IDEAS home Printed from https://ideas.repec.org/a/eee/socmed/v35y1992i12p1469-1476.html
   My bibliography  Save this article

Led (astray) by genetic maps: The cartography of the human genome and health care

Author

Listed:
  • Lippman, A.

Abstract

Advocates of projects to map the human genome claim that the information produced will illuminate the causes of human disease, improve treatment and, in general, increase our health and well-being. While concerns about the costs of mapping and the possible discriminatory and eugenic applications of the information it will provide have received some attention, assumptions implicit in the biomedical discourse in which its 'benefits' are proposed and which are shaping definitions of illness and health, normality and abnormality, have not yet been adequately analyzed. This paper examines how the genetic stories about mapping and its potential products being told in the biomedical (and popular) literature continue a tradition of reductionism and determinism. This new 'cartography', by adopting the blueprint as a metaphor for genes, leads to restricted conceptions of health and illness, reinforces inequities in the distribution of health and, by privatizing and individualizing responsibility for health, creates and legitimizes a new arena for social control.

Suggested Citation

  • Lippman, A., 1992. "Led (astray) by genetic maps: The cartography of the human genome and health care," Social Science & Medicine, Elsevier, vol. 35(12), pages 1469-1476, December.
  • Handle: RePEc:eee:socmed:v:35:y:1992:i:12:p:1469-1476
    as

    Download full text from publisher

    File URL: http://www.sciencedirect.com/science/article/pii/0277-9536(92)90049-V
    Download Restriction: Full text for ScienceDirect subscribers only
    ---><---

    As the access to this document is restricted, you may want to search for a different version of it.

    Citations

    Citations are extracted by the CitEc Project, subscribe to its RSS feed for this item.
    as


    Cited by:

    1. Vailly, Joëlle, 2006. "Genetic screening as a technique of government: The case of neonatal screening for cystic fibrosis in France," Social Science & Medicine, Elsevier, vol. 63(12), pages 3092-3101, December.
    2. Seabrook, Jamie A. & Avison, William R., 2010. "Genotype-environment interaction and sociology: Contributions and complexities," Social Science & Medicine, Elsevier, vol. 70(9), pages 1277-1284, May.
    3. Green, Sara & Carusi, Annamaria & Hoeyer, Klaus, 2022. "Plastic diagnostics: The remaking of disease and evidence in personalized medicine," Social Science & Medicine, Elsevier, vol. 304(C).
    4. Arribas-Ayllon, Michael, 2016. "After geneticization," Social Science & Medicine, Elsevier, vol. 159(C), pages 132-139.
    5. Vincenzo Pavone & Flor Arias, 2010. "Pre-Implantation Genetic Testing in Spain: beyond the geneticization thesis," Working Papers 1012, Instituto de Políticas y Bienes Públicos (IPP), CSIC.
    6. Schnittker, Jason, 2008. "An uncertain revolution: Why the rise of a genetic model of mental illness has not increased tolerance," Social Science & Medicine, Elsevier, vol. 67(9), pages 1370-1381, November.
    7. Faure, Marlyn C. & Matshabane, Olivia P. & Marshall, Patricia & Appelbaum, Paul S. & Stein, Dan J. & Engel, Mark E. & de Vries, Jantina, 2019. "Does genetics matter for disease-related stigma? The impact of genetic attribution on stigma associated with rheumatic heart disease in the Western Cape, South Africa," Social Science & Medicine, Elsevier, vol. 243(C).
    8. Easter, Michele M., 2012. "“Not all my fault”: Genetics, stigma, and personal responsibility for women with eating disorders," Social Science & Medicine, Elsevier, vol. 75(8), pages 1408-1416.
    9. Matthew W. Hughey & Devon R. Goss, 2015. "A Level Playing Field? Media Constructions of Athletics, Genetics, and Race," The ANNALS of the American Academy of Political and Social Science, , vol. 661(1), pages 182-211, September.

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:eee:socmed:v:35:y:1992:i:12:p:1469-1476. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Catherine Liu (email available below). General contact details of provider: http://www.elsevier.com/wps/find/journaldescription.cws_home/315/description#description .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.