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Author: Jonathan Michael Kaplan
Publisher: Routledge
ISBN: 1317721705
Category : Medical
Languages : en
Pages : 237
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Book Description
In The Limits and Lies of Human Genetic Research, Jonathan Kaplan weighs in on the controversial subject of the roles genes play in determining aspects of physical and behavioral human variation. Limits and Lies makes the case that neither the information we have on genes, nor on the environment, is sufficient to explain the complex variations among humans.
Author: Jonathan Michael Kaplan
Publisher: Routledge
ISBN: 1317721705
Category : Medical
Languages : en
Pages : 237
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Book Description
In The Limits and Lies of Human Genetic Research, Jonathan Kaplan weighs in on the controversial subject of the roles genes play in determining aspects of physical and behavioral human variation. Limits and Lies makes the case that neither the information we have on genes, nor on the environment, is sufficient to explain the complex variations among humans.
Author: Jonathan Michael Kaplan
Publisher: Psychology Press
ISBN: 9780415926386
Category : Medical
Languages : en
Pages : 224
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Book Description
First Published in 2000. Routledge is an imprint of Taylor & Francis, an informa company.
Author: Joseph S. Alper
Publisher: Johns Hopkins University Press+ORM
ISBN: 080187758X
Category : Medical
Languages : en
Pages : 440
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Book Description
This bioethics anthology exploring the questions and controversies surrounding the innovations of 21st century genetics. When the Human Genome Project completed its work in the early 2000s, it was hailed as a watershed moment in the history of medicine. But not everyone felt the same optimism about where the breakthrough might lead. The Double-Edged Helix explores the impact of recent genetic discoveries on society as a whole as well as individual populations and communities. This volume outlines potential positive and negative effects of genetic research on minorities, individuals with disabilities, and those of diverse sexual orientations. Presenting a wide array of perspectives, contributors address the medical and ethical implications of newly available technologies, from prenatal genetic screenings to the so-called “gay gene” debates. They emphasize the need to ensure that genetics research does not lead to discrimination against people on the basis of their DNA. A Choice Magazine Outstanding Academic Title
Author: Marc Lappé
Publisher:
ISBN:
Category : Science
Languages : en
Pages : 264
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Book Description
Author: Lois Wingerson
Publisher: Bantam
ISBN:
Category : Medical
Languages : en
Pages : 424
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Book Description
In this timely, provocative new book, Lois Wingerson explores advances in human genetic research--and how these advances are redefining the way we view ourselves and our world. Every week brings word of new genetic findings. It no longer startles us to read that a gene has been identified that predisposes an individual to breast cancer, to colon cancer, to Alzheimer's disease. From physical illnesses to behavioral traits, the mapping of our genes is moving with astonishing rapidity. Soon we will have extraordinary amounts of information about our most intimate selves. But--as this insightful, sometimes disturbing book makes clear--this new knowledge raises serious ethical, legal, and personal questions none of us can afford to ignore. On the heels of each new finding comes the capacity to test for the disorder the gene may activate, then the test itself--and then the questions. Just because the test is available, should we have it? The tests are often marketed by for-profit companies. Who is to determine what conditions warrant testing? Should it be up to the individual? A group of experts? A government agency? If a person learns he or she carries the gene for a particular disorder, what then? And, in the age of medical claim forms and computer networks, who else has access to that information? What if an employer finds out? If an insurance carrier denies future coverage? What about conceiving a child? Subjecting the fetus to prenatal genetic testing? If treatments for the condition lie well in the future, what benefit is it to know you or your child carry that gene? As the latest genetic breakthroughs make their way from the scientists' laboratories into individuals' lives, we will all face questions like these. In clear and accessible language, "Unnatural Selection takes us into the world of the researchers, physicians, ethicists, families, and people like ourselves as they contemplate the promise and consider the pitfalls of this exploding field of knowledge.
Author: Ruth Hubbard
Publisher: Beacon Press
ISBN: 9780807004319
Category : Science
Languages : en
Pages : 260
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Book Description
How Genetic Information Is Produced and Manipulated by Scientists, Physicians, Employers, Insurance Companies, Educators, and Law Enforcers
Author: John Meany
Publisher: Heinemann-Raintree Library
ISBN: 9781432916749
Category : Juvenile Nonfiction
Languages : en
Pages : 60
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Book Description
Can our DNA predict our future health? What are the dangers of cloning? What would you do about genetically modified food? People look at genetic research and claim that it can cause problems. They say that once certain genetic experiments and procedures are allowed, genetic research might be hard to control. Will the scientists know when to stop? But many people do not agree. They say that genetic research has the chance to create cures for diseases. It might help us feed the hungry. Do we have the right to delay research that could help those suffering from Alzheimer's or Parkinson's disease? People have been arguing about genetic research since DNA was discovered. Have you ever thought about genetic research? Are the advantages worth the risks? This book does not tell you what to think. But it will help you join in the debate. Features of the series: Techniques for thinking critically and creatively A wealth of facts and opinions Ideas for organizing debates and discussions Book jacket.
Author: Justin Healey
Publisher:
ISBN: 9781921507045
Category : Bioethics
Languages : en
Pages : 44
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Book Description
Since the 2003 mapping of the human genome, science has prompted complex challenges over how to maximise the benefit and minimise the harm when implementing rapidly expanding genetic-based knowledge. Are scientific advances being held back from producing miracle cures, or are we letting the genome out of the bottle? This fascinating book explains the fundamentals of human genetics and explores a range of considerations and dilemmas including: the limitations in personal genetic testing for diseases; privacy and the ownership of genetic information; the potential for genetic discrimination; setting restrictions in the application of genetic technologies, e.g. reproductive cloning, stem cell research using embryos, and genetic enhancements; patenting and the commercialisation of bioetchnology products; and forensic DNA databanks.Includes: Glossary; Fast Facts; Web Links; Index
Author: California. Legislature. Senate. Select Committee on Genetics and Public Policy
Publisher:
ISBN:
Category : Biotechnology
Languages : en
Pages : 118
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Book Description
Author: Celeste Michelle Condit
Publisher: Univ of Wisconsin Press
ISBN: 9780299163648
Category : Genetics
Languages : en
Pages : 348
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Book Description
The Meanings of the Gene is a compelling look at societal hopes and fears about genetics in the course of the twentieth century. The work of scientists and doctors in advancing genetic research and its applications has been accompanied by plenty of discussion in the popular press—from Good Housekeeping and Forbes to Ms. and the Congressional Record—about such topics as eugenics, sterilization, DNA, genetic counseling, and sex selection. By demonstrating the role of rhetoric and ideology in public discussions about genetics, Condit raises the controversial question, Who shapes decisions about genetic research and its consequences for humans—scientists, or the public? Analyzing hundreds of stories from American magazines—and, later, television news—from the 1910s to the 1990s, Condit identifies three central and enduring public worries about genetics: that genes are deterministic arbiters of human fate; that genetics research can be used for discriminatory ends; and that advances in genetics encourage perfectionistic thinking about our children. Other key public concerns that Condit highlights are the complexity of genetic decision-making and potential for invasion of privacy; conflict over the human genetic code and experimentation with DNA; and family genetics and reproductive decisions. Her analysis reveals a persistent debate in the popular media between themes of genetic determinism (such as eugenics) and more egalitarian views that place genes within the complexity of biological and social life. The Meanings of the Gene offers an insightful view of our continuing efforts to grapple with our biological natures and to define what it means, and will mean in the future, to be human.
