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Author: Mack Lipkin
Publisher: Springer Science & Business Media
ISBN: 1468421182
Category : Medical
Languages : en
Pages : 171
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Book Description
The "Genetics, Man, and Society" symposium was a collaborative effort of the Task Force on Genetics and Reproduction at Yale University and the Youth Council of the American Association for the Advancement of Science (A. A. A. S. ). The Task Force on Genetics and Reproduction at Yale is a voluntary, inter-professional organization engaged in examination of ethical and social implications of medical and basic genetics. It is similar in purpose to the Hastings Institute of Society, Ethics, and Life Sciences and the Kennedy Center for the Study of Bioethics at Georgetown. The Youth Council of A. A. A. S. was a committee of the A. A. A. S. concerned with problems of young persons. The Youth Council had significant impact on the A. A. A. S. through the constitutional reform and a number of innovative programs including the Congressional Fellows and Regional Centers Program, and the Committees on Minorities and Women. The symposium was initially conceived by William Drayton and Richard A. Tropp and was arranged by us. The Task Force took primary responsibility for format and for selecting and inviting speakers. The Youth Council made the arrangements, raised the necessary funds and represented the organizers for post-symposium use of the materials including printed and taped publications. This volume contains the edited proceedings of the symposium plus the editors' perspective on it.
Author: Mack Lipkin
Publisher: Springer Science & Business Media
ISBN: 1468421182
Category : Medical
Languages : en
Pages : 171
Get Book Here
Book Description
The "Genetics, Man, and Society" symposium was a collaborative effort of the Task Force on Genetics and Reproduction at Yale University and the Youth Council of the American Association for the Advancement of Science (A. A. A. S. ). The Task Force on Genetics and Reproduction at Yale is a voluntary, inter-professional organization engaged in examination of ethical and social implications of medical and basic genetics. It is similar in purpose to the Hastings Institute of Society, Ethics, and Life Sciences and the Kennedy Center for the Study of Bioethics at Georgetown. The Youth Council of A. A. A. S. was a committee of the A. A. A. S. concerned with problems of young persons. The Youth Council had significant impact on the A. A. A. S. through the constitutional reform and a number of innovative programs including the Congressional Fellows and Regional Centers Program, and the Committees on Minorities and Women. The symposium was initially conceived by William Drayton and Richard A. Tropp and was arranged by us. The Task Force took primary responsibility for format and for selecting and inviting speakers. The Youth Council made the arrangements, raised the necessary funds and represented the organizers for post-symposium use of the materials including printed and taped publications. This volume contains the edited proceedings of the symposium plus the editors' perspective on it.
Author: Institute of Medicine
Publisher: National Academies Press
ISBN: 0309047986
Category : Medical
Languages : en
Pages : 353
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Book Description
Raising hopes for disease treatment and prevention, but also the specter of discrimination and "designer genes," genetic testing is potentially one of the most socially explosive developments of our time. This book presents a current assessment of this rapidly evolving field, offering principles for actions and research and recommendations on key issues in genetic testing and screening. Advantages of early genetic knowledge are balanced with issues associated with such knowledge: availability of treatment, privacy and discrimination, personal decision-making, public health objectives, cost, and more. Among the important issues covered: Quality control in genetic testing. Appropriate roles for public agencies, private health practitioners, and laboratories. Value-neutral education and counseling for persons considering testing. Use of test results in insurance, employment, and other settings.
Author: Christina Schües
Publisher: transcript Verlag
ISBN: 3839459885
Category : Philosophy
Languages : en
Pages : 379
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Book Description
Prenatal diagnosis, especially noninvasive prenatal testing (NIPT), has changed the experience of pregnancy, prenatal care and responsibilities in Israel and Germany in different ways. These differences reflect the countries' historical legacies, medico-legal policies, normative and cultural identities. Building on this observation, the contributors of this book present conversations between leading scholars from Israel and Germany based on an empirical bioethical perspective, analyses about the reshaping of 'life' by biomedicine, and philosophical reflections on socio-cultural claims and epistemic horizons of responsibilities. Practices and discussions of reproductive medicine transform the concepts of responsibility and irresponsibility.
Author: Malte Dreyer
Publisher: BRILL
ISBN: 9004311890
Category : Social Science
Languages : en
Pages : 292
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Book Description
Genetic Transparency? tackles the question of who has, or should have access to personal genomic information. Genomic science is revolutionary in how it changes the way we live, individually and together, and how it changes the shape of society. If this is so, then – the authors of this volume claim – the rules that regulate genetic transparency should be debated carefully, openly and critically. It is important to see that the social and cultural meanings of DNA and genetic sequences are much richer than can be accounted for by purely biomedical knowledge. In this book, an international group of leading genomics experts and scholars from the humanities and social sciences discuss how the new accessibility of genomic information affects interpersonal relationships, our self-understandings, ethics, law, and healthcare systems. Contributors are: Kirsten Brukamp, Gabrielle Christenhusz, Lorraine Cowley, Malte Dreyer, Jeanette Erdmann, Andrei Famenka, Teresa Finlay, Caroline Fündling, Shannon Gibson, Cathy Herbrand, Angeliki Kerasidou, Lene Koch, Fruzsina Molnár-Gábor, Tim Ohnhäuser, Christoph Rehmann-Sutter, Benedikt Reiz, Vasilja Rolfes, Sara Tocchetti
Author: Aviad E. Raz
Publisher: Springer
ISBN: 331932733X
Category : Philosophy
Languages : en
Pages : 128
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Book Description
This book is a comprehensive, empirically-grounded exploration of the relationship between bioethics, culture, and the perspective of being affected. It provides a new outlook on how complex “bioethical” issues become questions of everyday life. The authors focus on two contexts, genetic testing and end-of-life care, to locate and demonstrate emerging themes of responsibility, such as self-responsibility, responsibility for kin, and the responsibility of society. Within these themes, the duty to know versus the right not to know one's genetic fate (in the context of genetic testing), or the sanctity of life versus self-determination (in the context of end of life care) are identified as culturally embedded dilemmas that are very much relevant for lay persons. Furthermore, cultural factors such as religion, history, utopian and dystopian views of biomedical technologies, outlooks on the body and on health/illness, and citizenship are examined. Health issues are increasingly becoming a question of assessing risk and responsibility: How can we better prepare ourselves for the future? We all make such assessments in a way that combines personal inclinations, professional recommendations, and cultural framings. There is still much to be learned about the interplay between these three dimensions.
Author: Thomas Lemke
Publisher: Routledge
ISBN: 1134056982
Category : Science
Languages : en
Pages : 185
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Book Description
Over the past 15 years, a series of empirical studies in different countries have shown that our increasing genetic knowledge leads to new forms of exclusion, disadvantaging and stigmatization. The spectrum of this "genetic discrimination" ranges from disadvantages at work, via problems with insurance policies, to difficulties with adoption agencies. The empirical studies on the problem of genetic discrimination have not gone unnoticed. Since the beginning of the 1990s, a series of legislative initiatives and statements, both on the national level and on the part of international and supranational organizations and commissions, have been put forward as ways of protecting people from genetic discrimination. This is the first book to critically evaluate the empirical evidence and the theoretical usefulness of the concept of "genetic discrimination." It discusses the advantages and limitations of adopting the concept, and offers a more complex account distinguishing between several dimensions and forms of genetic discrimination.
Author: Barbara Prainsack
Publisher: Routledge
ISBN: 1317129423
Category : Social Science
Languages : en
Pages : 221
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Book Description
Recent debate about the ethical and regulatory dimensions of developments in genetics has sidelined societal and cultural aspects, which arguably are indispensable for a nuanced understanding of the complexities of the topic. Regulatory and ethical debates benefit from taking seriously this ’third dimension’ of culture, which often determines the configurations and limits of the space within which scientific, ethical and legal debate can take place. To fill this gap, this volume brings together contributions exploring the mutual relationships between genetics, markets, societies and identities in genetics and genomics. It draws upon the recent transdisciplinary debate on how socio-cultural factors influence understandings of ’genetics2.0' and shows how individual and collective identities are challenged or reinforced by cultural meanings and practices of genetics. This book will become a standard reference for everyone seeking to make sense of the controversies and shifts in the field of genetics in the second decade of the twenty-first century.
Author: Bernhard Wieser
Publisher: transcript Verlag
ISBN: 3839437660
Category : Social Science
Languages : en
Pages : 365
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Book Description
Understanding the significance of genetic factors for our lives requires an analysis that goes beyond biological aspects. It is especially necessary to take into account how human beings relate to others and to themselves. Who we are is a result of social action and the ways in which human beings constitute themselves as subjects. Seen from this perspective, genetic medicine is a social practice that shapes how we think about us, how we conduct our behaviour and how we care for our children. This book scrutinises practices by which individuals become knowledgeable about their genes and constitute them as responsible decision makers.
Author: Kathryn Paige Harden
Publisher: Princeton University Press
ISBN: 0691190801
Category : Philosophy
Languages : en
Pages : 312
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Book Description
A provocative and timely case for how the science of genetics can help create a more just and equal society In recent years, scientists like Kathryn Paige Harden have shown that DNA makes us different, in our personalities and in our health—and in ways that matter for educational and economic success in our current society. In The Genetic Lottery, Harden introduces readers to the latest genetic science, dismantling dangerous ideas about racial superiority and challenging us to grapple with what equality really means in a world where people are born different. Weaving together personal stories with scientific evidence, Harden shows why our refusal to recognize the power of DNA perpetuates the myth of meritocracy, and argues that we must acknowledge the role of genetic luck if we are ever to create a fair society. Reclaiming genetic science from the legacy of eugenics, this groundbreaking book offers a bold new vision of society where everyone thrives, regardless of how one fares in the genetic lottery.
Author: Michael Arribas-Ayllon
Publisher: Routledge
ISBN: 1134026285
Category : Law
Languages : en
Pages : 267
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Book Description
Advances in molecular genetics have led to the increasing availability of genetic testing for a variety of inherited disorders. While this new knowledge presents many obvious health benefits to prospective individuals and their families it also raises complex ethical and moral dilemmas for families as well as genetic professionals. This book explores the ways in which genetic testing generates not only probabilities of potential futures, but also enjoys new forms of social, individual and professional responsibility. Concerns about confidentiality and informed consent involving children, the assessment of competence and maturity, the ability to engage in shared decision-making through acts of disclosure and choice, are just some of the issues that are examined in detail.
