Informed Consent in the Genomics Era

Matthias Wjst and colleagues argue that traditional informed consent may no longer be appropriate when dealing with long-term studies using biological material.

[1]  C. Weill Can consultation of both experts and the public help developing public policy? Some aspects of the debate in France , 2003 .

[2]  Bartha Maria Knoppers,et al.  Biobanking: International Norms , 2005, Journal of Law, Medicine & Ethics.

[3]  Eric M Meslin,et al.  Research Ethics Recommendations for Whole-Genome Research: Consensus Statement , 2008, PLoS biology.

[4]  S. Krimsky,et al.  Science in the private interest: has the lure of profits corrupted biomedical research? , 2006, IEEE Technology and Society Magazine.

[5]  G. Church,et al.  From genetic privacy to open consent , 2008, Nature Reviews Genetics.

[6]  R. Tutton,et al.  Genetic Databases : Socio-Ethical Issues in the Collection and Use of DNA , 2004 .

[7]  A. Petersen 'Biobanks' "engagements": engendering trust or engineering consent?' , 2007, Genomics, society, and policy.

[8]  C. Gieger,et al.  KORA-gen - Resource for Population Genetics, Controls and a Broad Spectrum of Disease Phenotypes , 2005 .

[9]  B. Knoppers Biobanks: simplifying consent. , 2004, Nature reviews. Genetics.

[10]  S. Funtowicz,et al.  Science for the Post-Normal Age , 1993, Commonplace.

[11]  B. Knoppers Consent revisited: points to consider. , 2005, Health law review.

[12]  Russ B Altman,et al.  Confidentiality in Genome Research , 2006, Science.

[13]  Heidi Ledford Human-subjects research: Trial and error , 2007, Nature.

[14]  Timothy Caulfield,et al.  Biobanks and Blanket Consent: The Proper Place of the Public Good and Public Perception Rationales , 2007 .

[15]  Vilhjalmur Arnason,et al.  Coding and Consent: Moral Challenges of the Database Project in Iceland , 2004, Bioethics.

[16]  J. Edwards Taking 'public understanding' seriously , 2002 .

[17]  J. Kaye,et al.  Lessons from European population genetic databases: comparing the law in Estonia, Iceland, Sweden and the United Kingdom. , 2005, European journal of health law.

[18]  Kenneth D. Mandl,et al.  Reestablishing the Researcher-Patient Compact , 2007, Science.

[19]  S. Reiser The Patient as Partner: A Theory of Human-Experimentation Ethics , 1988 .

[20]  F. Stern,et al.  THE ANATOMY OF THE NUREMBERG TRIALS , 1993, The Military Law and the Law of War Review.

[21]  John Gillott,et al.  Genetic Databases: Socio-Ethical Issues in the Collection and Use of DNA , 2005 .

[22]  P S Appelbaum,et al.  Two models of implementing informed consent. , 1988, Archives of internal medicine.

[23]  H. R. Abbing International Declaration on Human Genetic Data. , 2004, European journal of health law.

[24]  N. Null International Declaration on Human Genetic Data , 2004 .