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- 2024
-
Mark
MDM2 amplification in rod-shaped chromosomes provides clues to early stages of circularized gene amplification in liposarcoma
(
- Contribution to journal › Article
-
Mark
Gene amplification in neoplasia : A cytogenetic survey of 80 131 cases
(
- Contribution to journal › Article
- 2023
-
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
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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
A cryptic EWSR1::DDIT3 fusion in myxoid liposarcoma: Potential pitfalls with FISH and cytogenetics
(
- Contribution to journal › Article
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Mark
Diagnostic Yield From a Nationwide Implementation of Precision Medicine for all Children With Cancer
(
- Contribution to journal › Article
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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
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Mark
Tetraploidization Increases the Motility and Invasiveness of Cancer Cells
(
- 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
- 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
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
Amplification of ERBB2 (HER2) in embryonal rhabdomyosarcoma : A potential treatment target in rare cases?
(
- 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
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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
HUGO Gene Nomenclature Committee (HGNC) recommendations for the designation of gene fusions
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
Genomic and transcriptomic characterization of desmoplastic small round cell tumors
(
- Contribution to journal › Article
- 2020
-
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
-
Mark
PHF1 fusions cause distinct gene expression and chromatin accessibility profiles in ossifying fibromyxoid tumors and mesenchymal cells
(
- Contribution to journal › Article
-
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
- 2019
-
Mark
PRDM10 -rearranged Soft Tissue Tumor : A Clinicopathologic Study of 9 Cases
(
- Contribution to journal › Article
-
Mark
Cancer chromosome breakpoints cluster in gene-rich genomic regions
(
- Contribution to journal › Article
-
Mark
Aberrant receptor tyrosine kinase signaling in lipofibromatosis : a clinicopathological and molecular genetic study of 20 cases
(
- Contribution to journal › Article
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Mark
Gene fusion involving the insulin-like growth factor 1 receptor in an ALK-negative inflammatory myofibroblastic tumour
(
- 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
- 2018
-
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
-
Mark
The hidden genomic and transcriptomic plasticity of giant marker chromosomes in cancer
(
- Contribution to journal › Article
-
Mark
Different patterns of clonal evolution among different sarcoma subtypes followed for up to 25 years
(
- Contribution to journal › Article
-
Mark
Inferior survival for patients with malignant peripheral nerve sheath tumors defined by aberrant TP53
(
- Contribution to journal › Article
-
Mark
Neuroblastoma with flat genomic profile : A question of representativity?
(
- Contribution to journal › Article
- 2017
-
Mark
Frequent low-level mutations of Protein Kinase D2 in angiolipoma
(
- Contribution to journal › Article
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Mark
In-depth genetic analysis of sclerosing epithelioid fibrosarcoma reveals recurrent genomic alterations and potential treatment targets
(
- Contribution to journal › Article
-
Mark
Frequent miRNA-convergent fusion gene events in breast cancer
(
- Contribution to journal › Article
-
Mark
Scattered genomic amplification in dedifferentiated liposarcoma
(
- 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
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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
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Mark
RNA sequencing of sarcomas with simple karyotypes: identification and enrichment of fusion transcripts.
(
- Contribution to journal › Article
-
Mark
Ring chromosomes, breakpoint clusters, and neocentromeres in sarcomas.
(
- Contribution to journal › Article
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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
The emerging complexity of gene fusions in cancer.
(
- Contribution to journal › Scientific review
-
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
Recurrent PRDM10 Gene Fusions in Undifferentiated Pleomorphic Sarcoma.
(
- 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
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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
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Mark
Primary mesenchymal stem cells in human transplanted lungs are CD90/CD105 perivascularly located tissue-resident cells.
(
- Contribution to journal › Article
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Mark
Permanent activation of HMGA2 in lipomas mimics its temporal physiological activation linked to the gain of adipose tissue
(
- 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
Rearrangements of chromosome bands 15q12-q21 are secondary to HMGA2 deregulation in conventional lipoma.
(
- 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
-
Mark
Recurrent EWSR1-CREB3L1 Gene Fusions in Sclerosing Epithelioid Fibrosarcoma.
(
- Contribution to journal › Article
-
Mark
A novel SERPINE1-FOSB fusion gene results in transcriptional up-regulation of FOSB in pseudomyogenic haemangioendothelioma.
(
- 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
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
- 2013
-
Mark
Assessment of Fusion Gene Status in Sarcomas Using a Custom Made Fusion Gene Microarray
(
- Contribution to journal › Article
-
Mark
Cytogenetic and single nucleotide polymorphism array findings in soft tissue tumors in infants
(
- 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
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Mark
Survival meta-analyses for >1800 malignant peripheral nerve sheath tumor patients with and without neurofibromatosis type 1.
(
- 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
- 2012
-
Mark
Smooth muscle actin expression in primary bone tumours
(
- 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
Homozygous deletions of cadherin genes in chondrosarcoma-an array comparative genomic hybridization study
(
- 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
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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
Molecular genetic characterization of the 11q13 breakpoint in a desmoplastic fibroma of bone
(
- Contribution to journal › Article
-
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
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
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
SNP array and FISH findings in two pleomorphic hyalinizing angiectatic tumors.
(
- Contribution to journal › Article
-
Mark
Disease-associated patterns of disomic chromosomes in hyperhaploid neoplasms.
(
- Contribution to journal › Article
- 2011
-
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
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
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
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
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
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
The t(X;6) in subungual exostosis results in transcriptional deregulation of the gene for insulin receptor substrate 4.
(
- Contribution to journal › Article
-
Mark
FUS-CREB3L2/L1-Positive Sarcomas Show a Specific Gene Expression Profile with Upregulation of CD24 and FOXL1.
(
- Contribution to journal › Article
-
Mark
MUC4 Is a Highly Sensitive and Specific Marker for Low-grade Fibromyxoid Sarcoma.
(
- Contribution to journal › Article
-
Mark
Translocation t(7;19)(q22;q13)-a recurrent chromosome aberration in pseudomyogenic hemangioendothelioma?
(
- Contribution to journal › Article
- 2010
-
Mark
Genetic Abnormalities of the Transcription Factor T (Brachyury) in Sporadic Chordomas
2010) Annual Meeting of the Association-for-Molecular-Pathology In The Journal Of Molecular Diagnostics 12(6). p.906-906(
- Contribution to journal › Published meeting abstract
-
Mark
Epigenetic target genes in malignant peripheral nerve sheath tumours identified as surrogate prognostic biomarkers
2010) 21st Meeting of the European-Association-for-Cancer-Research In EJC Supplements 8(5). p.163-163(
- Contribution to journal › Published meeting abstract
-
Mark
Prognostic value of gene expression targeted by gain of 17q sequences in malignant peripheral nerve sheath tumours
2010) 21st Meeting of the European-Association-for-Cancer-Research In EJC Supplements 8(5). p.122-122(
- Contribution to journal › Published meeting abstract
-
Mark
Heterogeneous and Complex Rearragements of the Long Arm of Chromosome 6 in Chondromyxoid Fibroma
2010) 99th Annual Meeting of the United-States-and-Canadian-Academy-of-Pathology In Modern Pathology 23(Suppl. 1). p.27-27(
- Contribution to journal › Published meeting abstract
-
Mark
Heterogeneous and Complex Rearragements of the Long Arm of Chromosome 6 in Chondromyxoid Fibroma
2010) 99th Annual Meeting of the United-States-and-Canadian-Academy-of-Pathology In Laboratory Investigation 90(Suppl. 1). p.27-27(
- Contribution to journal › Published meeting abstract
-
Mark
Heterogeneous and Complex Rearrangements of Chromosome Arm 6q in Chondromyxoid Fibroma. Delineation of Breakpoints and Analysis of Candidate Target Genes.
(
- Contribution to journal › Article
-
Mark
In Vivo and In Vitro Implications of the Transcription Factor T (Brachyury) in Pathogenesis of Sporadic Chordomas
2010) 198th Scientific Meeting of the Pathological-Society-of-Great Britain-and-Ireland In Journal of Pathology 222. p.6-6(
- Contribution to journal › Published meeting abstract
-
Mark
Characterization of an alternative transcript of the human CREB3L2 gene.
(
- Contribution to journal › Article
-
Mark
Concomitant deletions of tumor suppressor genes MEN1 and AIP are essential for the pathogenesis of the brown fat tumor hibernoma.
(
- Contribution to journal › Article
-
Mark
Generation of trisomies in cancer cells by multipolar mitosis and incomplete cytokinesis.
(
- Contribution to journal › Article
-
Mark
Genomic Changes in Chromosomes 10, 16, and X in Malignant Peripheral Nerve Sheath Tumors Identify a High-Risk Patient Group.
(
- Contribution to journal › Article
-
Mark
Genomic characteristics of soft tissue sarcomas.
(
- Contribution to journal › Article
-
Mark
Fusion of the FUS and CREB3L2 genes in a supernumerary ring chromosome in low-grade fibromyxoid sarcoma.
(
- Contribution to journal › Article
- 2009
-
Mark
Comparison of cisplatin sensitivity and the 18F fluoro-2-deoxy 2 glucose uptake with proliferation parameters and gene expression in squamous cell carcinoma cell lines of the head and neck
(
- Contribution to journal › Article
-
Mark
Molecular Characterization Of The 12Q13.3-14.1 Recurrent Breakpoint Region On Ring Chromosomes 12 In Atypical Lipomatous Tumors
2009) 3rd Marie Curie-Genome Architecture in Relation to Disease Meeting (MC-GARD) In Cellular Oncology 31(2). p.113-113(
- Contribution to journal › Published meeting abstract
-
Mark
No Genomic Aberrations in Langerhans Cell Histiocytosis as Assessed by Diverse Molecular Technologies
(
- Contribution to journal › Article
-
Mark
Germline and somatic NF1 mutations in sporadic and NF1-associated malignant peripheral nerve sheath tumours
(
- Contribution to journal › Article
-
Mark
Characterization of a Hotspot Region on Chromosome 12 for Amplification in Ring Chromosomes in Atypical Lipomatous Tumors
(
- Contribution to journal › Article
-
Mark
Balanced and Unbalanced Rearrangement of Chromosome Arm 6q in Chondromyxoid Fibroma (CMF): Delineation of Breakpoints and Analysis of Candidate Target Genes
2009) 98th Annual Meeting of the United-States-and-Canadian-Academy-of-Pathology In Laboratory Investigation 89(S1). p.21-21(
- Contribution to journal › Published meeting abstract
-
Mark
Identification of p53 as a strong predictor of survival for patients with malignant peripheral nerve sheath tumors
(
- Contribution to journal › Article
-
Mark
Cytogenetic Analysis of 101 Giant Cell Tumors of Bone: Nonrandom Patterns of Telomeric Associations and Other Structural Aberrations
(
- Contribution to journal › Article
-
Mark
Clonal chromosome aberrations in a sialoblastoma
(
- Contribution to journal › Letter
-
Mark
Translocation-related sarcomas.
(
- Contribution to journal › Article
-
Mark
Two genetic pathways, t(1;10) and amplification of 3p11-12, in myxoinflammatory fibroblastic sarcoma, haemosiderotic fibrolipomatous tumour, and morphologically similar lesions.
(
- Contribution to journal › Article
-
Mark
Genomic profiling of chondrosarcoma: chromosomal patterns in central and peripheral tumors.
(
- Contribution to journal › Article
-
Mark
Low-grade fibromyxoid sarcoma is difficult to diagnose by fine needle aspiration cytology: a cytomorphological study of eight cases.
(
- Contribution to journal › Article
-
Mark
Telomeric associations correlate with telomere length reduction and clonal chromosome aberrations in giant cell tumor of bone.
(
- Contribution to journal › Article
-
Mark
Characterization of the human CREB3L2 gene promoter
(
- Contribution to journal › Article
-
Mark
Bidirectionality and transcriptional activity of the EWSR1 promoter region
(
- Contribution to journal › Article
-
Mark
Expression levels of HMGA2 in adipocytic tumors correlate with morphologic and cytogenetic subgroups.
(
- Contribution to journal › Article
- 2008
-
Mark
The utility of fluorescence in situ hybridization (FISH) in the diagnosis of myxoid soft tissue neoplasms
(
- Contribution to journal › Article
-
Mark
Molecular identification of COL6A3-CSF1 fusion transcripts in tenosynovial giant cell tumors
(
- Contribution to journal › Article
-
Mark
Mesenchymal Stromal Cells (MSC) Isolated from Human Osteosarcomas Show a High Progenitor Cell Frequency, Typical MSC Morphology, Surface Marker Profile, and Differentiation Capacity, and They Are Considerably Affected by Tyrosine Kinase Inhibitors in Vitro
(
- Contribution to journal › Published meeting abstract
-
Mark
Fusion of the COL1A1 and USP6 genes in a benign bone tumor.
(
- Contribution to journal › Article
-
Mark
Heterogeneous genetic profiles in soft tissue myoepitheliomas
(
- Contribution to journal › Article
-
Mark
Deep-seated ordinary and atypical lipomas - Histopathology, cytogenetics, clinical features, and outcome in 215 tumours of the extremity and trunk wall
(
- Contribution to journal › Article
-
Mark
The POU5F1P1 pseudogene encodes a putative protein similar to POU5F1 isoform 1.
(
- Contribution to journal › Article
-
Mark
A PCR/restriction digestion assay for the detection of the transcript variants 1 and 2 of POU5F1.
(
- Contribution to journal › Article
-
Mark
High-resolution molecular cytogenetic analysis of Wilms tumors highlights diagnostic difficulties among small round cell kidney tumors.
(
- Contribution to journal › Article
-
Mark
POU5F1, encoding a key regulator of stem cell pluripotency, is fused to EWSR1 in hidradenoma of the skin and mucoepidermoid carcinoma of the salivary glands.
(
- Contribution to journal › Article
-
Mark
Selection of Influential Genetic Markers Among a Large Number of Candidates Based on Effect Estimation Rather than Hypothesis Testing: An Approach for Genome-Wide Association Studies.
(
- Contribution to journal › Article
-
Mark
Frequent deletion of the CDKN2A locus in chordoma: analysis of chromosomal imbalances using array comparative genomic hybridisation.
(
- Contribution to journal › Article
-
Mark
Increased sensitivity to bleomycin in upper aerodigestive tract mucosa of head and neck squamous cell carcinoma patients.
(
- Contribution to journal › Article
-
Mark
Cytogenetic and molecular cytogenetic findings in lipoblastoma.
(
- Contribution to journal › Article
-
Mark
An endometrial stromal sarcoma cell line with the JAZF1/PHF1 chimera
(
- Contribution to journal › Article
- 2007
-
Mark
Concurrent gain of 17q and the MYC oncogene in a medullomyoblastoma
(
- Contribution to journal › Article
-
Mark
Assessment of the clinical and molecular impact of different cytogenetic subgroups in a series of 272 lipomas with abnormal karyotype
(
- Contribution to journal › Article
-
Mark
Characterization of the native CREB3L2 transcription factor and the FUS/CREB3L2 chimera
(
- Contribution to journal › Article
-
Mark
Genetic intratumour heterogeneity in high-grade brain tumours is associated with telomere-dependent mitotic instability.
(
- Contribution to journal › Article
-
Mark
Tiling resolution array comparative genomic hybridization analysis of a fibrosarcoma of bone.
(
- Contribution to journal › Article
-
Mark
Unstable translocation (8;22) in a case of giant cell reparative granuloma.
(
- Contribution to journal › Article
-
Mark
Cytogenetic findings in pediatric renal cell carcinoma
(
- Contribution to journal › Article
-
Mark
Fusion genes in angiomatoid fibrous histiocytoma
(
- Contribution to journal › Article
-
Mark
Comparison of the proximal promoter regions of the PAX3 and PAX7 genes
(
- Contribution to journal › Article
-
Mark
Successful treatment of a child with t(15;19)-positive tumor.
(
- Contribution to journal › Article
-
Mark
The impact of translocations and gene fusions on cancer causation.
(
- Contribution to journal › Scientific review
- 2006
-
Mark
Truncation and fusion of HMGA2 in lipomas with rearrangements of 5q32-->q33 and 12q14-->q15.
(
- Contribution to journal › Article
-
Mark
Expression profiling of Wilms tumors reveals new candidate genes for different clinical parameters
(
- Contribution to journal › Article
-
Mark
Fine-needle aspiration of neurilemoma (schwannoma). A clinicocytopathologic study of 116 patients
(
- Contribution to journal › Article
-
Mark
FISH mapping of i(7q) in acute leukemias and myxoid liposarcoma reveals clustered breakpoints in 7p11.2 : implications for formation and pathogenetic outcome of the idic(7)(p11.2)
(
- Contribution to journal › Article
-
Mark
Rearrangement of the COL12A1 and COL4A5 genes in subungual exostosis: molecular cytogenetic delineation of the tumor-specific translocation t(X;6)(q13-14;q22)
(
- Contribution to journal › Article
-
Mark
Molecular cytogenetic characterization of the 11q13 amplicon in head and neck squamous cell carcinoma.
(
- Contribution to journal › Article
-
Mark
Fusion of the Tumor-Suppressor Gene CHEK2 and the Gene for the Regulatory Subunit B of Protein Phosphatase 2 PPP2R2A in Childhood Teratoma.
(
- Contribution to journal › Article
-
Mark
Prognostic significance of chromosome aberrations in high-grade soft tissue sarcomas
(
- Contribution to journal › Article
-
Mark
Fusion of the SEC31L1 and ALK genes in an inflammatory myofibroblastic tumor.
(
- Contribution to journal › Article
-
Mark
Genomic profiling of bone and soft tissue tumors with supernumerary ring chromosomes using tiling resolution bacterial artificial chromosome microarrays.
(
- Contribution to journal › Article
-
Mark
Gene copy number changes in dermatofibrosarcoma protuberans - a fine-resolution study using array comparative genomic hybridization
(
- Contribution to journal › Article
-
Mark
Identification of a novel amplicon at distal 17q containing the BIRC5/SURVIVIN gene in malignant peripheral nerve sheath tumours
(
- Contribution to journal › Article
-
Mark
Gene expression profiles relate to SS18/SSX fusion type in synovial sarcoma
(
- Contribution to journal › Article
-
Mark
Cytogenetic abnormalities in 106 oral squamous cell carcinomas
(
- Contribution to journal › Article
- 2005
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Mark
Clear cell hidradenoma of the skin - a third tumor type with a t(11;19)-associated TORC1-MAML2 gene fusion
(
- Contribution to journal › Article
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Mark
Prevalence estimates of recurrent balanced cytogenetic aberrations and gene fusions in unselected patients with neoplastic disorders.
(
- Contribution to journal › Article
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Mark
Fusion of the EWSR1 and ATF1 genes without expression of the MITF-M transcript in angiomatoid fibrous histiocytoma
(
- Contribution to journal › Article
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Mark
Biallelic somatic inactivation of the NF1 gene through chromosomal translocations in a sporadic neurofibroma
(
- Contribution to journal › Article
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Mark
Clinicopathologic and molecular genetic characterization of low-grade fibromyxoid sarcoma, and cloning of a novel FUS/CREB3L1 fusion gene
(
- Contribution to journal › Article
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Mark
Core-needle biopsy performed by the cytopathologist : a technique to complement fine-needle aspiration of soft tissue and bone lesions
(
- Contribution to journal › Article
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Mark
Absence of mutations of the BRAF gene in malignant melanoma of soft parts (clear cell sarcoma of tendons and aponeuroses)
(
- Contribution to journal › Article
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Mark
Structural and numerical chromosome changes in colon cancer develop through telomere-mediated anaphase bridges, not through mitotic multipolarity.
(
- Contribution to journal › Article
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Mark
Atypical lipomatous tumor with rare structural rearrangements involving chromosomes 8 and 12
(
- Contribution to journal › Article
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Mark
Karyotypic evolution and tumor progression in head and neck squamous cell carcinomas.
(
- Contribution to journal › Article
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Mark
Molecular cytogenetic characterization of an ins(4;X) occurring as the sole abnormality in an aggressive, poorly differentiated soft tissue sarcoma.
(
- Contribution to journal › Article
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Mark
Fusion of the HMGA2 and NFIB genes in lipoma
(
- Contribution to journal › Article
- 2004
-
Mark
Activation of the GLI Oncogene through Fusion with the beta-Actin Gene (ACTB) in a Group of Distinctive Pericytic Neoplasms: Pericytoma with t(7;12).
(
- Contribution to journal › Article
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Mark
Molecular cytogenetic characterization of recurrent translocation breakpoints in bizarre parosteal osteochondromatous proliferation (Nora's lesion).
(
- Contribution to journal › Article
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Mark
Amplification of chromosome 1 sequences in lipomatous tumors and other sarcomas
(
- Contribution to journal › Article
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Mark
A novel FISH assay for SS18-SSX fusion type in synovial sarcoma
(
- Contribution to journal › Article
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Mark
Retained heterodisomy for chromosome 12 in atypical lipomatous tumors: implications for ring chromosome formation.
(
- Contribution to journal › Article
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Mark
Clinical and biological importance of cytogenetic abnormalities in childhood and adult acute lymphoblastic leukemia
(
- Contribution to journal › Scientific review
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Mark
Molecular genetic characterization of the genomic ACTB-GLI fusion in pericytoma with t(7;12).
(
- Contribution to journal › Article
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Mark
Statistical analyses of karyotypic complexity in head and neck squamous cell carcinoma.
(
- Contribution to journal › Article
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Mark
Fusion genes and rearranged genes as a linear function of chromosome aberrations in cancer
(
- Contribution to journal › Article
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Mark
Genetic characterization of bone and soft tissue tumors
(
- Contribution to journal › Article
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Mark
Expression of DOL54 is not restricted to myxoid liposarcomas with the FUS-DDIT3 chimera but is found in various sarcomas.1
(
- Contribution to journal › Article
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Mark
Combined binary ratio labeling fluorescence in situ hybridization analysis of chordoma
(
- Contribution to journal › Article
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Mark
Mitotic instability associated with late genomic changes in bone and soft tissue tumours.
(
- Contribution to journal › Article
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Mark
The chimeric FUS/CREB3l2 gene is specific for low-grade fibromyxoid sarcoma.
(
- Contribution to journal › Article
- 2003
-
Mark
Fusion of the FUS and BBF2H7 genes in low grade fibromyxoid sarcoma
(
- Contribution to journal › Article
-
Mark
Clustering of deletions on chromosome 13 in benign and low-malignant lipomatous tumors
(
- Contribution to journal › Article
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Mark
A novel fusion gene, SS18L1/SSX1, in synovial sarcoma
(
- Contribution to journal › Article
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Mark
Topoisomerase-II alpha is upregulated in malignant peripheral nerve sheath tumors and associated with clinical outcome
(
- Contribution to journal › Article
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Mark
Comparative cytogenetic and DNA flow cytometric analysis of 242 primary breast carcinomas
(
- Contribution to journal › Article
-
Mark
Fusion, disruption, and expression of HMGA2 in bone and soft tissue chondromas
(
- Contribution to journal › Article
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Mark
Extraskeletal myxoid chondrosarcoma with neuroendocrine differentiation: a case report with fine-needle aspiration biopsy, histopathology, electron microscopy, and cytogenetics.
(
- Contribution to journal › Article
-
Mark
Ring chromosomes and low-grade gene amplification in an atypical lipomatous tumor with minimal nuclear atypia
(
- Contribution to journal › Article
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Mark
Cytogenetic findings and clinical course in a consecutive series of Wilms tumors
(
- Contribution to journal › Article
- 2002
-
Mark
Cytogenetic aberrations and their prognostic impact in chondrosarcoma
(
- Contribution to journal › Article
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Mark
Cyclin D1 amplification in chromosomal band 11q13 is associated with overrepresentation of 3q21-q29 in head and neck carcinomas.
(
- Contribution to journal › Article
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Mark
Differentially amplified chromosome 12 sequences in low- and high-grade osteosarcoma.
(
- Contribution to journal › Article
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Mark
Molecular genetic characterization of the EWS/CHN and RBP56/CHN fusion genes in extraskeletal myxoid chondrosarcoma.
(
- Contribution to journal › Article
-
Mark
Centrosomal abnormalities, multipolar mitoses, and chromosomal instability in head and neck tumours with dysfunctional telomeres.
(
- Contribution to journal › Article
-
Mark
Molecular genetic characterization of the EWS/ATF1 fusion gene in clear cell sarcoma of tendons and aponeuroses.
(
- Contribution to journal › Article
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Mark
Correlation between clinicopathological features and karyotype in 100 cartilaginous and chordoid tumours. A report from the Chromosomes and Morphology (CHAMP) Collaborative Study Group
(
- Contribution to journal › Article
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Mark
Chromosomal translocations involving 11q13 contribute to cyclin D1 overexpression in squamous cell carcinoma of the head and neck
(
- Contribution to journal › Article
-
Mark
Solid tumor cytogenetics
2002) p.704-704(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Congenital and inherited syndromes associated with bone and soft tissue tumours
2002) p.349-349(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Enchondromatosis: Ollier disease and Maffucci syndrome
2002) p.356-356(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Chordoma
2002) p.316-316(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Synovial chondromatosis
2002) p.246-246(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Prognostically important chromosomal aberrations in soft tissue sarcomas: a report of the Chromosomes and Morphology (CHAMP) Study Group.
(
- Contribution to journal › Article
-
Mark
Karyotypic heterogeneity and clonal evolution in squamous cell carcinomas of the head and neck.
(
- Contribution to journal › Article
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Mark
Molecular cytogenetic mapping of recurrent chromosomal breakpoints in tenosynovial giant cell tumors.
(
- Contribution to journal › Article
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Mark
Fusion of RDC1 with HMGA2 in lipomas as the result of chromosome aberrations involving 2q35-37 and 12q13-15.
(
- Contribution to journal › Article
- 2001
-
Mark
Cloning of the der(17)t(X;17)(p11;q25) alveolar soft part sarcoma identifies the ASPL-TFE3 gene fusion, a new molecular diagnostic marker
(
- Contribution to journal › Article
-
Mark
Characterization of chromosome aberrations in salivary gland tumors by FISH, including multicolor COBRA-FISH
(
- Contribution to journal › Article
-
Mark
Comparative genomic hybridization of postirradiation sarcomas
(
- Contribution to journal › Article
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Mark
Multivariate analyses of genomic imbalances in solid tumors reveal distinct and converging pathways of karyotypic evolution
(
- Contribution to journal › Article
-
Mark
Biallelic inactivation of TP53 rarely contributes to the development of malignant peripheral nerve sheath tumors
(
- Contribution to journal › Article
-
Mark
Abnormal nuclear shape in solid tumors reflects mitotic instability
(
- Contribution to journal › Article
-
Mark
The der(17)t(X;17)(p11;q25) of human alveolar soft part sarcoma fuses the TFE3 transcription factor gene to ASPL, a novel gene at 17q25
(
- Contribution to journal › Article
-
Mark
Trisomy 7 accumulates with age in solid tumors and non-neoplastic synovia
(
- Contribution to journal › Article
-
Mark
No EWS/FLI1 fusion transcripts in giant-cell tumors of bone
(
- Contribution to journal › Article
-
Mark
Telomere dysfunction triggers extensive DNA fragmentation and evolution of complex chromosome abnormalities in human malignant tumors
(
- Contribution to journal › Article
-
Mark
Clinical impact of molecular and cytogenetic findings in synovial sarcoma
(
- Contribution to journal › Article
-
Mark
Distinct cytologic features of spindle cell lipoma - A cytologic-histologic study with clinical, radiologic, electron microscopic, and cytogenetic correlations
(
- Contribution to journal › Article
-
Mark
Analysis of the distribution and frequency of trisomy 7 in vivo in synovia from patients with osteoarthritis and pigmented villonodular synovitis
(
- Contribution to journal › Article
-
Mark
DNA copy number amplifications in sarcomas with homogeneously staining regions and double minutes
(
- Contribution to journal › Article
-
Mark
Cytogenetic and fluorescence in situ hybridization characterization of chromosome 8 rearrangements in head and neck squamous cell carcinomas
(
- Contribution to journal › Article
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Mark
Calcium pyrophosphate dihydrate crystal deposition disease in the temporomandibular joint: Diagnostic difficulties and clonal chromosome aberrations in a case followed up for 5 years
(
- Contribution to journal › Article
-
Mark
The tumor-associated gene HMGIC is expressed in normal and osteoarthritis-affected synovia
(
- Contribution to journal › Article
- 2000
-
Mark
Cytogenetics of hepatoblastoma: further characterization of 1q rearrangements by fluorescence in situ hybridization: an international collaborative study
(
- Contribution to journal › Article
-
Mark
Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity
(
- Contribution to journal › Article
-
Mark
Radiation-associated sarcomas are characterized by complex karyotypes with frequent rearrangements of chromosome arm 3p
(
- Contribution to journal › Article
-
Mark
Cytogenetic heterogeneity and clonal evolution in synchronous bilateral breast carcinomas and their lymph node metastases from a male patient without any detectable BRCA2 germline mutation
(
- Contribution to journal › Article
- 1999
-
Mark
Chromosomal aberrations in breast cancer: a comparison between cytogenetics and comparative genomic hybridization
(
- Contribution to journal › Article
-
Mark
Unique cytological features and chromosome aberrations in chondroid lipoma: a case report based on fine-needle aspiration cytology, histopathology, electron microscopy, chromosome banding, and molecular cytogenetics
(
- Contribution to journal › Article
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Mark
Hibernomas are characterized by homozygous deletions in the multiple endocrine neoplasia type I region. Metaphase fluorescence in situ hybridization reveals complex rearrangements not detected by conventional cytogenetics
(
- Contribution to journal › Article
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Mark
Cytogenetic aberrations in Ewing sarcoma: are secondary changes associated with clinical outcome?
(
- Contribution to journal › Article
-
Mark
Variable stability of chromosomes containing amplified alpha-satellite sequences in human mesenchymal tumours
(
- Contribution to journal › Article
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Mark
The structure and dynamics of ring chromosomes in human neoplastic and non-neoplastic cells
(
- Contribution to journal › Article