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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

The Journal of pathology, 2008-05, Vol.215 (1), p.78-86

2008

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POU5FI, encoding a key regulator of stem cell pluripotency, is fused to EWSRI in hidradenoma of the skin and mucoepidermoid carcinoma of the salivary glands

The Journal of pathology, 2008-05, Vol.215 (1), p.78-86

2008

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Frequent deletion of the CDKN2A locus in chordoma: analysis of chromosomal imbalances using array comparative genomic hybridisation

British journal of cancer, 2008-01, Vol.98 (2), p.434-442

2008

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Identification of a novel amplicon at distal 17q containing the BIRC5/SURVIVIN gene in malignant peripheral nerve sheath tumours

The Journal of pathology, 2006-08, Vol.209 (4), p.492-500

2006

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Genomic profiling of bone and soft tissue tumors with supernumerary ring chromosomes using tiling resolution bacterial artificial chromosome microarrays

Oncogene, 2006-11, Vol.25 (53), p.7106-7116

2006

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Generation of human cortical neurons from a new immortal fetal neural stem cell line

Experimental cell research, 2007-02, Vol.313 (3), p.588-601

2007

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Molecular cytogenetic mapping of recurrent chromosomal breakpoints in tenosynovial giant cell tumors

Virchows Archiv : an international journal of pathology, 2002-11, Vol.441 (5), p.475-480

2002

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Telomere shortening and mitotic dysfunction generate cytogenetic heterogeneity in a subgroup of renal cell carcinomas

British journal of cancer, 2004-07, Vol.91 (2), p.327-332

2004

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Comprehensive genetic analysis identifies a pathognomonic NAB2/STAT6 fusion gene, nonrandom secondary genomic imbalances, and a characteristic gene expression profile in solitary fibrous tumor

Genes chromosomes & cancer, 2013-10, Vol.52 (10), p.873-886

2013

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Centrosomal abnormalities, multipolar mitoses, and chromosomal instability in head and neck tumours with dysfunctional telomeres

British journal of cancer, 2002-07, Vol.87 (2), p.202-207

2002

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Fusion of the HMGA2 and NFIB genes in lipoma

Virchows Archiv : an international journal of pathology, 2005-11, Vol.447 (5), p.855-858

2005

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Correlation between clinicopathological features and karyotype in lipomatous tumors. A report of 178 cases from the Chromosomes and Morphology (CHAMP) Collaborative Study Group

The American journal of pathology, 1996-02, Vol.148 (2), p.623-630

1996

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Conserved mechanism of PLAG1 activation in salivary gland tumors with and without chromosome 8q12 abnormalities : Identification of SII as a new fusion partner gene

Cancer research (Chicago, Ill.), 1999-02, Vol.59 (4), p.918-923

1999

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Different patterns of clonal evolution among different sarcoma subtypes followed for up to 25 years

Nature communications, 2018-09, Vol.9 (1), p.3662-8, Article 3662

2018

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Truncation and fusion of HMGA2 in lipomas with rearrangements of 5q32→q33 and 12q14→q15

Cytogenetic and genome research, 2006-01, Vol.112 (1-2), p.60-66

2006

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Recurrent PRDM10 gene fusions in undifferentiated pleomorphic sarcoma

Clinical cancer research, 2015-02, Vol.21 (4), p.864-869

2015

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Telomeric associations correlate with telomere length reduction and clonal chromosome aberrations in giant cell tumor of bone

Cytogenetic and genome research, 2009-01, Vol.124 (2), p.121-127

2009

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Gene copy number changes in dermatofibrosarcoma protuberans – a fine-resolution study using array comparative genomic hybridization

Cytogenetic and genome research, 2006-11, Vol.115 (3-4), p.283-288

2006

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Recurrent Rearrangement of the PHF1 Gene in Ossifying Fibromyxoid Tumors

The American journal of pathology, 2012-09, Vol.181 (3), p.1069-1077

2012

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Structural and Numerical Chromosome Changes in Colon Cancer Develop through Telomere-Mediated Anaphase Bridges, Not through Mitotic Multipolarity

Proceedings of the National Academy of Sciences - PNAS, 2005-04, Vol.102 (15), p.5541-5546

2005

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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)

Cytogenetic and genome research, 2006-01, Vol.114 (2), p.126-130

2006

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Clinicopathologic and molecular genetic characterization of low-grade fibromyxoid sarcoma, and cloning of a novel FUS/CREB3L1 fusion gene

Laboratory investigation, 2005-03, Vol.85 (3), p.408-415

2005

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Genetic intratumour heterogeneity in high-grade brain tumours is associated with telomere-dependent mitotic instability

Neuropathology and applied neurobiology, 2007-08, Vol.33 (4), p.440-454

2007

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Telomere Dysfunction Triggers Extensive DNA Fragmentation and Evolution of Complex Chromosome Abnormalities in Human Malignant Tumors

Proceedings of the National Academy of Sciences - PNAS, 2001-10, Vol.98 (22), p.12683-12688

2001

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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

Cancer genetics, 2020-02, Vol.241, p.34-41

2020

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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

POU5FI, encoding a key regulator of stem cell pluripotency, is fused to EWSRI in hidradenoma of the skin and mucoepidermoid carcinoma of the salivary glands

Frequent deletion of the CDKN2A locus in chordoma: analysis of chromosomal imbalances using array comparative genomic hybridisation

Identification of a novel amplicon at distal 17q containing the BIRC5/SURVIVIN gene in malignant peripheral nerve sheath tumours

Genomic profiling of bone and soft tissue tumors with supernumerary ring chromosomes using tiling resolution bacterial artificial chromosome microarrays

Generation of human cortical neurons from a new immortal fetal neural stem cell line

Molecular cytogenetic mapping of recurrent chromosomal breakpoints in tenosynovial giant cell tumors

Telomere shortening and mitotic dysfunction generate cytogenetic heterogeneity in a subgroup of renal cell carcinomas

Comprehensive genetic analysis identifies a pathognomonic NAB2/STAT6 fusion gene, nonrandom secondary genomic imbalances, and a characteristic gene expression profile in solitary fibrous tumor

Centrosomal abnormalities, multipolar mitoses, and chromosomal instability in head and neck tumours with dysfunctional telomeres

Fusion of the HMGA2 and NFIB genes in lipoma

Correlation between clinicopathological features and karyotype in lipomatous tumors. A report of 178 cases from the Chromosomes and Morphology (CHAMP) Collaborative Study Group

Conserved mechanism of PLAG1 activation in salivary gland tumors with and without chromosome 8q12 abnormalities : Identification of SII as a new fusion partner gene

Different patterns of clonal evolution among different sarcoma subtypes followed for up to 25 years

Truncation and fusion of HMGA2 in lipomas with rearrangements of 5q32→q33 and 12q14→q15

Recurrent PRDM10 gene fusions in undifferentiated pleomorphic sarcoma

Telomeric associations correlate with telomere length reduction and clonal chromosome aberrations in giant cell tumor of bone

Gene copy number changes in dermatofibrosarcoma protuberans – a fine-resolution study using array comparative genomic hybridization

Recurrent Rearrangement of the PHF1 Gene in Ossifying Fibromyxoid Tumors

Structural and Numerical Chromosome Changes in Colon Cancer Develop through Telomere-Mediated Anaphase Bridges, Not through Mitotic Multipolarity

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)

Clinicopathologic and molecular genetic characterization of low-grade fibromyxoid sarcoma, and cloning of a novel FUS/CREB3L1 fusion gene

Genetic intratumour heterogeneity in high-grade brain tumours is associated with telomere-dependent mitotic instability

Telomere Dysfunction Triggers Extensive DNA Fragmentation and Evolution of Complex Chromosome Abnormalities in Human Malignant Tumors

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

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