J
Jane Kaye
Researcher at University of Oxford
Publications - 151
Citations - 24672
Jane Kaye is an academic researcher from University of Oxford. The author has contributed to research in topics: Biobank & Data sharing. The author has an hindex of 42, co-authored 145 publications receiving 18345 citations. Previous affiliations of Jane Kaye include University of Malaya & Mount Vernon Hospital.
Papers
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Journal ArticleDOI
eRegistries: governance for electronic maternal and child health registries.
Sonja Myhre,Jane Kaye,Lee A. Bygrave,Margunn Aanestad,Buthaina Ghanem,Patricia Mechael,Frederik Frøen,Frederik Frøen +7 more
TL;DR: This research utilizes findings from two web-based surveys, completed in 2015 that targeted public health officials and health care providers in 76 countries with high global maternal and child mortality burden and found that the prevailing legal landscape is characterized by inadequate data security safeguards and weak support for core privacy principles.
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Australian Aboriginal and Torres Strait Islander Collections of Genetic Heritage: The Legal, Ethical and Practical Considerations of a Dynamic Consent Approach to Decision Making.
TL;DR: Dynamic consent (DC) as mentioned in this paper is both a model and a specific web-based tool that enables clear, granular communication and recording of participant consent choices over time, and it enables individual consent choices to be expressed and recorded over time.
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Can i access my personal genome? the current legal position in the uk
TL;DR: The authors describe the policy implications in this area and conclude that, for now, the law appears to strike an appropriate balance, but new policy will need to be developed to address this issue.
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Genetic testing without consent: the implications of the new Human Tissue Act 2004
Anneke Lucassen,Jane Kaye +1 more
TL;DR: Despite its focus on consent the new Human Tissue Act 2004 allows for testing without consent where a relative could benefit, and should take measures to limit the potential harm that can be caused.
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Exploring the potential duty of care in clinical genomics under UK law.
Colin Mitchell,Corrette Ploem,Victoria Chico,Elizabeth Ormondroyd,Alison Hall,Susan E. Wallace,Michael Fay,Deirdre Goodwin,Jessica Bell,Simon Phillips,Jenny C. Taylor,Raoul C.M. Hennekam,Jane Kaye +12 more
TL;DR: The way that UK law may respond to three key challenges of genome-wide sequencing is explored and new legal duties in relation to feedback of findings that are unrelated to the presenting condition are established.