Genetic Databases

Socio-Ethical Issues in the Collection and Use of DNA

Inbunden, Engelska, 2004

AvOonagh Corrigan,Richard Tutton,UK) Corrigan, Oonagh (University of Plymouth,UK) Tutton, Richard (University of Nottingham

3 009 kr

Beställningsvara. Skickas inom 10-15 vardagar. Fri frakt för medlemmar vid köp för minst 249 kr.

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.

Produktinformation

Utgivningsdatum2004-03-18
Mått156 x 234 x 17 mm
Vikt570 g
FormatInbunden
SpråkEngelska
Antal sidor224
FörlagTaylor & Francis Ltd
ISBN9780415316798

Tillhör följande kategorier

Sociologi och antropologi inom Samhälle och politik

Oonagh Corrigan is a sociologist with a research interest in social and ethical issues surrounding developments in genetics and the pharmaceutical industry. In particular much of her work to date has focussed on the implications for human subjects involved in biomedical research and on regulatory mechanisms designed to protect such subjects. Richard Tutton is a research fellow in the Science and Technology Studies Unit (SATSU) in the Department of Sociology at the University of York. He has been researching the various social and ethical implications of developments in human genetics for several years

1. Introduction: Public Participation in Genetic Databases 2. Persons, Property and Gift: Exploring Languages of Tissue Donation to Biomedical Research 3. Blood Donation for Genetic Research: What Can we Learn From Donor's 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

Du kanske också är intresserad av

Genetic Databases

Oonagh Corrigan, Richard Tutton, UK) Corrigan, Oonagh (University of Plymouth, UK) Tutton, Richard (University of Nottingham

Häftad

939 kr

The Limits of Consent

Oonagh Corrigan, John McMillan, Kathleen Liddell, Martin Richards, Charles Weijer, UK) Corrigan, Oonagh (Senior Lecturer in Clinical Education Research, Peninsula College of Medicine and Dentistry, University of Plymouth, UK) McMillan, John (Senior Lecturer in Medical Ethics, Philosophy Department and Hull York Medical School, University of Hull, UK) Liddell, Kathleen (University Lecturer, Faculty of Law, University of Cambridge, UK) Richards, Martin (Emeritus Professor of Family Research, University of Cambridge, Canada) Weijer, Charles (Professor, Departments of Philosophy and Medicine, University of Western Ontario

Inbunden

2 439 kr