363 results on '"Vears, Danya"'
Search Results
2. Clinician perspectives on policy approaches to genetic risk disclosure in families
3. The Parliamentary Inquiry into Mitochondrial Donation Law Reform (Maeve’s Law) Bill 2021 in Australia: A Qualitative Analysis
4. Ethics of artificial intelligence in prenatal and pediatric genomic medicine
5. Predictive psychiatric genetic testing in minors : an exploration of the non-medical benefits
6. Correction: Clinician perspectives on policy approaches to genetic risk disclosure in families
7. Dealing with ambivalence in the practice of advanced genetic healthcare: towards an ethical choreography
8. Inductive content analysis: A guide for beginning qualitative researchers
9. Should secondary pharmacogenomic variants be actively screened and reported when diagnostic genome-wide sequencing is performed in a child?
10. What's in a name? Justifying terminology for genomic findings beyond the initial test indication: A scoping review
11. Disclosure of genetic risk in the family: A survey of the Flemish general population
12. Adolescents’ Capacity to Make Decisions in Healthcare: Perspectives of Serbian Primary Care Physicians
13. Australian public perspectives on genomic data storage and sharing: Benefits, concerns and access preferences
14. ‘Diagnostic shock’: the impact of results from ultrarapid genomic sequencing of critically unwell children on aspects of family functioning
15. Informing relatives of their genetic risk: an examination of the Belgian legal context
16. Reanalysis of genomic data in rare disease: current practice and attitudes among Australian clinical and laboratory genetics services
17. Australian public perspectives on genomic newborn screening: which conditions should be included?
18. Prospective cohort study of genomic newborn screening: BabyScreen+ pilot study protocol
19. The pros and cons of storing babies’ DNA
20. Consent for rapid genomic sequencing for critically ill children: legal and ethical issues
21. Genetic testing for psychiatric illness in children: ethical issues
22. GA4GH: International policies and standards for data sharing across genomic research and healthcare
23. Australian Public Perspectives on Genomic Newborn Screening: Risks, Benefits, and Preferences for Implementation
24. Analysis of laboratory reporting practices using a quality assessment of a virtual patient
25. Human Genetics Society of Australasia Position Statement: Predictive and Presymptomatic Genetic Testing in Adults and Children.
26. Exploration of genetic health professional - laboratory specialist interactions in diagnostic genomic sequencing
27. Should Secondary Pharmacogenomic Variants Be Actively Screened and Reported When Diagnostic Genome-Wide Sequencing Is Performed in a Child?
28. Ethics of artificial intelligence in prenatal and pediatric genomic medicine
29. Genetics experience impacts attitudes towards germline gene editing: a survey of over 1500 members of the public
30. Communicating genetic information to family members: analysis of consent forms for diagnostic genomic sequencing
31. Genetic health professionals’ experiences with initiating reanalysis of genomic sequence data
32. Searching for secondary findings: considering actionability and preserving the right not to know
33. Attitudes of publics who are unwilling to donate DNA data for research
34. The Parliamentary Inquiry into Mitochondrial Donation Law Reform (Maeve’s Law) Bill 2021 in Australia: A Qualitative Analysis
35. Are We Ready for Whole Population Genomic Sequencing of Asymptomatic Newborns?
36. Analysis of VUS reporting, variant reinterpretation and recontact policies in clinical genomic sequencing consent forms
37. Reporting practices for variants of uncertain significance from next generation sequencing technologies
38. Storing paediatric genomic data for sequential interrogation across the lifespan
39. Intensive Care Clinicians’ Perspectives on Ethical Challenges Raised by Rapid Genomic Testing in Critically Ill Infants
40. Human Genetics Society of Australasia Position Statement: Genetic Carrier Testing for Recessive Conditions
41. Australian public perspectives on genomic data governance: responsibility, regulation, and logistical considerations
42. Rapid Genomic Testing in Intensive Care: Health Professionals’ Perspectives on Ethical Challenges
43. Rapid genomic testing in critically ill patients with genetic conditions: position statement by the Human Genetics Society of Australasia
44. Key informant perspectives on implementing genomic newborn screening: a qualitative study guided by the Action, Actor, Context, Target, Time framework
45. Consent for rapid genomic sequencing for critically ill children: legal and ethical issues
46. Attitudes of European Geneticists Regarding Expanded Carrier Screening
47. Why genomics researchers are sometimes morally required to hunt for secondary findings
48. Current Ethical Issues Related to the Implementation of Whole-Exome and Whole-Genome Sequencing
49. A systematic analysis of online marketing materials used by providers of expanded carrier screening
50. Health, wealth and behavioural change: an exploration of role responsibilities in the wake of epigenetics
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