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Robert Cook-Deegan

Showing results (91-100 of 116) with videos related to

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Plos One|October 14, 2021
A survey of U.S. public perspectives on facial recognition technology and facial imaging data practices in health and research contextsSara H Katsanis, Peter Claes, Megan Doerr, et al.
Applied & Translational Genomics|September 27, 2016
Barriers to clinical adoption of next generation sequencing: Perspectives of a policy Delphi panelDonna A Messner, Jennifer Al Naber, Pei Koay, et al.
IEEE Transactions on Technology and Society|April 1, 2022
U.S. Adult Perspectives on Facial Images, DNA, and Other BiometricsSara H Katsanis, Peter Claes, Megan Doerr, et al.
JCO Precision Oncology|August 8, 2024
"I Just Assumed This Was Already Being Done": Canadian Patient Preferences for Enhanced Data Sharing for Precision OncologySamantha Pollard, Morgan Ehman, Anna Hermansen, et al.
Plos Medicine|September 26, 2008
Ethical and practical issues associated with aggregating databasesDavid R Karp, Shelley Carlin, Robert Cook-Deegan, et al.
The New England Journal of Medicine|July 17, 2009
Disclosure of APOE genotype for risk of Alzheimer's diseaseRobert C Green, J Scott Roberts, L Adrienne Cupples, et al.
The American Journal of Bioethics : AJOB|August 26, 2015
Broad Consent for Research With Biological Samples: Workshop ConclusionsChristine Grady, Lisa Eckstein, Ben Berkman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 18, 2008
Incorporating ethnicity into genetic risk assessment for Alzheimer disease: the REVEAL study experienceKurt D Christensen, J Scott Roberts, Charmaine D M Royal, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 16, 2014
A randomized noninferiority trial of condensed protocols for genetic risk disclosure of Alzheimer's diseaseRobert C Green, Kurt D Christensen, L Adrienne Cupples, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 21, 2017
A randomized controlled trial of disclosing genetic risk information for Alzheimer disease via telephoneKurt D Christensen, Wendy R Uhlmann, J Scott Roberts, et al.
Pageof 12

Showing results (91-100 of 116) with videos related to

Sort By:
Pageof 12
Plos One|October 14, 2021
A survey of U.S. public perspectives on facial recognition technology and facial imaging data practices in health and research contextsSara H Katsanis, Peter Claes, Megan Doerr, et al.
Applied & Translational Genomics|September 27, 2016
Barriers to clinical adoption of next generation sequencing: Perspectives of a policy Delphi panelDonna A Messner, Jennifer Al Naber, Pei Koay, et al.
IEEE Transactions on Technology and Society|April 1, 2022
U.S. Adult Perspectives on Facial Images, DNA, and Other BiometricsSara H Katsanis, Peter Claes, Megan Doerr, et al.
JCO Precision Oncology|August 8, 2024
"I Just Assumed This Was Already Being Done": Canadian Patient Preferences for Enhanced Data Sharing for Precision OncologySamantha Pollard, Morgan Ehman, Anna Hermansen, et al.
Plos Medicine|September 26, 2008
Ethical and practical issues associated with aggregating databasesDavid R Karp, Shelley Carlin, Robert Cook-Deegan, et al.
The New England Journal of Medicine|July 17, 2009
Disclosure of APOE genotype for risk of Alzheimer's diseaseRobert C Green, J Scott Roberts, L Adrienne Cupples, et al.
The American Journal of Bioethics : AJOB|August 26, 2015
Broad Consent for Research With Biological Samples: Workshop ConclusionsChristine Grady, Lisa Eckstein, Ben Berkman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 18, 2008
Incorporating ethnicity into genetic risk assessment for Alzheimer disease: the REVEAL study experienceKurt D Christensen, J Scott Roberts, Charmaine D M Royal, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 16, 2014
A randomized noninferiority trial of condensed protocols for genetic risk disclosure of Alzheimer's diseaseRobert C Green, Kurt D Christensen, L Adrienne Cupples, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 21, 2017
A randomized controlled trial of disclosing genetic risk information for Alzheimer disease via telephoneKurt D Christensen, Wendy R Uhlmann, J Scott Roberts, et al.
Pageof 12