376 results on '"Metcalfe, Sylvia A."'
Search Results
2. Ensuring best practice in genomics education: A theory- and empirically informed evaluation framework
3. Investigating genomic medicine practice and perceptions amongst Australian non-genetics physicians to inform education and implementation
4. Social and physical predictors of mental health impact in adult women who have an FMR1 premutation
5. General practitioners' views on genomics, practice and education: A qualitative interview study
6. Lessons learnt from implementing change in newborn bloodspot screening processes over more than a decade: Midwives, genetics and education
7. Detection of skewed X-chromosome inactivation in Fragile X syndrome and X chromosome aneuploidy using quantitative melt analysis.
8. Australians’ perspectives on support around use of personal genomic testing: Findings from the Genioz study
9. Genetic counselling, patient education, and informed decision-making in the genomic era
10. Australians’ views and experience of personal genomic testing: survey findings from the Genioz study
11. Australians’ views on personal genomic testing: focus group findings from the Genioz study
12. Australian Genomics: Outcomes of a 5-year national program to accelerate the integration of genomics in healthcare
13. Carrier testing in children and adolescents
14. Evidence linking FMR1 mRNA and attentional demands of stepping and postural control in women with the premutation
15. Analyzing communication in genetic consultations—A systematic review
16. Quality Issues in Clinical Genetic Services in Australia
17. Exploring inhibitory deficits in female premutation carriers of fragile X syndrome: Through eye movements
18. Genetics in general practice
19. Klinefelter syndrome: A general practice perspective
20. The Social Imperative for Community Genetic Screening: An Australian Perspective
21. Responsible implementation of expanded carrier screening
22. “It gives them more options”: preferences for preconception genetic carrier screening for fragile X syndrome in primary healthcare
23. Key informants' perspectives of implementing chromosomal microarrays into clinical practice in Australia
24. Current practice and attitudes of Australian obstetricians toward population-based carrier screening for inherited conditions
25. There's Cancer in the Family
26. Fragile X population carrier screening
27. Clinical audit of genetic testing and referral patterns for fragile X and associated conditions
28. Ensuring best practice in genomics education and evaluation: reporting item standards for education and its evaluation in genomics (RISE2 Genomics)
29. Development of a fragile X syndrome (FXS) knowledge scale: towards a modified multidimensional measure of informed choice for FXS population carrier screening
30. “He didn’t say that thalassaemia might come up” — β-thalassaemia carriers’ experiences and attitudes
31. Measuring physician practice, preparedness and preferences for genomic medicine: a national survey
32. The expectations and realities of nutrigenomic testing in australia: A qualitative study
33. Carrier screening in preconception consultation in primary care
34. Development of a questionnaire for evaluating genetics education in general practice
35. “It’s Challenging on a Personal Level”—Exploring the ‘Lived Experience’ of Australian and Canadian Prenatal Genetic Counselors
36. “Testing Times, Challenging Choices”: An Australian Study of Prenatal Genetic Counseling
37. Prenatal β-thalassemia carrier screening in Australia: healthcare professionalsʼ perspectives of clinical practice
38. Impaired response inhibition is associated with self-reported symptoms of depression, anxiety, and ADHD in female FMR1 premutation carriers
39. The Importance of Program Evaluation: How Can it be Applied to Diverse Genetics Education Settings?
40. The expectations and realities of nutrigenomic testing in australia: A qualitative study
41. From Expectations to Experiences: Consumer Autonomy and Choice in Personal Genomic Testing
42. Integrating genetics as practices of primary care
43. Cognitive-motor interference during postural control indicates at-risk cerebellar profiles in females with the FMR1 premutation
44. “Taking Its Toll”: The Challenges of Working in Fetal Medicine
45. Considerations for Reporting Genome Results to Patients
46. “Itʼs about having the choice”: Stakeholder perceptions of population-based genetic carrier screening for fragile X syndrome
47. Age and CGG-repeat length are associated with neuromotor impairments in at-risk females with the FMR1 premutation
48. Editorial: Educating Health Professionals in Genomic Medicine: Evidence-Based Strategies and Approaches
49. Human Genetics Society of Australasia Position Statement: Online DNA Testing
50. Development of an Evidence-Based, Theory-Informed National Survey of Physician Preparedness for Genomic Medicine and Preferences for Genomics Continuing Education
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