참고문헌
- Kang DH, Lee KM. Current status of genomic epidemiology research. Korean J Prev Med 2003; 36(3): 213-222 (Korean)
- Beskow LM, Burke W, Merz JF, Barr PA, Terry S, Penchaszadeh VB, Gostin LO, Gwinn M, Khoury MJ. Informed consent for population-based research involving genetics. JAMA 2001; 286(18): 2315-2321 https://doi.org/10.1001/jama.286.18.2315
- Clayton EW, Steinberg KK, Khoury MJ, Thomson E, Andrews L, Kahn MJ, Kopelman LM, Weiss JO. Informed consent for genetic research on stored tissue samples. JAMA 1995; 274(22): 1786-1792 https://doi.org/10.1001/jama.274.22.1786
- Wertz DC. Archived specimens: A platform for discussion. Community Genet 1999; 2(2-3): 51-60 https://doi.org/10.1159/000016187
- Hong YC, Lee KH. Specimen storage and analysis for genomic epidemiology. Korean J Prev Med 2003; 36(3): 209-221 (Korean)
- Austin MA, Harding S, McElroy C. Genebanks: A comparison of eight proposed international genetic databases. Community Genet 2003; 6(1): 37-45 https://doi.org/10.1159/000069544
- CIOMS. Special Ethical Considerations for Epidemiological Research. 2006 [cited 2007 Feb 27]; Available from: URL:http://www.cioms.ch/special_ethical_consideration.pdf
- SACGHS. Policy Issues Associated with Undertaking a Large U.S. Population Cohort Project on Genes, Environment, and Disease. 2006
- Caulfield T, Upshur RE, Daar A. DNA databanks and consent: A suggested policy option involving an authorization model. BMC Med Ethics 2003; 4: E1 https://doi.org/10.1186/1472-6939-4-1
- Williams G, Schroeder D. Human genetic banking: altruism, benefit and consent. New Genet Soc 2004; 23(1): 89-103 https://doi.org/10.1080/1463677042000189598
- Clayton EW. Informed consent and biobanks. J Law Med Ethics 2005; 33(1): 15-21 https://doi.org/10.1111/j.1748-720X.2005.tb00206.x
- Beskow LM. Ethical, Legal and Social Issues in the Design and Conduct of Human Genome Epidemiology Studies. In: Khoury MJ, Little J, Burke W, Editors. Human Genome Epidemiology: A Scientific Foundation for Using Genetic Information to Improve Health and Prevent Disease. New York: Oxford University Press; 2004. p. 58-76
- Hansson MG, Dillner J, Bartram CR, Carlson JA, Helgesson G. Should donors be allowed to give broad consent to future biobank research? Lancet Oncol 2006; 7(3): 266-269 https://doi.org/10.1016/S1470-2045(06)70618-0
- Summary of the Official Norwegian Report NOU 2005:1-Good Research, Better Health [cited 2007 Feb 27]; Available from: URL: http://www.helsetilsynet.no/upload/english/nou_2005_1_english%20summary.pdf
- National Bioethics Advisory Commission. Research Involving Human Biological Materials: Ethical Issues and Policy Guidance, Vol. 1. Rockville, MD: National Bioethics Advisory Commission; 1999. p. 55-76
- HUGO Ethics Committee. Statement on DNA sampling: Control and access. 1998 [cited 2007 Feb 27]; Available from: URL:http://www.hugo-international.org/Statement_on_DNA_Sampling.html
- Kaye J. Abandoning Informed Consent: The Case of Genetic Research in Population Collections. In: Corrigan O, Tutton R. Editors. Genetic Databases: Socio-ethical Issues in the Collection and Use of DNA London, New York: Routledge; 2004. p. 117-138
- UK Biobank. Ethics and Governance Framework ver 2. 2006 [cited 2007 Feb 27]; Available from: URL:http://www.ukbiobank.ac.uk/docs/EGF_Version2_July%202006.pdf
- Korea. Bioetics and Biosafety Act. 2005 (Korean)
- United Nations Educational, Scientific, and Cultural Organization(UNESCO). Human Genetic Data: Preliminary Study by the IBC on its Collection, Processing, Storage and Use. 2002 [cited 2007 Feb 27]; Available from: URL: http://portal.unesco.org/shs/en/ev.php-URL_ID=2138&URL_DO=DO_TOPIC&URL_SECTION=201.html
- HUGO Ethics Committee. Statement on DNA sampling: control and access. London. 1998 [cited 2007 Feb 27]; Available from: URL: http://www.hugo-international.org/Statement_on_DNA_Sampling.html
- Buchanan A. An ethical framework for biological samples policy. In: National Bioethics Advisory Committee, editors. Research Involving Human Biological Materials: Ethical Issues and Policy Guidance, Vol II. Rockville, MD: National Bioethics Advisory Commission; 2000. p. B-1-B-35
- Knoppers BM. Biobanking: international norms. J Law Med Ethics 2005; 33(1): 7-14 https://doi.org/10.1111/j.1748-720X.2005.tb00205.x
- Office for Human Research Protections (OHRP), Department of Health and Human Services (HHS). Guidance on Research Involving Coded Private Information or Biological Specimens [cited 2007 Feb 27]; Available from: URL:http://www.hhs.gov/ohrp/humansubjects/guidance/cdebiol.pdf
- HUGO Intellectual Property Committee. Statement on Patenting on Patenting Issues Related To Early Release of Sequence Data. 1997[cited 2007 Feb 27]; Available from: URL:http://www.hugo-international.org/PDFs/Statement%20on%20Patenting%20Issues%20Relating%20to%20Raw%20Sequence%20Dat.pdf
- Convention for the protection of human rights and dignity of the human being with regard to the application of biology and medicine: Convention on human rights and biomedicine. Council of Europe Convention of Biomedicine. Hum Reprod 1997; 12(9): 2076-2080 https://doi.org/10.1093/humrep/12.9.2076
- HUGO Ethics Committee. Statement on Benefit-Sharing. 2000 [cited 2007 Feb 27]; Available from: URL:http://www.hugo-international.org/Statement_on_Benefit_Sharing.htm
- Mannvernd. A Landmark Decision by the Icelandic Supreme Court. 2004 [cited 2007 Feb 27]; Available from: URL:http://www.mannvernd.is/english/lawsuits/Mannvernd_PressRelease_SupremeCourt.pdf
- Estonian Genome Project [cited 2007 Feb 27]; Available from: URL:http://www.geenivaramu.ee
- UK Biobank. The UK Biobank Ethics and Governance Framework. 2004 [cited 2007 Feb 27]; Available from: URL:http://www.ukbiobank.ac.uk/docs/egf-summary.doc
- Human Genetics Commission. Inside Information: Balancing Interests in the Use of Personal Genetic Data. London.: 2002 [cited 2007 Feb 27]; Available from: URL:http://www.hgc.gov.uk/UploadDocs/DocPub/Document/insideinformation_summary.pdf
- CARTaGENE [cited 2007 Feb 27]; Available from: URL:http://www.cartagene.qc.ca