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2. “I just wanted more”: Hereditary cancer syndromes patients’ perspectives on the utility of circulating tumour DNA testing for cancer screening

3. A Genomic Counseling Model for Population-Based Sequencing: A Pre-Post Intervention Study

4. Genetics providers’ perspectives on the use of digital tools in clinical practice

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

8. “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

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

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

11. Public knowledge of SARS-CoV-2 serological and viral lineage laboratory testing and result interpretation: A GENCOV study cross-sectional survey

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

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

22. “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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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