Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Don Chalmers

Showing results (11-20 of 28) with videos related to

Pageof 3
Sort By:
Public Understanding of Science (Bristol, England)|February 21, 2014
Public reaction to direct-to-consumer online genetic tests: Comparing attitudes, trust and intentions across commercial and conventional providersChristine Critchley, Dianne Nicol, Margaret Otlowski, et al.
Journal of Law and Medicine|April 23, 2013
Personalised medicine in the genome eraDon Chalmers, Dianne Nicol, Margaret Otlowski, et al.
Journal of Law and Medicine|March 7, 2014
Body ownership and researchRebekah E McWhirter, Dianne Nicol, Don Chalmers, et al.
Journal of Law and Medicine|September 4, 2020
Australian Perspectives on the Ethical and Regulatory Considerations for Responsible Data Sharing in Response to the COVID-19 PandemicDianne Nicol, Don Chalmers, Christine Critchley, et al.
Plos Computational Biology|July 19, 2012
Data sharing in the post-genomic world: the experience of the International Cancer Genome Consortium (ICGC) Data Access Compliance Office (DACO)Yann Joly, Edward S Dove, Bartha M Knoppers, et al.
European Journal of Human Genetics : EJHG|October 25, 2019
Public reactions to direct-to-consumer genetic health tests: A comparison across the US, UK, Japan and AustraliaJan Charbonneau, Dianne Nicol, Don Chalmers, et al.
Journal of Empirical Research on Human Research Ethics : JERHRE|May 20, 2020
A Scenario-Based Methodology for Analyzing the Ethical, Legal, and Social Issues in Genomic Data SharingRebekah McWhirter, Lisa Eckstein, Don Chalmers, et al.
European Journal of Human Genetics : EJHG|January 21, 2016
A decision tool to guide the ethics review of a challenging breed of emerging genomic projectsYann Joly, Derek So, Gladys Osien, et al.
Nature|February 7, 2020
Genomics: data sharing needs an international code of conductMark Phillips, Fruzsina Molnár-Gábor, Jan O Korbel, et al.
Journal of Personalized Medicine|January 8, 2015
Community engagement for big epidemiology: deliberative democracy as a toolRebekah E McWhirter, Christine R Critchley, Dianne Nicol, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
Public Understanding of Science (Bristol, England)|February 21, 2014
Public reaction to direct-to-consumer online genetic tests: Comparing attitudes, trust and intentions across commercial and conventional providersChristine Critchley, Dianne Nicol, Margaret Otlowski, et al.
Journal of Law and Medicine|April 23, 2013
Personalised medicine in the genome eraDon Chalmers, Dianne Nicol, Margaret Otlowski, et al.
Journal of Law and Medicine|March 7, 2014
Body ownership and researchRebekah E McWhirter, Dianne Nicol, Don Chalmers, et al.
Journal of Law and Medicine|September 4, 2020
Australian Perspectives on the Ethical and Regulatory Considerations for Responsible Data Sharing in Response to the COVID-19 PandemicDianne Nicol, Don Chalmers, Christine Critchley, et al.
Plos Computational Biology|July 19, 2012
Data sharing in the post-genomic world: the experience of the International Cancer Genome Consortium (ICGC) Data Access Compliance Office (DACO)Yann Joly, Edward S Dove, Bartha M Knoppers, et al.
European Journal of Human Genetics : EJHG|October 25, 2019
Public reactions to direct-to-consumer genetic health tests: A comparison across the US, UK, Japan and AustraliaJan Charbonneau, Dianne Nicol, Don Chalmers, et al.
Journal of Empirical Research on Human Research Ethics : JERHRE|May 20, 2020
A Scenario-Based Methodology for Analyzing the Ethical, Legal, and Social Issues in Genomic Data SharingRebekah McWhirter, Lisa Eckstein, Don Chalmers, et al.
European Journal of Human Genetics : EJHG|January 21, 2016
A decision tool to guide the ethics review of a challenging breed of emerging genomic projectsYann Joly, Derek So, Gladys Osien, et al.
Nature|February 7, 2020
Genomics: data sharing needs an international code of conductMark Phillips, Fruzsina Molnár-Gábor, Jan O Korbel, et al.
Journal of Personalized Medicine|January 8, 2015
Community engagement for big epidemiology: deliberative democracy as a toolRebekah E McWhirter, Christine R Critchley, Dianne Nicol, et al.
Pageof 3