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1.

Concordance of International Regulation of Pediatric Health Research.

Rothstein, Mark A; Patrinos, Dimitri; Brothers, Kyle B; Clayton, Ellen Wright; Joly, Yann; Zawati, Ma'n H; Andanda, Pamela; Arawi, Thalia; Castañeda, Mireya; Chalmers, Don; Chen, Haidan; Ghaly, Mohammed; Hatanaka, Ryoko; Hendriks, Aart C; Ho, Calvin W L; Kaye, Jane; Krekora-Zajac, Dorota; Lee, Won Bok; Mattsson, Titti; Nicolás, Pilar; Nnamuchi, Obiajulu; Rial-Sebbag, Emmanuelle; Siegal, Gil; Wathuta, Jane M; Knoppers, Bartha Maria.

J Pediatr; 260: 113524, 2023 09.

Artículo en Inglés | MEDLINE | ID: mdl-37245625

2.

Provenance and risk in transfer of biological materials.

Nielsen, Jane; Bubela, Tania; Chalmers, Don R C; Johns, Amber; Kahl, Linda; Kamens, Joanne; Lawson, Charles; Liddicoat, John; McWhirter, Rebekah; Monotti, Ann; Scheibner, James; Whitton, Tess; Nicol, Dianne.

PLoS Biol; 16(8): e2006031, 2018 08.

Artículo en Inglés | MEDLINE | ID: mdl-30102688

3.

Genomics: data sharing needs an international code of conduct.

Phillips, Mark; Molnár-Gábor, Fruzsina; Korbel, Jan O; Thorogood, Adrian; Joly, Yann; Chalmers, Don; Townend, David; Knoppers, Bartha M.

Nature; 578(7793): 31-33, 2020 02.

Artículo en Inglés | MEDLINE | ID: mdl-32025008

4.

Australian Perspectives on the Ethical and Regulatory Considerations for Responsible Data Sharing in Response to the COVID-19 Pandemic.

Nicol, Dianne; Chalmers, Don; Critchley, Christine; Eckstein, Lisa; Nielsen, Jane; Otlowski, Margaret.

J Law Med; 27(4): 829-838, 2020 Aug.

Artículo en Inglés | MEDLINE | ID: mdl-32880401

5.

Including all voices in international data-sharing governance.

Kaye, Jane; Terry, Sharon F; Juengst, Eric; Coy, Sarah; Harris, Jennifer R; Chalmers, Don; Dove, Edward S; Budin-Ljøsne, Isabelle; Adebamowo, Clement; Ogbe, Emilomo; Bezuidenhout, Louise; Morrison, Michael; Minion, Joel T; Murtagh, Madeleine J; Minari, Jusaku; Teare, Harriet; Isasi, Rosario; Kato, Kazuto; Rial-Sebbag, Emmanuelle; Marshall, Patricia; Koenig, Barbara; Cambon-Thomsen, Anne.

Hum Genomics; 12(1): 13, 2018 03 07.

Artículo en Inglés | MEDLINE | ID: mdl-29514717

6.

Has the biobank bubble burst? Withstanding the challenges for sustainable biobanking in the digital era.

Chalmers, Don; Nicol, Dianne; Kaye, Jane; Bell, Jessica; Campbell, Alastair V; Ho, Calvin W L; Kato, Kazuto; Minari, Jusaku; Ho, Chih-Hsing; Mitchell, Colin; Molnár-Gábor, Fruzsina; Otlowski, Margaret; Thiel, Daniel; Fullerton, Stephanie M; Whitton, Tess.

BMC Med Ethics; 17(1): 39, 2016 07 12.

Artículo en Inglés | MEDLINE | ID: mdl-27405974

7.

Is Australia Well Equipped to Deal with Future Clinical Trials?

Eckstein, Lisa; Chalmers, Don.

J Law Med; 24(2): 337-41, 2016.

Artículo en Inglés | MEDLINE | ID: mdl-30137707

8.

Public reaction to direct-to-consumer online genetic tests: Comparing attitudes, trust and intentions across commercial and conventional providers.

Critchley, Christine; Nicol, Dianne; Otlowski, Margaret; Chalmers, Don.

Public Underst Sci; 24(6): 731-50, 2015 Aug.

Artículo en Inglés | MEDLINE | ID: mdl-24553439

9.

Personalised medicine in the genome era.

Chalmers, Don; Nicol, Dianne; Otlowski, Margaret; Critchley, Christine.

J Law Med; 20(3): 577-94, 2013 Mar.

Artículo en Inglés | MEDLINE | ID: mdl-23600190

10.

Body ownership and research.

McWhirter, Rebekah E; Nicol, Dianne; Chalmers, Don; Dickinson, Joanne L.

J Law Med; 21(2): 323-9, 2013 Dec.

Artículo en Inglés | MEDLINE | ID: mdl-24597380

11.

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

McWhirter, Rebekah; Eckstein, Lisa; Chalmers, Don; Critchley, Christine; Nielsen, Jane; Otlowski, Margaret; Nicol, Dianne.

J Empir Res Hum Res Ethics; 15(4): 355-364, 2020 10.

Artículo en Inglés | MEDLINE | ID: mdl-32425102

12.

Public reactions to direct-to-consumer genetic health tests: A comparison across the US, UK, Japan and Australia.

Charbonneau, Jan; Nicol, Dianne; Chalmers, Don; Kato, Kazuto; Yamamoto, Natsuko; Walshe, Jarrod; Critchley, Christine.

Eur J Hum Genet; 28(3): 339-348, 2020 03.

Artículo en Inglés | MEDLINE | ID: mdl-31645768

13.

Data sharing in the post-genomic world: the experience of the International Cancer Genome Consortium (ICGC) Data Access Compliance Office (DACO).

Joly, Yann; Dove, Edward S; Knoppers, Bartha M; Bobrow, Martin; Chalmers, Don.

PLoS Comput Biol; 8(7): e1002549, 2012.

Artículo en Inglés | MEDLINE | ID: mdl-22807659

14.

Human genetic research databases and biobanks: towards uniform terminology and Australian best practice.

Chalmers, Don; Nicol, Dianne.

J Law Med; 15(4): 538-55, 2008 Feb.

Artículo en Inglés | MEDLINE | ID: mdl-18365521

15.

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

Nicol, Dianne; Eckstein, Lisa; Morrison, Michael; Sherkow, Jacob S; Otlowski, Margaret; Whitton, Tess; Bubela, Tania; Burdon, Kathryn P; Chalmers, Don; Chan, Sarah; Charlesworth, Jac; Critchley, Christine; Crossley, Merlin; de Lacey, Sheryl; Dickinson, Joanne L; Hewitt, Alex W; Kamens, Joanne; Kato, Kazuto; Kleiderman, Erika; Kodama, Satoshi; Liddicoat, John; Mackey, David A; Newson, Ainsley J; Nielsen, Jane; Wagner, Jennifer K; McWhirter, Rebekah E.

Genome Med; 9(1): 85, 2017 09 25.

Artículo en Inglés | MEDLINE | ID: mdl-28946923

16.

A decision tool to guide the ethics review of a challenging breed of emerging genomic projects.

Joly, Yann; So, Derek; Osien, Gladys; Crimi, Laura; Bobrow, Martin; Chalmers, Don; Wallace, Susan E; Zeps, Nikolajs; Knoppers, Bartha.

Eur J Hum Genet; 24(8): 1099-103, 2016 08.

Artículo en Inglés | MEDLINE | ID: mdl-26785834

17.

Toward better governance of human genomic data.

O'Doherty, Kieran C; Shabani, Mahsa; Dove, Edward S; Bentzen, Heidi Beate; Borry, Pascal; Burgess, Michael M; Chalmers, Don; De Vries, Jantina; Eckstein, Lisa; Fullerton, Stephanie M; Juengst, Eric; Kato, Kazuto; Kaye, Jane; Knoppers, Bartha Maria; Koenig, Barbara A; Manson, Spero M; McGrail, Kimberlyn M; McGuire, Amy L; Meslin, Eric M; Nicol, Dianne; Prainsack, Barbara; Terry, Sharon F; Thorogood, Adrian; Burke, Wylie.

Nat Genet; 53(1): 2-8, 2021 01.

Artículo en Inglés | MEDLINE | ID: mdl-33414545

18.

Biobanking and Privacy Laws in Australia.

Chalmers, Don.

J Law Med Ethics; 43(4): 703-13, 2015.

Artículo en Inglés | MEDLINE | ID: mdl-26711411

19.

Professional self-regulation and guidelines in assisted reproduction.

Chalmers, Don.

J Law Med; 9(4): 414-28, 2002 May.

Artículo en Inglés | MEDLINE | ID: mdl-12194473

20.

The expectation gap, risk management and the Australian HREC system.

Chalmers, Don.

Monash Bioeth Rev; 21(3): S49-57, 2002 Jul.

Artículo en Inglés | MEDLINE | ID: mdl-15810194

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Concordance of International Regulation of Pediatric Health Research.

Provenance and risk in transfer of biological materials.

Genomics: data sharing needs an international code of conduct.

Australian Perspectives on the Ethical and Regulatory Considerations for Responsible Data Sharing in Response to the COVID-19 Pandemic.

Including all voices in international data-sharing governance.

Has the biobank bubble burst? Withstanding the challenges for sustainable biobanking in the digital era.

Is Australia Well Equipped to Deal with Future Clinical Trials?

Public reaction to direct-to-consumer online genetic tests: Comparing attitudes, trust and intentions across commercial and conventional providers.

Personalised medicine in the genome era.

Body ownership and research.

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

Public reactions to direct-to-consumer genetic health tests: A comparison across the US, UK, Japan and Australia.

Data sharing in the post-genomic world: the experience of the International Cancer Genome Consortium (ICGC) Data Access Compliance Office (DACO).

Human genetic research databases and biobanks: towards uniform terminology and Australian best practice.

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

A decision tool to guide the ethics review of a challenging breed of emerging genomic projects.

Toward better governance of human genomic data.

Biobanking and Privacy Laws in Australia.

Professional self-regulation and guidelines in assisted reproduction.

The expectation gap, risk management and the Australian HREC system.