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Your search keyword '"Gabrielle Samuel"' showing total 87 results

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1. Roadmap for low-carbon ultra-low temperature storage in biobanking

2. The Ubuntu Way: Ensuring Ethical AI Integration in Health Research [version 1; peer review: 2 approved, 1 approved with reservations]

3. UK health researchers’ considerations of the environmental impacts of their data-intensive practices and its relevance to health inequities

4. Drivers and constraints to environmental sustainability in UK-based biobanking: balancing resource efficiency and future value

5. The ethical challenges of diversifying genomic data: A qualitative evidence synthesis

6. The environmental impact of data-driven precision medicine initiatives

7. Democratic research: Setting up a research commons for a qualitative, comparative, longitudinal interview study during the COVID-19 pandemic

8. Ethics review of big data research: What should stay and what should be reformed?

9. The environmental sustainability of data-driven health research: A scoping review

10. Forensic DNA phenotyping in Europe: views 'on the ground' from those who have a professional stake in the technology

11. For what it's worth. Unearthing the values embedded in digital phenotyping for mental health

12. Responsible Open Science: Moving towards an Ethics of Environmental Sustainability

17. Systems thinking and efficiency under emissions constraints: Addressing rebound effects in digital innovation and policy.

19. Public Trust and Trustworthiness in Biobanking: The Need for More Reflexivity

20. Bringing ethics into governance: the case of the UK COVID-19 contact tracing app

21. Ecologies of Public Trust: The NHS COVID-19 Contact Tracing App

22. Reimagining research ethics to include environmental sustainability:a principled approach, including a case study of data-driven health research

23. Boundaries Between Research Ethics and Ethical Research Use in Artificial Intelligence Health Research

24. Digital Phenotyping for Mental Health: Reviewing the Challenges of Using Data to Monitor and Predict Mental Health Problems

25. Rethinking value construction in biomedicine and healthcare

26. Problematizing consent: searching genetic genealogy databases for law enforcement purposes

27. Population health AI researchers’ perceptions of the public portrayal of AI: A pilot study

28. Investigative genetic genealogy: can collective privacy and solidarity help?

29. COVID-19 contact tracing apps: UK public perceptions

30. The UK COVID-19 contact tracing app as both an emerging technology and public health intervention: The need to consider promissory discourses

31. Normative positions towards COVID-19 contact-tracing apps: Findings from a large-scale qualitative study in nine European countries

32. Responsible open science: moving towards an ethics of environmental sustainability

33. COVID-19 and contact tracing apps: ethical challenges for a social experiment on a global scale

34. Can digital data diagnose mental health problems? A sociological exploration of ‘digital phenotyping’

35. The impact of investigative genetic genealogy: perceptions of UK professional and public stakeholders

36. Defining ethical standards for the application of digital tools to population health research

37. Public trust and ‘ethics review’ as a commodity: the case of Genomics England Limited and the UK’s 100,000 genomes project

38. Guest Editorial: Ethical Issues in Social Media Research

39. COVID-19 and Contact Tracing Apps: Technological Fix or Social Experiment?

40. Data-Driven Unsustainability? An Interdisciplinary Perspective on Governing the Environmental Impacts of a Data-Driven Society

41. The Ethics Ecosystem: Personal Ethics, Network Governance and Regulating Actors Governing the Use of Social Media Research Data

42. Civil society stakeholder views on forensic DNA phenotyping: Balancing risks and benefits

43. Is It Time to Re-Evaluate the Ethics Governance of Social Media Research?

44. Ethical challenges around the use of social media data: Views of researchers and research ethics committee members

45. A response to the forensic genetics policy initiative's report 'Establishing Best Practice for Forensic DNA Databases'

46. From 'a fair game' to 'a form of covert research':Research Ethics Committee Members differing notions of consent and potential risk to participants within social media research

47. Perspectives on Achieving Institutional Trust in Personalized Medicine

48. Societal impact evaluation: Exploring evaluator perceptions of the characterization of impact under the REF2014: Table 1

49. Towards a national genomics medicine service: the challenges facing clinical-research hybrid practices and the case of the 100 000 genomes project

50. The future of societal impact assessment using peer review: pre-evaluation training, consensus building and inter-reviewer reliability

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