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Social Studies of Science
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July 6, 2019
Data as promise: Reconfiguring Danish public health through personalized medicine
Klaus Hoeyer
Sociology of Health & Illness
|
December 23, 2006
The power of ethics: a case study from Sweden on the social life of moral concerns in policy processes
Klaus Hoeyer
Social Science & Medicine (1982)
|
April 10, 2010
An anthropological analysis of European Union (EU) health governance as biopolitics: the case of the EU tissues and cells directive
Klaus Hoeyer
New Genetics and Society
|
April 30, 2004
'Science is really needed--that's all I know': informed consent and the non-verbal practices of collecting blood for genetic research in northern Sweden
Klaus Hoeyer
Science, Technology & Human Values
|
July 4, 2015
Regulatory Anatomy: How "Safety Logics" Structure European Transplant Medicine
Klaus Hoeyer
Medical Anthropology
|
April 13, 2005
The role of ethics in commercial genetic research: notes on the notion of commodification
Klaus Hoeyer
Biotechnology & Genetic Engineering Reviews
|
March 18, 2011
The ethics of research biobanking: a critical review of the literature
Klaus Hoeyer
Medical Anthropology Quarterly
|
August 8, 2020
Weak Data: The Social Biography of a Measurement Instrument and How It Failed to Ensure Accountability in Home Care
Klaus Hoeyer, Malene Bødker
Medicine, Health Care, and Philosophy
|
September 7, 2017
"That is why I have trust": unpacking what 'trust' means to participants in international genetic research in Pakistan and Denmark
Zainab Sheikh, Klaus Hoeyer
Scandinavian Journal of Public Health
|
December 7, 2017
The rise and fall of an opt-out system
Francisca Nordfalk, Klaus Hoeyer
Page
of 5
Search research articles
Search
Showing results (1-10 of 48) with videos related to
Sort By:
Page
of 5
Social Studies of Science
|
July 6, 2019
Data as promise: Reconfiguring Danish public health through personalized medicine
Klaus Hoeyer
Sociology of Health & Illness
|
December 23, 2006
The power of ethics: a case study from Sweden on the social life of moral concerns in policy processes
Klaus Hoeyer
Social Science & Medicine (1982)
|
April 10, 2010
An anthropological analysis of European Union (EU) health governance as biopolitics: the case of the EU tissues and cells directive
Klaus Hoeyer
New Genetics and Society
|
April 30, 2004
'Science is really needed--that's all I know': informed consent and the non-verbal practices of collecting blood for genetic research in northern Sweden
Klaus Hoeyer
Science, Technology & Human Values
|
July 4, 2015
Regulatory Anatomy: How "Safety Logics" Structure European Transplant Medicine
Klaus Hoeyer
Medical Anthropology
|
April 13, 2005
The role of ethics in commercial genetic research: notes on the notion of commodification
Klaus Hoeyer
Biotechnology & Genetic Engineering Reviews
|
March 18, 2011
The ethics of research biobanking: a critical review of the literature
Klaus Hoeyer
Medical Anthropology Quarterly
|
August 8, 2020
Weak Data: The Social Biography of a Measurement Instrument and How It Failed to Ensure Accountability in Home Care
Klaus Hoeyer, Malene Bødker
Medicine, Health Care, and Philosophy
|
September 7, 2017
"That is why I have trust": unpacking what 'trust' means to participants in international genetic research in Pakistan and Denmark
Zainab Sheikh, Klaus Hoeyer
Scandinavian Journal of Public Health
|
December 7, 2017
The rise and fall of an opt-out system
Francisca Nordfalk, Klaus Hoeyer
Page
of 5