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Nils Mandahl

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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TOP 3
Trombetta Domenico; Mertens Fredrik; Lonoce Angelo; D'Addabbo Pietro; Rennstam Karin; Mandahl Nils; Storlazzi Clelia Tiziana
Characterization of a hotspot region on chromosome 12 for amplification in ring chromosomes in atypical lipomatous tumors.
Brekke Helge R; Kolberg Matthias; Skotheim Rolf I; Hall Kirsten S; Bjerkehagen Bodil; Risberg Björn; Domanski Henryk A; Mandahl Nils; Liestøl Knut; Smeland Sigbjørn; Danielsen Håvard E; Mertens Fredrik; Lothe Ragnhild A
Identification of p53 as a strong predictor of survival for patients with malignant peripheral nerve sheath tumors.
Gorunova Ludmila; Vult von Steyern Fredrik; Storlazzi Clelia Tiziana; Bjerkehagen Bodil; Follerås Gunnar; Heim Sverre; Mandahl Nils; Mertens Fredrik
Cytogenetic analysis of 101 giant cell tumors of bone: nonrandom patterns of telomeric associations and other structural aberrations.

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All Publications

2009: Trombetta Domenico; Mertens Fredrik; Lonoce Angelo; D'Addabbo Pietro; Rennstam Karin; Mandahl Nils; Storlazzi Clelia Tiziana
Characterization of a hotspot region on chromosome 12 for amplification in ring chromosomes in atypical lipomatous tumors.
Genes, chromosomes & cancer 2009;48(11):993-1001.
2009: Brekke Helge R; Kolberg Matthias; Skotheim Rolf I; Hall Kirsten S; Bjerkehagen Bodil; Risberg Björn; Domanski Henryk A; Mandahl Nils; Liestøl Knut; Smeland Sigbjørn; Danielsen Håvard E; Mertens Fredrik; Lothe Ragnhild A
Identification of p53 as a strong predictor of survival for patients with malignant peripheral nerve sheath tumors.
Neuro-oncology 2009;11(5):514-28.
2009: Gorunova Ludmila; Vult von Steyern Fredrik; Storlazzi Clelia Tiziana; Bjerkehagen Bodil; Follerås Gunnar; Heim Sverre; Mandahl Nils; Mertens Fredrik
Cytogenetic analysis of 101 giant cell tumors of bone: nonrandom patterns of telomeric associations and other structural aberrations.
Genes, chromosomes & cancer 2009;48(7):583-602.
2009: Hallor Karolin H; Staaf Johan; Bovée Judith V M G; Hogendoorn Pancras C W; Cleton-Jansen Anne-Marie; Knuutila Sakari; Savola Suvi; Niini Tarja; Brosjö Otte; Bauer Henrik C F; Vult von Steyern Fredrik; Jonsson Kjell; Skorpil Mikael; Mandahl Nils; Mertens Fredrik
Genomic profiling of chondrosarcoma: chromosomal patterns in central and peripheral tumors.
Clinical cancer research : an official journal of the American Association for Cancer Research 2009;15(8):2685-94.
2009: Hallor Karolin H; Sciot Raf; Staaf Johan; Heidenblad Markus; Rydholm Anders; Bauer Henrik Cf; Aström Kristina; Domanski Henryk A; Meis Jeanne M; Kindblom Lars-Gunnar; Panagopoulos Ioannis; Mandahl Nils; Mertens Fredrik
Two genetic pathways, t(1;10) and amplification of 3p11-12, in myxoinflammatory fibroblastic sarcoma, haemosiderotic fibrolipomatous tumour, and morphologically similar lesions.
The Journal of pathology 2009;217(5):716-27.
2009: Möller Emely; Mandahl Nils; Iliszko Mariola; Mertens Fredrik; Panagopoulos Ioannis
Bidirectionality and transcriptional activity of the EWSR1 promoter region.
Oncology reports 2009;21(3):641-8.
2009: Bartuma Hammurabi; Panagopoulos Ioannis; Collin Anna; Trombetta Domenico; Domanski Henryk A; Mandahl Nils; Mertens Fredrik
Expression levels of HMGA2 in adipocytic tumors correlate with morphologic and cytogenetic subgroups.
Molecular cancer 2009;8():36.
2009: Gebre-Medhin S; Broberg K; Jonson T; Gorunova L; von Steyern F Vult; Brosjö O; Jin Y; Gisselsson D; Panagopoulos I; Mandahl N; Mertens F
Telomeric associations correlate with telomere length reduction and clonal chromosome aberrations in giant cell tumor of bone.
Cytogenetic and genome research 2009;124(2):121-7.
2008: Bartuma Hammurabi; Domanski Henryk A; Von Steyern Fredrik Vult; Kullendorff Carl-Magnus; Mandahl Nils; Mertens Fredrik
Cytogenetic and molecular cytogenetic findings in lipoblastoma.
Cancer genetics and cytogenetics 2008;183(1):60-3.
2008: Möller E; Stenman G; Mandahl N; Hamberg H; Mölne L; van den Oord J J; Brosjö O; Mertens F; Panagopoulos I
POU5F1, encoding a key regulator of stem cell pluripotency, is fused to EWSR1 in hidradenoma of the skin and mucoepidermoid carcinoma of the salivary glands.
The Journal of pathology 2008;215(1):78-86.
2008: Hallor K H; Staaf J; Jönsson G; Heidenblad M; Vult von Steyern F; Bauer H C F; Ijszenga M; Hogendoorn P C W; Mandahl N; Szuhai K; Mertens F
Frequent deletion of the CDKN2A locus in chordoma: analysis of chromosomal imbalances using array comparative genomic hybridisation.
British journal of cancer 2008;98(2):434-42.
2008: Panagopoulos Ioannis; Mertens Fredrik; Löfvenberg Richard; Mandahl Nils
Fusion of the COL1A1 and USP6 genes in a benign bone tumor.
Cancer genetics and cytogenetics 2008;180(1):70-3.
2008: Möller Emely; Mandahl Nils; Mertens Fredrik; Panagopoulos Ioannis
Molecular identification of COL6A3-CSF1 fusion transcripts in tenosynovial giant cell tumors.
Genes, chromosomes & cancer 2008;47(1):21-5.
2007: Mertens Fredrik; Wiebe Thomas; Adlercreutz Catharina; Mandahl Nils; French Christopher A
Successful treatment of a child with t(15;19)-positive tumor.
Pediatric blood & cancer 2007;49(7):1015-7.
2007: Möller Emely; Isaksson Margareth; Mandahl Nils; Mertens Fredrik; Panagopoulos Ioannis
Comparison of the proximal promoter regions of the PAX3 and PAX7 genes.
Cancer genetics and cytogenetics 2007;178(2):114-9.
2007: Persson Oscar; Krogh Morten; Saal Lao H; Englund Elisabet; Liu Jian; Parsons Ramon; Mandahl Nils; Borg Ake; Widegren Bengt; Salford Leif G
Microarray analysis of gliomas reveals chromosomal position-associated gene expression patterns and identifies potential immunotherapy targets.
Journal of neuro-oncology 2007;85(1):11-24.
2007: Johnsson Anna; Collin Anna; Rydholm Anders; Domanski Henryk A; Mertens Fredrik; Mandahl Nils
Unstable translocation (8;22) in a case of giant cell reparative granuloma.
Cancer genetics and cytogenetics 2007;177(1):59-63.
2007: Glanz C; Rebetz J; Stewénius Y; Persson A; Englund E; Mandahl N; Mertens F; Salford L G; Widegren B; Fan X; Gisselsson D
Genetic intratumour heterogeneity in high-grade brain tumours is associated with telomere-dependent mitotic instability.
Neuropathology and applied neurobiology 2007;33(4):440-54.
2007: Bartuma Hammurabi; Hallor Karolin H; Panagopoulos Ioannis; Collin Anna; Rydholm Anders; Gustafson Pelle; Bauer Henrik C F; Brosjö Otte; Domanski Henryk A; Mandahl Nils; Mertens Fredrik
Assessment of the clinical and molecular impact of different cytogenetic subgroups in a series of 272 lipomas with abnormal karyotype.
Genes, chromosomes & cancer 2007;46(6):594-606.
2007: Hallor Karolin H; Micci Francesca; Meis-Kindblom Jeanne M; Kindblom Lars-Gunnar; Bacchini Patrizia; Mandahl Nils; Mertens Fredrik; Panagopoulos Ioannis
Fusion genes in angiomatoid fibrous histiocytoma.
Cancer letters 2007;251(1):158-63.
2007: Panagopoulos Ioannis; Möller Emely; Dahlén Anna; Isaksson Margareth; Mandahl Nils; Vlamis-Gardikas Alexios; Mertens Fredrik
Characterization of the native CREB3L2 transcription factor and the FUS/CREB3L2 chimera.
Genes, chromosomes & cancer 2007;46(2):181-91.
2007: Hallor Karolin H; Heidenblad Markus; Brosjö Otte; Mandahl Nils; Mertens Fredrik
Tiling resolution array comparative genomic hybridization analysis of a fibrosarcoma of bone.
Cancer genetics and cytogenetics 2007;172(1):80-3.
2006: Heidenblad M; Hallor K H; Staaf J; Jönsson G; Borg A; Höglund M; Mertens F; Mandahl N
Genomic profiling of bone and soft tissue tumors with supernumerary ring chromosomes using tiling resolution bacterial artificial chromosome microarrays.
Oncogene 2006;25(53):7106-16.
2006: Storlazzi C T; Brekke H R; Mandahl N; Brosjö O; Smeland S; Lothe R A; Mertens F
Identification of a novel amplicon at distal 17q containing the BIRC5/SURVIVIN gene in malignant peripheral nerve sheath tumours.
The Journal of pathology 2006;209(4):492-500.
2006: Storlazzi Clelia Tiziana; Wozniak Agnieszka; Panagopoulos Ioannis; Sciot Raf; Mandahl Nils; Mertens Fredrik; Debiec-Rychter Maria
Rearrangement of the COL12A1 and COL4A5 genes in subungual exostosis: molecular cytogenetic delineation of the tumor-specific translocation t(X;6)(q13-14;q22).
International journal of cancer. Journal international du cancer 2006;118(8):1972-6.
2006: Panagopoulos Ioannis; Nilsson Therese; Domanski Henryk A; Isaksson Margareth; Lindblom Pia; Mertens Fredrik; Mandahl Nils
Fusion of the SEC31L1 and ALK genes in an inflammatory myofibroblastic tumor.
International journal of cancer. Journal international du cancer 2006;118(5):1181-6.
2006: Fernebro Josefin; Francis Princy; Edén Patrik; Borg Ake; Panagopoulos Ioannis; Mertens Fredrik; Vallon-Christersson Johan; Akerman Måns; Rydholm Anders; Bauer Henrik C F; Mandahl Nils; Nilbert Mef
Gene expression profiles relate to SS18/SSX fusion type in synovial sarcoma.
International journal of cancer. Journal international du cancer 2006;118(5):1165-72.
2006: Mertens Fredrik; Strömberg Ulf; Rydholm Anders; Gustafson Pelle; Bauer Henrik C F; Brosjö Otte; Mandahl Nils
Prognostic significance of chromosome aberrations in high-grade soft tissue sarcomas.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2006;24(2):315-20.
2006: Schaad K; Strömbeck B; Mandahl N; Andersen M K; Heim S; Mertens F; Johansson B
FISH mapping of i(7q) in acute leukemias and myxoid liposarcoma reveals clustered breakpoints in 7p11.2: implications for formation and pathogenetic outcome of the idic(7)(p11.2).
Cytogenetic and genome research 2006;114(2):126-30.
2006: Nilsson M; Mertens F; Höglund M; Mandahl N; Panagopoulos I
Truncation and fusion of HMGA2 in lipomas with rearrangements of 5q32-->q33 and 12q14-->q15.
Cytogenetic and genome research 2006;112(1-2):60-6.
2005: Storlazzi Clelia Tiziana; Von Steyern Fredrik Vult; Domanski Henryk A; Mandahl Nils; Mertens Fredrik
Biallelic somatic inactivation of the NF1 gene through chromosomal translocations in a sporadic neurofibroma.
International journal of cancer. Journal international du cancer 2005;117(6):1055-7.
2005: Nilsson M; Panagopoulos I; Mertens F; Mandahl N
Fusion of the HMGA2 and NFIB genes in lipoma.
Virchows Archiv : an international journal of pathology 2005;447(5):855-8.
2005: Surace Cecilia; Storlazzi Clelia Tiziana; Engellau Jacob; Domanski Henryk A; Gustafson Pelle; Panagopoulos Ioannis; D'Addabbo Pietro; Rocchi Mariano; Mandahl Nils; Mertens Fredrik
Molecular cytogenetic characterization of an ins(4;X) occurring as the sole abnormality in an aggressive, poorly differentiated soft tissue sarcoma.
Virchows Archiv : an international journal of pathology 2005;447(5):869-74.
2005: Hallor Karolin Hansén; Mertens Fredrik; Jin Yuesheng; Meis-Kindblom Jeanne M; Kindblom Lars-Gunnar; Behrendtz Mikael; Kalén Anders; Mandahl Nils; Panagopoulos Ioannis
Fusion of the EWSR1 and ATF1 genes without expression of the MITF-M transcript in angiomatoid fibrous histiocytoma.
Genes, chromosomes & cancer 2005;44(1):97-102.
2005: Höglund Mattias; Gisselsson David; Mandahl Nils; Mitelman Felix
Ewing tumours and synovial sarcomas have critical features of karyotype evolution in common with epithelial tumours.
International journal of cancer. Journal international du cancer 2005;116(3):401-6.
2005: Stewénius Ylva; Gorunova Ludmila; Jonson Tord; Larsson Nina; Höglund Mattias; Mandahl Nils; Mertens Fredrik; Mitelman Felix; Gisselsson David
Structural and numerical chromosome changes in colon cancer develop through telomere-mediated anaphase bridges, not through mitotic multipolarity.
Proceedings of the National Academy of Sciences of the United States of America 2005;102(15):5541-6.
2005: Nilsson Malin; Domanski Henryk; Mertens Fredrik; Mandahl Nils
Atypical lipomatous tumor with rare structural rearrangements involving chromosomes 8 and 12.
Oncology reports 2005;13(4):649-52.
2005: Mertens Fredrik; Fletcher Christopher D M; Antonescu Cristina R; Coindre Jean-Michel; Colecchia Maurizio; Domanski Henryk A; Downs-Kelly Erinn; Fisher Cyril; Goldblum John R; Guillou Louis; Reid Robin; Rosai Juan; Sciot Raf; Mandahl Nils; Panagopoulos Ioannis
Clinicopathologic and molecular genetic characterization of low-grade fibromyxoid sarcoma, and cloning of a novel FUS/CREB3L1 fusion gene.
Laboratory investigation; a journal of technical methods and pathology 2005;85(3):408-15.
2005: Panagopoulos Ioannis; Mertens Fredrik; Isaksson Margareth; Mandahl Nils
Absence of mutations of the BRAF gene in malignant melanoma of soft parts (clear cell sarcoma of tendons and aponeuroses).
Cancer genetics and cytogenetics 2005;156(1):74-6.
2004: Dahlén Anna; Mertens Fredrik; Mandahl Nils; Panagopoulos Ioannis
Molecular genetic characterization of the genomic ACTB-GLI fusion in pericytoma with t(7;12).
Biochemical and biophysical research communications 2004;325(4):1318-23.
2004: Nilsson Malin; Domanski Henryk A; Mertens Fredrik; Mandahl Nils
Molecular cytogenetic characterization of recurrent translocation breakpoints in bizarre parosteal osteochondromatous proliferation (Nora's lesion).
Human pathology 2004;35(9):1063-9.
2004: Surace Cecilia; Panagopoulos Ioannis; Pålsson Eva; Rocchi Mariano; Mandahl Nils; Mertens Fredrik
A novel FISH assay for SS18-SSX fusion type in synovial sarcoma.
Laboratory investigation; a journal of technical methods and pathology 2004;84(9):1185-92.
2004: Panagopoulos Ioannis; Mertens Fredrik; Isaksson Margareth; Mandahl Nils
Expression of DOL54 is not restricted to myxoid liposarcomas with the FUS-DDIT3 chimera but is found in various sarcomas.
Oncology reports 2004;12(1):107-10.
2004: Gisselsson D; Gorunova L; Höglund M; Mandahl N; Elfving P
Telomere shortening and mitotic dysfunction generate cytogenetic heterogeneity in a subgroup of renal cell carcinomas.
British journal of cancer 2004;91(2):327-32.
2004: Panagopoulos Ioannis; Storlazzi Clelia Tiziana; Fletcher Christopher D M; Fletcher Jonathan A; Nascimento Antonio; Domanski Henryk A; Wejde Johan; Brosjö Otte; Rydholm Anders; Isaksson Margareth; Mandahl Nils; Mertens Fredrik
The chimeric FUS/CREB3l2 gene is specific for low-grade fibromyxoid sarcoma.
Genes, chromosomes & cancer 2004;40(3):218-28.
2004: Kuzniacka Alina; Mertens Fredrik; Strömbeck Bodil; Wiegant Joop; Mandahl Nils
Combined binary ratio labeling fluorescence in situ hybridization analysis of chordoma.
Cancer genetics and cytogenetics 2004;151(2):178-81.
2004: Dahlén Anna; Fletcher Christopher D M; Mertens Fredrik; Fletcher Jonathan A; Perez-Atayde Antonio R; Hicks M John; Debiec-Rychter Maria; Sciot Raf; Wejde Johan; Wedin Rikard; Mandahl Nils; Panagopoulos Ioannis
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).
The American journal of pathology 2004;164(5):1645-53.
2004: Mandahl N; Mertens F; Panagopoulos I; Knuutila S
Genetic characterization of bone and soft tissue tumors.
Acta orthopaedica Scandinavica. Supplementum 2004;75(311):21-8.
2004: Nilsson Malin; Meza-Zepeda Leonardo A; Mertens Fredrik; Forus Anne; Myklebost Ola; Mandahl Nils
Amplification of chromosome 1 sequences in lipomatous tumors and other sarcomas.
International journal of cancer. Journal international du cancer 2004;109(3):363-9.
2004: Gisselsson David; Pålsson Eva; Yu Christina; Mertens Fredrik; Mandahl Nils
Mitotic instability associated with late genomic changes in bone and soft tissue tumours.
Cancer letters 2004;206(1):69-76.
2004: Mertens F; Panagopoulos I; Jonson T; Gisselsson D; Isaksson M; Domanski H A; Mandahl N
Retained heterodisomy for chromosome 12 in atypical lipomatous tumors: implications for ring chromosome formation.
Cytogenetic and genome research 2004;106(1):33-8.
2003: Skotheim Rolf I; Kallioniemi Anne; Bjerkhagen Bodil; Mertens Fredrik; Brekke Helge R; Monni Outi; Mousses Spyro; Mandahl Nils; Soeter Gunnar; Nesland Jahn M; Smeland Sigbjørn; Kallioniemi Olli-P; Lothe Ragnhild A
Topoisomerase-II alpha is upregulated in malignant peripheral nerve sheath tumors and associated with clinical outcome.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2003;21(24):4586-91.
2003: Dahlén Anna; Mertens Fredrik; Rydholm Anders; Brosjö Otte; Wejde Johan; Mandahl Nils; Panagopoulos Ioannis
Fusion, disruption, and expression of HMGA2 in bone and soft tissue chondromas.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2003;16(11):1132-40.
2003: Storlazzi Clelia Tiziana; Mertens Fredrik; Nascimento Antonio; Isaksson Margareth; Wejde Johan; Brosjo Otte; Mandahl Nils; Panagopoulos Ioannis
Fusion of the FUS and BBF2H7 genes in low grade fibromyxoid sarcoma.
Human molecular genetics 2003;12(18):2349-58.
2003: Storlazzi Clelia Tiziana; Mertens Fredrik; Domanski Henryk; Fletcher Christopher D M; Wiegant Joop; Mandahl Nils
Ring chromosomes and low-grade gene amplification in an atypical lipomatous tumor with minimal nuclear atypia.
International journal of oncology 2003;23(1):67-71.
2003: Fadl-Elmula Imad; Gorunova Ludmila; Mandahl Nils; Heim Sverre
Chromosomal abnormalities in inflammatory pseudotumor of the urinary bladder.
Cancer genetics and cytogenetics 2003;143(2):169-71.
2003: Storlazzi Clelia Tiziana; Mertens Fredrik; Mandahl Nils; Gisselsson David; Isaksson Margareth; Gustafson Pelle; Domanski Henryk A; Panagopoulos Ioannis
A novel fusion gene, SS18L1/SSX1, in synovial sarcoma.
Genes, chromosomes & cancer 2003;37(2):195-200.
2003: Dahlén Anna; Debiec-Rychter Maria; Pedeutour Florence; Domanski Henryk A; Höglund Mattias; Bauer Henrik C F; Rydholm Anders; Sciot Raf; Mandahl Nils; Mertens Fredrik
Clustering of deletions on chromosome 13 in benign and low-malignant lipomatous tumors.
International journal of cancer. Journal international du cancer 2003;103(5):616-23.
2002: Panagopoulos Ioannis; Mertens Fredrik; Isaksson Margareth; Domanski Henryk A; Brosjö Otte; Heim Sverre; Bjerkehagen Bodil; Sciot Raf; Dal Cin Paola; Fletcher Jonathan A; Fletcher Christopher D M; Mandahl Nils
Molecular genetic characterization of the EWS/CHN and RBP56/CHN fusion genes in extraskeletal myxoid chondrosarcoma.
Genes, chromosomes & cancer 2002;35(4):340-52.
2002: Nilsson M; Höglund M; Panagopoulos I; Sciot R; Dal Cin P; Debiec-Rychter M; Mertens F; Mandahl N
Molecular cytogenetic mapping of recurrent chromosomal breakpoints in tenosynovial giant cell tumors.
Virchows Archiv : an international journal of pathology 2002;441(5):475-80.
2002: Crnalic Sead; Panagopoulos Ioannis; Boquist Lennart; Mandahl Nils; Stenling Roger; Löfvenberg Richard
Establishment and characterisation of a human clear cell sarcoma model in nude mice.
International journal of cancer. Journal international du cancer 2002;101(6):505-11.
2002: Broberg Karin; Zhang Miao; Strömbeck Bodil; Isaksson Margareth; Nilsson Malin; Mertens Fredrik; Mandahl Nils; Panagopoulos Ioannis
Fusion of RDC1 with HMGA2 in lipomas as the result of chromosome aberrations involving 2q35-37 and 12q13-15.
International journal of oncology 2002;21(2):321-6.
2002: Rapp Timothy B; Yang Liu; Conrad Ernest U; Mandahl Nils; Chansky Howard A
RNA splicing mediated by YB-1 is inhibited by TLS/CHOP in human myxoid liposarcoma cells.
Journal of orthopaedic research : official publication of the Orthopaedic Research Society 2002;20(4):723-9.
2002: Mertens Fredrik; Strömberg Ulf; Mandahl Nils; Dal Cin Paola; De Wever Ivo; Fletcher Christopher D M; Mitelman Felix; Rosai Juan; Rydholm Anders; Sciot Raf; Tallini Giovanni; Van Den Berghe Herman; Vanni Roberta; Willén Helena
Prognostically important chromosomal aberrations in soft tissue sarcomas: a report of the Chromosomes and Morphology (CHAMP) Study Group.
Cancer research 2002;62(14):3980-4.
2002: Gisselsson D; Jonson T; Yu C; Martins C; Mandahl N; Wiegant J; Jin Y; Mertens F; Jin C
Centrosomal abnormalities, multipolar mitoses, and chromosomal instability in head and neck tumours with dysfunctional telomeres.
British journal of cancer 2002;87(2):202-7.
2002: Xie Yuntao; Skytting Björn; Nilsson Gunnar; Gasbarri Alessandra; Haslam Karl; Bartolazzi Armando; Brodin Bertha; Mandahl Nils; Larsson Olle
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.
Cancer research 2002;62(13):3861-7.
2002: Yang Ke; Lui Weng-Onn; Xie Yuntao; Zhang Anju; Skytting Björn; Mandahl Nils; Larsson Catharina; Larsson Olle
Co-existence of SYT-SSX1 and SYT-SSX2 fusions in synovial sarcomas.
Oncogene 2002;21(26):4181-90.
2002: Panagopoulos Ioannis; Mertens Fredrik; Dêbiec-Rychter Maria; Isaksson Margareth; Limon Janusz; Kardas Iwona; Domanski Henryk A; Sciot Raf; Perek Danuta; Crnalic Sead; Larsson Olle; Mandahl Nils
Molecular genetic characterization of the EWS/ATF1 fusion gene in clear cell sarcoma of tendons and aponeuroses.
International journal of cancer. Journal international du cancer 2002;99(4):560-7.
2002: Fadl-Elmula Imad; Kytola Soili; Leithy Mona E L; Abdel-Hameed Mohamed; Mandahl Nils; Elagib Atif; Ibrahim Muntaser; Larsson Catharina; Heim Sverre
Chromosomal aberrations in benign and malignant bilharzia-associated bladder lesions analyzed by comparative genomic hybridization.
BMC cancer 2002;2():5.
2002: Mandahl Nils; Gustafson Pelle; Mertens Fredrik; Akerman Måns; Baldetorp Bo; Gisselsson David; Knuutila Sakari; Bauer Henrik C F; Larsson Olle
Cytogenetic aberrations and their prognostic impact in chondrosarcoma.
Genes, chromosomes & cancer 2002;33(2):188-200.
2002: Gisselsson David; Pålsson Eva; Höglund Mattias; Domanski Henryk; Mertens Fredrik; Pandis Nikos; Sciot Raf; Dal Cin Paola; Bridge Julia A; Mandahl Nils
Differentially amplified chromosome 12 sequences in low- and high-grade osteosarcoma.
Genes, chromosomes & cancer 2002;33(2):133-40.
2002: Tallini Giovanni; Dorfman Howard; Brys Peter; Dal Cin Paola; De Wever Ivo; Fletcher Christopher D M; Jonson Kjell; Mandahl Nils; Mertens Fredrik; Mitelman Felix; Rosai Juan; Rydholm Anders; Samson Ignace; Sciot Raf; Van den Berghe Herman; Vanni Roberta; Willén Helena
Correlation between clinicopathological features and karyotype in 100 cartilaginous and chordoid tumours. A report from the Chromosomes and Morphology (CHAMP) Collaborative Study Group.
The Journal of pathology 2002;196(2):194-203.
2001: Dahlén A; Broberg K; Domanski H A; Toksvig-Larsen S; Lindstrand A; Mandahl N; Mertens F
Analysis of the distribution and frequency of trisomy 7 in vivo in synovia from patients with osteoarthritis and pigmented villonodular synovitis.
Cancer genetics and cytogenetics 2001;131(1):19-24.
2001: Höglund M; Säll T; Heim S; Mitelman F; Mandahl N; Fadl-Elmula I
Identification of cytogenetic subgroups and karyotypic pathways in transitional cell carcinoma.
Cancer research 2001;61(22):8241-6.
2001: Gisselsson D; Jonson T; Petersén A; Strömbeck B; Dal Cin P; Höglund M; Mitelman F; Mertens F; Mandahl N
Telomere dysfunction triggers extensive DNA fragmentation and evolution of complex chromosome abnormalities in human malignant tumors.
Proceedings of the National Academy of Sciences of the United States of America 2001;98(22):12683-8.
2001: Panagopoulos I; Mertens F; Domanski H A; Isaksson M; Brosjö O; Gustafson P; Mandahl N
No EWS/FLI1 fusion transcripts in giant-cell tumors of bone.
International journal of cancer. Journal international du cancer 2001;93(6):769-72.
2001: Panagopoulos I; Mertens F; Isaksson M; Limon J; Gustafson P; Skytting B; Akerman M; Sciot R; Dal Cin P; Samson I; Iliszko M; Ryoe J; Dêbiec-Rychter M; Szadowska A; Brosjö O; Larsson O; Rydholm A; Mandahl N
Clinical impact of molecular and cytogenetic findings in synovial sarcoma.
Genes, chromosomes & cancer 2001;31(4):362-72.
2001: Fadl-Elmula I; Kytölä S; Pan Y; Lui W O; Derienzo G; Forsberg L; Mandahl N; Gorunova L; Bergerheim U S; Heim S; Larsson C
Characterization of chromosomal abnormalities in uroepithelial carcinomas by G-banding, spectral karyotyping and FISH analysis.
International journal of cancer. Journal international du cancer 2001;92(6):824-31.
2001: Höglund M; Gisselsson D; Mandahl N; Johansson B; Mertens F; Mitelman F; Säll T
Multivariate analyses of genomic imbalances in solid tumors reveal distinct and converging pathways of karyotypic evolution.
Genes, chromosomes & cancer 2001;31(2):156-71.
2001: Lothe R A; Smith-Sørensen B; Hektoen M; Stenwig A E; Mandahl N; Saeter G; Mertens F
Biallelic inactivation of TP53 rarely contributes to the development of malignant peripheral nerve sheath tumors.
Genes, chromosomes & cancer 2001;30(2):202-6.
2001: Gisselsson D; Björk J; Höglund M; Mertens F; Dal Cin P; Akerman M; Mandahl N
Abnormal nuclear shape in solid tumors reflects mitotic instability.
The American journal of pathology 2001;158(1):199-206.
2000: Panagopoulos I; Mertens F; Isaksson M; Mandahl N
A novel FUS/CHOP chimera in myxoid liposarcoma.
Biochemical and biophysical research communications 2000;279(3):838-45.
2000: Sciot R; Dorfman H; Brys P; Dal Cin P; De Wever I; Fletcher C D; Jonson K; Mandahl N; Mertens F; Mitelman F; Rosai J; Rydholm A; Samson I; Tallini G; Van den Berghe H; Vanni R; Willén H
Cytogenetic-morphologic correlations in aneurysmal bone cyst, giant cell tumor of bone and combined lesions. A report from the CHAMP study group.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2000;13(11):1206-10.
2000: Fadl-Elmula I; Gorunova L; Mandahl N; Elfving P; Lundgren R; Mitelman F; Heim S
Karyotypic characterization of urinary bladder transitional cell carcinomas.
Genes, chromosomes & cancer 2000;29(3):256-65.
2000: Dal Cin P; Sciot R; Brys P; De Wever I; Dorfman H; Fletcher C D; Jonsson K; Mandahl N; Mertens F; Mitelman F; Rosai J; Rydholm A; Samson I; Tallini G; Van den Berghe H; Vanni R; Willen H
Recurrent chromosome aberrations in fibrous dysplasia of the bone: a report of the CHAMP study group. CHromosomes And MorPhology.
Cancer genetics and cytogenetics 2000;122(1):30-2.
2000: De Wever I; Dal Cin P; Fletcher C D; Mandahl N; Mertens F; Mitelman F; Rosai J; Rydholm A; Sciot R; Tallini G; Van Den Berghe H; Vanni R; Willén H
Cytogenetic, clinical, and morphologic correlations in 78 cases of fibromatosis: a report from the CHAMP Study Group. CHromosomes And Morphology.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2000;13(10):1080-5.
2000: Gisselsson D; Mandahl N; Pålsson E; Gorunova L; Höglund M
Locus-specific multifluor FISH analysis allows physical characterization of complex chromosome abnormalities in neoplasia.
Genes, chromosomes & cancer 2000;28(3):347-52.
2000: Gisselsson D; Pettersson L; Höglund M; Heidenblad M; Gorunova L; Wiegant J; Mertens F; Dal Cin P; Mitelman F; Mandahl N
Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity.
Proceedings of the National Academy of Sciences of the United States of America 2000;97(10):5357-62.
2000: Mertens F; Dal Cin P; De Wever I; Fletcher C D; Mandahl N; Mitelman F; Rosai J; Rydholm A; Sciot R; Tallini G; van Den Berghe H; Vanni R; Willén H
Cytogenetic characterization of peripheral nerve sheath tumours: a report of the CHAMP study group.
The Journal of pathology 2000;190(1):31-8.
2000: Mertens F; Larramendy M; Gustavsson A; Gisselsson D; Rydholm A; Brosjö O; Mitelman F; Knuutila S; Mandahl N
Radiation-associated sarcomas are characterized by complex karyotypes with frequent rearrangements of chromosome arm 3p.
Cancer genetics and cytogenetics 2000;116(2):89-96.
2000: Mandahl N; Fletcher C D; Dal Cin P; De Wever I; Mertens F; Mitelman F; Rosai J; Rydholm A; Sciot R; Tallini G; Van Den Berghe H; Vanni R; Willén H
Comparative cytogenetic study of spindle cell and pleomorphic leiomyosarcomas of soft tissues: a report from the CHAMP Study Group.
Cancer genetics and cytogenetics 2000;116(1):66-73.
1999: Panagopoulos I; Mencinger M; Dietrich C U; Bjerkehagen B; Saeter G; Mertens F; Mandahl N; Heim S
Fusion of the RBP56 and CHN genes in extraskeletal myxoid chondrosarcomas with translocation t(9;17)(q22;q11).
Oncogene 1999;18(52):7594-8.
1999: Fadl-Elmula I; Gorunova L; Mandahl N; Elfving P; Lundgren R; Rademark C; Heim S
Cytogenetic analysis of upper urinary tract transitional cell carcinomas.
Cancer genetics and cytogenetics 1999;115(2):123-7.
1999: Gisselsson D; Domanski H A; Höglund M; Carlén B; Mertens F; Willén H; Mandahl N
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.
The American journal of surgical pathology 1999;23(10):1300-4.
1999: Berner J M; Sørlie T; Mertens F; Henriksen J; Saeter G; Mandahl N; Brøgger A; Myklebost O; Lothe R A
Chromosome band 9p21 is frequently altered in malignant peripheral nerve sheath tumors: studies of CDKN2A and other genes of the pRB pathway.
Genes, chromosomes & cancer 1999;26(2):151-60.
1999: Gisselsson D; Höglund M; Mertens F; Mandahl N
Variable stability of chromosomes containing amplified alpha-satellite sequences in human mesenchymal tumours.
Chromosoma 1999;108(5):271-7.
1999: Fadl-Elmula I; Gorunova L; Mandahl N; Elfving P; Lundgren R; Mitelman F; Heim S
Cytogenetic monoclonality in multifocal uroepithelial carcinomas: evidence of intraluminal tumour seeding.
British journal of cancer 1999;81(1):6-12.
1999: Thelin-Järnum S; Lassen C; Panagopoulos I; Mandahl N; Aman P
Identification of genes differentially expressed in TLS-CHOP carrying myxoid liposarcomas.
International journal of cancer. Journal international du cancer 1999;83(1):30-3.
1999: Nilsson G; Skytting B; Xie Y; Brodin B; Perfekt R; Mandahl N; Lundeberg J; Uhlén M; Larsson O
The SYT-SSX1 variant of synovial sarcoma is associated with a high rate of tumor cell proliferation and poor clinical outcome.
Cancer research 1999;59(13):3180-4.
1999: Gisselsson D; Höglund M; Mertens F; Dal Cin P; Mandahl N
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.
The American journal of pathology 1999;155(1):61-6.
1999: Mandahl N; Mertens F; Mitelman F
Genetic changes in bone and soft tissue tumors.
Acta orthopaedica Scandinavica. Supplementum 1999;285():30-40.
1999: Sciot R; Rosai J; Dal Cin P; de Wever I; Fletcher C D; Mandahl N; Mertens F; Mitelman F; Rydholm A; Tallini G; van den Berghe H; Vanni R; Willén H
Analysis of 35 cases of localized and diffuse tenosynovial giant cell tumor: a report from the Chromosomes and Morphology (CHAMP) study group.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 1999;12(6):576-9.
1999: Petit M M; Schoenmakers E F; Huysmans C; Geurts J M; Mandahl N; Van de Ven W J
LHFP, a novel translocation partner gene of HMGIC in a lipoma, is a member of a new family of LHFP-like genes.
Genomics 1999;57(3):438-41.
1999: Gisselsson D; Höglund M; Mertens F; Johansson B; Dal Cin P; Van den Berghe H; Earnshaw W C; Mitelman F; Mandahl N
The structure and dynamics of ring chromosomes in human neoplastic and non-neoplastic cells.
Human genetics 1999;104(4):315-25.
1999: Broberg K; Höglund M; Limon J; Lindstrand A; Toksvig-Larsen S; Mandahl N; Mertens F
Rearrangement of the neoplasia-associated gene HMGIC in synovia from patients with osteoarthritis.
Genes, chromosomes & cancer 1999;24(3):278-82.
1999: Kullendorff C M; Mertens F; Donnér M; Wiebe T; Akerman M; Mandahl N
Cytogenetic aberrations in Ewing sarcoma: are secondary changes associated with clinical outcome?
Medical and pediatric oncology 1999;32(2):79-83.
1998: Gisselsson D; Andreasson P; Meis-Kindblom J M; Kindblom L G; Mertens F; Mandahl N
Amplification of 12q13 and 12q15 sequences in a sclerosing epithelioid fibrosarcoma.
Cancer genetics and cytogenetics 1998;107(2):102-6.
1998: Gisselsson D; Höglund M; O'Brien K P; Dumanski J P; Mertens F; Mandahl N
A case of dermatofibrosarcoma protuberans with a ring chromosome 5 and a rearranged chromosome 22 containing amplified COL1A1 and PDGFB sequences.
Cancer letters 1998;133(2):129-34.
1998: Gisselsson D; Höglund M; Mertens F; Mitelman F; Mandahl N
Chromosomal organization of amplified chromosome 12 sequences in mesenchymal tumors detected by fluorescence in situ hybridization.
Genes, chromosomes & cancer 1998;23(3):203-12.
1998: O'Brien K P; Seroussi E; Dal Cin P; Sciot R; Mandahl N; Fletcher J A; Turc-Carel C; Dumanski J P
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.
Genes, chromosomes & cancer 1998;23(2):187-93.
1998: Mertens F; Kullendorff C M; Moëll C; Alumets J; Mandahl N
Complex karyotype in a childhood adrenocortical carcinoma.
Cancer genetics and cytogenetics 1998;105(2):190-2.
1998: Fadl-Elmula I; Bonaldi L; Gorunova L; Mandahl N; Elfving P; Heim S
Cytogenetic heterogeneity in a second primary radiation-induced bladder carcinoma: ten karyotypically unrelated clones.
Cancer genetics and cytogenetics 1998;105(2):134-7.
1998: Fadl-Elmula I; Gorunova L; Mandahl N; Elfving P; Heim S
Chromosome abnormalities in squamous cell carcinoma of the urethra.
Genes, chromosomes & cancer 1998;23(1):72-3.
1998: Jin C; Jin Y; Höglund M; Wennerberg J; Akervall J; Willén R; Dictor M; Mandahl N; Mitelman F; Mertens F
Cytogenetic and molecular genetic demonstration of polyclonality in an acinic cell carcinoma.
British journal of cancer 1998;78(3):292-5.
1998: Jin Y; Höglund M; Jin C; Martins C; Wennerberg J; Akervall J; Mandahl N; Mitelman F; Mertens F
FISH characterization of head and neck carcinomas reveals that amplification of band 11q13 is associated with deletion of distal 11q.
Genes, chromosomes & cancer 1998;22(4):312-20.
1998: Dal Cin P; Sciot R; Fletcher C D; Samson I; De Vos R; Mandahl N; Willén H; Larsson O; Van den Berghe H
Inflammatory leiomyosarcoma may be characterized by specific near-haploid chromosome changes.
The Journal of pathology 1998;185(1):112-5.
1998: Jin Y; Mertens F; Persson B; Warloe T; Gullestad H P; Salemark L; Jin C; Jonsson N; Risberg B; Mandahl N; Mitelman F; Heim S
Nonrandom numerical chromosome abnormalities in basal cell carcinomas.
Cancer genetics and cytogenetics 1998;103(1):35-42.
1998: Mandahl N; Mertens F; Willén H; Rydholm A; Kreicbergs A; Mitelman F
Nonrandom pattern of telomeric associations in atypical lipomatous tumors with ring and giant marker chromosomes.
Cancer genetics and cytogenetics 1998;103(1):25-34.
1998: Mertens F; Fletcher C D; Dal Cin P; De Wever I; Mandahl N; Mitelman F; Rosai J; Rydholm A; Sciot R; Tallini G; Van den Berghe H; Vanni R; Willén H
Cytogenetic analysis of 46 pleomorphic soft tissue sarcomas and correlation with morphologic and clinical features: a report of the CHAMP Study Group. Chromosomes and MorPhology.
Genes, chromosomes & cancer 1998;22(1):16-25.
1998: Fadl-Elmula I; Gorunova L; Lundgren R; Mandahl N; Forsby N; Mitelman F; Heim S
Chromosomal abnormalities in two bladder carcinomas with secondary squamous cell differentiation.
Cancer genetics and cytogenetics 1998;102(2):125-30.
1998: Mertens F; Kullendorff C M; Hjorth L; Alumets J; Mandahl N
Trisomy 3 as the sole karyotypic change in a pediatric immature teratoma.
Cancer genetics and cytogenetics 1998;102(1):83-5.
1998: Jin Y; Jin C; Arheden K; Larsson O; Bauer H F; Mandahl N; Mertens F
Unbalanced chromosomal rearrangements in a metastasizing salivary gland tumor with benign histology.
Cancer genetics and cytogenetics 1998;102(1):59-64.
1998: Willén H; Akerman M; Dal Cin P; De Wever I; Fletcher C D; Mandahl N; Mertens F; Mitelman F; Rosai J; Rydholm A; Sciot R; Tallini G; Van den Berghe H; Vanni R
Comparison of chromosomal patterns with clinical features in 165 lipomas: a report of the CHAMP study group.
Cancer genetics and cytogenetics 1998;102(1):46-9.
1998: Kullendorff C M; Donner M; Mertens F; Mandahl N
Chromosomal aberrations in a consecutive series of childhood rhabdomyosarcoma.
Medical and pediatric oncology 1998;30(3):156-9.
1998: Schuborg C; Mertens F; Rydholm A; Brosjö O; Dictor M; Mitelman F; Mandahl N
Cytogenetic analysis of four angiosarcomas from deep and superficial soft tissue.
Cancer genetics and cytogenetics 1998;100(1):52-6.
1998: Broberg K; Höglund M; Lindstrand A; Toksvig-Larsen S; Mandahl N; Mertens F
Polyclonal expansion of cells with trisomy 7 in synovia from patients with osteoarthritis.
Cytogenetics and cell genetics 1998;83(1-2):30-4.
1997: Broberg K; Limon J; Pålsson E; Lindstrand A; Toksvig-Larsen S; Mandahl N; Mertens F
Clonal chromosome aberrations are present in vivo in synovia and osteophytes from patients with osteoarthritis.
Human genetics 1997;101(3):295-8.
1997: Elfving P; Mandahl N; Lundgren R; Limon J; Bak-Jensen E; Fernö M; Olsson H; Mitelman F
Prognostic implications of cytogenetic findings in kidney cancer.
British journal of urology 1997;80(5):698-706.
1997: Panagopoulos I; Lassen C; Isaksson M; Mitelman F; Mandahl N; Aman P
Characteristic sequence motifs at the breakpoints of the hybrid genes FUS/CHOP, EWS/CHOP and FUS/ERG in myxoid liposarcoma and acute myeloid leukemia.
Oncogene 1997;15(11):1357-62.
1997: Mitelman F; Johansson B; Mandahl N; Mertens F
Clinical significance of cytogenetic findings in solid tumors.
Cancer genetics and cytogenetics 1997;95(1):1-8.
1997: Sciot R; Akerman M; Dal Cin P; De Wever I; Fletcher C D; Mandahl N; Mertens F; Mitelman F; Rosai J; Rydholm A; Tallini G; Van den Berghe H; Vanni R; Willen H
Cytogenetic analysis of subcutaneous angiolipoma: further evidence supporting its difference from ordinary pure lipomas: a report of the CHAMP Study Group.
The American journal of surgical pathology 1997;21(4):441-4.
1997: Jin C; Jin Y; Wennerberg J; Akervall J; Dictor M; Mandahl N; Heim S; Mitelman F; Mertens F
Cytogenetic analysis of inverted nasal papillomas and demonstration of genetic convergence during in vitro passaging.
International journal of cancer. Journal international du cancer 1997;70(6):668-73.
1997: Jin C; Jin Y; Wennerberg J; Akervall J; Grenthe B; Mandahl N; Heim S; Mitelman F; Mertens F
Clonal chromosome aberrations accumulate with age in upper aerodigestive tract mucosa.
Mutation research 1997;374(1):63-72.
1997: Jin Y; Merterns F; Persson B; Gullestad H P; Jin C; Warloe T; Salemark L; Jonsson N; Risberg B; Mandahl N; Mitelman F; Heim S
The reciprocal translocation t(9;16)(q22;p13) is a primary chromosome abnormality in basal cell carcinomas.
Cancer research 1997;57(3):404-6.
1997: Simon M P; Pedeutour F; Sirvent N; Grosgeorge J; Minoletti F; Coindre J M; Terrier-Lacombe M J; Mandahl N; Craver R D; Blin N; Sozzi G; Turc-Carel C; O'Brien K P; Kedra D; Fransson I; Guilbaud C; Dumanski J P
Deregulation of the platelet-derived growth factor B-chain gene via fusion with collagen gene COL1A1 in dermatofibrosarcoma protuberans and giant-cell fibroblastoma.
Nature genetics 1997;15(1):95-8.
1997: Choong P F; Rydholm A; Mertens F; Mandahl N
Musculoskeletal oncology--advances in cytogenetics and molecular genetics and their clinical implications.
Acta oncologica (Stockholm, Sweden) 1997;36(3):245-54.
1996: Mertens F; Pålsson E; Lindstrand A; Toksvig-Larsen S; Knuutila S; Larramendy M L; el-Rifai W; Limon J; Mitelman F; Mandahl N
Evidence of somatic mutations in osteoarthritis.
Human genetics 1996;98(6):651-6.
1996: Aman P; Panagopoulos I; Lassen C; Fioretos T; Mencinger M; Toresson H; Höglund M; Forster A; Rabbitts T H; Ron D; Mandahl N; Mitelman F
Expression patterns of the human sarcoma-associated genes FUS and EWS and the genomic structure of FUS.
Genomics 1996;37(1):1-8.
1996: Panagopoulos I; Aman P; Mertens F; Mandahl N; Rydholm A; Bauer H F; Mitelman F
Genomic PCR detects tumor cells in peripheral blood from patients with myxoid liposarcoma.
Genes, chromosomes & cancer 1996;17(2):102-7.
1996: Lothe R A; Karhu R; Mandahl N; Mertens F; Saeter G; Heim S; Borresen-Dale A L; Kallioniemi O P
Gain of 17q24-qter detected by comparative genomic hybridization in malignant tumors from patients with von Recklinghausen's neurofibromatosis.
Cancer research 1996;56(20):4778-81.
1996: Rosai J; Akerman M; Dal Cin P; DeWever I; Fletcher C D; Mandahl N; Mertens F; Mitelman F; Rydholm A; Sciot R; Tallini G; Van den Berghe H; Van de Ven W; Vanni R; Willen H
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).
The American journal of surgical pathology 1996;20(10):1182-9.
1996: Mandahl N; Akerman M; Aman P; Dal Cin P; De Wever I; Fletcher C D; Mertens F; Mitelman F; Rosai J; Rydholm A; Sciot R; Tallini G; Van den Berghe H; Van de Ven W; Vanni R; Willén H
Duplication of chromosome segment 12q15-24 is associated with atypical lipomatous tumors: a report of the CHAMP collaborative study group. CHromosomes And MorPhology.
International journal of cancer. Journal international du cancer 1996;67(5):632-5.
1996: Tallini G; Akerman M; Dal Cin P; De Wever I; Fletcher C D; Mandahl N; Mertens F; Mitelman F; Rosai J; Rydholm A; Sciot R; Van den Berghe H; Van den Ven W; Vanni R; Willen H
Combined morphologic and karyotypic study of 28 myxoid liposarcomas. Implications for a revised morphologic typing, (a report from the CHAMP Group).
The American journal of surgical pathology 1996;20(9):1047-55.
1996: Petit M M; Mols R; Schoenmakers E F; Mandahl N; Van de Ven W J
LPP, the preferred fusion partner gene of HMGIC in lipomas, is a novel member of the LIM protein gene family.
Genomics 1996;36(1):118-29.
1996: Akerman M; Dreinhöfer K; Rydholm A; Willén H; Mertens F; Mitelman F; Mandahl N
Cytogenetic studies on fine-needle aspiration samples from osteosarcoma and Ewing's sarcoma.
Diagnostic cytopathology 1996;15(1):17-22.
1996: Mertens F; Jonsson K; Willén H; Rydholm A; Kreicbergs A; Eriksson L; Olsson-Sandin G; Mitelman F; Mandahl N
Chromosome rearrangements in synovial chondromatous lesions.
British journal of cancer 1996;74(2):251-4.
1996: Choong P F; Mandahl N; Mertens F; Willén H; Alvegård T; Kreicbergs A; Mitelman F; Rydholm A
19p+ marker chromosome correlates with relapse in malignant fibrous histiocytoma.
Genes, chromosomes & cancer 1996;16(2):88-93.
1996: Akerman M; Willén H; Carlén B; Mandahl N; Mertens F
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.
Cytopathology : official journal of the British Society for Clinical Cytology 1996;7(3):187-200.
1996: Jin Y; Mertens F; Jin C; Wennerberg J; Mandahl N; Heim S; Mitelman F
Clonal chromosome abnormalities in two chemodectomas.
Genes, chromosomes & cancer 1996;15(3):178-81.
1996: Panagopoulos I; Höglund M; Mertens F; Mandahl N; Mitelman F; Aman P
Fusion of the EWS and CHOP genes in myxoid liposarcoma.
Oncogene 1996;12(3):489-94.
1996: Fletcher C D; Akerman M; Dal Cin P; de Wever I; Mandahl N; Mertens F; Mitelman F; Rosai J; Rydholm A; Sciot R; Tallini G; van den Berghe H; van de Ven W; Vanni R; Willen H
Correlation between clinicopathological features and karyotype in lipomatous tumors. A report of 178 cases from the Chromosomes and Morphology (CHAMP) Collaborative Study Group.
The American journal of pathology 1996;148(2):623-30.
1995: Gorunova L; Johansson B; Dawiskiba S; Andrén-Sandberg A; Jin Y; Mandahl N; Heim S; Mitelman F
Massive cytogenetic heterogeneity in a pancreatic carcinoma: fifty-four karyotypically unrelated clones.
Genes, chromosomes & cancer 1995;14(4):259-66.
1995: Mertens F; Willén H; Rydholm A; Brosjö O; Carlén B; Mitelman F; Mandahl N
Trisomy 20 is a primary chromosome aberration in desmoid tumors.
International journal of cancer. Journal international du cancer 1995;63(4):527-9.
1995: Akervall J A; Jin Y; Wennerberg J P; Zätterström U K; Kjellén E; Mertens F; Willén R; Mandahl N; Heim S; Mitelman F
Chromosomal abnormalities involving 11q13 are associated with poor prognosis in patients with squamous cell carcinoma of the head and neck.
Cancer 1995;76(5):853-9.
1995: Panagopoulos I; Mandahl N; Mitelman F; Aman P
Two distinct FUS breakpoint clusters in myxoid liposarcoma and acute myeloid leukemia with the translocations t(12;16) and t(16;21).
Oncogene 1995;11(6):1133-7.
1995: Nilbert M; Rydholm A; Mitelman F; Meltzer P S; Mandahl N
Characterization of the 12q13-15 amplicon in soft tissue tumors.
Cancer genetics and cytogenetics 1995;83(1):32-6.
1995: Gorunova L; Johansson B; Dawiskiba S; Andrén-Sandberg A; Mandahl N; Heim S; Mitelman F
Cytogenetically detected clonal heterogeneity in a duodenal adenocarcinoma.
Cancer genetics and cytogenetics 1995;82(2):146-50.
1995: Jin Y; Mertens F; Jin C; Akervall J; Wennerberg J; Gorunova L; Mandahl N; Heim S; Mitelman F
Nonrandom chromosome abnormalities in short-term cultured primary squamous cell carcinomas of the head and neck.
Cancer research 1995;55(14):3204-10.
1995: Mertens F; Rydholm A; Bauer H F; Limon J; Nedoszytko B; Szadowska A; Willén H; Heim S; Mitelman F; Mandahl N
Cytogenetic findings in malignant peripheral nerve sheath tumors.
International journal of cancer. Journal international du cancer 1995;61(6):793-8.
1995: Mertens F; Heim S; Kullendorff C M; Donnér M; Hägerstrand I; Mitelman F; Mandahl N
Clonal karyotypic evolution in a pediatric neurofibrosarcoma.
Cancer genetics and cytogenetics 1995;81(2):135-8.
1995: Johansson M; Jin Y; Mandahl N; Hambraeus G; Johansson L; Mitelman F; Heim S
Cytogenetic analysis of short-term cultured squamous cell carcinomas of the lung.
Cancer genetics and cytogenetics 1995;81(1):46-55.
1995: Jin Y; Mertens F; Arheden K; Mandahl N; Wennerberg J; Dictor M; Heim S; Mitelman F
Karyotypic features of malignant tumors of the nasal cavity and paranasal sinuses.
International journal of cancer. Journal international du cancer 1995;60(5):637-41.
1995: Mertens F; Heim S; Mandahl N; Mitelman F; Brun A; Strömblad L G; Kullendorff C M; Donnér M
Recurrent chromosomal imbalances in choroid plexus tumors.
Cancer genetics and cytogenetics 1995;80(1):83-4.
1995: Pandis N; Jin Y; Gorunova L; Petersson C; Bardi G; Idvall I; Johansson B; Ingvar C; Mandahl N; Mitelman F
Chromosome analysis of 97 primary breast carcinomas: identification of eight karyotypic subgroups.
Genes, chromosomes & cancer 1995;12(3):173-85.
1995: Jin Y; Mertens F; Mandahl N; Wennerberg J; Dictor M; Heim S; Mitelman F
Tetraploidization and progressive loss of 6q in a squamous cell carcinoma of the parotid gland.
Cancer genetics and cytogenetics 1995;79(2):157-9.
1995: Aspberg F; Mertens F; Bauer H C; Lindholm J; Mitelman F; Mandahl N
Near-haploidy in two malignant fibrous histiocytomas.
Cancer genetics and cytogenetics 1995;79(2):119-22.
1995: Choong P F; Willén H; Nilbert M; Mertens F; Mandahl N; Carlén B; Rydholm A
Pigmented villonodular synovitis. Monoclonality and metastasis--a case for neoplastic origin?
Acta orthopaedica Scandinavica 1995;66(1):64-8.
1995: Elfving P; Aman P; Mandahl N; Lundgren R; Mitelman F
Trisomy 7 in nonneoplastic epithelial kidney cells.
Cytogenetics and cell genetics 1995;69(1-2):90-6.
1995: Höglund M; Mitelman F; Mandahl N
A human 12p-derived cosmid hybridizing to subsets of human and chimpanzee telomeres.
Cytogenetics and cell genetics 1995;70(1-2):88-91.
1994: Panagopoulos I; Mandahl N; Ron D; Höglund M; Nilbert M; Mertens F; Mitelman F; Aman P
Characterization of the CHOP breakpoints and fusion transcripts in myxoid liposarcomas with the 12;16 translocation.
Cancer research 1994;54(24):6500-3.
1994: Orndal C; Rydholm A; Willén H; Mitelman F; Mandahl N
Cytogenetic intratumor heterogeneity in soft tissue tumors.
Cancer genetics and cytogenetics 1994;78(2):127-37.
1994: Mertens F; Albert A; Heim S; Lindholm J; Brosjö O; Mitelman F; Mandahl N
Clonal structural chromosome aberrations in fibrous dysplasia.
Genes, chromosomes & cancer 1994;11(4):271-2.
1994: Panagopoulos I; Aman P; Fioretos T; Höglund M; Johansson B; Mandahl N; Heim S; Behrendtz M; Mitelman F
Fusion of the FUS gene with ERG in acute myeloid leukemia with t(16;21)(p11;q22).
Genes, chromosomes & cancer 1994;11(4):256-62.
1994: Gorunova L; Mertens F; Mandahl N; Jonsson N; Persson B; Heim S; Mitelman F
Cytogenetic heterogeneity in a clear cell hidradenoma of the skin.
Cancer genetics and cytogenetics 1994;77(1):26-32.
1994: Bardi G; Aman P; Johansson B; Pandis N; Mandahl N; Bak-Jensen E; Björkman A; Sjögren H O; Andrén-Sandberg A; Mitelman F
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.
Cancer genetics and cytogenetics 1994;76(1):29-32.
1994: Bardi G; Gorunova L; Limon J; Nedoszytko B; Johansson B; Pandis N; Mandahl N; Bak-Jensen E; Andrén-Sandberg A; Rys J
Abnormal karyotypes in three carcinomas of the gallbladder.
Cancer genetics and cytogenetics 1994;76(1):15-8.
1994: Mertens F; Rydholm A; Brosjö O; Willén H; Mitelman F; Mandahl N
Hibernomas are characterized by rearrangements of chromosome bands 11q13-21.
International journal of cancer. Journal international du cancer 1994;58(4):503-5.
1994: Jin Y; Mertens F; Limon J; Mandahl N; Wennerberg J; Dictor M; Heim S; Mitelman F
Characteristic karyotypic features in lacrimal and salivary gland carcinomas.
British journal of cancer 1994;70(1):42-7.
1994: Johansson B; Bardi G; Pandis N; Gorunova L; Bäckman P L; Mandahl N; Dawiskiba S; Andrén-Sandberg A; Heim S; Mitelman F
Karyotypic pattern of pancreatic adenocarcinomas correlates with survival and tumour grade.
International journal of cancer. Journal international du cancer 1994;58(1):8-13.
1994: Mertens F; Mandahl N; Mitelman F; Heim S
Cytogenetic analysis in the examination of solid tumors in children.
Pediatric hematology and oncology 1994;11(4):361-77.
1994: Johansson M; Dietrich C; Mandahl N; Hambraeus G; Johansson L; Clausen P P; Mitelman F; Heim S
Karyotypic characterization of bronchial large cell carcinomas.
International journal of cancer. Journal international du cancer 1994;57(4):463-7.
1994: Mertens F; Kreicbergs A; Rydholm A; Willén H; Carlén B; Mitelman F; Mandahl N
Clonal chromosome aberrations in three sacral chordomas.
Cancer genetics and cytogenetics 1994;73(2):147-51.
1994: Nilbert M; Rydholm A; Willén H; Mitelman F; Mandahl N
MDM2 gene amplification correlates with ring chromosome in soft tissue tumors.
Genes, chromosomes & cancer 1994;9(4):261-5.
1994: Mandahl N; Höglund M; Mertens F; Rydholm A; Willén H; Brosjö O; Mitelman F
Cytogenetic aberrations in 188 benign and borderline adipose tissue tumors.
Genes, chromosomes & cancer 1994;9(3):207-15.
1994: Nilbert M; Mandahl N; Aman P; Rydholm A; Mitelman F
No rearrangements of the CHOP gene in malignant fibrous histiocytoma.
Cancer genetics and cytogenetics 1994;72(2):155-6.
1994: Mertens F; Rydholm A; Kreicbergs A; Willén H; Jonsson K; Heim S; Mitelman F; Mandahl N
Loss of chromosome band 8q24 in sporadic osteocartilaginous exostoses.
Genes, chromosomes & cancer 1994;9(1):8-12.
1994: Mandahl N; Mertens F; Willén H; Rydholm A; Brosjö O; Mitelman F
A new cytogenetic subgroup in lipomas: loss of chromosome 16 material in spindle cell and pleomorphic lipomas.
Journal of cancer research and clinical oncology 1994;120(12):707-11.
1993: Bardi G; Johansson B; Pandis N; Mandahl N; Bak-Jensen E; Lindström C; Törnqvist A; Frederiksen H; Andrén-Sandberg A; Mitelman F
Cytogenetic analysis of 52 colorectal carcinomas--non-random aberration pattern and correlation with pathologic parameters.
International journal of cancer. Journal international du cancer 1993;55(3):422-8.
1993: Orndal C; Mandahl N; Willén H; Rydholm A; Mitelman F
Cytogenetic evolution in primary tumors, local recurrences, and pulmonary metastases of two soft tissue sarcomas.
Clinical & experimental metastasis 1993;11(5):401-8.
1993: Mertens F; Mandahl N; Orndal C; Baldetorp B; Bauer H C; Rydholm A; Wiebe T; Willén H; Akerman M; Heim S
Cytogenetic findings in 33 osteosarcomas.
International journal of cancer. Journal international du cancer 1993;55(1):44-50.
1993: Johansson M; Dietrich C; Mandahl N; Hambraeus G; Johansson L; Clausen P P; Mitelman F; Heim S
Recombinations of chromosomal bands 6p21 and 14q24 characterise pulmonary hamartomas.
British journal of cancer 1993;67(6):1236-41.
1993: Bardi G; Johansson B; Pandis N; Mandahl N; Bak-Jensen E; Andrén-Sandberg A; Mitelman F; Heim S
Karyotypic abnormalities in tumours of the pancreas.
British journal of cancer 1993;67(5):1106-12.
1993: Mandahl N; Orndal C; Heim S; Willén H; Rydholm A; Bauer H C; Mitelman F
Aberrations of chromosome segment 12q13-15 characterize a subgroup of hemangiopericytomas.
Cancer 1993;71(10):3009-13.
1993: Jin Y; Mertens F; Mandahl N; Heim S; Olegård C; Wennerberg J; Biörklund A; Mitelman F
Chromosome abnormalities in eighty-three head and neck squamous cell carcinomas: influence of culture conditions on karyotypic pattern.
Cancer research 1993;53(9):2140-6.
1993: Mertens F; Orndal C; Mandahl N; Heim S; Bauer H F; Rydholm A; Tufvesson A; Willén H; Mitelman F
Chromosome aberrations in tenosynovial giant cell tumors and nontumorous synovial tissue.
Genes, chromosomes & cancer 1993;6(4):212-7.
1993: Johansson B; Heim S; Mandahl N; Mertens F; Mitelman F
Trisomy 7 in nonneoplastic cells.
Genes, chromosomes & cancer 1993;6(4):199-205.
1993: Johansson M; Heim S; Mandahl N; Hambraeus G; Johansson L; Mitelman F
Cytogenetic analysis of six bronchial carcinoids.
Cancer genetics and cytogenetics 1993;66(1):33-8.
1993: Pandis N; Jin Y; Limon J; Bardi G; Idvall I; Mandahl N; Mitelman F; Heim S
Interstitial deletion of the short arm of chromosome 3 as a primary chromosome abnormality in carcinomas of the breast.
Genes, chromosomes & cancer 1993;6(3):151-5.
1993: Mandahl N; Baldetorp B; Fernö M; Akerman M; Rydholm A; Heim S; Willén H; Killander D; Mitelman F
Comparative cytogenetic and DNA flow cytometric analysis of 150 bone and soft-tissue tumors.
International journal of cancer. Journal international du cancer 1993;53(3):358-64.
1993: Mandahl N; Willén H; Rydholm A; Heim S; Mitelman F
Rearrangement of band q13 on both chromosomes 12 in a periosteal chondroma.
Genes, chromosomes & cancer 1993;6(2):121-3.
1993: Bardi G; Johansson B; Pandis N; Bak-Jensen E; Orndal C; Heim S; Mandahl N; Andrén-Sandberg A; Mitelman F
Cytogenetic aberrations in colorectal adenocarcinomas and their correlation with clinicopathologic features.
Cancer 1993;71(2):306-14.
1993: Pandis N; Heim S; Bardi G; Idvall I; Mandahl N; Mitelman F
Chromosome analysis of 20 breast carcinomas: cytogenetic multiclonality and karyotypic-pathologic correlations.
Genes, chromosomes & cancer 1993;6(1):51-7.
1993: Orndal C; Mandahl N; Rydholm A; Willén H; Brosjö O; Mitelman F
Chromosome aberrations and cytogenetic intratumor heterogeneity in chondrosarcomas.
Journal of cancer research and clinical oncology 1993;120(1-2):51-6.
1992: Elfving P; Lundgren R; Cigudosa J C; Heim S; Mandahl N; Mitelman F
Trisomy 7 in nonneoplastic kidney tissue cultured with and without epidermal growth factor.
Cancer genetics and cytogenetics 1992;64(1):99-100.
1992: Carlén B; Orndal C; Willén H; Mandahl N
The ultrastructure of fresh and cultured cells in fifteen soft tissue and bone tumors.
Anticancer research 1992;12(6B):2185-90.
1992: Aman P; Ron D; Mandahl N; Fioretos T; Heim S; Arheden K; Willén H; Rydholm A; Mitelman F
Rearrangement of the transcription factor gene CHOP in myxoid liposarcomas with t(12;16)(q13;p11).
Genes, chromosomes & cancer 1992;5(4):278-85.
1992: Johansson M; Jin Y; Heim S; Mandahl N; Hambraeus G; Johansson L; Mitelman F
Pseudodiploid karyotypes in adenosquamous carcinomas of the lung.
Cancer genetics and cytogenetics 1992;63(2):95-6.
1992: Bardi G; Johansson B; Pandis N; Heim S; Mandahl N; Hägerstrand I; Holmin T; Andrén-Sandberg A; Mitelman F
Trisomy 7 in nonneoplastic focal steatosis of the liver.
Cancer genetics and cytogenetics 1992;63(1):22-4.
1992: Pandis N; Heim S; Bardi G; Idvall I; Mandahl N; Mitelman F
Whole-arm t(1;16) and i(1q) as sole anomalies identify gain of 1q as a primary chromosomal abnormality in breast cancer.
Genes, chromosomes & cancer 1992;5(3):235-8.
1992: Bardi G; Johansson B; Pandis N; Heim S; Mandahl N; Bak-Jensen E; Frederiksen H; Andrén-Sandberg A; Mitelman F
Recurrent chromosome aberrations in abdominal smooth muscle tumors.
Cancer genetics and cytogenetics 1992;62(1):43-6.
1992: Pandis N; Heim S; Bardi G; Limon J; Mandahl N; Mitelman F
Improved technique for short-term culture and cytogenetic analysis of human breast cancer.
Genes, chromosomes & cancer 1992;5(1):14-20.
1992: Olegård C; Mandahl N; Heim S; Willén H; Leifsson B; Mitelman F
Embryonal rhabdomyosarcoma with 100 chromosomes but no structural aberrations.
Cancer genetics and cytogenetics 1992;60(2):198-201.
1992: Orndal C; Mandahl N; Rydholm A; Willén H; Brosjö O; Heim S; Mitelman F
Supernumerary ring chromosomes in five bone and soft tissue tumors of low or borderline malignancy.
Cancer genetics and cytogenetics 1992;60(2):170-5.
1992: Orndal C; Mandahl N; Carlén B; Willén H; Wennerberg J; Heim S; Mitelman F
Near-haploid clones in a malignant fibrous histiocytoma.
Cancer genetics and cytogenetics 1992;60(2):147-51.
1992: Johansson B; Bardi G; Heim S; Mandahl N; Mertens F; Bak-Jensen E; Andrén-Sandberg A; Mitelman F
Nonrandom chromosomal rearrangements in pancreatic carcinomas.
Cancer 1992;69(7):1674-81.
1992: Mertens F; Jin Y; Heim S; Mandahl N; Jonsson N; Mertens O; Persson B; Salemark L; Wennerberg J; Mitelman F
Clonal structural chromosome aberrations in nonneoplastic cells of the skin and upper aerodigestive tract.
Genes, chromosomes & cancer 1992;4(3):235-40.
1992: Lundgren R; Heim S; Mandahl N; Anderson H; Mitelman F
Chromosome abnormalities are associated with unfavorable outcome in prostatic cancer patients.
The Journal of urology 1992;147(3 Pt 2):784-8.
1992: Pejovic T; Himmelmann A; Heim S; Mandahl N; Flodérus U M; Furgyik S; Elmfors B; Helm G; Willén H; Mitelman F
Prognostic impact of chromosome aberrations in ovarian cancer.
British journal of cancer 1992;65(2):282-6.
1992: Bardi G; Johansson B; Pandis N; Heim S; Mandahl N; Andrén-Sandberg A; Hägerstrand I; Mitelman F
Cytogenetic findings in three primary hepatocellular carcinomas.
Cancer genetics and cytogenetics 1992;58(2):191-5.
1992: Bardi G; Johansson B; Pandis N; Heim S; Mandahl N; Békássy A; Hägerstrand I; Mitelman F
Trisomy 2 as the sole chromosomal abnormality in a hepatoblastoma.
Genes, chromosomes & cancer 1992;4(1):78-80.
1992: Pejovic T; Heim S; Mandahl N; Baldetorp B; Elmfors B; Flodérus U M; Furgyik S; Helm G; Himmelmann A; Willén H
Chromosome aberrations in 35 primary ovarian carcinomas.
Genes, chromosomes & cancer 1992;4(1):58-68.
1992: Lundgren R; Mandahl N; Heim S; Limon J; Henrikson H; Mitelman F
Cytogenetic analysis of 57 primary prostatic adenocarcinomas.
Genes, chromosomes & cancer 1992;4(1):16-24.
1991: Lindström E; Salford L G; Heim S; Mandahl N; Strömblad S; Brun A; Mitelman F
Trisomy 7 and sex chromosome loss need not be representative of tumor parenchyma cells in malignant glioma.
Genes, chromosomes & cancer 1991;3(6):474-9.
1991: Limon J; Mrozek K; Mandahl N; Nedoszytko B; Verhest A; Rys J; Niezabitowski A; Babinska M; Nosek H; Ochalek T
Cytogenetics of synovial sarcoma: presentation of ten new cases and review of the literature.
Genes, chromosomes & cancer 1991;3(5):338-45.
1991: Pandis N; Heim S; Bardi G; Flodérus U M; Willén H; Mandahl N; Mitelman F
Chromosome analysis of 96 uterine leiomyomas.
Cancer genetics and cytogenetics 1991;55(1):11-8.
1991: Bardi G; Johansson B; Pandis N; Heim S; Mandahl N; Andrén-Sandberg A; Hägerstrand I; Mitelman F
Trisomy 7 in short-term cultures of colorectal adenocarcinomas.
Genes, chromosomes & cancer 1991;3(2):149-52.
1991: Pejovic T; Heim S; Mandahl N; Elmfors B; Furgyik S; Flodérus U M; Helm G; Willén H; Mitelman F
Bilateral ovarian carcinoma: cytogenetic evidence of unicentric origin.
International journal of cancer. Journal international du cancer 1991;47(3):358-61.
1991: Mertens F; Heim S; Mandahl N; Johansson B; Mertens O; Persson B; Salemark L; Wennerberg J; Jonsson N; Mitelman F
Cytogenetic analysis of 33 basal cell carcinomas.
Cancer research 1991;51(3):954-7.
1991: Higashi K; Jin Y; Johansson M; Heim S; Mandahl N; Biörklund A; Wennerberg J; Hambraeus G; Johansson L; Mitelman F
Rearrangement of 9p13 as the primary chromosomal aberration in adenoid cystic carcinoma of the respiratory tract.
Genes, chromosomes & cancer 1991;3(1):21-3.
1991: Orndal C; Carlén B; Akerman M; Willén H; Mandahl N; Heim S; Rydholm A; Mitelman F
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.
Cytopathology : official journal of the British Society for Clinical Cytology 1991;2(5):261-70.
1990: Pandis N; Heim S; Bardi G; Flodérus U M; Willén H; Mandahl N; Mitelman F
Parallel karyotypic evolution and tumor progression in uterine leiomyoma.
Genes, chromosomes & cancer 1990;2(4):311-7.
1990: Rydholm A; Mandahl N; Heim S; Kreicbergs A; Willén H; Mitelman F
Malignant fibrous histiocytomas with a 19p+ marker chromosome have increased relapse rate.
Genes, chromosomes & cancer 1990;2(4):296-9.
1990: Pejovic T; Heim S; Orndal C; Jin Y S; Mandahl N; Willén H; Mitelman F
Simple numerical chromosome aberrations in well-differentiated malignant epithelial tumors.
Cancer genetics and cytogenetics 1990;49(1):95-101.
1990: Nilbert M; Heim S; Mandahl N; Flodérus U M; Willén H; Mitelman F
Characteristic chromosome abnormalities, including rearrangements of 6p, del(7q), +12, and t(12;14), in 44 uterine leiomyomas.
Human genetics 1990;85(6):605-11.
1990: Mandahl N; Heim S; Willén H; Rydholm A; Mitelman F
Supernumerary ring chromosome as the sole cytogenetic abnormality in a dermatofibrosarcoma protuberans.
Cancer genetics and cytogenetics 1990;49(2):273-5.
1990: Limon J; Mrózek K; Heim S; Elfving P; Nedoszytko B; Babinska M; Mandahl N; Lundgren R; Mitelman F
On the significance of trisomy 7 and sex chromosome loss in renal cell carcinoma.
Cancer genetics and cytogenetics 1990;49(2):259-63.
1990: Orndal C; Johansson M; Heim S; Mandahl N; Månsson B; Alumets J; Mitelman F
Parathyroid adenoma with t(1;5)(p22;q32) as the sole clonal chromosome abnormality.
Cancer genetics and cytogenetics 1990;48(2):225-8.
1990: Nilbert M; Mandahl N; Heim S; Rydholm A; Helm G; Willén H; Baldetorp B; Mitelman F
Complex karyotypic changes, including rearrangements of 12q13 and 14q24, in two leiomyosarcomas.
Cancer genetics and cytogenetics 1990;48(2):217-23.
1990: Pandis N; Heim S; Bardi G; Mandahl N; Mitelman F
High resolution mapping of consistent leiomyoma breakpoints in chromosomes 12 and 14 to 12q15 and 14q24.1.
Genes, chromosomes & cancer 1990;2(3):227-30.
1990: Jin Y S; Higashi K; Mandahl N; Heim S; Wennerberg J; Biörklund A; Dictor M; Mitelman F
Frequent rearrangement of chromosomal bands 1p22 and 11q13 in squamous cell carcinomas of the head and neck.
Genes, chromosomes & cancer 1990;2(3):198-204.
1990: Johansson B; Mertens F; Heim S; Kristoffersson U; Mandahl N; Nilsson P G; Mitelman F
Cytogenetic findings in acute megakaryoblastic leukemia (ANLL-M7).
Cancer genetics and cytogenetics 1990;48(1):119-23.
1990: Eneroth M; Mandahl N; Heim S; Willén H; Rydholm A; Alberts K A; Mitelman F
Localization of the chromosomal breakpoints of the t(12;16) in liposarcoma to subbands 12q13.3 and 16p11.2.
Cancer genetics and cytogenetics 1990;48(1):101-7.
1990: Johansson B; Mertens F; Fioretos T; Heim S; Kristoffersson U; Mandahl N; Bartram C R; Mitelman F
Remarkably long survival of a patient with Ph1-positive chronic myeloid leukemia and 5' bcr rearrangement.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1990;4(6):448-9.
1990: Limon J; Lundgren R; Elfving P; Heim S; Kristoffersson U; Mandahl N; Mitelman F
An improved technique for short-term culturing of human prostatic adenocarcinoma tissue for cytogenetic analysis.
Cancer genetics and cytogenetics 1990;46(2):191-9.
1990: Pejovic T; Heim S; Mandahl N; Flodérus U M; Willén H; Mitelman F
Complex karyotypic anomalies, including an i(5p) marker chromosome, in malignant mixed mesodermal tumor of the ovary.
Cancer genetics and cytogenetics 1990;46(1):65-9.
1990: Pejovic T; Heim S; Mandahl N; Elmfors B; Flodérus U M; Furgyik S; Helm G; Willén H; Mitelman F
Trisomy 12 is a consistent chromosomal aberration in benign ovarian tumors.
Genes, chromosomes & cancer 1990;2(1):48-52.
1990: Kristoffersson U; Heim S; Johnsson A; Mandahl N; Olsson H; Akerman M; Mitelman F
Deletion of 14q in non-Hodgkin's lymphoma.
European journal of haematology 1990;44(4):261-4.
1990: Heim S; Békàssy A N; Garwicz S; Heldrup J; Kristoffersson U; Mandahl N; Wiebe T; Mitelman F
Bone marrow karyotypes in 94 children with acute leukemia.
European journal of haematology 1990;44(4):227-33.
1990: Orndal C; Mandahl N; Rydholm A; Nilbert M; Heim S; Akerman M; Mitelman F
Chromosomal evolution and tumor progression in a myxoid liposarcoma.
Acta orthopaedica Scandinavica 1990;61(2):99-105.
1990: Nilbert M; Heim S; Mandahl N; Flodérus U M; Willén H; Mitelman F
Trisomy 12 in uterine leiomyomas. A new cytogenetic subgroup.
Cancer genetics and cytogenetics 1990;45(1):63-6.
1990: Mandahl N; Jin Y S; Heim S; Willén H; Wennerberg J; Biörklund A; Mitelman F
Trisomy 5 and loss of the Y chromosome as the sole cytogenetic anomalies in a cavernous hemangioma/angiosarcoma.
Genes, chromosomes & cancer 1990;1(4):315-6.
1990: Mertens F; Johansson B; Heim S; Kristoffersson U; Mandahl N; Turesson I; Malm C; Othzén A; Bartram C R; Catovsky D
Trisomy 14 in atypical chronic myeloid leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1990;4(2):117-20.
1990: Jin Y S; Heim S; Mandahl N; Biörklund A; Wennerberg J; Mitelman F
Multiple clonal chromosome aberrations in squamous cell carcinomas of the larynx.
Cancer genetics and cytogenetics 1990;44(2):209-16.
1990: Mandahl N; Heim S; Arheden K; Rydholm A; Willén H; Mitelman F
Chromosomal rearrangements in chondromatous tumors.
Cancer 1990;65(2):242-8.
1990: Nilbert M; Jin Y S; Heim S; Mandahl N; Flodérus U M; Willén H; Mitelman F
Chromosome rearrangements in two uterine sarcomas.
Cancer genetics and cytogenetics 1990;44(1):27-35.
1990: Jin Y S; Heim S; Mandahl N; Biörklund A; Wennerberg J; Mitelman F
Unrelated clonal chromosomal aberrations in carcinomas of the oral cavity.
Genes, chromosomes & cancer 1990;1(3):209-15.
1990: Elfving P; Cigudosa J C; Lundgren R; Limon J; Mandahl N; Kristoffersson U; Heim S; Mitelman F
Trisomy 7, trisomy 10, and loss of the Y chromosome in short-term cultures of normal kidney tissue.
Cytogenetics and cell genetics 1990;53(2-3):123-5.
1989: Pejovic T; Heim S; Mandahl N; Elmfors B; Flodérus U M; Furgyik S; Helm G; Willén H; Mitelman F
Consistent occurrence of a 19p+ marker chromosome and loss of 11p material in ovarian seropapillary cystadenocarcinomas.
Genes, chromosomes & cancer 1989;1(2):167-71.
1989: Nilbert M; Heim S; Mandahl N; Flodérus U M; Willén H; Baldetorp B; Mitelman F
Complex karyotypic anomalies in a bizarre leiomyoma of the uterus.
Genes, chromosomes & cancer 1989;1(2):131-4.
1989: Mandahl N; Heim S; Rydholm A; Willén H; Mitelman F
Structural chromosome aberrations in an adamantinoma.
Cancer genetics and cytogenetics 1989;42(2):187-90.
1989: Nilbert M; Heim S; Mandahl N; Flodérus U M; Willén H; Mitelman F
Different karyotypic abnormalities, t(1;6) and del(7), in two uterine leiomyomas from the same patient.
Cancer genetics and cytogenetics 1989;42(1):51-3.
1989: Mandahl N; Heim S; Brosjö O; Bauer H C; Tribukait B; Rydholm A; Mitelman F
Cytogenetic and quantitative DNA analysis of primary and xenografted human osteosarcomas.
Cancer genetics and cytogenetics 1989;42(1):27-34.
1989: Arheden K; Mandahl N; Heim S; Mitelman F
The INT1 oncogene is not rearranged or amplified in lipomas with structural chromosomal abnormalities of 12q13-15.
Cancer genetics and cytogenetics 1989;42(1):143-6.
1989: Mandahl N; Heim S; Willén H; Rydholm A; Eneroth M; Nilbert M; Kreicbergs A; Mitelman F
Characteristic karyotypic anomalies identify subtypes of malignant fibrous histiocytoma.
Genes, chromosomes & cancer 1989;1(1):9-14.
1989: Kristoffersson U; Heim S; Mandahl N; Akerman M; Mitelman F
Multiple clonal chromosome aberrations in two thymomas.
Cancer genetics and cytogenetics 1989;41(1):93-8.
1989: Lundgren R; Elfving P; Heim S; Kristoffersson U; Mandahl N; Mitelman F
A squamous cell bladder carcinoma with karyotypic abnormalities reminiscent of transitional cell carcinoma.
The Journal of urology 1989;142(2 Pt 1):374-6.
1989: Mertens F; Heim S; Mandahl N; Johansson B; Rydholm A; Biörklund A; Wennerberg J; Jonsson N; Mitelman F
Clonal chromosome aberrations in a keratoacanthoma and a basal cell papilloma.
Cancer genetics and cytogenetics 1989;39(2):227-32.
1989: Arheden K; Nilbert M; Heim S; Mandahl N; Mitelman F
No amplification or rearrangement of INT1, GLI, or COL2A1 in uterine leiomyomas with t(12;14)(q14-15;q23-24).
Cancer genetics and cytogenetics 1989;39(2):195-201.
1989: Limon J; Lundgren R; Elfving P; Heim S; Kristoffersson U; Mandahl N; Mitelman F
Double minutes in two primary adenocarcinomas of the prostate.
Cancer genetics and cytogenetics 1989;39(2):191-4.
1989: Heim S; Mertens F; Jin Y S; Mandahl N; Johansson B; Biörklund A; Wennerberg J; Jonsson N; Mitelman F
Diverse chromosome abnormalities in squamous cell carcinomas of the skin.
Cancer genetics and cytogenetics 1989;39(1):69-76.
1989: Jin Y S; Heim S; Mandahl N; Biörklund A; Wennerberg J; Willén R; Mitelman F
Two unrelated clonal chromosome rearrangements in a nasal papilloma.
Cancer genetics and cytogenetics 1989;39(1):29-34.
1989: Arheden K; Rønne M; Mandahl N; Heim S; Kinzler K W; Vogelstein B; Mitelman F
In situ hybridization localizes the human putative oncogene GLI to chromosome subbands 12q13.3-14.1.
Human genetics 1989;82(1):1-2.
1989: Mertens F; Heim S; Jin Y S; Johansson B; Mandahl N; Biörklund A; Wennerberg J; Jonsson N; Mitelman F
Basosquamous papilloma. A benign epithelial skin tumor with multiple cytogenetic clones.
Cancer genetics and cytogenetics 1989;37(2):235-9.
1989: Johansson B; Mandahl N; Heim S; Mertens F; Andrén-Sandberg A; Mitelam F
Chromosome abnormalities in a pancreatic adenocarcinoma.
Cancer genetics and cytogenetics 1989;37(2):209-13.
1989: Nilbert M; Mandahl N; Heim S; Rydholm A; Willén H; Mitelman F
Cytogenetic abnormalities in an angioleiomyoma.
Cancer genetics and cytogenetics 1989;37(1):61-4.
1989: Heim S; Mandahl N; Jin Y; Strömblad S; Lindström E; Salford L G; Mitelman F
Trisomy 7 and sex chromosome loss in human brain tissue.
Cytogenetics and cell genetics 1989;52(3-4):136-8.
1989: Heim S; Caron M; Jin Y; Mandahl N; Mitelman F
Genetic convergence during serial in vitro passage of a polyclonal squamous cell carcinoma.
Cytogenetics and cell genetics 1989;52(3-4):133-5.
1988: Jin Y; Heim J; Mandahl N; Biörklund A; Wennerberg J; Mitelman F
Inversion inv(4)(p15q26) in a squamous cell carcinoma of the hypopharynx.
Cancer genetics and cytogenetics 1988;36(2):233-4.
1988: Nilbert M; Heim S; Mandahl N; Flodérus U M; Willén H; Akerman M; Mitelman F
Ring formation and structural rearrangements of chromosome 1 as secondary changes in uterine leiomyomas with t(12;14)(q14-15;q23-24).
Cancer genetics and cytogenetics 1988;36(2):183-90.
1988: Kristoffersson U; Heim S; Mandahl N; Olsson H; Akerman M; Mitelman F
Trisomy 5 and t(5;14)(q11;q32) as the sole abnormalities in two different clones from a centroblastic non-Hodgkin's lymphoma.
Cancer genetics and cytogenetics 1988;36(2):173-6.
1988: Heim S; Jin Y; Mandahl N; Biörklund A; Wennerberg J; Jonsson N; Mitelman F
Multiple unrelated clonal chromosome abnormalities in an in situ squamous cell carcinoma of the skin.
Cancer genetics and cytogenetics 1988;36(2):149-53.
1988: Heim S; Mandahl N; Rydholm A; Willén H; Mitelman F
Different karyotypic features characterize different clinico-pathologic subgroups of benign lipogenic tumors.
International journal of cancer. Journal international du cancer 1988;42(6):863-7.
1988: Heim S; Mandahl N; Mitelman F
Genetic convergence and divergence in tumor progression.
Cancer research 1988;48(21):5911-6.
1988: Billström R; Thiede T; Hansen S; Heim S; Kristoffersson U; Mandahl N; Mitelman F
Bone marrow karyotype and prognosis in primary myelodysplastic syndromes.
European journal of haematology 1988;41(4):341-6.
1988: Akerman M; Alvegård T; Eliasson J; Garwicz S; Mandahl N; Rydholm A; Willén H
A case of Ewing's sarcoma diagnosed by fine needle aspiration. Light microscopy, electron microscopy and chromosomal analysis.
Acta orthopaedica Scandinavica 1988;59(5):589-92.
1988: Heim S; Mandahl N; Arheden K; Giovanella B C; Yim S O; Stehlin J S; Mitelman F
Multiple karyotypic abnormalities, including structural rearrangements of 11p, in cell lines from malignant melanomas.
Cancer genetics and cytogenetics 1988;35(1):5-20.
1988: Lundgren R; Kristoffersson U; Heim S; Mandahl N; Mitelman F
Multiple structural chromosome rearrangements, including del(7q) and del(10q), in an adenocarcinoma of the prostate.
Cancer genetics and cytogenetics 1988;35(1):103-8.
1988: Nilbert M; Mandahl N; Heim S; Rydholm A; Willén H; Akerman M; Mitelman F
Chromosome abnormalities in leiomyosarcomas.
Cancer genetics and cytogenetics 1988;34(2):209-18.
1988: Kristoffersson U; Lagergren J; Heim S; Mandahl N
Four copies of 8p in a mentally retarded boy with the mosaic karyotype 47,XY, + i(8p)/46,XY.
Clinical genetics 1988;34(3):201-3.
1988: Karlsson I; Mandahl N; Heim S; Rydholm A; Willén H; Mitelman F
Complex chromosome rearrangements in an extraabdominal desmoid tumor.
Cancer genetics and cytogenetics 1988;34(2):241-5.
1988: Mertens F; Johansson B; Heim S; Mandahl N; Rydholm A; Mitelman F
Bands involved in primary chromosome rearrangements in sarcomas are not constitutionally liable to breakage in sarcoma patients.
Human genetics 1988;79(4):309-14.
1988: Mandahl N; Heim S; Arheden K; Rydholm A; Willén H; Mitelman F
Three major cytogenetic subgroups can be identified among chromosomally abnormal solitary lipomas.
Human genetics 1988;79(3):203-8.
1988: Mertens F; Johansson B; Heim S; Mandahl N; Rydholm A; Mitelman F
Normal frequency of chromosome breakage in lymphocytes from patients with musculoskeletal sarcoma.
Cancer genetics and cytogenetics 1988;33(2):299-304.
1988: Mitelman F; Prigogina E L; Fleischman E W; Frenkel M A; Garwicz S; Heim S; Ilyinskaya G W; Kristoffersson U; Mandahl N; Volkova M A
A new specific chromosomal rearrangement, t(11;20)(p15;q11), in myeloblastic leukemia with maturation.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1988;2(7):430-2.
1988: Jin Y S; Mandahl N; Heim S; Schüller H; Mitelman F
Isochromosomes i(8q) or i(9q) in three adenocarcinomas of the lung.
Cancer genetics and cytogenetics 1988;33(1):11-7.
1988: Jin Y S; Mandahl N; Heim S; Biörklund A; Wennerberg J; Mitelman F
t(6;7)(q23;p22) as the sole chromosomal anomaly in a vocal cord carcinoma.
Cancer genetics and cytogenetics 1988;32(2):305-7.
1988: Heim S; Nilbert M; Vanni R; Floderus U M; Mandahl N; Liedgren S; Lecca U; Mitelman F
A specific translocation, t(12;14)(q14-15;q23-24), characterizes a subgroup of uterine leiomyomas.
Cancer genetics and cytogenetics 1988;32(1):13-7.
1988: Jin Y S; Heim S; Mandahl N; Biörklund A; Wennerberg J; Mitelman F
Multiple apparently unrelated clonal chromosome abnormalities in a squamous cell carcinoma of the tongue.
Cancer genetics and cytogenetics 1988;32(1):93-100.
1988: Mandahl N; Heim S; Arheden K; Rydholm A; Willén H; Mitelman F
Multiple karyotypic rearrangements, including t(X;18)(p11;q11), in a fibrosarcoma.
Cancer genetics and cytogenetics 1988;30(2):323-7.
1988: Heim S; Kristoffersson U; Mandahl N; Malm C; Mitelman F
Variant translocation t(3;15)(q21;q22) in a patient with acute promyelocytic leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1988;2(1):65-7.
1988: Jin Y S; Mandahl N; Heim S; Biörklund A; Wennerberg J; Mitelman F
Unique karyotypic abnormalities in a squamous cell carcinoma of the larynx.
Cancer genetics and cytogenetics 1988;30(1):177-9.
1988: Mandahl N; Heim S; Arheden K; Rydholm A; Willén H; Mitelman F
Rings, dicentrics, and telomeric association in histiocytomas.
Cancer genetics and cytogenetics 1988;30(1):23-33.
1988: Arheden K; Mandahl N; Strömbeck B; Isaksson M; Mitelman F
Chromosome localization of the human oncogene INT1 to 12q13 by in situ hybridization.
Cytogenetics and cell genetics 1988;47(1-2):86-7.
1988: Nilbert M; Heim S; Mandahl N; Flodérus U M; Willén H; Mitelman F
Karyotypic rearrangements in 20 uterine leiomyomas.
Cytogenetics and cell genetics 1988;49(4):300-4.
1988: Arheden K; Tommerup N; Mandahl N; Heim S; Winther J; Jensen O A; Prause J U; Mitelman F
Amplification of the human putative oncogene INT1 in primary retinoblastoma tumors.
Cytogenetics and cell genetics 1988;48(3):174-7.
1987: Heim S; Alimena G; Billström R; Diverio D; Kristoffersson U; Mandahl N; Nanni M; Mitelman F
Tetraploid karyotype (92,XXYY) in two patients with acute lymphoblastic leukemia.
Cancer genetics and cytogenetics 1987;29(1):129-33.
1987: Heim S; Avanzi G C; Billström R; Kristoffersson U; Mandahl N; Bekassy A N; Garwicz S; Wiebe T; Pegoraro L; Falda M
A new specific chromosomal rearrangement, t(8;16) (p11;p13), in acute monocytic leukaemia.
British journal of haematology 1987;66(3):323-6.
1987: Heim S; Békàssy A N; Garwicz S; Heldrup J; Wiebe T; Kristoffersson U; Mandahl N; Mitelman F
New structural chromosomal rearrangements in congenital leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1987;1(1):16-23.
1986: Heim S; Kristoffersson U; Mandahl N; Mitelman F; Bekassy A N; Garwicz S; Heldrup J; Wiebe T
Reciprocal translocation (11;19)(q23;p13) in congenital acute lymphoblastic leukemia.
Cancer genetics and cytogenetics 1986;23(3):239-44.
1986: Heim S; Kristoffersson U; Mandahl N; Mitelman F; Bekassy A N; Garwicz S; Wiebe T
High resolution banding analysis of the reciprocal translocation t(6;9) in acute nonlymphocytic leukemia.
Cancer genetics and cytogenetics 1986;22(3):195-201.
1985: Heim S; Billström R; Kristoffersson U; Mandahl N; Strömbeck B; Mitelman F
Variant Ph translocations in chronic myeloid leukemia.
Cancer genetics and cytogenetics 1985;18(3):215-27.

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