Ioannis Panagopoulos
- Head engineer
- +47 22 93 44 24
Publications 2024
RUNX1::MIR99AHG Chimera in Acute Myeloid Leukemia
Genes Chromosomes Cancer, 63 (9), e23272
DOI 10.1002/gcc.23272, PubMed 39324493
Accurate and comprehensive evaluation of O6-methylguanine-DNA methyltransferase promoter methylation by nanopore sequencing
Neuropathol Appl Neurobiol, 50 (3), e12984
DOI 10.1111/nan.12984, PubMed 38783575
Genetic characterization of intramuscular myxomas
Pathol Oncol Res, 30, 1611553
DOI 10.3389/pore.2024.1611553, PubMed 38317844
Fusion of Platelet Derived Growth Factor Receptor Alpha (PDGFRA) With Ubiquitin Specific Peptidase 8 (USP8) in a Calcified Chondroid Mesenchymal Neoplasm Harboring t(4;15)(q12;q21) as a Sole Aberration
Cancer Genomics Proteomics, 21 (3), 252-259
DOI 10.21873/cgp.20444, PubMed 38670591
Genetic Characterization of Pediatric Mixed Phenotype Acute Leukemia (MPAL)
Cancer Genomics Proteomics, 21 (1), 1-11
DOI 10.21873/cgp.20424, PubMed 38151288
Genetic Heterogeneity in Cellular Angiofibromas
Genes Chromosomes Cancer, 63 (8), e23262
DOI 10.1002/gcc.23262, PubMed 39120141
Germline MYOF1::WNK4 and VPS25::MYOF1 Chimeras Generated by the Constitutional Translocation t(17;19)(q21;p13) in Two Siblings With Myelodysplastic Syndrome
Cancer Genomics Proteomics, 21 (3), 272-284
DOI 10.21873/cgp.20446, PubMed 38670586
Acute Lymphoblastic Leukemia With Near-haploid Karyotype and Philadelphia Chromosome
Anticancer Res, 44 (4), 1389-1397
DOI 10.21873/anticanres.16935, PubMed 38537997
Publications 2023
Genomic Complexity as a Biomarker to De-Escalate Adjuvant Imatinib Treatment in High-Risk Gastrointestinal Stromal Tumor
JCO Precis Oncol, 7, e2200351
DOI 10.1200/PO.22.00351, PubMed 36724411
Genetic Pathways in Peritoneal Mesothelioma Tumorigenesis
Cancer Genomics Proteomics, 20 (4), 363-374
DOI 10.21873/cgp.20388, PubMed 37400148
Pathogenetic Dichotomy in Angioleiomyoma
Cancer Genomics Proteomics, 20 (6), 556-566
DOI 10.21873/cgp.20405, PubMed 37889065
Fusion of the High-mobility Group AT-Hook 2 (HMGA2) and the Gelsolin (GSN) Genes in Lipomas With t(9;12)(q33;q14) Chromosomal Translocation
In Vivo, 37 (2), 524-530
DOI 10.21873/invivo.13110, PubMed 36881074
Chromosome Translocation t(10;19)(q26;q13) in a CIC-sarcoma
In Vivo, 37 (1), 57-69
DOI 10.21873/invivo.13054, PubMed 36593014
Recurrent 8q11-13 Aberrations Leading to PLAG1 Rearrangements, Including Novel Chimeras HNRNPA2B1::PLAG1 and SDCBP::PLAG1, in Lipomatous Tumors
Cancer Genomics Proteomics, 20 (2), 171-181
DOI 10.21873/cgp.20372, PubMed 36870688
Novel MYCBP::EHD2 and RUNX1::ZNF780A Fusion Genes in T-cell Acute Lymphoblastic Leukemia
Cancer Genomics Proteomics, 20 (1), 51-63
DOI 10.21873/cgp.20364, PubMed 36581344
Acute Undifferentiated Leukemia With a Balanced t(5;10)(q35;p12) Resulting in Fusion of HNRNPH1 With MLLT10
Cancer Genomics Proteomics, 20 (4), 354-362
DOI 10.21873/cgp.20387, PubMed 37400142
Fusion of the Genes for Interferon Regulatory Factor 2 Binding Protein 2 (IRF2BP2) and Caudal Type Homeobox 1 (CDX1) in a Chondrogenic Tumor
In Vivo, 37 (6), 2459-2463
DOI 10.21873/invivo.13352, PubMed 37905608
Publications 2022
Endometrial Carcinoma: Molecular Cytogenetics and Transcriptomic Profile
Cancers (Basel), 14 (14)
DOI 10.3390/cancers14143536, PubMed 35884597
Cytogenetic and molecular analyses of 291 gastrointestinal stromal tumors: site-specific cytogenetic evolution as evidence of pathogenetic heterogeneity
Oncotarget, 13, 508-517
DOI 10.18632/oncotarget.28209, PubMed 35284037
A Novel Cryptic t(2;3)(p21;q25) Translocation Fuses the WWTR1 and PRKCE Genes in Uterine Leiomyoma With 3q- as the Sole Visible Chromosome Abnormality
Cancer Genomics Proteomics, 19 (5), 636-646
DOI 10.21873/cgp.20348, PubMed 35985686
Fusion of the HMGA2 and BNC2 Genes in Uterine Leiomyoma With t(9;12)(p22;q14)
In Vivo, 36 (6), 2654-2661
DOI 10.21873/invivo.13000, PubMed 36309352
Presence of a t(12;18)(q14;q21) Chromosome Translocation and Fusion of the Genes for High-mobility Group AT-Hook 2 (HMGA2) and WNT Inhibitory Factor 1 (WIF1) in Infrapatellar Fat Pad Cells from a Patient With Hoffa's Disease
Cancer Genomics Proteomics, 19 (5), 584-590
DOI 10.21873/cgp.20343, PubMed 35985683
Recurrent Fusion of the Genes for High-mobility Group AT-hook 2 (HMGA2) and Nuclear Receptor Co-repressor 2 (NCOR2) in Osteoclastic Giant Cell-rich Tumors of Bone
Cancer Genomics Proteomics, 19 (2), 163-177
DOI 10.21873/cgp.20312, PubMed 35181586
Fusion of High Mobility Group AT-hook 2 Gene (HMGA2) With the Chromosome 12 Open Reading Frame 42 Gene (C12orf42) in an Aggressive Angiomyxoma With del(12)(q14q23) as the Sole Cytogenetic Anomaly
Cancer Genomics Proteomics, 19 (5), 576-583
DOI 10.21873/cgp.20342, PubMed 35985684
Chromosomal Translocation t(5;12)(p13;q14) Leading to Fusion of High-mobility Group AT-hook 2 Gene With Intergenic Sequences From Chromosome Sub-Band 5p13.2 in Benign Myoid Neoplasms of the Breast: A Second Case
Cancer Genomics Proteomics, 19 (4), 445-455
DOI 10.21873/cgp.20331, PubMed 35732319
Neoplasia-associated Chromosome Translocations Resulting in Gene Truncation
Cancer Genomics Proteomics, 19 (6), 647-672
DOI 10.21873/cgp.20349, PubMed 36316036
Functional temozolomide sensitivity testing of patient-specific glioblastoma stem cell cultures is predictive of clinical outcome
Transl Oncol, 26, 101535
DOI 10.1016/j.tranon.2022.101535, PubMed 36115076
Publications 2021
Rare KMT2A-ELL and Novel ZNF56-KMT2A Fusion Genes in Pediatric T-cell Acute Lymphoblastic Leukemia
Cancer Genomics Proteomics, 18 (2), 121-131
DOI 10.21873/cgp.20247, PubMed 33608309
Therapy-induced Deletion in 11q23 Leading to Fusion of KMT2A With ARHGEF12 and Development of B Lineage Acute Lymphoplastic Leukemia in a Child Treated for Acute Myeloid Leukemia Caused by t(9;11)(p21;q23)/KMT2A-MLLT3
Cancer Genomics Proteomics, 18 (1), 67-81
DOI 10.21873/cgp.20242, PubMed 33419897
Therapy-related Myeloid Leukemia With the Translocation t(8;19)(p11;q13) Leading to a KAT6A-LEUTX Fusion Gene
Anticancer Res, 41 (4), 1753-1760
DOI 10.21873/anticanres.14940, PubMed 33813379
Several Fusion Genes Identified in a Spermatic Cord Leiomyoma With Rearrangements of Chromosome Arms 3p and 21q
Cancer Genomics Proteomics, 18 (4), 531-542
DOI 10.21873/cgp.20278, PubMed 34183386
Fusion of the Paired Box 3 (PAX3) and Myocardin (MYOCD) Genes in Pediatric Rhabdomyosarcoma
Cancer Genomics Proteomics, 18 (6), 723-734
DOI 10.21873/cgp.20293, PubMed 34697065
Monosomy 13 in Mammary Myofibroblastoma
Anticancer Res, 41 (8), 3747-3751
DOI 10.21873/anticanres.15166, PubMed 34281833
Interstitial Deletions Generating Fusion Genes
Cancer Genomics Proteomics, 18 (3), 167-196
DOI 10.21873/cgp.20251, PubMed 33893073
Publications 2020
Mutation analysis and genomic imbalances of cells found in effusion fluids from patients with ovarian cancer
Oncol Lett, 20 (3), 2273-2279
DOI 10.3892/ol.2020.11782, PubMed 32782545
TYRO3 Truncation Resulting From a t(10;15)(p11;q15) Chromosomal Translocation in Pediatric Acute Myeloid Leukemia
Anticancer Res, 40 (11), 6115-6121
DOI 10.21873/anticanres.14632, PubMed 33109549
Rare cause of small bowel obstruction secondary to epiploic appendagitis: Diagnostic dilemma and role of minimal invasive surgery
Int J Surg Case Rep, 78, 30-33
DOI 10.1016/j.ijscr.2020.11.140, PubMed 33310465
Cytogenetic and Molecular Study of an Adult Sclerosing Rhabdomyosarcoma of the Extremity: MYOD1-mutation and Clonal Evolution
Cancer Genomics Proteomics, 17 (5), 563-569
DOI 10.21873/cgp.20212, PubMed 32859634
A Small-Molecule Tankyrase Inhibitor Reduces Glioma Stem Cell Proliferation and Sphere Formation
Cancers (Basel), 12 (6)
DOI 10.3390/cancers12061630, PubMed 32575464
Molecular pathogenesis and prognostication of "low-grade'' and "high-grade" endometrial stromal sarcoma
Genes Chromosomes Cancer, 60 (3), 160-167
DOI 10.1002/gcc.22907, PubMed 33099834
Fusion of the Lumican (LUM) Gene With the Ubiquitin Specific Peptidase 6 (USP6) Gene in an Aneurysmal Bone Cyst Carrying a t(12;17)(q21;p13) Chromosome Translocation
Cancer Genomics Proteomics, 17 (5), 555-561
DOI 10.21873/cgp.20211, PubMed 32859633
NDRG1-PLAG1 and TRPS1-PLAG1 Fusion Genes in Chondroid Syringoma
Cancer Genomics Proteomics, 17 (3), 237-248
DOI 10.21873/cgp.20184, PubMed 32345665
Recurrent Fusion of the GRB2 Associated Binding Protein 1 (GAB1) Gene With ABL Proto-oncogene 1 (ABL1) in Benign Pediatric Soft Tissue Tumors
Cancer Genomics Proteomics, 17 (5), 499-508
DOI 10.21873/cgp.20206, PubMed 32859628
Chromosome Translocation t(14;21)(q11;q22) Activates Both OLIG1 and OLIG2 in Pediatric T-cell Lymphoblastic Malignancies and May Signify Adverse Prognosis
Cancer Genomics Proteomics, 17 (1), 41-48
DOI 10.21873/cgp.20166, PubMed 31882550
Chronic Expanding Hematoma with a t(11;19)(q13;q13) Chromosomal Translocation
Anticancer Res, 40 (1), 97-100
DOI 10.21873/anticanres.13930, PubMed 31892557
FOS-ANKH and FOS-RUNX2 Fusion Genes in Osteoblastoma
Cancer Genomics Proteomics, 17 (2), 161-168
DOI 10.21873/cgp.20176, PubMed 32108038
Fusion of the COL4A5 Gene With NR2F2-AS1 in a Hemangioma Carrying a t(X;15)(q22;q26) Chromosomal Translocation
Cancer Genomics Proteomics, 17 (4), 383-390
DOI 10.21873/cgp.20197, PubMed 32576583
An Unbalanced Chromosome Translocation Between 7p22 and 12q13 Leads to ACTB-GLI1 Fusion in Pericytoma
Anticancer Res, 40 (3), 1239-1245
DOI 10.21873/anticanres.14065, PubMed 32132020
Publications 2019
18F-Fluciclovine PET/CT in Suspected Residual or Recurrent High-Grade Glioma
Clin Nucl Med, 44 (8), 605-611
DOI 10.1097/RLU.0000000000002641, PubMed 31274605
MGMT promoter methylation is a rare epigenetic change in malignant effusions
Cytopathology, 31 (1), 12-15
DOI 10.1111/cyt.12782, PubMed 31808217
Novel GTF2I-PDGFRB and IKZF1-TYW1 fusions in pediatric leukemia with normal karyotype
Exp Hematol Oncol, 8, 12
DOI 10.1186/s40164-019-0136-y, PubMed 31161074
Genetic Characterization of Myoid Hamartoma of the Breast
Cancer Genomics Proteomics, 16 (6), 563-568
DOI 10.21873/cgp.20158, PubMed 31659109
Fusion of the COL1A1 and FYN Genes in Epithelioid Osteoblastoma
Cancer Genomics Proteomics, 16 (5), 361-368
DOI 10.21873/cgp.20141, PubMed 31467230
Fusion of the Genes PHF1 and TFE3 in Malignant Chondroid Syringoma
Cancer Genomics Proteomics, 16 (5), 345-351
DOI 10.21873/cgp.20139, PubMed 31467228
Fusion of the Genes WWTR1 and FOSB in Pseudomyogenic Hemangioendothelioma
Cancer Genomics Proteomics, 16 (4), 293-298
DOI 10.21873/cgp.20134, PubMed 31243110
Molecular Genetic Characterization of Acute Myeloid Leukemia With Trisomy 4 as the Sole Chromosome Abnormality
Cancer Genomics Proteomics, 16 (3), 175-178
DOI 10.21873/cgp.20123, PubMed 31018948
Publications 2018
Identification of novel cyclin gene fusion transcripts in endometrioid ovarian carcinomas
Int J Cancer, 143 (6), 1379-1387
DOI 10.1002/ijc.31418, PubMed 29633253
The microRNA miR-192/215 family is upregulated in mucinous ovarian carcinomas
Sci Rep, 8 (1), 11069
DOI 10.1038/s41598-018-29332-7, PubMed 30038317
Identification of an EPC2-PHF1 fusion transcript in low-grade endometrial stromal sarcoma
Oncotarget, 9 (27), 19203-19208
DOI 10.18632/oncotarget.24969, PubMed 29721194
Expression and clinical role of the dipeptidyl peptidases DPP8 and DPP9 in ovarian carcinoma
Virchows Arch, 474 (2), 177-185
DOI 10.1007/s00428-018-2487-x, PubMed 30467600
MGMT Gene Promoter Methylation Status - Assessment of Two Pyrosequencing Kits and Three Methylation-specific PCR Methods for their Predictive Capacity in Glioblastomas
Cancer Genomics Proteomics, 15 (6), 437-446
DOI 10.21873/cgp.20102, PubMed 30343277
K27/G34 versus K28/G35 in histone H3-mutant gliomas: A note of caution
Acta Neuropathol, 136 (1), 175-176
DOI 10.1007/s00401-018-1867-2, PubMed 29766298
PAN3-PSMA2 fusion resulting from a novel t(7;13)(p14;q12) chromosome translocation in a myelodysplastic syndrome that evolved into acute myeloid leukemia
Exp Hematol Oncol, 7, 7
DOI 10.1186/s40164-018-0099-4, PubMed 29560286
Consistent Involvement of Chromosome 13 in Angiolipoma
Cancer Genomics Proteomics, 15 (1), 61-65
DOI 10.21873/cgp.20065, PubMed 29275363
RUNX1-PDCD6 fusion resulting from a novel t(5;21)(p15;q22) chromosome translocation in myelodysplastic syndrome secondary to chronic lymphocytic leukemia
PLoS One, 13 (4), e0196181
DOI 10.1371/journal.pone.0196181, PubMed 29672642
Pyrosequencing Analysis of MGMT Promoter Methylation in Meningioma
Cancer Genomics Proteomics, 15 (5), 379-385
DOI 10.21873/cgp.20096, PubMed 30194078
Cytogenetics of Spindle Cell/Pleomorphic Lipomas: Karyotyping and FISH Analysis of 31 Tumors
Cancer Genomics Proteomics, 15 (3), 193-200
DOI 10.21873/cgp.20077, PubMed 29695401
Publications 2017
Genomic imbalances are involved in miR-30c and let-7a deregulation in ovarian tumors: implications for HMGA2 expression
Oncotarget, 8 (13), 21554-21560
DOI 10.18632/oncotarget.15795, PubMed 28423547
Recurrent fusion transcripts in squamous cell carcinomas of the vulva
Oncotarget, 8 (10), 16843-16850
DOI 10.18632/oncotarget.15167, PubMed 28186972
RNA-sequencing identifies novel GREB1-NCOA2 fusion gene in a uterine sarcoma with the chromosomal translocation t(2;8)(p25;q13)
Genes Chromosomes Cancer, 57 (4), 176-181
DOI 10.1002/gcc.22518, PubMed 29218853
ZC3H7B-BCOR high-grade endometrial stromal sarcomas: a report of 17 cases of a newly defined entity
Mod Pathol, 31 (4), 674-684
DOI 10.1038/modpathol.2017.162, PubMed 29192652
Fusion of the genes BRD8 and PHF1 in endometrial stromal sarcoma
Genes Chromosomes Cancer, 56 (12), 841-845
DOI 10.1002/gcc.22485, PubMed 28758277
Loss of chromosome 13 material in cellular angiofibromas indicates pathogenetic similarity with spindle cell lipomas
Diagn Pathol, 12 (1), 17
DOI 10.1186/s13000-017-0607-6, PubMed 28193293
Genetic heterogeneity in leiomyomas of deep soft tissue
Oncotarget, 8 (30), 48769-48781
DOI 10.18632/oncotarget.17953, PubMed 28591699
Cytogenetic Analysis of a Pseudoangiomatous Pleomorphic/Spindle Cell Lipoma
Anticancer Res, 37 (5), 2219-2223
DOI 10.21873/anticanres.11557, PubMed 28476785
Karyotyping and analysis of GNAS locus in intramuscular myxomas
Oncotarget, 8 (13), 22086-22094
DOI 10.18632/oncotarget.14986, PubMed 28160572
Identification of SETD2-NF1 fusion gene in a pediatric spindle cell tumor with the chromosomal translocation t(3;17)(p21;q12)
Oncol Rep, 37 (6), 3181-3188
DOI 10.3892/or.2017.5628, PubMed 28498454
Fusion of the genes ataxin 2 like, ATXN2L, and Janus kinase 2, JAK2, in cutaneous CD4 positive T-cell lymphoma
Oncotarget, 8 (61), 103775-103784
DOI 10.18632/oncotarget.21790, PubMed 29262599
FAM53B truncation caused by t(10;19)(q26;q13) chromosome translocation in acute lymphoblastic leukemia
Oncol Lett, 13 (4), 2216-2220
DOI 10.3892/ol.2017.5705, PubMed 28454383
DEK-NUP214-Fusion Identified by RNA-Sequencing of an Acute Myeloid Leukemia with t(9;12)(q34;q15)
Cancer Genomics Proteomics, 14 (6), 437-443
DOI 10.21873/cgp.20053, PubMed 29109093
Rearrangement of the Chromatin Organizer Special AT-rich Binding Protein 1 Gene, SATB1, Resulting from a t(3;5)(p24;q14) Chromosomal Translocation in Acute Myeloid Leukemia
Anticancer Res, 37 (2), 693-698
DOI 10.21873/anticanres.11365, PubMed 28179318
Publications 2016
Expressions of miR-30c and let-7a are inversely correlated with HMGA2 expression in squamous cell carcinoma of the vulva
Oncotarget, 7 (51), 85058-85062
DOI 10.18632/oncotarget.13187, PubMed 27835588
Molecular characterization of the t(4;12)(q27~28;q14~15) chromosomal rearrangement in lipoma
Oncol Lett, 12 (3), 1701-1704
DOI 10.3892/ol.2016.4834, PubMed 27588119
A novel truncated form of HMGA2 in tumors of the ovaries
Oncol Lett, 12 (2), 1559-1563
DOI 10.3892/ol.2016.4805, PubMed 27446471
Upregulation of INS-IGF2 read-through expression and identification of a novel INS-IGF2 splice variant in insulinomas
Oncol Rep, 36 (5), 2653-2662
DOI 10.3892/or.2016.5132, PubMed 27667266
Cytogenetic and molecular profile of endometrial stromal sarcoma
Genes Chromosomes Cancer, 55 (11), 834-46
DOI 10.1002/gcc.22380, PubMed 27219024
Novel fusion genes and chimeric transcripts in ependymal tumors
Genes Chromosomes Cancer, 55 (12), 944-953
DOI 10.1002/gcc.22392, PubMed 27401149
Fusion of the HMGA2 and C9orf92 genes in myolipoma with t(9;12)(p22;q14)
Diagn Pathol, 11, 22
DOI 10.1186/s13000-016-0472-8, PubMed 26857357
Rare MLL-ELL fusion transcripts in childhood acute myeloid leukemia-association with young age and myeloid sarcomas?
Exp Hematol Oncol, 5, 8
DOI 10.1186/s40164-016-0037-2, PubMed 26949571
Recurrent fusion of the genes FN1 and ALK in gastrointestinal leiomyomas
Mod Pathol, 29 (11), 1415-1423
DOI 10.1038/modpathol.2016.129, PubMed 27469327
Gene fusions AHRR-NCOA2, NCOA2-ETV4, ETV4-AHRR, P4HA2-TBCK, and TBCK-P4HA2 resulting from the translocations t(5;8;17)(p15;q13;q21) and t(4;5)(q24;q31) in a soft tissue angiofibroma
Oncol Rep, 36 (5), 2455-2462
DOI 10.3892/or.2016.5096, PubMed 27633981
RUNX1 truncation resulting from a cryptic and novel t(6;21)(q25;q22) chromosome translocation in acute myeloid leukemia: A case report
Oncol Rep, 36 (5), 2481-2488
DOI 10.3892/or.2016.5119, PubMed 27667292
Publications 2015
HMGA2 expression pattern and TERT mutations in tumors of the vulva
Oncol Rep, 33 (6), 2675-80
DOI 10.3892/or.2015.3882, PubMed 25823555
Fusion genes with ALK as recurrent partner in ependymoma-like gliomas: a new brain tumor entity?
Neuro Oncol, 17 (10), 1365-73
DOI 10.1093/neuonc/nov039, PubMed 25795305
Rearrangement of chromosome bands 12q14~15 causing HMGA2-SOX5 gene fusion and HMGA2 expression in extraskeletal osteochondroma
Oncol Rep, 34 (2), 577-84
DOI 10.3892/or.2015.4035, PubMed 26043835
Novel KAT6B-KANSL1 fusion gene identified by RNA sequencing in retroperitoneal leiomyoma with t(10;17)(q22;q21)
PLoS One, 10 (1), e0117010
DOI 10.1371/journal.pone.0117010, PubMed 25621995
Fusion of the genes EWSR1 and PBX3 in retroperitoneal leiomyoma with t(9;22)(q33;q12)
PLoS One, 10 (4), e0124288
DOI 10.1371/journal.pone.0124288, PubMed 25875009
The recurrent chromosomal translocation t(12;18)(q14~15;q12~21) causes the fusion gene HMGA2-SETBP1 and HMGA2 expression in lipoma and osteochondrolipoma
Int J Oncol, 47 (3), 884-90
DOI 10.3892/ijo.2015.3099, PubMed 26202160
LAMTOR1-PRKCD and NUMA1-SFMBT1 fusion genes identified by RNA sequencing in aneurysmal benign fibrous histiocytoma with t(3;11)(p21;q13)
Cancer Genet, 208 (11), 545-51
DOI 10.1016/j.cancergen.2015.07.007, PubMed 26432191
Fusion of the TBL1XR1 and HMGA1 genes in splenic hemangioma with t(3;6)(q26;p21)
Int J Oncol, 48 (3), 1242-50
DOI 10.3892/ijo.2015.3310, PubMed 26708416
Recurrent 12q13-15 chromosomal aberrations, high frequency of isocitrate dehydrogenase 1 mutations, and absence of high mobility group AT-hook 2 expression in periosteal chondromas
Oncol Lett, 10 (1), 163-167
DOI 10.3892/ol.2015.3197, PubMed 26170993
Acute appendicitis from the shadows of Lemierre disease
Int J Colorectal Dis, 30 (11), 1593-4
DOI 10.1007/s00384-015-2141-x, PubMed 25665516
Novel ZEB2-BCL11B Fusion Gene Identified by RNA-Sequencing in Acute Myeloid Leukemia with t(2;14)(q22;q32)
PLoS One, 10 (7), e0132736
DOI 10.1371/journal.pone.0132736, PubMed 26186352
Publications 2014
MEAF6/PHF1 is a recurrent gene fusion in endometrial stromal sarcoma
Cancer Lett, 347 (1), 75-8
DOI 10.1016/j.canlet.2014.01.030, PubMed 24530230
Low frequency of ESRRA-C11orf20 fusion gene in ovarian carcinomas
PLoS Biol, 12 (2), e1001784
DOI 10.1371/journal.pbio.1001784, PubMed 24504521
Several fusion genes identified by whole transcriptome sequencing in a spindle cell sarcoma with rearrangements of chromosome arm 12q and MDM2 amplification
Int J Oncol, 45 (5), 1829-36
DOI 10.3892/ijo.2014.2605, PubMed 25176350
Novel CSF1-S100A10 fusion gene and CSF1 transcript identified by RNA sequencing in tenosynovial giant cell tumors
Int J Oncol, 44 (5), 1425-32
DOI 10.3892/ijo.2014.2326, PubMed 24604026
Chromosome aberrations and HEY1-NCOA2 fusion gene in a mesenchymal chondrosarcoma
Oncol Rep, 32 (1), 40-4
DOI 10.3892/or.2014.3180, PubMed 24839999
The "grep" command but not FusionMap, FusionFinder or ChimeraScan captures the CIC-DUX4 fusion gene from whole transcriptome sequencing data on a small round cell tumor with t(4;19)(q35;q13)
PLoS One, 9 (6), e99439
DOI 10.1371/journal.pone.0099439, PubMed 24950227
Novel TNS3-MAP3K3 and ZFPM2-ELF5 fusion genes identified by RNA sequencing in multicystic mesothelioma with t(7;17)(p12;q23) and t(8;11)(q23;p13)
Cancer Lett, 357 (2), 502-9
DOI 10.1016/j.canlet.2014.12.002, PubMed 25484136
Sequential combination of karyotyping and RNA-sequencing in the search for cancer-specific fusion genes
Int J Biochem Cell Biol, 53, 462-5
DOI 10.1016/j.biocel.2014.05.018, PubMed 24863361
Comparison between karyotyping-FISH-reverse transcription PCR and RNA-sequencing-fusion gene identification programs in the detection of KAT6A-CREBBP in acute myeloid leukemia
PLoS One, 9 (5), e96570
DOI 10.1371/journal.pone.0096570, PubMed 24798186
Publications 2013
Genomic aberration patterns and expression profiles of squamous cell carcinomas of the vulva
Genes Chromosomes Cancer, 52 (6), 551-63
DOI 10.1002/gcc.22053, PubMed 23404381
Myeloid leukemia with t(7;21)(p22;q22) and 5q deletion
Oncol Rep, 30 (4), 1549-52
DOI 10.3892/or.2013.2623, PubMed 23877199
Cryptic FUS-ERG fusion identified by RNA-sequencing in childhood acute myeloid leukemia
Oncol Rep, 30 (6), 2587-92
DOI 10.3892/or.2013.2751, PubMed 24068373
Fusion of ZMYND8 and RELA genes in acute erythroid leukemia
PLoS One, 8 (5), e63663
DOI 10.1371/journal.pone.0063663, PubMed 23667654
Fusion of the ZC3H7B and BCOR genes in endometrial stromal sarcomas carrying an X;22-translocation
Genes Chromosomes Cancer, 52 (7), 610-8
DOI 10.1002/gcc.22057, PubMed 23580382
RNA sequencing identifies fusion of the EWSR1 and YY1 genes in mesothelioma with t(14;22)(q32;q12)
Genes Chromosomes Cancer, 52 (8), 733-40
DOI 10.1002/gcc.22068, PubMed 23630070
Publications 2012
High-throughput sequencing identifies an NFIA/CBFA2T3 fusion gene in acute erythroid leukemia with t(1;16)(p31;q24)
Leukemia, 27 (4), 980-2
DOI 10.1038/leu.2012.266, PubMed 23032695
Whole-transcriptome sequencing identifies novel IRF2BP2-CDX1 fusion gene brought about by translocation t(1;5)(q42;q32) in mesenchymal chondrosarcoma
PLoS One, 7 (11), e49705
DOI 10.1371/journal.pone.0049705, PubMed 23185413
t(12;13)(q14;q31) leading to HMGA2 upregulation in acute myeloid leukaemia
Br J Haematol, 157 (6), 769-71
DOI 10.1111/j.1365-2141.2012.09081.x, PubMed 22404713
Novel fusion of MYST/Esa1-associated factor 6 and PHF1 in endometrial stromal sarcoma
PLoS One, 7 (6), e39354
DOI 10.1371/journal.pone.0039354, PubMed 22761769
A novel TCF3-HLF fusion transcript in acute lymphoblastic leukemia with a t(17;19)(q22;p13)
Cancer Genet, 205 (12), 669-72
DOI 10.1016/j.cancergen.2012.10.004, PubMed 23181981
Publications 2010
HIF1alpha isoforms in benign and malignant prostate tissue and their correlation to neuroendocrine differentiation
BMC Cancer, 10, 385
DOI 10.1186/1471-2407-10-385, PubMed 20663134
Absence of the JAZF1/SUZ12 chimeric transcript in the immortalized non-neoplastic endometrial stromal cell line T HESCs
Oncol Lett, 1 (6), 947-950
DOI 10.3892/ol.2010.185, PubMed 22870092
Characterization of an alternative transcript of the human CREB3L2 gene
Oncol Rep, 24 (5), 1133-9
DOI 10.3892/or_00000964, PubMed 20878102
Publications 2009
Expression levels of HMGA2 in adipocytic tumors correlate with morphologic and cytogenetic subgroups
Mol Cancer, 8, 36
DOI 10.1186/1476-4598-8-36, PubMed 19508721
t(19;22)(q13;q12) Translocation leading to the novel fusion gene EWSR1-ZNF444 in soft tissue myoepithelial carcinoma
Genes Chromosomes Cancer, 48 (12), 1051-6
DOI 10.1002/gcc.20706, PubMed 19760602
Telomeric associations correlate with telomere length reduction and clonal chromosome aberrations in giant cell tumor of bone
Cytogenet Genome Res, 124 (2), 121-7
DOI 10.1159/000207516, PubMed 19420923
Two genetic pathways, t(1;10) and amplification of 3p11-12, in myxoinflammatory fibroblastic sarcoma, haemosiderotic fibrolipomatous tumour, and morphologically similar lesions
J Pathol, 217 (5), 716-27
DOI 10.1002/path.2513, PubMed 19199331
Genomic characteristics of soft tissue sarcomas
Virchows Arch, 456 (2), 129-39
DOI 10.1007/s00428-009-0736-8, PubMed 19189124
t(3;21)(q22;q22) leading to truncation of the RYK gene in atypical chronic myeloid leukemia
Cancer Lett, 277 (2), 205-11
DOI 10.1016/j.canlet.2008.12.016, PubMed 19168282
The expression of pluripotency marker Oct 3/4 in prostate cancer and benign prostate hyperplasia
Prostate, 69 (9), 909-16
DOI 10.1002/pros.20934, PubMed 19274762
Bidirectionality and transcriptional activity of the EWSR1 promoter region
Oncol Rep, 21 (3), 641-8
PubMed 19212622
Application of risk management techniques for the remediation of an old mining site in Greece
Waste Manag, 29 (5), 1739-46
DOI 10.1016/j.wasman.2008.11.017, PubMed 19136246
Characterization of the human CREB3L2 gene promoter
Oncol Rep, 21 (3), 615-24
PubMed 19212619
Publications 2008
Detection of a t(1;22)(q23;q12) translocation leading to an EWSR1-PBX1 fusion gene in a myoepithelioma
Genes Chromosomes Cancer, 47 (7), 558-64
DOI 10.1002/gcc.20559, PubMed 18383210
BRAF mutations are very rare in B- and T-cell pediatric acute lymphoblastic leukemias
Leukemia, 22 (8), 1619-21
DOI 10.1038/leu.2008.14, PubMed 18273045
Low-grade fibromyxoid sarcoma is difficult to diagnose by fine needle aspiration cytology: a cytomorphological study of eight cases
Cytopathology, 20 (5), 304-14
DOI 10.1111/j.1365-2303.2008.00587.x, PubMed 18637810
When the genome plays dice: circumvention of the spindle assembly checkpoint and near-random chromosome segregation in multipolar cancer cell mitoses
PLoS One, 3 (4), e1871
DOI 10.1371/journal.pone.0001871, PubMed 18392149
Bone marrow ectopic expression of a non-coding RNA in childhood T-cell acute lymphoblastic leukemia with a novel t(2;11)(q11.2;p15.1) translocation
Mol Cancer, 7, 80
DOI 10.1186/1476-4598-7-80, PubMed 18947387
Heterogeneous genetic profiles in soft tissue myoepitheliomas
Mod Pathol, 21 (11), 1311-9
DOI 10.1038/modpathol.2008.124, PubMed 18604193
A novel fusion 5'AFF3/3'BCL2 originated from a t(2;18)(q11.2;q21.33) translocation in follicular lymphoma
Oncogene, 27 (47), 6187-90
DOI 10.1038/onc.2008.214, PubMed 18622426
Molecular identification of COL6A3-CSF1 fusion transcripts in tenosynovial giant cell tumors
Genes Chromosomes Cancer, 47 (1), 21-5
DOI 10.1002/gcc.20501, PubMed 17918257
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
J Pathol, 215 (1), 78-86
DOI 10.1002/path.2327, PubMed 18338330
An endometrial stromal sarcoma cell line with the JAZF1/PHF1 chimera
Cancer Genet Cytogenet, 185 (2), 74-7
DOI 10.1016/j.cancergencyto.2008.04.020, PubMed 18722875
Fusion of the COL1A1 and USP6 genes in a benign bone tumor
Cancer Genet Cytogenet, 180 (1), 70-3
DOI 10.1016/j.cancergencyto.2007.09.017, PubMed 18068538
The POU5F1P1 pseudogene encodes a putative protein similar to POU5F1 isoform 1
Oncol Rep, 20 (5), 1029-33
PubMed 18949397
A PCR/restriction digestion assay for the detection of the transcript variants 1 and 2 of POU5F1
Genes Chromosomes Cancer, 47 (6), 521-9
DOI 10.1002/gcc.20555, PubMed 18335506
The fatty acid amide hydrolase (FAAH) Pro129Thr polymorphism is not associated with severe obesity in Greek subjects
Horm Metab Res, 40 (12), 907-10
DOI 10.1055/s-0028-1087169, PubMed 18819056
High-resolution molecular cytogenetic analysis of Wilms tumors highlights diagnostic difficulties among small round cell kidney tumors
Genes Chromosomes Cancer, 47 (10), 845-52
DOI 10.1002/gcc.20587, PubMed 18615675
Promoter analysis of epigenetically controlled genes in bladder cancer
Genes Chromosomes Cancer, 47 (5), 368-78
DOI 10.1002/gcc.20542, PubMed 18196590
Publications 2007
Assessment of the clinical and molecular impact of different cytogenetic subgroups in a series of 272 lipomas with abnormal karyotype
Genes Chromosomes Cancer, 46 (6), 594-606
DOI 10.1002/gcc.20445, PubMed 17370328
Tiling resolution array comparative genomic hybridization, expression and methylation analyses of dup(1q) in Burkitt lymphomas and pediatric high hyperdiploid acute lymphoblastic leukemias reveal clustered near-centromeric breakpoints and overexpression of genes in 1q22-32.3
Hum Mol Genet, 16 (18), 2215-25
DOI 10.1093/hmg/ddm173, PubMed 17613536
Molecular cytogenetic characterization of t(14;19)(q32;p13), a new recurrent translocation in B cell malignancies
Virchows Arch, 450 (5), 559-65
DOI 10.1007/s00428-007-0407-6, PubMed 17406891
Comparison of the proximal promoter regions of the PAX3 and PAX7 genes
Cancer Genet Cytogenet, 178 (2), 114-9
DOI 10.1016/j.cancergencyto.2007.06.006, PubMed 17954266
Fusion of NUP98 and the SET binding protein 1 (SETBP1) gene in a paediatric acute T cell lymphoblastic leukaemia with t(11;18)(p15;q12)
Br J Haematol, 136 (2), 294-6
DOI 10.1111/j.1365-2141.2006.06410.x, PubMed 17233820
Characterization of the native CREB3L2 transcription factor and the FUS/CREB3L2 chimera
Genes Chromosomes Cancer, 46 (2), 181-91
DOI 10.1002/gcc.20395, PubMed 17117415
Characterisation of genomic translocation breakpoints and identification of an alternative TCF3/PBX1 fusion transcript in t(1;19)(q23;p13)-positive acute lymphoblastic leukaemias
Br J Haematol, 138 (2), 196-201
DOI 10.1111/j.1365-2141.2007.06644.x, PubMed 17593026
Upregulation of the SOX5 by promoter swapping with the P2RY8 gene in primary splenic follicular lymphoma
Leukemia, 21 (10), 2221-5
DOI 10.1038/sj.leu.2404784, PubMed 17554380
Publications 2006
Midline carcinoma with t(15;19) and BRD4-NUT fusion oncogene in a 30-year-old female with response to docetaxel and radiotherapy
BMC Cancer, 6, 69
DOI 10.1186/1471-2407-6-69, PubMed 16542442
Gene expression profiles relate to SS18/SSX fusion type in synovial sarcoma
Int J Cancer, 118 (5), 1165-72
DOI 10.1002/ijc.21475, PubMed 16152617
Fusion genes in angiomatoid fibrous histiocytoma
Cancer Lett, 251 (1), 158-63
DOI 10.1016/j.canlet.2006.11.014, PubMed 17188428
Fusion of the tumor-suppressor gene CHEK2 and the gene for the regulatory subunit B of protein phosphatase 2 PPP2R2A in childhood teratoma
Neoplasia, 8 (5), 413-8
DOI 10.1593/neo.06139, PubMed 16790090
C2028T polymorphism in exon 12 and dinucleotide repeat polymorphism in intron 13 of the HIF-1alpha gene define HIF-1alpha protein expression in non-small cell lung cancer
Lung Cancer, 53 (3), 257-62
DOI 10.1016/j.lungcan.2006.05.025, PubMed 16837101
Consistent rearrangement of chromosomal band 6p21 with generation of fusion genes JAZF1/PHF1 and EPC1/PHF1 in endometrial stromal sarcoma
Cancer Res, 66 (1), 107-12
DOI 10.1158/0008-5472.CAN-05-2485, PubMed 16397222
Deregulation of HMGA2 in an aggressive angiomyxoma with t(11;12)(q23;q15)
Virchows Arch, 448 (6), 838-42
DOI 10.1007/s00428-006-0186-5, PubMed 16568309
Truncation and fusion of HMGA2 in lipomas with rearrangements of 5q32-->q33 and 12q14-->q15
Cytogenet Genome Res, 112 (1-2), 60-6
DOI 10.1159/000087514, PubMed 16276091
MLL/GAS7 fusion in a pediatric case of t(11;17)(q23;p13)-positive precursor B-cell acute lymphoblastic leukemia
Haematologica, 91 (9), 1287-8
PubMed 16956839
Fusion of the SEC31L1 and ALK genes in an inflammatory myofibroblastic tumor
Int J Cancer, 118 (5), 1181-6
DOI 10.1002/ijc.21490, PubMed 16161041
Fusion of ETV6 with an intronic sequence of the BAZ2A gene in a paediatric pre-B acute lymphoblastic leukaemia with a cryptic chromosome 12 rearrangement
Br J Haematol, 133 (3), 270-5
DOI 10.1111/j.1365-2141.2006.06020.x, PubMed 16643428
A novel and cytogenetically cryptic t(7;21)(p22;q22) in acute myeloid leukemia results in fusion of RUNX1 with the ubiquitin-specific protease gene USP42
Leukemia, 20 (2), 224-9
DOI 10.1038/sj.leu.2404076, PubMed 16357831
Confirmation of the high frequency of the TMPRSS2/ERG fusion gene in prostate cancer
Genes Chromosomes Cancer, 45 (7), 717-9
DOI 10.1002/gcc.20329, PubMed 16575875
t(3;12)(q26;q14) in polycythemia vera is associated with upregulation of the HMGA2 gene
Leukemia, 20 (12), 2190-2
DOI 10.1038/sj.leu.2404418, PubMed 17024113
Rearrangement of the COL12A1 and COL4A5 genes in subungual exostosis: molecular cytogenetic delineation of the tumor-specific translocation t(X;6)(q13-14;q22)
Int J Cancer, 118 (8), 1972-6
DOI 10.1002/ijc.21586, PubMed 16284948
Publications 2005
Fusion of the EWSR1 and ATF1 genes without expression of the MITF-M transcript in angiomatoid fibrous histiocytoma
Genes Chromosomes Cancer, 44 (1), 97-102
DOI 10.1002/gcc.20201, PubMed 15884099
Clinicopathologic and molecular genetic characterization of low-grade fibromyxoid sarcoma, and cloning of a novel FUS/CREB3L1 fusion gene
Lab Invest, 85 (3), 408-15
DOI 10.1038/labinvest.3700230, PubMed 15640831
Fusion of the HMGA2 and NFIB genes in lipoma
Virchows Arch, 447 (5), 855-8
DOI 10.1007/s00428-005-0037-9, PubMed 16133369
Absence of mutations of the BRAF gene in malignant melanoma of soft parts (clear cell sarcoma of tendons and aponeuroses)
Cancer Genet Cytogenet, 156 (1), 74-6
DOI 10.1016/j.cancergencyto.2004.04.008, PubMed 15588860
Molecular cytogenetic characterization of an ins(4;X) occurring as the sole abnormality in an aggressive, poorly differentiated soft tissue sarcoma
Virchows Arch, 447 (5), 869-74
DOI 10.1007/s00428-005-0041-0, PubMed 16133367
Publications 2004
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)
Am J Pathol, 164 (5), 1645-53
DOI 10.1016/s0002-9440(10)63723-6, PubMed 15111311
Molecular genetic characterization of the genomic ACTB-GLI fusion in pericytoma with t(7;12)
Biochem Biophys Res Commun, 325 (4), 1318-23
DOI 10.1016/j.bbrc.2004.10.172, PubMed 15555571
Genetic characterization of bone and soft tissue tumors
Acta Orthop Scand Suppl, 75 (311), 21-8
DOI 10.1080/00016470410001708290, PubMed 15188662
Retained heterodisomy for chromosome 12 in atypical lipomatous tumors: implications for ring chromosome formation
Cytogenet Genome Res, 106 (1), 33-8
DOI 10.1159/000078557, PubMed 15218238
MLL/GRAF fusion in an infant acute monocytic leukemia (AML M5b) with a cytogenetically cryptic ins(5;11)(q31;q23q23)
Genes Chromosomes Cancer, 41 (4), 400-4
DOI 10.1002/gcc.20097, PubMed 15382263
Expression of DOL54 is not restricted to myxoid liposarcomas with the FUS-DDIT3 chimera but is found in various sarcomas
Oncol Rep, 12 (1), 107-10
PubMed 15201968
The chimeric FUS/CREB3l2 gene is specific for low-grade fibromyxoid sarcoma
Genes Chromosomes Cancer, 40 (3), 218-28
DOI 10.1002/gcc.20037, PubMed 15139001
Vascular endothelial growth factor gene polymorphisms and pre-eclampsia
Mol Hum Reprod, 10 (5), 321-4
DOI 10.1093/molehr/gah048, PubMed 14997002
A novel FISH assay for SS18-SSX fusion type in synovial sarcoma
Lab Invest, 84 (9), 1185-92
DOI 10.1038/labinvest.3700142, PubMed 15208645
Publications 2003
Fusion, disruption, and expression of HMGA2 in bone and soft tissue chondromas
Mod Pathol, 16 (11), 1132-40
DOI 10.1097/01.MP.0000092954.42656.94, PubMed 14614053
Cytogenetic and molecular genetic analyses of endometrial stromal sarcoma: nonrandom involvement of chromosome arms 6p and 7p and confirmation of JAZF1/JJAZ1 gene fusion in t(7;17)
Cancer Genet Cytogenet, 144 (2), 119-24
DOI 10.1016/s0165-4608(03)00025-6, PubMed 12850374
Fusion of the NUP98 gene and the homeobox gene HOXC13 in acute myeloid leukemia with t(11;12)(p15;q13)
Genes Chromosomes Cancer, 36 (1), 107-12
DOI 10.1002/gcc.10139, PubMed 12461755
Genomic characterization of MOZ/CBP and CBP/MOZ chimeras in acute myeloid leukemia suggests the involvement of a damage-repair mechanism in the origin of the t(8;16)(p11;p13)
Genes Chromosomes Cancer, 36 (1), 90-8
DOI 10.1002/gcc.10137, PubMed 12461753
Prevalence of hemochromatosis gene (HFE) mutations in Greece
Acta Haematol, 109 (3), 137-40
DOI 10.1159/000069289, PubMed 12714823
Formation of trisomies and their parental origin in hyperdiploid childhood acute lymphoblastic leukemia
Blood, 102 (8), 3010-5
DOI 10.1182/blood-2003-05-1444, PubMed 12829594
A novel chromosomal translocation t(3;7)(q26;q21) in myeloid leukemia resulting in overexpression of EVI1
Ann Hematol, 83 (2), 78-83
DOI 10.1007/s00277-003-0778-y, PubMed 14551738
A novel fusion gene, SS18L1/SSX1, in synovial sarcoma
Genes Chromosomes Cancer, 37 (2), 195-200
DOI 10.1002/gcc.10210, PubMed 12696068
Fusion of the FUS and BBF2H7 genes in low grade fibromyxoid sarcoma
Hum Mol Genet, 12 (18), 2349-58
DOI 10.1093/hmg/ddg237, PubMed 12915480
Publications 2002
Fusion of RDC1 with HMGA2 in lipomas as the result of chromosome aberrations involving 2q35-37 and 12q13-15
Int J Oncol, 21 (2), 321-6
PubMed 12118328
Establishment and characterisation of a human clear cell sarcoma model in nude mice
Int J Cancer, 101 (6), 505-11
DOI 10.1002/ijc.10588, PubMed 12237889
Molecular cytogenetic mapping of recurrent chromosomal breakpoints in tenosynovial giant cell tumors
Virchows Arch, 441 (5), 475-80
DOI 10.1007/s00428-002-0640-y, PubMed 12447678
Expression of NUP98/TOP1, but not of TOP1/NUP98, in a treatment-related myelodysplastic syndrome with t(10;20;11)(q24;q11;p15)
Genes Chromosomes Cancer, 34 (2), 249-54
DOI 10.1002/gcc.10066, PubMed 11979559
RT-PCR analysis of acute myeloid leukemia with t(8;16)(p11;p13): identification of a novel MOZ/CBP transcript and absence of CBP/MOZ expression
Genes Chromosomes Cancer, 35 (4), 372-4
DOI 10.1002/gcc.10131, PubMed 12378533
Molecular genetic characterization of the EWS/ATF1 fusion gene in clear cell sarcoma of tendons and aponeuroses
Int J Cancer, 99 (4), 560-7
DOI 10.1002/ijc.10404, PubMed 11992546
Molecular genetic characterization of the EWS/CHN and RBP56/CHN fusion genes in extraskeletal myxoid chondrosarcoma
Genes Chromosomes Cancer, 35 (4), 340-52
DOI 10.1002/gcc.10127, PubMed 12378528
Fusion of the FUS and ATF1 genes in a large, deep-seated angiomatoid fibrous histiocytoma
Diagn Mol Pathol, 11 (3), 157-62
DOI 10.1097/00019606-200209000-00006, PubMed 12218455
Publications 2001
Fusion of the homeobox gene HLXB9 and the ETV6 gene in infant acute myeloid leukemias with the t(7;12)(q36;p13)
Cancer Res, 61 (14), 5374-7
PubMed 11454678
Fusion of the BCR and the fibroblast growth factor receptor-1 (FGFR1) genes as a result of t(8;22)(p11;q11) in a myeloproliferative disorder: the first fusion gene involving BCR but not ABL
Genes Chromosomes Cancer, 32 (4), 302-10
DOI 10.1002/gcc.1195, PubMed 11746971
Fusion of the MORF and CBP genes in acute myeloid leukemia with the t(10;16)(q22;p13)
Hum Mol Genet, 10 (4), 395-404
DOI 10.1093/hmg/10.4.395, PubMed 11157802
No EWS/FLI1 fusion transcripts in giant-cell tumors of bone
Int J Cancer, 93 (6), 769-72
DOI 10.1002/ijc.1415, PubMed 11519035
Clinical impact of molecular and cytogenetic findings in synovial sarcoma
Genes Chromosomes Cancer, 31 (4), 362-72
DOI 10.1002/gcc.1155, PubMed 11433527
Publications 2000
Lentivirus vector gene expression during ES cell-derived hematopoietic development in vitro
J Virol, 74 (22), 10778-84
DOI 10.1128/jvi.74.22.10778-10784.2000, PubMed 11044122
RT-PCR analysis of the MOZ-CBP and CBP-MOZ chimeric transcripts in acute myeloid leukemias with t(8;16)(p11;p13)
Genes Chromosomes Cancer, 28 (4), 415-24
DOI 10.1002/1098-2264(200008)28:4<415::aid-gcc7>3.0.co;2-i, PubMed 10862050
A novel FUS/CHOP chimera in myxoid liposarcoma
Biochem Biophys Res Commun, 279 (3), 838-45
DOI 10.1006/bbrc.2000.4026, PubMed 11162437
Acute myeloid leukemia with inv(8)(p11q13)
Leuk Lymphoma, 39 (5-6), 651-6
DOI 10.3109/10428190009113397, PubMed 11342350
Genetic characterization of angiomatoid fibrous histiocytoma identifies fusion of the FUS and ATF-1 genes induced by a chromosomal translocation involving bands 12q13 and 16p11
Cancer Genet Cytogenet, 121 (2), 109-16
DOI 10.1016/s0165-4608(00)00237-5, PubMed 11063792
Publications 1999
Epiretinal membrane in association with Takayasu disease
Acta Ophthalmol Scand, 77 (4), 483-4
DOI 10.1034/j.1600-0420.1999.770430.x, PubMed 10463431
A novel PCR-based approach for the detection of the Huntington disease associated trinucleotide repeat expansion
Hum Mutat, 13 (3), 232-6
DOI 10.1002/(SICI)1098-1004(1999)13:3<232::AID-HUMU7>3.0.CO;2-N, PubMed 10090478
A methylation PCR approach for detection of fragile X syndrome
Hum Mutat, 14 (1), 71-9
DOI 10.1002/(SICI)1098-1004(1999)14:1<71::AID-HUMU9>3.0.CO;2-5, PubMed 10447261
Fusion of the RBP56 and CHN genes in extraskeletal myxoid chondrosarcomas with translocation t(9;17)(q22;q11)
Oncogene, 18 (52), 7594-8
DOI 10.1038/sj.onc.1203155, PubMed 10602519
Identification of genes differentially expressed in TLS-CHOP carrying myxoid liposarcomas
Int J Cancer, 83 (1), 30-3
DOI 10.1002/(sici)1097-0215(19990924)83:1<30::aid-ijc6>3.0.co;2-4, PubMed 10449603
Publications 1998
Expression analysis and chromosomal mapping of a novel human gene, APRIL, encoding an acidic protein rich in leucines
Biochim Biophys Acta, 1395 (2), 176-80
DOI 10.1016/s0167-4781(97)00165-6, PubMed 9473664
Publications 1997
Additional evidence of a variant translocation t(12;22) with EWS/CHOP fusion in myxoid liposarcoma: clinicopathological features
J Pathol, 182 (4), 437-41
DOI 10.1002/(SICI)1096-9896(199708)182:4<437::AID-PATH882>3.0.CO;2-X, PubMed 9306965
Characterization and chromosomal mapping of the human TFG gene involved in thyroid carcinoma
Genomics, 41 (3), 327-31
DOI 10.1006/geno.1997.4625, PubMed 9169129
Characteristic sequence motifs at the breakpoints of the hybrid genes FUS/CHOP, EWS/CHOP and FUS/ERG in myxoid liposarcoma and acute myeloid leukemia
Oncogene, 15 (11), 1357-62
DOI 10.1038/sj.onc.1201281, PubMed 9315104
Variable FHIT transcripts in non-neoplastic tissues
Genes Chromosomes Cancer, 19 (4), 215-9
DOI 10.1002/(sici)1098-2264(199708)19:4<215::aid-gcc2>3.0.co;2-#, PubMed 9258655
Publications 1996
Expression patterns of the human sarcoma-associated genes FUS and EWS and the genomic structure of FUS
Genomics, 37 (1), 1-8
DOI 10.1006/geno.1996.0513, PubMed 8921363
NRAS mutations are rare in acute myeloid leukaemias with t(8;21) or inv(16)
Eur J Haematol, 56 (1-2), 68-71
DOI 10.1111/j.1600-0609.1996.tb00297.x, PubMed 8599996
Genomic PCR detects tumor cells in peripheral blood from patients with myxoid liposarcoma
Genes Chromosomes Cancer, 17 (2), 102-7
DOI 10.1002/(SICI)1098-2264(199610)17:2<102::AID-GCC5>3.0.CO;2-9, PubMed 8913727
Fusion of the EWS and CHOP genes in myxoid liposarcoma
Oncogene, 12 (3), 489-94
PubMed 8637704
The FHIT and PTPRG genes are deleted in benign proliferative breast disease associated with familial breast cancer and cytogenetic rearrangements of chromosome band 3p14
Cancer Res, 56 (21), 4871-5
PubMed 8895736
Publications 1995
Two distinct FUS breakpoint clusters in myxoid liposarcoma and acute myeloid leukemia with the translocations t(12;16) and t(16;21)
Oncogene, 11 (6), 1133-7
PubMed 7566973
Cloning and sequencing of a cDNA encoding rat D-dopachrome tautomerase
FEBS Lett, 373 (3), 203-6
DOI 10.1016/0014-5793(95)01041-c, PubMed 7589466
Publications 1994
Fusion of the FUS gene with ERG in acute myeloid leukemia with t(16;21)(p11;q22)
Genes Chromosomes Cancer, 11 (4), 256-62
DOI 10.1002/gcc.2870110408, PubMed 7533529
Characterization of the CHOP breakpoints and fusion transcripts in myxoid liposarcomas with the 12;16 translocation
Cancer Res, 54 (24), 6500-3
PubMed 7987849