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Neuropathology : Official Journal of the Japanese Society of Neuropathology|March 3, 2016
Gliosarcomas lack BRAFV600E mutation, but a subset exhibit β-catenin nuclear localizationKatherine E Schwetye, Nancy M Joseph, Hussam Al-Kateb, et al.
Diabetes|May 22, 2007
Multiple variants in vascular endothelial growth factor (VEGFA) are risk factors for time to severe retinopathy in type 1 diabetes: the DCCT/EDIC genetics studyHussam Al-Kateb, Lucia Mirea, Xinlei Xie, et al.
Circulation Research|May 23, 2002
Mutation in the ARH gene and a chromosome 13q locus influence cholesterol levels in a new form of digenic-recessive familial hypercholesterolemiaHussam Al-Kateb, Sylvia Bähring, Katrin Hoffmann, et al.
The Journal of Molecular Diagnostics : JMD|May 13, 2014
Detection of gene rearrangements in targeted clinical next-generation sequencingHaley J Abel, Hussam Al-Kateb, Catherine E Cottrell, 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.
Clinical Lymphoma, Myeloma & Leukemia|May 1, 2019
Future of Personalized Therapy Targeting Aberrant Signaling Pathways in Multiple MyelomaFaiz Anwer, Kevin Mathew Gee, Ahmad Iftikhar, et al.
Clinical Genetics|December 4, 2023
CAMTA1-related disorder: Phenotypic and molecular characterization of 26 new individuals and literature reviewHussam Al-Kateb, P Y Billie Au, Siren Berland, et al.
Cancer|October 28, 2014
Clinical next-generation sequencing in patients with non-small cell lung cancerIan S Hagemann, Siddhartha Devarakonda, Christina M Lockwood, et al.
Human Pathology|May 24, 2025
Morphologic and immunophenotypic characterization of conventional FLCN-mutated tumors (FMT) compared to a series of 8 non-conventional FMTSounak Gupta, Surendra Dasari, Wei Shen, et al.
Mayo Clinic Proceedings|February 13, 2026
Utility of Next-Generation Sequencing in Renal Neoplasia, Including Tumors With Clear Cytoplasm and Rare Phenotypes (ELOC/MITF Alterations and Mismatch Repair Deficiency)Michael McCarthy, Antonina A Wojcik, Emily G Barr Fritcher, et al.
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