Achieving Justice in Genomic Translation ReThinking the Pathway to Benefit
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Achieving Justice in Genomic Translation ReThinking the Pathway to Benefit Description
This book examines the ethical and social issues that arise in the conduct of genetic research, from the discovery phase, through development and delivery research, to health outcomes.
Details
| OPC | PDHNSZ2 |
|---|---|
| Codes | 0195390385 (ISBN-10) |
| 9780195390384 (ISBN) |
Disclaimer: The information below is provided by various external sources and should be used as a guide only.
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.
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.
Alternative names:
- ISBN Achieving Justice in Genomic Translation ( Re-Thinking the Pathway to Benefit ) 224 pages English
- ISBN Achieving Justice in Genomic Translation ( Re-Thinking the Pathway to Benefit ) 224 pages English
Detailed Product Information
Features
| Language version | English |
|---|---|
| Release date (DD/MM/YYYY) | 13/10/2011 |
| Number of pages | 224 pages |
| Written by | Wylie Burke, Kelly A. Edwards, Sara Goering, Suzanne Holland, Susan Brown Trinidad |
| Publisher | Oxford University Press |
| Suggested gender | Any gender |
| International Standard Book Number (ISBN) | 9780195390384 |
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