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Life Sciences, Society and Policy
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November 18, 2015
The evolution of withdrawal: negotiating research relationships in biobanking
Karen Melham, Linda Briceno Moraia, Colin Mitchell, et al.
European Journal of Health Law
|
September 8, 2005
Lessons from European population genetic databases: comparing the law in Estonia, Iceland, Sweden and the United Kingdom
Susan M C Gibbons, Hördur Helgi Helgason, Jane Kaye, et al.
Pharmacogenomics
|
June 4, 2008
Sample, data use and protection in biobanking in Europe: legal issues
Eleni Zika, Tobias Schulte In den Bäumen, Jane Kaye, et al.
European Journal of Human Genetics : EJHG
|
May 8, 2014
Dynamic consent: a patient interface for twenty-first century research networks
Jane Kaye, Edgar A Whitley, David Lund, et al.
Genetic Testing and Molecular Biomarkers
|
February 2, 2017
Returning Results in Biobank Research: Global Trends and Solutions
Eva De Clercq, Jane Kaye, Susan M Wolf, et al.
Journal of Community Genetics
|
January 25, 2018
Desiderata for digital consent in genomic research
Carlos Luis Parra-Calderón, Jane Kaye, Alberto Moreno-Conde, et al.
European Journal of Health Law
|
December 2, 2011
Consent forms in genomics: the difference between law and practice
Paula Boddington, Liam Curren, Jane Kaye, et al.
Journal of Law and Medicine
|
January 8, 2021
Clinical Decision Support Systems and Medico-Legal Liability in Recall and Treatment: A Fresh Examination
Megan Prictor, Mark Taylor, Jane Kaye, et al.
European Journal of Health Law
|
September 30, 2010
Identifiability, genomics and U.K. data protection law
Liam Curren, Paula Boddington, Heather Gowans, et al.
Journal of Medical Internet Research
|
April 17, 2016
Patient Perspectives on Sharing Anonymized Personal Health Data Using a Digital System for Dynamic Consent and Research Feedback: A Qualitative Study
Karen Spencer, Caroline Sanders, Edgar A Whitley, et al.
Page
of 10
Search research articles
Search
Showing results (31-40 of 99) with videos related to
Sort By:
Page
of 10
Life Sciences, Society and Policy
|
November 18, 2015
The evolution of withdrawal: negotiating research relationships in biobanking
Karen Melham, Linda Briceno Moraia, Colin Mitchell, et al.
European Journal of Health Law
|
September 8, 2005
Lessons from European population genetic databases: comparing the law in Estonia, Iceland, Sweden and the United Kingdom
Susan M C Gibbons, Hördur Helgi Helgason, Jane Kaye, et al.
Pharmacogenomics
|
June 4, 2008
Sample, data use and protection in biobanking in Europe: legal issues
Eleni Zika, Tobias Schulte In den Bäumen, Jane Kaye, et al.
European Journal of Human Genetics : EJHG
|
May 8, 2014
Dynamic consent: a patient interface for twenty-first century research networks
Jane Kaye, Edgar A Whitley, David Lund, et al.
Genetic Testing and Molecular Biomarkers
|
February 2, 2017
Returning Results in Biobank Research: Global Trends and Solutions
Eva De Clercq, Jane Kaye, Susan M Wolf, et al.
Journal of Community Genetics
|
January 25, 2018
Desiderata for digital consent in genomic research
Carlos Luis Parra-Calderón, Jane Kaye, Alberto Moreno-Conde, et al.
European Journal of Health Law
|
December 2, 2011
Consent forms in genomics: the difference between law and practice
Paula Boddington, Liam Curren, Jane Kaye, et al.
Journal of Law and Medicine
|
January 8, 2021
Clinical Decision Support Systems and Medico-Legal Liability in Recall and Treatment: A Fresh Examination
Megan Prictor, Mark Taylor, Jane Kaye, et al.
European Journal of Health Law
|
September 30, 2010
Identifiability, genomics and U.K. data protection law
Liam Curren, Paula Boddington, Heather Gowans, et al.
Journal of Medical Internet Research
|
April 17, 2016
Patient Perspectives on Sharing Anonymized Personal Health Data Using a Digital System for Dynamic Consent and Research Feedback: A Qualitative Study
Karen Spencer, Caroline Sanders, Edgar A Whitley, et al.
Page
of 10