349 results on '"Turbitt, Erin"'
Search Results
2. A survey of genetic and palliative care health professionals’ views of integrating genetics into palliative care
3. Approaching discussions about genetics with palliative patients and their families: a qualitative exploration with genetic health professionals
4. Parents’ perspectives on conversations about prognosis and an assessment of prognostic information available online: A mixed-methods study
5. A mixed-methods assessment of the Australasian Society of Genetic Counselors (ASGC) Mentor Program
6. The Parent PrU: A measure to assess personal utility of pediatric genomic results
7. The PrU: Development and validation of a measure to assess personal utility of genomic results
8. Free Online Decision Tools to Support Parents Making Decisions About Their Children's Chronic Health Condition: An Environmental Scan
9. Do online decision aids reflect new prenatal screening and testing options? An environmental scan and content analysis
10. Views and experiences of palliative care clinicians in addressing genetics with individuals and families: a qualitative study
11. Dyadic concordance and associations of beliefs with intentions to learn carrier results from genomic sequencing
12. Race, ethnicity, and ancestry reporting in genetic counseling research: A focused mapping review and synthesis
13. Parent clinical trial priorities for fragile X syndrome: a best–worst scaling
14. Precision Public Health Initiatives in Cancer: Proceedings from the Transdisciplinary Conference for Future Leaders in Precision Public Health
15. Parents' preferences for receiving and discussing prognostic genetic information regarding their children's neurodevelopmental condition: A qualitative study.
16. Parents' preferences for receiving and discussing prognostic genetic information regarding their children's neurodevelopmental condition: A qualitative study
17. Extending an Antiracism Lens to the Implementation of Precision Public Health Interventions
18. Advancing precision public health using human genomics: examples from the field and future research opportunities
19. Genetic counseling, genetic testing, and risk perceptions for breast and colorectal cancer: Results from the 2015 National Health Interview Survey
20. Australians’ perspectives on support around use of personal genomic testing: Findings from the Genioz study
21. The Parent PrU: a measure to assess personal utility of pediatric genomic results
22. Genetic testing decisions in non-western cultures: an opportunity for intergenerational decision making
23. Psychosocial, attitudinal, and demographic correlates of cancer-related germline genetic testing in the 2017 Health Information National Trends Survey
24. Ethnic identity and engagement with genome sequencing research
25. Australians’ views and experience of personal genomic testing: survey findings from the Genioz study
26. Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study
27. Special Issue: “Genetic Counseling and Genetic Testing in Precision Medicine”
28. Motivations to learn genomic information are not exceptional: Lessons from behavioral science
29. Judgment and Decision Making in Genome Sequencing
30. List of Contributors
31. Adaptation of couples living with a high risk of breast/ovarian cancer and the association with risk-reducing surgery
32. Australians’ views on personal genomic testing: focus group findings from the Genioz study
33. A randomized controlled study of a consent intervention for participating in an NIH genome sequencing study
34. Data from Uptake of Genetic Testing Among Patients with Cancer At Risk for Lynch Syndrome in the National Health Interview Survey
35. Supplementary Table S1 and S2 from Uptake of Genetic Testing Among Patients with Cancer At Risk for Lynch Syndrome in the National Health Interview Survey
36. Do Teachers Question the Reality of Pain in Their Students? A Survey Using the Concept of Pain Inventory-Proxy (COPI-Proxy)
37. General practitioner perspectives on referrals to paediatric public specialty clinics
38. Use of home visiting GP services by paediatric patients presenting at emergency departments
39. Co-payments and parental decisionmaking: A cross-sectional survey of the impact on general practice and emergency department presentations
40. Models of communication for polygenic scores and associated psychosocial and behavioral effects on recipients: A systematic review
41. Genetic Testing and Other Healthcare Use by Black and White Individuals in a Genomic Sequencing Study
42. Evidence linking FMR1 mRNA and attentional demands of stepping and postural control in women with the premutation
43. Australasian Genetic Counselors’ Perceptions of Their Role in Supporting Clients’ Behavior Change
44. Feasibility of Coping Effectiveness Training for Caregivers of Children with Autism Spectrum Disorder: a Genetic Counseling Intervention
45. A qualitative exploration of parent decision making about new genetic tests for children with diagnosed neurodevelopmental disorders
46. Teacher-led Pain Science Education in schools – a pilot feasibility Stepped wedge cluster randomised clinical trial
47. The global imperative to address vaccine-preventable diseases
48. Translating pain science education to the classroom: Teachers’ perceptions and experiences to inform co-design for professional development
49. Spousal Concordance in Genome Sequencing Beliefs and Intentions and Spousal Influence on Individuals’ Genome Sequencing Intentions
50. Genetic counsellors’ perceptions and readiness for their role in changing patient health behaviour
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