biobanking: empirical data from a Swedish population-based study

(2010) P. A. Melas et al.   JOURNAL OF MEDICAL ETHICS

The Havasupai Indian Tribe Case — Lessons for Research Involving Stored Biologic Samples

(2010) Michelle M. Mello et al.   NEW ENGLAND JOURNAL OF MEDICINE

Structuring Public Engagement for Effective Input in Policy Development on Human Tissue Biobanking

(2010) K.C. O’Doherty et al.   Public Health Genomics

Researchers to Return Blood Samples to the Yanomamo

(2010) J. Couzin-Frankel   SCIENCE

Who's minding the shop? The role of Canadian research ethics boards in the creation and uses of registries and biobanks

(2009) Elaine Gibson et al.   BMC Medical Ethics

Researchers' preferences and attitudes on ethical aspects of genomics research: a comparative study between the USA and Spain

(2009) M Ruiz-Canela et al.   JOURNAL OF MEDICAL ETHICS

“Broad” consent, exceptions to consent and the question of using biological samples for research purposes different from the initial collection purpose

(2009) Carlo Petrini   SOCIAL SCIENCE & MEDICINE

Opt-out plus, the patients' choice: preferences of cancer patients concerning information and consent regimen for future research with biological samples archived in the context of treatment

(2008) E Vermeulen et al.   JOURNAL OF CLINICAL PATHOLOGY

US and Scottish Health Professionals' Attitudes toward DNA Biobanking

(2008) D. A. Leiman et al.   JOURNAL OF THE AMERICAN MEDICAL INFORMATICS ASSOCIATION

Informed consent in biobank research: A deliberative approach to the debate

(2008) David M. Secko et al.   SOCIAL SCIENCE & MEDICINE