본문 바로가기
KERD
논문KCI 등재

유전체 코호트 연구의 윤리적 고려 사항

Ethical Considerations in Genomic Cohort Study

1

조회

0

다운로드

4

인용

0

참고문헌

참고문헌 (32)

  1. Kang DH, "Current status of genomic epidemiology research", 36(3), pp.213~222 (2003)
  2. Beskow LM, "Informed consent for population- based research involving genetics", 286(18), pp.2315~2321 (2001)
  3. Clayton EW, "Informed consent for genetic research on stored tissue samples", 274(22), pp.1786~1792 (1995)
  4. Wertz DC, "Archived specimens: A platform for discussion", 2(2-3), pp.51~60 (1999)
  5. Hong YC, "Specimen storage and analysis for genomic epidemiology", 36(3), pp.209~221 (2003)
  6. Austin MA, "Genebanks:A comparison of eight proposed international genetic databases", 6(1), pp.37~45 (2003)
  7. CIOMS, "Special Ethical Considerations for Epidemiological Research. 2006" (2007)
  8. SACGHS, "Policy Issues Associated with Undertaking a Large U.S" (2006)
  9. Caulfield T, "DNA databanks and consent: A suggested policy option involving an authorization model", 4, pp.E1~ (2003)
  10. Williams G, "Human genetic banking: altruism, benefit and consent", 23(1), pp.89~103 (2004)
  11. Clayton EW, "Informed consent and biobanks", 33(1), pp.15~21 (2005)
  12. Beskow LM, "Ethical, Legal and Social Issues in the Design and Conduct of Human Genome Epidemiology Studies", pp.58~76 (2004), New York: Oxford University Press
  13. Hansson MG, "Should donors be allowed to give broad consent to future biobank research?", 7(3), pp.266~269
  14. "Summary of the Official Norwegian Report NOU 2005:1-Good Research, Better Health" (2007)
  15. National Bioethics Advisory Commission, "Research Involving Human Biological Materials: Ethical Issues and Policy Guidance", 1, pp.55~76 (1999), Rockville, MD: National Bioethics Advisory Commission
  16. HUGO Ethics Committee, "Statement on DNA sampling: Control and access. 1998" (2007)
  17. Kaye J, "Abandoning Informed Consent: The Case of Genetic Research in Population Collections", pp.117~138 (2004), New York: Routledge
  18. UK Biobank, "Ethics and Governance Framework ver 2. 2006" (2007)
  19. Korea, "Bioetics and Biosafety Act" (2005)
  20. United Nations Educational, Scientific, and Cultural Organization(UNESCO), "Human Genetic Data: Preliminary Study by the IBC on its Collection, Processing, Storage and Use. 2002" (2007)
  21. HUGO Ethics Committee, "Statement on DNA sampling: control and access. London. 1998" (2007)
  22. Buchanan A, "An ethical framework for biological samples policy", II, pp.B-1~B-35 (2000), Rockville, MD: National Bioethics Advisory Commission
  23. Knoppers BM, "Biobanking: international norms", 33(1), pp.7~14 (2005)
  24. Office for Human Research Protections (OHRP), Department of Health and Human Services (HHS), "Guidance on Research Involving Coded Private Information or Biological Specimens" (2007)
  25. HUGO Intellectual Property Committee, "Statement on Patenting on Patenting Issues Related To Early Release of Sequence Data. 1997" (2007)
  26. 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", 12(9), pp.2076~2080 (1997)
  27. HUGO Ethics Committee, "Statement on Benefit-Sharing. 2000" (2007)
  28. Mannvernd, "A Landmark Decision by the Icelandic Supreme Court. 2004" (2007)
  29. ; Available from: URL:http:, , www.geenivaramu. ee, 2007, ~[DOI]
  30. UK Biobank, "The UK Biobank Ethics and Governance Framework. 2004" (2007)
  31. Human Genetics Commission, "Inside Information: Balancing Interests in the Use of Personal Genetic Data. London.: 2002" (2007)
  32. ; Available from: URL:http:, , www.cartagene.qc.ca, 2008, ~[DOI]

관련 논문AI추천

이 간행물의 다른 논문 (14건)