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Public Understanding of Science (Bristol, England)|August 19, 2020
Examining diversity in public willingness to participate in offshore human biobanking: An Australian mixed methods studyChristine Critchley, Miriam Wiersma, Wendy Lipworth, 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 One|February 19, 2021
Determining the willingness of Australians to export their corneas on deathHeather M Machin, Lisa Buckland, Christine Critchley, 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|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.
The Medical Journal of Australia|April 9, 2009
The influence of depression and anxiety on outcomes after an intervention for prediabetesMichael Kyrios, Susan M Moore, Naomi Hackworth, et al.
Human Genetics|August 18, 2018
Australia: regulating genomic data sharing to promote public trustLisa Eckstein, Donald Chalmers, Christine Critchley, et al.
Human Genetics|August 24, 2018
Correction to: Australia: regulating genomic data sharing to promote public trustLisa Eckstein, Donald Chalmers, Christine Critchley, et al.
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