Collection
Ethics, Law, and Society in Human Genomics
This thematic series addresses current and emerging issues in human genomics, such as data sharing, personalized and precision medicine, and feedback of findings. The series welcomed submissions which explicitly dealt with how the issues are framed (e.g., in terms of ethical principles such as autonomy, justice and solidarity), including discussions of the possibilities and challenges of harnessing genomic research for public good.
Editors
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Professor Ruth Chadwick
University of Manchester, UK
Articles (10 in this collection)
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Including all voices in international data-sharing governance
Authors (first, second and last of 22)
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Attitudes of stakeholders in psychiatry towards the inclusion of children in genomic research
Authors (first, second and last of 6)
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APPLaUD: access for patients and participants to individual level uninterpreted genomic data
Authors (first, second and last of 12)
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Identify Down syndrome transcriptome associations using integrative analysis of microarray database and correlation-interaction network
Authors (first, second and last of 12)
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Ethical frameworks for obtaining informed consent in tumour profiling: an evidence-based case for Singapore
Authors (first, second and last of 5)
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Falling giants and the rise of gene editing: ethics, private interests and the public good
Authors (first, second and last of 6)
