Recurrent EP300-BCOR Fusions in Pediatric Gliomas With Distinct Clinicopathologic Features

Author:

Torre Matthew12,Meredith David M2,Dubuc Adrian3,Solomon David A4,Perry Arie4,Vasudevaraja Varshini5,Serrano Jonathan5,Snuderl Matija5,Ligon Keith L12,Alexandrescu Sanda12

Affiliation:

1. Department of Pathology, Boston Children’s Hospital and Harvard Medical School, Boston, Massachusetts

2. Department of Pathology

3. Center for Advanced Molecular Diagnostics, Brigham and Women’s Hospital Harvard Medical School, Boston, Massachusetts

4. Department of Pathology, University of California, San Francisco, California

5. Department of Pathology, NYU Langone Health, New York, New York

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Clinical Neurology,Neurology,General Medicine,Pathology and Forensic Medicine

Reference27 articles.

1. Clarifying the impact of polycomb complex component disruption in human cancers;Yamamoto;Mol Cancer Res,2014

2. Recurrent BCOR internal tandem duplication and BCOR or BCL6 expression distinguish primitive myxoid mesenchymal tumor of infancy from congenital infantile fibrosarcoma;Santiago;Mod Pathol,2017

3. Clear cell sarcomas of the kidney are characterised by BCOR gene abnormalities, including exon 15 internal tandem duplications and BCOR-CCNB3 gene fusion;Wong;Histopathology,2018

4. BCOR-CCNB3 fusion positive sarcomas: A clinicopathologic and molecular analysis of 36 cases with comparison to morphologic spectrum and clinical behavior of other round cell sarcomas;Kao;Am J Surg Pathol,2018

5. ZC3H7B-BCOR-rearranged endometrial stromal sarcomas: A distinct subset merits its own classification?;Mansor;Int J Gynecol Pathol,2018

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