Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
Birch, Kean
2007.
THEVIRTUALBIOECONOMY.
Distinktion: Journal of Social Theory,
Vol. 8,
Issue. 1,
p.
83.
Rose, Nikolas
2007.
Molecular Biopolitics, Somatic Ethics and the Spirit of Biocapital.
Social Theory & Health,
Vol. 5,
Issue. 1,
p.
3.
Wahlberg, Ayo
2007.
MEASURING PROGRESS.
Distinktion: Journal of Social Theory,
Vol. 8,
Issue. 1,
p.
65.
Dixon-Woods, Mary
Wilson, Duncan
Jackson, Clare
Cavers, Debbie
and
Pritchard-Jones, Kathy
2008.
Human Tissue and ‘the Public’: The Case of Childhood Cancer Tumour Banking.
BioSocieties,
Vol. 3,
Issue. 1,
p.
57.
Rose, Nikolas
2008.
Race, Risk and Medicine in the Age of ‘Your Own Personal Genome’.
BioSocieties,
Vol. 3,
Issue. 4,
p.
423.
Fitzgerald, Ruth
2008.
Biological citizenship at the periphery: parenting children with genetic disorders.
New Genetics and Society,
Vol. 27,
Issue. 3,
p.
251.
Barr, Michael
and
Rose, Diana
2008.
The great ambivalence: factors likely to affect service user and public acceptability of the pharmacogenomics of antidepressant medication.
Sociology of Health & Illness,
Vol. 30,
Issue. 6,
p.
944.
Amsler, Sarah
2008.
The Blackwell Encyclopedia of Sociology.
Williams, Simon J.
Gabe, Jonathan
and
Davis, Peter
2008.
The sociology of pharmaceuticals: progress and prospects.
Sociology of Health & Illness,
Vol. 30,
Issue. 6,
p.
813.
Shields, Rob
2008.
Hope and Fear in Biotechnology.
Space and Culture,
Vol. 11,
Issue. 2,
p.
125.
Burges Watson, Duika
Moreira, Tiago
and
Murtagh, Madeleine
2009.
Little bottles and the promise of probiotics.
Health: An Interdisciplinary Journal for the Social Study of Health, Illness and Medicine,
Vol. 13,
Issue. 2,
p.
219.
Tutton, Richard
2009.
Social Aspects of Genetic Testing Technologies.
Sociology Compass,
Vol. 3,
Issue. 6,
p.
972.
Rose, Nikolas
2009.
Normality and Pathology in a Biomedical Age.
The Sociological Review,
Vol. 57,
Issue. 2_suppl,
p.
66.
Raz, Aviad E.
and
Schicktanz, Silke
2009.
Diversity and uniformity in genetic responsibility: moral attitudes of patients, relatives and lay people in Germany and Israel.
Medicine, Health Care and Philosophy,
Vol. 12,
Issue. 4,
p.
433.
Martin, Graham P.
2009.
Whose health, whose care, whose say? Some comments on public involvement in new NHS commissioning arrangements.
Critical Public Health,
Vol. 19,
Issue. 1,
p.
123.
Adams, Vincanne
Murphy, Michelle
and
Clarke, Adele E
2009.
Anticipation: Technoscience, life, affect, temporality.
Subjectivity,
Vol. 28,
Issue. 1,
p.
246.
Raz, Aviad E.
and
Schicktanz, Silke
2009.
Lay perceptions of genetic testing in Germany and Israel: the interplay of national culture and individual experience.
New Genetics and Society,
Vol. 28,
Issue. 4,
p.
401.
Raz, Aviad E.
2010.
Commentary: a sociologist's view on community genetics.
Journal of Community Genetics,
Vol. 1,
Issue. 1,
p.
3.
Brown, Patrick
and
Calnan, Michael
2010.
Political Accountability of Explicit Rationing: Legitimacy Problems Faced by Nice.
Journal of Health Services Research & Policy,
Vol. 15,
Issue. 2,
p.
65.
Meleo-Erwin, Zoë C.
2010.
Fat Bodies, Qualitative Research and the Spirit of Participatory Action Research.
International Review of Qualitative Research,
Vol. 3,
Issue. 3,
p.
335.