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Round cell sarcomas beyond E wing: emerging entities
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1096-911x(199709)29:3<170::aid-mpo3>3.0.co;2-aopenalex-snapshot
Undifferentiated sarcomas of children: Pathology and clinical behavior—an Intergroup Rhabdomyosarcoma Study
inferredcites →https://doi.org/10.1002/(sici)1097-0142(19990201)85:3<725::aid-cncr23>3.0.co;2-2openalex-snapshot
Extraskeletal Ewing's sarcoma
inferredcites →https://doi.org/10.1002/(sici)1098-2264(199602)15:2<115::aid-gcc6>3.0.co;2-6openalex-snapshot
Fusion of an ETS‐family gene, EIAF, to EWS by t(17;22)(q12;q12) chromosome translocation in an undifferentiated sarcoma of infancy
inferredcites →https://doi.org/10.1002/gcc.20945openalex-snapshot
High prevalence of CIC fusion with double‐homeobox (DUX4) transcription factors in EWSR1 ‐negative undifferentiated small blue round cell sarcomas
inferredcites →https://doi.org/10.1002/gcc.22050openalex-snapshot
Recurrent NCOA2 gene rearrangements in congenital/infantile spindle cell rhabdomyosarcoma
inferredcites →https://doi.org/10.1002/j.1460-2075.1993.tb06137.xopenalex-snapshot
Combinatorial generation of variable fusion proteins in the Ewing family of tumours.
inferredcites →https://doi.org/10.1006/geno.2002.6690openalex-snapshot
Genomic Analysis of Human Chromosome 10q and 4q Telomeres Suggests a Common Origin
inferredcites →https://doi.org/10.1007/s00428-009-0854-3openalex-snapshot
Soft tissue tumors associated with EWSR1 translocation
inferredcites →https://doi.org/10.1007/s10024-002-0022-0openalex-snapshot
Aberrant Immunohistochemical Expression in Nonrhabdomyosarcoma Soft Tissue Sarcomas of Infancy: Retrospective Review of Clinical Material
inferredcites →https://doi.org/10.1007/s11060-004-4598-2openalex-snapshot
CIC, a gene involved in cerebellar development and ErbB signaling, is significantly expressed in medulloblastomas
inferredcites →https://doi.org/10.1016/0046-8177(94)90149-xopenalex-snapshot
MIC2 analysis in pediatric lymphomas and leukemias
inferredcites →https://doi.org/10.1016/0165-4608(92)90005-sopenalex-snapshot
12q13 abnormality in rhabdomyosarcoma
inferredcites →https://doi.org/10.1016/0165-4608(95)00240-5openalex-snapshot
t(4;19)(q35;q13.1): A recurrent change in primitive mesenchymal tumors?
inferredcites →https://doi.org/10.1016/j.ajhg.2010.01.035openalex-snapshot
Worldwide Population Analysis of the 4q and 10q Subtelomeres Identifies Only Four Discrete Interchromosomal Sequence Transfers in Human Evolution
inferredcites →https://doi.org/10.1016/j.cancergencyto.2009.06.002openalex-snapshot
Ewing sarcoma–peripheral neuroectodermal tumor of the kidney with a FUS–ERG fusion transcript
inferredcites →https://doi.org/10.1016/j.cancergencyto.2009.06.011openalex-snapshot
Fusion of EWSR1 with the DUX4 facioscapulohumeral muscular dystrophy region resulting from t(4;22)(q35;q12) in a case of embryonal rhabdomyosarcoma
inferredcites →https://doi.org/10.1016/j.cancergencyto.2009.06.015openalex-snapshot
Detailed cytogenetic and array analysis of pediatric primitive sarcomas reveals a recurrent CIC–DUX4 fusion gene event
inferredcites →https://doi.org/10.1016/j.humpath.2009.04.013openalex-snapshot
Undifferentiated sarcoma: does it exist? A clinicopathologic study of 7 pediatric cases and review of literature
inferredcites →https://doi.org/10.1016/j.humpath.2011.04.023openalex-snapshot
The CIC-DUX4 fusion transcript is present in a subgroup of pediatric primitive round cell sarcomas
inferredcites →https://doi.org/10.1016/s0169-328x(02)00439-4openalex-snapshot
CIC, a member of a novel subfamily of the HMG-box superfamily, is transiently expressed in developing granule neurons
inferredcites →https://doi.org/10.1016/s0888-7543(05)80363-5openalex-snapshot
Genomic structure of the EWS gene and its relationship to EWSR1, a site of tumor-associated chromosome translocation
inferredcites →https://doi.org/10.1038/359162a0openalex-snapshot
Gene fusion with an ETS DNA-binding domain caused by chromosome translocation in human tumours
inferredcites →https://doi.org/10.1038/labinvest.3780194openalex-snapshot
Variability in Gene Expression Patterns of Ewing Tumor Cell Lines Differing in EWS-FLI1 Fusion Type
inferredcites →https://doi.org/10.1038/modpathol.2010.201openalex-snapshot
A novel t(4;22)(q31;q12) produces an EWSR1–SMARCA5 fusion in extraskeletal Ewing sarcoma/primitive neuroectodermal tumor
inferredcites →https://doi.org/10.1038/modpathol.2012.97openalex-snapshot
Expression of ERG, an Ets family transcription factor, identifies ERG-rearranged Ewing sarcoma
inferredcites →https://doi.org/10.1038/ncb1913openalex-snapshot
BCOR regulates mesenchymal stem cell function by epigenetic mechanisms
inferredcites →https://doi.org/10.1038/ng.1107openalex-snapshot
A new subtype of bone sarcoma defined by BCOR-CCNB3 gene fusion
inferredcites →https://doi.org/10.1038/onc.2010.205openalex-snapshot
Recent advances in the molecular pathogenesis of Ewing's sarcoma
inferredcites →https://doi.org/10.1038/sj.onc.1200933openalex-snapshot
A new member of the ETS family fused to EWS in Ewing tumors
inferredcites →https://doi.org/10.1038/sj.onc.1203762openalex-snapshot
A novel zinc finger gene is fused to EWS in small round cell tumor
inferredcites →https://doi.org/10.1038/sj.onc.1204598openalex-snapshot
Biology of EWS/ETS fusions in Ewing's family tumors
inferredcites →https://doi.org/10.1056/nejm199408043310503openalex-snapshot
The Ewing Family of Tumors -- A Subgroup of Small-Round-Cell Tumors Defined by Specific Chimeric Transcripts
inferredcites →https://doi.org/10.1073/pnas.90.12.5752openalex-snapshot
Ewing sarcoma 11;22 translocation produces a chimeric transcription factor that requires the DNA-binding domain encoded by FLI1 for transformation.
inferredcites →https://doi.org/10.1074/jbc.m203951200openalex-snapshot
Characterization and Expression of Mammalian Cyclin B3, a Prepachytene Meiotic Cyclin
inferredcites →https://doi.org/10.1093/hmg/ddl136openalex-snapshot
Fusion between CIC and DUX4 up-regulates PEA3 family genes in Ewing-like sarcomas with t(4;19)(q35;q13) translocation
inferredcites →https://doi.org/10.1097/00000478-199902000-00004openalex-snapshot
Adamantinoma-like Ewing's Sarcoma: Genomic Confirmation, Phenotypic Drift
inferredcites →https://doi.org/10.1097/00000478-200003000-00010openalex-snapshot
Cytokeratin Immunoreactivity in Ewing's Sarcoma
inferredcites →https://doi.org/10.1097/01.pas.0000167056.13614.62openalex-snapshot
Morphologic and Immunophenotypic Diversity in Ewing Family Tumors
inferredcites →https://doi.org/10.1097/pas.0b013e3181706252openalex-snapshot
Primary Extraskeletal Ewing Family Tumor With Complex Epithelial Differentiation: A Unique Case Arising in the Lateral Neck Presenting With Horner Syndrome
inferredcites →https://doi.org/10.1097/pas.0b013e318206b67bopenalex-snapshot
ERG Transcription Factor as an Immunohistochemical Marker for Vascular Endothelial Tumors and Prostatic Carcinoma
inferredcites →https://doi.org/10.1097/pas.0b013e31828e5168openalex-snapshot
Adamantinoma-like Ewing Family Tumor of Soft Tissue Associated With the Vagus Nerve
inferredcites →https://doi.org/10.1126/science.1189044openalex-snapshot
A Unifying Genetic Model for Facioscapulohumeral Muscular Dystrophy
inferredcites →https://doi.org/10.1158/1078-0432.ccr-08-2184openalex-snapshot
The NFATc2 Gene Is Involved in a Novel Cloned Translocation in a Ewing Sarcoma Variant That Couples Its Function in Immunology to Oncology
inferredcites →https://doi.org/10.1200/jco.1996.14.4.1245openalex-snapshot
Does expression of different EWS chimeric transcripts define clinically distinct risk groups of Ewing tumor patients?
inferredcites →https://doi.org/10.1200/jco.1998.16.4.1248openalex-snapshot
EWS-FLI1 fusion transcript structure is an independent determinant of prognosis in Ewing's sarcoma.
inferredcites →https://doi.org/10.1200/jco.1999.17.6.1809openalex-snapshot
EWS-FLI1 and EWS-ERG Gene Fusions Are Associated With Similar Clinical Phenotypes in Ewing's Sarcoma
inferredcites →https://doi.org/10.1200/jco.2009.23.3585openalex-snapshot
Impact of EWS-ETS Fusion Type on Disease Progression in Ewing's Sarcoma/Peripheral Primitive Neuroectodermal Tumor: Prospective Results From the Cooperative Euro-E.W.I.N.G. 99 Trial
inferredcites →https://doi.org/10.1242/dev.129.4.993openalex-snapshot
EGFR signalling inhibits Capicua-dependent repression during specification ofDrosophilawing veins
inferredcites →https://doi.org/10.1371/journal.pgen.1001181openalex-snapshot
Facioscapulohumeral Dystrophy: Incomplete Suppression of a Retrotransposed Gene
inferredcites →https://doi.org/10.2350/07-06-0296.1openalex-snapshot
Translocation (4;19)(q35;q13.1)–Associated Primitive round Cell Sarcoma: Report of a Case and Review of the Literature
inferredcites →https://doi.org/10.2353/jmoldx.2007.070009openalex-snapshot
Ewing Sarcoma with Novel Translocation t(2;16) Producing an In-Frame Fusion of FUS and FEV
inferredcites →https://doi.org/10.2353/jmoldx.2007.070053openalex-snapshot
Undifferentiated Small Round Cell Sarcomas with Rare EWS Gene Fusions
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4197931openalex-extracted
A Global CollaboRAtive Study of CIC-Rearranged, BCOR::CCNB3-Rearranged and Other Ultra-Rare Unclassified Undifferentiated Round Cell Sarcomas (GRACefUl)
inferred← citeshttps://doi.org/10.1002/9780470015902.a0025221openalex-snapshot
Molecular Genetics of Ewing Sarcoma
inferred← citeshttps://doi.org/10.1002/9781119000822.hfcm113.pub2openalex-snapshot
Soft Tissue Sarcomas
inferred← citeshttps://doi.org/10.1002/cncr.29090openalex-snapshot
Systemic levels of neuropeptide Y and dipeptidyl peptidase activity in patients with Ewing sarcoma—Associations with tumor phenotype and survival
inferred← citeshttps://doi.org/10.1002/gcc.22336openalex-snapshot
Ewing sarcoma with ERG gene rearrangements: A molecular study focusing on the prevalence of FUS‐ERG and common pitfalls in detecting EWSR1‐ERG fusions by FISH
inferred← citeshttps://doi.org/10.1002/gcc.22668openalex-snapshot
Novel MXD4–NUTM1 fusion transcript identified in primary ovarian undifferentiated small round cell sarcoma
inferred← citeshttps://doi.org/10.1002/gcc.22828openalex-snapshot
Ewing sarcoma with FEV gene rearrangements is a rare subset with predilection for extraskeletal locations and aggressive behavior
inferred← citeshttps://doi.org/10.1002/gcc.22857openalex-snapshot
The clinical heterogeneity of round cell sarcomas with EWSR1 / FUS gene fusions: Impact of gene fusion type on clinical features and outcome
inferred← citeshttps://doi.org/10.1002/gcc.23050openalex-snapshot
Ewing sarcoma and related FET family translocation‐associated round cell tumors: A century of clinical and scientific progress
inferred← citeshttps://doi.org/10.1002/gcc.23215openalex-snapshot
Expanding the molecular landscape of undifferentiated sarcomas of bone with a novel EWSR1‐SSX3 gene fusion
inferred← citeshttps://doi.org/10.1002/ijc.34051openalex-snapshot
The landscape of genetic aberrations in myxofibrosarcoma
inferred← citeshttps://doi.org/10.1002/jcp.27558openalex-snapshot
Ewing‐like sarcoma: An emerging family of round cell sarcomas
inferred← citeshttps://doi.org/10.1002/jcp.27853openalex-snapshot
Forkhead box O4 transcription factor in human neoplasms: Cannot afford to lose the novel suppressor
inferred← citeshttps://doi.org/10.1002/jcu.70232openalex-snapshot
Prenatal Diagnosis of a Fetal Spinal Malignant Small Round Cell Tumor: Ultrasound, Fetal MRI , and Immunohistochemical Findings
inferred← citeshttps://doi.org/10.1002/jso.23853openalex-snapshot
Contemporary diagnostics: Sarcoma pathology update
inferred← citeshttps://doi.org/10.1002/nbm.4000openalex-snapshot
Probabilistic classification of tumour habitats in soft tissue sarcoma
inferred← citeshttps://doi.org/10.1002/path.5053openalex-snapshot
Transcriptomic definition of molecular subgroups of small round cell sarcomas
inferred← citeshttps://doi.org/10.1002/path.5071openalex-snapshot
Genetic analyses of undifferentiated small round cell sarcoma identifies a novel sarcoma subtype with a recurrent CRTC1‐SS18 gene fusion
inferred← citeshttps://doi.org/10.1002/pbc.26096openalex-snapshot
Comparison of clinical features and outcomes in patients with extraskeletal versus skeletal localized Ewing sarcoma: A report from the Children's Oncology Group
inferred← citeshttps://doi.org/10.1002/pbc.26524openalex-snapshot
Results for patients with sarcoma not otherwise specified and other diagnoses than Ewing sarcoma treated according to the Euro‐EWING 99 trial
inferred← citeshttps://doi.org/10.1007/978-1-4471-6578-1_25openalex-snapshot
Ewing’s Sarcoma Family of Tumors
inferred← citeshttps://doi.org/10.1007/978-1-4939-1807-2_15openalex-snapshot
Tumors of Smooth Muscle, of Skeletal Muscle, and of Unknown Origin and Tumor-Like Conditions of the Vulva
inferred← citeshttps://doi.org/10.1007/978-3-030-28315-5_28openalex-snapshot
Ewing’s Sarcoma Family of Tumors
inferred← citeshttps://doi.org/10.1007/978-3-030-29676-6_39openalex-snapshot
Small Blue Round Cell Tumors
inferred← citeshttps://doi.org/10.1007/978-3-031-45024-2_29openalex-snapshot
Markers and Immunoprofile of Ewing Sarcoma/Primitive Neuroectodermal Tumors (PNET) and Ewing-Like Sarcoma Tumors
inferred← citeshttps://doi.org/10.1007/978-3-031-67675-8_22openalex-snapshot
Soft Tissue and Bone Tumors of the Head and Neck
inferred← citeshttps://doi.org/10.1007/978-3-319-33679-4_3openalex-snapshot
The Biology of AYA Cancers
inferred← citeshttps://doi.org/10.1007/978-981-15-3773-8_10openalex-snapshot
Rare Peritoneal Tumours: Histopathological Diagnosis and Patterns of Peritoneal Dissemination
inferred← citeshttps://doi.org/10.1007/s00117-016-0116-8openalex-snapshot
Ewing-Sarkom, fibrogene Tumoren, Riesenzelltumor, Hämangiom des Skeletts
inferred← citeshttps://doi.org/10.1007/s00292-015-0010-6openalex-snapshot
Molekularpathologie der Weichgewebstumoren: Beitrag zur Diagnostik und Therapieprädiktion
inferred← citeshttps://doi.org/10.1007/s00292-016-0184-6openalex-snapshot
Grading von Weichgewebe- und Knochensarkomen
inferred← citeshttps://doi.org/10.1007/s00292-018-0421-2openalex-snapshot
Ewing-Sarkome und Ewing-artige Sarkome
inferred← citeshttps://doi.org/10.1007/s00292-020-00838-0openalex-snapshot
Fluoreszenz-in-situ-Hybridisierung bei der Diagnostik von Weichgewebs- und Knochentumoren
inferred← citeshttps://doi.org/10.1007/s00401-014-1312-0openalex-snapshot
Unusual primary cerebral localization of a CIC–DUX4 translocation tumor of the Ewing sarcoma family
inferred← citeshttps://doi.org/10.1007/s00428-014-1613-7openalex-snapshot
Malignant round cell tumor of bone with EWSR1-NFATC2 gene fusion
inferred← citeshttps://doi.org/10.1007/s00428-014-1627-1openalex-snapshot
The combination of CD99 and NKX2.2, a transcriptional target of EWSR1-FLI1, is highly specific for the diagnosis of Ewing sarcoma
inferred← citeshttps://doi.org/10.1007/s00428-017-2072-8openalex-snapshot
Histological and immunohistochemical characteristics of undifferentiated small round cell sarcomas associated with CIC-DUX4 and BCOR-CCNB3 fusion genes
inferred← citeshttps://doi.org/10.1007/s00428-019-02678-7openalex-snapshot
Update on selected advances in the immunohistochemical and molecular genetic analysis of soft tissue tumors
inferred← citeshttps://doi.org/10.1007/s00428-019-02720-8openalex-snapshot
Ewing sarcoma and Ewing-like tumors
inferred← citeshttps://doi.org/10.1007/s00428-025-04055-zopenalex-snapshot
Sinonasal EWSR1::POU2AF3 sarcoma: a case report and literature review
inferred← citeshttps://doi.org/10.1007/s00432-019-02895-2openalex-snapshot
DNA methylation profiling distinguishes Ewing-like sarcoma with EWSR1–NFATc2 fusion from Ewing sarcoma
inferred← citeshttps://doi.org/10.1007/s00432-023-05585-2openalex-snapshot
A rare Ewing-like small round cell tumor in prostate: a case report and literature review
inferred← citeshttps://doi.org/10.1007/s11864-020-00785-1openalex-snapshot
Small Round Blue Cell Sarcoma Other Than Ewing Sarcoma: What Should an Oncologist Know?
inferred← citeshttps://doi.org/10.1007/s12105-014-0558-0openalex-snapshot
Adamantinoma-Like Ewing Sarcoma Mimicking Basal Cell Adenocarcinoma of the Parotid Gland: A Case Report and Review of the Literature
inferred← citeshttps://doi.org/10.1007/s12105-017-0808-zopenalex-snapshot
Head and Neck Round Cell Sarcomas: A Comparative Clinicopathologic Analysis of 2 Molecular Subsets: Ewing and CIC-Rearranged Sarcomas
inferred← citeshttps://doi.org/10.1007/s12105-022-01521-xopenalex-snapshot
Top 10 Histological Mimics of Neuroendocrine Carcinoma You Should Not Miss in the Head and Neck
inferred← citeshttps://doi.org/10.1007/s12262-015-1399-0openalex-snapshot
Extraosseous Ewing Sarcoma: Diagnosis, Prognosis and Optimal Management
inferred← citeshttps://doi.org/10.1007/s13193-023-01793-xopenalex-snapshot
Case Report: Primary Ewing Sarcoma of the Penis
inferred← citeshttps://doi.org/10.1007/s13193-024-02084-9openalex-snapshot
Adamantinoma-Like Ewing Sarcoma Arising in the Neck of Pancreas: A Rare Case Report with Literature Review
inferred← citeshttps://doi.org/10.1016/b978-0-12-416721-6.00024-8openalex-snapshot
Markers for bone sarcomas
inferred← citeshttps://doi.org/10.1016/b978-0-12-821666-8.00017-7openalex-snapshot
Markers for bone sarcomas
inferred← citeshttps://doi.org/10.1016/b978-0-323-37675-4.50184-8openalex-snapshot
Undifferentiated Round Cell Sarcoma With CIC-DUX4 Translocation
inferred← citeshttps://doi.org/10.1016/b978-0-323-44941-0.00014-xopenalex-snapshot
Mesenchymal Tumors of the Central Nervous System
inferred← citeshttps://doi.org/10.1016/b978-0-323-52480-3.50060-3openalex-snapshot
Primary Ewing Sarcoma, Thyroid
inferred← citeshttps://doi.org/10.1016/b978-0-323-53114-6.00009-2openalex-snapshot
Soft-Tissue Tumors of the Head and Neck
inferred← citeshttps://doi.org/10.1016/b978-0-323-71257-6.00003-4openalex-snapshot
Neoplasms of the Sinonasal Tract
inferred← citeshttps://doi.org/10.1016/b978-1-4557-3382-8.00003-7openalex-snapshot
Neoplasms of the Sinonasal Tract
inferred← citeshttps://doi.org/10.1016/j.acthis.2015.03.011openalex-snapshot
Immunohistochemistry as potential diagnostic pitfall in the most common solid tumors of children and adolescents
inferred← citeshttps://doi.org/10.1016/j.adcanc.2021.100008openalex-snapshot
Pathogenesis of Ewing sarcoma: Existing and emerging trends
inferred← citeshttps://doi.org/10.1016/j.anndiagpath.2016.03.002openalex-snapshot
Defining Ewing and Ewing-like small round cell tumors (SRCT): The need for molecular techniques in their categorization and differential diagnosis. A study of 200 cases
inferred← citeshttps://doi.org/10.1016/j.annpat.2014.11.001openalex-snapshot
Tumeurs de la famille Ewing/PNET : vers un nouveau paradigme ?
inferred← citeshttps://doi.org/10.1016/j.biocel.2014.04.022openalex-snapshot
Round cell sarcomas – Biologically important refinements in subclassification
inferred← citeshttps://doi.org/10.1016/j.clon.2017.02.010openalex-snapshot
Advances in the Pathology and Molecular Biology of Sarcomas and the Impact on Treatment
inferred← citeshttps://doi.org/10.1016/j.currproblcancer.2019.05.006openalex-snapshot
Diagnostic classification of soft tissue malignancies: A review and update from a surgical pathology perspective
inferred← citeshttps://doi.org/10.1016/j.ehpc.2019.200329openalex-snapshot
Two cases of poorly differentiated synovial sarcoma arising from the chest wall - One case of Ewing sarcoma-like small cell type with death 4 years after the first presentation and one case of high-grade spindle cell type receiving postoperative adjuvant chemotherapy
inferred← citeshttps://doi.org/10.1016/j.ejca.2023.01.003openalex-snapshot
A global collaboRAtive study of CIC-rearranged, BCOR::CCNB3-rearranged and other ultra-rare unclassified undifferentiated small round cell sarcomas (GRACefUl)
inferred← citeshttps://doi.org/10.1016/j.humpath.2016.07.038openalex-snapshot
Diagnostic utility of cyclin D1 in the diagnosis of small round blue cell tumors in children and adolescents
inferred← citeshttps://doi.org/10.1016/j.humpath.2016.09.004openalex-snapshot
Targeted next-generation sequencing of CIC-DUX4 soft tissue sarcomas demonstrates low mutational burden and recurrent chromosome 1p loss
inferred← citeshttps://doi.org/10.1016/j.humpath.2018.03.020openalex-snapshot
EWSR1-NFATC2 gene fusion in a soft tissue tumor with epithelioid round cell morphology and abundant stroma: a case report and review of the literature
inferred← citeshttps://doi.org/10.1016/j.ijscr.2016.10.014openalex-snapshot
Ewing sarcoma/primitive neuroectodermal tumor of the kidney
inferred← citeshttps://doi.org/10.1016/j.ijscr.2019.09.016openalex-snapshot
Primary renal Ewing’s sarcoma in a young male treated completely by surgical excision without chemotherapeutic agents
inferred← citeshttps://doi.org/10.1016/j.jasc.2017.12.002openalex-snapshot
Cytologic diagnosis of round cell sarcomas in the era of ancillary testing: an updated review
inferred← citeshttps://doi.org/10.1016/j.jmoldx.2024.02.002openalex-snapshot
Machine Learning–Supported Diagnosis of Small Blue Round Cell Sarcomas Using Targeted RNA Sequencing
inferred← citeshttps://doi.org/10.1016/j.modpat.2024.100656openalex-snapshot
Superficial Neurocristic FET::ETS Fusion Tumor: Expanding the Clinicopathological and Molecular Genetic Spectrum of a Recently Described Entity
inferred← citeshttps://doi.org/10.1016/j.mpdhp.2016.10.007openalex-snapshot
Paraspinal mesenchymal tumors: the overlap between neuropathology and soft tissue pathology
inferred← citeshttps://doi.org/10.1016/j.mpdhp.2017.08.003openalex-snapshot
Molecular testing of sarcomas
inferred← citeshttps://doi.org/10.1016/j.mpsur.2016.11.004openalex-snapshot
Pathology of paediatric bone tumours
inferred← citeshttps://doi.org/10.1016/j.neuchi.2024.101562openalex-snapshot
Primary intradural Extraosseous Ewing’s sarcoma of the cauda equina: A case report and literature review
inferred← citeshttps://doi.org/10.1016/j.oooo.2014.05.023openalex-snapshot
Neuroblastoma-like schwannoma of the lower labial mucosa: a rare morphologic variant of peripheral nerve sheath tumor
inferred← citeshttps://doi.org/10.1016/j.path.2017.04.001openalex-snapshot
Ewing Sarcoma, an Update on Molecular Pathology with Therapeutic Implications
inferred← citeshttps://doi.org/10.1016/j.path.2023.07.001openalex-snapshot
Sarcomas with EWSR1::Non-ETS Fusion (EWSR1::NFATC2 and EWSR1::PATZ1)
inferred← citeshttps://doi.org/10.1016/j.pathol.2017.08.003openalex-snapshot
A diagnostic approach to bone tumours
inferred← citeshttps://doi.org/10.1016/j.pathol.2019.09.015openalex-snapshot
Undifferentiated round cell sarcomas with CIC-DUX4 gene fusion: expanding the clinical spectrum
inferred← citeshttps://doi.org/10.1016/j.prp.2016.11.015openalex-snapshot
Primary CIC-DUX4 round cell sarcoma of the kidney: A treatment-refractory tumor with poor outcome
inferred← citeshttps://doi.org/10.1016/j.prp.2022.153773openalex-snapshot
CIC rearranged sarcomas: A single institution experience of the potential pitfalls in interpreting CIC FISH results
inferred← citeshttps://doi.org/10.1016/j.prp.2024.155209openalex-snapshot
The utility of FISH analysis in the diagnosis of BCOR-rearranged sarcomas
inferred← citeshttps://doi.org/10.1016/j.rmcr.2026.102469openalex-snapshot
Temporary airway stenting as a bridge to chemotherapy in primary mediastinal Ewing's sarcoma with critical tracheal compression: A case report
inferred← citeshttps://doi.org/10.1016/j.suronc.2018.05.016openalex-snapshot
Extraskeletal versus Skeletal Ewing Sarcoma in the adult population: Controversies in care
inferred← citeshttps://doi.org/10.1038/bjc.2017.4openalex-snapshot
The spectrum of EWSR1-rearranged neoplasms at a tertiary sarcoma centre; assessing 772 tumour specimens and the value of current ancillary molecular diagnostic modalities
inferred← citeshttps://doi.org/10.1038/modpathol.2014.139openalex-snapshot
BCOR–CCNB3 fusions are frequent in undifferentiated sarcomas of male children
inferred← citeshttps://doi.org/10.1038/modpathol.2014.83openalex-snapshot
CIC-DUX sarcomas demonstrate frequent MYC amplification and ETS-family transcription factor expression
inferred← citeshttps://doi.org/10.1038/modpathol.2016.119openalex-snapshot
Small round blue cell tumors of the sinonasal tract: a differential diagnosis approach
inferred← citeshttps://doi.org/10.1038/modpathol.2016.140openalex-snapshot
Evaluation of ETV4 and WT1 expression in CIC-rearranged sarcomas and histologic mimics
inferred← citeshttps://doi.org/10.1038/s41379-018-0045-3openalex-snapshot
Array-based DNA-methylation profiling in sarcomas with small blue round cell histology provides valuable diagnostic information
inferred← citeshttps://doi.org/10.1038/s41379-018-0139-yopenalex-snapshot
Limited biopsies of soft tissue tumors: the contemporary role of immunohistochemistry and molecular diagnostics
inferred← citeshttps://doi.org/10.1038/s41379-020-00684-8openalex-snapshot
EWSR1-PATZ1-rearranged sarcoma: a report of nine cases of spindle and round cell neoplasms with predilection for thoracoabdominal soft tissues and frequent expression of neural and skeletal muscle markers
inferred← citeshttps://doi.org/10.1038/s41379-020-0542-zopenalex-snapshot
NFATc2-rearranged sarcomas: clinicopathologic, molecular, and cytogenetic study of 7 cases with evidence of AGGRECAN as a novel diagnostic marker
inferred← citeshttps://doi.org/10.1038/s41379-021-00740-xopenalex-snapshot
Correction to: EWSR1-PATZ1-rearranged sarcoma: a report of nine cases of spindle and round cell neoplasms with predilection for thoracoabdominal soft tissues and frequent expression of neural and skeletal muscle markers
inferred← citeshttps://doi.org/10.1038/s41525-021-00210-yopenalex-snapshot
Integrated diagnosis based on transcriptome analysis in suspected pediatric sarcomas
inferred← citeshttps://doi.org/10.1038/s41698-021-00177-0openalex-snapshot
Multiscale-omic assessment of EWSR1-NFATc2 fusion positive sarcomas identifies the mTOR pathway as a potential therapeutic target
inferred← citeshttps://doi.org/10.1038/s41698-025-00878-wopenalex-snapshot
Immunologic correlates in a CIC::DUX4 fusion-positive sarcoma responsive to dual immune checkpoint blockade
inferred← citeshttps://doi.org/10.1053/j.semdp.2016.08.008openalex-snapshot
Pediatric soft tissue tumor pathology: A happy morpho-molecular union
inferred← citeshttps://doi.org/10.1080/01913123.2020.1737610openalex-snapshot
Ultrastructure of CIC-DUX4 sarcoma: the first pathological report
inferred← citeshttps://doi.org/10.1097/md9.0000000000000243openalex-snapshot
Isolated right oculomotor nerve palsy as the first presenting manifestation of metastatic renal Ewing’s sarcoma
inferred← citeshttps://doi.org/10.1097/mnm.0000000000001031openalex-snapshot
PET-CT imaging features that differentiate between positive and negative EWSR1 translocation in Ewing sarcoma
inferred← citeshttps://doi.org/10.1097/pap.0000000000000091openalex-snapshot
Clinical Applications of Molecular Markers in Bone Tumors
inferred← citeshttps://doi.org/10.1097/pas.0000000000000223openalex-snapshot
BCOR-CCNB3 (Ewing-like) Sarcoma
inferred← citeshttps://doi.org/10.1097/pas.0000000000000286openalex-snapshot
A Novel CIC-FOXO4 Gene Fusion in Undifferentiated Small Round Cell Sarcoma
inferred← citeshttps://doi.org/10.1097/pas.0000000000000591openalex-snapshot
Novel BCOR-MAML3 and ZC3H7B-BCOR Gene Fusions in Undifferentiated Small Blue Round Cell Sarcomas
inferred← citeshttps://doi.org/10.1097/pas.0000000000000772openalex-snapshot
DUX4 Immunohistochemistry Is a Highly Sensitive and Specific Marker for CIC-DUX4 Fusion-positive Round Cell Tumor
inferred← citeshttps://doi.org/10.1097/pas.0000000000001183openalex-snapshot
Spindle and Round Cell Sarcoma With EWSR1-PATZ1 Gene Fusion
inferred← citeshttps://doi.org/10.1097/pas.0000000000001260openalex-snapshot
EWSR1-NFATC2 Translocation-associated Sarcoma Clinicopathologic Findings in a Rare Aggressive Primary Bone or Soft Tissue Tumor
inferred← citeshttps://doi.org/10.1097/pas.0000000000001441openalex-snapshot
NKX3-1 Is a Useful Immunohistochemical Marker of EWSR1-NFATC2 Sarcoma and Mesenchymal Chondrosarcoma
inferred← citeshttps://doi.org/10.1097/pas.0000000000002403openalex-snapshot
The Extensive Case Series of 21 CIC::DUX4, 18 BCOR::CCNB3 and 148 Ewing’s Sarcomas From a Single Center
inferred← citeshttps://doi.org/10.1097/pat.0000000000000049openalex-snapshot
Promiscuous genes involved in recurrent chromosomal translocations in soft tissue tumours
inferred← citeshttps://doi.org/10.1111/1346-8138.16157openalex-snapshot
Case of CIC‐DUX4 sarcoma of the skin: Histological simulant of epithelioid angiosarcoma
inferred← citeshttps://doi.org/10.1111/ajco.12980openalex-snapshot
FISH analysis of selected soft tissue tumors: Diagnostic experience in a tertiary center
inferred← citeshttps://doi.org/10.1111/crj.12235openalex-snapshot
Askin's tumour in pregnancy with dismal prognosis
inferred← citeshttps://doi.org/10.1111/cup.13788openalex-snapshot
Primary cutaneous Ewing sarcoma with diffuse S100 / SOX10 positivity and pseudoalveolar pattern: An extraordinarily rare case highlighting a potential pitfall with significant repercussions
inferred← citeshttps://doi.org/10.1111/cup.14781openalex-snapshot
Dermal CIC ‐Rearranged Sarcoma With Neuroendocrine Differentiation Mimicking Merkel Cell Carcinoma
inferred← citeshttps://doi.org/10.1111/his.12650openalex-snapshot
Massive osseous and cartilaginous metaplasia of soft tissue Ewing sarcoma in adult: report of two cases
inferred← citeshttps://doi.org/10.1111/his.12985openalex-snapshot
CIC – DUX 4 fusion‐positive round‐cell sarcomas of soft tissue and bone: a single‐institution morphological and molecular analysis of seven cases
inferred← citeshttps://doi.org/10.1111/his.13001openalex-snapshot
BCOR – CCNB 3‐positive soft tissue sarcoma with round‐cell and spindle‐cell histology: a series of four cases highlighting the pitfall of mimicking poorly differentiated synovial sarcoma
inferred← citeshttps://doi.org/10.1111/his.13031openalex-snapshot
Atypical Ewing sarcoma breakpoint region 1 fluorescence in‐situ hybridization signal patterns in bone and soft tissue tumours: diagnostic experience with 135 cases
inferred← citeshttps://doi.org/10.1111/his.13112openalex-snapshot
The utility of ETV 1, ETV 4 and ETV 5 RNA in‐situ hybridization in the diagnosis of CIC – DUX sarcomas
inferred← citeshttps://doi.org/10.1111/pin.13142openalex-snapshot
Modeling fusion gene‐associated sarcoma: Advantages for understanding sarcoma biology and pathology
inferred← citeshttps://doi.org/10.1136/jitc-2020-000653openalex-snapshot
Role of immunotherapy in Ewing sarcoma
inferred← citeshttps://doi.org/10.1155/2019/9386390openalex-snapshot
EWSR1-NFATC2 and FUS-NFATC2 Gene Fusion-Associated Mesenchymal Tumors: Clinicopathologic Correlation and Literature Review
inferred← citeshttps://doi.org/10.1158/0008-5472.can-16-3351openalex-snapshot
CIC-DUX4 Induces Small Round Cell Sarcomas Distinct from Ewing Sarcoma
inferred← citeshttps://doi.org/10.1158/1078-0432.ccr-15-3028openalex-snapshot
Genomic EWSR1 Fusion Sequence as Highly Sensitive and Dynamic Plasma Tumor Marker in Ewing Sarcoma
inferred← citeshttps://doi.org/10.1159/000524260openalex-snapshot
The Small Round Cell Sarcomas Complexities and Desmoplastic Presentation
inferred← citeshttps://doi.org/10.1172/jci.insight.152293openalex-snapshot
WEE1 kinase is a therapeutic vulnerability in CIC-DUX4 undifferentiated sarcoma
inferred← citeshttps://doi.org/10.1177/01455613221132392openalex-snapshot
Clinical Characteristics of Children with Nasal BCOR-Rearranged Ewing-like Sarcoma: A Case Report and Literature Review
inferred← citeshttps://doi.org/10.1177/1066896916668637openalex-snapshot
Desmoplastic Small Round Cell Tumor
inferred← citeshttps://doi.org/10.1177/1066896918755009openalex-snapshot
Malignant Ewing-Like Neoplasm With an EWSR1-KLF15 Fusion: At the Crossroads of a Myoepithelial Carcinoma and a Ewing-Like Sarcoma. A Case Report With Treatment Options
inferred← citeshttps://doi.org/10.1177/1066896919827093openalex-snapshot
Bone Sarcoma With EWSR1-NFATC2 Fusion: Sarcoma With Varied Morphology and Amplification of Fusion Gene Distinct From Ewing Sarcoma
inferred← citeshttps://doi.org/10.1177/1066896920929081openalex-snapshot
An EWSR1-CREB3L1 Fusion Gene in Extraskeletal Undifferentiated Round Cell Sarcoma Expands the Spectrum of Genetic Landscape in the “Ewing-Like” Undifferentiated Round Cell Sarcomas
inferred← citeshttps://doi.org/10.1177/10668969251410957openalex-snapshot
Androgen Receptor Positive EWSR1 :: FEV -Rearranged Prostatic Ewing Sarcoma Mimicking High-Grade Neuroendocrine Carcinoma
inferred← citeshttps://doi.org/10.1177/1093526617698263openalex-snapshot
BCOR-CCNB3 Undifferentiated Sarcoma—Does Immunohistochemistry Help in the Identification?
inferred← citeshttps://doi.org/10.1177/10935266241249344openalex-snapshot
Decoding BCOR -ITD Sarcomas: Case Report of a Rare Pediatric Tumor With Challenges in Diagnosis
inferred← citeshttps://doi.org/10.1186/s12885-019-6465-8openalex-snapshot
Loss of Stag2 cooperates with EWS-FLI1 to transform murine Mesenchymal stem cells
inferred← citeshttps://doi.org/10.1186/s13000-016-0502-6openalex-snapshot
RETRACTED ARTICLE: Paediatric Ewing-like sarcoma arising from the cranium – a unique diagnostic challenge
inferred← citeshttps://doi.org/10.1186/s13000-016-0549-4openalex-snapshot
Retraction Note: Paediatric Ewing-like sarcoma arising from the cranium – a unique diagnostic challenge
inferred← citeshttps://doi.org/10.1186/s13000-024-01443-yopenalex-snapshot
Report and literature review of four cases of EWSR1::NFATC2 round cell sarcoma
inferred← citeshttps://doi.org/10.1200/edbk_175378openalex-snapshot
Advances in the Treatment of Pediatric Bone Sarcomas
inferred← citeshttps://doi.org/10.12659/ajcr.892551openalex-snapshot
High-Grade Undifferentiated Small Round Cell Sarcoma with t(4;19)(q35;q13.1) CIC-DUX4 Fusion: Emerging Entities of Soft Tissue Tumors with Unique Histopathologic Features – A Case Report and Literature Review
inferred← citeshttps://doi.org/10.12998/wjcc.v12.i16.2887openalex-snapshot
Clinicopathological analysis of EWSR1/FUS::NFATC2 rearranged sarcoma in the left forearm: A case report
inferred← citeshttps://doi.org/10.12998/wjcc.v7.i20.3372openalex-snapshot
Ureteral Ewing’s sarcoma in an elderly woman: A case report
inferred← citeshttps://doi.org/10.1586/14737159.2014.946909openalex-snapshot
Molecular diagnosis of soft tissue neoplasia: clinical applications and recent advances
inferred← citeshttps://doi.org/10.18632/oncotarget.20098openalex-snapshot
Robust diagnosis of Ewing sarcoma by immunohistochemical detection of super-enhancer-driven EWSR1-ETS targets
inferred← citeshttps://doi.org/10.2147/ott.s155523openalex-snapshot
Renal Ewing sarcoma/primitive neuroectodermal tumor in a pregnant woman who underwent robot-assisted laparoscopic nephrectomy: a case report and literature review
inferred← citeshttps://doi.org/10.2147/ott.s213233openalex-snapshot
Management of Ewing Sarcoma Family of Tumors: A Short Description of a Rare Primitive Uterine pPNET and Literature Review
inferred← citeshttps://doi.org/10.21682/2311-1267-2022-9-4-102-106openalex-snapshot
Sarcoma of the right femur with heterogeneous morphology similar to myoepithelial carcinoma and amplification of the EWSR1 gene in a 14-year-old boy. Clinical observation and literature review
inferred← citeshttps://doi.org/10.2350/15-07-1666-misc.1openalex-snapshot
The Evolution of Pediatric Soft Tissue Sarcoma Classification in the Last 50 Years
inferred← citeshttps://doi.org/10.24287/1726-1708-2022-21-3-84-89openalex-snapshot
Sarcoma with BCOR gene alterations (BCOR-ITD) of the L3 vertebra in an 8-year-old boy
inferred← citeshttps://doi.org/10.25259/asjo-2023-7-(466)openalex-snapshot
BCOR overexpression in pediatric sarcomas- a morphologic continuum of mixed round and spindle cell tumors
inferred← citeshttps://doi.org/10.31729/jnma.7523openalex-snapshot
Extraosseous Ewing Sarcoma in a Pelvic Region: A Case Report
inferred← citeshttps://doi.org/10.3389/fonc.2022.1047738openalex-snapshot
Case report: Ewing sarcoma with EWSR–ERG fusion elevates procalcitonin extremely in the long term without infection
inferred← citeshttps://doi.org/10.3389/fped.2020.591257openalex-snapshot
Case Report: Primary Ewing Sarcoma of the Penis With Multiple Metastases
inferred← citeshttps://doi.org/10.3389/freae.2024.1427399openalex-snapshot
Quantification of tumour-infiltrating immune cells through deconvolution of DNA methylation data in Ewing sarcomas
inferred← citeshttps://doi.org/10.3389/fsurg.2023.1180107openalex-snapshot
Renal primitive neuroectodermal tumor: A rare case with a good prognosis
inferred← citeshttps://doi.org/10.3390/cancers12030644openalex-snapshot
High Specificity of BCL11B and GLG1 for EWSR1-FLI1 and EWSR1-ERG Positive Ewing Sarcoma
inferred← citeshttps://doi.org/10.3390/cancers14215411openalex-snapshot
CIC-Rearranged Sarcomas: An Intriguing Entity That May Lead the Way to the Comprehension of More Common Cancers
inferred← citeshttps://doi.org/10.3390/ijms27156864openalex-snapshot
Artificial Intelligence-Based Histopathological Analysis to Assist Pathologists in Diagnosing Ewing Sarcoma and Selected Tumor Entities Using Tissue Microarrays
inferred← citeshttps://doi.org/10.3892/mco.2022.2510openalex-snapshot
BCOR‑CCNB3 sarcoma arising in the proximal tibia: A case report
inferred← citeshttps://doi.org/10.4103/ijmr.ijmr_2144_18openalex-snapshot
Clinicopathologic features of undifferentiated round cell sarcomas of bone & soft tissues
inferred← citeshttps://doi.org/10.4103/ijpm.ijpm_267_20openalex-snapshot
FISH for EWSR1 in Ewing's sarcoma family of tumors
inferred← citeshttps://doi.org/10.4149/neo_2018_171107n716openalex-snapshot
An undifferentiated sarcoma with BCOR-CCNB3 fusion transcript - pathological and clinical retrospective study
inferred← citeshttps://doi.org/10.4172/2161-0681.1000244openalex-snapshot
Female New-Born with Undifferentiated Sarcoma Defined by Bcor-Ccnb3 Fusion Transcript
inferred← citeshttps://doi.org/10.4172/2476-2024.1000110openalex-snapshot
Diagnostic Challenges in Pediatric Round Blue Cell Tumors of the Bone
inferred← citeshttps://doi.org/10.5334/jbsr.3249openalex-snapshot
Pediatric Patient with a Diagnosis of Pelvic Extraosseous Ewing’s Sarcoma: A Case Report
inferred← citeshttps://doi.org/10.5430/jst.v5n2p105openalex-snapshot
Irinotecan and temozolomide in adults with recurrent sarcoma
inferred← citeshttps://doi.org/10.55418/9781933477275-13openalex-snapshot
Nonepithelial and Miscellaneous Neoplasms
inferred← citeshttps://doi.org/10.5858/arpa.2014-0367-rsopenalex-snapshot
Ewing Sarcoma/Primitive Neuroectodermal Tumor of the Kidney: A Rare and Lethal Entity
inferred← citeshttps://doi.org/10.7759/cureus.35389openalex-snapshot
A Rare Case of Lower Limb Sarcoma With BCOR-CCNB3 Mutation: Diagnosis and Treatment
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