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Research Square
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March 30, 2023
Big Advocacy, Little Recognition: The Hidden Work of Black Patients in Precision Medicine
Lynette Hammond Gerido, Kenneth Resnicow, Elena Stoffel, et al.
The Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics
|
April 18, 2019
What is a Medical Information Commons?
Juli M Bollinger, Peter D Zuk, Mary A Majumder, et al.
Personalized Medicine
|
December 13, 2017
Barriers to clinical adoption of next-generation sequencing: a policy Delphi panel's solutions
Donna A Messner, Pei Koay, Jennifer Al Naber, et al.
Journal of Community Genetics
|
September 29, 2023
Big advocacy, little recognition: the hidden work of Black patients in precision medicine
Lynette Hammond Gerido, Kenneth Resnicow, Elena M Stoffel, et al.
Journal of Personalized Medicine
|
April 10, 2015
Perspectives on genetic and genomic technologies in an academic medical center: the duke experience
Sara Huston Katsanis, Mollie A Minear, Allison Vorderstrasse, et al.
Journal of Contemporary Medical Education
|
August 4, 2015
Perceptions of Personalized Medicine in an Academic Health System: Educational Findings
Allison Vorderstrasse, Sara Huston Katsanis, Mollie A Minear, et al.
Journal of Personalized Medicine
|
August 6, 2021
Challenges to Building a Gene Variant Commons to Assess Hereditary Cancer Risk: Results of a Modified Policy Delphi Panel Deliberation
Mary A Majumder, Matthew L Blank, Janis Geary, et al.
The Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics
|
April 18, 2019
Hopeful and Concerned: Public Input on Building a Trustworthy Medical Information Commons
Patricia A Deverka, Dierdre Gilmore, Jennifer Richmond, et al.
Frontiers in Big Data
|
February 23, 2023
Fresh takes on five health data sharing domains: Quality, privacy, equity, incentives, and sustainability
Christi J Guerrini, Mary A Majumder, Jill O Robinson, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 19, 2022
Balancing openness with Indigenous data sovereignty: An opportunity to leave no one behind in the journey to sequence all of life
Ann M Mc Cartney, Jane Anderson, Libby Liggins, et al.
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of 12
Search research articles
Search
Showing results (81-90 of 116) with videos related to
Sort By:
Page
of 12
Research Square
|
March 30, 2023
Big Advocacy, Little Recognition: The Hidden Work of Black Patients in Precision Medicine
Lynette Hammond Gerido, Kenneth Resnicow, Elena Stoffel, et al.
The Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics
|
April 18, 2019
What is a Medical Information Commons?
Juli M Bollinger, Peter D Zuk, Mary A Majumder, et al.
Personalized Medicine
|
December 13, 2017
Barriers to clinical adoption of next-generation sequencing: a policy Delphi panel's solutions
Donna A Messner, Pei Koay, Jennifer Al Naber, et al.
Journal of Community Genetics
|
September 29, 2023
Big advocacy, little recognition: the hidden work of Black patients in precision medicine
Lynette Hammond Gerido, Kenneth Resnicow, Elena M Stoffel, et al.
Journal of Personalized Medicine
|
April 10, 2015
Perspectives on genetic and genomic technologies in an academic medical center: the duke experience
Sara Huston Katsanis, Mollie A Minear, Allison Vorderstrasse, et al.
Journal of Contemporary Medical Education
|
August 4, 2015
Perceptions of Personalized Medicine in an Academic Health System: Educational Findings
Allison Vorderstrasse, Sara Huston Katsanis, Mollie A Minear, et al.
Journal of Personalized Medicine
|
August 6, 2021
Challenges to Building a Gene Variant Commons to Assess Hereditary Cancer Risk: Results of a Modified Policy Delphi Panel Deliberation
Mary A Majumder, Matthew L Blank, Janis Geary, et al.
The Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics
|
April 18, 2019
Hopeful and Concerned: Public Input on Building a Trustworthy Medical Information Commons
Patricia A Deverka, Dierdre Gilmore, Jennifer Richmond, et al.
Frontiers in Big Data
|
February 23, 2023
Fresh takes on five health data sharing domains: Quality, privacy, equity, incentives, and sustainability
Christi J Guerrini, Mary A Majumder, Jill O Robinson, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 19, 2022
Balancing openness with Indigenous data sovereignty: An opportunity to leave no one behind in the journey to sequence all of life
Ann M Mc Cartney, Jane Anderson, Libby Liggins, et al.
Page
of 12