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Novel low‐grade renal spindle cell neoplasm with HEY1::NCOA2 fusion that is distinct from mesenchymal chondrosarcoma

Genes chromosomes & cancer, 2023-03, Vol.62 (3), p.171-175

2023

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Detecting disease‐defining gene fusions in unclassified round cell sarcomas using anchored multiplex PCR/targeted RNA next‐generation sequencing—Molecular and clinicopathological characterization of 16 cases

Genes chromosomes & cancer, 2019-10, Vol.58 (10), p.713-722

2019

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A novel MBTD1‐PHF1 gene fusion in endometrial stromal sarcoma: A case report and literature review

Genes chromosomes & cancer, 2020-07, Vol.59 (7), p.428-432

2020

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Characterization of novel USP6 gene rearrangements in a subset of so-called cellular fibroma of tendon sheath

Modern pathology, 2021-01, Vol.34 (1), p.13-19

2021

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6q25.1 (TAB2) microdeletion is a risk factor for hypoplastic left heart: a case report that expands the phenotype

BMC cardiovascular disorders, 2020-03, Vol.20 (1), p.137-7, Article 137

2020

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Droplet Digital PCR (ddPCR) as a Novel Technology in Detecting CTNNB1 Mutations in Desmoid Fibromatosis

Applied immunohistochemistry & molecular morphology, 2022-11, Vol.30 (10), p.662-667

2022

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Assessing Genomic Copy Number Alterations as Best Practice for Renal Cell Neoplasia: An Evidence-Based Review from the Cancer Genomics Consortium Workgroup

Cancer genetics, 2020-06, Vol.244, p.40-54

2020

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Loss of the flagellum happened only once in the fungal lineage: phylogenetic structure of kingdom Fungi inferred from RNA polymerase II subunit genes

BMC evolutionary biology, 2006-09, Vol.6, p.74

2006

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Pediatric Low-Grade Spindle Cell Neoplasm With A Novel AK5::ALK Fusion: A Case Report

Annals of otology, rhinology & laryngology, 2023-04, Vol.132 (4), p.470-475

2023

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Deletion of FUNDC2 and CMC4 on Chromosome Xq28 Is Sufficient to Cause Hypergonadotropic Hypogonadism in Men

Frontiers in genetics, 2020-09, Vol.11, p.557341-557341

2020

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Body plan evolution of ascomycetes, as inferred from an RNA polymerase II phylogeny

Proceedings of the National Academy of Sciences - PNAS, 2004-03, Vol.101 (13), p.4507-4512

2004

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Inflammatory myofibroblastic tumor of the mesentery with a SQSTM1::ALK fusion responding to alectinib

Cancer reports, 2023-03, Vol.6 (3), p.e1792-n/a

2023

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Using RPB1 sequences to improve phylogenetic inference among mushrooms (Inocybe, Agaricales)

American journal of botany, 2002-04, Vol.89 (4), p.688-698

2002

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Spindle Cell Neoplasm With a Novel MN1::TAF3 Fusion: A Rare Case in a Toddler

Journal of pediatric hematology/oncology, 2024-11, Vol.46 (8), p.442-445

2024

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Neurotrophic Receptor Tyrosine Kinase 2 (NTRK2) Alterations in Low-Grade Gliomas: Report of a Novel Gene Fusion Partner in a Pilocytic Astrocytoma and Review of the Literature

Case reports in pathology, 2020, Vol.2020 (2020), p.1-7

2020

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Gene fusion analysis in renal cell carcinoma by FusionPlex RNA‐sequencing and correlations of molecular findings with clinicopathological features

Genes chromosomes & cancer, 2020-01, Vol.59 (1), p.40-49

2020

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Myoepithelial carcinoma of the parotid gland with a novel CTCF::NCOA2 fusion

Genes chromosomes & cancer, 2023-03, Vol.62 (3), p.161-166

2023

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Clinical Validation of FusionPlex RNA Sequencing and Its Utility in the Diagnosis and Classification of Hematologic Neoplasms

The Journal of molecular diagnostics : JMD, 2023-12, Vol.25 (12), p.932-944

2023

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Sporadic oncocytic tumors with features intermediate between oncocytoma and chromophobe renal cell carcinoma: comprehensive clinicopathological and genomic profiling

Human pathology, 2020-10, Vol.104, p.18-29

2020

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Recurrent genetic alterations in hepatitis C-associated hepatocellular carcinoma detected by genomic microarray: a genetic, clinical and pathological correlation study

Molecular cytogenetics, 2014-11, Vol.7 (1), p.81-81, Article 81

2014

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Calcified chondroid mesenchymal neoplasms with FN1-receptor tyrosine kinase gene fusions including FGFR2, FGFR1, MERTK, NTRK1, and TEK: a molecular and clinicopathologic analysis

Modern pathology, 2021-07, Vol.34 (7), p.1373-1383

2021

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ALK rearranged renal cell carcinoma (ALK-RCC): a multi-institutional study of twelve cases with identification of novel partner genes CLIP1, KIF5B and KIAA1217

Modern pathology, 2020-12, Vol.33 (12), p.2564-2579

2020

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Amplification of DNA damage-inducible transcript 3 (DDIT3) is associated with myxoid liposarcoma-like morphology and homologous lipoblastic differentiation in dedifferentiated liposarcoma

Modern pathology, 2019-04, Vol.32 (4), p.585-592

2019

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GAB1::ABL1 fusions define a distinctive soft tissue neoplasm, with variable perineurial differentiation, and a predilection for children and young adults

Genes chromosomes & cancer, 2023-08, Vol.62 (8), p.449-459

2023

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Novel BRAF gene fusions and activating point mutations in spindle cell sarcomas with histologic overlap with infantile fibrosarcoma

Modern pathology, 2021-08, Vol.34 (8), p.1530-1540

2021

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Novel low‐grade renal spindle cell neoplasm with HEY1::NCOA2 fusion that is distinct from mesenchymal chondrosarcoma

Detecting disease‐defining gene fusions in unclassified round cell sarcomas using anchored multiplex PCR/targeted RNA next‐generation sequencing—Molecular and clinicopathological characterization of 16 cases

A novel MBTD1‐PHF1 gene fusion in endometrial stromal sarcoma: A case report and literature review

Characterization of novel USP6 gene rearrangements in a subset of so-called cellular fibroma of tendon sheath

6q25.1 (TAB2) microdeletion is a risk factor for hypoplastic left heart: a case report that expands the phenotype

Droplet Digital PCR (ddPCR) as a Novel Technology in Detecting CTNNB1 Mutations in Desmoid Fibromatosis

Assessing Genomic Copy Number Alterations as Best Practice for Renal Cell Neoplasia: An Evidence-Based Review from the Cancer Genomics Consortium Workgroup

Loss of the flagellum happened only once in the fungal lineage: phylogenetic structure of kingdom Fungi inferred from RNA polymerase II subunit genes

Pediatric Low-Grade Spindle Cell Neoplasm With A Novel AK5::ALK Fusion: A Case Report

Deletion of FUNDC2 and CMC4 on Chromosome Xq28 Is Sufficient to Cause Hypergonadotropic Hypogonadism in Men

Body plan evolution of ascomycetes, as inferred from an RNA polymerase II phylogeny

Inflammatory myofibroblastic tumor of the mesentery with a SQSTM1::ALK fusion responding to alectinib

Using RPB1 sequences to improve phylogenetic inference among mushrooms (Inocybe, Agaricales)

Spindle Cell Neoplasm With a Novel MN1::TAF3 Fusion: A Rare Case in a Toddler

Neurotrophic Receptor Tyrosine Kinase 2 (NTRK2) Alterations in Low-Grade Gliomas: Report of a Novel Gene Fusion Partner in a Pilocytic Astrocytoma and Review of the Literature

Gene fusion analysis in renal cell carcinoma by FusionPlex RNA‐sequencing and correlations of molecular findings with clinicopathological features

Myoepithelial carcinoma of the parotid gland with a novel CTCF::NCOA2 fusion

Clinical Validation of FusionPlex RNA Sequencing and Its Utility in the Diagnosis and Classification of Hematologic Neoplasms

Sporadic oncocytic tumors with features intermediate between oncocytoma and chromophobe renal cell carcinoma: comprehensive clinicopathological and genomic profiling

Recurrent genetic alterations in hepatitis C-associated hepatocellular carcinoma detected by genomic microarray: a genetic, clinical and pathological correlation study

Calcified chondroid mesenchymal neoplasms with FN1-receptor tyrosine kinase gene fusions including FGFR2, FGFR1, MERTK, NTRK1, and TEK: a molecular and clinicopathologic analysis

ALK rearranged renal cell carcinoma (ALK-RCC): a multi-institutional study of twelve cases with identification of novel partner genes CLIP1, KIF5B and KIAA1217

Amplification of DNA damage-inducible transcript 3 (DDIT3) is associated with myxoid liposarcoma-like morphology and homologous lipoblastic differentiation in dedifferentiated liposarcoma

GAB1::ABL1 fusions define a distinctive soft tissue neoplasm, with variable perineurial differentiation, and a predilection for children and young adults

Novel BRAF gene fusions and activating point mutations in spindle cell sarcomas with histologic overlap with infantile fibrosarcoma

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