Co-determination of donors in biobanks

Principles and Practice in Biobank Governance

Volumn , Issue , 2009, Pages 69-78

  Gundermann, Lukas ^b   Stockter, Ulrich ^a  

^a UNIVERSITY OF COLOGNE   (Germany)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

EID: 73449135066     PISSN: None     EISSN: None     Source Type: Book    
DOI: None     Document Type: Chapter

References (12)

1. Caulfield, T. 2007. Biobanks and Blanket Consent: The Proper Place of the Public Good and Public Perception Rationales. King's Law Journal, 18, 209-226.
2. Caulfield, T. and Brownsword, R. 2005. Human Dignity: A Guide to Policy Making in the Biotechnology Era? Nature Reviews Genetics, 7, 72-76.
3. Elger, B. and Mauron, A. 2003. A Presumed-Consent Model for Regulating Informed Consent of Genetic Research Involving DNA Banking, in Population and Genetics: Legal and Socio-Ethical Perspectives, edited by B. Knoppers. Leiden/Boston: Martinus Nijhoff Publishers, 269-295.
4. Gertz, R. 2004. An Analysis of the Icelandic Supreme Court Judgement on the Health Sector Database Act. SCRIPT-ed 1(2), 241-258. [Online] Available at: http://www.law.ed.ac.uk/ahrc/script-ed/issue2/iceland.pdf [accessed 16 March 2009].
5. Gibbons, S. and Kaye, J. 2007. Governing Genetic Databases: Collection, Storage and Use. King's Law Journal, 18, 201-208.
6. Johnsson, L. et al. 2008. Patients' Refusal to Consent to Storage and Use of Samples in Swedish Biobanks: Cross Sectional Study. British Medical Journal, 337, a345.
7. Kaye, J. 2004. Abandoning Informed Consent, in Genetic Databases: Socioethical Issues in the Collection and Use of DNA, edited by R. Tutton and O. Corrigan. London/New York: Routledge, 117-138.
8. Laurie, G. 2008. Consent for Biobanking: Lack of Dissent When Opting in Doesn't Necessarily Support 'Opt Out'. British Medical Journal, 337, 186-187.
9. Nõmper, A. 2005. Open Consent - A New Form of Informed Consent for Population Genetic Databases, Tallinn. [Online] Available at: http://dspace.utlib.ee/dspace/bitstream/10062/818/5/nomper.pdf [accessed 16 March 2009].
10. Reischl J. et al. 2006. Pharmacogenetic Research and Data Protection - Challenges and Solutions. Pharmacogenomics Journal, 6, 1-9.
11. Robertson, J. 1999. Privacy Issues in Second Stage Genomics. Jurimetrics, 40, 59-76.
12. Wendler, D. 2006. One-time General Consent for Research on Biological Samples. British Medical Journal, 332, 544-547.