344 results on '"Best, Stephanie"'
Search Results
2. Reanalysis of genomic data, how do we do it now and what if we automate it? A qualitative study
3. The value of genomic testing in severe childhood speech disorders
4. Noninvasive pediatric blood pressure assessment: exploring the clinicians’ perspective
5. Using a theory informed approach to design, execute, and evaluate implementation strategies to support offering reproductive genetic carrier screening in Australia
6. Determining the utility of diagnostic genomics: a conceptual framework
7. Scaling-up and future sustainability of a national reproductive genetic carrier screening program
8. Aligning intuition and theory: a novel approach to identifying the determinants of behaviours necessary to support implementation of evidence into practice
9. Determining priority indicators of utility for genomic testing in rare disease: A Delphi study
10. Translating Women’s Health Research into Policy and Practice
11. The more you do it, the easier it gets: using behaviour change theory to support health care professionals offering reproductive genetic carrier screening
12. Co-designing interventions to ‘live well’: experiences and perceptions of the Genetic, Undiagnosed and Rare Disease (GUaRD) community
13. Implementation and Evaluation of a National Multidisciplinary Kidney Genetics Clinic Network Over 10 Years
14. Calibrating variant curation by clinical context based on factors that influence patients’ tolerance of uncertainty
15. “Somewhere to turn to with my questions”: A pre-post pilot of an information linker service for caregivers who have a child with a Developmental and Epileptic Encephalopathy
16. Barriers to and Facilitators of Implementing Guidelines for Detecting Familial Hypercholesterolaemia in Australia
17. How does the genomic naive public perceive whole genomic testing for health purposes? A scoping review
18. Australian public perspectives on genomic newborn screening: which conditions should be included?
19. Aligning organisational priorities and implementation science for cancer research
20. Eliciting parental preferences and values for the return of additional findings from genomic sequencing
21. Reanalysis of genomic data in rare disease: current practice and attitudes among Australian clinical and laboratory genetics services
22. FEASIBILITY OF SCHOOL-BASED SCREENING FOR HIGH BLOOD PRESSURE IN CHILDREN: THE HEALTHY HEARTS @ SCHOOL STUDY
23. Implementation and evaluation of a national multidisciplinary kidney genetics clinic network over ten years
24. Standardizing variation: Scaling up clinical genomics in Australia
25. Australian public perspectives on genomic data storage and sharing: Benefits, concerns and access preferences
26. A systematic review of geographical inequities for accessing clinical genomic and genetic services for non-cancer related rare disease
27. The mobilisation of professional identity: A scoping and lexical review
28. Improving the way we do action research in quality improvement
29. Prospective cohort study of genomic newborn screening: BabyScreen+ pilot study protocol
30. Australian public perspectives on genomic newborn screening: Which conditions should be included?
31. Preferences and values for rapid genomic testing in critically ill infants and children: a discrete choice experiment
32. Organizational perspectives on implementing complex health interventions: clinical genomics in Australia
33. "It's fundamental to the work that we do": Genetic counselors' perceptions of their role in clients' mental well‐being.
34. Understanding genomic health information: how to meet the needs of the culturally and linguistically diverse community—a mixed methods study
35. Interprofessional teamwork: the role of professional identity and signature pedagogy – a mixed methods study
36. Australian Public Perspectives on Genomic Newborn Screening: Risks, Benefits, and Preferences for Implementation
37. Using Implementation Science Frameworks to Guide the Use of Electronic Patient-Reported Outcome Symptom Monitoring in Routine Cancer Care
38. Team Around the Patient: multi-professional opportunities to support care delivery in hospitals.
39. We need to stand together on the shoulders of giants: consolidating effective approaches for translating genomics into practice with implementation science
40. Extending an Antiracism Lens to the Implementation of Precision Public Health Interventions
41. Attitudes and Practices of Australian Nephrologists Toward Implementation of Clinical Genomics
42. Quality of life in caregivers of a child with a developmental and epileptic encephalopathy.
43. Learning from scaling up ultra-rapid genomic testing for critically ill children to a national level
44. A dynamic systems view of clinical genomics: a rich picture of the landscape in Australia using a complexity science lens
45. The long and winding road: perspectives of people and parents of children with mitochondrial conditions negotiating management after diagnosis
46. Enabling mental health student nurses to work co-productively
47. An Investigation of Barriers and Enablers for Genetics in Speech-Language Pathology Explored Through a Case Study of Childhood Apraxia of Speech
48. The personal utility and uptake of genomic sequencing in pediatric and adult conditions: eliciting societal preferences with three discrete choice experiments
49. Prudence or speed: Health and social care innovation in rural Wales
50. Clinical genomic testing: what matters to key stakeholders?
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