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Jane Kaye (1962-)

Name	Jane Kaye
Zeit	1962- (Lebensdaten)
Geschlecht	weiblich
Akademischer Grad bzw. Titel	Dr.
Weitere Angaben	Ph.D. University of Oxford . Director of the Centre for Law, Health and Emerging Technologies at Oxford: (HeLEX), the Department of Public Health at the University of Oxford
Quelle	Homepage: http://www.law.ox.ac.uk/profile/jane.kaye LoC-NA
Datensatztyp	Person
GND-Nummer	140087575
Datensatz-ID	140087575
Beteiligt an alle anzeigen Moving beyond Technical Issues to Stakeholder Involvement: Key Areas for Consideration in the Development of Human-Centred and Trusted AI in Healthcare Discovery of drug–omics associations in type 2 diabetes with generative deep-learning models The practice of active patient involvement in rare disease research using ICT: experiences and lessons from the RUDY JAPAN project Toward better governance of human genomic data ‘CTRL’: an online, Dynamic Consent and participant engagement platform working towards solving the complexities of consent in genomic research Reflections on dynamic consent in biomedical research: the story so far Governance of research consortia: challenges of implementing Responsible Research and Innovation within Europe Discovery of biomarkers for glycaemic deterioration before and after the onset of type 2 diabetes: descriptive characteristics of the epidemiological studies within the IMI DIRECT Consortium Motivations for data sharing—views of research participants from four European countries: A DIRECT study Balancing Data Subjects’ Rights and Public Interest Research: : Examining the Interplay between UK Law, EU Human Rights Law and the GDPR Sharing data for future research—engaging participants’ views about data governance beyond the original project: a DIRECT Study The governance structure for data access in the DIRECT consortium: an innovative medicines initiative (IMI) project Including all voices in international data-sharing governance Desiderata for digital consent in genomic research Dynamic Consent: a potential solution to some of the challenges of modern biomedical research Health-related quality of life and a cost-utility simulation of adults in the UK with osteogenesis imperfecta, X-linked hypophosphatemia and fibrous dysplasia Using digital technologies to engage with medical research: views of myotonic dystrophy patients in Japan Has the biobank bubble burst? Withstanding the challenges for sustainable biobanking in the digital era Challenges and opportunities for ELSI early career researchers Citizen science or scientific citizenship? Disentangling the uses of public engagement rhetoric in national research initiatives Challenges and opportunities for ELSI early career researchers Consent for Biobanking: The Legal Frameworks of Countries in the BioSHaRE-EU Project StemBANCC: Governing Access to Material and Data in a Large Stem Cell Research Consortium The emerging need for family-centric initiatives for obtaining consent in personal genome research Building a data sharing model for global genomic research Towards a data sharing Code of Conduct for international genomic research

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Jane Kaye (1962-)

Moving beyond Technical Issues to Stakeholder Involvement: Key Areas for Consideration in the Development of Human-Centred and Trusted AI in Healthcare

Discovery of drug–omics associations in type 2 diabetes with generative deep-learning models

The practice of active patient involvement in rare disease research using ICT: experiences and lessons from the RUDY JAPAN project

Toward better governance of human genomic data

‘CTRL’: an online, Dynamic Consent and participant engagement platform working towards solving the complexities of consent in genomic research

Reflections on dynamic consent in biomedical research: the story so far

Governance of research consortia: challenges of implementing Responsible Research and Innovation within Europe

Discovery of biomarkers for glycaemic deterioration before and after the onset of type 2 diabetes: descriptive characteristics of the epidemiological studies within the IMI DIRECT Consortium

Motivations for data sharing—views of research participants from four European countries: A DIRECT study

Balancing Data Subjects’ Rights and Public Interest Research: : Examining the Interplay between UK Law, EU Human Rights Law and the GDPR

Sharing data for future research—engaging participants’ views about data governance beyond the original project: a DIRECT Study

The governance structure for data access in the DIRECT consortium: an innovative medicines initiative (IMI) project

Including all voices in international data-sharing governance

Desiderata for digital consent in genomic research

Dynamic Consent: a potential solution to some of the challenges of modern biomedical research

Health-related quality of life and a cost-utility simulation of adults in the UK with osteogenesis imperfecta, X-linked hypophosphatemia and fibrous dysplasia

Using digital technologies to engage with medical research: views of myotonic dystrophy patients in Japan

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

Challenges and opportunities for ELSI early career researchers

Citizen science or scientific citizenship? Disentangling the uses of public engagement rhetoric in national research initiatives

Challenges and opportunities for ELSI early career researchers

Consent for Biobanking: The Legal Frameworks of Countries in the BioSHaRE-EU Project

StemBANCC: Governing Access to Material and Data in a Large Stem Cell Research Consortium

The emerging need for family-centric initiatives for obtaining consent in personal genome research

Building a data sharing model for global genomic research

Towards a data sharing Code of Conduct for international genomic research