26 results on '"Best, Stephanie"'
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2. Reanalysis of genomic data, how do we do it now and what if we automate it? A qualitative study
3. Evaluation of research co-design in health: a systematic overview of reviews and development of a framework
4. Shaping the future of kidney genetics in Australia: proceedings from the KidGen policy implementation workshop 2023
5. Australian public perspectives on genomic newborn screening: which conditions should be included?
6. Aligning organisational priorities and implementation science for cancer research
7. Eliciting parental preferences and values for the return of additional findings from genomic sequencing
8. The value of genomic testing in severe childhood speech disorders
9. Using a theory informed approach to design, execute, and evaluate implementation strategies to support offering reproductive genetic carrier screening in Australia
10. Determining the utility of diagnostic genomics: a conceptual framework
11. Scaling-up and future sustainability of a national reproductive genetic carrier screening program
12. Aligning intuition and theory: a novel approach to identifying the determinants of behaviours necessary to support implementation of evidence into practice
13. The more you do it, the easier it gets: using behaviour change theory to support health care professionals offering reproductive genetic carrier screening
14. Co-designing interventions to ‘live well’: experiences and perceptions of the Genetic, Undiagnosed and Rare Disease (GUaRD) community
15. How does the genomic naive public perceive whole genomic testing for health purposes? A scoping review
16. A systematic review of geographical inequities for accessing clinical genomic and genetic services for non-cancer related rare disease
17. Preferences and values for rapid genomic testing in critically ill infants and children: a discrete choice experiment
18. Understanding genomic health information: how to meet the needs of the culturally and linguistically diverse community—a mixed methods study
19. Learning from scaling up ultra-rapid genomic testing for critically ill children to a national level
20. A dynamic systems view of clinical genomics: a rich picture of the landscape in Australia using a complexity science lens
21. The long and winding road: perspectives of people and parents of children with mitochondrial conditions negotiating management after diagnosis
22. The personal utility and uptake of genomic sequencing in pediatric and adult conditions: eliciting societal preferences with three discrete choice experiments
23. Clinical genomic testing: what matters to key stakeholders?
24. Attitudes of Australian health professionals towards rapid genomic testing in neonatal and paediatric intensive care
25. Building a learning community of Australian clinical genomics: a social network study of the Australian Genomic Health Alliance
26. Habit Reversal Training and Acceptance and Commitment Therapy for Tourette Syndrome: A Pilot Project
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