27 results on '"Eisen, Andrea"'
Search Results
2. Mainstream Model of Genetic Testing for Prostate Cancer at a Large Tertiary Cancer Centre
3. Analysis of Factors Associated With Pathological Complete Response in Patients With HER2-Positive Breast Cancer Receiving Neoadjuvant Chemotherapy
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
6. Validation of the International Breast Cancer Intervention Study (IBIS) model in the High Risk Ontario Breast Screening Program: A retrospective cohort study
7. High Risk Breast Cancer Screening is a Double Edged Sword: A Qualitative Study of Patient Perspectives on the Ontario High Risk Breast Cancer Screening Program
8. Breastfeeding and the risk of epithelial ovarian cancer among women with a BRCA1 or BRCA2 mutation
9. Age-specific ovarian cancer risks among women with a BRCA1 or BRCA2 mutation
10. Breast screening for survivors of breast cancer: A systematic review
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
17. P538: Curious but cautious: Patients’ preferences for all types of clinically actionable genomic incidental results
18. P523: Returning all clinically relevant findings from genomic sequencing: Preliminary results from the incidental genomics RCT
19. P409: Clinical utility of genomic sequencing for hereditary cancer syndromes: An observational chart review
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)
23. Cognitive markers of dementia risk in middle-aged women with bilateral salpingo-oophorectomy prior to menopause
24. Clinical Management Recommendations for Surveillance and Risk-Reduction Strategies for Hereditary Breast and Ovarian Cancer Among Individuals Carrying a Deleterious BRCA1 or BRCA2 Mutation
25. The risk of ovarian cancer after breast cancer in BRCA1 and BRCA2 carriers
26. What Comes Next? A Cohort Profile of Women Who Have Undergone BRCA1 and BRCA2 Testing in Ontario, Canada
27. Perceptions of Receptivity: Exploring Tobacco Use and Smoking Cessation Best Practices from the Perspectives of Individuals with Lung Cancer and Health Care Professionals: Findings from Phase I
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