• English
    • français
    • Deutsch
    • español
    • português (Brasil)
    • Bahasa Indonesia
    • русский
    • العربية
    • 中文
  • English 
    • English
    • français
    • Deutsch
    • español
    • português (Brasil)
    • Bahasa Indonesia
    • русский
    • العربية
    • 中文
  • Login
View Item 
  •   Home
  • Ethics collections
  • Health Ethics
  • View Item
  •   Home
  • Ethics collections
  • Health Ethics
  • View Item
JavaScript is disabled for your browser. Some features of this site may not work without it.

Browse

All of the LibraryCommunitiesPublication DateTitlesSubjectsAuthorsThis CollectionPublication DateTitlesSubjectsAuthorsProfilesView

My Account

LoginRegister

The Library

AboutNew SubmissionSubmission GuideSearch GuideRepository PolicyContact

RECONFIGURING NATURE: ISSUES AND DEBATES IN THE NEW GENETICS

  • CSV
  • RefMan
  • EndNote
  • BibTex
  • RefWorks
Author(s)
Glasner, Peter, ed.
Keywords
Genetics
Nature
Concept of Health
Social Control of Science and Technology
Cloning
Genetics, Molecular Biology and Microbiology
Genetic Screening / Genetic Testing
Behavioral Genetics
Neurosciences and Mental Health Therapies
Animal Experimentation
Information Science Ethics
Informed Consent
Economics of Health Care
Health Care for Particular Diseases or Groups
Show allShow less

Full record
Show full item record
URI
http://hdl.handle.net/20.500.12424/263411
Online Access
http://hdl.handle.net/10822/547564
Abstract
List of tables and figures -- List of contributors -- Acknowledgements -- Ch. 1. Introduction: what's new about the `new genetics'? / Peter Glasner and Harry Rothman -- Pt. I. Literacy, public understanding and the media -- Ch. 2. The gene shop at Manchester airport / Mairi Levitt -- Ch. 3. Public understanding of genetic engineering in Germany / Jurgen Hampel -- Ch. 4. Predictive medicine, genetics and schizophrenia / John Turney and Jill Turner -- Pt. II. Commercialisation and health -- Ch. 5. Pharmacogenetics: implications for drug development, patients and society / Alun McCarthy -- Ch. 6. The use of large biological sample collections in genetics research: issues for public policy / Paul Martin and Jane Kaye -- Pt. III. Gen-ethics: human genetic banking -- Ch. 7. DNA sampling and banking in clinical genetics and genetic research / Kare Berg -- Ch. 8. Human genetic banking and the limits of informed consent / Garrath Williams and Doris Schroeder -- Ch. 9. Regulation and social perceptions of genetic data banking in Germany / Juergen Simon and Susanne Braun -- Pt. IV. Genetic screening -- Ch. 10. Genetic and nongenetic medical information: is there a moral difference in the context of insurance? / Veikko Launis -- Ch. 11. New practices of screening in the field of cancergenetics: a co-evolutionary perspective / Dirk Stemerding and Annemiek Nelis -- Ch. 12. Lumping and splitting revisited: or what happens when the new genetics meets disease classification /Adam M. Hedgecoe -- Pt. V. Cloning and xenotransplantation -- Ch. 13. What we know and what we don't about cloning and society / Sarah Franklin -- Ch. 14. Containing contradictions: debating nature, controversy and biotechnology / Nik Brown -- Ch. 15. Constructing the scientific citizen: science and democracy in the biosciences / Alan Irwin -- Ch. 16. Conclusion / Peter Glasner -- Index
Date
2011-07-12
Identifier
oai:repository.library.georgetown.edu:10822/547564
ISBN 0-7546-3237-7
Aldershot, Hampshire/Burlington, VT: Ashgate, 2004. 330 p.
http://hdl.handle.net/10822/547564
ISBN
0754632377
Collections
Health Ethics

entitlement

 

Related items

Showing items related by title, author, creator and subject.

  • Thumbnail

    Al-muwakabah al-Shar'iyah li mu'tayat al-handasah al-wirathíyah

    Abu Ghuddah, 'Abd al-Sattar (2016-01-08)
    This paper was submitted to the symposium held by the Islamic Organization for Medical Sciences (IOMS) in Kuwait during the period 13-15 October 1998 on genetics. The paper presents detailed juristic answers for different questions raised by the applications of genetic engineering such as prenatal diagnostic testing especially in case of endogamous marriage, gene therapy, genetic privacy and selective abortion.
  • Thumbnail

    Al-Wirathah Wa Al-Handasah Al-Wirathiyah Wa Al-Jinum Al-Bashari Wa Al-'Ilaj Al-Jini: Ru'yah Islamiyah (Al-Juz' Al-Awwal) Al-Wirathah Wa Al-Handasah Al-Wirathiyah Wa Al-Jinum Al-Bashari Genetics, Genetic Engineering, Human Genome and Genetic Therapy: An Islamic Perspective (Vol. 1) Genetics, Genetic Engineering and the Human Genome

    Jundi, Ahmad Raja'i (2016-01-08)
  • Thumbnail

    Privacy-preserving genomic testing in the clinic: A model using HIV treatment

    Mclaren P.J.; Raisaro J.L.; Aouri M.; Rotger M.; Ayday E.; Bartha I.; Delgado M.B.; Vallet Y.; Günthard H.F.; Cavassini M.; et al. (Nature Publishing Group, 2018-04-12)
    Purpose:The implementation of genomic-based medicine is hindered by unresolved questions regarding data privacy and delivery of interpreted results to health-care practitioners. We used DNA-based prediction of HIV-related outcomes as a model to explore critical issues in clinical genomics.Methods:We genotyped 4,149 markers in HIV-positive individuals. Variants allowed for prediction of 17 traits relevant to HIV medical care, inference of patient ancestry, and imputation of human leukocyte antigen (HLA) types. Genetic data were processed under a privacy-preserving framework using homomorphic encryption, and clinical reports describing potentially actionable results were delivered to health-care providers.Results:A total of 230 patients were included in the study. We demonstrated the feasibility of encrypting a large number of genetic markers, inferring patient ancestry, computing monogenic and polygenic trait risks, and reporting results under privacy-preserving conditions. The average execution time of a multimarker test on encrypted data was 865 ms on a standard computer. The proportion of tests returning potentially actionable genetic results ranged from 0 to 54%.Conclusions:The model of implementation presented herein informs on strategies to deliver genomic test results for clinical care. Data encryption to ensure privacy helps to build patient trust, a key requirement on the road to genomic-based medicine. © 2015 American College of Medical Genetics and Genomics.
DSpace software (copyright © 2002 - 2021)  DuraSpace
Quick Guide | Contact Us
Open Repository is a service operated by 
Atmire NV
 

Export search results

The export option will allow you to export the current search results of the entered query to a file. Different formats are available for download. To export the items, click on the button corresponding with the preferred download format.

By default, clicking on the export buttons will result in a download of the allowed maximum amount of items.

To select a subset of the search results, click "Selective Export" button and make a selection of the items you want to export. The amount of items that can be exported at once is similarly restricted as the full export.

After making a selection, click one of the export format buttons. The amount of items that will be exported is indicated in the bubble next to export format.