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Further description of two patients with biallelic variants in NADSYN1 in association with cardiac and vertebral anomalies

American journal of medical genetics. Part A, 2022-08, Vol.188 (8), p.2479-2484

2022

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Epithelioid Angiomyolipoma With Prominent Papillary Architecture Mimicking Renal Cell Carcinoma: A Case Report

International journal of surgical pathology, 2024-02, Vol.32 (1), p.206-208

2024

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Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis

The New England journal of medicine, 2020-10, Vol.383 (18), p.1746-1756

2020

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Platelet depletion and aspirin treatment protect mice in a two-event model of transfusion-related acute lung injury

The Journal of clinical investigation, 2009-11, Vol.119 (11), p.3450-3461

2009

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The Immunomodulatory Adapter Proteins DAP12 and Fc Receptor γ-Chain (FcRγ) Regulate Development of Functional Osteoclasts through the Syk Tyrosine Kinase

Proceedings of the National Academy of Sciences - PNAS, 2004-04, Vol.101 (16), p.6158-6163

2004

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Hyperactivated MyD88 signaling in dendritic cells, through specific deletion of Lyn kinase, causes severe autoimmunity and inflammation

Proceedings of the National Academy of Sciences - PNAS, 2013-08, Vol.110 (35), p.E3311-E3320

2013

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CRTC1–MAML2 fusion in mucoepidermoid carcinoma of the breast

Histopathology, 2019-02, Vol.74 (3), p.463-473

2019

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Preference for secondary findings in prenatal and pediatric exome sequencing

Prenatal diagnosis, 2022-05, Vol.42 (6), p.753-761

2022

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The utility of pathologic examination and comprehensive phenotyping for accurate diagnosis with perinatal exome sequencing

Prenatal diagnosis, 2022-09, Vol.42 (10), p.1288-1294

2022

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Exome sequencing vs targeted gene panels for the evaluation of nonimmune hydrops fetalis

American journal of obstetrics and gynecology, 2022-01, Vol.226 (1), p.128.e1-128.e11

2022

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Neutrophil-specific deletion of Syk kinase results in reduced host defense to bacterial infection

Blood, 2009-11, Vol.114 (23), p.4871-4882

2009

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Genomic analysis in myeloid sarcoma and comparison with paired acute myeloid leukemia

Human pathology, 2021-02, Vol.108, p.76-83

2021

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Neutrophils and their Fc gamma receptors are essential in a mouse model of transfusion-related acute lung injury

The Journal of clinical investigation, 2006-06, Vol.116 (6), p.1615-1623

2006

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Polyoma virus-associated carcinomas of the urologic tract: a clinicopathologic and molecular study

Modern pathology, 2018-09, Vol.31 (9), p.1429-1441

2018

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Deletion of Syk in neutrophils prevents immune complex arthritis

The Journal of immunology (1950), 2011-10, Vol.187 (8), p.4319-4330

2011

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Fusion driven JMML: a novel CCDC88C-FLT3 fusion responsive to sorafenib identified by RNA sequencing

Leukemia, 2020-02, Vol.34 (2), p.662-666

2020

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Molecularly Classified Uterine FIGO Grade 3 Endometrioid Carcinomas Show Distinctive Clinical Outcomes But Overlapping Morphologic Features

The American journal of surgical pathology, 2021-03, Vol.45 (3), p.421

2021

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Genomic profiling of malignant phyllodes tumors reveals aberrations in FGFR1 and PI-3 kinase/RAS signaling pathways and provides insights into intratumoral heterogeneity

Modern pathology, 2016-09, Vol.29 (9), p.1012-1027

2016

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Well-differentiated papillary mesothelioma of the peritoneum is genetically defined by mutually exclusive mutations in TRAF7 and CDC42

Modern pathology, 2019-01, Vol.32 (1), p.88-99

2019

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Adenomatoid tumors of the male and female genital tract are defined by TRAF7 mutations that drive aberrant NF-kB pathway activation

Modern pathology, 2018-04, Vol.31 (4), p.660-673

2018

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Multinodular and vacuolating neuronal tumor of the cerebrum is a clonal neoplasm defined by genetic alterations that activate the MAP kinase signaling pathway

Acta neuropathologica, 2018-03, Vol.135 (3), p.485-488

2018

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The genetic landscape of anaplastic pleomorphic xanthoastrocytoma

Brain pathology (Zurich, Switzerland), 2019-01, Vol.29 (1), p.85-96

2019

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Primary intracranial sarcomas with DICER1 mutation often contain prominent eosinophilic cytoplasmic globules and can occur in the setting of neurofibromatosis type 1

Acta neuropathologica, 2019-03, Vol.137 (3), p.521-525

2019

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EML4::ALK fusions in complex lymphatic malformations

Pediatric blood & cancer, 2023-09, Vol.70 (9), p.e30516-n/a

2023

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Further description of two patients with biallelic variants in NADSYN1 in association with cardiac and vertebral anomalies

Epithelioid Angiomyolipoma With Prominent Papillary Architecture Mimicking Renal Cell Carcinoma: A Case Report

Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis

Platelet depletion and aspirin treatment protect mice in a two-event model of transfusion-related acute lung injury

The Immunomodulatory Adapter Proteins DAP12 and Fc Receptor γ-Chain (FcRγ) Regulate Development of Functional Osteoclasts through the Syk Tyrosine Kinase

Hyperactivated MyD88 signaling in dendritic cells, through specific deletion of Lyn kinase, causes severe autoimmunity and inflammation

CRTC1–MAML2 fusion in mucoepidermoid carcinoma of the breast

Preference for secondary findings in prenatal and pediatric exome sequencing

The utility of pathologic examination and comprehensive phenotyping for accurate diagnosis with perinatal exome sequencing

Exome sequencing vs targeted gene panels for the evaluation of nonimmune hydrops fetalis

Neutrophil-specific deletion of Syk kinase results in reduced host defense to bacterial infection

Genomic analysis in myeloid sarcoma and comparison with paired acute myeloid leukemia

Neutrophils and their Fc gamma receptors are essential in a mouse model of transfusion-related acute lung injury

Polyoma virus-associated carcinomas of the urologic tract: a clinicopathologic and molecular study

Deletion of Syk in neutrophils prevents immune complex arthritis

Fusion driven JMML: a novel CCDC88C-FLT3 fusion responsive to sorafenib identified by RNA sequencing

Molecularly Classified Uterine FIGO Grade 3 Endometrioid Carcinomas Show Distinctive Clinical Outcomes But Overlapping Morphologic Features

Genomic profiling of malignant phyllodes tumors reveals aberrations in FGFR1 and PI-3 kinase/RAS signaling pathways and provides insights into intratumoral heterogeneity

Well-differentiated papillary mesothelioma of the peritoneum is genetically defined by mutually exclusive mutations in TRAF7 and CDC42

Adenomatoid tumors of the male and female genital tract are defined by TRAF7 mutations that drive aberrant NF-kB pathway activation

Multinodular and vacuolating neuronal tumor of the cerebrum is a clonal neoplasm defined by genetic alterations that activate the MAP kinase signaling pathway

The genetic landscape of anaplastic pleomorphic xanthoastrocytoma

Primary intracranial sarcomas with DICER1 mutation often contain prominent eosinophilic cytoplasmic globules and can occur in the setting of neurofibromatosis type 1

EML4::ALK fusions in complex lymphatic malformations

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