1 – 100 of 269
- show: 100
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2024
-
Mark
Gene amplification in neoplasia : A cytogenetic survey of 80 131 cases
(
- Contribution to journal › Article
-
Mark
MDM2 amplification in rod-shaped chromosomes provides clues to early stages of circularized gene amplification in liposarcoma
(
- Contribution to journal › Article
- 2023
-
Mark
A cryptic EWSR1::DDIT3 fusion in myxoid liposarcoma: Potential pitfalls with FISH and cytogenetics
(
- Contribution to journal › Article
-
Mark
A cloud-based resource for genome coordinate-based exploration and large-scale analysis of chromosome aberrations and gene fusions in cancer
(
- Contribution to journal › Article
-
Mark
Epithelioid and Spindle Cell Hemangioma : Clinicopathologic Analysis of 18 Primary Bone and Soft Tissue Tumors Highlighting a Predilection for the Hands and Feet, Frequent Multicentricity, and Benign Behavior
(
- Contribution to journal › Article
-
Mark
Transcriptomic subtyping of malignant peripheral nerve sheath tumours highlights immune signatures, genomic profiles, patient survival and therapeutic targets
(
- Contribution to journal › Article
-
Mark
Insertion of the CXXC domain of KMT2A into YAP1 : An unusual mechanism behind the formation of a chimeric oncogenic protein
(
- Contribution to journal › Article
-
Mark
Tetraploidization Increases the Motility and Invasiveness of Cancer Cells
(
- Contribution to journal › Article
-
Mark
Diagnostic Yield From a Nationwide Implementation of Precision Medicine for all Children With Cancer
(
- Contribution to journal › Article
- 2022
-
Mark
Overlapping morphological, immunohistochemical and genetic features of superficial CD34-positive fibroblastic tumor and PRDM10-rearranged soft tissue tumor
(
- Contribution to journal › Article
-
Mark
Amplification of ERBB2 (HER2) in embryonal rhabdomyosarcoma : A potential treatment target in rare cases?
(
- Contribution to journal › Article
-
Mark
Signatures of copy number alterations in human cancer
(
- Contribution to journal › Article
-
Mark
The diagnostic utility of DNA copy number analysis of core needle biopsies from soft tissue and bone tumors
(
- Contribution to journal › Article
-
Mark
Superficial CD34-Positive Fibroblastic Tumor : A Clinicopathologic, Immunohistochemical, and Molecular Study of 59 Cases
(
- Contribution to journal › Article
- 2021
-
Mark
BL1391 : an established cell line from a human malignant peripheral nerve sheath tumor with unique genomic features
(
- Contribution to journal › Article
-
Mark
“Inflammatory Leiomyosarcoma” and “Histiocyte-rich Rhabdomyoblastic Tumor” : a clinicopathological, immunohistochemical and genetic study of 13 cases, with a proposal for reclassification as “Inflammatory Rhabdomyoblastic Tumor”
(
- Contribution to journal › Article
-
Mark
Genomic and transcriptomic characterization of desmoplastic small round cell tumors
(
- Contribution to journal › Article
-
Mark
HUGO Gene Nomenclature Committee (HGNC) recommendations for the designation of gene fusions
(
- Contribution to journal › Debate/Note/Editorial
- 2020
-
Mark
Recurrent Fusions Between YAP1 and KMT2A in Morphologically Distinct Neoplasms Within the Spectrum of Low-grade Fibromyxoid Sarcoma and Sclerosing Epithelioid Fibrosarcoma
(
- Contribution to journal › Article
-
Mark
PHF1 fusions cause distinct gene expression and chromatin accessibility profiles in ossifying fibromyxoid tumors and mesenchymal cells
(
- Contribution to journal › Article
-
Mark
Deep sequencing of myxoinflammatory fibroblastic sarcoma
(
- Contribution to journal › Article
-
Mark
Genomic and transcriptomic features of dermatofibrosarcoma protuberans : Unusual chromosomal origin of the COL1A1-PDGFB fusion gene and synergistic effects of amplified regions in tumor development
(
- Contribution to journal › Article
- 2019
-
Mark
Aberrant receptor tyrosine kinase signaling in lipofibromatosis : a clinicopathological and molecular genetic study of 20 cases
(
- Contribution to journal › Article
-
Mark
Cancer chromosome breakpoints cluster in gene-rich genomic regions
(
- Contribution to journal › Article
-
Mark
PRDM10 -rearranged Soft Tissue Tumor : A Clinicopathologic Study of 9 Cases
(
- Contribution to journal › Article
-
Mark
Undifferentiated pleomorphic sarcomas with PRDM10 fusions have a distinct gene expression profile
(
- Contribution to journal › Article
-
Mark
Most gene fusions in cancer are stochastic events
(
- Contribution to journal › Article
-
Mark
Gene fusion involving the insulin-like growth factor 1 receptor in an ALK-negative inflammatory myofibroblastic tumour
(
- Contribution to journal › Article
- 2018
-
Mark
Different patterns of clonal evolution among different sarcoma subtypes followed for up to 25 years
(
- Contribution to journal › Article
-
Mark
Neuroblastoma with flat genomic profile : A question of representativity?
(
- Contribution to journal › Article
-
Mark
Inferior survival for patients with malignant peripheral nerve sheath tumors defined by aberrant TP53
(
- Contribution to journal › Article
-
Mark
The hidden genomic and transcriptomic plasticity of giant marker chromosomes in cancer
(
- Contribution to journal › Article
-
Mark
Inflammatory leiomyosarcoma is a distinct tumor characterized by near-haploidization, few somatic mutations, and a primitive myogenic gene expression signature
(
- Contribution to journal › Article
- 2017
-
Mark
Frequent low-level mutations of Protein Kinase D2 in angiolipoma
(
- Contribution to journal › Article
-
Mark
Scattered genomic amplification in dedifferentiated liposarcoma
(
- Contribution to journal › Article
-
Mark
Frequent miRNA-convergent fusion gene events in breast cancer
(
- Contribution to journal › Article
-
Mark
In-depth genetic analysis of sclerosing epithelioid fibrosarcoma reveals recurrent genomic alterations and potential treatment targets
(
- Contribution to journal › Article
- 2016
-
Mark
Genetic heterogeneity in rhabdomyosarcoma revealed by SNP array analysis.
(
- Contribution to journal › Article
-
Mark
Comprehensive genetic analysis of a pediatric pleomorphic myxoid liposarcoma reveals near-haploidization and loss of the RB1 gene.
(
- Contribution to journal › Article
-
Mark
Gene fusions in soft tissue tumors: Recurrent and overlapping pathogenetic themes.
(
- Contribution to journal › Scientific review
-
Mark
FN1-EGF gene fusions are recurrent in calcifying aponeurotic fibroma.
(
- Contribution to journal › Article
-
Mark
Primary Pseudomyogenic Hemangioendothelioma of Bone.
(
- Contribution to journal › Article
- 2015
-
Mark
Methylated RASSF1A in malignant peripheral nerve sheath tumors identifies neurofibromatosis type 1 patients with inferior prognosis.
(
- Contribution to journal › Article
-
Mark
The emerging complexity of gene fusions in cancer.
(
- Contribution to journal › Scientific review
-
Mark
Recurrent PRDM10 Gene Fusions in Undifferentiated Pleomorphic Sarcoma.
(
- Contribution to journal › Article
-
Mark
Gene fusion detection in formalin-fixed paraffin-embedded benign fibrous histiocytomas using fluorescence in situ hybridization and RNA sequencing.
(
- Contribution to journal › Article
-
Mark
Ring chromosomes, breakpoint clusters, and neocentromeres in sarcomas.
(
- Contribution to journal › Article
-
Mark
Protein expression of BIRC5, TK1, and TOP2A in malignant peripheral nerve sheath tumours - A prognostic test after surgical resection.
(
- Contribution to journal › Article
-
Mark
RNA sequencing of sarcomas with simple karyotypes: identification and enrichment of fusion transcripts.
(
- Contribution to journal › Article
-
Mark
Non-fibrosing sclerosing epithelioid fibrosarcoma: An unusual variant.
2015) In Histopathology(
- Contribution to journal › Letter
-
Mark
Soft tissue tumors
2015) p.583-614(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Tumors of bone
2015) p.566-582(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Tumors of the skin
2015) p.555-565(
- Chapter in Book/Report/Conference proceeding › Book chapter
- 2014
-
Mark
Nuclear expression of STAT6 distinguishes solitary fibrous tumor from histologic mimics
(
- Contribution to journal › Article
-
Mark
Permanent activation of HMGA2 in lipomas mimics its temporal physiological activation linked to the gain of adipose tissue
(
- Contribution to journal › Article
-
Mark
Primary mesenchymal stem cells in human transplanted lungs are CD90/CD105 perivascularly located tissue-resident cells.
(
- Contribution to journal › Article
-
Mark
Integrative Genome and Transcriptome Analyses Reveal Two Distinct Types of Ring Chromosome in Soft Tissue Sarcomas.
(
- Contribution to journal › Article
-
Mark
Rearrangements of chromosome bands 15q12-q21 are secondary to HMGA2 deregulation in conventional lipoma.
(
- Contribution to journal › Article
-
Mark
Myoepithelioma of bone with a novel FUS-POU5F1 fusion gene
(
- Contribution to journal › Article
-
Mark
Evolving techniques for gene fusion detection in soft tissue tumours.
(
- Contribution to journal › Scientific review
-
Mark
Recurrent EWSR1-CREB3L1 Gene Fusions in Sclerosing Epithelioid Fibrosarcoma.
(
- Contribution to journal › Article
-
Mark
GRIA2 is a novel diagnostic marker for solitary fibrous tumour identified through gene expression profiling
(
- Contribution to journal › Article
-
Mark
Sequencing IDH1/2 glioma mutation hotspots in gliomas and malignant peripheral nerve sheath tumors.
(
- Contribution to journal › Letter
-
Mark
A novel SERPINE1-FOSB fusion gene results in transcriptional up-regulation of FOSB in pseudomyogenic haemangioendothelioma.
(
- Contribution to journal › Article
-
Mark
Fusions involving protein kinase C and membrane-associated proteins in benign fibrous histiocytoma.
(
- Contribution to journal › Article
-
Mark
Exomic analysis of myxoid liposarcomas, synovial sarcomas, and osteosarcomas
(
- Contribution to journal › Article
- 2013
-
Mark
Assessment of Fusion Gene Status in Sarcomas Using a Custom Made Fusion Gene Microarray
(
- Contribution to journal › Article
-
Mark
A Benign Vascular Tumor With a New Fusion Gene: EWSR1-NFATC1 in Hemangioma of the Bone.
(
- Contribution to journal › Article
-
Mark
Cytogenetic and single nucleotide polymorphism array findings in soft tissue tumors in infants
(
- Contribution to journal › Article
-
Mark
TERT promoter mutations occur frequently in gliomas and a subset of tumors derived from cells with low rates of self-renewal
(
- Contribution to journal › Article
-
Mark
Survival meta-analyses for >1800 malignant peripheral nerve sheath tumor patients with and without neurofibromatosis type 1.
(
- Contribution to journal › Article
-
Mark
WHO Classification of Tumours of Soft Tissue and Bone : WHO Classification of Tumours, vol. 5
Fletcher, Christopher ; Bridge, JA ; Hogendoorn, PCW and Mertens, Fredrik LU (2013)
- Book/Report › Anthology (editor)
- 2012
-
Mark
Smooth muscle actin expression in primary bone tumours
(
- Contribution to journal › Article
-
Mark
Homozygous deletions of cadherin genes in chondrosarcoma-an array comparative genomic hybridization study
(
- Contribution to journal › Article
-
Mark
Malignant fibrous histiocytoma and fibrosarcoma of bone: a re-assessment in the light of currently employed morphological, immunohistochemical and molecular approaches
(
- Contribution to journal › Article
-
Mark
Identification of a novel, recurrent HEY1-NCOA2 fusion in mesenchymal chondrosarcoma based on a genome-wide screen of exon-level expression data
(
- Contribution to journal › Article
-
Mark
MUC4 Is a Sensitive and Extremely Useful Marker for Sclerosing Epithelioid Fibrosarcoma: Association With FUS Gene Rearrangement.
(
- Contribution to journal › Article
-
Mark
Molecular genetic characterization of the 11q13 breakpoint in a desmoplastic fibroma of bone
(
- Contribution to journal › Article
-
Mark
Retained heterodisomy is associated with high gene expression in hyperhaploid inflammatory leiomyosarcoma.
(
- Contribution to journal › Article
-
Mark
FOSL1 as a candidate target gene for 11q12 rearrangements in desmoplastic fibroblastoma.
(
- Contribution to journal › Article
-
Mark
The MDM2 SNP309 G allele is not preferentially amplified in bone and soft tissue tumors.
(
- Contribution to journal › Article
-
Mark
Recurrent Rearrangement of the PHF1 Gene in Ossifying Fibromyxoid Tumors.
(
- Contribution to journal › Article
-
Mark
Fusion of the AHRR and NCOA2 genes through a recurrent translocation t(5;8)(p15;q13) in soft tissue angiofibroma results in upregulation of aryl hydrocarbon receptor target genes.
(
- Contribution to journal › Article
-
Mark
Biphasic, Hyperdiploid Breast Tumors in Children: A Distinct Entity?
2012) In Journal of Pediatric Hematology/Oncology(
- Contribution to journal › Article
-
Mark
A novel GTF2I/NCOA2 fusion gene emphasizes the role of NCOA2 in soft tissue angiofibroma development.
2012) In Genes, Chromosomes and Cancer(
- Contribution to journal › Letter
-
Mark
Analysis of giant cell tumour of bone cells for Noonan syndrome/Cherubism-related mutations.
2012) In Journal of Oral Pathology & Medicine(
- Contribution to journal › Article
-
Mark
Disease-associated patterns of disomic chromosomes in hyperhaploid neoplasms.
(
- Contribution to journal › Article
-
Mark
SNP array and FISH findings in two pleomorphic hyalinizing angiectatic tumors.
(
- Contribution to journal › Article
- 2011
-
Mark
MUC4 Is a Highly Sensitive and Specific Marker for Low-Grade Fibromyxoid Sarcoma
2011) Annual Meeting on the United States and Canadian-Academy-of-Pathology, 2011 In Laboratory Investigation 91. p.12-12(
- Contribution to journal › Published meeting abstract
-
Mark
Chromosome banding analysis of cells from fine-needle aspiration biopsy samples from soft tissue and bone tumors: is it clinically meaningful?
(
- Contribution to journal › Article
-
Mark
Mesenchymal stromal cells from primary osteosarcoma are non-malignant and strikingly similar to their bone marrow counterparts.
(
- Contribution to journal › Article
-
Mark
Tumor-Infiltrating Macrophages Are Associated with Metastasis Suppression in High-Grade Osteosarcoma: A Rationale for Treatment with Macrophage-Activating Agents
2011) Annual Meeting on the United States and Canadian-Academy-of-Pathology, 2011 In Laboratory Investigation 91(Feb 26 - Mar 4, 2011). p.10-10(
- Contribution to journal › Published meeting abstract
-
Mark
Role of the transcription factor T (brachyury) in the pathogenesis of sporadic chordoma: a genetic and functional-based study
(
- Contribution to journal › Article
-
Mark
Tumor-Infiltrating Macrophages Are Associated with Metastasis Suppression in High-Grade Osteosarcoma: A Rationale for Treatment with Macrophage Activating Agents
(
- Contribution to journal › Article
-
Mark
Malignant Fibrous Histiocytoma and Fibrosarcoma of Bone in 2011: What's New?
2011) Annual Meeting on the United States and Canadian-Academy-of-Pathology, 2011 In Laboratory Investigation 91. p.20-20(
- Contribution to journal › Published meeting abstract
-
Mark
Identification of a Novel, Recurrent HEY1-NCOA2 Fusion in Mesenchymal Chondrosarcoma Based on a Genome-Wide Screen of Exon-Level Expression Data
2011) Annual Meeting on the United States and Canadian-Academy-of-Pathology, 2011 In Laboratory Investigation 91. p.23-23(
- Contribution to journal › Published meeting abstract
-
Mark
Gene expression and single nucleotide polymorphism array analyses of spindle cell lipomas and conventional lipomas with 13q14 deletion.
(
- Contribution to journal › Article
-
Mark
HMGA2 and MDM2 expression in lipomatous tumors with partial, low-level amplification of sequences from the long arm of chromosome 12.
(
- Contribution to journal › Article
-
Mark
MUC4 Is a Highly Sensitive and Specific Marker for Low-grade Fibromyxoid Sarcoma.
(
- Contribution to journal › Article
-
Mark
The t(X;6) in subungual exostosis results in transcriptional deregulation of the gene for insulin receptor substrate 4.
(
- Contribution to journal › Article