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Digital Health
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June 27, 2018
Towards 'Engagement 2.0': Insights from a study of dynamic consent with biobank participants
Harriet Ja Teare, Michael Morrison, Edgar A Whitley, et al.
Life Sciences, Society and Policy
|
September 29, 2015
'Pop-Up' Governance: developing internal governance frameworks for consortia: the example of UK10K
Jane Kaye, Dawn Muddyman, Carol Smee, et al.
Genome Medicine
|
September 15, 2009
Planning for translational research in genomics
Naomi Hawkins, Jantina de Vries, Paula Boddington, et al.
Science (New York, N.Y.)
|
November 22, 2008
The path forward for DNA data
Paula Boddington, Naomi Hawkins, Catherine Heeney, et al.
European Journal of Human Genetics : EJHG
|
November 6, 2009
Ethical implications of the use of whole genome methods in medical research
Jane Kaye, Paula Boddington, Jantina de Vries, et al.
Nature Reviews. Genetics
|
March 25, 2009
Data sharing in genomics--re-shaping scientific practice
Jane Kaye, Catherine Heeney, Naomi Hawkins, et al.
Regenerative Medicine
|
October 5, 2017
The European General Data Protection Regulation: challenges and considerations for iPSC researchers and biobanks
Michael Morrison, Jessica Bell, Carol George, et al.
Medical Law Review
|
October 19, 2013
Can I access my personal genome? The current legal position in the UK
Jane Kaye, Nadja Kanellopoulou, Naomi Hawkins, et al.
JMIR Research Protocols
|
December 14, 2017
Participant-Centric Initiatives and Medical Research: Scoping Review Protocol
Victoria Coathup, Nao Hamakawa, Teresa Finlay, et al.
The Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics
|
April 29, 2020
Australian Aboriginal and Torres Strait Islander Collections of Genetic Heritage: The Legal, Ethical and Practical Considerations of a Dynamic Consent Approach to Decision Making
Megan Prictor, Sharon Huebner, Harriet J A Teare, et al.
Page
of 10
Search research articles
Search
Showing results (21-30 of 99) with videos related to
Sort By:
Page
of 10
Digital Health
|
June 27, 2018
Towards 'Engagement 2.0': Insights from a study of dynamic consent with biobank participants
Harriet Ja Teare, Michael Morrison, Edgar A Whitley, et al.
Life Sciences, Society and Policy
|
September 29, 2015
'Pop-Up' Governance: developing internal governance frameworks for consortia: the example of UK10K
Jane Kaye, Dawn Muddyman, Carol Smee, et al.
Genome Medicine
|
September 15, 2009
Planning for translational research in genomics
Naomi Hawkins, Jantina de Vries, Paula Boddington, et al.
Science (New York, N.Y.)
|
November 22, 2008
The path forward for DNA data
Paula Boddington, Naomi Hawkins, Catherine Heeney, et al.
European Journal of Human Genetics : EJHG
|
November 6, 2009
Ethical implications of the use of whole genome methods in medical research
Jane Kaye, Paula Boddington, Jantina de Vries, et al.
Nature Reviews. Genetics
|
March 25, 2009
Data sharing in genomics--re-shaping scientific practice
Jane Kaye, Catherine Heeney, Naomi Hawkins, et al.
Regenerative Medicine
|
October 5, 2017
The European General Data Protection Regulation: challenges and considerations for iPSC researchers and biobanks
Michael Morrison, Jessica Bell, Carol George, et al.
Medical Law Review
|
October 19, 2013
Can I access my personal genome? The current legal position in the UK
Jane Kaye, Nadja Kanellopoulou, Naomi Hawkins, et al.
JMIR Research Protocols
|
December 14, 2017
Participant-Centric Initiatives and Medical Research: Scoping Review Protocol
Victoria Coathup, Nao Hamakawa, Teresa Finlay, et al.
The Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics
|
April 29, 2020
Australian Aboriginal and Torres Strait Islander Collections of Genetic Heritage: The Legal, Ethical and Practical Considerations of a Dynamic Consent Approach to Decision Making
Megan Prictor, Sharon Huebner, Harriet J A Teare, et al.
Page
of 10