379 results on '"Vears, Danya F."'
Search Results
2. Reanalysis of genomic data in rare disease: current practice and attitudes among Australian clinical and laboratory genetics services
3. Analysis of public perceptions on the use of artificial intelligence in genomic medicine
4. Australian public perspectives on genomic newborn screening: which conditions should be included?
5. Doctor–Parent Disagreement for Preterm Infants Born in the Grey Zone: Do Ethical Frameworks Help?
6. Clinician perspectives on policy approaches to genetic risk disclosure in families
7. Predictive psychiatric genetic testing in minors : an exploration of the non-medical benefits
8. The Parliamentary Inquiry into Mitochondrial Donation Law Reform (Maeve’s Law) Bill 2021 in Australia: A Qualitative Analysis
9. Inductive content analysis: A guide for beginning qualitative researchers
10. Boundary-work in genomic medicine: Safeguarding the future of diagnostic next-generation sequencing in the clinic
11. Correction: Clinician perspectives on policy approaches to genetic risk disclosure in families
12. Ethics of artificial intelligence in prenatal and pediatric genomic medicine
13. Dealing with ambivalence in the practice of advanced genetic healthcare: towards an ethical choreography
14. Disclosure of genetic risk in the family: A survey of the Flemish general population
15. Adolescents’ Capacity to Make Decisions in Healthcare: Perspectives of Serbian Primary Care Physicians
16. Australian public perspectives on genomic data storage and sharing: Benefits, concerns and access preferences
17. ‘Diagnostic shock’: the impact of results from ultrarapid genomic sequencing of critically unwell children on aspects of family functioning
18. Informing relatives of their genetic risk: an examination of the Belgian legal context
19. The patient with 41 reports: Analysis of laboratory exome sequencing reporting of a “virtual patient”
20. GA4GH: International policies and standards for data sharing across genomic research and healthcare
21. Disclosure of genetic information to family members: a systematic review of normative documents
22. Analysis of laboratory reporting practices using a quality assessment of a virtual patient
23. Alleviating the confusion around content analysis: A comment in response to Wainstein, Elliott & Austin 2023.
24. Exploration of genetic health professional - laboratory specialist interactions in diagnostic genomic sequencing
25. Prospective cohort study of genomic newborn screening: BabyScreen+ pilot study protocol
26. Genetics experience impacts attitudes towards germline gene editing: a survey of over 1500 members of the public
27. Communicating genetic information to family members: analysis of consent forms for diagnostic genomic sequencing
28. Genetic health professionals’ experiences with initiating reanalysis of genomic sequence data
29. Australian public perspectives on genomic newborn screening: Which conditions should be included?
30. Australian Public Perspectives on Genomic Newborn Screening: Risks, Benefits, and Preferences for Implementation
31. A systematic analysis of online marketing materials used by providers of expanded carrier screening
32. Searching for secondary findings: considering actionability and preserving the right not to know
33. Ethics of artificial intelligence in prenatal and pediatric genomic medicine
34. Reporting practices for variants of uncertain significance from next generation sequencing technologies
35. Growing complexity of (expanded) carrier screening: Direct-to-consumer, physician-mediated, and clinic-based offers
36. Human Genetics Society of Australasia Position Statement: Predictive and Presymptomatic Genetic Testing in Adults and Children.
37. Analysis of VUS reporting, variant reinterpretation and recontact policies in clinical genomic sequencing consent forms
38. Health, wealth and behavioural change: an exploration of role responsibilities in the wake of epigenetics
39. Readability of informed consent forms for whole-exome and whole-genome sequencing
40. The Parliamentary Inquiry into Mitochondrial Donation Law Reform (Maeve’s Law) Bill 2021 in Australia: A Qualitative Analysis
41. Are We Ready for Whole Population Genomic Sequencing of Asymptomatic Newborns?
42. Parents’ experiences with requesting carrier testing for their unaffected children
43. Current Ethical Issues Related to the Implementation of Whole-Exome and Whole-Genome Sequencing
44. Why genomics researchers are sometimes morally required to hunt for secondary findings
45. Are We Ready for Whole Population Genomic Sequencing of Asymptomatic Newborns?
46. Human Genetics Society of Australasia Position Statement: Genetic Carrier Testing for Recessive Conditions
47. Australian public perspectives on genomic data governance: responsibility, regulation, and logistical considerations
48. Rapid Genomic Testing in Intensive Care: Health Professionals’ Perspectives on Ethical Challenges
49. A practical checklist for return of results from genomic research in the European context
50. Carrier testing in children and adolescents
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