Nils Mandahl
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Nils Mandahl's Degrees
- Bachelors Biology University of California, Berkeley
- PhD Genetics Stanford University
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(Suggest an Edit or Addition)Nils Mandahl's Published Works
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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
- TERT promoter mutations occur frequently in gliomas and a subset of tumors derived from cells with low rates of self-renewal (2013) (1148)
- Fusion of CHOP to a novel RNA-binding protein in human myxoid liposarcoma (1993) (883)
- 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)
- Deregulation of the platelet-derived growth factor β-chain gene via fusion with collagen gene COL1A1 in dermatof ibrosarcoma protuberans and giant-cell fibroblastoma (1997) (506)
- 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)
- 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)
- Rearrangement of the transcription factor gene CHOP in myxoid liposarcomas with t(12;16)(q13;p11) (1992) (304)
- 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)
- 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)
- Oncogenic conversion of a novel orphan nuclear receptor by chromosome translocation. (1995) (213)
- LPP, the preferred fusion partner gene of HMGIC in lipomas, is a novel member of the LIM protein gene family. (1996) (207)
- Chromosome analysis of 97 primary breast carcinomas: Identification of eight karyotypic subgroups (1995) (205)
- Abnormal nuclear shape in solid tumors reflects mitotic instability. (2001) (200)
- 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)
- 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)
- The chimeric FUS/CREB3l2 gene is specific for low‐grade fibromyxoid sarcoma (2004) (188)
- Cytogenetic analysis of 57 primary prostatic adenocarcinomas (1992) (184)
- Various regions within the alpha‐helical domain of the COL1A1 gene are fused to the second exon of the PDGFB gene in dermatofibrosarcomas and giant‐cell fibroblastomas (1998) (178)
- Trisomy 7 in nonneoplastic cells (1993) (178)
- The SYT-SSX1 variant of synovial sarcoma is associated with a high rate of tumor cell proliferation and poor clinical outcome. (1999) (174)
- Cytogenetic analysis of 46 pleomorphic soft tissue sarcomas and correlation with morphologic and clinical features: A report of the CHAMP study group (1998) (169)
- Expression patterns of the human sarcoma-associated genes FUS and EWS and the genomic structure of FUS. (1996) (163)
- Fusion of the FUS and BBF2H7 genes in low grade fibromyxoid sarcoma. (2003) (160)
- Conserved mechanism of PLAG1 activation in salivary gland tumors with and without chromosome 8q12 abnormalities: identification of SII as a new fusion partner gene. (1999) (159)
- A specific translocation, t(12;14)(q14-15;q23-24), characterizes a subgroup of uterine leiomyomas. (1988) (156)
- A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications. (2002) (152)
- Genetic convergence and divergence in tumor progression. (1988) (149)
- Trisomy 7 and sex chromosome loss in human brain tissue. (1989) (147)
- 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)
- Chromosome analysis of 96 uterine leiomyomas. (1991) (138)
- 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)
- Trisomy 7, trisomy 10, and loss of the Y chromosome in short-term cultures of normal kidney tissue. (1990) (135)
- 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)
- Fusion of the FUS gene with ERG in acute myeloid leukemia with t(16;21)(p11;q22) (1994) (130)
- Chromosomal abnormalities involving 11q13 are associated with poor prognosis in patients with squamous cell carcinoma of the head and neck (1995) (128)
- Fusion of the EWSR1 and ATF1 genes without expression of the MITF‐M transcript in angiomatoid fibrous histiocytoma (2005) (123)
- Characteristic karyotypic anomalies identify subtypes of malignant fibrous histiocytoma (1989) (120)
- 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)
- Rings, dicentrics, and telomeric association in histiocytomas. (1988) (118)
- Correlation between clinicopathological features and karyotype in spindle cell sarcomas. A report of 130 cases from the CHAMP study group. (1999) (117)
- Analysis of 35 cases of localized and diffuse tenosynovial giant cell tumor: a report from the Chromosomes and Morphology (CHAMP) study group. (1999) (117)
- 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 rearrangement of the PHF1 gene in ossifying fibromyxoid tumors. (2012) (113)
- Recurrent t(16;17)(q22;p13) in aneurysmal bone cysts. (1999) (113)
- Characterization of the 12q13-15 amplicon in soft tissue tumors. (1995) (113)
- Translocation t(9;22)(q22;q12) is a primary cytogenetic abnormality in extraskeletal myxoid chondrosarcoma (1995) (112)
- 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)
- Additional evidence of a variant translocation t(12;22) with EWS/CHOP fusion in myxoid liposarcoma: clinicopathological features (1997) (110)
- 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)
- 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)
- Whole‐arm t(1;16) and i(1q) as sole anomalies identify gain of 1 q as a primary chromosomal abnormality in breast cancer (1992) (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)
- 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)
- LHFP, a novel translocation partner gene of HMGIC in a lipoma, is a member of a new family of LHFP-like genes. (1999) (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)
- Supernumerary ring chromosomes in five bone and soft tissue tumors of low or borderline malignancy. (1992) (97)
- Characterization of the CHOP breakpoints and fusion transcripts in myxoid liposarcomas with the 12;16 translocation. (1994) (97)
- Ring chromosomes in parosteal osteosarcoma contain sequences from 12q13–15: A combined cytogenetic and comparative genomic hybridization study (1996) (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)
- Chromosomal rearrangements in chondromatous tumors (1990) (95)
- MDM2 gene amplification correlates with ring chromosomes in soft tissue tumors (1994) (94)
- Reciprocal translocation t(3;12)(q27;q13) in lipoma. (1986) (94)
- Lipomas have characteristic structural chromosomal rearrangements of 12q13‐q14 (1987) (94)
- Nonrandom chromosomal rearrangements in pancreatic carcinomas (1992) (93)
- Multiple structural chromosome rearrangements, including del(7q) and del(10q), in an adenocarcinoma of the prostate. (1988) (92)
- Three major cytogenetic subgroups can be identified among chromosomally abnormal solitary lipomas (1988) (91)
- Fusion genes in angiomatoid fibrous histiocytoma. (2007) (90)
- Cytogenetic characterization of peripheral nerve sheath tumours: a report of the CHAMP study group. (2000) (89)
- Marker ring chromosome--a new cytogenetic abnormality characterizing lipogenic tumors? (1987) (88)
- Chromosome aberrations in 35 primary ovarian carcinomas (1992) (88)
- Fusion of the RBP56 and CHN genes in extraskeletal myxoid chondrosarcomas with translocation t(9;17)(q22;q11) (1999) (88)
- Exomic analysis of myxoid liposarcomas, synovial sarcomas, and osteosarcomas (2014) (88)
- Fusion, Disruption, and Expression of HMGA2 in Bone and Soft Tissue Chondromas (2003) (86)
- Chromosome analysis of 20 breast carcinomas: Cytogenetic multiclonality and karyotypic‐pathologic correlations (1993) (85)
- Cytogenetic intratumor heterogeneity in soft tissue tumors. (1994) (85)
- Karyotypic abnormalities in tumours of the pancreas. (1993) (84)
- Cytogenetic findings in 33 osteosarcomas (1993) (84)
- Chromosome aberrations in tenosynovial giant cell tumors and nontumorous synovial tissue (1993) (83)
- Identification of cytogenetic subgroups and karyotypic pathways in transitional cell carcinoma. (2001) (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)
- Recombinations of chromosomal bands 6p21 and 14q24 characterise pulmonary hamartomas. (1993) (81)
- Differentially amplified chromosome 12 sequences in low‐ and high‐grade osteosarcoma (2002) (81)
- Cytogenetic aberrations in colorectal adenocarcinomas and their correlation with clinicopathologic features (1993) (80)
- Supernumerary ring chromosome as the sole cytogenetic abnormality in a dermatofibrosarcoma protuberans. (1990) (80)
- Molecular identification of COL6A3‐CSF1 fusion transcripts in tenosynovial giant cell tumors (2008) (80)
- A novel fusion gene, SS18L1/SSX1, in synovial sarcoma (2003) (80)
- 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)
- Cytogenetic analysis of 52 colorectal carcinomas‐‐non‐random aberration pattern and correlation with pathologic parameters (1993) (78)
- Overexpression of the hepatocyte growth factor (HGF) receptor (Met) and presence of a truncated and activated intracellular HGF receptor fragment in locally aggressive/malignant human musculoskeletal tumors. (2000) (77)
- Assessment of the clinical and molecular impact of different cytogenetic subgroups in a series of 272 lipomas with abnormal karyotype (2007) (77)
- A new specific chromosomal rearrangement, t(8;16) (p11;p13), in acute monocytic leukaemia (1987) (76)
- 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)
- Chromosome abnormalities in bilateral breast carcinomas. Cytogenetic evaluation of the clonal origin of multiple primary tumors (1995) (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)
- Identification of genes differentially expressed in TLS‐CHOP carrying myxoid liposarcomas (1999) (73)
- Aberrations of chromosome segment 12q13–15 characterize a subgroup of hemangiopericytomas (1993) (72)
- Loss of chromosome band 8q24 in sporadic osteocartilaginous exostoses (1994) (71)
- Genomic Profiling of Chondrosarcoma: Chromosomal Patterns in Central and Peripheral Tumors (2009) (71)
- Cytogenetic evidence of clonality in cutaneous benign fibrous histiocytomas: a report of the CHAMP Study Group (2000) (69)
- Trisomy 21 in neoplastic cells. (2005) (67)
- Topoisomerase-II alpha is upregulated in malignant peripheral nerve sheath tumors and associated with clinical outcome. (2003) (66)
- Karyotypic characterization of urinary bladder transitional cell carcinomas (2000) (66)
- Multiple apparently unrelated clonal chromosome abnormalities in a squamous cell carcinoma of the tongue. (1988) (66)
- Cytogenetic aberrations and their prognostic impact in chondrosarcoma (2002) (65)
- Karyotypic rearrangements in 20 uterine leiomyomas. (1988) (65)
- Radiation-associated sarcomas are characterized by complex karyotypes with frequent rearrangements of chromosome arm 3p. (2000) (65)
- Variant Ph translocations in chronic myeloid leukemia. (1985) (65)
- Hibernomas are characterized by rearrangements of chromosome bands 11q13‐21 (1994) (65)
- Gene expression profiles relate to SS18/SSX fusion type in synovial sarcoma (2006) (64)
- Cytogenetic characterization of peripheral nerve sheath tumours: a report of the CHAMP study group (2000) (64)
- Cytogenetic monoclonality in multifocal uroepithelial carcinomas: evidence of intraluminal tumour seeding (1999) (64)
- 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)
- Prognostic implication of cytogenetic findings in 106 patients with non-Hodgkin lymphoma. (1987) (63)
- Characteristic sequence motifs at the breakpoints of the hybrid genes FUS/CHOP, EWS/CHOP and FUS/ERG in myxoid liposarcoma and acute myeloid leukemia (1997) (63)
- Frequent rearrangement of chromosomal bands 1p22 and 11q13 in squamous cell carcinomas of the head and neck (1990) (62)
- Bone marrow karyotype and prognosis in primary myelodysplastic syndromes (1988) (61)
- A new chromosome type replacing the double minutes in a mouse tumor. (1978) (61)
- Chromosome aberrations in 35 primary ovarian carcinomas. (1992) (60)
- Trisomy 12 in uterine leiomyomas. A new cytogenetic subgroup. (1990) (60)
- SYT-SSX is critical for cyclin D1 expression in synovial sarcoma cells: a gain of function of the t(X;18)(p11.2;q11.2) translocation. (2002) (59)
- Trisomy 12 is a consistent chromosomal aberration in benign ovarian tumors (1990) (59)
- Comparative cytogenetic study of spindle cell and pleomorphic leiomyosarcomas of soft tissues: a report from the CHAMP Study Group. (2000) (59)
- Consistent occurrence of a 19p+ marker chromosome and loss of 11p material in ovarian seropapillary cystadenocarcinomas (1989) (59)
- Chromosomal Abnormality T(9;22)(Q22;Q12) In an Extraskeletal Myxoid Chondrosarcoma Characterized By Fine Needle Aspiration Cytology, Electron Microscopy, Immunohistochemistry and Dna Flow Cytometry (1991) (58)
- Cytogenetic analysis of multifocal breast carcinomas: detection of karyotypically unrelated clones as well as clonal similarities between tumour foci. (1994) (58)
- Malignant fibrous histiocytomas with a 19p+ marker chromosome have increased relapse rate (1990) (57)
- Amplification of chromosome 1 sequences in lipomatous tumors and other sarcomas (2004) (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)
- A novel FUS/CHOP chimera in myxoid liposarcoma. (2000) (56)
- Cytogenetics and molecular genetics of bone and soft tissue tumors. (1996) (56)
- 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)
- Characteristic chromosome abnormalities, including rearrangements of 6p, del(7q), +12, and t(12;14), in 44 uterine leiomyomas (1990) (55)
- Clonal chromosome abnormalities in two liposarcomas. (1987) (55)
- Bilateral ovarian carcinoma: Cytogenetic evidence of unicentric origin (1991) (55)
- 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)
- Nonrandom numerical chromosome aberrations (+8, +11, +17, +20) in infantile fibrosarcoma. (1989) (54)
- Biallelic inactivation of TP53 rarely contributes to the development of malignant peripheral nerve sheath tumors (2001) (54)
- Ring formation and structural rearrangements of chromosome 1 as secondary changes in uterine leiomyomas with t(12;14)(q14-15;q23-24). (1988) (53)
- Cytogenetic analysis of 101 giant cell tumors of bone: Nonrandom patterns of telomeric associations and other structural aberrations (2009) (53)
- Chromosome rearrangements in synovial chondromatous lesions. (1996) (53)
- Double minute chromosomes are not centromeric regions of the host chromosomes. (2009) (53)
- Monoclonal origin of endometriotic cysts (1995) (52)
- Cytogenetic and molecular cytogenetic findings in lipoblastoma. (2008) (51)
- Two distinct FUS breakpoint clusters in myxoid liposarcoma and acute myeloid leukemia with the translocations t(12;16) and t(16;21). (1995) (51)
- Amplification of 12q13 and 12q15 sequences in a sclerosing epithelioid fibrosarcoma. (1998) (51)
- Experimental elimination and recovery of double minute chromosomes in malignant cell populations. (2009) (51)
- Genomic profiling of bone and soft tissue tumors with supernumerary ring chromosomes using tiling resolution bacterial artificial chromosome microarrays (2006) (51)
- On the significance of trisomy 7 and sex chromosome loss in renal cell carcinoma. (1990) (51)
- Characterization of the native CREB3L2 transcription factor and the FUS/CREB3L2 chimera (2007) (51)
- Generation of human cortical neurons from a new immortal fetal neural stem cell line. (2007) (50)
- 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)
- 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)
- Fusion of RDC1 with HMGA2 in lipomas as the result of chromosome aberrations involving 2q35-37 and 12q13-15. (2002) (47)
- Isochromosomes i(8q) or i(9q) in three adenocarcinomas of the lung. (1988) (47)
- Characteristic karyotypic features in lacrimal and salivary gland carcinomas. (1994) (47)
- Multiple unrelated clonal chromosome abnormalities in an in situ squamous cell carcinoma of the skin. (1988) (47)
- Multiple karyotypic rearrangements, including t(X;18)(p11;q11), in a fibrosarcoma. (1988) (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)
- Rearrangement of band q13 on both chromosomes 12 in a periosteal chondroma (1993) (45)
- Identification of p53 as a strong predictor of survival for patients with malignant peripheral nerve sheath tumors. (2009) (45)
- Multiple clonal chromosome aberrations in squamous cell carcinomas of the larynx. (1990) (44)
- Co-existence of SYT-SSX1 and SYT-SSX2 fusions in synovial sarcomas (2002) (44)
- Rearrangement of 9p13 as the primary chromosomal aberration in adenoid cystic carcinoma of the respiratory tract (1991) (44)
- Simple numerical chromosome aberrations in well-differentiated malignant epithelial tumors. (1990) (43)
- Massive cytogenetic heterogeneity in a pancreatic carcinoma: Fifty‐four karyotypically unrelated clones (1995) (43)
- Variation in C-stained chromosome regions in European hedgehogs (Insectivora, Mammalia). (2009) (43)
- Clonal chromosome aberrations in three sacral chordomas. (1994) (42)
- Localization of the chromosomal breakpoints of the t(12;16) in liposarcoma to subbands 12q13.3 and 16p11.2. (1990) (42)
- Trisomy 7 in Short‐Term Cultures of Colorectal Adenocarcinomas (1991) (42)
- Recurrent chromosome aberrations in abdominal smooth muscle tumors. (1992) (42)
- A new cytogenetic subgroup in lipomas: loss of chromosome 16 material in spindle cell and pleomorphic lipomas (2005) (41)
- Diverse chromosome abnormalities in squamous cell carcinomas of the skin. (1989) (41)
- Fusion of the HMGA2 and NFIB genes in lipoma (2005) (41)
- Characterization of chromosomal abnormalities in uroepithelial carcinomas by G‐banding, spectral karyotyping and FISH analysis (2001) (41)
- Fusions involving protein kinase C and membrane-associated proteins in benign fibrous histiocytoma. (2014) (41)
- Bone marrow karyotypes in 94 children with acute leukemia (1990) (41)
- Truncation and fusion of HMGA2 in lipomas with rearrangements of 5q32→q33 and 12q14→q15 (2005) (40)
- Trisomy 2 as the sole chromosomal abnormality in a hepatoblastoma (1992) (40)
- Cytogenetic aberrations in Ewing sarcoma: are secondary changes associated with clinical outcome? (1999) (40)
- Chromosome abnormalities are associated with unfavorable outcome in prostatic cancer patients. (1992) (40)
- Different karyotypic features characterize different clinicopathologic subgroups of benign lipogenic tumors (1988) (39)
- Cytogenetic findings in three primary hepatocellular carcinomas. (1992) (39)
- Prognostic implications of cytogenetic findings in kidney cancer. (1997) (39)
- Genetic heterogeneity in rhabdomyosarcoma revealed by SNP array analysis (2016) (39)
- 19p + marker chromosome correlates with relapse in malignant fibrous histiocytoma (1996) (39)
- New structural chromosomal rearrangements in congenital leukemia. (1987) (38)
- Chromosomal aberrations in a consecutive series of childhood rhabdomyosarcoma. (1998) (38)
- Telomere shortening and mitotic dysfunction generate cytogenetic heterogeneity in a subgroup of renal cell carcinomas (2004) (38)
- Cytogenetic analysis of four angiosarcomas from deep and superficial soft tissue. (1998) (38)
- High resolution banding analysis of the reciprocal translocation t(6;9) in acute nonlymphocytic leukemia. (1986) (38)
- Chromosome abnormalities in a pancreatic adenocarcinoma. (1989) (38)
- Complex karyotypic changes, including rearrangements of 12q13 and 14q24, in two leiomyosarcomas. (1990) (38)
- Molecular genetic characterization of the genomic ACTB-GLI fusion in pericytoma with t(7;12). (2004) (37)
- Chromosome localization of the human oncogene INT1 to 12q13 by in situ hybridization. (1988) (37)
- The t(X;6) in subungual exostosis results in transcriptional deregulation of the gene for insulin receptor substrate 4 (2011) (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)
- Chromosome rearrangements in two uterine sarcomas. (1990) (37)
- Genomic characteristics of soft tissue sarcomas (2010) (36)
- Clinical significance of genetic imbalances revealed by comparative genomic hybridization in chondrosarcomas. (1999) (36)
- Nonrandom pattern of telomeric associations in atypical lipomatous tumors with ring and giant marker chromosomes. (1998) (36)
- Double minutes in two primary adenocarcinomas of the prostate. (1989) (35)
- Chromosomal abnormalities in giant cell tumors of bone. (1991) (35)
- Unique karyotypic abnormalities in a squamous cell carcinoma of the larynx. (1988) (35)
- Different karyotypic abnormalities, t(1;6) and del(7), in two uterine leiomyomas from the same patient. (1989) (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)
- Cytogenetic analysis of upper urinary tract transitional cell carcinomas. (1999) (34)
- Trisomy 7 in nonneoplastic epithelial kidney cells. (1995) (34)
- Comparative genomic hybridization of postirradiation sarcomas (2001) (34)
- Clonal chromosome aberrations accumulate with age in upper aerodigestive tract mucosa. (1997) (34)
- Karyotypic features of malignant tumors of the nasal cavity and paranasal sinuses (1995) (34)
- Clonal structural chromosome aberrations in nonneoplastic cells of the skin and upper aerodigestive tract (1992) (33)
- RNA splicing mediated by YB‐1 is inhibited by TLS/CHOP in human myxoid liposarcoma cells (2002) (33)
- Cytogenetic analysis of short-term cultured squamous cell carcinomas of the lung. (1995) (33)
- Cytogenetics of uterine sarcomas: presentation of eight new cases and review of the literature. (1998) (32)
- Nonrandom secondary chromosome-aberrations in liposarcomas with t(12, 16). (1994) (32)
- Prognostic impact of chromosome aberrations in ovarian cancer. (1992) (32)
- Trisomy 20 is a primary chromosome aberration in desmoid tumors (1995) (32)
- Complex chromosome rearrangements in an extraabdominal desmoid tumor. (1988) (32)
- Q-, G- and C-band patterns of the mink chromosomes. (2009) (30)
- Evidence of somatic mutations in osteoarthritis (1996) (30)
- Biallelic somatic inactivation of the NF1 gene through chromosomal translocations in a sporadic neurofibroma (2005) (30)
- Analysis of the distribution and frequency of trisomy 7 in vivo in synovia from patients with osteoarthritis and pigmented villonodular synovitis. (2001) (29)
- Isolation and characterization of radiation hybrids for human chromosome 12. (1995) (29)
- Chromosomal abnormalities in two bladder carcinomas with secondary squamous cell differentiation. (1998) (29)
- Inflammatory leiomyosarcoma may be characterized by specific near‐haploid chromosome changes (1998) (29)
- Structural chromosome aberrations in a case of angioleiomyoma. (1986) (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)
- The gene for the human putative apoE receptor is on chromosome 12 in the segment q13-14. (1989) (28)
- A comparative chromosome study by means of G-, C-, and NOR-bandings of the weasel, the pygmy weasel and the stoat (Mustela, Carnivora, Mammalia). (2009) (28)
- Genomic PCR detects tumor cells in peripheral blood from patients with myxoid liposarcoma (1996) (28)
- 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)
- A novel FISH assay for SS18–SSX fusion type in synovial sarcoma (2004) (27)
- Trichorhinophalangeal syndrome type I: symptoms and signs, radiology and genetics. (1986) (27)
- Cytogenetic analysis in the examination of solid tumors in children. (1994) (27)
- Chromosomal aberrations in benign and malignant Bilharzia-associated bladder lesions analyzed by comparative genomic hybridization (2002) (27)
- Near-haploidy in two malignant fibrous histiocytomas. (1995) (27)
- Multiple cytogenetic abnormalities in a case of osteosarcoma. (1986) (27)
- Comparative cytogenetic and dna flow cytometric analysis of 150 bone and soft‐tissue tumors (1993) (27)
- Unbalanced t(1;16) as the sole karyotypic abnormality in a breast carcinoma and its lymph node metastasis. (1994) (26)
- Polyclonal expansion of cells with trisomy 7 in synovia from patients with osteoarthritis (1999) (26)
- Nonrandom secondary chromosome-aberrations in synovial sarcomas with t(x-18). (1995) (26)
- Amplification and overexpression of the hepatocyte growth factor receptor (HGFR/MET) in rat DMBA sarcomas (1999) (26)
- t(3;6;14)(p21;p21;q24) as the sole clonal chromosome abnormality in a hamartoma of the lung. (1992) (26)
- Chromosome abnormalities in leiomyosarcomas. (1988) (26)
- Combined binary ratio labeling fluorescence in situ hybridization analysis of chordoma. (2004) (26)
- Disease‐associated patterns of disomic chromosomes in hyperhaploid neoplasms (2012) (25)
- Trisomy 14 in atypical chronic myeloid leukemia. (1990) (25)
- The reciprocal translocation t(9;16)(q22;p13) is a primary chromosome abnormality in basal cell carcinomas. (1997) (25)
- Microarray analysis of gliomas reveals chromosomal position-associated gene expression patterns and identifies potential immunotherapy targets (2007) (24)
- Structural chromosomal abnormalities of 3q in myelodysplastic syndrome/acute myeloid leukaemia with Sweet's syndrome (1990) (24)
- Chromosomal evolution and tumor progression in a myxoid liposarcoma. (1990) (24)
- No amplification or rearrangement of INT1, GLI, or COL2A1 in uterine leiomyomas with t(12;14)(q14-15;q23-24). (1989) (24)
- An improved technique for short-term culturing of human prostatic adenocarcinoma tissue for cytogenetic analysis. (1990) (24)
- Retained heterodisomy is associated with high gene expression in hyperhaploid inflammatory leiomyosarcoma. (2012) (23)
- Cytogenetic studies in Hodgkin's disease. (2009) (23)
- Multiple clonal chromosome aberrations in two thymomas. (1989) (23)
- Effects of continuous trichloroethylene inhalation on different strains of mice. (2009) (23)
- Karyotypic characterization of bronchial large cell carcinomas (1994) (22)
- Cytogenetic findings in acute megakaryoblastic leukemia (ANLL-M7). (1990) (22)
- Translocation 11;19 in a mucoepidermoid tumor of the lung. (1995) (22)
- Genetic convergence during serial in vitro passage of a polyclonal squamous cell carcinoma. (1989) (21)
- Fusion of the FUS and CREB3L2 genes in a supernumerary ring chromosome in low-grade fibromyxoid sarcoma. (2010) (21)
- Chromosome analysis in 100 cases of first trimester trophoblast sampling (1985) (21)
- Tetraploid karyotype (92,XXYY) in two patients with acute lymphoblastic leukemia. (1987) (21)
- Unbalanced chromosomal rearrangements in a metastasizing salivary gland tumor with benign histology. (1998) (21)
- In situ hybridization localizes the human putative oncogene GLI to chromosome subbands 12q13.3–14.1 (1989) (20)
- Histologic—cytogenetic correlations in uterine leiomyomas (1991) (20)
- High resolution analysis of the 5q-marker chromosome in refractory anemia. (2008) (20)
- Trisomy 7 in nonneoplastic focal steatosis of the liver. (1992) (20)
- Nonrandom numerical chromosome abnormalities in basal cell carcinomas. (1998) (20)
- Variable stability of chromosomes containing amplified α-satellite sequences in human mesenchymal tumours (1999) (20)
- Cytogenetic abnormalities in an angioleiomyoma. (1989) (19)
- Multiple karyotypic abnormalities, including structural rearrangements of 11p, in cell lines from malignant melanomas. (1988) (19)
- t(6;7)(q23;p22) as the sole chromosomal anomaly in a vocal cord carcinoma. (1988) (19)
- Separate karyotypic features in a local recurrence and a metastasis of a fibrosarcoma. (1989) (19)
- Telomeric associations correlate with telomere length reduction and clonal chromosome aberrations in giant cell tumor of bone (2009) (19)
- Clonal chromosome aberrations are present in vivo in synovia and osteophytes from patients with osteoarthritis (1997) (19)
- Parathyroid adenoma with t(1;5)(p22;q32) as the sole clonal chromosome abnormality. (1990) (19)
- Clonal chromosome-aberrations in fibrocystic breast disease-associated with increased risk of cancer. (1994) (19)
- Structural chromosome aberrations in an adamantinoma. (1989) (19)
- Ring chromosomes and low-grade gene amplification in an atypical lipomatous tumor with minimal nuclear atypia. (2003) (19)
- Gene copy number changes in dermatofibrosarcoma protuberans – a fine-resolution study using array comparative genomic hybridization (2006) (19)
- Basosquamous papilloma. A benign epithelial skin tumor with multiple cytogenetic clones. (1989) (18)
- Most gene fusions in cancer are stochastic events (2019) (18)
- Clonal chromosome aberrations in a keratoacanthoma and a basal cell papilloma. (1989) (18)
- Frequent rearrangement of chromosomal bands 1p22 and 11q13 in squamous cell carcinomas of the head and neck. (1991) (18)
- 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)
- Amplification of the human putative oncogene INT1 in primary retinoblastoma tumors. (1988) (17)
- High resolution mapping of consistent leiomyoma breakpoints in chromosomes 12 and 14 to 12q15 and 14q24.1 (1990) (17)
- High resolution chromosome analysis of constitutional and acquired t(15;17) maps c-erbA to subband 17q11.2. (1986) (17)
- Karyotypic abnormalities in adenocarcinomas of the lung. (1994) (16)
- Cytogenetic heterogeneity in a clear cell hidradenoma of the skin. (1994) (16)
- Locus‐specific multifluor FISH analysis allows physical characterization of complex chromosome abnormalities in neoplasia (2000) (16)
- Translocation (2;3)(p21;p26) as the sole anomaly in a benign localized fibrous mesothelioma. (1996) (16)
- DNA copy number amplifications in sarcomas with homogeneously staining regions and double minutes. (2001) (15)
- A case of Ewing's sarcoma diagnosed by fine needle aspiration. Light microscopy, electron microscopy and chromosomal analysis. (1988) (15)
- Cytogenetic analysis of six bronchial carcinoids. (1993) (14)
- Integrative genome and transcriptome analyses reveal two distinct types of ring chromosome in soft tissue sarcomas. (2014) (14)
- Near-haploid clones in a malignant fibrous histiocytoma. (1992) (14)
- Reclassification and subtyping of so-called malignant fibrous histiocytoma of bone: comparison with cytogenetic features (2011) (14)
- Complex karyotypic anomalies, including an i(5p) marker chromosome, in malignant mixed mesodermal tumor of the ovary. (1990) (14)
- Cytogenetic heterogeneity and clonal evolution in a recurrent fibrosarcoma (1993) (14)
- Comparison of the proximal promoter regions of the PAX3 and PAX7 genes. (2007) (14)
- Localization of nucleolar organizing regions in European hedgehogs (Insectivora, Mammalia). (2009) (14)
- 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)
- Chromosomal abnormalities in inflammatory pseudotumor of the urinary bladder. (2003) (13)
- Unstable translocation (8;22) in a case of giant cell reparative granuloma. (2007) (13)
- Genetic intratumour heterogeneity in high‐grade brain tumours is associated with telomere‐dependent mitotic instability (2007) (13)
- Inversion inv(4)(p15q26) in a squamous cell carcinoma of the hypopharynx. (1988) (13)
- RNA sequencing of sarcomas with simple karyotypes: identification and enrichment of fusion transcripts (2015) (12)
- Molecular genetic characterization of the 11q13 breakpoint in a desmoplastic fibroma of bone. (2012) (12)
- Cytogenetically detected clonal heterogeneity in a duodenal adenocarcinoma. (1995) (12)
- Trisomy 7 in nonneoplastic kidney tissue cultured with and without epidermal growth factor. (1992) (12)
- Cytogenetic evolution in primary tumors, local recurrences, and pulmonary metastases of two soft tissue sarcomas (1993) (12)
- A new specific chromosomal rearrangement, t(11;20)(p15;q11), in myeloblastic leukemia with maturation. (1988) (12)
- Characterization of a hotspot region on chromosome 12 for amplification in ring chromosomes in atypical lipomatous tumors (2009) (12)
- 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)
- No rearrangements of the CHOP gene in malignant fibrous histiocytoma. (1994) (11)
- Ullrich-Noonan syndrome. (2009) (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)
- Embryonal rhabdomyosarcoma with 100 chromosomes but no structural aberrations. (1992) (11)
- Cytogenetic and quantitative DNA analysis of primary and xenografted human osteosarcomas. (1989) (11)
- The INT1 oncogene is not rearranged or amplified in lipomas with structural chromosomal abnormalities of 12q13-15. (1989) (11)
- Rearrangement of the neoplasia‐associated gene HMGIC in synovia from patients with osteoarthritis (1999) (11)
- Tetraploidization and progressive loss of 6q in a squamous cell carcinoma of the parotid gland. (1995) (10)
- Variant translocation t(3;15)(q21;q22) in a patient with acute promyelocytic leukemia. (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)
- Recurrent chromosomal imbalances in choroid plexus tumors. (1995) (10)
- Telomeric association in a malignant fibrous histiocytoma (2004) (10)
- Cytogenetic heterogeneity in a second primary radiation-induced bladder carcinoma: ten karyotypically unrelated clones. (1998) (10)
- Normal frequency of chromosome breakage in lymphocytes from patients with musculoskeletal sarcoma. (1988) (10)
- Prognostic significance of chromosome aberrations in high-grade soft tissue sarcomas. (2006) (10)
- Different patterns of clonal evolution among different sarcoma subtypes followed for up to 25 years (2018) (10)
- Trisomy 3 as the sole karyotypic change in a pediatric immature teratoma. (1998) (10)
- Cytogenetic and molecular genetic demonstration of polyclonality in an acinic cell carcinoma. (1998) (10)
- Ewing tumours and synovial sarcomas have critical features of karyotype evolution in common with epithelial tumours (2005) (10)
- Late appearing 5q--marker in refractory anemia. (1987) (9)
- Genetic characterization of bone and soft tissue tumors (2004) (9)
- A human 12p-derived cosmid hybridizing to subsets of human and chimpanzee telomeres. (1995) (9)
- Cytogenetic characterization of a periampullary adenocarcinoma of the pancreas, its liver metastasis, and a cell line established from the metastasis in a patient with Gardner's syndrome (1994) (9)
- Chromosome abnormalities in solid tumors (1989) (9)
- Musculoskeletal oncology--advances in cytogenetics and molecular genetics and their clinical implications. (1997) (9)
- Two unrelated clonal chromosome rearrangements in a nasal papilloma. (1989) (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)
- Cytogenetic analysis of inverted nasal papillomas and demonstration of genetic convergence during in vitro passaging (1997) (8)
- In vitro chromosome studies in the root vole (Microtus oeconomus). (2009) (8)
- Trisomy 5 and t(5;14)(q11;q32) as the sole abnormalities in two different clones from a centroblastic non-Hodgkin's lymphoma. (1988) (8)
- Cancer chromosome breakpoints cluster in gene‐rich genomic regions (2018) (8)
- Molecular cytogenetic characterization of an ins(4;X) occurring as the sole abnormality in an aggressive, poorly differentiated soft tissue sarcoma (2005) (8)
- Chromosome aberrations and cytogenetic intratumor heterogeneity in chondrosarcomas (2005) (8)
- A squamous cell bladder carcinoma with karyotypic abnormalities reminiscent of transitional cell carcinoma. (1989) (7)
- Clonal karyotypic evolution in a pediatric neurofibrosarcoma. (1995) (7)
- New chromosomal rearrangement, t(12;22)(p13;q12), in acute nonlymphocytic leukemia. (1991) (7)
- Inferior survival for patients with malignant peripheral nerve sheath tumors defined by aberrant TP53 (2018) (7)
- Genetic changes in bone and soft tissue tumors. (1993) (7)
- Abnormal karyotypes in three carcinomas of the gallbladder. (1994) (6)
- Soft tissue tumors: Lipoma / benign lipomatous tumors (2011) (6)
- Isolation and regional localization of cosmid linking clones from human chromosome 12. (1994) (6)
- Establishment and characterisation of a human clear cell sarcoma model in nude mice (2002) (6)
- Tiling resolution array comparative genomic hybridization analysis of a fibrosarcoma of bone. (2007) (6)
- Reciprocal translocation (11;19)(q23;p13) in congenital acute lymphoblastic leukemia. (1986) (6)
- Retained heterodisomy for chromosome 12 in atypical lipomatous tumors: implications for ring chromosome formation (2004) (6)
- Chromosome abnormalities in a carcinoma in pleomorphic adenoma of the lacrimal gland. (1991) (5)
- Increased frequency of chromosome aberrations in long-term cultured cerebrospinal fluid lymphocytes of patients with multiple sclerosis (1991) (5)
- 387 Chromosomal abnormalities involving 11Q13 are associated with poor prognosis in squamous cell carcinoma of the head and neck (1995) (5)
- Four cytogenetic subgroups can be identified in lipomas (1989) (5)
- Expression of DOL54 is not restricted to myxoid liposarcomas with the FUS-DDIT3 chimera but is found in various sarcomas. (2004) (5)
- Normal frequency of structural chromosome aberrations in fibroblasts from patients with non-Hodgkin's lymphoma. (2008) (5)
- G-and C-banded chromosomes of Tupaia chinensis (Mammalia, primates). (2009) (4)
- Constitutional C-band polymorphism in lymphocytes from patients with chronic myeloid leukemia. (2008) (4)
- Clonal chromosome aberrations accumulate with age in upper aerodigestive tract mucosa (1996) (4)
- Atypical lipomatous tumor with rare structural rearrangements involving chromosomes 8 and 12. (2005) (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)
- Identification of SII as a New Fusion Partner Gene Tumors with and without Chromosome 8 q 12 Abnormalities : Activation in Salivary Gland PLAG 1 Conserved Mechanism of Updated (1999) (3)
- Do clonal chromosome abnormalities prognosticate early relapse in Hodgkin's disease? (1988) (3)
- Normal high-resolution karyotypes in three patients with the Holt-Oram syndrome. (1987) (3)
- Cytogenetic analysis of pancreatic adenocarcinomas (1991) (3)
- Chromosome abnormalities in squamous cell carcinoma of the urethra (1998) (3)
- GLI1 (glioma-associated oncogene homolog 1) (2011) (3)
- Pseudodiploid karyotypes in adenosquamous carcinomas of the lung. (1992) (3)
- 16th European Colloqium on Animal Cytogenetics and Gene Mapping (2004) (3)
- Soft Tissue Tumors (2015) (3)
- In situ hybridization localizes the human type II alpha 1 collagen gene (COL2A1) to 12q13. (2008) (3)
- Clinical Significance of Cytogenetic Findings in Solid Tumors (1997) (2)
- Cytogenetic findings in a malignant fibrous histiocytoma of the breast. (1999) (2)
- C-Band Variation in Hypertensive Men (1985) (2)
- Erratum: Improved technique for short-term culture and cytogenetic analysis of human breast cancer (Genes Chrom Cancer 5:14-20, (1992)) (1992) (2)
- Cytogenetic findings in pediatric germ-cell tumors. (1995) (2)
- No abnormal C-band polymorphism in lung cancer patients. (2008) (2)
- Cytogenetic and single nucleotide polymorphism array findings in soft tissue tumors in infants. (2013) (2)
- ACTB (Actin, beta) (2011) (2)
- Cytogenetic analysis of basal cell carcinoma (1991) (2)
- Soft tissue tumors: Low grade fibromyxoid sarcoma (2011) (1)
- 83 The specific translocation t(12;14)(q14–15;q23–24) and other clonal chromosome rearrangements in 20 uterine leiomyomas (1989) (1)
- Clonal chromosome abnormalities in two chemodectomas (1996) (1)
- Bands involved in primary chromosome rearrangements in sarcomas are not constitutionally liable to breakage in sarcoma patients (1988) (1)
- [Cytogenetic diagnosis of tumors. Clinical significance of chromosome aberrations]. (1997) (1)
- Phyllis Jean McAlpine, Ph.D, FCCMG (1999) (1)
- Chromosomes in orthopedic tumors. (1990) (1)
- Clonal chromosome abnormalities in two chemodectomas. (1996) (1)
- Cytogenetic intra-tumor heterogenetty in three large sarcomas (1991) (1)
- Subject Index Vol. 52, 1989 (1989) (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)
- Trisomy 12 is a consistent chromosomal change in benign tumors of the ovary (1991) (1)
- Consistent occurrence of 19+ marker chromosomes in ovarian seropapillary cystadenocarcinomas (1991) (1)
- Fibrohistiocytic tumors have characteristic karyotypic anomalies which correlate with clinico-pathologic parameters (1991) (1)
- Short communication Cytogenetic and molecular cytogenetic findings in lipoblastoma (2008) (1)
- O27: Genomic profiling of bone and soft tissue tumors with supernumerary ring chromosomes using tiling resolution BAC microarrays (2005) (1)
- The MDM2 SNP309 G allele is not preferentially amplified in bone and soft tissue tumors. (2012) (1)
- Detection of recurrence and clonal evolution of ANLL-M4 by high resolution banding analysis of the unique reciprocal translocation t(6;9) in a teenager girl (1986) (1)
- Rearrangements of chromosome bands 15q12-q21 are secondary to HMGA2 deregulation in conventional lipoma. (2014) (1)
- Giemsa‐negative chromosome bands preferentially recombine in cancer‐associated translocations and gene fusions (2022) (0)
- Influence of choice of tissue culture technique on karytotypic pattern in head and neck squamous cell carcinomas (1992) (0)
- Genetic Convergence and Divergence in Tumor Progression 1 (2006) (0)
- Research Expression levels of HMGA 2 in adipocytic tumors correlate with morphologic and cytogenetic subgroups (2017) (0)
- 38th Biennial American Cytogenetics Conference (2004) (0)
- 10 Multiple cytogenetic clones in squamous cell carcinomas (1989) (0)
- Structural and numerical chromosome changes in colorectal cancer develop through telomere-mediated anaphase bridging and not through mitotic multipolarity " (2005) (0)
- Scattered genomic amplification in dedifferentiated liposarcoma (2017) (0)
- Chromosome Aberrations in Human Neoplasia (1992) (0)
- Cytogenetic Analysis of 33 Basal Cell Carcinomas 1 (2006) (0)
- Soft tissue tumors: Liposarcoma / malignant lipomatous tumors (2011) (0)
- Invited Lectures (2009) (0)
- Contents, Vol. 52, 1989 (1989) (0)
- Cytogenetic analysis of adenocarcinomas of the lung (1994) (0)
- 46 Ring chromosomes in soft tissue tumors (1987) (0)
- ISCN (2009): Important revisions and new additions to molecular methods for copy number detection for cytogenetic analysis (2009) (0)
- Call for Nomination of Members of the International Standing Committee of Human Cytogenomic Nomenclature (2018) (0)
- The prognostic implication of cytogenetic findings in non‐Hodgkin lymphomas (1986) (0)
- Loss of material from the long arm of chromosome 16 characterizes spindle cell and pleomorphic lipomas (1995) (0)
- Karyotypic characteristics of uterine leiomyoma (1991) (0)
- Subject Index Vol. 20, 1978 (1978) (0)
- Cytogenetic multiclonality in primary breast carcinomas (1992) (0)
- Multiple cytogenetically unrelated clones in short-term cultures from squamous cell carcinomas (1989) (0)
- Cytogenetics of malignant bone and soft tissue tumors (1992) (0)
- 18 Different cytogenetic subgroups among benign lipogenic tumors (1987) (0)
- Admixture of intact or lysed platelets to lymphocyte cultures results in higher chromosome aberration frequencies. (2008) (0)
- Amplification of INT1 in retinoblastomas (1989) (0)
- AbstractFour cytogenetic subgroups can be identified in lipomas (1989) (0)
- Two variants of the TLS-CHOP fusion transcript in myxoid liposarcomas with the 12;16 translocation (1994) (0)
- Pseudo- and neardiploid karyotypes in adenosquamous carcinomas of the lung (1991) (0)
- Cytogenetically unrelated clones in pancreatic carcinomas (1994) (0)
- Different patterns of clonal evolution among different sarcoma subtypes followed for up to 25 years (2018) (0)
- Samuel A. Latt, 1938–1988 (1988) (0)
- Cytogenetic characterization of a periampullary adenocarcinoma of the pancreas, its liver metastasis, and a cell line established from the metastasis and a cell line established from the metastasis in a patient with Gardner's syndrome. (1994) (0)
- syndrome typeI:symptoms andsigns, radiology andgenetics (1986) (0)
- Chromosome 5 abnormalities in large cell carcinomas of the lung (1992) (0)
- Unique Cytologic and Chromosome Aberrations in Chondroid Lipoma (2000) (0)
- The ultrastructure of fresh and cultured cells in fifteen soft tissue and bone tumors. (1992) (0)
- Tumorigenesis and Neoplastic Progression Recurrent Rearrangement of the PHF 1 Gene in Ossifying Fibromyxoid Tumors (2012) (0)
- 107 Clonal chromosome aberrations in two thymomas (1989) (0)
- Cytogenetic analysis of colon carcinomas (1991) (0)
- Brief Gene Mapping Reports A / B / C (2003) (0)
- Soft tissue tumors: Pericytoma with t(7;12) (2011) (0)
- Contents Vol. 115, 2006 (2006) (0)
- Chromosome abnormalities in mesenchymal neoplasms (1986) (0)
- Tumors of bone (2015) (0)
- Soft Tissue Tumors: Low grade fibromyxoid (2005) (0)
- Subject Index, Vol. 69, 1995 (2004) (0)
- Characteristic karyotypic features in non-squamous cell carcinomas of the head and neck (1994) (0)
- Cytogenetic aberrations in colorectal carcinomas and their correlation with survival (1992) (0)
- Cytogenetic characterization, frequency and distribution of rob t(1;29) in some Italian and Portuguese cattle breeds (2004) (0)
- Author Index / Subject Index Vol. 49, 1988 (1988) (0)
- Chop in liposarcoma, variations on a theme (1996) (0)
- Secondary chromosome aberrations in synovial sarcoma with t(X;18) (1995) (0)
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What Schools Are Affiliated With Nils Mandahl?
Nils Mandahl is affiliated with the following schools:
