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1. Molecular and Immunophenotypic Correlates of Metastatic Epithelioid Angiomyolipoma Include Alterations of TP53, RB1, and ATRX

2. Prospective evaluation of genome sequencing to compare conventional cytogenetics in acute myeloid leukemia

6. Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC)

7. Genomic attributes of prostate cancer across primary and metastatic noncastrate and castrate resistant disease states: a next generation sequencing study of 183 patients

11. Next generation sequencing-based identification of fusion-driven renal neoplasia: A single institution experience

12. 534 Responses to immunotherapy based on programmed death-ligand 1 (PD-L1) copy number variation (CNV) status in patients with advanced non-small cell lung cancer (NSCLC)

14. Constitutional chromosome rearrangements that mimic the 2017 world health organization “acute myeloid leukemia with recurrent genetic abnormalities”: A study of three cases and review of the literature

15. Myeloid malignancies with 5q and 7q deletions are associated with extreme genomic complexity, biallelic TP53 variants, and very poor prognosis

20. Mate pair sequencing outperforms fluorescence in situ hybridization in the genomic characterization of multiple myeloma

22. ATRIP11:: FLT3gene fusion in a patient with myeloid/lymphoid neoplasm with eosinophilia and tyrosine kinase gene fusions: a case report and review of the literature

23. Optical Genome Mapping in Acute Myeloid Leukemia: A Multicenter Evaluation

24. 44. An international landscape of cancer NGS reporting practices

27. Molecular and Immunophenotypic Correlates of Metastatic Epithelioid Angiomyolipoma Include Alterations of TP53, RB1, and ATRX

28. Characterization of unusual iAMP21 B‐lymphoblastic leukemia ( iAMP21‐ALL ) from the Mayo Clinic and Children's Oncology Group

29. A TRIP11:: FLT3 gene fusion in a patient with myeloid/lymphoid neoplasm with eosinophilia and tyrosine kinase gene fusions: a case report and review of the literature.

30. 35. Atypical FISH patterns clarified by RNAseq in solid tumor specimens

31. 15. Standard procedure for the curation and maintenance of cancer-specific gene lists

33. Assessment of Risk of Hereditary Predisposition in Patients With Melanoma and/or Mesothelioma and Renal Neoplasia

35. 24. Clinical utility of mate pair sequencing as a reflex test in B-lymphoblastic leukemia/lymphoma

36. Optical genome mapping for assessment of genomic aberrations in acute myeloid leukemia: a multicenter evaluation

37. 12. Analysis of the clinical utility of mate pair sequencing to further characterize congenital chromosome abnormalities

39. A National Multicenter Evaluation of the Clinical Utility of Optical Genome Mapping for Assessment of Genomic Aberrations in Acute Myeloid Leukemia

40. Clinical Value of Next Generation Sequencing in the Detection of Recurring Structural Rearrangements and Copy Number Abnormalities in Acute Myeloid Leukemia

41. Collaborative, Multidisciplinary Evaluation of Cancer Variants Through Virtual Molecular Tumor Boards Informs Local Clinical Practices

42. Abstract 5707: A standard operating procedure for the interpretation of oncogenicity/pathogenicity of somatic mutations

43. Abstract 3215: ClinGen somatic cancer working group: Disseminating standardized cancer molecular diagnostic data and evidence through global collaboration and expert curation

44. Abstract 3222: The Virtual Molecular Tumor Board of the Variant Interpretation for Cancer Consortium: A systematic gateway connecting cancer genome interpretation and progress in genomic knowledgebases in cancer

45. Abstract 1096: Harmonization standards from the Variant Interpretation for Cancer Consortium

46. 46. ClinGen somatic cancer working group: Enhancing standardized interpretation of cancer genetic data for clinical use

47. 59. Integrating cytogenomic and sequence variants in the GA4GH variation representation specification

48. 42. Genomic gymnastics: Using RNAseq and mate pair sequencing to collaboratively decipher structural variation

49. 20. A resource for our clinical genomics community: The Compendium of Cancer Genome Aberrations (CCGA)

50. 67. NUP98 rearrangements in hematologic malignancies: A 4-year review from the genomics laboratory

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