Numrah Fadra

发表

Confirming Variants in Next-Generation Sequencing Panel Testing by Sanger Sequencing.

Eric W. Klee, Matthew J. Ferber, Devin Oglesbee, 2015, The Journal of molecular diagnostics : JMD.

Impact of RNA degradation on fusion detection by RNA-seq

Asha A. Nair, J. Jen, A. Nair, 2016, BMC Genomics.

Development and Verification of an RNA Sequencing (RNA-Seq) Assay for the Detection of Gene Fusions in Tumors.

Gavin R. Oliver, Jesse S. Voss, Asha A. Nair, 2018, The Journal of molecular diagnostics : JMD.

Structure–function analysis of hepatitis C virus envelope glycoproteins E1 and E2

Sergei L. Kosakovsky Pond, N. Pattabiraman, R. Mazumder, 2015, Journal of biomolecular structure & dynamics.

Multiple isodicentric Y chromosomes in myeloid malignancies: a unique cytogenetic entity and potential therapeutic target

Gavin R. Oliver, M. Patnaik, K. Halling, 2018, Leukemia & lymphoma.

Transcriptomic and immunophenotypic characterization of two cases of adamantinoma‐like Ewing sarcoma of the thyroid gland

M. Rivera, Kay Minn, K. Halling, 2023, Histopathology.

RNA-seq Reveals Differences in Expressed Tumor Mutational Burden in Colorectal and Endometrial Cancer With and Without Defective DNA Mismatch Repair.

Jesse S. Voss, Asha A. Nair, J. Jen, 2021, The Journal of molecular diagnostics : JMD.

Preemptive Pharmacogenomic Testing for Precision Medicine: A Comprehensive Analysis of Five Actionable Pharmacogenomic Genes Using Next-Generation DNA Sequencing and a Customized CYP2D6 Genotyping Cascade.

Yuan Ji, Richard M Weinshilboum, Linnea M Baudhuin, 2016, The Journal of molecular diagnostics : JMD.

Uterine inflammatory Myofibroblastic tumors in pregnant women with and without involvement of the placenta: a study of six cases with identification of a novel TIMP3-RET fusion.

A. Clayton, G. Keeney, J. K. Schoolmeester, 2020, Human pathology.

LPCAT1-TERT fusions are uniquely recurrent in epithelioid trophoblastic tumors and positively regulate cell growth

Gavin R. Oliver, Jesse S. Voss, J. Jen, 2021, PloS one.

Preemptive Pharmacogenomic Testing for Precision Medicine: A Comprehensive Analysis of Five Actionable Pharmacogenomic Genes Using Next-Generation DNA Sequencing and a Customized CYP2D6 Genotyping Cascade.

P. Caraballo, R. Weinshilboum, J. Black, 2016, The Journal of molecular diagnostics : JMD.

Clinical Validation of a Next Generation Sequencing Panel Test for Hereditary Colorectal Cancer

M. Ferber, Numrah Fadra, Brittany C Thomas, 2016 .

Clinical Validation of Tagmentation-Based Genome Sequencing for Germline Disorders.

E. Thorland, H. Kearney, Shawn McClelland, 2023, The Journal of molecular diagnostics : JMD.

Ancillary immunohistochemical and molecular testing in the classification of cutaneous sweat gland/duct neoplasms: a validation study with emphasis on histomorphologic correlation and pathological diagnosis.

N. Comfere, Numrah Fadra, C. Wieland, 2024, Human pathology.

RNA sequencing identifies a novel USP9X‐USP6 promoter swap gene fusion in a primary aneurysmal bone cyst

Asha A. Nair, P. Blackburn, A. Nair, 2019, Genes, chromosomes & cancer.

Polymorphous Low-Grade Neuroepithelial Tumor of the Young (PLNTY): Molecular Profiling Confirms Frequent MAPK Pathway Activation.

Asha A. Nair, C. Ida, T. Kaufmann, 2021, Journal of neuropathology and experimental neurology.

Chondroid Synoviocytic Neoplasm: A Clinicopathologic, Immunohistochemical and Molecular Genetic Study of a Distinctive Tumor of Synoviocytes.

A. Folpe, Numrah Fadra, Rohini Mopuri, 2024, Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc.