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437 results on '"Schrader, Kasmintan A."'

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1. Whole genome and transcriptome integrated analyses guide clinical care of pediatric poor prognosis cancers

2. Optimising clinical care through CDH1-specific germline variant curation: improvement of clinical assertions and updated curation guidelines

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

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

14. The Pancreatic Cancer Early Detection (PRECEDE) Study is a Global Effort to Drive Early Detection: Baseline Imaging Findings in High-Risk Individuals

16. Long-Read Sequencing of an Advanced Cancer Cohort Resolves Rearrangements, Unravels Haplotypes, and Reveals Methylation Landscapes

18. Improved structural variant interpretation for hereditary cancer susceptibility using long-read sequencing

19. 2023 Canadian Urological Association guideline: Genetic testing in prostate cancer

20. Current and new frontiers in hereditary cancer surveillance: Opportunities for liquid biopsy

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

23. “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

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

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

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

27. P658: Detection of variant parent-of-origin in diverse hereditary cancer syndromes using only the proband’s blood sample

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

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

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

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

34. Data from A Recurrent ERCC3 Truncating Mutation Confers Moderate Risk for Breast Cancer

35. Supplementary Figures 1 - 6, Tables 1 - 2 from A Recurrent ERCC3 Truncating Mutation Confers Moderate Risk for Breast Cancer

36. Supplementary Table 5 from Homologous Recombination Deficiency and Platinum-Based Therapy Outcomes in Advanced Breast Cancer

37. Supplementary Information from Homologous Recombination Deficiency and Platinum-Based Therapy Outcomes in Advanced Breast Cancer

38. Optimising clinical care through CDH1-specific germline variant curation: improvement of clinical assertions and updated curation guidelines.

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. O35: Parent-of-origin-aware genomic analysis infers segregation of pathogenic variants in SDHD without parental data*

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

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

47. Optimising clinical care throughCDH1-specific germline variant curation: improvement of clinical assertions and updated curation guidelines

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