129 results on '"Shickh, Salma"'
Search Results
2. Great expectations: patients’ preferences for clinically significant results from genomic sequencing
3. Genetics Adviser: The development and usability testing of a new patient digital health application to support clinical genomic testing
4. “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
5. A comprehensive genomic reporting structure for communicating all clinically significant primary and secondary findings
6. Widening the lens of actionability: A qualitative study of primary care providers’ views and experiences of managing secondary genomic findings
7. Challenges and practical solutions for managing secondary genomic findings in primary care
8. Patient and public preferences for being recontacted with updated genomic results: a mixed methods study
9. The clinical utility of exome and genome sequencing across clinical indications: a systematic review
10. Effect of genetics clinical decision support tools on health-care providers’ decision making: a mixed-methods systematic review
11. Beyond medically actionable results: an analytical pipeline for decreasing the burden of returning all clinically significant secondary findings
12. Clinical and psychological outcomes of receiving a variant of uncertain significance from multigene panel testing or genomic sequencing: a systematic review and meta-analysis
13. Variant classification changes over time in BRCA1 and BRCA2
14. c.1289G>A (p.Arg430His) variant in the epsilon isoform of the GFAP gene in a patient with adult onset Alexander disease
15. Theory‐based behavior change intervention to increase uptake of risk‐reducing salpingo‐oophorectomy in women with a BRCA1 or BRCA2 pathogenic variant: The PREVENT randomized controlled trial
16. “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
17. Development of patient “profiles” to tailor counseling for incidental genomic sequencing results
18. P564: Doing no harm: Exploring the psychosocial impacts of receiving secondary findings from whole exome sequencing
19. P547: The clinician-reported Genetic testing Utility InDEX (C-GUIDE): Establishing content validity for a new measure for sequencing-based newborn screening
20. P555: Clinical utility returning of all types of medically relevant genomic sequencing findings: An observational study
21. P538: Curious but cautious: Patients’ preferences for all types of clinically actionable genomic incidental results
22. P523: Returning all clinically relevant findings from genomic sequencing: Preliminary results from the incidental genomics RCT
23. A model for the return and referral of all clinically significant secondary findings of genomic sequencing
24. How do members of the public expect to use variants of uncertain significance in their health care? A population-based survey
25. P409: Clinical utility of genomic sequencing for hereditary cancer syndromes: An observational chart review
26. P397: Clinical utility of all types of medically relevant secondary findings: A systematic evidence review
27. P382: Professionals’ perspectives on the use of digital tools to support patient recontact in clinical genetics
28. P543: Comparing the analytical performance of exome sequencing and traditional panel testing in a cancer population
29. Correction: Variant classification changes over time in BRCA1 and BRCA2
30. From the patient to the population: Use of genomics for population screening
31. Patient-facing digital tools for delivering genetic services: a systematic review
32. “Doctors shouldn’t have to cheat the system”: Clinicians’ real-world experiences of the utility of genomic sequencing
33. A comprehensive genomic reporting structure for communicating all clinically significant primary and secondary findings
34. Genetics Adviser: a protocol for a mixed-methods randomised controlled trial evaluating a digital platform for genetics service delivery
35. Patient-facing digital tools for delivering genetic services: a systematic review.
36. eP502: How will returning variants of uncertain significance impact healthcare use? A cross-sectional survey
37. eP392: A comprehensive genomic test reporting structure for communicating cancer and incidental findings
38. eP513: “Doctors shouldn’t have to cheat the system”: Clinicians’ real-world experiences of the utility of genomic sequencing
39. eP299: Genetics adviser: The development and usability testing of a new patient-centered digital health application to support clinical genomic testing
40. “I just wanted more”: Hereditary cancer syndromes patients’ perspectives on the utility of circulating tumour DNA testing for cancer screening
41. The role of digital tools in the delivery of genomic medicine: enhancing patient-centered care
42. "Game Changer": Health Professionals' Views on the Clinical Utility of Circulating Tumor DNA Testing in Hereditary Cancer Syndrome Management.
43. Widening the lens of actionability: A qualitative study of primary care providers’ views and experiences of managing secondary genomic findings
44. Beyond medically actionable results: an analytical pipeline for decreasing the burden of returning all clinically significant secondary findings
45. Exome and genome sequencing in adults with undiagnosed disease: a prospective cohort study
46. Effectiveness of the Genomics ADvISER decision aid for the selection of secondary findings from genomic sequencing: a randomized clinical trial
47. Health outcomes, utility and costs of returning incidental results from genomic sequencing in a Canadian cancer population: protocol for a mixed-methods randomised controlled trial
48. Exome and genome sequencing in adults with undiagnosed disease: a prospective cohort study.
49. Evaluation of a decision aid for incidental genomic results, the Genomics ADvISER: protocol for a mixed methods randomised controlled trial
50. Quality of life drives patients’ preferences for secondary findings from genomic sequencing
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