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Beth A Pitel

Showing results (41-50 of 48) with videos related to

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Human Pathology|December 25, 2023
Next generation sequencing-based identification of fusion-driven renal neoplasia: A single institution experienceBurak Tekin, Christopher D Hofich, Beth A Pitel, et al.
The Journal of Molecular Diagnostics : JMD|February 2, 2025
Clinical Validation of the TruSight Oncology 500 Assay for the Detection and Reporting of Pan-Cancer BiomarkersHussam Al-Kateb, Shannon M Knight, Gopinath Sivasankaran, et al.
American Journal of Hematology|January 11, 2020
Clinical utility of fluorescence in situ hybridization-based diagnosis of BCR-ABL1 like (Philadelphia chromosome like) B-acute lymphoblastic leukemiaTheodora Anagnostou, Ryan A Knudson, Kathryn E Pearce, et al.
European Urology|April 19, 2025
Renal Neoplasia in Birt-Hogg-Dubé Syndrome: Integrated Histopathologic, Bulk, and Single-cell Transcriptomic AnalysisSounak Gupta, Surendra Dasari, Rachel R Warren, et al.
Nature Genetics|April 5, 2020
A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancerAlex H Wagner, Brian Walsh, Georgia Mayfield, et al.
The Journal of Molecular Diagnostics : JMD|November 9, 2024
SARCP, a Clinical Next-Generation Sequencing Assay for the Detection of Gene Fusions in Sarcomas: A Description of the First 652 CasesMazen A Atiq, Jagadheshwar Balan, Patrick R Blackburn, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 1, 2022
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)Peter Horak, Malachi Griffith, Arpad M Danos, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 5, 2022
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)Peter Horak, Malachi Griffith, Arpad M Danos, et al.
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Showing results (41-50 of 48) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 48 results.
Human Pathology|December 25, 2023
Next generation sequencing-based identification of fusion-driven renal neoplasia: A single institution experienceBurak Tekin, Christopher D Hofich, Beth A Pitel, et al.
The Journal of Molecular Diagnostics : JMD|February 2, 2025
Clinical Validation of the TruSight Oncology 500 Assay for the Detection and Reporting of Pan-Cancer BiomarkersHussam Al-Kateb, Shannon M Knight, Gopinath Sivasankaran, et al.
American Journal of Hematology|January 11, 2020
Clinical utility of fluorescence in situ hybridization-based diagnosis of BCR-ABL1 like (Philadelphia chromosome like) B-acute lymphoblastic leukemiaTheodora Anagnostou, Ryan A Knudson, Kathryn E Pearce, et al.
European Urology|April 19, 2025
Renal Neoplasia in Birt-Hogg-Dubé Syndrome: Integrated Histopathologic, Bulk, and Single-cell Transcriptomic AnalysisSounak Gupta, Surendra Dasari, Rachel R Warren, et al.
Nature Genetics|April 5, 2020
A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancerAlex H Wagner, Brian Walsh, Georgia Mayfield, et al.
The Journal of Molecular Diagnostics : JMD|November 9, 2024
SARCP, a Clinical Next-Generation Sequencing Assay for the Detection of Gene Fusions in Sarcomas: A Description of the First 652 CasesMazen A Atiq, Jagadheshwar Balan, Patrick R Blackburn, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 1, 2022
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)Peter Horak, Malachi Griffith, Arpad M Danos, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 5, 2022
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)Peter Horak, Malachi Griffith, Arpad M Danos, et al.
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