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Genetic Databases Socio ethical Issues in the Collection and Use of DNA 1st Edition by Oonagh Corrigan, Richard Tutton ISBN 0415316804 9780415316804

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Genetic Databases Socio ethical Issues in the Collection and Use of DNA 1st Edition Oonagh Corrigan Digital Instant Download

Author(s): Oonagh Corrigan, Richard Tutton
ISBN(s): 9780415316804, 0415316804
Edition: 1
File Details: PDF, 2.66 MB
Year: 2004
Language: english
SKU: EB-2413382 Category: Tags: ,

Genetic Databases Socio ethical Issues in the Collection and Use of DNA 1st Edition by Oonagh Corrigan, Richard Tutton – Ebook PDF Instant Download/Delivery: 0415316804, 9780415316804
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ISBN 10: 0415316804 
ISBN 13: 9780415316804
Author: Oonagh Corrigan, Richard Tutton

Genetic Databases offers a timely analysis of the underlying tensions, contradictions and limitations of the current regulatory frameworks for, and policy debates about, genetic databases. Drawing on original empirical research and theoretical debates in the fields of sociology, anthropology and legal studies, the contributors to this book challenge the prevailing orthodoxy of informed consent and explore the relationship between personal privacy and the public good. They also consider the multiple meanings attached to human tissue and the role of public consultations and commercial involvement in the creation and use of genetic databases. The authors argue that policy and regulatory frameworks produce a representation of participation that is often at odds with the experiences and understandings of those taking part. The findings present a serious challenge for public policy to provide mechanisms to safeguard the welfare of individuals participating in genetic databases.

Genetic Databases Socio ethical Issues in the Collection and Use of DNA 1st Table of contents:

  1. Introduction Public participation in genetic databases
  2. Person, property and gift Exploring languages of tissue donation to biomedical research
  3. Blood donation for genetic research What can we learn from donors’ narratives?
  4. Levels and styles of participation in genetic databases A case study of the North Cumbria Community Genetics Project
  5. Informed consent The contradictory ethical safeguards in pharmacogenetics
  6. Ambiguous gifts Public anxiety, informed consent and biobanks
  7. Abandoning informed consent The case of genetic research in population collections
  8. Children’s participation in genetic epidemiology Consent and control
  9. ‘Public consent’ or ‘scientific citizenship’? What counts as public participation in population-based DNA collections?
  10. Tissue collection and the pharmaceutical industry Investigating corporate biobanks

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Tags: Oonagh Corrigan, Richard Tutton, Genetic Databases