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Human Genetics|August 18, 2018
Australia: regulating genomic data sharing to promote public trustLisa Eckstein, Donald Chalmers, Christine Critchley, et al.Journal of Law and Medicine|January 8, 2021
Don Chalmers: His Contributions to Legal Research and Education, Health Law, and Research Ethics, Locally and GloballyDianne Nicol, Yann Joly, Jane Kaye, et al.BMC Medical Ethics|August 18, 2020
Public trust and global biobank networksLisa Dive, Christine Critchley, Margaret Otlowski, et al.Translational Vision Science & Technology|March 2, 2016
Ethical Considerations for the Return of Incidental Findings in Ophthalmic Genomic ResearchEmmanuelle Souzeau, Kathryn P Burdon, David A Mackey, et al.The Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics|March 4, 2022
Anti-Selection & Genetic Testing in Insurance: An Interdisciplinary PerspectiveDexter Golinghorst, Aisling de Paor, Yann Joly, et al.BMC Medical Ethics|August 14, 2025
Opportunities for a national genomic data governance framework in Australia: a systematic reviewFabian Cannizzo, Miranda E Vidgen, Rebekah McWhirter, et al.European Journal of Human Genetics : EJHG|July 31, 2019
Correction to: Genetic discrimination by Australian insurance companies: a survey of consumer experiencesJane Tiller, Susan Morris, Toni Rice, et al.American Journal of Medical Genetics. Part A|February 14, 2024
Australian researcher's perspectives on the Australian industry-led moratorium on genetic tests in life insuranceTatiane Yanes, Marisa Blencoe, Antonia Howard, et al.European Journal of Human Genetics : EJHG|July 9, 2019
Genetic discrimination by Australian insurance companies: a survey of consumer experiencesJane Tiller, Susan Morris, Toni Rice, 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 6