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154 results on '"Clausen, Marc"'

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1. Genetics Adviser: The development and usability testing of a new patient digital health application to support clinical genomic testing

4. Genome screening, reporting, and genetic counseling for healthy populations

5. A comprehensive genomic reporting structure for communicating all clinically significant primary and secondary findings

10. Prospective cohort study of genomic newborn screening: BabyScreen+ pilot study protocol

14. Development of patient “profiles” to tailor counseling for incidental genomic sequencing results

15. “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

16. P892: “Should I let them know I have this?”: Concerns and experiences of genetic discrimination amongst individuals with hereditary cancer syndromes

17. P881: Revealing the hidden costs: Exploring the financial toxicity of hereditary cancer syndromes

18. P867: “I worry I don’t have control”: The psychosocial impacts of living with a hereditary cancer syndrome

19. P862: How to conduct equitable genetics research to include underserved populations: A systematic review of best practices

20. P733: Comparative analysis of DNA variant classifications between the GENCOV COVID-19 genome study and the ClinVar database

21. P710: Phenome-wide association study (PheWAS) for the Canadian HostSeq Biobank

22. P709: Self reported vs genetic ancestry from the GENCOV COVID-19 genomic sequencing study

23. P574: Summary of findings from comprehensive genome sequencing performed in a healthy population cohort*

25. P555: Clinical utility returning of all types of medically relevant genomic sequencing findings: An observational study

26. P553: How do patients with hereditary cancer syndromes navigate the healthcare system? A qualitative comparative study across Canada

28. P523: Returning all clinically relevant findings from genomic sequencing: Preliminary results from the incidental genomics RCT

30. A model for the return and referral of all clinically significant secondary findings of genomic sequencing

31. A second update on mapping the human genetic architecture of COVID-19

33. P436: Population genome screening identifies previously undiagnosed disease: A case series

34. P409: Clinical utility of genomic sequencing for hereditary cancer syndromes: An observational chart review

35. P375: Fragmented systems of care: An overview of Canadian health system care models for hereditary cancer syndromes

36. P406: Partnering with patients to explore the psychosocial and socioeconomic impacts of hereditary cancer syndromes

38. P391: What are patients’ perspectives on the privacy and security of digital genomic tools? A qualitative study

39. P357: Replication of genetic variation associated with COVID-19 clinical outcomes: The GENCOV Prospective Cohort Study

40. P382: Professionals’ perspectives on the use of digital tools to support patient recontact in clinical genetics

41. P543: Comparing the analytical performance of exome sequencing and traditional panel testing in a cancer population

42. Genome screening, reporting, and genetic counseling for healthy populations

44. “Doctors shouldn’t have to cheat the system”: Clinicians’ real-world experiences of the utility of genomic sequencing

45. Genetics Adviser: a protocol for a mixed-methods randomised controlled trial evaluating a digital platform for genetics service delivery

46. eP502: How will returning variants of uncertain significance impact healthcare use? A cross-sectional survey

47. eP392: A comprehensive genomic test reporting structure for communicating cancer and incidental findings

49. eP294: Return of genome sequencing results in ostensibly healthy COVID-19 positive individuals: GENCOV Study Canada

50. eP299: Genetics adviser: The development and usability testing of a new patient-centered digital health application to support clinical genomic testing

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