CyberGenetics

Regular price €198.40
Quantity:
Delivery/Collection within 10-20 working days
Shipping & Delivery
23andMe Research
A01=Anna Harris
A01=Sally Wyatt
A01=Susan Kelly
ancestry
Author_Anna Harris
Author_Sally Wyatt
Author_Susan Kelly
biopolitics
Category=JB
Category=JBFV
Category=JHB
COMT Gene
consumers
counselors
digital technologies
DNA Exchange
DTC Genetic Testing
eq_bestseller
eq_isMigrated=1
eq_isMigrated=2
eq_nobargain
eq_non-fiction
eq_society-politics
FAQ Section
Genetic Counselling
Genetic Counselling Profession
Genetic Counselling Services
genetic data
genetic technologies
Genetic Testing
Genetic Testing Companies
genetic testing online
Genetic Testing Product
Genetic Testing Services
Genome Sequencing Technologies
genomics
governments
health
healthcare organisations
illness
interdisciplinary
Internal Validation Experiments
internet platforms
medical research
Medical Research Participation
mental health
methodologies
New Genetics
new media
Online
Online Genetic
Online Genetic Testing
Online Research Participation
participatory medical practices
paternity
personal genomics
Research Articles
research participation
Schizophrenia Aetiology
Schizophrenia Genetics
science
SNP Profile
social data
social life
Spatial Temporal Relations
study
subjectivities
Young Man
YouTube

Product details

  • ISBN 9781138946514
  • Weight: 385g
  • Dimensions: 156 x 234mm
  • Publication Date: 29 Apr 2016
  • Publisher: Taylor & Francis Ltd
  • Publication City/Country: GB
  • Product Form: Hardback
Secure checkout Fast Shipping Easy returns

Online genetic testing services are increasingly being offered to consumers who are becoming exposed to, and knowledgeable about, new kinds of genetic technologies, as the launch of a 23andme genetic testing product in the UK testifies. Genetic research breakthroughs, cheek swabbing forensic pathologists and celebrities discovering their ancestral roots are littered throughout the North American, European and Australasian media landscapes. Genetic testing is now capturing the attention, and imagination, of hundreds of thousands of people who can not only buy genetic tests online, but can also go online to find relatives, share their results with strangers, sign up for personal DNA-based musical scores, and take part in research. This book critically examines this market of direct-to-consumer (DTC) genetic testing from a social science perspective, asking, what happens when genetics goes online?

With a focus on genetic testing for disease, the book is about the new social arrangements which emerge when a traditionally clinical practice (genetic testing) is taken into new spaces (the internet). It examines the intersections of new genetics and new media by drawing from three different fields: internet studies; the sociology of health; and science and technology studies.

While there has been a surge of research activity concerning DTC genetic testing, particularly in sociology, ethics and law, this is the first scholarly monograph on the topic, and the first book which brings together the social study of genetics and the social study of digital technologies. This book thus not only offers a new overview of this field, but also offers a unique contribution by attending to the digital, and by drawing upon empirical examples from our own research of DTC genetic testing websites (using online methods) and in-depth interviews in the United Kingdom with people using healthcare services.

Anna Harris completed a medical degree at the University of Tasmania, and a Masters and PhD in Medical Anthropology at the University of Melbourne. She has been a post-doctoral researcher at the Universities of Maastricht and Exeter. She has published in clinical and social science journals, and her own blog.

Susan Kelly is Associate Professor in Sociology, University of Exeter and Senior Research Fellow in Egenis (Exeter Centre for the Study of the Life Sciences). She earned a PhD in Sociology from the University of California, San Francisco, followed by a post-doctoral position in the Stanford Center for Biomedical Ethics.

Sally Wyatt is Programme Leader of the e-Humanities Group of the Royal Netherlands Academy of Arts and Sciences, and Professor of Digital Cultures in Development at Maastricht University. She is the founding co-editor (with Andrew Webster) of the Health, Technology & Society series published by Palgrave Macmillan.

More from this author