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NTRK fusion detection across multiple assays and 33,997 cases: diagnostic implications and pitfalls

Modern pathology, 2020-01, Vol.33 (1), p.38-46

2020

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Detection of NTRK Fusions: Merits and Limitations of Current Diagnostic Platforms

Cancer research (Chicago, Ill.), 2019-07, Vol.79 (13), p.3163-3168

2019

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Sulfated Glycosaminoglycans Accelerate Transthyretin Amyloidogenesis by Quaternary Structural Conversion

Biochemistry (Easton), 2011-02, Vol.50 (6), p.1001-1015

2011

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Evaluation of the rapid Idylla IDH1-2 mutation assay in FFPE glioma samples

Diagnostic pathology, 2024-05, Vol.19 (1), p.70-70, Article 70

2024

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Towards a single-assay approach: a combined DNA/RNA sequencing panel eliminates diagnostic redundancy and detects clinically-relevant fusions in neuropathology

Acta neuropathologica communications, 2022-11, Vol.10 (1), p.167-167, Article 167

2022

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The Emerging Molecular Landscape of Urothelial Carcinoma

Surgical pathology clinics, 2016-09, Vol.9 (3), p.391-404

2016

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Challenges in the Diagnosis of Urothelial Carcinoma Variants: Can Emerging Molecular Data Complement Pathology Review?

Urology (Ridgewood, N.J.), 2017-04, Vol.102, p.7-16

2017

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Practical Considerations for Oncogenic Fusion Detection and Reporting in Solid Tumors

The journal of applied laboratory medicine, 2024-01, Vol.9 (1), p.116-123

Solomon, James P

2024

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TRK Fusions Are Enriched in Cancers with Uncommon Histologies and the Absence of Canonical Driver Mutations

Clinical cancer research, 2020-04, Vol.26 (7), p.1624-1632

2020

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Her2/neu Status Determination in Breast Cancer: A Single Institutional Experience Using a Dual-Testing Approach With Immunohistochemistry and Fluorescence In Situ Hybridization

American journal of clinical pathology, 2017-04, Vol.147 (4), p.432-437

2017

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Comparison of RNA-Based Next-Generation Sequencing Assays for the Detection of NTRK Gene Fusions

The Journal of molecular diagnostics : JMD, 2021-11, Vol.23 (11), p.1443-1451

2021

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Apocrine Variant of Pleomorphic Lobular Carcinoma In Situ: Further Clinical, Histopathologic, Immunohistochemical, and Molecular Characterization of an Emerging Entity

The American journal of surgical pathology, 2020-08, Vol.44 (8), p.1092

2020

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Aβ induces astrocytic glutamate release, extrasynaptic NMDA receptor activation, and synaptic loss

Proceedings of the National Academy of Sciences - PNAS, 2013-07, Vol.110 (27), p.E2518-E2527

2013

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Use of the Afirma Xpression Atlas for cytologically indeterminate, Afirma Genomic Sequencing Classifier suspicious thyroid nodules: Clinicopathologic analysis with postoperative molecular testing

American journal of clinical pathology, 2024-05, Vol.161 (5), p.463-468

2024

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Diagnostic interobserver agreement for thyroid fine-needle aspirates: Effects of reviewer experience and molecular diagnostics

American journal of clinical pathology, 2024-04

2024

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Morphologic and Molecular Characteristics of Bladder Cancer

Surgical pathology clinics, 2015-12, Vol.8 (4), p.663-676

2015

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Bioinformatically Expanded Next-Generation Sequencing Analysis Optimizes Identification of Therapeutically Relevant MET Copy Number Alterations in >50,000 Tumors

Clinical cancer research, 2022-11, Vol.28 (21), p.4649-4659

2022

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Molecular Diagnostics of Non-Hodgkin Lymphoma

The cancer journal (Sudbury, Mass.), 2020-05, Vol.26 (3), p.186

2020

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Anaplastic Transformation of Papillary Thyroid Cancer in the Retroperitoneum

Case reports in pathology, 2015-01, Vol.2015, p.241308-4

2015

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Gelsolin amyloidosis: genetics, biochemistry, pathology and possible strategies for therapeutic intervention

Critical reviews in biochemistry and molecular biology, 2012-05, Vol.47 (3), p.282-296

2012

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A Rare PDGFRA Exon 15 Germline Mutation Identified in a Patient With Phenotypic Manifestations Concerning for GIST-Plus Syndrome: A Case Report and Review of Literature

International journal of surgical pathology, 2023-09, Vol.31 (6), p.1139-1145

2023

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Clinical Experience of Cerebrospinal Fluid–Based Liquid Biopsy Demonstrates Superiority of Cell-Free DNA over Cell Pellet Genomic DNA for Molecular Profiling

The Journal of molecular diagnostics : JMD, 2021-06, Vol.23 (6), p.742-752

2021

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Her2/neu Status Determination in Breast Cancer

American journal of clinical pathology, 2017-04, Vol.147 (4), p.432-437

2017

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Heparin Binds 8 kDa Gelsolin Cross-β-Sheet Oligomers and Accelerates Amyloidogenesis by Hastening Fibril Extension

Biochemistry (Easton), 2011-04, Vol.50 (13), p.2486-2498

2011

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Combining molecular testing and the Bethesda category III:VI ratio for thyroid fine‐needle aspirates: A quality‐assurance metric for evaluating diagnostic performance in a cytopathology laboratory

Cancer cytopathology, 2022-04, Vol.130 (4), p.259-274

2022

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NTRK fusion detection across multiple assays and 33,997 cases: diagnostic implications and pitfalls

Detection of NTRK Fusions: Merits and Limitations of Current Diagnostic Platforms

Sulfated Glycosaminoglycans Accelerate Transthyretin Amyloidogenesis by Quaternary Structural Conversion

Evaluation of the rapid Idylla IDH1-2 mutation assay in FFPE glioma samples

Towards a single-assay approach: a combined DNA/RNA sequencing panel eliminates diagnostic redundancy and detects clinically-relevant fusions in neuropathology

The Emerging Molecular Landscape of Urothelial Carcinoma

Challenges in the Diagnosis of Urothelial Carcinoma Variants: Can Emerging Molecular Data Complement Pathology Review?

Practical Considerations for Oncogenic Fusion Detection and Reporting in Solid Tumors

TRK Fusions Are Enriched in Cancers with Uncommon Histologies and the Absence of Canonical Driver Mutations

Her2/neu Status Determination in Breast Cancer: A Single Institutional Experience Using a Dual-Testing Approach With Immunohistochemistry and Fluorescence In Situ Hybridization

Comparison of RNA-Based Next-Generation Sequencing Assays for the Detection of NTRK Gene Fusions

Apocrine Variant of Pleomorphic Lobular Carcinoma In Situ: Further Clinical, Histopathologic, Immunohistochemical, and Molecular Characterization of an Emerging Entity

Aβ induces astrocytic glutamate release, extrasynaptic NMDA receptor activation, and synaptic loss

Use of the Afirma Xpression Atlas for cytologically indeterminate, Afirma Genomic Sequencing Classifier suspicious thyroid nodules: Clinicopathologic analysis with postoperative molecular testing

Diagnostic interobserver agreement for thyroid fine-needle aspirates: Effects of reviewer experience and molecular diagnostics

Morphologic and Molecular Characteristics of Bladder Cancer

Bioinformatically Expanded Next-Generation Sequencing Analysis Optimizes Identification of Therapeutically Relevant MET Copy Number Alterations in >50,000 Tumors

Molecular Diagnostics of Non-Hodgkin Lymphoma

Anaplastic Transformation of Papillary Thyroid Cancer in the Retroperitoneum

Gelsolin amyloidosis: genetics, biochemistry, pathology and possible strategies for therapeutic intervention

A Rare PDGFRA Exon 15 Germline Mutation Identified in a Patient With Phenotypic Manifestations Concerning for GIST-Plus Syndrome: A Case Report and Review of Literature

Clinical Experience of Cerebrospinal Fluid–Based Liquid Biopsy Demonstrates Superiority of Cell-Free DNA over Cell Pellet Genomic DNA for Molecular Profiling

Her2/neu Status Determination in Breast Cancer

Heparin Binds 8 kDa Gelsolin Cross-β-Sheet Oligomers and Accelerates Amyloidogenesis by Hastening Fibril Extension

Combining molecular testing and the Bethesda category III:VI ratio for thyroid fine‐needle aspirates: A quality‐assurance metric for evaluating diagnostic performance in a cytopathology laboratory

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