Fredrik Mertens
#125,158
Most Influential Person Now
Researcher
Fredrik Mertens's AcademicInfluence.com Rankings
Fredrik Mertenscomputer-science Degrees
Computer Science
#5214
World Rank
#5508
Historical Rank
Computational Linguistics
#671
World Rank
#683
Historical Rank
Machine Learning
#1296
World Rank
#1316
Historical Rank
Artificial Intelligence
#1530
World Rank
#1559
Historical Rank
Download Badge
Computer Science
Fredrik Mertens's Degrees
- Masters Computer Science Stanford University
- Bachelors Computer Science University of California, Berkeley
Similar Degrees You Can Earn
Why Is Fredrik Mertens Influential?
(Suggest an Edit or Addition)Fredrik Mertens's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Pathology and genetics of tumours of soft tissue and bone (2002) (4672)
- The impact of translocations and gene fusions on cancer causation (2007) (1272)
- TERT promoter mutations occur frequently in gliomas and a subset of tumors derived from cells with low rates of self-renewal (2013) (1148)
- A breakpoint map of recurrent chromosomal rearrangements in human neoplasia (1997) (707)
- Nuclear expression of STAT6 distinguishes solitary fibrous tumor from histologic mimics (2014) (540)
- 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 (2001) (523)
- The emerging complexity of gene fusions in cancer (2015) (487)
- Chromosomal imbalance maps of malignant solid tumors: a cytogenetic survey of 3185 neoplasms. (1997) (469)
- Mitelman database of chromosome aberrations and gene fusions in cancer (2014) (452)
- Telomere dysfunction triggers extensive DNA fragmentation and evolution of complex chromosome abnormalities in human malignant tumors (2001) (431)
- Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity. (2000) (407)
- Tumor-Infiltrating Macrophages Are Associated with Metastasis Suppression in High-Grade Osteosarcoma: A Rationale for Treatment with Macrophage Activating Agents (2011) (353)
- Correlation between clinicopathological features and karyotype in lipomatous tumors. A report of 178 cases from the Chromosomes and Morphology (CHAMP) Collaborative Study Group. (1996) (341)
- Fusion genes and rearranged genes as a linear function of chromosome aberrations in cancer (2004) (333)
- MUC4 Is a Highly Sensitive and Specific Marker for Low-grade Fibromyxoid Sarcoma (2011) (298)
- Fusion of the EWS and CHOP genes in myxoid liposarcoma. (1996) (293)
- Clinicopathologic and molecular genetic characterization of low-grade fibromyxoid sarcoma, and cloning of a novel FUS/CREB3L1 fusion gene (2005) (271)
- Identification of a novel, recurrent HEY1‐NCOA2 fusion in mesenchymal chondrosarcoma based on a genome‐wide screen of exon‐level expression data (2012) (258)
- Amplification of cyclin D1 in squamous cell carcinoma of the head and neck and the prognostic value of chromosomal abnormalities and cyclin D1 overexpression (1997) (237)
- Comprehensive genetic analysis identifies a pathognomonic NAB2/STAT6 fusion gene, nonrandom secondary genomic imbalances, and a characteristic gene expression profile in solitary fibrous tumor (2013) (215)
- MUC4 Is a Sensitive and Extremely Useful Marker for Sclerosing Epithelioid Fibrosarcoma: Association With FUS Gene Rearrangement (2012) (207)
- Abnormal nuclear shape in solid tumors reflects mitotic instability. (2001) (200)
- Eighth International Workshop on Human Gene Mapping (1984) (195)
- Atlas of Genetics and Cytogenetics in Oncology and Haematology (2005) (195)
- Structural and numerical chromosome changes in colon cancer develop through telomere-mediated anaphase bridges, not through mitotic multipolarity. (2005) (192)
- Survival meta-analyses for >1800 malignant peripheral nerve sheath tumor patients with and without neurofibromatosis type 1 (2012) (192)
- Cytogenetic deletion maps of hematologic neoplasms: Circumstantial evidence for tumor suppressor Loci (1993) (190)
- Isochromosomes in neoplasia (1994) (189)
- The chimeric FUS/CREB3l2 gene is specific for low‐grade fibromyxoid sarcoma (2004) (188)
- Combined morphologic and karyotypic study of 59 atypical lipomatous tumors. Evaluation of their relationship and differential diagnosis with other adipose tissue tumors (a report of the CHAMP Study Group). (1996) (188)
- Primary vs. secondary neoplasia‐associated chromosomal abnormalities—balanced rearrangements vs. genomic imbalances? (1996) (182)
- Trisomy 7 in nonneoplastic cells (1993) (178)
- Role of the transcription factor T (brachyury) in the pathogenesis of sporadic chordoma: a genetic and functional‐based study (2011) (175)
- Cytogenetic evolution patterns in non-Hodgkin's lymphoma. (1995) (170)
- Cytogenetic analysis of 46 pleomorphic soft tissue sarcomas and correlation with morphologic and clinical features: A report of the CHAMP study group (1998) (169)
- Fusion of the FUS and BBF2H7 genes in low grade fibromyxoid sarcoma. (2003) (160)
- A novel SERPINE1–FOSB fusion gene results in transcriptional up‐regulation of FOSB in pseudomyogenic haemangioendothelioma (2014) (154)
- Chromosome abnormalities in eighty-three head and neck squamous cell carcinomas: influence of culture conditions on karyotypic pattern. (1993) (143)
- Clinical significance of cytogenetic findings in solid tumors. (1997) (140)
- Molecular genetic characterization of the EWS/ATF1 fusion gene in clear cell sarcoma of tendons and aponeuroses (2002) (138)
- Two genetic pathways, t(1;10) and amplification of 3p11–12, in myxoinflammatory fibroblastic sarcoma, haemosiderotic fibrolipomatous tumour, and morphologically similar lesions (2009) (136)
- Successful treatment of a child with t(15;19)‐positive tumor (2007) (135)
- Cytogenetic aberrations in 188 benign and borderline adipose tissue tumors (1994) (132)
- Chromosomal abnormalities involving 11q13 are associated with poor prognosis in patients with squamous cell carcinoma of the head and neck (1995) (128)
- Cytogenetics of secondary myelodysplasia (sMDS) and acute nonlymphocvtic leukemia (sANLL) (1991) (127)
- Fusion of the EWSR1 and ATF1 genes without expression of the MITF‐M transcript in angiomatoid fibrous histiocytoma (2005) (123)
- Fusion of the SEC31L1 and ALK genes in an inflammatory myofibroblastic tumor (2006) (120)
- Clinical impact of molecular and cytogenetic findings in synovial sarcoma (2001) (118)
- Analysis of 35 cases of localized and diffuse tenosynovial giant cell tumor: a report from the Chromosomes and Morphology (CHAMP) study group. (1999) (117)
- Correlation between clinicopathological features and karyotype in spindle cell sarcomas. A report of 130 cases from the CHAMP study group. (1999) (117)
- Germline and somatic NF1 mutations in sporadic and NF1‐associated malignant peripheral nerve sheath tumours (2009) (115)
- The structure and dynamics of ring chromosomes in human neoplastic and non-neoplastic cells (1999) (115)
- Correlation between clinicopathological features and karyotype in 100 cartilaginous and chordoid tumours. A report from the Chromosomes and Morphology (CHAMP) Collaborative Study Group (2002) (114)
- Recurrent t(16;17)(q22;p13) in aneurysmal bone cysts. (1999) (113)
- Recurrent rearrangement of the PHF1 gene in ossifying fibromyxoid tumors. (2012) (113)
- 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 (2012) (111)
- Recurrent t(16;17)(q22;p13) in aneurysmal bone cysts (1999) (111)
- 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). (2004) (110)
- Recurrent EWSR1-CREB3L1 Gene Fusions in Sclerosing Epithelioid Fibrosarcoma (2014) (110)
- Geographic heterogeneity of neoplasia‐associated chromosome aberrations (1991) (109)
- Secondary chromosomal abnormalities in acute leukemias. (1994) (106)
- Cytogenetic-Morphologic Correlations in Aneurysmal Bone Cyst, Giant Cell Tumor of Bone and Combined Lesions. A Report from the CHAMP Study Group (2000) (106)
- Clustering of deletions on chromosome 13 in benign and low‐malignant lipomatous tumors (2003) (105)
- Cytogenetic, Clinical, and Morphologic Correlations in 78 Cases of Fibromatosis: A Report from the CHAMP Study Group (2000) (105)
- Frequent deletion of the CDKN2A locus in chordoma: analysis of chromosomal imbalances using array comparative genomic hybridisation (2007) (104)
- Multivariate analyses of genomic imbalances in solid tumors reveal distinct and converging pathways of karyotypic evolution (2001) (103)
- Molecular genetic characterization of the EWS/CHN and RBP56/CHN fusion genes in extraskeletal myxoid chondrosarcoma (2002) (103)
- Pigmented villonodular synovitis. Monoclonality and metastasis--a case for neoplastic origin? (1995) (101)
- Translocation t(7;19)(q22;q13)−a recurrent chromosome aberration in pseudomyogenic hemangioendothelioma? (2011) (101)
- Combined morphologic and karyotypic study of 28 myxoid liposarcomas. Implications for a revised morphologic typing, (a report from the CHAMP Group). (1996) (101)
- Nonrandom chromosome abnormalities in short-term cultured primary squamous cell carcinomas of the head and neck. (1995) (101)
- Clear cell hidradenoma of the skin—a third tumor type with a t(11;19)‐associated TORC1–MAML2 gene fusion (2005) (99)
- 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 (2008) (99)
- Characterization of the CHOP breakpoints and fusion transcripts in myxoid liposarcomas with the 12;16 translocation. (1994) (97)
- Expression profiling of Wilms tumors reveals new candidate genes for different clinical parameters (2006) (97)
- Ring chromosomes in parosteal osteosarcoma contain sequences from 12q13–15: A combined cytogenetic and comparative genomic hybridization study (1996) (96)
- Karyotypic patterns in chronic myeloproliferative disorders: report on 74 cases and review of the literature. (1991) (96)
- Molecular cytogenetic characterization of recurrent translocation breakpoints in bizarre parosteal osteochondromatous proliferation (Nora's lesion). (2004) (96)
- Centrosomal abnormalities, multipolar mitoses, and chromosomal instability in head and neck tumours with dysfunctional telomeres (2002) (95)
- Lipomas have characteristic structural chromosomal rearrangements of 12q13‐q14 (1987) (94)
- Gene fusions in soft tissue tumors: Recurrent and overlapping pathogenetic themes (2016) (90)
- Fusion genes in angiomatoid fibrous histiocytoma. (2007) (90)
- Cytogenetic characterization of peripheral nerve sheath tumours: a report of the CHAMP study group. (2000) (89)
- Exomic analysis of myxoid liposarcomas, synovial sarcomas, and osteosarcomas (2014) (88)
- Fusion of the RBP56 and CHN genes in extraskeletal myxoid chondrosarcomas with translocation t(9;17)(q22;q11) (1999) (88)
- Core‐needle biopsy performed by the cytopathologist (2005) (87)
- Fusion, Disruption, and Expression of HMGA2 in Bone and Soft Tissue Chondromas (2003) (86)
- Cytogenetic findings in 33 osteosarcomas (1993) (84)
- Chromosome aberrations in tenosynovial giant cell tumors and nontumorous synovial tissue (1993) (83)
- Cytogenetic analysis of subcutaneous angiolipoma: further evidence supporting its difference from ordinary pure lipomas: a report of the CHAMP Study Group. (1997) (83)
- Chromosomal organization of amplified chromosome 12 sequences in mesenchymal tumors detected by fluorescence in situ hybridization (1998) (82)
- Gain of 17q24-qter detected by comparative genomic hybridization in malignant tumors from patients with von Recklinghausen's neurofibromatosis. (1996) (82)
- No genomic aberrations in Langerhans cell histiocytosis as assessed by diverse molecular technologies (2009) (81)
- Karyotypic heterogeneity and clonal evolution in squamous cell carcinomas of the head and neck. (2002) (81)
- Differentially amplified chromosome 12 sequences in low‐ and high‐grade osteosarcoma (2002) (81)
- A novel fusion gene, SS18L1/SSX1, in synovial sarcoma (2003) (80)
- Molecular identification of COL6A3‐CSF1 fusion transcripts in tenosynovial giant cell tumors (2008) (80)
- Prevalence estimates of recurrent balanced cytogenetic aberrations and gene fusions in unselected patients with neoplastic disorders (2005) (79)
- Chromosome band 9p21 is frequently altered in malignant peripheral nerve sheath tumors: Studies of CDKN2A and other genes of the pRB pathway (1999) (79)
- Molecular cytogenetic mapping of recurrent chromosomal breakpoints in tenosynovial giant cell tumors (2002) (78)
- Translocation-related sarcomas. (2009) (78)
- Assessment of the clinical and molecular impact of different cytogenetic subgroups in a series of 272 lipomas with abnormal karyotype (2007) (77)
- Cytogenetic findings in malignant peripheral nerve sheath tumors (1995) (75)
- Absence of mutations of the BRAF gene in malignant melanoma of soft parts (clear cell sarcoma of tendons and aponeuroses). (2005) (74)
- FISH characterization of head and neck carcinomas reveals that amplification of band 11q13 is associated with deletion of distal 11q (1998) (73)
- Generation of trisomies in cancer cells by multipolar mitosis and incomplete cytokinesis (2010) (73)
- Loss of chromosome band 8q24 in sporadic osteocartilaginous exostoses (1994) (71)
- Genomic Profiling of Chondrosarcoma: Chromosomal Patterns in Central and Peripheral Tumors (2009) (71)
- FUS-CREB3L2/L1–Positive Sarcomas Show a Specific Gene Expression Profile with Upregulation of CD24 and FOXL1 (2011) (70)
- Cytogenetic evidence of clonality in cutaneous benign fibrous histiocytomas: a report of the CHAMP Study Group (2000) (69)
- Malignant fibrous histiocytoma and fibrosarcoma of bone: a re-assessment in the light of currently employed morphological, immunohistochemical and molecular approaches (2012) (68)
- The FHIT and PTPRG genes are deleted in benign proliferative breast disease associated with familial breast cancer and cytogenetic rearrangements of chromosome band 3p14. (1996) (67)
- Distinct cytologic features of spindle cell lipoma (2001) (67)
- Clinical and biological importance of cytogenetic abnormalities in childhood and adult acute lymphoblastic leukemia (2004) (66)
- Topoisomerase-II alpha is upregulated in malignant peripheral nerve sheath tumors and associated with clinical outcome. (2003) (66)
- In-depth Genetic Analysis of Sclerosing Epithelioid Fibrosarcoma Reveals Recurrent Genomic Alterations and Potential Treatment Targets (2017) (66)
- Radiation-associated sarcomas are characterized by complex karyotypes with frequent rearrangements of chromosome arm 3p. (2000) (65)
- Hibernomas are characterized by rearrangements of chromosome bands 11q13‐21 (1994) (65)
- Cytogenetic aberrations and their prognostic impact in chondrosarcoma (2002) (65)
- Gene fusion detection in formalin-fixed paraffin-embedded benign fibrous histiocytomas using fluorescence in situ hybridization and RNA sequencing (2015) (64)
- Cytogenetic characterization of peripheral nerve sheath tumours: a report of the CHAMP study group (2000) (64)
- Gene expression profiles relate to SS18/SSX fusion type in synovial sarcoma (2006) (64)
- Characterization of chromosome aberrations in salivary gland tumors by FISH, including multicolor COBRA‐FISH (2001) (63)
- 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. (1999) (63)
- Fine‐needle aspiration of neurilemoma (schwannoma). A clinicocytopathologic study of 116 patients (2006) (63)
- Comparative cytogenetic study of spindle cell and pleomorphic leiomyosarcomas of soft tissues: a report from the CHAMP Study Group. (2000) (59)
- Cytogenetic abnormalities in 106 oral squamous cell carcinomas. (2006) (59)
- Correlation between karyotypic pattern and clinicopathologic features in 125 breast cancer cases (1996) (58)
- Amplification of chromosome 1 sequences in lipomatous tumors and other sarcomas (2004) (57)
- Cytogenetic comparison of primary tumors and lymph node metastases in breast cancer patients (1998) (57)
- The POU5F1P1 pseudogene encodes a putative protein similar to POU5F1 isoform 1. (2008) (57)
- Identification of a novel amplicon at distal 17q containing the BIRC5/SURVIVIN gene in malignant peripheral nerve sheath tumours (2006) (57)
- Genomic changes in chromosomes 10, 16, and X in malignant peripheral nerve sheath tumors identify a high-risk patient group. (2010) (57)
- Concomitant deletions of tumor suppressor genes MEN1 and AIP are essential for the pathogenesis of the brown fat tumor hibernoma (2010) (57)
- Deep-seated ordinary and atypical lipomas: histopathology, cytogenetics, clinical features, and outcome in 215 tumours of the extremity and trunk wall. (2008) (57)
- Comparison of chromosomal patterns with clinical features in 165 lipomas: a report of the CHAMP study group. (1998) (56)
- Fine needle aspiration (FNA) of synovial sarcoma—a comparative histological–cytological study of 15 cases, including immunohistochemical, electron microscopic and cytogenetic examination and DNA‐ploidy analysis (1996) (56)
- A novel FUS/CHOP chimera in myxoid liposarcoma. (2000) (56)
- Primary Pseudomyogenic Hemangioendothelioma of Bone (2016) (55)
- Clonal chromosome abnormalities in two liposarcomas. (1987) (55)
- Biallelic inactivation of TP53 rarely contributes to the development of malignant peripheral nerve sheath tumors (2001) (54)
- 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. (1999) (54)
- Cytogenetic analysis of 101 giant cell tumors of bone: Nonrandom patterns of telomeric associations and other structural aberrations (2009) (53)
- Tenth International Workshop on Human Gene Mapping (1988) (53)
- Chromosome rearrangements in synovial chondromatous lesions. (1996) (53)
- Mesenchymal stromal cells from primary osteosarcoma are non‐malignant and strikingly similar to their bone marrow counterparts (2011) (52)
- FN1–EGF gene fusions are recurrent in calcifying aponeurotic fibroma (2016) (51)
- Characterization of the native CREB3L2 transcription factor and the FUS/CREB3L2 chimera (2007) (51)
- Cytogenetic and molecular cytogenetic findings in lipoblastoma. (2008) (51)
- Genomic profiling of bone and soft tissue tumors with supernumerary ring chromosomes using tiling resolution bacterial artificial chromosome microarrays (2006) (51)
- Amplification of 12q13 and 12q15 sequences in a sclerosing epithelioid fibrosarcoma. (1998) (51)
- A novel GTF2I/NCOA2 fusion gene emphasizes the role of NCOA2 in soft tissue angiofibroma development (2013) (49)
- Cytogenetic analysis of 33 basal cell carcinomas. (1991) (49)
- Rearrangement of the COL12A1 and COL4A5 genes in subungual exostosis: molecular cytogenetic delineation of the tumor‐specific translocationt(X;6)(q13‐14;q22) (2006) (49)
- Constitutional chromosome instability and cancer risk. (1989) (49)
- Heterogeneous genetic profiles in soft tissue myoepitheliomas (2008) (48)
- Gene expression and single nucleotide polymorphism array analyses of spindle cell lipomas and conventional lipomas with 13q14 deletion (2011) (48)
- Signatures of copy number alterations in human cancer (2021) (48)
- Chromosomal aberrations in breast cancer: A comparison between cytogenetics and comparative genomic hybridization (1999) (47)
- Abnormal cell cycle regulation in malignancy. (1999) (47)
- Fusion of RDC1 with HMGA2 in lipomas as the result of chromosome aberrations involving 2q35-37 and 12q13-15. (2002) (47)
- Characteristic karyotypic features in lacrimal and salivary gland carcinomas. (1994) (47)
- Recurrent PRDM10 Gene Fusions in Undifferentiated Pleomorphic Sarcoma (2014) (47)
- Recurrent chromosome aberrations in fibrous dysplasia of the bone: a report of the CHAMP study group. CHromosomes And MorPhology. (2000) (46)
- Identification of p53 as a strong predictor of survival for patients with malignant peripheral nerve sheath tumors. (2009) (45)
- Aberrant receptor tyrosine kinase signaling in lipofibromatosis: a clinicopathological and molecular genetic study of 20 cases (2018) (44)
- Nonrandom pattern of cytogenetic abnormalities in squamous cell carcinoma of the larynx (2000) (44)
- Molecular cytogenetic characterization of the 11q13 amplicon in head and neck squamous cell carcinoma (2006) (42)
- Clonal chromosome aberrations in three sacral chordomas. (1994) (42)
- Diverse chromosome abnormalities in squamous cell carcinomas of the skin. (1989) (41)
- Fusion of the HMGA2 and NFIB genes in lipoma (2005) (41)
- Fusions involving protein kinase C and membrane-associated proteins in benign fibrous histiocytoma. (2014) (41)
- A new cytogenetic subgroup in lipomas: loss of chromosome 16 material in spindle cell and pleomorphic lipomas (2005) (41)
- Evolving techniques for gene fusion detection in soft tissue tumours (2014) (40)
- Trisomy 7 accumulates with age in solid tumors and non‐neoplastic synovia (2001) (40)
- Cytogenetic aberrations in Ewing sarcoma: are secondary changes associated with clinical outcome? (1999) (40)
- Truncation and fusion of HMGA2 in lipomas with rearrangements of 5q32→q33 and 12q14→q15 (2005) (40)
- Cytogenetics of hepatoblastoma: further characterization of 1q rearrangements by fluorescence in situ hybridization: an international collaborative study. (2000) (40)
- Primary mesenchymal stem cells in human transplanted lungs are CD90/CD105 perivascularly located tissue-resident cells (2014) (40)
- Genetic heterogeneity in rhabdomyosarcoma revealed by SNP array analysis (2016) (39)
- Spectral karyotyping and chromosome banding studies of primary breast carcinomas and their lymph node metastases. (2000) (39)
- Recurrent Fusions Between YAP1 and KMT2A in Morphologically Distinct Neoplasms Within the Spectrum of Low-grade Fibromyxoid Sarcoma and Sclerosing Epithelioid Fibrosarcoma (2020) (39)
- 19p + marker chromosome correlates with relapse in malignant fibrous histiocytoma (1996) (39)
- Chromosome abnormalities in a pancreatic adenocarcinoma. (1989) (38)
- Chromosomal aberrations in a consecutive series of childhood rhabdomyosarcoma. (1998) (38)
- Cytogenetic analysis of four angiosarcomas from deep and superficial soft tissue. (1998) (38)
- Molecular genetic characterization of the genomic ACTB-GLI fusion in pericytoma with t(7;12). (2004) (37)
- Dichotomy of hyperdiploid acute lymphoblastic leukemia on the basis of the distribution of gained chromosomes. (1996) (37)
- A case of dermatofibrosarcoma protuberans with a ring chromosome 5 and a rearranged chromosome 22 containing amplified COL1A1 and PDGFB sequences. (1998) (37)
- Mitotic instability associated with late genomic changes in bone and soft tissue tumours. (2004) (37)
- The t(X;6) in subungual exostosis results in transcriptional deregulation of the gene for insulin receptor substrate 4 (2011) (37)
- Clinical significance of genetic imbalances revealed by comparative genomic hybridization in chondrosarcomas. (1999) (36)
- No EWS/FLI1 fusion transcripts in giant‐cell tumors of bone (2001) (36)
- Cytogenetic studies on fine‐needle aspiration samples from osteosarcoma and Ewing's sarcoma (1996) (36)
- Nonrandom pattern of telomeric associations in atypical lipomatous tumors with ring and giant marker chromosomes. (1998) (36)
- Variable FHIT transcripts in non‐neoplastic tissues (1997) (36)
- Genomic characteristics of soft tissue sarcomas (2010) (36)
- FOSL1 as a candidate target gene for 11q12 rearrangements in desmoplastic fibroblastoma (2012) (35)
- Expression levels of HMGA2 in adipocytic tumors correlate with morphologic and cytogenetic subgroups (2009) (35)
- Duplication of chromosome segment 12q15‐24 is associated with atypical lipomatous tumors. A report of the CHAMP collaborative study group (1996) (35)
- Karyotypic abnormalities in fibroadenomas of the breast (1997) (34)
- Clonal chromosome aberrations accumulate with age in upper aerodigestive tract mucosa. (1997) (34)
- GRIA2 is a novel diagnostic marker for solitary fibrous tumour identified through gene expression profiling (2014) (34)
- Karyotypic features of malignant tumors of the nasal cavity and paranasal sinuses (1995) (34)
- Comprehensive genetic analysis of a paediatric pleomorphic myxoid liposarcoma reveals near‐haploidization and loss of the RB1 gene (2016) (34)
- Comparative genomic hybridization of postirradiation sarcomas (2001) (34)
- Clonal structural chromosome aberrations in nonneoplastic cells of the skin and upper aerodigestive tract (1992) (33)
- Age- and gender-related heterogeneity of cancer chromosome aberrations. (1993) (33)
- Trisomy 20 is a primary chromosome aberration in desmoid tumors (1995) (32)
- Nonrandom secondary chromosome-aberrations in liposarcomas with t(12, 16). (1994) (32)
- Chromosome abnormalities in oral squamous cell carcinomas. (1993) (31)
- Myoepithelioma of bone with a novel FUS‐POU5F1 fusion gene (2014) (31)
- An endometrial stromal sarcoma cell line with the JAZF1/PHF1 chimera. (2008) (31)
- Cytogenetic findings and clinical course in a consecutive series of Wilms tumors. (2003) (31)
- Chromosomal translocations involving 11q13 contribute to cyclin D1 overexpression in squamous cell carcinoma of the head and neck. (2002) (31)
- Biallelic somatic inactivation of the NF1 gene through chromosomal translocations in a sporadic neurofibroma (2005) (30)
- Evidence of somatic mutations in osteoarthritis (1996) (30)
- Enchondromatosis: Ollier disease and Maffucci syndrome (2002) (30)
- A Benign Vascular Tumor With a New Fusion Gene: EWSR1-NFATC1 in Hemangioma of the Bone (2013) (30)
- Different patterns of chromosomal imbalances in metastasising and non‐metastasising primary breast carcinomas (1999) (30)
- Analysis of the distribution and frequency of trisomy 7 in vivo in synovia from patients with osteoarthritis and pigmented villonodular synovitis. (2001) (29)
- Ring marker containing 17q and chromosome 22 in a case of dermatofibrosarcoma protuberans. (1996) (28)
- Fusion of the COL1A1 and USP6 genes in a benign bone tumor. (2008) (28)
- Low‐grade fibromyxoid sarcoma is difficult to diagnose by fine needle aspiration cytology: a cytomorphological study of eight cases (2009) (28)
- Prognostically important chromosomal aberrations in soft tissue sarcomas: a report of the Chromosomes and Morphology (CHAMP) Study Group. (2002) (28)
- Protein expression of BIRC5, TK1, and TOP2A in malignant peripheral nerve sheath tumours – A prognostic test after surgical resection (2015) (28)
- Genomic PCR detects tumor cells in peripheral blood from patients with myxoid liposarcoma (1996) (28)
- HUGO Gene Nomenclature Committee (HGNC) recommendations for the designation of gene fusions (2021) (28)
- A novel FISH assay for SS18–SSX fusion type in synovial sarcoma (2004) (27)
- Near-haploidy in two malignant fibrous histiocytomas. (1995) (27)
- Centromere cleavage is a mechanism underlying isochromosome formation in skin and head and neck carcinomas (2000) (27)
- Cytogenetic analysis in the examination of solid tumors in children. (1994) (27)
- Polyclonal expansion of cells with trisomy 7 in synovia from patients with osteoarthritis (1999) (26)
- Cytogenetic and fluorescence in situ hybridization characterization of chromosome 1 rearrangements in head and neck carcinomas delineate a target region for deletions within 1p11-1p13. (1998) (26)
- Frequent low‐level mutations of protein kinase D2 in angiolipoma (2017) (26)
- Combined binary ratio labeling fluorescence in situ hybridization analysis of chordoma. (2004) (26)
- Nonrandom secondary chromosome-aberrations in synovial sarcomas with t(x-18). (1995) (26)
- Duplication 18p with mild influence on the phenotype. (1988) (25)
- Trisomy 14 in atypical chronic myeloid leukemia. (1990) (25)
- Cytogenetics of benign breast lesions (1998) (25)
- Inflammatory leiomyosarcoma is a distinct tumor characterized by near-haploidization, few somatic mutations, and a primitive myogenic gene expression signature (2018) (25)
- Disease‐associated patterns of disomic chromosomes in hyperhaploid neoplasms (2012) (25)
- Smooth muscle actin expression in primary bone tumours (2012) (24)
- The POU 5 F 1 P 1 pseudogene encodes a putative protein similar to POU 5 F 1 isoform 1 (24)
- Cytogenetic and fluorescence in situ hybridization characterization of chromosome 8 rearrangements in head and neck squamous cell carcinomas. (2001) (23)
- Retained heterodisomy is associated with high gene expression in hyperhaploid inflammatory leiomyosarcoma. (2012) (23)
- Extraskeletal myxoid chondrosarcoma with neuroendocrine differentiation: a case report with fine-needle aspiration biopsy, histopathology, electron microscopy, and cytogenetics. (2003) (23)
- PRDM10-rearranged Soft Tissue Tumor: A Clinicopathologic Study of 9 Cases (2019) (23)
- Cytogenetic findings in invasive breast carcinomas with prognostically favourable histology: A less complex karyotypic pattern? (1998) (23)
- Heterogeneous and complex rearrangements of chromosome arm 6q in chondromyxoid fibroma: delineation of breakpoints and analysis of candidate target genes. (2010) (23)
- Cytogenetic findings in acute megakaryoblastic leukemia (ANLL-M7). (1990) (22)
- Unbalanced chromosomal rearrangements in a metastasizing salivary gland tumor with benign histology. (1998) (21)
- A case of myelodysplastic syndrome with high platelet counts and a t(3;8)(q26;q24). (1987) (21)
- Fusion of the FUS and CREB3L2 genes in a supernumerary ring chromosome in low-grade fibromyxoid sarcoma. (2010) (21)
- Variable stability of chromosomes containing amplified α-satellite sequences in human mesenchymal tumours (1999) (20)
- Fusion of the tumor-suppressor gene CHEK2 and the gene for the regulatory subunit B of protein phosphatase 2 PPP2R2A in childhood teratoma. (2006) (20)
- Variable FHIT transcripts in non-neoplastic tissues. (1997) (20)
- Nonrandom numerical chromosome abnormalities in basal cell carcinomas. (1998) (20)
- Telomeric associations correlate with telomere length reduction and clonal chromosome aberrations in giant cell tumor of bone (2009) (19)
- Fluorescent in situ hybridisation (FISH) characterisation of pericentromeric breakpoints on chromosome 5 in head and neck squamous cell carcinomas. (1999) (19)
- PHF1 fusions cause distinct gene expression and chromatin accessibility profiles in ossifying fibromyxoid tumors and mesenchymal cells (2020) (19)
- Ring chromosomes and low-grade gene amplification in an atypical lipomatous tumor with minimal nuclear atypia. (2003) (19)
- Clonal chromosome aberrations are present in vivo in synovia and osteophytes from patients with osteoarthritis (1997) (19)
- Chromosome aberrations in prophylactic mastectomies from women belonging to breast cancer families (1996) (19)
- Gene copy number changes in dermatofibrosarcoma protuberans – a fine-resolution study using array comparative genomic hybridization (2006) (19)
- Statistical analyses of karyotypic complexity in head and neck squamous cell carcinoma. (2004) (18)
- Clonal chromosome aberrations in a keratoacanthoma and a basal cell papilloma. (1989) (18)
- Methylated RASSF1A in malignant peripheral nerve sheath tumors identifies neurofibromatosis type 1 patients with inferior prognosis (2014) (18)
- Basosquamous papilloma. A benign epithelial skin tumor with multiple cytogenetic clones. (1989) (18)
- Cyclin D1 amplification in chromosomal band 11q13 is associated with overrepresentation of 3q21–q29 in head and neck carcinomas (2002) (18)
- Most gene fusions in cancer are stochastic events (2019) (18)
- Clonal structural chromosome aberrations in fibrous dysplasia (1994) (17)
- Scattered genomic amplification in dedifferentiated liposarcoma (2017) (17)
- Chromosome banding analysis of cells from fine-needle aspiration biopsy samples from soft tissue and bone tumors: is it clinically meaningful? (2011) (17)
- 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. (2000) (17)
- Frequent miRNA-convergent fusion gene events in breast cancer (2017) (17)
- Undifferentiated pleomorphic sarcomas with PRDM10 fusions have a distinct gene expression profile (2019) (17)
- Cytogenetic heterogeneity in a clear cell hidradenoma of the skin. (1994) (16)
- Trisomy 13 as a primary chromosome aberration in acute leukemia. (1991) (16)
- Translocation (2;3)(p21;p26) as the sole anomaly in a benign localized fibrous mesothelioma. (1996) (16)
- Multiple polysomies in breast carcinomas: preferential gain of chromosomes 1, 5, 6, 7, 12, 16, 17, 18, and 19. (1999) (16)
- “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” (2020) (16)
- Centennial of Wilhelm Waldeyer’s introduction of the term “chromosome” (1988) (16)
- 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 (2008) (16)
- Cytogenetic changes in benign proliferative and nonproliferative lesions of the breast. (1998) (15)
- DNA copy number amplifications in sarcomas with homogeneously staining regions and double minutes. (2001) (15)
- Reclassification and subtyping of so-called malignant fibrous histiocytoma of bone: comparison with cytogenetic features (2011) (14)
- Comparison of the proximal promoter regions of the PAX3 and PAX7 genes. (2007) (14)
- Gene fusion involving the insulin‐like growth factor 1 receptor in an ALK‐negative inflammatory myofibroblastic tumour (2019) (14)
- Tandem duplication (1) (q11 → q22) in a male infant with multiple congenital malformations (1987) (14)
- Integrative genome and transcriptome analyses reveal two distinct types of ring chromosome in soft tissue sarcomas. (2014) (14)
- Calcium pyrophosphate dihydrate crystal deposition disease in the temporomandibular joint: diagnostic difficulties and clonal chromosome aberrations in a case followed up for 5 years. (2001) (13)
- SNP array and FISH findings in two pleomorphic hyalinizing angiectatic tumors. (2012) (13)
- High‐resolution molecular cytogenetic analysis of Wilms tumors highlights diagnostic difficulties among small round cell kidney tumors (2008) (13)
- Genetic intratumour heterogeneity in high‐grade brain tumours is associated with telomere‐dependent mitotic instability (2007) (13)
- Unstable translocation (8;22) in a case of giant cell reparative granuloma. (2007) (13)
- The Hidden Genomic and Transcriptomic Plasticity of Giant Marker Chromosomes in Cancer (2017) (13)
- 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) (2006) (13)
- The Tumor-Associated Gene HMGIC Is Expressed in Normal and Osteoarthritis-Affected Synovia (2001) (12)
- Karyotypic evolution and tumor progression in head and neck squamous cell carcinomas. (2005) (12)
- Characterization of a hotspot region on chromosome 12 for amplification in ring chromosomes in atypical lipomatous tumors (2009) (12)
- Normal level of spontaneous chromosome breakage in lymphocytes from patients with non-Hodgkin's lymphoma. (1988) (12)
- Molecular genetic characterization of the 11q13 breakpoint in a desmoplastic fibroma of bone. (2012) (12)
- RNA sequencing of sarcomas with simple karyotypes: identification and enrichment of fusion transcripts (2015) (12)
- A PCR/restriction digestion assay for the detection of the transcript variants 1 and 2 of POU5F1 (2008) (12)
- Rearrangement of the neoplasia‐associated gene HMGIC in synovia from patients with osteoarthritis (1999) (11)
- Frequency and distribution of mitomycin C-induced structural chromosome aberrations in lymphocytes from non-Hodgkin lymphoma patients. (1988) (11)
- 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 (2009) (11)
- A subgroup of breast carcinomas is cytogenetically characterized by trisomy 12. (1997) (11)
- 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. (2019) (11)
- Comparative cytogenetic and DNA flow cytometric analysis of 242 primary breast carcinomas. (2003) (11)
- HMGA2 and MDM2 expression in lipomatous tumors with partial, low-level amplification of sequences from the long arm of chromosome 12. (2011) (11)
- Complex karyotype in a childhood adrenocortical carcinoma. (1998) (11)
- Trisomy 3 as the sole karyotypic change in a pediatric immature teratoma. (1998) (10)
- Different patterns of clonal evolution among different sarcoma subtypes followed for up to 25 years (2018) (10)
- Deep sequencing of myxoinflammatory fibroblastic sarcoma (2020) (10)
- Ring chromosomes, breakpoint clusters, and neocentromeres in sarcomas (2015) (10)
- Cytogenetic and molecular genetic demonstration of polyclonality in an acinic cell carcinoma. (1998) (10)
- Chromosome aberrations in prophylactic mastectomies from women belonging to breast cancer families. (1996) (10)
- Recurrent chromosomal imbalances in choroid plexus tumors. (1995) (10)
- Tetraploidization and progressive loss of 6q in a squamous cell carcinoma of the parotid gland. (1995) (10)
- Normal frequency of chromosome breakage in lymphocytes from patients with musculoskeletal sarcoma. (1988) (10)
- No increased chromosome breakage in skin fibroblasts from patients with musculoskeletal sarcoma (1988) (10)
- Bidirectionality and transcriptional activity of the EWSR1 promoter region. (2009) (10)
- Remarkably long survival of a patient with Ph1-positive chronic myeloid leukemia and 5' bcr rearrangement. (1990) (10)
- Prognostic significance of chromosome aberrations in high-grade soft tissue sarcomas. (2006) (10)
- Permanent activation of HMGA2 in lipomas mimics its temporal physiological activation linked to the gain of adipose tissue (2014) (10)
- Musculoskeletal oncology--advances in cytogenetics and molecular genetics and their clinical implications. (1997) (9)
- Genetic characterization of bone and soft tissue tumors (2004) (9)
- Concurrent gain of 17q and the MYC oncogene in a medullomyoblastoma (2007) (9)
- Analysis of giant cell tumour of bone cells for Noonan syndrome/cherubism-related mutations. (2013) (9)
- The pathogenetic significance of acquired trisomy 8 is not reducible to amplification of a single chromosome band. (1995) (9)
- Cytogenetic findings in pediatric renal cell carcinoma. (2007) (8)
- POU 5 F 1 , encoding a key regulator of stem cell pluripotency , is fused to EWSR 1 in hidradenoma of the skin and mucoepidermoid carcinoma of the salivary glands (2008) (8)
- Cancer chromosome breakpoints cluster in gene‐rich genomic regions (2018) (8)
- Increased sensitivity to bleomycin in upper aerodigestive tract mucosa of head and neck squamous cell carcinoma patients. (2008) (8)
- Overlapping morphological, immunohistochemical and genetic features of superficial CD34-positive fibroblastic tumor and PRDM10-rearranged soft tissue tumor (2021) (8)
- Molecular cytogenetic characterization of an ins(4;X) occurring as the sole abnormality in an aggressive, poorly differentiated soft tissue sarcoma (2005) (8)
- Characterization of the human CREB3L2 gene promoter. (2009) (8)
- Cytogenetic analysis of inverted nasal papillomas and demonstration of genetic convergence during in vitro passaging (1997) (8)
- Complex karyotypes in flow cytometrically DNA-diploid squamous cell carcinomas of the head and neck. (1998) (8)
- Different cytogenetic patterns in skeletal breast cancer metastases (1996) (7)
- Inferior survival for patients with malignant peripheral nerve sheath tumors defined by aberrant TP53 (2018) (7)
- Clonal karyotypic evolution in a pediatric neurofibrosarcoma. (1995) (7)
- Chromosomal abnormalities in squamous cell carcinoma of the head and neck. (2000) (7)
- Genetic changes in bone and soft tissue tumors. (1993) (7)
- Clonal chromosome aberrations in a sialoblastoma. (2009) (7)
- Retained heterodisomy for chromosome 12 in atypical lipomatous tumors: implications for ring chromosome formation (2004) (6)
- The breakpoints of spontaneous chromosome aberrations in lymphocytes from patients with non-Hodgkin's lymphoma are nonrandomly distributed. (2008) (6)
- Complex karyotype with an 11q13 homogeneously staining region in esophageal squamous cell carcinoma. (1995) (6)
- Sequencing IDH1/2 glioma mutation hotspots in gliomas and malignant peripheral nerve sheath tumors. (2014) (6)
- Congenital and inherited syndromes associated with bone and soft tissue tumours (2002) (6)
- Extraskeletal Myxoid Chondrosarcoma with Neuroendocrine Differentiation: A Case Report with Fine-Needle Aspiration Biopsy, Histopathology, Electron Microscopy, and Cytogenetics (2003) (6)
- Tiling resolution array comparative genomic hybridization analysis of a fibrosarcoma of bone. (2007) (6)
- Positive Sarcomas Show a Specific Gene Expression Profile with Upregulation of CD 24 and FOXL 1 (2011) (6)
- Expression of DOL54 is not restricted to myxoid liposarcomas with the FUS-DDIT3 chimera but is found in various sarcomas. (2004) (5)
- Nervous system: Peripheral nerve sheath tumors (2011) (5)
- Breakprone chromosome bands in lymphocytes from sarcoma patients do not coincide with bands involved in primary sarcoma-associated chromosome rearrangements. (2008) (5)
- Non‐fibrosing sclerosing epithelioid fibrosarcoma: an unusual variant (2016) (5)
- Frequency and distribution of N-methyl-N'-nitro-N-nitrosoguanidine (MNNG)-induced structural chromosome aberrations in fibroblasts from sarcoma and non-Hodgkin's lymphoma patients. (1989) (5)
- Normal frequency of structural chromosome aberrations in fibroblasts from patients with non-Hodgkin's lymphoma. (2008) (5)
- Characterization of a malignant eccrine poroma by cytogenetic and fluorescence in situ hybridization techniques. (1998) (5)
- 387 Chromosomal abnormalities involving 11Q13 are associated with poor prognosis in squamous cell carcinoma of the head and neck (1995) (5)
- Influence of serum concentration on chromosome breakage frequency. (2008) (4)
- Assessment of Fusion Gene Status in Sarcomas Using a Custom Made Fusion Gene Microarray (2013) (4)
- Clonal chromosome aberrations accumulate with age in upper aerodigestive tract mucosa (1996) (4)
- Homozygous deletions of cadherin genes in chondrosarcoma-an array comparative genomic hybridization study. (2012) (4)
- Genomic and transcriptomic characterization of desmoplastic small round cell tumors (2021) (4)
- Breakprone chromosome bands in fibroblasts from patients with non-Hodgkin's lymphoma do not coincide with bands involved in primary rearrangements in non-Hodgkin's lymphomas. (2008) (4)
- Atypical lipomatous tumor with rare structural rearrangements involving chromosomes 8 and 12. (2005) (4)
- 16th European Colloqium on Animal Cytogenetics and Gene Mapping (2004) (3)
- Soft Tissue Tumors (2015) (3)
- GLI1 (glioma-associated oncogene homolog 1) (2011) (3)
- Superficial CD34-Positive Fibroblastic Tumor (2022) (3)
- Trisomy 16 as the primary chromosome aberration in a papilloma of the breast. (1998) (3)
- Different cytogenetic patterns in skeletal breast cancer metastases. (1996) (2)
- ACTB (Actin, beta) (2011) (2)
- Cytogenetic and single nucleotide polymorphism array findings in soft tissue tumors in infants. (2013) (2)
- CREB3L2 (cAMP responsive element binding protein 3-like 2) (2011) (2)
- Cytogenetic findings in pediatric germ-cell tumors. (1995) (2)
- Solid tumor cytogenetics (2002) (2)
- BL1391: an established cell line from a human malignant peripheral nerve sheath tumor with unique genomic features (2020) (2)
- Distribution of structural chromosome aberrations in skin fibroblasts from patients with benign mesenchymal tumors. (2008) (2)
- Cytogenetic analysis of basal cell carcinoma (1991) (2)
- 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. (2008) (2)
- Clinical Significance of Cytogenetic Findings in Solid Tumors (1997) (2)
- Phyllis Jean McAlpine, Ph.D, FCCMG (1999) (1)
- Short communication Cytogenetic and molecular cytogenetic findings in lipoblastoma (2008) (1)
- Clonal chromosome abnormalities in two chemodectomas (1996) (1)
- Rearrangements of chromosome bands 15q12-q21 are secondary to HMGA2 deregulation in conventional lipoma. (2014) (1)
- [Cytogenetic diagnosis of tumors. Clinical significance of chromosome aberrations]. (1997) (1)
- Neuroblastoma with flat genomic profile: a question of representativity? (2018) (1)
- Superficial CD 34-Positive Fibroblastic Tumor A Clinicopathologic , Immunohistochemical , and Molecular Study of 59 Cases (2022) (1)
- Core needle biopsy performed by the cytopathologist : a technique to complement fine needle aspiration of musculoskeletal tumors (2003) (1)
- Bone & Soft Tissue (2011) (1)
- RASSF1A and SCGB3A1 are common target genes for promoter hypermethylation in malignant peripheral nerve sheath tumors (2007) (1)
- Bands involved in primary chromosome rearrangements in sarcomas are not constitutionally liable to breakage in sarcoma patients (1988) (1)
- Clonal chromosome abnormalities in two chemodectomas. (1996) (1)
- 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 (2001) (1)
- Tumors of the skin (2015) (1)
- Characterization of an alternative transcript of the human CREB3L2 gene. (2010) (1)
- Amplification of ERBB2 (HER2) in embryonal rhabdomyosarcoma: A potential treatment target in rare cases? (2021) (1)
- 23. Soft Tissue Tumors (2010) (1)
- The MDM2 SNP309 G allele is not preferentially amplified in bone and soft tissue tumors. (2012) (1)
- O27: Genomic profiling of bone and soft tissue tumors with supernumerary ring chromosomes using tiling resolution BAC microarrays (2005) (1)
- Abstract LB-189: BIRC5 (Survivin) is a prognostic biomarker and potential drug target for patients with malignant peripheral nerve sheath tumors. (2013) (1)
- Soft Tissue Tumors: Angiofibroma (2013) (1)
- Soft tissue tumors: Low grade fibromyxoid sarcoma (2011) (1)
- Soft Tissue Tumors: Low grade fibromyxoid (2005) (0)
- Soft Tissue Tumors: t(X;20)(p11.23;q13.33) in Biphasic Synovial Sarcoma (2008) (0)
- Unique Cytologic and Chromosome Aberrations in Chondroid Lipoma (2000) (0)
- Cytogenetic characterization, frequency and distribution of rob t(1;29) in some Italian and Portuguese cattle breeds (2004) (0)
- Desmoid Fibromatosis in the Brachial Plexus Mimicking an Ulnar Nerve Entrapment (2019) (0)
- PO-340 Dysregulation of the TP53 network and PRC2 activity are independent poor prognostic factors in patients with malignant peripheral nerve sheath tumours (2018) (0)
- Bone: Subungual exostosis with t(X;6)(q13;q22) (2011) (0)
- Impaired GARNL4 and BCLAF1 expression: novel oncogenic mechanism in balanced rearrangement in chondromyxoid fibroma? (2008) (0)
- Secondary chromosome aberrations in synovial sarcoma with t(X;18) (1995) (0)
- Bone & Soft Tissue (2010) (0)
- Signatures of copy number alterations in human cancer (2022) (0)
- In Vivo and In Vitro Implications of the Transcription Factor T (Brachyury) in Pathogenesis of Sporadic Chordomas (2010) (0)
- Contents Vol. 115, 2006 (2006) (0)
- The diagnostic utility of DNA copy number analysis of core needle biopsies from soft tissue and bone tumors (2022) (0)
- Malignant Fibrous Histiocytoma and Fibrosarcoma of Bone in 2011: What's New? (2011) (0)
- Frequent miRNA-convergent fusion gene events in breast cancer (2017) (0)
- Different patterns of clonal evolution among different sarcoma subtypes followed for up to 25 years (2018) (0)
- Genetic Abnormalities of the Transcription Factor T (Brachyury) in Sporadic Chordomas (2010) (0)
- Balanced and Unbalanced Rearrangement of Chromosome Arm 6q in Chondromyxoid Fibroma (CMF): Delineation of Breakpoints and Analysis of Candidate Target Genes (2009) (0)
- BL1391: an established cell line from a human malignant peripheral nerve sheath tumor with unique genomic features (2020) (0)
- Table of Content Volume 55, Number 4, April 2016 (2016) (0)
- Array-CGH Analysis of Chondromyxoid Fibroma complementary to conventional cytogenetics points to recurrent involvement of chromosomal region 6q23 (2006) (0)
- Research Expression levels of HMGA 2 in adipocytic tumors correlate with morphologic and cytogenetic subgroups (2017) (0)
- 440: Genomic copy number changes and the prognostic impact of the encoded genes PTEN and BIRC5 in malignant peripheral nerve sheath tumours (2014) (0)
- Epithelioid and Spindle Cell Hemangioma (2022) (0)
- Structural and numerical chromosome changes in colorectal cancer develop through telomere-mediated anaphase bridging and not through mitotic multipolarity " (2005) (0)
- A cloud-based resource for genome coordinate-based exploration and large-scale analysis of chromosome aberrations and gene fusions in cancer. (2023) (0)
- Biphasic, Hyperdiploid Breast Tumors in Children: A Distinct Entity? (2013) (0)
- 38th Biennial American Cytogenetics Conference (2004) (0)
- Cytogenetic Analysis of 33 Basal Cell Carcinomas 1 (2006) (0)
- Short communication Cytogenetic findings in pediatric renal cell carcinoma (2007) (0)
- A cryptic EWSR1 :: DDIT3 fusion in myxoid liposarcoma: Potential pitfalls with FISH and cytogenetics (2022) (0)
- qter Detected by Comparative Genomic Hybridization in Malignant Tumors from Patients with von Recklinghausen ' s Neurofibromatosis ' (0)
- Scattered genomic amplification in dedifferentiated liposarcoma (2017) (0)
- Heterogeneous and Complex Rearragements of the Long Arm of Chromosome 6 in Chondromyxoid Fibroma (2010) (0)
- Brief Gene Mapping Reports A / B / C (2003) (0)
- Prognostic value of gene expression targeted by gain of 17q sequences in malignant peripheral nerve sheath tumours (2010) (0)
- Soft tissue tumors: Pericytoma with t(7;12) (2011) (0)
- Atlas of Genetics and Cytogenetics in Oncology and Haematology Soft Tissue Tumors : Angiofibroma (2013) (0)
- SS18L1 (synovial sarcoma translocation gene on chromosome 18-like 1) (2011) (0)
- Epigenetic target genes in malignant peripheral nerve sheath tumours identified as surrogate prognostic biomarkers (2010) (0)
- Tumors of bone (2015) (0)
- Characterization of the human CREB 3 L 2 gene promoter (0)
- Tumorigenesis and Neoplastic Progression Recurrent Rearrangement of the PHF 1 Gene in Ossifying Fibromyxoid Tumors (2012) (0)
- Molecular Characterization Of The 12Q13.3-14.1 Recurrent Breakpoint Region On Ring Chromosomes 12 In Atypical Lipomatous Tumors (2009) (0)
- Characteristic karyotypic features in non-squamous cell carcinomas of the head and neck (1994) (0)
This paper list is powered by the following services:
What Schools Are Affiliated With Fredrik Mertens?
Fredrik Mertens is affiliated with the following schools:
