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27 results on '"Eisen, Andrea"'

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1. Incidence of endometrial cancer in BRCA mutation carriers

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

5. “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

8. Breastfeeding and the risk of epithelial ovarian cancer among women with a BRCA1 or BRCA2 mutation

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

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

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

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

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

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

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

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

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

22. P054: Creation of the Ontario Hereditary Cancer Research Network (OHCRN)

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