Genomics and Public Health: Legal and Socio-Ethical Perspectives
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Genomics and Public Health: Legal and Socio-Ethical Perspectives By Bartha Maria Knoppers
Publisher: Martinus Nijhoff | ISBN: 9004155597 | edition 2006 | PDF | 344 pages | 2,7 mb
When genomics and public health are integrated into society, it will create as many responsibilities as rights for citizens, researchers, and decision makers. Indeed, the expression of genetic risk factors in both common and infectious diseases is of great interest to public health. Policy development in this area needs to tackle crucial themes such as: research and its application to public health and genomic medicine, the authority of the state, the right to privacy, and the roles and responsibilities of citizens and the State. Considering the current fears of a world-wide pandemic, this book is a timely and insightful exploration of both research possibilities and the role of the state. It will help to understand the limits of possible state access to bio-banks and data. It examines the issue of the possible use of newborn screening programmes by public health authorities.
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