26 results on '"Clausen, Marc"'
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2. Genetics Adviser: The development and usability testing of a new patient digital health application to support clinical genomic testing.
3. Public knowledge of SARS-CoV-2 serological and viral lineage laboratory testing and result interpretation: A GENCOV study cross-sectional survey
4. “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
5. How do members of the public expect to use variants of uncertain significance in their health care? A population-based survey
6. P373: Patients’ and parents’ perspectives on the use of digital tools to deliver genetic services
7. P436: Population genome screening identifies previously undiagnosed disease: A case series
8. P409: Clinical utility of genomic sequencing for hereditary cancer syndromes: An observational chart review
9. P375: Fragmented systems of care: An overview of Canadian health system care models for hereditary cancer syndromes
10. P406: Partnering with patients to explore the psychosocial and socioeconomic impacts of hereditary cancer syndromes
11. O54: Reimagining genetics service delivery: Genetics providers’ perspectives on the integration of digital tools into clinical practice
12. P391: What are patients’ perspectives on the privacy and security of digital genomic tools? A qualitative study
13. P357: Replication of genetic variation associated with COVID-19 clinical outcomes: The GENCOV Prospective Cohort Study
14. P382: Professionals’ perspectives on the use of digital tools to support patient recontact in clinical genetics
15. P543: Comparing the analytical performance of exome sequencing and traditional panel testing in a cancer population
16. “Doctors shouldn’t have to cheat the system”: Clinicians’ real-world experiences of the utility of genomic sequencing
17. eP502: How will returning variants of uncertain significance impact healthcare use? A cross-sectional survey
18. eP392: A comprehensive genomic test reporting structure for communicating cancer and incidental findings
19. eP513: “Doctors shouldn’t have to cheat the system”: Clinicians’ real-world experiences of the utility of genomic sequencing
20. eP294: Return of genome sequencing results in ostensibly healthy COVID-19 positive individuals: GENCOV Study Canada
21. eP299: Genetics adviser: The development and usability testing of a new patient-centered digital health application to support clinical genomic testing
22. eP325: Medically actionable DNA variation from the GENCOV COVID-19 Genome Sequencing Study
23. Challenges and practical solutions for managing secondary genomic findings in primary care
24. The role of digital tools in the delivery of genomic medicine: enhancing patient-centered care
25. Health-care practitioners’ preferences for the return of secondary findings from next-generation sequencing: a discrete choice experiment
26. Effectiveness of the Genomics ADvISER decision aid for the selection of secondary findings from genomic sequencing: a randomized clinical trial
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