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"CRISPR babies": What does this mean for science and Canada?

Canadian Medical Association journal (CMAJ), 2019-01, Vol.191 (4), p.E91-E92

2019

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Trust in genomic data sharing among members of the general public in the UK, USA, Canada and Australia

Human genetics, 2019-12, Vol.138 (11-12), p.1237-1246

2019

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The author who wasn't there? Fairness and attribution in publications following access to population biobanks

PloS one, 2018-03, Vol.13 (3), p.e0194997-e0194997

2018

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Members of the public in the USA, UK, Canada and Australia expressing genetic exceptionalism say they are more willing to donate genomic data

European journal of human genetics : EJHG, 2020-04, Vol.28 (4), p.424-434

2020

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Attitudes of publics who are unwilling to donate DNA data for research

European journal of medical genetics, 2019-05, Vol.62 (5), p.316-323

2019

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Overcoming barriers to facilitate the regulation of multi-centre regenerative medicine clinical trials

Stem cell research & therapy, 2018-11, Vol.9 (1), p.307-307, Article 307

2018

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Human germline genome editing is illegal in Canada, but could it be desirable for some members of the rare disease community?

Journal of community genetics, 2020-04, Vol.11 (2), p.129-138

2020

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APPLaUD: access for patients and participants to individual level uninterpreted genomic data

Human genomics, 2018-02, Vol.12 (1), p.7-7, Article 7

2018

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Re-contact Following Withdrawal of Minors from Research

Canadian journal of bioethics = revue canadienne de bioéthique, 2022-01, Vol.5 (1), p.45-53

2022

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'Your DNA, Your Say': global survey gathering attitudes toward genomics: design, delivery and methods

Personalized medicine, 2018-07, Vol.15 (4), p.311-318

2018

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Canada's Assisted Human Reproduction Act: Pragmatic Reforms in Support of Research

Frontiers in medicine, 2019-07, Vol.6, p.157

2019

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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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The ‘serious’ factor in germline modification

Journal of medical ethics, 2019-08, Vol.45 (8), p.508-513

2019

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Realigning gene editing with clinical research ethics: What the "CRISPR Twins" debacle means for Chinese and international research ethics governance

Accountability in research, 2019-05, Vol.26 (4), p.257-264

2019

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Human gene editing: revisiting Canadian policy

npj Regenerative medicine, 2017-01, Vol.2 (1), p.3-2, Article 3

2017

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Recruiting terminally ill patients into non-therapeutic oncology studies: views of health professionals

BMC medical ethics, 2012-12, Vol.13 (1), p.33-33, Article 33

2012

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Heritable Genome Editing: Who Speaks for “Future” Children?

CRISPR journal, 2019-10, Vol.2 (5), p.285-292

2019

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‘Serious’ factor—a relevant starting point for further debate: a response

Journal of medical ethics, 2020-02, Vol.46 (2), p.153-155

2020

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A blueprint for the next generation of ELSI research, training, and outreach in regenerative medicine

npj Regenerative medicine, 2017-07, Vol.2 (1), p.21-4, Article 21

2017

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Unpacking the notion of "serious" genetic conditions: towards implementation in reproductive decision-making?

European journal of human genetics : EJHG, 2024-08

2024

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Going Back to Basics: What is the Target of Prenatal Screening?

American journal of bioethics, 2023-03, Vol.23 (3), p.50-52

2023

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Of the Rights and Best Interests of Future Generations

American journal of bioethics, 2020-08, Vol.20 (8), p.38-40

2020

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Genetically Enhanced Minors: Whose Responsibility?

American journal of bioethics, 2018-06, Vol.18 (6), p.1-3

2018

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Global Public Perceptions of Genomic Data Sharing: What Shapes the Willingness to Donate DNA and Health Data?

American journal of human genetics, 2020-10, Vol.107 (4), p.743-752

2020

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The Serious Factor in Expanded Prenatal Genetic Testing

American journal of bioethics, 2022-02, Vol.22 (2), p.23-25

2022

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"CRISPR babies": What does this mean for science and Canada?

Trust in genomic data sharing among members of the general public in the UK, USA, Canada and Australia

The author who wasn't there? Fairness and attribution in publications following access to population biobanks

Members of the public in the USA, UK, Canada and Australia expressing genetic exceptionalism say they are more willing to donate genomic data

Attitudes of publics who are unwilling to donate DNA data for research

Overcoming barriers to facilitate the regulation of multi-centre regenerative medicine clinical trials

Human germline genome editing is illegal in Canada, but could it be desirable for some members of the rare disease community?

APPLaUD: access for patients and participants to individual level uninterpreted genomic data

Re-contact Following Withdrawal of Minors from Research

'Your DNA, Your Say': global survey gathering attitudes toward genomics: design, delivery and methods

Canada's Assisted Human Reproduction Act: Pragmatic Reforms in Support of Research

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

The ‘serious’ factor in germline modification

Realigning gene editing with clinical research ethics: What the "CRISPR Twins" debacle means for Chinese and international research ethics governance

Human gene editing: revisiting Canadian policy

Recruiting terminally ill patients into non-therapeutic oncology studies: views of health professionals

Heritable Genome Editing: Who Speaks for “Future” Children?

‘Serious’ factor—a relevant starting point for further debate: a response

A blueprint for the next generation of ELSI research, training, and outreach in regenerative medicine

Unpacking the notion of "serious" genetic conditions: towards implementation in reproductive decision-making?

Going Back to Basics: What is the Target of Prenatal Screening?

Of the Rights and Best Interests of Future Generations

Genetically Enhanced Minors: Whose Responsibility?

Global Public Perceptions of Genomic Data Sharing: What Shapes the Willingness to Donate DNA and Health Data?

The Serious Factor in Expanded Prenatal Genetic Testing

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