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Research Involvement and Engagement
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February 2, 2021
The practice of active patient involvement in rare disease research using ICT: experiences and lessons from the RUDY JAPAN project
Nao Hamakawa, Atsushi Kogetsu, Moeko Isono, et al.
Journal of Medical Internet Research
|
November 23, 2023
Public Preferences for Digital Health Data Sharing: Discrete Choice Experiment Study in 12 European Countries
Roberta Biasiotto, Jennifer Viberg Johansson, Melaku Birhanu Alemu, et al.
Science (New York, N.Y.)
|
May 4, 2019
Consent insufficient for data release
Dianne Nicol, Lisa Eckstein, Heidi Beate Bentzen, et al.
BMC Pregnancy and Childbirth
|
January 22, 2016
eRegistries: Electronic registries for maternal and child health
J Frederik Frøen, Sonja L Myhre, Michael J Frost, et al.
British Journal of Sports Medicine
|
November 20, 2015
Direct-to-consumer genetic testing for predicting sports performance and talent identification: Consensus statement
Nick Webborn, Alun Williams, Mike McNamee, et al.
Annals of Internal Medicine
|
February 19, 2019
Are Requirements to Deposit Data in Research Repositories Compatible With the European Union's General Data Protection Regulation?
Deborah Mascalzoni, Heidi Beate Bentzen, Isabelle Budin-Ljøsne, et al.
Human Genomics
|
March 9, 2018
Including all voices in international data-sharing governance
Jane Kaye, Sharon F Terry, Eric Juengst, et al.
Plos Biology
|
March 28, 2008
Research ethics recommendations for whole-genome research: consensus statement
Timothy Caulfield, Amy L McGuire, Mildred Cho, et al.
The Journal of Pediatrics
|
May 28, 2023
Concordance of International Regulation of Pediatric Health Research
Mark A Rothstein, Dimitri Patrinos, Kyle B Brothers, et al.
Nature Genetics
|
January 8, 2021
Toward better governance of human genomic data
Kieran C O'Doherty, Mahsa Shabani, Edward S Dove, et al.
Page
of 10
Search research articles
Search
Showing results (81-90 of 99) with videos related to
Sort By:
Page
of 10
Research Involvement and Engagement
|
February 2, 2021
The practice of active patient involvement in rare disease research using ICT: experiences and lessons from the RUDY JAPAN project
Nao Hamakawa, Atsushi Kogetsu, Moeko Isono, et al.
Journal of Medical Internet Research
|
November 23, 2023
Public Preferences for Digital Health Data Sharing: Discrete Choice Experiment Study in 12 European Countries
Roberta Biasiotto, Jennifer Viberg Johansson, Melaku Birhanu Alemu, et al.
Science (New York, N.Y.)
|
May 4, 2019
Consent insufficient for data release
Dianne Nicol, Lisa Eckstein, Heidi Beate Bentzen, et al.
BMC Pregnancy and Childbirth
|
January 22, 2016
eRegistries: Electronic registries for maternal and child health
J Frederik Frøen, Sonja L Myhre, Michael J Frost, et al.
British Journal of Sports Medicine
|
November 20, 2015
Direct-to-consumer genetic testing for predicting sports performance and talent identification: Consensus statement
Nick Webborn, Alun Williams, Mike McNamee, et al.
Annals of Internal Medicine
|
February 19, 2019
Are Requirements to Deposit Data in Research Repositories Compatible With the European Union's General Data Protection Regulation?
Deborah Mascalzoni, Heidi Beate Bentzen, Isabelle Budin-Ljøsne, et al.
Human Genomics
|
March 9, 2018
Including all voices in international data-sharing governance
Jane Kaye, Sharon F Terry, Eric Juengst, et al.
Plos Biology
|
March 28, 2008
Research ethics recommendations for whole-genome research: consensus statement
Timothy Caulfield, Amy L McGuire, Mildred Cho, et al.
The Journal of Pediatrics
|
May 28, 2023
Concordance of International Regulation of Pediatric Health Research
Mark A Rothstein, Dimitri Patrinos, Kyle B Brothers, et al.
Nature Genetics
|
January 8, 2021
Toward better governance of human genomic data
Kieran C O'Doherty, Mahsa Shabani, Edward S Dove, et al.
Page
of 10