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