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Sverre Heim

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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Micci Francesca; Haugom Lisbeth; Ahlquist Terje; Abeler Vera M; Trope Claes G; Lothe Ragnhild A; Heim Sverre
Tumor spreading to the contralateral ovary in bilateral ovarian carcinoma is a late event in clonal evolution.
Brandal Petter; Panagopoulos Ioannis; Bjerkehagen Bodil; Heim Sverre
t(19;22)(q13;q12) Translocation leading to the novel fusion gene EWSR1-ZNF444 in soft tissue myoepithelial carcinoma.
Dahlback Hanne-Sofie S; Brandal Petter; Meling Torstein R; Gorunova Ludmila; Scheie David; Heim Sverre
Genomic aberrations in 80 cases of primary glioblastoma multiforme: Pathogenetic heterogeneity and putative cytogenetic pathways.

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All Publications

2010: Micci Francesca; Haugom Lisbeth; Ahlquist Terje; Abeler Vera M; Trope Claes G; Lothe Ragnhild A; Heim Sverre
Tumor spreading to the contralateral ovary in bilateral ovarian carcinoma is a late event in clonal evolution.
Journal of oncology 2010;2010():646340.
2009: Brandal Petter; Panagopoulos Ioannis; Bjerkehagen Bodil; Heim Sverre
t(19;22)(q13;q12) Translocation leading to the novel fusion gene EWSR1-ZNF444 in soft tissue myoepithelial carcinoma.
Genes, chromosomes & cancer 2009;48(12):1051-6.
2009: Dahlback Hanne-Sofie S; Brandal Petter; Meling Torstein R; Gorunova Ludmila; Scheie David; Heim Sverre
Genomic aberrations in 80 cases of primary glioblastoma multiforme: Pathogenetic heterogeneity and putative cytogenetic pathways.
Genes, chromosomes & cancer 2009;48(10):908-24.
2009: Karrman Kristina; Forestier Erik; Heyman Mats; Andersen Mette K; Autio Kirsi; Blennow Elisabeth; Borgström Georg; Ehrencrona Hans; Golovleva Irina; Heim Sverre; Heinonen Kristiina; Hovland Randi; Johannsson Johann H; Kerndrup Gitte; Nordgren Ann; Palmqvist Lars; Johansson Bertil;
Clinical and cytogenetic features of a population-based consecutive series of 285 pediatric T-cell acute lymphoblastic leukemias: rare T-cell receptor gene rearrangements are associated with poor outcome.
Genes, chromosomes & cancer 2009;48(9):795-805.
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: Micci Francesca; Panagopoulos Ioannis; Haugom Lisbeth; Andersen Hege Kilen; Tjønnfjord Geir E; Beiske Klaus; Heim Sverre
t(3;21)(q22;q22) leading to truncation of the RYK gene in atypical chronic myeloid leukemia.
Cancer letters 2009;277(2):205-11.
2008: Cerveira Nuno; Micci Francesca; Santos Joana; Pinheiro Manuela; Correia Cecília; Lisboa Susana; Bizarro Susana; Norton Lucília; Glomstein Anders; Asberg Ann E; Heim Sverre; Teixeira Manuel R
Molecular characterization of the MLL-SEPT6 fusion gene in acute myeloid leukemia: identification of novel fusion transcripts and cloning of genomic breakpoint junctions.
Haematologica 2008;93(7):1076-80.
2008: Brandal Petter; Panagopoulos Ioannis; Bjerkehagen Bodil; Gorunova Ludmila; Skjeldal Sigmund; Micci Francesca; Heim Sverre
Detection of a t(1;22)(q23;q12) translocation leading to an EWSR1-PBX1 fusion gene in a myoepithelioma.
Genes, chromosomes & cancer 2008;47(7):558-64.
2008: Forestier Erik; Heyman Mats; Andersen Mette K; Autio Kirsi; Blennow Elisabeth; Borgström Georg; Golovleva Irina; Heim Sverre; Heinonen Kristina; Hovland Randi; Johannsson Johann H; Kerndrup Gitte; Nordgren Ann; Rosenquist Richard; Swolin Birgitta; Johansson Bertil;
Outcome of ETV6/RUNX1-positive childhood acute lymphoblastic leukaemia in the NOPHO-ALL-1992 protocol: frequent late relapses but good overall survival.
British journal of haematology 2008;140(6):665-72.
2008: Micci Francesca; Haugom Lisbeth; Abeler Vera M; Tropé Claes G; Danielsen Håvard E; Heim Sverre
Consistent numerical chromosome aberrations in thecofibromas of the ovary.
Virchows Archiv : an international journal of pathology 2008;452(3):269-76.
2008: Forestier Erik; Gauffin Fredrika; Andersen Mette K; Autio Kirsi; Borgström Georg; Golovleva Irina; Gustafsson Britt; Heim Sverre; Heinonen Kristina; Heyman Mats; Hovland Randi; Johannsson Johann H; Kerndrup Gitte; Rosenquist Richard; Schoumans Jacqueline; Swolin Birgitta; Johansson Bertil; Nordgren Ann;
Clinical and cytogenetic features of pediatric dic(9;20)(p13.2;q11.2)-positive B-cell precursor acute lymphoblastic leukemias: a Nordic series of 24 cases and review of the literature.
Genes, chromosomes & cancer 2008;47(2):149-58.
2007: Micci Francesca; Bjerkehagen Bodil; Heim Sverre
Pairwise comparison of genomic imbalances between primary and recurrent well differentiated liposarcomas.
Cancer genetics and cytogenetics 2007;178(2):163-7.
2007: Aamot Hege Vangstein; Torlakovic Emina Emilia; Eide Marianne Brodtkorb; Holte Harald; Heim Sverre
Non-Hodgkin lymphoma with t(14;18): clonal evolution patterns and cytogenetic-pathologic-clinical correlations.
Journal of cancer research and clinical oncology 2007;133(7):455-70.
2007: Ikonomou Ida Münster; Aamot Hege Vangstein; Heim Sverre; Fosså Alexander; Delabie Jan
Granulomatous slack skin with a translocation t(3;9)(q12;p24).
The American journal of surgical pathology 2007;31(5):803-6.
2007: Micci Francesca; Panagopoulos Ioannis; Tjønnfjord Geir E; Kolstad Arne; Delabie Jan; Beiske Klaus; Heim Sverre
Molecular cytogenetic characterization of t(14;19)(q32;p13), a new recurrent translocation in B cell malignancies.
Virchows Archiv : an international journal of pathology 2007;450(5):559-65.
2007: Forestier Erik; Andersen Mette K; Autio Kirsi; Blennow Elisabeth; Borgström Georg; Golovleva Irina; Heim Sverre; Heinonen Kristina; Hovland Randi; Johannsson Johann H; Kerndrup Gitte; Nordgren Ann; Rosenquist Richard; Swolin Birgitta; Johansson Bertil;
Cytogenetic patterns in ETV6/RUNX1-positive pediatric B-cell precursor acute lymphoblastic leukemia: A Nordic series of 245 cases and review of the literature.
Genes, chromosomes & cancer 2007;46(5):440-50.
2007: Micci Francesca; Haugom Lisbeth; Abeler Vera M; Bjerkehagen Bodil; Heim Sverre
Trisomy 7 in postoperative spindle cell nodules.
Cancer genetics and cytogenetics 2007;174(2):147-50.
2007: Torres Lurdes; Ribeiro Franclim R; Pandis Nikos; Andersen Johan A; Heim Sverre; Teixeira Manuel R
Intratumor genomic heterogeneity in breast cancer with clonal divergence between primary carcinomas and lymph node metastases.
Breast cancer research and treatment 2007;102(2):143-55.
2007: Micci F; Heim S
Pathogenetic mechanisms in endometrial stromal sarcoma.
Cytogenetic and genome research 2007;118(2-4):190-5.
2007: Lundin C; Heidenblad M; Strombeck B; Borg A; Hovland R; Heim S; Johansson B
Tiling resolution array CGH of dic(7;9)(p11 approximately 13;p11 approximately 13) in B-cell precursor acute lymphoblastic leukemia reveals clustered breakpoints at 7p11.2 approximately 12.1 and 9p13.1.
Cytogenetic and genome research 2007;118(1):13-8.
2006: Karrman Kristina; Forestier Erik; Andersen Mette K; Autio Kirsi; Borgström Georg; Heim Sverre; Heinonen Kristina; Hovland Randi; Kerndrup Gitte; Johansson Bertil;
High incidence of the ETV6/RUNX1 fusion gene in paediatric precursor B-cell acute lymphoblastic leukaemias with trisomy 21 as the sole cytogenetic change: a Nordic series of cases diagnosed 1989-2005.
British journal of haematology 2006;135(3):352-4.
2006: Ikonomou Ida Münster; Tierens Anne; Troen Gunhild; Aamot Hege Vangstein; Heim Sverre; Lauritzsen Grete F; Vålerhaugen Helen; Delabie Jan
Peripheral T-cell lymphoma with involvement of the expanded mantle zone.
Virchows Archiv : an international journal of pathology 2006;449(1):78-87.
2006: Torlakovic E E; Aamot H V; Heim S
A marginal zone phenotype in follicular lymphoma with t(14;18) is associated with secondary cytogenetic aberrations typical of marginal zone lymphoma.
The Journal of pathology 2006;209(2):258-64.
2006: Micci Francesca; Panagopoulos Ioannis; Bjerkehagen Bodil; Heim Sverre
Deregulation of HMGA2 in an aggressive angiomyxoma with t(11;12)(q23;q15).
Virchows Archiv : an international journal of pathology 2006;448(6):838-42.
2006: Aamot Hege Vangstein; Tjønnfjord Geir E; Delabie Jan; Heim Sverre
Molecular cytogenetic analysis of leukemic mantle cell lymphoma with a cryptic t(11;14).
Cancer genetics and cytogenetics 2006;165(2):172-5.
2006: Brandal Petter; Bjerkehagen Bodil; Heim Sverre
Rearrangement of chromosomal region 8q11-13 in lipomatous tumours: correlation with lipoblastoma morphology.
The Journal of pathology 2006;208(3):388-94.
2006: Brandal Petter; Lie Agnes Kathrine; Bassarova Assia; Svindland Aud; Risberg Bjørn; Danielsen Håvard; Heim Sverre
Genomic aberrations in mucinous tubular and spindle cell renal cell carcinomas.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2006;19(2):186-94.
2006: Micci Francesca; Panagopoulos Ioannis; Bjerkehagen Bodil; Heim Sverre
Consistent rearrangement of chromosomal band 6p21 with generation of fusion genes JAZF1/PHF1 and EPC1/PHF1 in endometrial stromal sarcoma.
Cancer research 2006;66(1):107-12.
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.
2005: Aamot Hege Vangstein; Micci Francesca; Holte Harald; Delabie Jan; Heim Sverre
G-banding and molecular cytogenetic analyses of marginal zone lymphoma.
British journal of haematology 2005;130(6):890-901.
2005: Aamot Hege Vangstein; Bjørnslett Merete; Delabie Jan; Heim Sverre
t(14;22)(q32;q11) in non-Hodgkin lymphoma and myeloid leukaemia: molecular cytogenetic investigations.
British journal of haematology 2005;130(6):845-51.
2005: Kleivi Kristine; Diep Chieu B; Pandis Nikos; Heim Sverre; Teixeira Manuel R; Lothe Ragnhild A
TP53 mutations are associated with a particular pattern of genomic imbalances in breast carcinomas.
The Journal of pathology 2005;207(1):14-9.
2005: Brandal Petter; Busund Lill-Tove; Heim Sverre
Chromosome abnormalities in juxtaglomerular cell tumors.
Cancer 2005;104(3):504-10.
2005: Brandal Petter; Bjerkehagen Bodil; Danielsen Håvard; Heim Sverre
Chromosome 7 abnormalities are common in chordomas.
Cancer genetics and cytogenetics 2005;160(1):15-21.
2005: Teixeira Manuel R; Heim Sverre
Multiple numerical chromosome aberrations in cancer: what are their causes and what are their consequences?
Seminars in cancer biology 2005;15(1):3-12.
2004: Teixeira Manuel R; Ribeiro Franclim R; Eknaes Mette; Waehre Håkon; Stenwig Anna E; Giercksky Karl E; Heim Sverre; Lothe Ragnhild A
Genomic analysis of prostate carcinoma specimens obtained via ultrasound-guided needle biopsy may be of use in preoperative decision-making.
Cancer 2004;101(8):1786-93.
2004: Brandal Petter; Bjerkehagen Bodil; Heim Sverre
Molecular cytogenetic characterization of tenosynovial giant cell tumors.
Neoplasia (New York, N.Y.) 2004;6(5):578-83.
2004: Teixeira M R; Ribeiro F R; Torres L; Pandis N; Andersen J A; Lothe R A; Heim S
Assessment of clonal relationships in ipsilateral and bilateral multiple breast carcinomas by comparative genomic hybridisation and hierarchical clustering analysis.
British journal of cancer 2004;91(4):775-82.
2004: Bardi Georgia; Fenger Claus; Johansson Bertil; Mitelman Felix; Heim Sverre
Tumor karyotype predicts clinical outcome in colorectal cancer patients.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2004;22(13):2623-34.
2004: Micci Francesca; Teixeira Manuel R; Haugom Lisbeth; Kristensen Gunnar; Abeler Vera M; Heim Sverre
Genomic aberrations in carcinomas of the uterine corpus.
Genes, chromosomes & cancer 2004;40(3):229-46.
2003: Adeyinka Adewale; Baldetorp Bo; Mertens Fredrik; Olsson Håkan; Johannsson Oskar; Heim Sverre; Pandis Nikos
Comparative cytogenetic and DNA flow cytometric analysis of 242 primary breast carcinomas.
Cancer genetics and cytogenetics 2003;147(1):62-7.
2003: Brandal Petter; Micci Francesca; Bjerkehagen Bodil; Eknaes Mette; Larramendy Marcelo; Lothe Ragnhild A; Knuutila Sakari; Heim Sverre
Molecular cytogenetic characterization of desmoid tumors.
Cancer genetics and cytogenetics 2003;146(1):1-7.
2003: Micci Francesca; Teixeira Manuel R; Scheistrøen Marit; Abeler Vera M; Heim Sverre
Cytogenetic characterization of tumors of the vulva and vagina.
Genes, chromosomes & cancer 2003;38(2):137-48.
2003: Kildal Wanja; Kraggerud Sigrid Marie; Abeler Vera M; Heim Sverre; Tropé Claés G; Kristensen Gunnar B; Risberg Bjørn; Lothe Ragnhild A; Danielsen Håvard E
Genome profiles of bilateral dysgerminomas, a unilateral gonadoblastoma, and a metastasis from a 46, XY phenotypic female.
Human pathology 2003;34(9):946-9.
2003: Micci Francesca; Walter Claudia U; Teixeira Manuel R; Panagopoulos Ioannis; Bjerkehagen Bodil; Saeter Gunnar; Heim Sverre
Cytogenetic and molecular genetic analyses of endometrial stromal sarcoma: nonrandom involvement of chromosome arms 6p and 7p and confirmation of JAZF1/JJAZ1 gene fusion in t(7;17).
Cancer genetics and cytogenetics 2003;144(2):119-24.
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: Ioannidis P; Mahaira L; Papadopoulou A; Teixeira M R; Heim S; Andersen J A; Evangelou E; Dafni U; Pandis N; Trangas T
CRD-BP: a c-Myc mRNA stabilizing protein with an oncofetal pattern of expression.
Anticancer research 2003;23(3A):2179-83.
2003: Forestier Erik; Heim Sverre; Blennow Elisabeth; Borgström Georg; Holmgren Gösta; Heinonen Kristiina; Johannsson Johann; Kerndrup Gitte; Andersen Mette Klarskov; Lundin Catarina; Nordgren Ann; Rosenquist Richard; Swolin Birgitta; Johansson Bertil;
Cytogenetic abnormalities in childhood acute myeloid leukaemia: a Nordic series comprising all children enrolled in the NOPHO-93-AML trial between 1993 and 2001.
British journal of haematology 2003;121(4):566-77.
2003: Papadopoulou Anna; Trangas Theoni; Teixeira Manuel R; Heim Sverre; Dimitriadis Euthimios; Tsarouha Haroula; Andersen Johan A; Evangelou Evangelos; Ioannidis Panayiotis; Agnantis Niki J; Pandis Nikos
Telomerase activity and genetic alterations in primary breast carcinomas.
Neoplasia (New York, N.Y.) 2003;5(2):170-8.
2003: Ioannidis Panayotis; Mahaira Louisa; Papadopoulou Anna; Teixeira Manuel R; Heim Sverre; Andersen Johan A; Evangelou Evangelos; Dafni Urania; Pandis Nikos; Trangas Theoni
8q24 Copy number gains and expression of the c-myc mRNA stabilizing protein CRD-BP in primary breast carcinomas.
International journal of cancer. Journal international du cancer 2003;104(1):54-9.
2003: Ikonomou Ida Münster; Nesland Jahn M; Schjølseth Svein Arve; Heim Sverre; Delabie Jan
Mantle cell lymphoma with Homer-Wright rosettes.
Virchows Archiv : an international journal of pathology 2003;442(2):179-82.
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: Aamot H; Micci F; Holte H; Delabie J; Heim S
M-FISH cytogenetic analysis of non-Hodgkin lymphomas with t(14;18)(q32;q21) and add(1)(p36) as a secondary abnormality shows that the extra material often comes from chromosome arm 17q.
Leukemia & lymphoma 2002;43(5):1051-6.
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: Kleivi Kristine; Lothe Ragnhild A; Heim Sverre; Tsarouha Haroula; Kraggerud Sigrid M; Pandis Nikos; Papadopoulou Anna; Andersen Johan; Jakobsen Kjetill S; Teixeira Manuel R
Genome profiling of breast cancer cells selected against in vitro shows copy number changes.
Genes, chromosomes & cancer 2002;33(3):304-9.
2002: Teixeira Manuel R; Pandis Nikos; Heim Sverre
Cytogenetic clues to breast carcinogenesis.
Genes, chromosomes & cancer 2002;33(1):1-16.
2002: Micci F; Teixeira M R; Bjerkehagen B; Heim S
Characterization of supernumerary rings and giant marker chromosomes in well-differentiated lipomatous tumors by a combination of G-banding, CGH, M-FISH, and chromosome- and locus-specific FISH.
Cytogenetic and genome research 2002;97(1-2):13-9.
2001: Micci F; Teixeira M R; Heim S
Complete cytogenetic characterization of the human breast cancer cell line MA11 combining G-banding, comparative genomic hybridization, multicolor fluorescence in situ hybridization, RxFISH, and chromosome-specific painting.
Cancer genetics and cytogenetics 2001;131(1):25-30.
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: 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: Bomme L; Lothe R A; Bardi G; Fenger C; Kronborg O; Heim S
Assessments of clonal composition of colorectal adenomas by FISH analysis of chromosomes 1, 7, 13 and 20.
International journal of cancer. Journal international du cancer 2001;92(6):816-23.
2001: Teixeira M R; Tsarouha H; Kraggerud S M; Pandis N; Dimitriadis E; Andersen J A; Lothe R A; Heim S
Evaluation of breast cancer polyclonality by combined chromosome banding and comparative genomic hybridization analysis.
Neoplasia (New York, N.Y.) 2001;3(3):204-14.
2000: Panagopoulos I; Teixeira M R; Micci F; Hammerstrøm J; Isaksson M; Johansson B; Mitelman F; Heim S
Acute myeloid leukemia with inv(8)(p11q13).
Leukemia & lymphoma 2000;39(5-6):651-6.
2000: Thorstensen L; Qvist H; Heim S; Liefers G J; Nesland J M; Giercksky K E; Lothe R A
Evaluation of 1p losses in primary carcinomas, local recurrences and peripheral metastases from colorectal cancer patients.
Neoplasia (New York, N.Y.) 2000;2(6):514-22.
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: Panagopoulos I; Isaksson M; Lindvall C; Björkholm M; Ahlgren T; Fioretos T; Heim S; Mitelman F; Johansson B
RT-PCR analysis of the MOZ-CBP and CBP-MOZ chimeric transcripts in acute myeloid leukemias with t(8;16)(p11;p13).
Genes, chromosomes & cancer 2000;28(4):415-24.
2000: Forestier E; Johansson B; Gustafsson G; Borgström G; Kerndrup G; Johannsson J; Heim S
Prognostic impact of karyotypic findings in childhood acute lymphoblastic leukaemia: a Nordic series comparing two treatment periods. For the Nordic Society of Paediatric Haematology and Oncology (NOPHO) Leukaemia Cytogenetic Study Group.
British journal of haematology 2000;110(1):147-53.
2000: Teixeira M R; Micci F; Dietrich C U; Heim S
Detailed genome-wide screening for inter- and intrachromosomal abnormalities by sequential G-banding and RxFISH color banding of the same metaphase cells.
Cancer genetics and cytogenetics 2000;119(2):94-101.
2000: Kraggerud S M; Szymanska J; Abeler V M; Kaern J; Eknaes M; Heim S; Teixeira M R; Tropé C G; Peltomäki P; Lothe R A
DNA copy number changes in malignant ovarian germ cell tumors.
Cancer research 2000;60(11):3025-30.
2000: Teixeira M R; Waehre H; Lothe R A; Stenwig A E; Pandis N; Giercksky K E; Heim S
High frequency of clonal chromosome abnormalities in prostatic neoplasms sampled by prostatectomy or ultrasound-guided needle biopsy.
Genes, chromosomes & cancer 2000;28(2):211-9.
2000: Forestier E; Johansson B; Borgström G; Kerndrup G; Johansson J; Heim S
Cytogenetic findings in a population-based series of 787 childhood acute lymphoblastic leukemias from the Nordic countries. The NOPHO Leukemia Cytogenetic Study Group.
European journal of haematology 2000;64(3):194-200.
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: Bjerkehagen B; Dietrich C; Reed W; Micci F; Saeter G; Berner A; Nesland J M; Heim S
Extraskeletal myxoid chondrosarcoma: multimodal diagnosis and identification of a new cytogenetic subgroup characterized by t(9;17)(q22;q11).
Virchows Archiv : an international journal of pathology 1999;435(5):524-30.
1999: Larsen J B; Schrøder H D; Sørensen A G; Bjerre P; Heim S
Simple numerical chromosome aberrations characterize pituitary adenomas.
Cancer genetics and cytogenetics 1999;114(2):144-9.
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: Tsarouha H; Pandis N; Bardi G; Teixeira M R; Andersen J A; Heim S
Karyotypic evolution in breast carcinomas with i(1)(q10) and der(1;16)(q10;p10) as the primary chromosome abnormality.
Cancer genetics and cytogenetics 1999;113(2):156-61.
1999: Teixeira M R; Micci F; Dietrich C U; Heim S
Cross-species color banding characterization of chromosomal rearrangements in leukemias with incomplete G-band karyotypes.
Genes, chromosomes & cancer 1999;26(1):13-9.
1999: Micci F; Teixeira M R; Dietrich C U; Saeter G; Bjerkehagen B; Heim S
Combined RxFISH/G-banding allows refined karyotyping of solid tumors.
Human genetics 1999;104(5):370-5.
1999: Teixeira M R; Kristensen G B; Abeler V M; Heim S
Karyotypic findings in tumors of the vulva and vagina.
Cancer genetics and cytogenetics 1999;111(1):87-91.
1998: Bomme L; Bardi G; Pandis N; Fenger C; Kronborg O; Heim S
Cytogenetic analysis of colorectal adenomas: karyotypic comparisons of synchronous tumors.
Cancer genetics and cytogenetics 1998;106(1):66-71.
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: Teixeira M R; Pandis N; Dietrich C U; Reed W; Andersen J; Qvist H; Heim S
Chromosome banding analysis of gynecomastias and breast carcinomas in men.
Genes, chromosomes & cancer 1998;23(1):16-20.
1998: Adeyinka A; Mertens F; Idvall I; Bondeson L; Ingvar C; Heim S; Mitelman F; Pandis N
Cytogenetic findings in invasive breast carcinomas with prognostically favourable histology: a less complex karyotypic pattern?
International journal of cancer. Journal international du cancer 1998;79(4):361-4.
1998: Bardi G; Rizou H; Michailakis E; Dietrich C; Pandis N; Heim S
Cytogenetic findings in three primary hepatocellular carcinomas.
Cancer genetics and cytogenetics 1998;104(2):165-6.
1998: Teixeira M R; Qvist H; Bøhler P J; Pandis N; Heim S
Cytogenetic analysis shows that carcinosarcomas of the breast are of monoclonal origin.
Genes, chromosomes & cancer 1998;22(2):145-51.
1998: Pandis N; Teixeira M R; Adeyinka A; Rizou H; Bardi G; Mertens F; Andersen J A; Bondeson L; Sfikas K; Qvist H; Apostolikas N; Mitelman F; Heim S
Cytogenetic comparison of primary tumors and lymph node metastases in breast cancer patients.
Genes, chromosomes & cancer 1998;22(2):122-9.
1998: Teixeira M R; Giercksky K E; Ikonomou I M; Heim S
Translocation (3;3)(p14;q29) as the primary chromosome abnormality in a peritoneal mesothelioma.
Cancer genetics and cytogenetics 1998;103(1):73-5.
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: 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: Bomme L; Heim S; Bardi G; Fenger C; Kronborg O; Brøgger A; Lothe R A
Allelic imbalance and cytogenetic deletion of 1p in colorectal adenomas: a target region identified between DIS199 and DIS234.
Genes, chromosomes & cancer 1998;21(3):185-94.
1997: Dietrich C U; Pandis N; Rizou H; Petersson C; Bardi G; Qvist H; Apostolikas N; Bøhler P J; Andersen J A; Idvall I; Mitelman F; Heim S
Cytogenetic findings in phyllodes tumors of the breast: karyotypic complexity differentiates between malignant and benign tumors.
Human pathology 1997;28(12):1379-82.
1997: Gerdes A M; Pandis N; Bomme L; Dietrich C U; Teixeira M R; Bardi G; Heim S
Fluorescence in situ hybridization of old G-banded and mounted chromosome preparations.
Cancer genetics and cytogenetics 1997;98(1):9-15.
1997: Adeyinka A; Pandis N; Bardi G; Bonaldi L; Mertens F; Mitelman F; Heim S
A subgroup of breast carcinomas is cytogenetically characterized by trisomy 12.
Cancer genetics and cytogenetics 1997;97(2):119-21.
1997: Forestier E; Gustafsson G; von Heideman A; Heim S; Hernell O; Mitelman F; Nordenson I; Swolin B; Söderhäll S
Prognostic impact of bone marrow karyotype in childhood acute lymphoblastic leukaemia: Swedish experiences 1986-91.
Acta paediatrica (Oslo, Norway : 1992) 1997;86(8):819-25.
1997: Bardi G; Parada L A; Bomme L; Pandis N; Johansson B; Willén R; Fenger C; Kronborg O; Mitelman F; Heim S
Cytogenetic findings in metastases from colorectal cancer.
International journal of cancer. Journal international du cancer 1997;72(4):604-7.
1997: Heim S; Teixeira M R; Dietrich C U; Pandis N
Cytogenetic polyclonality in tumors of the breast.
Cancer genetics and cytogenetics 1997;95(1):16-9.
1997: Pandis N; Bardi G; Mitelman F; Heim S
Deletion of the short arm of chromosome 3 in breast tumors.
Genes, chromosomes & cancer 1997;18(4):241-5.
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: Teixeira M R; Pandis N; Bardi G; Andersen J A; Bøhler P J; Qvist H; Heim S
Discrimination between multicentric and multifocal breast carcinoma by cytogenetic investigation of macroscopically distinct ipsilateral lesions.
Genes, chromosomes & cancer 1997;18(3):170-4.
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: Teixeira M R; Qvist H; Giercksky K E; Bøhler P J; Heim S
Cytogenetic analysis of several pseudomyxoma peritonei lesions originating from a mucinous cystadenoma of the appendix.
Cancer genetics and cytogenetics 1997;93(2):157-9.
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: Petersson C; Pandis N; Rizou H; Mertens F; Dietrich C U; Adeyinka A; Idvall I; Bondeson L; Georgiou G; Ingvar C; Heim S; Mitelman F
Karyotypic abnormalities in fibroadenomas of the breast.
International journal of cancer. Journal international du cancer 1997;70(3):282-6.
1997: Bardi G; Parada L A; Bomme L; Pandis N; Willén R; Johansson B; Jeppsson B; Beroukas K; Heim S; Mitelman F
Cytogenetic comparisons of synchronous carcinomas and polyps in patients with colorectal cancer.
British journal of cancer 1997;76(6):765-9.
1996: Pejovic T; Iosif C S; Mitelman F; Heim S
Karyotypic characteristics of borderline malignant tumors of the ovary: trisomy 12, trisomy 7, and r(1) as nonrandom features.
Cancer genetics and cytogenetics 1996;92(2):95-8.
1996: Bomme L; Bardi G; Pandis N; Fenger C; Kronborg O; Heim S
Chromosome abnormalities in colorectal adenomas: two cytogenetic subgroups characterized by deletion of 1p and numerical aberrations.
Human pathology 1996;27(11):1192-7.
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: Köhler M; Johansson B; Garwicz S; Heim S; Mitelman F
No FISH evidence for trisomy 7 in normal or leukemic bone marrow.
Cancer genetics and cytogenetics 1996;88(2):133-5.
1996: Adeyinka A; Pandis N; Nilsson J; Idvall I; Mertens F; Petersson C; Heim S; Mitelman F
Different cytogenetic patterns in skeletal breast cancer metastases.
Genes, chromosomes & cancer 1996;16(1):72-4.
1996: Heim S
Transient acute monoblastic leukemia with reciprocal (8;16)(p11;p13) translocation.
Pediatric hematology and oncology 1996;13(3):203-4.
1996: Pejovic T; Alm P; Iosif S C; Mitelman F; Heim S
Cytogenetic findings in four malignant mixed mesodermal tumors of the ovary.
Cancer genetics and cytogenetics 1996;88(1):53-6.
1996: Pandis N; Idvall I; Bardi G; Jin Y; Gorunova L; Mertens F; Olsson H; Ingvar C; Beroukas K; Mitelman F; Heim S
Correlation between karyotypic pattern and clincopathologic features in 125 breast cancer cases.
International journal of cancer. Journal international du cancer 1996;66(2):191-6.
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: Andreasson P; Johansson B; Arheden K; Tedgård U; Ljung R; Heim S; Mitelmann F
Emergence of novel transient clonal chromosomal bone marrow changes in remission of acute lymphoblastic leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1996;10(2):378-83.
1996: Teixeira M R; Pandis N; Bardi G; Andersen J A; Heim S
Karyotypic comparisons of multiple tumorous and macroscopically normal surrounding tissue samples from patients with breast cancer.
Cancer research 1996;56(4):855-9.
1996: Johansson B; Fioretos T; Garwicz S; Heim S; Mitelman F
t(3;21)(q26;q22) with AML1 rearrangement in a de novo childhood acute monoblastic leukaemia.
British journal of haematology 1996;92(2):429-31.
1996: Teixeira M R; Pandis N; Gerdes A M; Dietrich C U; Bardi G; Andersen J A; Graversen H P; Mitelman F; Heim S
Cytogenetic abnormalities in an in situ ductal carcinoma and five prophylactically removed breasts from members of a family with hereditary breast cancer.
Breast cancer research and treatment 1996;38(2):177-82.
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: Lothe R A; Andersen S N; Hofstad B; Meling G I; Peltomäki P; Heim S; Brøgger A; Vatn M; Rognum T O; Børresen A L
Deletion of 1p loci and microsatellite instability in colorectal polyps.
Genes, chromosomes & cancer 1995;14(3):182-8.
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: Johansson B; Arheden K; Höglund M; Othzén A; Békássy A N; Turesson I; Heim S; Mitelman F
Fluorescence in situ hybridization analysis of whole-arm 7;12 translocations in hematologic malignancies.
Genes, chromosomes & cancer 1995;14(1):56-62.
1995: Teixeira M R; Pandis N; Bardi G; Andersen J A; Mitelman F; Heim S
Clonal heterogeneity in breast cancer: karyotypic comparisons of multiple intra- and extra-tumorous samples from 3 patients.
International journal of cancer. Journal international du cancer 1995;63(1):63-8.
1995: Pandis N; Teixeira M R; Gerdes A M; Limon J; Bardi G; Andersen J A; Idvall I; Mandahl N; Mitelman F; Heim S
Chromosome abnormalities in bilateral breast carcinomas. Cytogenetic evaluation of the clonal origin of multiple primary tumors.
Cancer 1995;76(2):250-8.
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: Pandis N; Karaiskos C; Bardi G; Sfikas K; Tserkezoglou A; Fotiou S; Heim S
Chromosome analysis of uterine adenomyosis. Detection of the leiomyoma-associated del(7q) in three cases.
Cancer genetics and cytogenetics 1995;80(2):118-20.
1995: Bardi G; Pandis N; Schousboe K; Hølund B; Heim S
Near-diploid karyotypes with recurrent chromosome abnormalities characterize early-stage endometrial cancer.
Cancer genetics and cytogenetics 1995;80(2):110-4.
1995: Karaiskos C; Pandis N; Bardi G; Sfikas K; Tserkezoglou A; Fotiou S; Heim S
Cytogenetic findings in uterine epithelioid leiomyomas.
Cancer genetics and cytogenetics 1995;80(2):103-6.
1995: Hasle H; Heim S; Schroeder H; Schmiegelow K; Ostergaard E; Kerndrup G
Transient pancytopenia preceding acute lymphoblastic leukemia (pre-ALL).
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1995;9(4):605-8.
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: 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: Bardi G; Sukhikh T; Pandis N; Fenger C; Kronborg O; Heim S
Karyotypic characterization of colorectal adenocarcinomas.
Genes, chromosomes & cancer 1995;12(2):97-109.
1995: Dietrich C U; Pandis N; Teixeira M R; Bardi G; Gerdes A M; Andersen J A; Heim S
Chromosome abnormalities in benign hyperproliferative disorders of epithelial and stromal breast tissue.
International journal of cancer. Journal international du cancer 1995;60(1):49-53.
1994: Dietrich C U; Pandis N; Bardi G; Teixeira M R; Soukhikh T; Petersson C; Andersen J A; Heim S
Karyotypic changes in phyllodes tumors of the breast.
Cancer genetics and cytogenetics 1994;78(2):200-6.
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: Teixeira M R; Pandis N; Bardi G; Andersen J A; Mandahl N; Mitelman F; Heim S
Cytogenetic analysis of multifocal breast carcinomas: detection of karyotypically unrelated clones as well as clonal similarities between tumour foci.
British journal of cancer 1994;70(5):922-7.
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: Pandis N; Bardi G; Heim S
Interrelationship between methodological choices and conceptual models in solid tumor cytogenetics.
Cancer genetics and cytogenetics 1994;76(2):77-84.
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: Bardi G; Sukhikh T; Pandis N; Hølund B; Heim S
Complex karyotypic abnormalities in a primary carcinoma of the fallopian tube.
Genes, chromosomes & cancer 1994;10(3):207-9.
1994: Bomme L; Bardi G; Pandis N; Fenger C; Kronborg O; Heim S
Clonal karyotypic abnormalities in colorectal adenomas: clues to the early genetic events in the adenoma-carcinoma sequence.
Genes, chromosomes & cancer 1994;10(3):190-6.
1994: Hagmar L; Brøgger A; Hansteen I L; Heim S; Högstedt B; Knudsen L; Lambert B; Linnainmaa K; Mitelman F; Nordenson I
Cancer risk in humans predicted by increased levels of chromosomal aberrations in lymphocytes: Nordic study group on the health risk of chromosome damage.
Cancer research 1994;54(11):2919-22.
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: Köhler M; Johansson B; Ludvigsson J; Aman P; Heim S; Mitelman F
Acute myeloid leukemia (AML-M1) with multiple trisomies and t(8;21)(q22;q22).
Cancer genetics and cytogenetics 1994;73(1):79-81.
1994: Dietrich C U; Pandis N; Andersen J A; Heim S
Chromosome abnormalities in adenolipomas of the breast: karyotypic evidence that the mesenchymal component constitutes the neoplastic parenchyma.
Cancer genetics and cytogenetics 1994;72(2):146-50.
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.
1993: Aman P; Pejovic T; Wennborg A; Heim S; Mitelman F
Mapping of the 19p13 breakpoint in an ovarian carcinoma between the INSR and TCF3 loci.
Genes, chromosomes & cancer 1993;8(2):134-6.
1993: Dietrich C U; Pandis N; Bjerre P; Schrøder H D; Heim S
Simple numerical chromosome aberrations in two pituitary adenomas.
Cancer genetics and cytogenetics 1993;69(2):118-21.
1993: Fioretos T; Nilsson P G; Aman P; Heim S; Kristoffersson U; Malm C; Simonsson B; Turesson I; Mitelman F
Clinical impact of breakpoint position within M-bcr in chronic myeloid leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1993;7(8):1225-31.
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: Dietrich C U; Jacobsen B B; Starklint H; Heim S
Clonal karyotypic evolution in an embryonal rhabdomyosarcoma with trisomy 8 as the primary chromosomal abnormality.
Genes, chromosomes & cancer 1993;7(4):240-4.
1993: Bajalica S; Sørensen A G; Pedersen N T; Heim S; Brøndum-Nielsen K
Chromosome painting as a supplement to cytogenetic banding analysis in non-Hodgkin's lymphoma.
Genes, chromosomes & cancer 1993;7(4):231-9.
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: Bardi G; Pandis N; Fenger C; Kronborg O; Bomme L; Heim S
Deletion of 1p36 as a primary chromosomal aberration in intestinal tumorigenesis.
Cancer research 1993;53(8):1895-8.
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: Pejovic T; Heim S; Alm P; Iosif S; Himmelmann A; Skjaerris J; Mitelman F
Isochromosome 1q as the sole karyotypic abnormality in a Sertoli cell tumor of the ovary.
Cancer genetics and cytogenetics 1993;65(1):79-80.
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.
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: Heim S; Sørensen A G; Christensen B E; Pedersen N T
Re-emergence in remission of primary clone in acute myelogenous leukaemias with multiple chromosomal aberrations at diagnosis.
British journal of haematology 1992;82(2):332-6.
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: Heim S
Is cancer cytogenetics reducible to the molecular genetics of cancer cells?
Genes, chromosomes & cancer 1992;5(3):188-96.
1992: Heim S; Mitelman F
Cytogenetic analysis in the diagnosis of acute leukemia.
Cancer 1992;70(6 Suppl):1701-9.
1992: Bajalica S; Brøndum-Nielsen K; Sørensen A G; Pedersen N T; Heim S
Identification of a whole-arm translocation by in situ hybridization with directly fluorochrome-labeled probes in a myelodysplastic syndrome.
Genes, chromosomes & cancer 1992;5(2):128-31.
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: Fioretos T; Heim S; Garwicz S; Ludvigsson J; Mitelman F
Molecular analysis of Philadelphia-positive childhood chronic myeloid leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1992;6(7):723-5.
1992: Mitelman F; Heim S
Quantitative acute leukemia cytogenetics.
Genes, chromosomes & cancer 1992;5(1):57-66.
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: Heim S; Christensen B E; Fioretos T; Sørensen A G; Pedersen N T
Acute myelomonocytic leukemia with inv(16)(p13q22) complicating Philadelphia chromosome positive chronic myeloid leukemia.
Cancer genetics and cytogenetics 1992;59(1):35-8.
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: Bardi G; Pandis N; Mandahl N; Heim S; Sfikas K; Willén H; Panagiotopoulos G; Rydholm A; Mitelman F
Chromosomal abnormalities in giant cell tumors of bone.
Cancer genetics and cytogenetics 1991;57(2):161-7.
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: Mertens F; Sallerfors B; Heim S; Johansson B; Kristoffersson U; Malm C; Mitelman F
Trisomy 13 as a primary chromosome aberration in acute leukemia.
Cancer genetics and cytogenetics 1991;56(1):39-44.
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: Johansson B; Mertens F; Heim S; Kristoffersson U; Mitelman F
Cytogenetics of secondary myelodysplasia (sMDS) and acute nonlymphocytic leukemia (sANLL).
European journal of haematology 1991;47(1):17-27.
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: Mertens F; Johansson B; Heim S; Kristoffersson U; Mitelman F
Karyotypic patterns in chronic myeloproliferative disorders: report on 74 cases and review of the literature.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1991;5(3):214-20.
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: 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: Nibert M; Heim S
Uterine leiomyoma cytogenetics.
Genes, chromosomes & cancer 1990;2(1):3-13.
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: Brøgger A; Hagmar L; Hansteen I L; Heim S; Högstedt B; Knudsen L; Lambert B; Linnainmaa K; Mitelman F; Nordenson I
An inter-Nordic prospective study on cytogenetic endpoints and cancer risk. Nordic Study Group on the Health Risk of Chromosome Damage.
Cancer genetics and cytogenetics 1990;45(1):85-92.
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: Heim S; Johansson B; Mertens F
Constitutional chromosome instability and cancer risk.
Mutation research 1989;221(1):39-51.
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; Mitelman F
Cytogenetically unrelated clones in hematological neoplasms.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1989;3(1):6-8.
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: 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: Mitelman F; Heim S
Consistent involvement of only 71 of the 329 chromosomal bands of the human genome in primary neoplasia-associated rearrangements.
Cancer research 1988;48(24 Pt 1):7115-9.
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: 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: 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; 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.

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