420 results on '"Hallowell, Nina"'
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2. Training Ethically Responsible AI Researchers: a Case Study
3. Inalienable data: Ethical imaginaries of de-identified health data ownership
4. Democratising or disrupting diagnosis? Ethical issues raised by the use of AI tools for rare disease diagnosis
5. “I don’t think people are ready to trust these algorithms at face value”: trust and the use of machine learning algorithms in the diagnosis of rare disease
6. Public governance of medical artificial intelligence research in the UK: an integrated multi-scale model
7. Eating to live or living to eat: The meaning of hunger following gastric surgery
8. Ethical preparedness in genomic medicine: how NHS clinical scientists navigate ethical issues
9. COVID-19 and Contact Tracing Apps: Ethical Challenges for a Social Experiment on a Global Scale
10. Delivering genomic medicine in the United Kingdom National Health Service: a systematic review and narrative synthesis
11. Negotiating jurisdictional boundaries in response to new genetic possibilities in breast cancer care: The creation of an ‘oncogenetic taskscape’
12. Research or clinical care : what's the difference?
13. Moving into the mainstream: healthcare professionals’ views of implementing treatment focussed genetic testing in breast cancer care
14. High-risk women’s risk perception after receiving personalized polygenic breast cancer risk information
15. Patients’ Views of Treatment-Focused Genetic Testing (TFGT): Some Lessons for the Mainstreaming of BRCA1 and BRCA2 Testing
16. Artificial intelligence and medical research databases: ethical review by data access committees
17. Therapeutic appropriation: a new concept in the ethics of clinical research
18. Clinician–researchers and custodians of scarce resources: a qualitative study of health professionals’ views on barriers to the involvement of teenagers and young adults in cancer trials
19. Big data phenotyping in rare diseases: some ethical issues
20. Making Sense of SNPs: Women’s Understanding and Experiences of Receiving a Personalized Profile of Their Breast Cancer Risks
21. A practical checklist for return of results from genomic research in the European context
22. Providing recurrence risk counselling for parents after diagnosis of a serious genetic condition caused by an apparently de novo mutation in their child: a qualitative investigation of the PREGCARE strategy with UK clinical genetics practitioners
23. Artificial intelligence and medical research databases: ethical review by data access committees
24. An analysis of semantic agreement : the case for studying folk-linguistic descriptions of talk
25. Ambassadors of hope, research pioneers and agents of change—individuals’ expectations and experiences of taking part in a randomised trial of an innovative health technology: longitudinal qualitative study
26. Germline mismatch repair (MMR) gene analyses from English NHS regional molecular genomics laboratories 1996–2020: development of a national resource of patient-level genomics laboratory records
27. High-risk individuals’ perceptions of reproductive genetic testing for CDH1 mutations
28. The Psychosocial Impact of Undergoing Prophylactic Total Gastrectomy (PTG) to Manage the Risk of Hereditary Diffuse Gastric Cancer (HDGC)
29. A qualitative study of patients’ perceptions of the value of molecular diagnosis for familial hypercholesterolemia (FH)
30. Revealing the results of whole-genome sequencing and whole-exome sequencing in research and clinical investigations: some ethical issues
31. Correction: Delivering genomic medicine in the UK National Health Service: a systematic review and narrative synthesis
32. Return of results from genomic research: a practical tool
33. What ethical and legal principles should guide the genotyping of children as part of a personalised screening programme for common cancer?
34. Better governance, better access: practising responsible data sharing in the METADAC governance infrastructure
35. An investigation of the factors effecting high-risk individuals’ decision-making about prophylactic total gastrectomy and surveillance for hereditary diffuse gastric cancer (HDGC)
36. Timing and context: important considerations in the return of genetic results to research participants
37. AIgorithmic Ethics: A Technically Sweet Solution to a Non-Problem
38. How do index patients participating in genetic screening programmes for familial hypercholesterolemia (FH) interpret their DNA results? A UK-based qualitative interview study
39. The ethical challenges of artificial intelligence-driven digital pathology
40. Understanding the outcomes of multi-centre clinical trials: A qualitative study of health professional experiences and views
41. Managing expectations, rights, and duties in large-scale genomics initiatives: a European comparison
42. The ethical challenges of artificial intelligence‐driven digital pathology
43. Perceptions And Experiences Of Taking Oral Hypoglycaemic Agents Among People Of Pakistani And Indian Origin: Qualitative Study
44. Negotiating present and future selves: managing the risk of hereditary ovarian cancer by prophylactic surgery
45. Understanding the ethical and legal considerations of Digital Pathology
46. Feasibility and design of a trial regarding the optimal mode of delivery for preterm birth: the CASSAVA multiple methods study
47. Distinguishing research from clinical care in cancer genetics: Theoretical justifications and practical strategies
48. Digital/computational phenotyping: What are the differences in the science and the ethics?
49. The ethics of genomic medicine: redefining values and norms in the UK and France
50. Looking different, feeling different: women’s reactions to risk-reducing breast and ovarian surgery
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