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The Right to Liberty in a Pandemic

University of Queensland law journal, 2021-12, Vol.40 (2), p.159-179

McWhirter, Rebekah

2021

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Understanding public reactions to commercialization of biobanks and use of biobank resources

Social science & medicine (1982), 2016-08, Vol.162, p.79-87

2016

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Performance data and informed consent: a duty to disclose?

Medical journal of Australia, 2017-08, Vol.207 (3), p.100-101

McWhirter, Rebekah E

2017

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Expertise, public health and the European Convention on Human Rights: 'Vavricka' v 'Czech Republic'

Modern law review, 2023-07, Vol.86 (4), p.1035-1048

2023

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Australian Attitudes Towards Waivers of Consent Within the Context of Genomic Data Sharing

Journal of empirical research on human research ethics, 2024-07, Vol.19 (3), p.113-123

2024

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Informed consent and performance data : clinician experience as a material risk

University of New South Wales law journal, 2017-01, Vol.40 (2), p.566-589

McWhirter, Rebekah

2017

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Identifying public expectations of genetic biobanks

Public understanding of science (Bristol, England), 2017-08, Vol.26 (6), p.671-687

2017

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Context matters in genomic data sharing: a qualitative investigation into responses from the Australian public

BMC medical genomics, 2023-04, Vol.15 (Suppl 3), p.275-16, Article 275

2023

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General practitioner perceptions of assessment and reporting of absolute cardiovascular disease risk via pathology services: a qualitative study

Family practice, 2021-03, Vol.38 (2), p.173-179

2021

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Reversing the 'quasi-tribunal' role of human research ethics committees: A waiver of consent case study

University of New South Wales law journal, 2023-07, Vol.46 (2), p.498-534

2023

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Australian human research ethics committee members' confidence in reviewing genomic research applications

European journal of human genetics : EJHG, 2021-12, Vol.29 (12), p.1811-1818

2021

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All in the Blood: A Review of Aboriginal Australians’ Cultural Beliefs About Blood and Implications for Biospecimen Research

Journal of empirical research on human research ethics, 2015-10, Vol.10 (4), p.347-359

2015

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A Scenario-Based Methodology for Analyzing the Ethical, Legal, and Social Issues in Genomic Data Sharing

Journal of empirical research on human research ethics, 2020-10, Vol.15 (4), p.355-364

2020

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General practitioners maintain a focus on blood pressure management rather than absolute cardiovascular disease risk management

Journal of evaluation in clinical practice, 2021-12, Vol.27 (6), p.1353-1360

2021

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Integration of absolute cardiovascular disease risk assessment into routine blood cholesterol testing at pathology services

Family practice, 2020-10, Vol.37 (5), p.675-681

2020

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Margaret Brazier, Law and Healing: A History of a Stormy Marriage

Medical law review, 2024-05, Vol.32 (2), p.281-286

McWhirter, Rebekah

2024

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Moving Forward on Consent Practices in Australia

Journal of bioethical inquiry, 2018-06, Vol.15 (2), p.243-257

2018

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Provenance and risk in transfer of biological materials

PLoS biology, 2018-08, Vol.16 (8), p.e2006031-e2006031

2018

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Community engagement for big epidemiology: deliberative democracy as a tool

Journal of personalized medicine, 2014-11, Vol.4 (4), p.459-474

2014

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Recurrence patterns identify aggressive form of human papillomavirus‐dependent vulvar cancer

Australian & New Zealand journal of obstetrics & gynaecology, 2020-04, Vol.60 (2), p.231-237

2020

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Key challenges in bringing CRISPR-mediated somatic cell therapy into the clinic

Genome medicine, 2017-09, Vol.9 (1), p.85-85, Article 85

2017

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Ethical genetic research in Indigenous communities: challenges and successful approaches

Trends in molecular medicine, 2012-12, Vol.18 (12), p.702-708

2012

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Self-directed multimedia process for delivering participant informed consent

BMJ open, 2020-07, Vol.10 (7), p.e036977-e036977

2020

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Vaccine Hesitancy: Public Trust, Expertise, and the War on Science by Maya J. Goldenberg

International journal of feminist approaches to bioethics, 2022-02, Vol.15 (1), p.202-205

McWhirter, Rebekah

2022

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Genome-wide homozygosity and multiple sclerosis in Orkney and Shetland Islanders

European journal of human genetics : EJHG, 2012-02, Vol.20 (2), p.198-202

2012

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The Right to Liberty in a Pandemic

Understanding public reactions to commercialization of biobanks and use of biobank resources

Performance data and informed consent: a duty to disclose?

Expertise, public health and the European Convention on Human Rights: 'Vavricka' v 'Czech Republic'

Australian Attitudes Towards Waivers of Consent Within the Context of Genomic Data Sharing

Informed consent and performance data : clinician experience as a material risk

Identifying public expectations of genetic biobanks

Context matters in genomic data sharing: a qualitative investigation into responses from the Australian public

General practitioner perceptions of assessment and reporting of absolute cardiovascular disease risk via pathology services: a qualitative study

Reversing the 'quasi-tribunal' role of human research ethics committees: A waiver of consent case study

Australian human research ethics committee members' confidence in reviewing genomic research applications

All in the Blood: A Review of Aboriginal Australians’ Cultural Beliefs About Blood and Implications for Biospecimen Research

A Scenario-Based Methodology for Analyzing the Ethical, Legal, and Social Issues in Genomic Data Sharing

General practitioners maintain a focus on blood pressure management rather than absolute cardiovascular disease risk management

Integration of absolute cardiovascular disease risk assessment into routine blood cholesterol testing at pathology services

Margaret Brazier, Law and Healing: A History of a Stormy Marriage

Moving Forward on Consent Practices in Australia

Provenance and risk in transfer of biological materials

Community engagement for big epidemiology: deliberative democracy as a tool

Recurrence patterns identify aggressive form of human papillomavirus‐dependent vulvar cancer

Key challenges in bringing CRISPR-mediated somatic cell therapy into the clinic

Ethical genetic research in Indigenous communities: challenges and successful approaches

Self-directed multimedia process for delivering participant informed consent

Vaccine Hesitancy: Public Trust, Expertise, and the War on Science by Maya J. Goldenberg

Genome-wide homozygosity and multiple sclerosis in Orkney and Shetland Islanders

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