Results of the Inquiry and Citation Review
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2. Girelli, D., et al., The interaction between MTHFR 677 C-->T genotype and folate status is a determinant of coronary atherosclerosis risk. J Nutr, 2003. 133(5): p. 1281-5.
3. Kim, Y.I., Folate and carcinogenesis: evidence, mechanisms, and implications. J Nutr Biochem, 1999. 10(2): p. 66-88.
4. Khoury, M.J., et al., Do we need genomic research for the prevention of common diseases with environmental causes? Am J Epidemiol, 2005. 161(9): p. 799-805.
5. UNESCO: Explanatory Memorandum on the Elaboration of the Preliminary Draft Declaration on the Universal Norms on Bioethics. SHS/EST/CIB-CIGB/05/CONF.202/4, Paris, February 2005.
6. Chadwick, R. and K. Berg, Solidarity and equity: new ethical frameworks for genetic databases. Nat Rev Genet, 2001. 2(4): p. 318-21.
7. UNESCO (Working group of the International Bioethics Committee (IBC) on Confidentiality and Genetic Data): Report on Confidentiality and Genetic Data. Paris, 30 June 2000. BIO-503/99/CIB-6/GT-2/3.
8. Clayton, E.W., Why the use of anonymous samples for research matters. J Law Med Ethics, 1995. 23(4): p. 375-7.
9. World Medical Association (WMA): Declaration of Helsinki - Ethical Principles for Medical Research Involving Human Subjects. adopted 1964, amended last time 2000, Clarification on Paragraph 29 in 2002, on Paragraph 30 in 2004.
10. Council of Europe: Convention on Human Rights and Biomedicine. Oviedo, 4.IV.1997.
11. Council for International Organisations of Medical Sciences (CIOMS): International Ethical Guidelines for Biomedical Research Involving Human Subjects. Geneva, 2002.
12. UNESCO: Universal declaration on the human genome and human rights, 11 November, 1997.
13. UNESCO (Working Group of the International Bioethics Committee (IBC) on Genetic Data): Human Genetic Data: Preliminary Study by the IBC on its Collection, Processing, Storage and Use. SHS-503/01/CIB-8/3 (Rev. 2), Paris, 15 May 2002.
14. UNESCO: International Declaration on Human Genetic Data, 16 October 2003.
15. UNESCO (International Bioethics Committee (IBC)): Preliminary Draft Declaration on Universal Norms on Bioethics. SHS/EST/CIB-EXTR/05/Conf.202/2. Paris, 9 February 2005.
16. European Union: The 25 Recommendations on the Ethical, Legal and Social Implications of Genetic Testing, Brussels 2004.
17. Ordovas, J.M. and D. Corella, Genes, diet and plasma lipids: the evidence from observational studies. World Rev Nutr Diet, 2004. 93: p. 41-76.
18. Muller, M. and S. Kersten, Nutrigenomics: goals and strategies. Nat Rev Genet, 2003. 4(4): p. 315-22.
19. Ordovas, J.M. and D. Corella, Nutritional genomics. Annu Rev Genomics Hum Genet, 2004. 5: p. 71-118.
20. Mathers, J.C., Nutrition and cancer prevention: diet-gene interactions. Proc Nutr Soc, 2003. 62(3): p. 605-10.
21. Mathers, J.C., Chairman's introduction: what can we expect to learn from genomics? Proc Nutr Soc, 2004. 63(1): p. 1-4.
22. Deutsche Forschungsgemeinschaft, Senate Commission on Genetic Research: Predictive genetic diagnosis Scientific background, practical and social implementation. Bonn 2003.
23. Hirtzlin, I., et al., An empirical survey on biobanking of human genetic material and data in six EU countries. Eur J Hum Genet, 2003. 11(6): p. 475-88.
24. European Society of Human Genetic, Data storage and DNA banking for biomedical research: technical, social and ethical issues. Eur J Hum Genet, 2003. 11 Suppl 2: p. S8-10.
25. Godard, B., et al., Data storage and DNA banking for biomedical research: informed consent, confidentiality, quality issues, ownership, return of benefits. A professional perspective. Eur J Hum Genet, 2003. 11 Suppl 2: p. S88-122.
26. EMEA (European Agency for the Evaluation of Medicinal Products) CPMP, 'Position Paper on Terminology in Pharmacogenetics' EMEA/CPMP/3070/01, November 2002.
27. ASHG report. Statement on informed consent for genetic research. The American Society of Human Genetics. Am J Hum Genet, 1996. 59(2): p. 471-4.
28. Directive 95/46/EC of the European Parliament and of the Council of 24 October 1995 on the protection of individuals with regard to the processing of personal data and on the free movement of such data. Official Journal L 281 , 23/11/1995, P. 0031 - 0050.
29. Swedish Ministry of Health and Social Affairs (2002): Biobanks in Medical Care Act (2002:297).
30. Regidor, E., The use of personal data from medical records and biological materials: ethical perspectives and the basis for legal restrictions in health research. Soc Sci Med, 2004. 59(9): p. 1975-84.
31. German National Ethics Council (2004). Biobanks for research; Nationaler Ethikrat Berlin.
32. Deschenes, M., et al., Human genetic research, DNA banking and consent: a question of 'form'? Clin Genet, 2001. 59(4): p. 221-39.
33. World Health Organization: Proposed International Guidelines on Ethical Issues in Medical Genetics and Genetic Services, Geneva, 15-16 December 1997.
34. Human Genome Organization (HUGO): Statement on DNA sampling: Control and access. Genome Digest March 1999: 6(1):8.
35. Clayton, E.W., et al., Informed consent for genetic research on stored tissue samples. Jama, 1995. 274(22): p. 1786-92.