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Clinicopathologic and Genomic Analysis of TP53 -Mutated Endometrial Carcinomas

Clinical cancer research, 2021-05, Vol.27 (9), p.2613-2623

2021

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A Pan-Cancer Study of Somatic TERT Promoter Mutations and Amplification in 30,773 Tumors Profiled by Clinical Genomic Sequencing

The Journal of molecular diagnostics : JMD, 2021-02, Vol.23 (2), p.253-263

2021

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Genetic and epigenetic landscape of IDH-wildtype glioblastomas with FGFR3-TACC3 fusions

Acta neuropathologica communications, 2020-11, Vol.8 (1), p.186-186, Article 186

2020

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Antibiotics are associated with worse outcomes in lung cancer patients treated with chemotherapy and immunotherapy

NPJ precision oncology, 2024-07, Vol.8 (1), p.143-9, Article 143

2024

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Genomic landscape of endometrial carcinomas of no specific molecular profile

Modern pathology, 2022-09, Vol.35 (9), p.1269-1278

2022

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Molecular clarification of brainstem astroblastoma with EWSR1-BEND2 fusion in a 38-year-old man

Free Neuropathology, 2021-01, Vol.2

2021

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Enhanced specificity of clinical high-sensitivity tumor mutation profiling in cell-free DNA via paired normal sequencing using MSK-ACCESS

Nature communications, 2021-06, Vol.12 (1), p.3770-3770, Article 3770

2021

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Comprehensive Next-Generation Sequencing Unambiguously Distinguishes Separate Primary Lung Carcinomas From Intrapulmonary Metastases: Comparison with Standard Histopathologic Approach

Clinical cancer research, 2019-12, Vol.25 (23), p.7113-7125

2019

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Myxoid pleomorphic liposarcoma is distinguished from other liposarcomas by widespread loss of heterozygosity and significantly worse overall survival: a genomic and clinicopathologic study

Modern pathology, 2022-11, Vol.35 (11), p.1644-1655

2022

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Chromoplexy Is a Frequent Early Clonal Event in EWSR1-Rearranged Round Cell Sarcomas That Can Be Detected Using Clinically Validated Targeted Sequencing Panels

Cancer research (Chicago, Ill.), 2024-05, Vol.84 (9), p.1504

2024

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Identification of prognostic molecular biomarkers in 157 HPV‐positive and HPV‐negative squamous cell carcinomas of the oropharynx

International journal of cancer, 2019-12, Vol.145 (11), p.3152-3162

2019

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FGFR2::TACC2 fusion as a novel KIT‐independent mechanism of targeted therapy failure in a multidrug‐resistant gastrointestinal stromal tumor

Genes chromosomes & cancer, 2022-07, Vol.61 (7), p.412-419

2022

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Deep Learning–Based Objective and Reproducible Osteosarcoma Chemotherapy Response Assessment and Outcome Prediction

The American journal of pathology, 2023-03, Vol.193 (3), p.341-349

2023

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Survival of Locally Advanced MSI-high Gastric Cancer Patients Treated With Perioperative Chemotherapy: A Retrospective Cohort Study

Annals of surgery, 2023-05, Vol.277 (5), p.798

2023

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RUNX2 (6p21.1) amplification in osteosarcoma

Human pathology, 2019-12, Vol.94, p.23-28

2019

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Evaluation of a Reflex Testing Algorithm for Suspected Heparin-Induced Thrombocytopenia

American journal of clinical pathology, 2017-11, Vol.148 (5), p.390-397

2017

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Combination Therapy With MDM2 and MEK Inhibitors Is Effective in Patient-Derived Models of Lung Adenocarcinoma With Concurrent Oncogenic Drivers and MDM2 Amplification

Journal of thoracic oncology, 2023-09, Vol.18 (9), p.1165-1183

2023

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Defining Novel DNA Virus-Tumor Associations and Genomic Correlates Using Prospective Clinical Tumor/Normal Matched Sequencing Data

The Journal of molecular diagnostics : JMD, 2022-05, Vol.24 (5), p.515-528

2022

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JAK2, PD-L1, and PD-L2 (9p24.1) amplification in metastatic mucosal and cutaneous melanomas with durable response to immunotherapy

Human pathology, 2019-06, Vol.88, p.87-91

2019

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A contemporary guide to chromosomal copy number profiling in the diagnosis of renal cell carcinoma

Urologic oncology, 2022-12, Vol.40 (12), p.512-524

2022

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Secondary renal neoplasia following chemotherapy or radiation in pediatric patients

Human pathology, 2020-09, Vol.103, p.1-13

2020

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Next-Generation Sequencing-Based Assessment of JAK2, PD-L1, and PD-L2 Copy Number Alterations at 9p24.1 in Breast Cancer: Potential Implications for Clinical Management

The Journal of molecular diagnostics : JMD, 2019-03, Vol.21 (2), p.307-317

2019

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RAS/MAPK Pathway Driver Alterations Are Significantly Associated With Oncogenic KIT Mutations in Germ-cell Tumors

Urology (Ridgewood, N.J.), 2020-10, Vol.144, p.111-116

2020

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Clinicopathologic and Genomic Analysis of TP53 -Mutated Endometrial Carcinomas

A Pan-Cancer Study of Somatic TERT Promoter Mutations and Amplification in 30,773 Tumors Profiled by Clinical Genomic Sequencing

Genetic and epigenetic landscape of IDH-wildtype glioblastomas with FGFR3-TACC3 fusions

Antibiotics are associated with worse outcomes in lung cancer patients treated with chemotherapy and immunotherapy

Genomic landscape of endometrial carcinomas of no specific molecular profile

Molecular clarification of brainstem astroblastoma with EWSR1-BEND2 fusion in a 38-year-old man

Enhanced specificity of clinical high-sensitivity tumor mutation profiling in cell-free DNA via paired normal sequencing using MSK-ACCESS

Comprehensive Next-Generation Sequencing Unambiguously Distinguishes Separate Primary Lung Carcinomas From Intrapulmonary Metastases: Comparison with Standard Histopathologic Approach

Myxoid pleomorphic liposarcoma is distinguished from other liposarcomas by widespread loss of heterozygosity and significantly worse overall survival: a genomic and clinicopathologic study

Chromoplexy Is a Frequent Early Clonal Event in EWSR1-Rearranged Round Cell Sarcomas That Can Be Detected Using Clinically Validated Targeted Sequencing Panels

Identification of prognostic molecular biomarkers in 157 HPV‐positive and HPV‐negative squamous cell carcinomas of the oropharynx

FGFR2::TACC2 fusion as a novel KIT‐independent mechanism of targeted therapy failure in a multidrug‐resistant gastrointestinal stromal tumor

Deep Learning–Based Objective and Reproducible Osteosarcoma Chemotherapy Response Assessment and Outcome Prediction

Survival of Locally Advanced MSI-high Gastric Cancer Patients Treated With Perioperative Chemotherapy: A Retrospective Cohort Study

Clinical and molecular features of acquired resistance to immunotherapy in non-small cell lung cancer

Assessment of isochromosome 12p and 12p abnormalities in germ cell tumors using fluorescence in situ hybridization, single-nucleotide polymorphism arrays, and next-generation sequencing/mate-pair sequencing

RUNX2 (6p21.1) amplification in osteosarcoma

Evaluation of a Reflex Testing Algorithm for Suspected Heparin-Induced Thrombocytopenia

Combination Therapy With MDM2 and MEK Inhibitors Is Effective in Patient-Derived Models of Lung Adenocarcinoma With Concurrent Oncogenic Drivers and MDM2 Amplification

Defining Novel DNA Virus-Tumor Associations and Genomic Correlates Using Prospective Clinical Tumor/Normal Matched Sequencing Data

JAK2, PD-L1, and PD-L2 (9p24.1) amplification in metastatic mucosal and cutaneous melanomas with durable response to immunotherapy

A contemporary guide to chromosomal copy number profiling in the diagnosis of renal cell carcinoma

Secondary renal neoplasia following chemotherapy or radiation in pediatric patients

Next-Generation Sequencing-Based Assessment of JAK2, PD-L1, and PD-L2 Copy Number Alterations at 9p24.1 in Breast Cancer: Potential Implications for Clinical Management

RAS/MAPK Pathway Driver Alterations Are Significantly Associated With Oncogenic KIT Mutations in Germ-cell Tumors

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