Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Beth A Pitel

Showing results (11-20 of 48) with videos related to

Pageof 5
Sort By:
Cold Spring Harbor Molecular Case Studies|June 5, 2019
Elucidating a false-negative <i>MYC</i> break-apart fluorescence in situ hybridization probe study by next-generation sequencing in a patient with high-grade B-cell lymphoma with <i>IGH/MYC</i> and <i>IGH/BCL2</i> rearrangementsJess F Peterson, Beth A Pitel, Stephanie A Smoley, et al.
Cancer Genetics|August 23, 2020
Integrated genomic analysis using chromosomal microarray, fluorescence in situ hybridization and mate pair analyses: Characterization of a cryptic t(9;22)(p24.1;q11.2)/BCR-JAK2 in myeloid/lymphoid neoplasm with eosinophiliaJessica S Snider, Iya Znoyko, Kathryn G Lindsey, et al.
Translational Oncology|June 3, 2026
RNA-Based and DNA-Based Next-Generation Sequencing of KIT and PDGFRA Mutations in Gastrointestinal Stromal Tumors: Analytical Performance and Epidemiologic InsightsSoumya Jaladi, Saba Alvand, Beth A Pitel, et al.
Human Pathology|September 30, 2018
Use of mate-pair sequencing to characterize a complex cryptic BCR/ABL1 rearrangement observed in a newly diagnosed case of chronic myeloid leukemiaJess F Peterson, Beth A Pitel, Stephanie A Smoley, et al.
The Journal of Molecular Diagnostics : JMD|December 20, 2025
Development and Clinical Validation of OncCNV: A Pipeline for Comprehensive Genome-Wide Analysis of Oncogene Amplifications, Homozygous Deletions, and Biallelic Inactivation of Tumor Suppressor Genes Using the TruSight Oncology 500 KitStephanie A Smoley, Gopinath Sivasankaran, Mallika Gandham, et al.
Cold Spring Harbor Molecular Case Studies|January 10, 2023
A <i>TRIP11:: FLT3</i> gene fusion in a patient with myeloid/lymphoid neoplasm with eosinophilia and tyrosine kinase gene fusions: a case report and review of the literatureElise R Venable, Marie-France Gagnon, Beth A Pitel, et al.
Blood Advances|April 25, 2019
Characterization of a cryptic <i>IGH/CCND1</i> rearrangement in a case of mantle cell lymphoma with negative <i>CCND1</i> FISH studiesJess F Peterson, Linda B Baughn, Rhett P Ketterling, et al.
JAMA Network Open|November 12, 2021
Assessment of Risk of Hereditary Predisposition in Patients With Melanoma and/or Mesothelioma and Renal NeoplasiaSounak Gupta, Lori A Erickson, Christine M Lohse, et al.
Genes, Chromosomes & Cancer|February 2, 2019
Acute leukemias harboring KMT2A/MLLT10 fusion: a 10-year experience from a single genomics laboratoryJess F Peterson, William R Sukov, Beth A Pitel, et al.
The Journal of Molecular Diagnostics : JMD|September 3, 2025
Evaluation of Atypical FISH Findings by RNA SequencingBeth A Pitel, Saba Alvand, Mark A Montanari, et al.
Pageof 5

Showing results (11-20 of 48) with videos related to

Sort By:
Pageof 5
Cold Spring Harbor Molecular Case Studies|June 5, 2019
Elucidating a false-negative <i>MYC</i> break-apart fluorescence in situ hybridization probe study by next-generation sequencing in a patient with high-grade B-cell lymphoma with <i>IGH/MYC</i> and <i>IGH/BCL2</i> rearrangementsJess F Peterson, Beth A Pitel, Stephanie A Smoley, et al.
Cancer Genetics|August 23, 2020
Integrated genomic analysis using chromosomal microarray, fluorescence in situ hybridization and mate pair analyses: Characterization of a cryptic t(9;22)(p24.1;q11.2)/BCR-JAK2 in myeloid/lymphoid neoplasm with eosinophiliaJessica S Snider, Iya Znoyko, Kathryn G Lindsey, et al.
Translational Oncology|June 3, 2026
RNA-Based and DNA-Based Next-Generation Sequencing of KIT and PDGFRA Mutations in Gastrointestinal Stromal Tumors: Analytical Performance and Epidemiologic InsightsSoumya Jaladi, Saba Alvand, Beth A Pitel, et al.
Human Pathology|September 30, 2018
Use of mate-pair sequencing to characterize a complex cryptic BCR/ABL1 rearrangement observed in a newly diagnosed case of chronic myeloid leukemiaJess F Peterson, Beth A Pitel, Stephanie A Smoley, et al.
The Journal of Molecular Diagnostics : JMD|December 20, 2025
Development and Clinical Validation of OncCNV: A Pipeline for Comprehensive Genome-Wide Analysis of Oncogene Amplifications, Homozygous Deletions, and Biallelic Inactivation of Tumor Suppressor Genes Using the TruSight Oncology 500 KitStephanie A Smoley, Gopinath Sivasankaran, Mallika Gandham, et al.
Cold Spring Harbor Molecular Case Studies|January 10, 2023
A <i>TRIP11:: FLT3</i> gene fusion in a patient with myeloid/lymphoid neoplasm with eosinophilia and tyrosine kinase gene fusions: a case report and review of the literatureElise R Venable, Marie-France Gagnon, Beth A Pitel, et al.
Blood Advances|April 25, 2019
Characterization of a cryptic <i>IGH/CCND1</i> rearrangement in a case of mantle cell lymphoma with negative <i>CCND1</i> FISH studiesJess F Peterson, Linda B Baughn, Rhett P Ketterling, et al.
JAMA Network Open|November 12, 2021
Assessment of Risk of Hereditary Predisposition in Patients With Melanoma and/or Mesothelioma and Renal NeoplasiaSounak Gupta, Lori A Erickson, Christine M Lohse, et al.
Genes, Chromosomes & Cancer|February 2, 2019
Acute leukemias harboring KMT2A/MLLT10 fusion: a 10-year experience from a single genomics laboratoryJess F Peterson, William R Sukov, Beth A Pitel, et al.
The Journal of Molecular Diagnostics : JMD|September 3, 2025
Evaluation of Atypical FISH Findings by RNA SequencingBeth A Pitel, Saba Alvand, Mark A Montanari, et al.
Pageof 5