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BRAF mutation and CDKN2A deletion define a clinically distinct subgroup of childhood secondary high-grade glioma

Journal of clinical oncology, 2015-03, Vol.33 (9), p.1015-1022

2015

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Multiplex Detection of Pediatric Low-Grade Glioma Signature Fusion Transcripts and Duplications Using the NanoString nCounter System

Journal of neuropathology and experimental neurology, 2017-07, Vol.76 (7), p.562-570

2017

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Recurrent Cytogenetic Abnormalities in Acute Lymphoblastic Leukemia

Methods in molecular biology (Clifton, N.J.), 2017-01, Vol.1541, p.257

Shago, Mary

2017

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An aggressive central giant cell granuloma in a pediatric patient: case report and review of literature

Journal of otolaryngology-head and neck surgery, 2019-07, Vol.48 (1), p.32-32

2019

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Universal Poor Survival in Children With Medulloblastoma Harboring Somatic TP53 Mutations

Journal of clinical oncology, 2010-03, Vol.28 (8), p.1345-1350

2010

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Myeloproliferative Neoplasm Driven by ETV6-ABL1 in an Adolescent with Recent History of Burkitt Leukemia

Current oncology (Toronto), 2023-06, Vol.30 (7), p.5946-5952

2023

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Primary Undifferentiated Sarcoma of the Kidney Harboring a Novel Variant of CIC-DUX4 Gene Fusion

The American journal of surgical pathology, 2016-09, Vol.40 (9), p.1298-1301

2016

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Chromosome Preparation for Acute Lymphoblastic Leukemia

Methods in molecular biology (Clifton, N.J.), 2017-01, Vol.1541, p.19

Shago, Mary

2017

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Genome assembly comparison identifies structural variants in the human genome

Nature genetics, 2006-12, Vol.38 (12), p.1413-1418

2006

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Identifying Genes Regulated in a Myc-dependent Manner

The Journal of biological chemistry, 2002-10, Vol.277 (40), p.36921-36930

2002

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Frequency and outcome of pediatric acute lymphoblastic leukemia with ZNF384 gene rearrangements including a novel translocation resulting in an ARID1B/ZNF384 gene fusion

Pediatric blood & cancer, 2016-11, Vol.63 (11), p.1915-1921

2016

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Mammary analog secretory carcinoma of salivary gland origin with the ETV6 gene rearrangement by FISH: expanded morphologic and immunohistochemical spectrum of a recently described entity

The American journal of surgical pathology, 2012-01, Vol.36 (1), p.27-34

2012

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CUL7 is a novel antiapoptotic oncogene

Cancer research (Chicago, Ill.), 2007-10, Vol.67 (20), p.9616-9622

2007

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Integrated Molecular and Clinical Analysis of 1,000 Pediatric Low-Grade Gliomas

Cancer cell, 2020-04, Vol.37 (4), p.569-583.e5

2020

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The clinical impact of copy number variants in inherited bone marrow failure syndromes

Npj genomic medicine, 2017-05, Vol.2 (1), p.1-8, Article 18

2017

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Structural Variation of Chromosomes in Autism Spectrum Disorder

American journal of human genetics, 2008-02, Vol.82 (2), p.477-488

2008

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Immunohistochemistry for ATRX Can Miss ATRX Mutations: Lessons From Neuroblastoma

The American journal of surgical pathology, 2019-09, Vol.43 (9), p.1203

2019

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Rearrangement bursts generate canonical gene fusions in bone and soft tissue tumors

Science (American Association for the Advancement of Science), 2018-08, Vol.361 (6405)

2018

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The diploid genome sequence of an individual human

PLoS biology, 2007-09, Vol.5 (10), p.e254-e254

2007

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Pediatric fibromyxoid soft tissue tumor with PLAG1 fusion: A novel entity?

Genes chromosomes & cancer, 2021-04, Vol.60 (4), p.263-271

2021

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Inhibition of nuclear hormone receptor activity by calreticulin

Nature (London), 1994-02, Vol.367 (6462), p.480-483

1994

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Prognostic Importance of Cytogenetic Subgroups in Relapse Risk Stratification in Children and Young Adults with First Relapsed B-ALL: A Children's Oncology Group Study AALL1331

Blood, 2022-11, Vol.140 (Supplement 1), p.3476-3477

2022

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Fluorescent In Situ Hybridization for TP53 in the Diagnosis of Pediatric Osteogenic Sarcoma

The American journal of surgical pathology, 2018-06, Vol.42 (6), p.744-749

2018

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Minimal residual disease comparison between Ig/TCR PCR versus NGS assays in children with Philadelphia chromosome-positive acute lymphoblastic leukemia: A report from the COG AALL1631 study

Journal of clinical oncology, 2022-06, Vol.40 (16_suppl), p.10023-10023

2022

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BRAF mutation and CDKN2A deletion define a clinically distinct subgroup of childhood secondary high-grade glioma

Multiplex Detection of Pediatric Low-Grade Glioma Signature Fusion Transcripts and Duplications Using the NanoString nCounter System

Recurrent Cytogenetic Abnormalities in Acute Lymphoblastic Leukemia

An aggressive central giant cell granuloma in a pediatric patient: case report and review of literature

Universal Poor Survival in Children With Medulloblastoma Harboring Somatic TP53 Mutations

Myeloproliferative Neoplasm Driven by ETV6-ABL1 in an Adolescent with Recent History of Burkitt Leukemia

Primary Undifferentiated Sarcoma of the Kidney Harboring a Novel Variant of CIC-DUX4 Gene Fusion

Chromosome Preparation for Acute Lymphoblastic Leukemia

The impact of category, cytopathology and cytogenetics on development and progression of clonal and malignant myeloid transformation in inherited bone marrow failure syndromes

Genome assembly comparison identifies structural variants in the human genome

Identifying Genes Regulated in a Myc-dependent Manner

Frequency and outcome of pediatric acute lymphoblastic leukemia with ZNF384 gene rearrangements including a novel translocation resulting in an ARID1B/ZNF384 gene fusion

Mammary analog secretory carcinoma of salivary gland origin with the ETV6 gene rearrangement by FISH: expanded morphologic and immunohistochemical spectrum of a recently described entity

CUL7 is a novel antiapoptotic oncogene

Integrated Molecular and Clinical Analysis of 1,000 Pediatric Low-Grade Gliomas

The clinical impact of copy number variants in inherited bone marrow failure syndromes

Structural Variation of Chromosomes in Autism Spectrum Disorder

Immunohistochemistry for ATRX Can Miss ATRX Mutations: Lessons From Neuroblastoma

Rearrangement bursts generate canonical gene fusions in bone and soft tissue tumors

The diploid genome sequence of an individual human

Pediatric fibromyxoid soft tissue tumor with PLAG1 fusion: A novel entity?

Inhibition of nuclear hormone receptor activity by calreticulin

Prognostic Importance of Cytogenetic Subgroups in Relapse Risk Stratification in Children and Young Adults with First Relapsed B-ALL: A Children's Oncology Group Study AALL1331

Fluorescent In Situ Hybridization for TP53 in the Diagnosis of Pediatric Osteogenic Sarcoma

Minimal residual disease comparison between Ig/TCR PCR versus NGS assays in children with Philadelphia chromosome-positive acute lymphoblastic leukemia: A report from the COG AALL1631 study

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