Author

Publication

2011 - Oxford University Press, Oxford, England

Language

English

Word Count

53,000 words, Guess

Page Count

212 pages

Identifiers

and 2 more
  • Better World Books9780195390384
  • Open LibraryOL25138382M

Classifications

  • DDC174.2/96042
  • LCCQH438.7 .A26 2011
  • LCCQH438.7.A26 2011

Description

This book explores implicit choices made by researchers, policy makers, and funders regarding who benefits from society's investment in health research. The authors focus specifically on genetic research and examine whether such research tends to reduce or exacerbate existing health disparities. Using case examples to illustrate the issues, the authors trace the path of genetics research from discovery, through development and delivery, to health outcomes. Topics include breast cancer screening and treatment, autism research, pharmacogenetics, prenatal testing, newborn screening, and youth suicide prevention. Each chapter emphasizes the societal context of genetic research and illustrates how science might change if attention were paid to the needs of marginalized populations. Written by experts in genetics, health, and philosophy, this book argues that the scientific enterprise has a responsibility to respond to community needs to assure that research innovations achieve much needed health impacts.

Subjects

Other Editions

  • Achieving justice in genomic translation: rethinking the pathway to benefitOxford University Press2011-01-01

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