366 results on '"Carroll, June C."'
Search Results
2. Opportunistic genomic screening has clinical utility: An interventional cohort study
3. Genetics Adviser: The development and usability testing of a new patient digital health application to support clinical genomic testing
4. Great expectations: patients’ preferences for clinically significant results from genomic sequencing
5. “I don’t need any more unknowns hanging over my head”: Views of patients with cancer on variants of uncertain significance and low/moderate risk results from genomic sequencing
6. A comprehensive genomic reporting structure for communicating all clinically significant primary and secondary findings
7. Widening the lens of actionability: A qualitative study of primary care providers’ views and experiences of managing secondary genomic findings
8. Challenges and practical solutions for managing secondary genomic findings in primary care
9. Anticipating the primary care role in genomic medicine: expectations of genetics health professionals
10. The role of digital tools in the delivery of genomic medicine: enhancing patient-centered care
11. Effect of genetics clinical decision support tools on health-care providers’ decision making: a mixed-methods systematic review
12. Hereditary colorectal cancer screening: A 10-year longitudinal cohort study following an educational intervention
13. Noninvasive Prenatal Testing for Trisomies 21, 18, and 13, Sex Chromosome Aneuploidies, and Microdeletions in Average-Risk Pregnancies: A Cost-Effectiveness Analysis
14. Effectiveness of the Genomics ADvISER decision aid for the selection of secondary findings from genomic sequencing: a randomized clinical trial
15. Family History Taking in Pediatric Practice : A Qualitative Interview Study
16. Developing clinical decision tools to implement chronic disease prevention and screening in primary care: the BETTER 2 program (building on existing tools to improve chronic disease prevention and screening in primary care)
17. Pregnant during the COVID-19 pandemic: an exploration of patients’ lived experiences
18. A framework to build capacity for a reflex-testing program for Lynch syndrome
19. Development of patient “profiles” to tailor counseling for incidental genomic sequencing results
20. Primary care providers’ lived experiences of genetics in practice
21. “I don’t need any more unknowns hanging over my head”: Cancer patients’ views on variants of uncertain significance and low/moderate risk results from genomic sequencing
22. Universal tumor screening for Lynch syndrome: health-care providers’ perspectives
23. Psychosocial Response to Uncertain Newborn Screening Results for Cystic Fibrosis
24. A secondary benefit: the reproductive impact of carrier results from newborn screening for cystic fibrosis
25. A model for the return and referral of all clinically significant secondary findings of genomic sequencing
26. Opinion commune de la SOGC et du CCGM sur le dépistage génétique en contexte de procréation : Mise à jour à l'intention de l'ensemble des prestataires canadiens de soins de santé maternelle et de services en procréation, à l'ère des tests offerts directement aux consommateurs
27. RETIRED: Joint SOGC–CCMG Opinion for Reproductive Genetic Carrier Screening: An Update for All Canadian Providers of Maternity and Reproductive Healthcare in the Era of Direct-to-Consumer Testing
28. Bridging the gap in genetics: a progressive model for primary to specialist care
29. Use of eConsult to enhance genetics service delivery in primary care: A multimethod study
30. 25 Genomic medicine in paediatric care for neurodevelopmental disorders: An assessment of practices, attitudes and education needs of Ontario paediatricians
31. Genetics Adviser: a protocol for a mixed-methods randomised controlled trial evaluating a digital platform for genetics service delivery
32. The Educational Needs and Professional Roles of Canadian Physicians and Nurses regarding Genetic Testing and Adult Onset Hereditary Disease
33. Finding the sweet spot: a qualitative study exploring patients' acceptability of chatbots in genetic service delivery.
34. Ensuring best practice in genomics education and evaluation: reporting item standards for education and its evaluation in genomics (RISE2 Genomics)
35. The current state of cancer family history collection tools in primary care: a systematic review
36. A Master Class in Family Doctor Leadership: Evaluating an Innovative Program
37. Experiences of patients with a disability in receiving primary health care
38. Benefits and burdens of newborn screening: public understanding and decision-making
39. Informing parents about expanded newborn screening: influences on provider involvement
40. Newborn screening for cystic fibrosis
41. Primary care providers’ role in newborn screening result notification for cystic fibrosis
42. Interactive Genetic Counseling Role-Play: A Novel Educational Strategy for Family Physicians
43. Widening the lens of actionability: A qualitative study of primary care providers’ views and experiences of managing secondary genomic findings
44. Applying the 2011 Canadian guidelines for breast cancer screening in practice
45. What does the feminization of family medicine mean?
46. Family history and breast cancer
47. GenetiKit: a randomized controlled trial to enhance delivery of genetics services by family physicians
48. Nicotine dependence as a risk factor for upper aerodigestive tract (UADT) cancers: A mediation analysis
49. The primary care physician role in cancer genetics: a qualitative study of patient experience
50. Systematic Review: Family History in Risk Assessment for Common Diseases
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