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

2. Eliciting parental preferences and values for the return of additional findings from genomic sequencing

4. Expanding the Australian Newborn Blood Spot Screening Program using genomic sequencing: do we want it and are we ready?

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

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

7. 'Game Changer': Health Professionals' Views on the Clinical Utility of Circulating Tumor DNA Testing in Hereditary Cancer Syndrome Management

9. Quality of life drives patients' preferences for secondary findings from genomic sequencing

10. Effectiveness of the Genomics ADvISER decision aid for the selection of secondary findings from genomic sequencing: a randomized clinical trial

18. Genome-wide sequencing in acutely ill infants: genomic medicine's critical application?

20. Q-SEA - a tool for quality assessment of ethics analyses conducted as part of health technology assessments

21. Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening

23. perceptions of gene expression profiling in breast cancer treatment decisions

24. Recommendations for the predictive genetic test in Huntington's disease

25. An equity checklist : a framework for health technology assessments

39. HotSpot Do these genes make me look fat? Obesity and melanocortin-4 receptor gene deficiencies.

40. "Should I let them know I have this?": Multifaceted genetic discrimination and limited awareness of legal protections amongst individuals with hereditary cancer syndromes.

41. Canadian College of Medical Geneticists: clinical practice advisory document - responsibility to recontact for reinterpretation of clinical genetic testing.

42. International policies guiding the selection, analysis, and clinical management of secondary findings from genomic sequencing: A systematic review.

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

45. The Key Features of a Genetic Nondiscrimination Policy: A Delphi Consensus Statement.

46. Genetics Navigator: protocol for a mixed methods randomized controlled trial evaluating a digital platform to deliver genomic services in Canadian pediatric and adult populations.

47. "I Just Assumed This Was Already Being Done": Canadian Patient Preferences for Enhanced Data Sharing for Precision Oncology.

48. Variant classification changes over time in the clinical molecular diagnostic laboratory setting.

49. A proposal for an inclusive working definition of genetic discrimination to promote a more coherent debate.

50. Genetics providers' perspectives on the use of digital tools in clinical practice.

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