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Author Details
Full Name
Don Chalmers
Affiliation
University of Tasmania
ORCID
Career Start Year
1993
Papers
42
H Index
13
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37245625
Concordance of International Regulation of Pediatric Health Research.
J Pediatr
2023
33414545
Toward better governance of human genomic data.
Nat Genet
2021
32425102
A Scenario-Based Methodology for Analyzing the Ethical, Legal, and Social Issues in Genomic Data Sharing.
J Empir Res Hum Res Ethics
2020
31645768
Public reactions to direct-to-consumer genetic health tests: A comparison across the US, UK, Japan and Australia.
Eur J Hum Genet
2020
32025008
Genomics: data sharing needs an international code of conduct.
Nature
2020
32880401
Australian Perspectives on the Ethical and Regulatory Considerations for Responsible Data Sharing in Response to the COVID-19 Pandemic.
J Law Med
2020
31048483
Consent insufficient for data release.
Science
2019
29514717
Including all voices in international data-sharing governance.
Hum Genomics
2018
30136006
Correction to: Australia: regulating genomic data sharing to promote public trust.
Hum Genet
2018
30102688
Provenance and risk in transfer of biological materials.
PLoS Biol
2018
30116956
Australia: regulating genomic data sharing to promote public trust.
Hum Genet
2018
28946923
Key challenges in bringing CRISPR-mediated somatic cell therapy into the clinic.
Genome Med
2017
28353264
Ethics and Governance of Stem Cell Banks.
Methods Mol Biol
2017
26785834
A decision tool to guide the ethics review of a challenging breed of emerging genomic projects.
Eur J Hum Genet
2016
30137707
Is Australia Well Equipped to Deal with Future Clinical Trials?
J Law Med
2016
27405974
Has the biobank bubble burst? Withstanding the challenges for sustainable biobanking in the digital era.
BMC Med Ethics
2016
24553439
Public reaction to direct-to-consumer online genetic tests: Comparing attitudes, trust and intentions across commercial and conventional providers.
Public Underst Sci
2015
26711411
Biobanking and Privacy Laws in Australia.
J Law Med Ethics
2015
24911490
The International Cancer Genome Consortium's evolving data-protection policies.
Nat Biotechnol
2014
27294026
To share or not to share is the question.
Appl Transl Genom
2014
25563457
Community engagement for big epidemiology: deliberative democracy as a tool.
J Pers Med
2014
24965440
A role for research ethics committees in exchanges of human biospecimens through material transfer agreements.
J Bioeth Inq
2014
23600190
Personalised medicine in the genome era.
J Law Med
2013
24597380
Body ownership and research.
J Law Med
2013
22582247
Research priorities. ELSI 2.0 for genomics and society.
Science
2012
23520913
Legal aspects of genetic databases for international biomedical research: the example of the International Cancer Genome Consortium (ICGC).
Rev Derecho Genoma Hum
2012
22807659
Data sharing in the post-genomic world: the experience of the International Cancer Genome Consortium (ICGC) Data Access Compliance Office (DACO).
PLoS Comput Biol
2012
20949382
Genetic research and biobanks.
Methods Mol Biol
2011
21410787
Viewpoint: are the research ethics committees working in the best interests of participants in an increasingly globalized research environment?
J Intern Med
2011
18365521
Human genetic research databases and biobanks: towards uniform terminology and Australian best practice.
J Law Med
2008
15807347
Research involving humans: a time for change?
J Law Med Ethics
2004
14562469
Embryonic stem cell research: can the law balance ethical, scientific and economic values? (Part I).
Rev Derecho Genoma Hum
2003
15032099
Embryonic stem cell research: can the law balance ethical, scientific and economic values? (Part II).
Rev Derecho Genoma Hum
2003
12194473
Professional self-regulation and guidelines in assisted reproduction.
J Law Med
2002
15810194
The expectation gap, risk management and the Australian HREC system.
Monash Bioeth Rev
2002
12116675
Consent, commercialisation and benefit-sharing.
J Law Med
2001
10026665
Ethics committees: is reform in order?
Med J Aust
1999
10451677
New national guidelines for ethics committees are on the way.
Med J Aust
1999
9612458
The death of a healthy volunteer in a human research project: implications for Australian clinical research.
Med J Aust
1998
9469189
Towards a consensual culture in the ethical review of research. Australian Health Ethics Committee.
Med J Aust
1998
8293226
Malpractice liability for the failure to adequately educate patients: the Australian law of "informed consent" and its implications for American ethics committees.
Camb Q Healthc Ethics
1993
11660490
Rogers v. Whitaker and informed consent in Australia: a fair dinkum duty of disclosure.
Med Law Rev
1993
1 - 42 of 42
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University of Tasmania
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Osaka University
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University of Washington School of Medicine
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Nikolajs Zeps
Queensland University of Technology
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Inserm, Toulouse Paul Sabatier University
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Simon Fraser University
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Institute for Human Virology
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