Section for Cancer Cytogenetics

Publications published since 1983 or in press from OUS - Section for Cancer Cytogenetics

437 publications found

Publications in press

1. Barbany G, Andersen MK, Autio K, Borgström G, Franco LC, Golovleva I, Heim S, Heinonen K, Hovland R, Johansson B, Johannsson JH, Kjeldsen E, Nordgren A, Palmqvist L, Forestier E, on behalf of the Nordic Society of Paediatric Haematology and Oncology (NOPHO), the Swedish Cytogenetic Leukaemia Study Group (SCLSG) and the NOPHO Leukaemia Cytogenetic Study Group (NLCSG)
   Additional aberrations of the ETV6 and RUNX1 genes have no prognostic impact in 229 t(12;21)(p13;q22)-positive B-cell precursor acute lymphoblastic leukaemias treated according to the NOPHO-ALL-2000 protocol
   Leuk Res (in press)
   PubMed 22521551
2. Nyquist KB, Panagopoulos I, Thorsen J, Roberto R, Wik HS, Tierens A, Heim S, Micci F
   t(12;13)(q14;q31) leading to HMGA2 upregulation in acute myeloid leukaemia
   Br J Haematol (in press)
   PubMed 22404713

Publications 2012

1. Ellingsen T, Hansen I, Thorsen J, Kuno Møller B, Tarp U, Jacobsen S, Lund Hetland M, Vestergaard A, Hørslev-Petersen K, Stengaard-Pedersen K (2012)
   Up-regulated dipeptidyl-peptidase IV (CD26) on monocytes was unaffected by effective DMARD treatment in early steroid and DMARD-naive rheumatoid arthritis
   Clin Exp Rheumatol, 30 (1), 58-63
   PubMed 22273590
2. Håvik AB, Brandal P, Honne H, Dahlback HS, Scheie D, Hektoen M, Meling TR, Helseth E, Heim S, Lothe RA, Lind GE (2012)
   MGMT promoter methylation in gliomas-assessment by pyrosequencing and quantitative methylation-specific PCR
   J Transl Med, 10, 36
   PubMed 22390413
3. Kildal W, Micci F, Risberg B, Abeler VM, Kristensen GB, Heim S, Danielsen HE (2012)
   Genomic imbalances in endometrial adenocarcinomas - comparison of DNA ploidy, karyotyping and comparative genomic hybridization
   Mol Oncol, 6 (1), 98-107
   PubMed 22062770

Publications 2011

1. Andersen MK, Autio K, Barbany G, Borgström G, Cavelier L, Golovleva I, Heim S, Heinonen K, Hovland R, Johannsson JH, Johansson B, Kjeldsen E, Nordgren A, Palmqvist L, Forestier E (2011)
   Paediatric B-cell precursor acute lymphoblastic leukaemia with t(1;19)(q23;p13): clinical and cytogenetic characteristics of 47 cases from the Nordic countries treated according to NOPHO protocols
   Br J Haematol, 155 (2), 235-43
   PubMed 21902680
2. Dahlback HS, Brandal P, Gorunova L, Widing E, Meling TR, Krossnes BK, Heim S (2011)
   Genomic aberrations in pediatric gliomas and embryonal tumors
   Genes Chromosomes Cancer, 50 (10), 788-99
   PubMed 21717527
3. Dahlback HS, Brandal P, Krossnes BK, Fric R, Meling TR, Meza-Zepeda LA, Danielsen HE, Heim S (2011)
   Multiple chromosomal monosomies are characteristic of giant cell ependymoma
   Hum Pathol, 42 (12), 2042-6
   PubMed 21683982
4. Dahlback HS, Gorunova L, Brandal P, Scheie D, Helseth E, Meling TR, Heim S (2011)
   Genomic aberrations in diffuse low-grade gliomas
   Genes Chromosomes Cancer, 50 (6), 409-20
   PubMed 21412929
5. Dahlback HS, Gorunova L, Micci F, Scheie D, Brandal P, Meling TR, Heim S (2011)
   Molecular cytogenetic analysis of a gliosarcoma with osseous metaplasia
   Cytogenet Genome Res, 134 (2), 88-95
   PubMed 21555877
6. Gorunova L, Bjerkehagen B, Heim S (2011)
   Paratesticular leiomyoma with a der(14)t(12;14)(q15;q24)
   Cancer Genet, 204 (8), 465-8
   PubMed 21962898
7. Kyriazoglou AI, Dimitriadis E, Arnogiannaki N, Brandal P, Heim S, Pandis N (2011)
   Similar cytogenetic findings in two synchronous secondary peripheral chondrosarcomas in a patient with multiple osteochondromas
   Cancer Genet, 204 (12), 677-81
   PubMed 22285020
8. Micci F, Thorsen J, Haugom L, Zeller B, Tierens A, Heim S (2011)
   Translocation t(1;16)(p31;q24) rearranging CBFA2T3 is specific for acute erythroid leukemia
   Leukemia, 25 (9), 1510-2
   PubMed 21606959
9. Møller P, Clark N, Mæhle L (2011)
   A SImplified method for Segregation Analysis (SISA) to determine penetrance and expression of a genetic variant in a family
   Hum Mutat, 32 (5), 568-71
   PubMed 21309035
10. Nyquist KB, Thorsen J, Zeller B, Haaland A, Trøen G, Heim S, Micci F (2011)
    Identification of the TAF15-ZNF384 fusion gene in two new cases of acute lymphoblastic leukemia with a t(12;17)(p13;q12)
    Cancer Genet, 204 (3), 147-52
    PubMed 21504714
11. Teixeira MR, Heim S (2011)
    Cytogenetic analysis of tumor clonality
    Adv Cancer Res, 112, 127-49
    PubMed 21925303
12. Thorsen J, Micci F, Heim S (2011)
    Identification of chromosomal breakpoints of cancer-specific translocations by rolling circle amplification and long-distance inverse PCR
    Cancer Genet, 204 (8), 458-61
    PubMed 21962896
13. Warsame AA, Aasheim HC, Nustad K, Trøen G, Tierens A, Wang V, Randen U, Dong HP, Heim S, Brech A, Delabie J (2011)
    Splenic marginal zone lymphoma with VH1-02 gene rearrangement expresses poly- and self-reactive antibodies with similar reactivity
    Blood, 118 (12), 3331-9
    PubMed 21725051

Publications 2010

1. Brandal P, Teixeira MR, Heim S (2010)
   Genotypic and phenotypic classification of cancer: How should the impact of the two diagnostic approaches best be balanced?
   Genes Chromosomes Cancer, 49 (9), 763-74
   PubMed 20607708
2. Micci F, Haugom L, Ahlquist T, Andersen HK, Abeler VM, Davidson B, Trope CG, Lothe RA, Heim S (2010)
   Genomic aberrations in borderline ovarian tumors
   J Transl Med, 8, 21
   PubMed 20184781
3. Micci F, Skotheim RI, Haugom L, Weimer J, Eibak AM, Abeler VM, Trope CG, Arnold N, Lothe RA, Heim S (2010)
   Array-CGH analysis of microdissected chromosome 19 markers in ovarian carcinoma identifies candidate target genes
   Genes Chromosomes Cancer, 49 (11), 1046-53
   PubMed 20725991
4. Santos J, Cerveira N, Bizarro S, Ribeiro FR, Correia C, Torres L, Lisboa S, Vieira J, Mariz JM, Norton L, Snijder S, Mellink CH, Buijs A, Shih LY, Strehl S, Micci F, Heim S, Teixeira MR (2010)
   Expression pattern of the septin gene family in acute myeloid leukemias with and without MLL-SEPT fusion genes
   Leuk Res, 34 (5), 615-21
   PubMed 19748670

Publications 2009

1. Gebre-Medhin S, Broberg K, Jonson T, Gorunova L, von Steyern FV, Brosjö O, Jin Y, Gisselsson D, Panagopoulos I, Mandahl N, Mertens F (2009)
   Telomeric associations correlate with telomere length reduction and clonal chromosome aberrations in giant cell tumor of bone
   Cytogenet Genome Res, 124 (2), 121-7
   PubMed 19420923
2. Micci F, Haugom L, Ahlquist T, Abeler VM, Trope CG, Lothe RA, Heim S (2009)
   Tumor spreading to the contralateral ovary in bilateral ovarian carcinoma is a late event in clonal evolution
   J Oncol, 2010, 646340
   PubMed 19759843
3. Skotheim RI, Thomassen GO, Eken M, Lind GE, Micci F, Ribeiro FR, Cerveira N, Teixeira MR, Heim S, Rognes T, Lothe RA (2009)
   A universal assay for detection of oncogenic fusion transcripts by oligo microarray analysis
   Mol Cancer, 8, 5
   PubMed 19152679

Publications 2008

1. Cerveira N, Micci F, Santos J, Pinheiro M, Correia C, Lisboa S, Bizarro S, Norton L, Glomstein A, Asberg AE, Heim S, Teixeira MR (2008)
   Molecular characterization of the MLL-SEPT6 fusion gene in acute myeloid leukemia: identification of novel fusion transcripts and cloning of genomic breakpoint junctions
   Haematologica, 93 (7), 1076-80
   PubMed 18492691
2. Danielsen SA, Lind GE, Bjørnslett M, Meling GI, Rognum TO, Heim S, Lothe RA (2008)
   Novel mutations of the suppressor gene PTEN in colorectal carcinomas stratified by microsatellite instability- and TP53 mutation- status
   Hum Mutat, 29 (11), E252-62
   PubMed 18781614
3. Fløisand Y, Normann AP, Heim S, Lund-Johansen F, Tjønnfjord GE (2008)
   High expression of CD7 on CD34+ cells is not linked to deletion of derivative chromosome 9 or lack of dendritic cells in chronic myeloid leukaemia
   Scand J Clin Lab Invest, 68 (2), 93-8
   PubMed 17852828

Publications 2007

1. Forestier E, Andersen MK, Autio K, Blennow E, Borgström G, Golovleva I, Heim S, Heinonen K, Hovland R, Johannsson JH, Kerndrup G, Nordgren A, Rosenquist R, Swolin B, Johansson B, Nordic Society of Pediatric Hematology and Oncology (NOPHO), Swedish Cytogenetic Leukemia Study Group (SCLSG), NOPHO Leukemia Cytogenetic Study Group (NLCSG) (2007)
   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, 46 (5), 440-50
   PubMed 17285576
2. Hallor KH, Micci F, Meis-Kindblom JM, Kindblom LG, Bacchini P, Mandahl N, Mertens F, Panagopoulos I (2007)
   Fusion genes in angiomatoid fibrous histiocytoma
   Cancer Lett, 251 (1), 158-63
   PubMed 17188428
3. Ikonomou IM, Aamot HV, Heim S, Fosså A, Delabie J (2007)
   Granulomatous slack skin with a translocation t(3;9)(q12;p24)
   Am J Surg Pathol, 31 (5), 803-6
   PubMed 17460466
4. Lundin C, Heidenblad M, Strombeck B, Borg A, Hovland R, Heim S, Johansson B (2007)
   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
   Cytogenet Genome Res, 118 (1), 13-8
   PubMed 17901695
5. McLaughlin JR, Risch HA, Lubinski J, Moller P, Ghadirian P, Lynch H, Karlan B, Fishman D, Rosen B, Neuhausen SL, Offit K, Kauff N, Domchek S, Tung N, Friedman E, Foulkes W, Sun P, Narod SA, Hereditary Ovarian Cancer Clinical Study Group (2007)
   Reproductive risk factors for ovarian cancer in carriers of BRCA1 or BRCA2 mutations: a case-control study
   Lancet Oncol, 8 (1), 26-34
   PubMed 17196508
6. Micci F, Bjerkehagen B, Heim S (2007)
   Pairwise comparison of genomic imbalances between primary and recurrent well differentiated liposarcomas
   Cancer Genet Cytogenet, 178 (2), 163-7
   PubMed 17954275
7. Micci F, Haugom L, Abeler VM, Bjerkehagen B, Heim S (2007)
   Trisomy 7 in postoperative spindle cell nodules
   Cancer Genet Cytogenet, 174 (2), 147-50
   PubMed 17452257
8. Micci F, Heim S (2007)
   Pathogenetic mechanisms in endometrial stromal sarcoma
   Cytogenet Genome Res, 118 (2-4), 190-5
   PubMed 18000370
9. Micci F, Panagopoulos I, Tjønnfjord GE, Kolstad A, Delabie J, Beiske K, Heim S (2007)
   Molecular cytogenetic characterization of t(14;19)(q32;p13), a new recurrent translocation in B cell malignancies
   Virchows Arch, 450 (5), 559-65
   PubMed 17406891
10. Stormorken AT, Clark N, Grindedal E, Maehle L, Møller P (2007)
    Prevention of colorectal cancer by colonoscopic surveillance in families with hereditary colorectal cancer
    Scand J Gastroenterol, 42 (5), 611-7
    PubMed 17454882
11. Torres L, Ribeiro FR, Pandis N, Andersen JA, Heim S, Teixeira MR (2007)
    Intratumor genomic heterogeneity in breast cancer with clonal divergence between primary carcinomas and lymph node metastases
    Breast Cancer Res Treat, 102 (2), 143-55
    PubMed 16906480
12. Wu Q, Lothe RA, Ahlquist T, Silins I, Tropé CG, Micci F, Nesland JM, Suo Z, Lind GE (2007)
    DNA methylation profiling of ovarian carcinomas and their in vitro models identifies HOXA9, HOXB5, SCGB3A1, and CRABP1 as novel targets
    Mol Cancer, 6, 45
    PubMed 17623056
13. Aamot HV, Torlakovic EE, Eide MB, Holte H, Heim S (2007)
    Non-Hodgkin lymphoma with t(14;18): clonal evolution patterns and cytogenetic-pathologic-clinical correlations
    J Cancer Res Clin Oncol, 133 (7), 455-70
    PubMed 17235551

Publications 2006

1. Brandal P, Bjerkehagen B, Heim S (2006)
   Rearrangement of chromosomal region 8q11-13 in lipomatous tumours: correlation with lipoblastoma morphology
   J Pathol, 208 (3), 388-94
   PubMed 16308870
2. Brandal P, Lie AK, Bassarova A, Svindland A, Risberg B, Danielsen H, Heim S (2006)
   Genomic aberrations in mucinous tubular and spindle cell renal cell carcinomas
   Mod Pathol, 19 (2), 186-94
   PubMed 16258504
3. Clausen OP, Aass HC, Beigi M, Purdie KJ, Proby CM, Brown VL, Mattingsdal M, Micci F, Kølvraa S, Bolund L, Deangelis PM (2006)
   Are keratoacanthomas variants of squamous cell carcinomas? A comparison of chromosomal aberrations by comparative genomic hybridization
   J Invest Dermatol, 126 (10), 2308-15
   PubMed 16728973
4. Friedman E, Kotsopoulos J, Lubinski J, Lynch HT, Ghadirian P, Neuhausen SL, Isaacs C, Weber B, Foulkes WD, Moller P, Rosen B, Kim-Sing C, Gershoni-Baruch R, Ainsworth P, Daly M, Tung N, Eisen A, Olopade OI, Karlan B, Saal HM, Garber JE, Rennert G, Gilchrist D, Eng C, Offit K et al. (2006)
   Spontaneous and therapeutic abortions and the risk of breast cancer among BRCA mutation carriers
   Breast Cancer Res, 8 (2), R15
   PubMed 16563180
5. Geirdal AØ, Maehle L, Heimdal K, Stormorken A, Møller P, Dahl AA (2006)
   Quality of life and its relation to cancer-related stress in women of families with hereditary cancer without demonstrated mutation
   Qual Life Res, 15 (3), 461-70
   PubMed 16547785
6. Ikonomou IM, Tierens A, Troen G, Aamot HV, Heim S, Lauritzsen GF, Vålerhaugen H, Delabie J (2006)
   Peripheral T-cell lymphoma with involvement of the expanded mantle zone
   Virchows Arch, 449 (1), 78-87
   PubMed 16633785
7. Karrman K, Forestier E, Andersen MK, Autio K, Borgström G, Heim S, Heinonen K, Hovland R, Kerndrup G, Johansson B, Nordic Society of Paediatric Haematology and Oncology (NOPHO) and the NOPHO Leukaemia Cytogenetic Study Group (NLCSG) (2006)
   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
   Br J Haematol, 135 (3), 352-4
   PubMed 16965388
8. Kotsopoulos J, Lubinski J, Neuhausen SL, Lynch HT, Rosen B, Ainsworth P, Moller P, Ghadirian P, Isaacs C, Karlan B, Sun P, Narod SA (2006)
   Hormone replacement therapy and the risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers
   Gynecol Oncol, 100 (1), 83-8
   PubMed 16137751
9. Micci F, Panagopoulos I, Bjerkehagen B, Heim S (2006)
   Consistent rearrangement of chromosomal band 6p21 with generation of fusion genes JAZF1/PHF1 and EPC1/PHF1 in endometrial stromal sarcoma
   Cancer Res, 66 (1), 107-12
   PubMed 16397222
10. Micci F, Panagopoulos I, Bjerkehagen B, Heim S (2006)
    Deregulation of HMGA2 in an aggressive angiomyxoma with t(11;12)(q23;q15)
    Virchows Arch, 448 (6), 838-42
    PubMed 16568309
11. Narod SA, Lubinski J, Ghadirian P, Lynch HT, Moller P, Foulkes WD, Rosen B, Kim-Sing C, Isaacs C, Domchek S, Sun P, Hereditary Breast Cancer Clinical Study Group (2006)
    Screening mammography and risk of breast cancer in BRCA1 and BRCA2 mutation carriers: a case-control study
    Lancet Oncol, 7 (5), 402-6
    PubMed 16648044
12. Rudkin TM, Hamel N, Galvez M, Hogervorst F, Gille JJ, Møller P, Apold J, Foulkes WD (2006)
    The frequent BRCA1 mutation 1135insA has multiple origins: a haplotype study in different populations
    BMC Med Genet, 7, 15
    PubMed 16509964
13. Schaad K, Strömbeck B, Mandahl N, Andersen MK, Heim S, Mertens F, Johansson B (2006)
    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)
    Cytogenet Genome Res, 114 (2), 126-30
    PubMed 16825763
14. Stormorken AT, Hoff G, Norstein J, Bowitz-Lothe IM, Hanslien E, Grindedal E, Møller P (2006)
    Estimated prevalence of hereditary cancers and the need for surveillance in a Norwegian county, Telemark
    Scand J Gastroenterol, 41 (1), 71-9
    PubMed 16373279
15. Torlakovic EE, Aamot HV, Heim S (2006)
    A marginal zone phenotype in follicular lymphoma with t(14;18) is associated with secondary cytogenetic aberrations typical of marginal zone lymphoma
    J Pathol, 209 (2), 258-64
    PubMed 16583359
16. Aamot HV, Tjønnfjord GE, Delabie J, Heim S (2006)
    Molecular cytogenetic analysis of leukemic mantle cell lymphoma with a cryptic t(11;14)
    Cancer Genet Cytogenet, 165 (2), 172-5
    PubMed 16527613

Publications 2005

1. Behboudi A, Winnes M, Gorunova L, van den Oord JJ, Mertens F, Enlund F, Stenman G (2005)
   Clear cell hidradenoma of the skin-a third tumor type with a t(11;19)--associated TORC1-MAML2 gene fusion
   Genes Chromosomes Cancer, 43 (2), 202-5
   PubMed 15729701
2. Brandal P, Bjerkehagen B, Danielsen H, Heim S (2005)
   Chromosome 7 abnormalities are common in chordomas
   Cancer Genet Cytogenet, 160 (1), 15-21
   PubMed 15949565
3. Brandal P, Busund LT, Heim S (2005)
   Chromosome abnormalities in juxtaglomerular cell tumors
   Cancer, 104 (3), 504-10
   PubMed 15968688
4. Cullinane CA, Lubinski J, Neuhausen SL, Ghadirian P, Lynch HT, Isaacs C, Weber B, Moller P, Offit K, Kim-Sing C, Friedman E, Randall S, Pasini B, Ainsworth P, Gershoni-Baruch R, Foulkes WD, Klijn J, Tung N, Rennert G, Olopade O, Couch F, Wagner T, Olsson H, Sun P, Weitzel JN et al. (2005)
   Effect of pregnancy as a risk factor for breast cancer in BRCA1/BRCA2 mutation carriers
   Int J Cancer, 117 (6), 988-91
   PubMed 15986445
5. Eisen A, Lubinski J, Klijn J, Moller P, Lynch HT, Offit K, Weber B, Rebbeck T, Neuhausen SL, Ghadirian P, Foulkes WD, Gershoni-Baruch R, Friedman E, Rennert G, Wagner T, Isaacs C, Kim-Sing C, Ainsworth P, Sun P, Narod SA (2005)
   Breast cancer risk following bilateral oophorectomy in BRCA1 and BRCA2 mutation carriers: an international case-control study
   J Clin Oncol, 23 (30), 7491-6
   PubMed 16234515
6. Geirdal AØ, Reichelt JG, Dahl AA, Heimdal K, Maehle L, Stormorken A, Møller P (2005)
   Psychological distress in women at risk of hereditary breast/ovarian or HNPCC cancers in the absence of demonstrated mutations
   Fam Cancer, 4 (2), 121-6
   PubMed 15951962
7. Heidenblad M, Lindgren D, Veltman JA, Jonson T, Mahlamäki EH, Gorunova L, van Kessel AG, Schoenmakers EF, Höglund M (2005)
   Microarray analyses reveal strong influence of DNA copy number alterations on the transcriptional patterns in pancreatic cancer: implications for the interpretation of genomic amplifications
   Oncogene, 24 (10), 1794-801
   PubMed 15688027
8. Hope Q, Bullock S, Evans C, Meitz J, Hamel N, Edwards SM, Severi G, Dearnaley D, Jhavar S, Southgate C, Falconer A, Dowe A, Muir K, Houlston RS, Engert JC, Roquis D, Sinnett D, Simard J, Heimdal K, Møller P, Maehle L, Badzioch M, Eeles RA, Easton DF, English DR et al. (2005)
   Macrophage scavenger receptor 1 999C>T (R293X) mutation and risk of prostate cancer
   Cancer Epidemiol Biomarkers Prev, 14 (2), 397-402
   PubMed 15734964
9. Kleivi K, Diep CB, Pandis N, Heim S, Teixeira MR, Lothe RA (2005)
   TP53 mutations are associated with a particular pattern of genomic imbalances in breast carcinomas
   J Pathol, 207 (1), 14-9
   PubMed 16007576
10. Stewénius Y, Gorunova L, Jonson T, Larsson N, Höglund M, Mandahl N, Mertens F, Mitelman F, Gisselsson D (2005)
    Structural and numerical chromosome changes in colon cancer develop through telomere-mediated anaphase bridges, not through mitotic multipolarity
    Proc Natl Acad Sci U S A, 102 (15), 5541-6
    PubMed 15809428
11. Stormorken AT, Bowitz-Lothe IM, Norèn T, Kure E, Aase S, Wijnen J, Apold J, Heimdal K, Møller P (2005)
    Immunohistochemistry identifies carriers of mismatch repair gene defects causing hereditary nonpolyposis colorectal cancer
    J Clin Oncol, 23 (21), 4705-12
    PubMed 16034045
12. Teixeira MR, Heim S (2005)
    Multiple numerical chromosome aberrations in cancer: what are their causes and what are their consequences?
    Semin Cancer Biol, 15 (1), 3-12
    PubMed 15613283
13. van der Klift H, Wijnen J, Wagner A, Verkuilen P, Tops C, Otway R, Kohonen-Corish M, Vasen H, Oliani C, Barana D, Moller P, Delozier-Blanchet C, Hutter P, Foulkes W, Lynch H, Burn J, Möslein G, Fodde R (2005)
    Molecular characterization of the spectrum of genomic deletions in the mismatch repair genes MSH2, MLH1, MSH6, and PMS2 responsible for hereditary nonpolyposis colorectal cancer (HNPCC)
    Genes Chromosomes Cancer, 44 (2), 123-38
    PubMed 15942939
14. Weitzel JN, Robson M, Pasini B, Manoukian S, Stoppa-Lyonnet D, Lynch HT, McLennan J, Foulkes WD, Wagner T, Tung N, Ghadirian P, Olopade O, Isaacs C, Kim-Sing C, Møller P, Neuhausen SL, Metcalfe K, Sun P, Narod SA (2005)
    A comparison of bilateral breast cancers in BRCA carriers
    Cancer Epidemiol Biomarkers Prev, 14 (6), 1534-8
    PubMed 15941968
15. Aamot HV, Bjørnslett M, Delabie J, Heim S (2005)
    t(14;22)(q32;q11) in non-Hodgkin lymphoma and myeloid leukaemia: molecular cytogenetic investigations
    Br J Haematol, 130 (6), 845-51
    PubMed 16156854
16. Aamot HV, Micci F, Holte H, Delabie J, Heim S (2005)
    G-banding and molecular cytogenetic analyses of marginal zone lymphoma
    Br J Haematol, 130 (6), 890-901
    PubMed 16156859

Publications 2004

1. Bardi G, Fenger C, Johansson B, Mitelman F, Heim S (2004)
   Tumor karyotype predicts clinical outcome in colorectal cancer patients
   J Clin Oncol, 22 (13), 2623-34
   PubMed 15226330
2. Brandal P, Bjerkehagen B, Heim S (2004)
   Molecular cytogenetic characterization of tenosynovial giant cell tumors
   Neoplasia, 6 (5), 578-83
   PubMed 15548367
3. Gisselsson D, Gorunova L, Höglund M, Mandahl N, Elfving P (2004)
   Telomere shortening and mitotic dysfunction generate cytogenetic heterogeneity in a subgroup of renal cell carcinomas
   Br J Cancer, 91 (2), 327-32
   PubMed 15162157
4. Heidenblad M, Schoenmakers EF, Jonson T, Gorunova L, Veltman JA, van Kessel AG, Höglund M (2004)
   Genome-wide array-based comparative genomic hybridization reveals multiple amplification targets and novel homozygous deletions in pancreatic carcinoma cell lines
   Cancer Res, 64 (9), 3052-9
   PubMed 15126341
5. Hendriks YM, Wagner A, Morreau H, Menko F, Stormorken A, Quehenberger F, Sandkuijl L, Møller P, Genuardi M, Van Houwelingen H, Tops C, Van Puijenbroek M, Verkuijlen P, Kenter G, Van Mil A, Meijers-Heijboer H, Tan GB, Breuning MH, Fodde R, Wijnen JT, Bröcker-Vriends AH, Vasen H (2004)
   Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance
   Gastroenterology, 127 (1), 17-25
   PubMed 15236168
6. Kotar K, Brunet JS, Møller P, Hugel L, Warner E, McLaughlin J, Wong N, Narod SA, Foulkes WD (2004)
   Ratio of female to male offspring of women tested for BRCA1 and BRCA2 mutations
   J Med Genet, 41 (8), e103
   PubMed 15286163
7. Micci F, Teixeira MR, Haugom L, Kristensen G, Abeler VM, Heim S (2004)
   Genomic aberrations in carcinomas of the uterine corpus
   Genes Chromosomes Cancer, 40 (3), 229-46
   PubMed 15139002
8. Møller P (2004)
   Costs and benefits of diagnosing familial breast cancer
   Ann Oncol, 15 Suppl 1, I55-I59
   PubMed 15280189
9. Teixeira MR, Ribeiro FR, Eknaes M, Waehre H, Stenwig AE, Giercksky KE, Heim S, Lothe RA (2004)
   Genomic analysis of prostate carcinoma specimens obtained via ultrasound-guided needle biopsy may be of use in preoperative decision-making
   Cancer, 101 (8), 1786-93
   PubMed 15386312
10. Teixeira MR, Ribeiro FR, Torres L, Pandis N, Andersen JA, Lothe RA, Heim S (2004)
    Assessment of clonal relationships in ipsilateral and bilateral multiple breast carcinomas by comparative genomic hybridisation and hierarchical clustering analysis
    Br J Cancer, 91 (4), 775-82
    PubMed 15266323

Publications 2003

1. Adeyinka A, Baldetorp B, Mertens F, Olsson H, Johannsson O, Heim S, Pandis N (2003)
   Comparative cytogenetic and DNA flow cytometric analysis of 242 primary breast carcinomas
   Cancer Genet Cytogenet, 147 (1), 62-7
   PubMed 14580772
2. Boyd M, Spenning HS, Mairs RJ (2003)
   Radiation and gene therapy: rays of hope for the new millennium?
   Curr Gene Ther, 3 (4), 319-39
   PubMed 12871020
3. Brandal P, Micci F, Bjerkehagen B, Eknaes M, Larramendy M, Lothe RA, Knuutila S, Heim S (2003)
   Molecular cytogenetic characterization of desmoid tumors
   Cancer Genet Cytogenet, 146 (1), 1-7
   PubMed 14499689
4. Fadl-Elmula I, Gorunova L, Mandahl N, Heim S (2003)
   Chromosomal abnormalities in inflammatory pseudotumor of the urinary bladder
   Cancer Genet Cytogenet, 143 (2), 169-71
   PubMed 12781452
5. Forestier E, Heim S, Blennow E, Borgström G, Holmgren G, Heinonen K, Johannsson J, Kerndrup G, Andersen MK, Lundin C, Nordgren A, Rosenquist R, Swolin B, Johansson B, Nordic Society of Paediatric Haematology and Oncology (NOPHO), Swedish Cytogenetic Leukaemia Study Group (SCLSG), NOPHO Leukaemia Cytogenetic Study Group (NLCSG) (2003)
   Cytogenetic abnormalities in childhood acute myeloid leukaemia: a Nordic series comprising all children enrolled in the NOPHO-93-AML trial between 1993 and 2001
   Br J Haematol, 121 (4), 566-77
   PubMed 12752097
6. Heimdal K, Maehle L, Apold J, Pedersen JC, Møller P (2003)
   The Norwegian founder mutations in BRCA1: high penetrance confirmed in an incident cancer series and differences observed in the risk of ovarian cancer
   Eur J Cancer, 39 (15), 2205-13
   PubMed 14522380
7. Ikonomou IM, Nesland JM, Schjølseth SA, Heim S, Delabie J (2003)
   Mantle cell lymphoma with Homer-Wright rosettes
   Virchows Arch, 442 (2), 179-82
   PubMed 12596071
8. Ioannidis P, Mahaira L, Papadopoulou A, Teixeira MR, Heim S, Andersen JA, Evangelou E, Dafni U, Pandis N, Trangas T (2003)
   8q24 Copy number gains and expression of the c-myc mRNA stabilizing protein CRD-BP in primary breast carcinomas
   Int J Cancer, 104 (1), 54-9
   PubMed 12532419
9. Ioannidis P, Mahaira L, Papadopoulou A, Teixeira MR, Heim S, Andersen JA, Evangelou E, Dafni U, Pandis N, Trangas T (2003)
   CRD-BP: a c-Myc mRNA stabilizing protein with an oncofetal pattern of expression
   Anticancer Res, 23 (3A), 2179-83
   PubMed 12894594
10. Jonson T, Heidenblad M, Håkansson P, Gorunova L, Johansson B, Fioretos T, Höglund M (2003)
    Pancreatic carcinoma cell lines with SMAD4 inactivation show distinct expression responses to TGFB1
    Genes Chromosomes Cancer, 36 (4), 340-52
    PubMed 12619158
11. Kildal W, Kraggerud SM, Abeler VM, Heim S, Tropé CG, Kristensen GB, Risberg B, Lothe RA, Danielsen HE (2003)
    Genome profiles of bilateral dysgerminomas, a unilateral gonadoblastoma, and a metastasis from a 46, XY phenotypic female
    Hum Pathol, 34 (9), 946-9
    PubMed 14562293
12. Micci F, Teixeira MR, Scheistrøen M, Abeler VM, Heim S (2003)
    Cytogenetic characterization of tumors of the vulva and vagina
    Genes Chromosomes Cancer, 38 (2), 137-48
    PubMed 12939741
13. Micci F, Walter CU, Teixeira MR, Panagopoulos I, Bjerkehagen B, Saeter G, Heim S (2003)
    Cytogenetic and molecular genetic analyses of endometrial stromal sarcoma: nonrandom involvement of chromosome arms 6p and 7p and confirmation of JAZF1/JJAZ1 gene fusion in t(7;17)
    Cancer Genet Cytogenet, 144 (2), 119-24
    PubMed 12850374
14. Normann AP, Egeland T, Madshus IH, Heim S, Tjønnfjord GE (2003)
    CD7 expression by CD34+ cells in CML patients, of prognostic significance?
    Eur J Haematol, 71 (4), 266-75
    PubMed 12950236
15. Papadopoulou A, Trangas T, Teixeira MR, Heim S, Dimitriadis E, Tsarouha H, Andersen JA, Evangelou E, Ioannidis P, Agnantis NJ, Pandis N (2003)
    Telomerase activity and genetic alterations in primary breast carcinomas
    Neoplasia, 5 (2), 170-8
    PubMed 12659690
16. Teixeira MR, Pandis N, Heim S (2003)
    Multicentric mammary carcinoma: evidence of monoclonal proliferation
    Cancer, 97 (3), 715-7; author reply 717
    PubMed 12548617

Publications 2002

1. Fadl-Elmula I, Kytola S, Leithy ME, Abdel-Hameed M, Mandahl N, Elagib A, Ibrahim M, Larsson C, Heim S (2002)
   Chromosomal aberrations in benign and malignant bilharzia-associated bladder lesions analyzed by comparative genomic hybridization
   BMC Cancer, 2, 5
   PubMed 11914143
2. Hallén M, Parada LA, Gorunova L, Pålsson B, Dictor M, Johansson B (2002)
   Cytogenetic abnormalities in a hemangiopericytoma of the spleen
   Cancer Genet Cytogenet, 136 (1), 62-5
   PubMed 12165454
3. Heidenblad M, Jonson T, Mahlamäki EH, Gorunova L, Karhu R, Johansson B, Höglund M (2002)
   Detailed genomic mapping and expression analyses of 12p amplifications in pancreatic carcinomas reveal a 3.5-Mb target region for amplification
   Genes Chromosomes Cancer, 34 (2), 211-23
   PubMed 11979555
4. Kleivi K, Lothe RA, Heim S, Tsarouha H, Kraggerud SM, Pandis N, Papadopoulou A, Andersen J, Jakobsen KS, Teixeira MR (2002)
   Genome profiling of breast cancer cells selected against in vitro shows copy number changes
   Genes Chromosomes Cancer, 33 (3), 304-9
   PubMed 11807988
5. Mahlamäki EH, Bärlund M, Tanner M, Gorunova L, Höglund M, Karhu R, Kallioniemi A (2002)
   Frequent amplification of 8q24, 11q, 17q, and 20q-specific genes in pancreatic cancer
   Genes Chromosomes Cancer, 35 (4), 353-8
   PubMed 12378529
6. Micci F, Teixeira MR, Bjerkehagen B, Heim S (2002)
   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
   Cytogenet Genome Res, 97 (1-2), 13-9
   PubMed 12438732
7. Møller P, Borg A, Evans DG, Haites N, Reis MM, Vasen H, Anderson E, Steel CM, Apold J, Goudie D, Howell A, Lalloo F, Maehle L, Gregory H, Heimdal K (2002)
   Survival in prospectively ascertained familial breast cancer: analysis of a series stratified by tumour characteristics, BRCA mutations and oophorectomy
   Int J Cancer, 101 (6), 555-9
   PubMed 12237897
8. Narod SA, Dubé MP, Klijn J, Lubinski J, Lynch HT, Ghadirian P, Provencher D, Heimdal K, Moller P, Robson M, Offit K, Isaacs C, Weber B, Friedman E, Gershoni-Baruch R, Rennert G, Pasini B, Wagner T, Daly M, Garber JE, Neuhausen SL, Ainsworth P, Olsson H, Evans G, Osborne M et al. (2002)
   Oral contraceptives and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers
   J Natl Cancer Inst, 94 (23), 1773-9
   PubMed 12464649
9. Panagopoulos I, Mertens F, Isaksson M, Domanski HA, Brosjö O, Heim S, Bjerkehagen B, Sciot R, Dal Cin P, Fletcher JA, Fletcher CD, Mandahl N (2002)
   Molecular genetic characterization of the EWS/CHN and RBP56/CHN fusion genes in extraskeletal myxoid chondrosarcoma
   Genes Chromosomes Cancer, 35 (4), 340-52
   PubMed 12378528
10. Teixeira MR, Pandis N, Heim S (2002)
    Cytogenetic clues to breast carcinogenesis
    Genes Chromosomes Cancer, 33 (1), 1-16
    PubMed 11746982
11. Aamot H, Micci F, Holte H, Delabie J, Heim S (2002)
    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
    Leuk Lymphoma, 43 (5), 1051-6
    PubMed 12148885

Publications 2001

1. Bomme L, Lothe RA, Bardi G, Fenger C, Kronborg O, Heim S (2001)
   Assessments of clonal composition of colorectal adenomas by FISH analysis of chromosomes 1, 7, 13 and 20
   Int J Cancer, 92 (6), 816-23
   PubMed 11351301
2. Fadl-Elmula I, Kytölä S, Pan Y, Lui WO, Derienzo G, Forsberg L, Mandahl N, Gorunova L, Bergerheim US, Heim S, Larsson C (2001)
   Characterization of chromosomal abnormalities in uroepithelial carcinomas by G-banding, spectral karyotyping and FISH analysis
   Int J Cancer, 92 (6), 824-31
   PubMed 11351302
3. Gorunova L, Dawiskiba S, Andrén-Sandberg A, Höglund M, Johansson B (2001)
   Extensive cytogenetic heterogeneity in a benign retroperitoneal schwannoma
   Cancer Genet Cytogenet, 127 (2), 148-54
   PubMed 11425455
4. Heim S, Teixeira MA, Pandis N (2001)
   Are some breast carcinomas polyclonal in origin?
   J Pathol, 194 (4), 395-7
   PubMed 11523045
5. Höglund M, Säll T, Heim S, Mitelman F, Mandahl N, Fadl-Elmula I (2001)
   Identification of cytogenetic subgroups and karyotypic pathways in transitional cell carcinoma
   Cancer Res, 61 (22), 8241-6
   PubMed 11719456
6. Jonson T, Albrechtsson E, Axelson J, Heidenblad M, Gorunova L, Johansson B, Höglund M (2001)
   Altered expression of TGFB receptors and mitogenic effects of TGFB in pancreatic carcinomas
   Int J Oncol, 19 (1), 71-81
   PubMed 11408925
7. Micci F, Teixeira MR, Heim S (2001)
   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 Genet Cytogenet, 131 (1), 25-30
   PubMed 11734314
8. Møller P, Heimdal K, Apold J, Fredriksen A, Borg A, Hovig E, Hagen A, Hagen B, Pedersen JC, Maehle L, Norwegian Inherited Breast Cancer Group, Norwegian Inherited Ovarian Cancer Group (2001)
   Genetic epidemiology of BRCA1 mutations in Norway
   Eur J Cancer, 37 (18), 2428-34
   PubMed 11720839
9. Teixeira MR, Tsarouha H, Kraggerud SM, Pandis N, Dimitriadis E, Andersen JA, Lothe RA, Heim S (2001)
   Evaluation of breast cancer polyclonality by combined chromosome banding and comparative genomic hybridization analysis
   Neoplasia, 3 (3), 204-14
   PubMed 11494114

Publications 2000

1. Fadl-Elmula I, Gorunova L, Mandahl N, Elfving P, Lundgren R, Mitelman F, Heim S (2000)
   Karyotypic characterization of urinary bladder transitional cell carcinomas
   Genes Chromosomes Cancer, 29 (3), 256-65
   PubMed 10992300
2. Forestier E, Johansson B, Borgström G, Kerndrup G, Johansson J, Heim S (2000)
   Cytogenetic findings in a population-based series of 787 childhood acute lymphoblastic leukemias from the Nordic countries. The NOPHO Leukemia Cytogenetic Study Group
   Eur J Haematol, 64 (3), 194-200
   PubMed 10997886
3. Forestier E, Johansson B, Gustafsson G, Borgström G, Kerndrup G, Johannsson J, Heim S (2000)
   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
   Br J Haematol, 110 (1), 147-53
   PubMed 10930992
4. Gisselsson D, Mandahl N, Pålsson E, Gorunova L, Höglund M (2000)
   Locus-specific multifluor FISH analysis allows physical characterization of complex chromosome abnormalities in neoplasia
   Genes Chromosomes Cancer, 28 (3), 347-52
   PubMed 10862042
5. Gisselsson D, Pettersson L, Höglund M, Heidenblad M, Gorunova L, Wiegant J, Mertens F, Dal Cin P, Mitelman F, Mandahl N (2000)
   Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity
   Proc Natl Acad Sci U S A, 97 (10), 5357-62
   PubMed 10805796
6. Jonson T, Mahlamäki EH, Karhu R, Gorunova L, Johansson B, Höglund M (2000)
   Characterization of genomically amplified segments using PCR: optimizing relative-PCR for reliable and simple gene expression and gene copy analyses
   Genes Chromosomes Cancer, 29 (2), 192-9
   PubMed 10959100
7. Koul A, Malander S, Loman N, Pejovic T, Heim S, Willen R, Johannsson O, Olsson H, Ridderheim M, Borg Å (2000)
   BRCA1 and BRCA2 mutations in ovarian cancer: Covariation with specific cytogenetic features
   Int J Gynecol Cancer, 10 (4), 289-295
   PubMed 11240689
8. Kraggerud SM, Szymanska J, Abeler VM, Kaern J, Eknaes M, Heim S, Teixeira MR, Tropé CG, Peltomäki P, Lothe RA (2000)
   DNA copy number changes in malignant ovarian germ cell tumors
   Cancer Res, 60 (11), 3025-30
   PubMed 10850452
9. Panagopoulos I, Isaksson M, Lindvall C, Björkholm M, Ahlgren T, Fioretos T, Heim S, Mitelman F, Johansson B (2000)
   RT-PCR analysis of the MOZ-CBP and CBP-MOZ chimeric transcripts in acute myeloid leukemias with t(8;16)(p11;p13)
   Genes Chromosomes Cancer, 28 (4), 415-24
   PubMed 10862050
10. Panagopoulos I, Teixeira MR, Micci F, Hammerstrøm J, Isaksson M, Johansson B, Mitelman F, Heim S (2000)
    Acute myeloid leukemia with inv(8)(p11q13)
    Leuk Lymphoma, 39 (5-6), 651-6
    PubMed 11342350
11. Teixeira MR, Micci F, Dietrich CU, Heim S (2000)
    Detailed genome-wide screening for inter- and intrachromosomal abnormalities by sequential G-banding and RxFISH color banding of the same metaphase cells
    Cancer Genet Cytogenet, 119 (2), 94-101
    PubMed 10867142
12. Teixeira MR, Waehre H, Lothe RA, Stenwig AE, Pandis N, Giercksky KE, Heim S (2000)
    High frequency of clonal chromosome abnormalities in prostatic neoplasms sampled by prostatectomy or ultrasound-guided needle biopsy
    Genes Chromosomes Cancer, 28 (2), 211-9
    PubMed 10825006
13. Thorstensen L, Qvist H, Heim S, Liefers GJ, Nesland JM, Giercksky KE, Lothe RA (2000)
    Evaluation of 1p losses in primary carcinomas, local recurrences and peripheral metastases from colorectal cancer patients
    Neoplasia, 2 (6), 514-22
    PubMed 11228544

Publications 1999

1. Bjerkehagen B, Dietrich C, Reed W, Micci F, Saeter G, Berner A, Nesland JM, Heim S (1999)
   Extraskeletal myxoid chondrosarcoma: multimodal diagnosis and identification of a new cytogenetic subgroup characterized by t(9;17)(q22;q11)
   Virchows Arch, 435 (5), 524-30
   PubMed 10592057
2. Fadl-Elmula I, Gorunova L, Mandahl N, Elfving P, Lundgren R, Mitelman F, Heim S (1999)
   Cytogenetic monoclonality in multifocal uroepithelial carcinomas: evidence of intraluminal tumour seeding
   Br J Cancer, 81 (1), 6-12
   PubMed 10487605
3. Fadl-Elmula I, Gorunova L, Mandahl N, Elfving P, Lundgren R, Rademark C, Heim S (1999)
   Cytogenetic analysis of upper urinary tract transitional cell carcinomas
   Cancer Genet Cytogenet, 115 (2), 123-7
   PubMed 10598145
4. Gorunova L, Parada LA, Limon J, Jin Y, Hallén M, Hägerstrand I, Iliszko M, Wajda Z, Johansson B (1999)
   Nonrandom chromosomal aberrations and cytogenetic heterogeneity in gallbladder carcinomas
   Genes Chromosomes Cancer, 26 (4), 312-21
   PubMed 10534766
5. Jonson T, Gorunova L, Dawiskiba S, Andrén-Sandberg A, Stenman G, ten Dijke P, Johansson B, Höglund M (1999)
   Molecular analyses of the 15q and 18q SMAD genes in pancreatic cancer
   Genes Chromosomes Cancer, 24 (1), 62-71
   PubMed 9892110
6. Larsen JB, Schrøder HD, Sørensen AG, Bjerre P, Heim S (1999)
   Simple numerical chromosome aberrations characterize pituitary adenomas
   Cancer Genet Cytogenet, 114 (2), 144-9
   PubMed 10549272
7. Micci F, Teixeira MR, Dietrich CU, Saeter G, Bjerkehagen B, Heim S (1999)
   Combined RxFISH/G-banding allows refined karyotyping of solid tumors
   Hum Genet, 104 (5), 370-5
   PubMed 10394927
8. Panagopoulos I, Mencinger M, Dietrich CU, Bjerkehagen B, Saeter G, Mertens F, Mandahl N, Heim S (1999)
   Fusion of the RBP56 and CHN genes in extraskeletal myxoid chondrosarcomas with translocation t(9;17)(q22;q11)
   Oncogene, 18 (52), 7594-8
   PubMed 10602519
9. Teixeira MR, Kristensen GB, Abeler VM, Heim S (1999)
   Karyotypic findings in tumors of the vulva and vagina
   Cancer Genet Cytogenet, 111 (1), 87-91
   PubMed 10326597
10. Teixeira MR, Micci F, Dietrich CU, Heim S (1999)
    Cross-species color banding characterization of chromosomal rearrangements in leukemias with incomplete G-band karyotypes
    Genes Chromosomes Cancer, 26 (1), 13-9
    PubMed 10441000
11. Tsarouha H, Pandis N, Bardi G, Teixeira MR, Andersen JA, Heim S (1999)
    Karyotypic evolution in breast carcinomas with i(1)(q10) and der(1;16)(q10;p10) as the primary chromosome abnormality
    Cancer Genet Cytogenet, 113 (2), 156-61
    PubMed 10484983

Publications 1998

1. Adeyinka A, Mertens F, Idvall I, Bondeson L, Ingvar C, Heim S, Mitelman F, Pandis N (1998)
   Cytogenetic findings in invasive breast carcinomas with prognostically favourable histology: a less complex karyotypic pattern?
   Int J Cancer, 79 (4), 361-4
   PubMed 9699527
2. Bardi G, Rizou H, Michailakis E, Dietrich C, Pandis N, Heim S (1998)
   Cytogenetic findings in three primary hepatocellular carcinomas
   Cancer Genet Cytogenet, 104 (2), 165-6
   PubMed 9666813
3. Bomme L, Bardi G, Pandis N, Fenger C, Kronborg O, Heim S (1998)
   Cytogenetic analysis of colorectal adenomas: karyotypic comparisons of synchronous tumors
   Cancer Genet Cytogenet, 106 (1), 66-71
   PubMed 9772912
4. Bomme L, Heim S, Bardi G, Fenger C, Kronborg O, Brøgger A, Lothe RA (1998)
   Allelic imbalance and cytogenetic deletion of 1p in colorectal adenomas: a target region identified between DIS199 and DIS234
   Genes Chromosomes Cancer, 21 (3), 185-94
   PubMed 9523193
5. Fadl-Elmula I, Bonaldi L, Gorunova L, Mandahl N, Elfving P, Heim S (1998)
   Cytogenetic heterogeneity in a second primary radiation-induced bladder carcinoma: ten karyotypically unrelated clones
   Cancer Genet Cytogenet, 105 (2), 134-7
   PubMed 9723030
6. Fadl-Elmula I, Gorunova L, Lundgren R, Mandahl N, Forsby N, Mitelman F, Heim S (1998)
   Chromosomal abnormalities in two bladder carcinomas with secondary squamous cell differentiation
   Cancer Genet Cytogenet, 102 (2), 125-30
   PubMed 9546064
7. Fadl-Elmula I, Gorunova L, Mandahl N, Elfving P, Heim S (1998)
   Chromosome abnormalities in squamous cell carcinoma of the urethra
   Genes Chromosomes Cancer, 23 (1), 72-3
   PubMed 9714000
8. Gorunova L, Höglund M, Andrén-Sandberg A, Dawiskiba S, Jin Y, Mitelman F, Johansson B (1998)
   Cytogenetic analysis of pancreatic carcinomas: intratumor heterogeneity and nonrandom pattern of chromosome aberrations
   Genes Chromosomes Cancer, 23 (2), 81-99
   PubMed 9739011
9. Heim S, Smeland EB (1998)
   [Molecular genetic diagnosis of leukemias and lymphomas]
   Tidsskr Nor Laegeforen, 118 (16), 2511-8
   PubMed 9667131
10. Höglund M, Gorunova L, Andrén-Sandberg A, Dawiskiba S, Mitelman F, Johansson B (1998)
    Cytogenetic and fluorescence in situ hybridization analyses of chromosome 19 aberrations in pancreatic carcinomas: frequent loss of 19p13.3 and gain of 19q13.1-13.2
    Genes Chromosomes Cancer, 21 (1), 8-16
    PubMed 9443037
11. Höglund M, Gorunova L, Jonson T, Dawiskiba S, Andrén-Sandberg A, Stenman G, Johansson B (1998)
    Cytogenetic and FISH analyses of pancreatic carcinoma reveal breaks in 18q11 with consistent loss of 18q12-qter and frequent gain of 18p
    Br J Cancer, 77 (11), 1893-9
    PubMed 9667665
12. Jin Y, Mertens F, Persson B, Warloe T, Gullestad HP, Salemark L, Jin C, Jonsson N, Risberg B, Mandahl N, Mitelman F, Heim S (1998)
    Nonrandom numerical chromosome abnormalities in basal cell carcinomas
    Cancer Genet Cytogenet, 103 (1), 35-42
    PubMed 9595042
13. Pandis N, Teixeira MR, Adeyinka A, Rizou H, Bardi G, Mertens F, Andersen JA, Bondeson L, Sfikas K, Qvist H, Apostolikas N, Mitelman F, Heim S (1998)
    Cytogenetic comparison of primary tumors and lymph node metastases in breast cancer patients
    Genes Chromosomes Cancer, 22 (2), 122-9
    PubMed 9598799
14. Teixeira MR, Giercksky KE, Ikonomou IM, Heim S (1998)
    Translocation (3;3)(p14;q29) as the primary chromosome abnormality in a peritoneal mesothelioma
    Cancer Genet Cytogenet, 103 (1), 73-5
    PubMed 9595051
15. Teixeira MR, Pandis N, Dietrich CU, Reed W, Andersen J, Qvist H, Heim S (1998)
    Chromosome banding analysis of gynecomastias and breast carcinomas in men
    Genes Chromosomes Cancer, 23 (1), 16-20
    PubMed 9713992
16. Teixeira MR, Qvist H, Bøhler PJ, Pandis N, Heim S (1998)
    Cytogenetic analysis shows that carcinosarcomas of the breast are of monoclonal origin
    Genes Chromosomes Cancer, 22 (2), 145-51
    PubMed 9598802

Publications 1997

1. Adeyinka A, Pandis N, Bardi G, Bonaldi L, Mertens F, Mitelman F, Heim S (1997)
   A subgroup of breast carcinomas is cytogenetically characterized by trisomy 12
   Cancer Genet Cytogenet, 97 (2), 119-21
   PubMed 9283594
2. Bardi G, Parada LA, Bomme L, Pandis N, Johansson B, Willén R, Fenger C, Kronborg O, Mitelman F, Heim S (1997)
   Cytogenetic findings in metastases from colorectal cancer
   Int J Cancer, 72 (4), 604-7
   PubMed 9259398
3. Bardi G, Parada LA, Bomme L, Pandis N, Willén R, Johansson B, Jeppsson B, Beroukas K, Heim S, Mitelman F (1997)
   Cytogenetic comparisons of synchronous carcinomas and polyps in patients with colorectal cancer
   Br J Cancer, 76 (6), 765-9
   PubMed 9310243
4. Dietrich CU, Pandis N, Rizou H, Petersson C, Bardi G, Qvist H, Apostolikas N, Bøhler PJ, Andersen JA, Idvall I, Mitelman F, Heim S (1997)
   Cytogenetic findings in phyllodes tumors of the breast: karyotypic complexity differentiates between malignant and benign tumors
   Hum Pathol, 28 (12), 1379-82
   PubMed 9416694
5. Forestier E, Gustafsson G, von Heideman A, Heim S, Hernell O, Mitelman F, Nordenson I, Swolin B, Söderhäll S (1997)
   Prognostic impact of bone marrow karyotype in childhood acute lymphoblastic leukaemia: Swedish experiences 1986-91
   Acta Paediatr, 86 (8), 819-25
   PubMed 9307160
6. Gerdes AM, Pandis N, Bomme L, Dietrich CU, Teixeira MR, Bardi G, Heim S (1997)
   Fluorescence in situ hybridization of old G-banded and mounted chromosome preparations
   Cancer Genet Cytogenet, 98 (1), 9-15
   PubMed 9309112
7. Heim S, Teixeira MR, Dietrich CU, Pandis N (1997)
   Cytogenetic polyclonality in tumors of the breast
   Cancer Genet Cytogenet, 95 (1), 16-9
   PubMed 9140449
8. Jin C, Jin Y, Wennerberg J, Akervall J, Dictor M, Mandahl N, Heim S, Mitelman F, Mertens F (1997)
   Cytogenetic analysis of inverted nasal papillomas and demonstration of genetic convergence during in vitro passaging
   Int J Cancer, 70 (6), 668-73
   PubMed 9096647
9. Jin C, Jin Y, Wennerberg J, Akervall J, Grenthe B, Mandahl N, Heim S, Mitelman F, Mertens F (1997)
   Clonal chromosome aberrations accumulate with age in upper aerodigestive tract mucosa
   Mutat Res, 374 (1), 63-72
   PubMed 9067416
10. Jin Y, Merterns F, Persson B, Gullestad HP, Jin C, Warloe T, Salemark L, Jonsson N, Risberg B, Mandahl N, Mitelman F, Heim S (1997)
    The reciprocal translocation t(9;16)(q22;p13) is a primary chromosome abnormality in basal cell carcinomas
    Cancer Res, 57 (3), 404-6
    PubMed 9012465
11. Mahlamäki EH, Höglund M, Gorunova L, Karhu R, Dawiskiba S, Andrén-Sandberg A, Kallioniemi OP, Johansson B (1997)
    Comparative genomic hybridization reveals frequent gains of 20q, 8q, 11q, 12p, and 17q, and losses of 18q, 9p, and 15q in pancreatic cancer
    Genes Chromosomes Cancer, 20 (4), 383-91
    PubMed 9408755
12. Pandis N, Bardi G, Mitelman F, Heim S (1997)
    Deletion of the short arm of chromosome 3 in breast tumors
    Genes Chromosomes Cancer, 18 (4), 241-5
    PubMed 9087563
13. Petersson C, Pandis N, Rizou H, Mertens F, Dietrich CU, Adeyinka A, Idvall I, Bondeson L, Georgiou G, Ingvar C, Heim S, Mitelman F (1997)
    Karyotypic abnormalities in fibroadenomas of the breast
    Int J Cancer, 70 (3), 282-6
    PubMed 9033628
14. Rasmussen K, Iversen JG, Heim S (1997)
    [Anders Jahre's 1997 medical awards]
    Tidsskr Nor Laegeforen, 117 (24), 3554-6
    PubMed 9411920
15. Teixeira MR, Pandis N, Bardi G, Andersen JA, Bøhler PJ, Qvist H, Heim S (1997)
    Discrimination between multicentric and multifocal breast carcinoma by cytogenetic investigation of macroscopically distinct ipsilateral lesions
    Genes Chromosomes Cancer, 18 (3), 170-4
    PubMed 9071569
16. Teixeira MR, Qvist H, Giercksky KE, Bøhler PJ, Heim S (1997)
    Cytogenetic analysis of several pseudomyxoma peritonei lesions originating from a mucinous cystadenoma of the appendix
    Cancer Genet Cytogenet, 93 (2), 157-9
    PubMed 9078301
17. Tranebjaerg L, Børresen-Dale AL, Hansteen IL, Heim S, Kvittingen EA, Møller P (1997)
    Genetic services in Norway
    Eur J Hum Genet, 5 Suppl 2, 130-4
    PubMed 9450210

Publications 1996

1. Adeyinka A, Pandis N, Nilsson J, Idvall I, Mertens F, Petersson C, Heim S, Mitelman F (1996)
   Different cytogenetic patterns in skeletal breast cancer metastases
   Genes Chromosomes Cancer, 16 (1), 72-4
   PubMed 9162201
2. Andreasson P, Johansson B, Arheden K, Tedgård U, Ljung R, Heim S, Mitelmann F (1996)
   Emergence of novel transient clonal chromosomal bone marrow changes in remission of acute lymphoblastic leukemia
   Leukemia, 10 (2), 378-83
   PubMed 8637252
3. Bomme L, Bardi G, Pandis N, Fenger C, Kronborg O, Heim S (1996)
   Chromosome abnormalities in colorectal adenomas: two cytogenetic subgroups characterized by deletion of 1p and numerical aberrations
   Hum Pathol, 27 (11), 1192-7
   PubMed 8912830
4. Heim S (1996)
   Genetic nomenclature: ISCN and ISGN
   Pediatr Hematol Oncol, 13 (2), iii
   PubMed 8721024
5. Heim S (1996)
   [Chromosome aberrations in solid tumors. Cytogenetic examinations are now available in Norway]
   Tidsskr Nor Laegeforen, 116 (19), 2295-6
   PubMed 8848778
6. Jin Y, Mertens F, Jin C, Wennerberg J, Mandahl N, Heim S, Mitelman F (1996)
   Clonal chromosome abnormalities in two chemodectomas
   Genes Chromosomes Cancer, 15 (3), 178-81
   PubMed 8721683
7. Johansson B, Fioretos T, Garwicz S, Heim S, Mitelman F (1996)
   t(3;21)(q26;q22) with AML1 rearrangement in a de novo childhood acute monoblastic leukaemia
   Br J Haematol, 92 (2), 429-31
   PubMed 8603012
8. Köhler M, Johansson B, Garwicz S, Heim S, Mitelman F (1996)
   No FISH evidence for trisomy 7 in normal or leukemic bone marrow
   Cancer Genet Cytogenet, 88 (2), 133-5
   PubMed 8640721
9. Lothe RA, Karhu R, Mandahl N, Mertens F, Saeter G, Heim S, Borresen-Dale AL, Kallioniemi OP (1996)
   Gain of 17q24-qter detected by comparative genomic hybridization in malignant tumors from patients with von Recklinghausen's neurofibromatosis
   Cancer Res, 56 (20), 4778-81
   PubMed 8840998
10. Pandis N, Idvall I, Bardi G, Jin Y, Gorunova L, Mertens F, Olsson H, Ingvar C, Beroukas K, Mitelman F, Heim S (1996)
    Correlation between karyotypic pattern and clincopathologic features in 125 breast cancer cases
    Int J Cancer, 66 (2), 191-6
    PubMed 8603810
11. Pejovic T, Alm P, Iosif SC, Mitelman F, Heim S (1996)
    Cytogenetic findings in four malignant mixed mesodermal tumors of the ovary
    Cancer Genet Cytogenet, 88 (1), 53-6
    PubMed 8630980
12. Pejovic T, Iosif CS, Mitelman F, Heim S (1996)
    Karyotypic characteristics of borderline malignant tumors of the ovary: trisomy 12, trisomy 7, and r(1) as nonrandom features
    Cancer Genet Cytogenet, 92 (2), 95-8
    PubMed 8976364
13. Teixeira MR, Heim S, Pandis N, Bardi G, Anderson JA (1996)
    Karyotypic comparisons of multiple tumorous and macroscopically normal surrounding tissue samples from patients with breast cancer. Reply
    Cancer Res., 56 (21), 5098
14. Teixeira MR, Pandis N, Bardi G, Andersen JA, Heim S (1996)
    Karyotypic comparisons of multiple tumorous and macroscopically normal surrounding tissue samples from patients with breast cancer
    Cancer Res, 56 (4), 855-9
    PubMed 8631024
15. Teixeira MR, Pandis N, Gerdes AM, Dietrich CU, Bardi G, Andersen JA, Graversen HP, Mitelman F, Heim S (1996)
    Cytogenetic abnormalities in an in situ ductal carcinoma and five prophylactically removed breasts from members of a family with hereditary breast cancer
    Breast Cancer Res Treat, 38 (2), 177-82
    PubMed 8861836

Publications 1995

1. Akervall JA, Jin Y, Wennerberg JP, Zätterström UK, Kjellén E, Mertens F, Willén R, Mandahl N, Heim S, Mitelman F (1995)
   Chromosomal abnormalities involving 11q13 are associated with poor prognosis in patients with squamous cell carcinoma of the head and neck
   Cancer, 76 (5), 853-9
   PubMed 8625189
2. Bardi G, Fenger C, Pandis N, Mitelman F, Heim S (1995)
   Karyotypic aberrations in an anal-canal malignant-melanoma and its local metastasis
   Int J Oncol, 6 (3), 555-7
   PubMed 21556570
3. Bardi G, Pandis N, Fenger C, Heim S (1995)
   Trisomy 7 as the sole cytogenetic aberration in the epithelial component of a colonic adenoma
   Cancer Genet Cytogenet, 82 (1), 82-4
   PubMed 7627942
4. Bardi G, Pandis N, Schousboe K, Hølund B, Heim S (1995)
   Near-diploid karyotypes with recurrent chromosome abnormalities characterize early-stage endometrial cancer
   Cancer Genet Cytogenet, 80 (2), 110-4
   PubMed 7736425
5. Bardi G, Sukhikh T, Pandis N, Fenger C, Kronborg O, Heim S (1995)
   Karyotypic characterization of colorectal adenocarcinomas
   Genes Chromosomes Cancer, 12 (2), 97-109
   PubMed 7535093
6. Dietrich C, Pandis N, Bardi G, Hagerstrand I, Andersen J, Mitelman F, Heim S (1995)
   Rearrangement of chromosomal bands-3p13-14 in 2 hamartomas of the breast
   Int J Oncol, 6 (3), 559-61
   PubMed 21556571
7. Dietrich CU, Pandis N, Teixeira MR, Bardi G, Gerdes AM, Andersen JA, Heim S (1995)
   Chromosome abnormalities in benign hyperproliferative disorders of epithelial and stromal breast tissue
   Int J Cancer, 60 (1), 49-53
   PubMed 7814151
8. Fischer E, Dalhoff E, Heim S, Hofbauer U, Tiziani HJ (1995)
   Absolute interferometric distance measurement using a FM-demodulation technique
   Appl Opt, 34 (25), 5589-94
   PubMed 21060384
9. Gorunova L, Johansson B, Dawiskiba S, Andrén-Sandberg A, Jin Y, Mandahl N, Heim S, Mitelman F (1995)
   Massive cytogenetic heterogeneity in a pancreatic carcinoma: fifty-four karyotypically unrelated clones
   Genes Chromosomes Cancer, 14 (4), 259-66
   PubMed 8605114
10. Gorunova L, Johansson B, Dawiskiba S, Andrén-Sandberg A, Mandahl N, Heim S, Mitelman F (1995)
    Cytogenetically detected clonal heterogeneity in a duodenal adenocarcinoma
    Cancer Genet Cytogenet, 82 (2), 146-50
    PubMed 7664244
11. Hasle H, Heim S, Schroeder H, Schmiegelow K, Ostergaard E, Kerndrup G (1995)
    Transient pancytopenia preceding acute lymphoblastic leukemia (pre-ALL)
    Leukemia, 9 (4), 605-8
    PubMed 7723392
12. Jin C, Mertens F, Jin Y, Wennerberg J, Heim S, Mitelman F (1995)
    Complex karyotype with an 11q13 homogeneously staining region in esophageal squamous cell carcinoma
    Cancer Genet Cytogenet, 82 (2), 175-6
    PubMed 7664250
13. Jin Y, Mertens F, Arheden K, Mandahl N, Wennerberg J, Dictor M, Heim S, Mitelman F (1995)
    Karyotypic features of malignant tumors of the nasal cavity and paranasal sinuses
    Int J Cancer, 60 (5), 637-41
    PubMed 7860137
14. Jin Y, Mertens F, Jin C, Akervall J, Wennerberg J, Gorunova L, Mandahl N, Heim S, Mitelman F (1995)
    Nonrandom chromosome abnormalities in short-term cultured primary squamous cell carcinomas of the head and neck
    Cancer Res, 55 (14), 3204-10
    PubMed 7606742
15. Jin Y, Mertens F, Mandahl N, Wennerberg J, Dictor M, Heim S, Mitelman F (1995)
    Tetraploidization and progressive loss of 6q in a squamous cell carcinoma of the parotid gland
    Cancer Genet Cytogenet, 79 (2), 157-9
    PubMed 7889511
16. Johansson B, Arheden K, Höglund M, Othzén A, Békássy AN, Turesson I, Heim S, Mitelman F (1995)
    Fluorescence in situ hybridization analysis of whole-arm 7;12 translocations in hematologic malignancies
    Genes Chromosomes Cancer, 14 (1), 56-62
    PubMed 8527385
17. Johansson M, Jin Y, Mandahl N, Hambraeus G, Johansson L, Mitelman F, Heim S (1995)
    Cytogenetic analysis of short-term cultured squamous cell carcinomas of the lung
    Cancer Genet Cytogenet, 81 (1), 46-55
    PubMed 7773960
18. Johansson M, Mandahl N, Johansson L, Hambraeus G, Mitelman F, Heim S (1995)
    Translocation 11;19 in a mucoepidermoid tumor of the lung
    Cancer Genet Cytogenet, 80 (1), 85-6
    PubMed 7697644
19. Karaiskos C, Pandis N, Bardi G, Sfikas K, Tserkezoglou A, Fotiou S, Heim S (1995)
    Cytogenetic findings in uterine epithelioid leiomyomas
    Cancer Genet Cytogenet, 80 (2), 103-6
    PubMed 7736423
20. Lothe RA, Andersen SN, Hofstad B, Meling GI, Peltomäki P, Heim S, Brøgger A, Vatn M, Rognum TO, Børresen AL (1995)
    Deletion of 1p loci and microsatellite instability in colorectal polyps
    Genes Chromosomes Cancer, 14 (3), 182-8
    PubMed 8589034
21. Mertens F, Heim S, Kullendorff CM, Donnér M, Hägerstrand I, Mitelman F, Mandahl N (1995)
    Clonal karyotypic evolution in a pediatric neurofibrosarcoma
    Cancer Genet Cytogenet, 81 (2), 135-8
    PubMed 7621409
22. Mertens F, Heim S, Mandahl N, Mitelman F, Brun A, Strömblad LG, Kullendorff CM, Donnér M (1995)
    Recurrent chromosomal imbalances in choroid plexus tumors
    Cancer Genet Cytogenet, 80 (1), 83-4
    PubMed 7697643
23. Mertens F, Mandahl N, Hagerstrand I, Kullendorff C, Heim S (1995)
    Cytogenetic findings in pediatric germ-cell tumors
    Int J Oncol, 6 (2), 401-4
    PubMed 21556551
24. Mertens F, Rydholm A, Bauer HF, Limon J, Nedoszytko B, Szadowska A, Willén H, Heim S, Mitelman F, Mandahl N (1995)
    Cytogenetic findings in malignant peripheral nerve sheath tumors
    Int J Cancer, 61 (6), 793-8
    PubMed 7790113
25. Pandis N, Jin Y, Gorunova L, Petersson C, Bardi G, Idvall I, Johansson B, Ingvar C, Mandahl N, Mitelman F (1995)
    Chromosome analysis of 97 primary breast carcinomas: identification of eight karyotypic subgroups
    Genes Chromosomes Cancer, 12 (3), 173-85
    PubMed 7536456
26. Pandis N, Karaiskos C, Bardi G, Sfikas K, Tserkezoglou A, Fotiou S, Heim S (1995)
    Chromosome analysis of uterine adenomyosis. Detection of the leiomyoma-associated del(7q) in three cases
    Cancer Genet Cytogenet, 80 (2), 118-20
    PubMed 7736427
27. Pandis N, Teixeira MR, Gerdes AM, Limon J, Bardi G, Andersen JA, Idvall I, Mandahl N, Mitelman F, Heim S (1995)
    Chromosome abnormalities in bilateral breast carcinomas. Cytogenetic evaluation of the clonal origin of multiple primary tumors
    Cancer, 76 (2), 250-8
    PubMed 8625100
28. Teixeira MR, Pandis N, Bardi G, Andersen JA, Mitelman F, Heim S (1995)
    Clonal heterogeneity in breast cancer: karyotypic comparisons of multiple intra- and extra-tumorous samples from 3 patients
    Int J Cancer, 63 (1), 63-8
    PubMed 7558454

Publications 1994

1. Aman P, Pejovic T, Heim S, Mitelman F (1994)
   The mullerian-inhibiting substance gene is transcribed in human ovarian carcinomas with and without 19p rearrangements
   Int J Oncol, 5 (2), 177-9
   PubMed 21559572
2. Bardi G, Gorunova L, Limon J, Nedoszytko B, Johansson B, Pandis N, Mandahl N, Bak-Jensen E, Andrén-Sandberg A, Rys J (1994)
   Abnormal karyotypes in three carcinomas of the gallbladder
   Cancer Genet Cytogenet, 76 (1), 15-8
   PubMed 8076343
3. Bardi G, Sukhikh T, Pandis N, Hølund B, Heim S (1994)
   Complex karyotypic abnormalities in a primary carcinoma of the fallopian tube
   Genes Chromosomes Cancer, 10 (3), 207-9
   PubMed 7522045
4. Bomme L, Bardi G, Pandis N, Fenger C, Kronborg O, Heim S (1994)
   Clonal karyotypic abnormalities in colorectal adenomas: clues to the early genetic events in the adenoma-carcinoma sequence
   Genes Chromosomes Cancer, 10 (3), 190-6
   PubMed 7522042
5. Dietrich CU, Pandis N, Andersen JA, Heim S (1994)
   Chromosome abnormalities in adenolipomas of the breast: karyotypic evidence that the mesenchymal component constitutes the neoplastic parenchyma
   Cancer Genet Cytogenet, 72 (2), 146-50
   PubMed 8143274
6. Dietrich CU, Pandis N, Bardi G, Teixeira MR, Soukhikh T, Petersson C, Andersen JA, Heim S (1994)
   Karyotypic changes in phyllodes tumors of the breast
   Cancer Genet Cytogenet, 78 (2), 200-6
   PubMed 7828153
7. Gorunova L, Mertens F, Mandahl N, Jonsson N, Persson B, Heim S, Mitelman F (1994)
   Cytogenetic heterogeneity in a clear cell hidradenoma of the skin
   Cancer Genet Cytogenet, 77 (1), 26-32
   PubMed 7923079
8. Hagmar L, Brøgger A, Hansteen IL, Heim S, Högstedt B, Knudsen L, Lambert B, Linnainmaa K, Mitelman F, Nordenson I (1994)
   Cancer risk in humans predicted by increased levels of chromosomal aberrations in lymphocytes: Nordic study group on the health risk of chromosome damage
   Cancer Res, 54 (11), 2919-22
   PubMed 8187078
9. Jin Y, Mertens F, Limon J, Mandahl N, Wennerberg J, Dictor M, Heim S, Mitelman F (1994)
   Characteristic karyotypic features in lacrimal and salivary gland carcinomas
   Br J Cancer, 70 (1), 42-7
   PubMed 8018539
10. Johansson B, Bardi G, Pandis N, Gorunova L, Bäckman PL, Mandahl N, Dawiskiba S, Andrén-Sandberg A, Heim S, Mitelman F (1994)
    Karyotypic pattern of pancreatic adenocarcinomas correlates with survival and tumour grade
    Int J Cancer, 58 (1), 8-13
    PubMed 8014018
11. Johansson M, Dietrich C, Mandahl N, Hambraeus G, Johansson L, Clausen PP, Mitelman F, Heim S (1994)
    Karyotypic characterization of bronchial large cell carcinomas
    Int J Cancer, 57 (4), 463-7
    PubMed 8181850
12. Johansson M, Karauzum S, Dietrich C, Mandahl N, Hambraeus G, Johansson L, Clausen P, Mitelman F, Heim S (1994)
    Karyotypic abnormalities in adenocarcinomas of the lung
    Int J Oncol, 5 (1), 17-26
    PubMed 21559552
13. Köhler M, Johansson B, Ludvigsson J, Aman P, Heim S, Mitelman F (1994)
    Acute myeloid leukemia (AML-M1) with multiple trisomies and t(8;21)(q22;q22)
    Cancer Genet Cytogenet, 73 (1), 79-81
    PubMed 8174079
14. Mertens F, Albert A, Heim S, Lindholm J, Brosjö O, Mitelman F, Mandahl N (1994)
    Clonal structural chromosome aberrations in fibrous dysplasia
    Genes Chromosomes Cancer, 11 (4), 271-2
    PubMed 7533532
15. Mertens F, Mandahl N, Mitelman F, Heim S (1994)
    Cytogenetic analysis in the examination of solid tumors in children
    Pediatr Hematol Oncol, 11 (4), 361-77
    PubMed 7947009
16. Mertens F, Rydholm A, Kreicbergs A, Willén H, Jonsson K, Heim S, Mitelman F, Mandahl N (1994)
    Loss of chromosome band 8q24 in sporadic osteocartilaginous exostoses
    Genes Chromosomes Cancer, 9 (1), 8-12
    PubMed 7507706
17. Panagopoulos I, Aman P, Fioretos T, Höglund M, Johansson B, Mandahl N, Heim S, Behrendtz M, Mitelman F (1994)
    Fusion of the FUS gene with ERG in acute myeloid leukemia with t(16;21)(p11;q22)
    Genes Chromosomes Cancer, 11 (4), 256-62
    PubMed 7533529
18. Pandis N, Bardi G, Heim S (1994)
    Interrelationship between methodological choices and conceptual models in solid tumor cytogenetics
    Cancer Genet Cytogenet, 76 (2), 77-84
    PubMed 7923072
19. Pandis N, Bardi G, Jin Y, Dietrich C, Johansson B, Andersen J, Mandahl N, Mitelman F, Heim S (1994)
    Unbalanced t(1;16) as the sole karyotypic abnormality in a breast carcinoma and its lymph node metastasis
    Cancer Genet Cytogenet, 75 (2), 158-9
    PubMed 8055484
20. Petersson C, Johansson B, Pandis N, Gorunova L, Ingvar C, Idvall I, Mandahl N, Mitelman F (1994)
    Clonal chromosome-aberrations in fibrocystic breast disease-associated with increased risk of cancer
    Int J Oncol, 5 (6), 1207-10
    PubMed 21559699
21. Teixeira MR, Pandis N, Bardi G, Andersen JA, Mandahl N, Mitelman F, Heim S (1994)
    Cytogenetic analysis of multifocal breast carcinomas: detection of karyotypically unrelated clones as well as clonal similarities between tumour foci
    Br J Cancer, 70 (5), 922-7
    PubMed 7947098

Publications 1993

1. Aman P, Pejovic T, Wennborg A, Heim S, Mitelman F (1993)
   Mapping of the 19p13 breakpoint in an ovarian carcinoma between the INSR and TCF3 loci
   Genes Chromosomes Cancer, 8 (2), 134-6
   PubMed 7504518
2. Bajalica S, Sørensen AG, Pedersen NT, Heim S, Brøndum-Nielsen K (1993)
   Chromosome painting as a supplement to cytogenetic banding analysis in non-Hodgkin's lymphoma
   Genes Chromosomes Cancer, 7 (4), 231-9
   PubMed 7692950
3. Bardi G, Johansson B, Pandis N, Bak-Jensen E, Orndal C, Heim S, Mandahl N, Andrén-Sandberg A, Mitelman F (1993)
   Cytogenetic aberrations in colorectal adenocarcinomas and their correlation with clinicopathologic features
   Cancer, 71 (2), 306-14
   PubMed 8422622
4. Bardi G, Johansson B, Pandis N, Mandahl N, Bak-Jensen E, Andrén-Sandberg A, Mitelman F, Heim S (1993)
   Karyotypic abnormalities in tumours of the pancreas
   Br J Cancer, 67 (5), 1106-12
   PubMed 8494707
5. Bardi G, Pandis N, Fenger C, Kronborg O, Bomme L, Heim S (1993)
   Deletion of 1p36 as a primary chromosomal aberration in intestinal tumorigenesis
   Cancer Res, 53 (8), 1895-8
   PubMed 8467511
6. Dietrich CU, Jacobsen BB, Starklint H, Heim S (1993)
   Clonal karyotypic evolution in an embryonal rhabdomyosarcoma with trisomy 8 as the primary chromosomal abnormality
   Genes Chromosomes Cancer, 7 (4), 240-4
   PubMed 7692951
7. Dietrich CU, Pandis N, Bjerre P, Schrøder HD, Heim S (1993)
   Simple numerical chromosome aberrations in two pituitary adenomas
   Cancer Genet Cytogenet, 69 (2), 118-21
   PubMed 8402547
8. Fioretos T, Nilsson PG, Aman P, Heim S, Kristoffersson U, Malm C, Simonsson B, Turesson I, Mitelman F (1993)
   Clinical impact of breakpoint position within M-bcr in chronic myeloid leukemia
   Leukemia, 7 (8), 1225-31
   PubMed 8350622
9. Jin Y, Mertens F, Mandahl N, Heim S, Olegård C, Wennerberg J, Biörklund A, Mitelman F (1993)
   Chromosome abnormalities in eighty-three head and neck squamous cell carcinomas: influence of culture conditions on karyotypic pattern
   Cancer Res, 53 (9), 2140-6
   PubMed 8481917
10. Johansson B, Heim S, Mandahl N, Mertens F, Mitelman F (1993)
    Trisomy 7 in nonneoplastic cells
    Genes Chromosomes Cancer, 6 (4), 199-205
    PubMed 7685621
11. Johansson M, Dietrich C, Mandahl N, Hambraeus G, Johansson L, Clausen PP, Mitelman F, Heim S (1993)
    Recombinations of chromosomal bands 6p21 and 14q24 characterise pulmonary hamartomas
    Br J Cancer, 67 (6), 1236-41
    PubMed 8512809
12. Johansson M, Heim S, Mandahl N, Hambraeus G, Johansson L, Mitelman F (1993)
    Cytogenetic analysis of six bronchial carcinoids
    Cancer Genet Cytogenet, 66 (1), 33-8
    PubMed 8467472
13. Mandahl N, Baldetorp B, Fernö M, Akerman M, Rydholm A, Heim S, Willén H, Killander D, Mitelman F (1993)
    Comparative cytogenetic and DNA flow cytometric analysis of 150 bone and soft-tissue tumors
    Int J Cancer, 53 (3), 358-64
    PubMed 8428789
14. Mandahl N, Orndal C, Heim S, Willén H, Rydholm A, Bauer HC, Mitelman F (1993)
    Aberrations of chromosome segment 12q13-15 characterize a subgroup of hemangiopericytomas
    Cancer, 71 (10), 3009-13
    PubMed 8490829
15. Mandahl N, Willén H, Rydholm A, Heim S, Mitelman F (1993)
    Rearrangement of band q13 on both chromosomes 12 in a periosteal chondroma
    Genes Chromosomes Cancer, 6 (2), 121-3
    PubMed 7680888
16. Mertens F, Mandahl N, Orndal C, Baldetorp B, Bauer HC, Rydholm A, Wiebe T, Willén H, Akerman M, Heim S (1993)
    Cytogenetic findings in 33 osteosarcomas
    Int J Cancer, 55 (1), 44-50
    PubMed 8344751
17. Mertens F, Orndal C, Mandahl N, Heim S, Bauer HF, Rydholm A, Tufvesson A, Willén H, Mitelman F (1993)
    Chromosome aberrations in tenosynovial giant cell tumors and nontumorous synovial tissue
    Genes Chromosomes Cancer, 6 (4), 212-7
    PubMed 7685623
18. Pandis N, Heim S, Bardi G, Idvall I, Mandahl N, Mitelman F (1993)
    Chromosome analysis of 20 breast carcinomas: cytogenetic multiclonality and karyotypic-pathologic correlations
    Genes Chromosomes Cancer, 6 (1), 51-7
    PubMed 7680222
19. Pandis N, Jin Y, Limon J, Bardi G, Idvall I, Mandahl N, Mitelman F, Heim S (1993)
    Interstitial deletion of the short arm of chromosome 3 as a primary chromosome abnormality in carcinomas of the breast
    Genes Chromosomes Cancer, 6 (3), 151-5
    PubMed 7682099
20. Pejovic T, Heim S, Alm P, Iosif S, Himmelmann A, Skjaerris J, Mitelman F (1993)
    Isochromosome 1q as the sole karyotypic abnormality in a Sertoli cell tumor of the ovary
    Cancer Genet Cytogenet, 65 (1), 79-80
    PubMed 8431922

Publications 1992

1. Aman P, Ron D, Mandahl N, Fioretos T, Heim S, Arheden K, Willén H, Rydholm A, Mitelman F (1992)
   Rearrangement of the transcription factor gene CHOP in myxoid liposarcomas with t(12;16)(q13;p11)
   Genes Chromosomes Cancer, 5 (4), 278-85
   PubMed 1283316
2. Bajalica S, Brøndum-Nielsen K, Sørensen AG, Pedersen NT, Heim S (1992)
   Identification of a whole-arm translocation by in situ hybridization with directly fluorochrome-labeled probes in a myelodysplastic syndrome
   Genes Chromosomes Cancer, 5 (2), 128-31
   PubMed 1381948
3. Bardi G, Johansson B, Pandis N, Heim S, Mandahl N, Andrén-Sandberg A, Hägerstrand I, Mitelman F (1992)
   Cytogenetic findings in three primary hepatocellular carcinomas
   Cancer Genet Cytogenet, 58 (2), 191-5
   PubMed 1312894
4. Bardi G, Johansson B, Pandis N, Heim S, Mandahl N, Bak-Jensen E, Frederiksen H, Andrén-Sandberg A, Mitelman F (1992)
   Recurrent chromosome aberrations in abdominal smooth muscle tumors
   Cancer Genet Cytogenet, 62 (1), 43-6
   PubMed 1521232
5. Bardi G, Johansson B, Pandis N, Heim S, Mandahl N, Békássy A, Hägerstrand I, Mitelman F (1992)
   Trisomy 2 as the sole chromosomal abnormality in a hepatoblastoma
   Genes Chromosomes Cancer, 4 (1), 78-80
   PubMed 1377013
6. Bardi G, Johansson B, Pandis N, Heim S, Mandahl N, Hägerstrand I, Holmin T, Andrén-Sandberg A, Mitelman F (1992)
   Trisomy 7 in nonneoplastic focal steatosis of the liver
   Cancer Genet Cytogenet, 63 (1), 22-4
   PubMed 1423221
7. Elfving P, Lundgren R, Cigudosa JC, Heim S, Mandahl N, Mitelman F (1992)
   Trisomy 7 in nonneoplastic kidney tissue cultured with and without epidermal growth factor
   Cancer Genet Cytogenet, 64 (1), 99-100
   PubMed 1458459
8. Fioretos T, Heim S, Garwicz S, Ludvigsson J, Mitelman F (1992)
   Molecular analysis of Philadelphia-positive childhood chronic myeloid leukemia
   Leukemia, 6 (7), 723-5
   PubMed 1625493
9. Heim S (1992)
   Cytogenetic findings in primary and secondary MDS
   Leuk Res, 16 (1), 43-6
   PubMed 1732669
10. Heim S (1992)
    Is cancer cytogenetics reducible to the molecular genetics of cancer cells?
    Genes Chromosomes Cancer, 5 (3), 188-96
    PubMed 1384669
11. Heim S, Christensen BE, Fioretos T, Sørensen AG, Pedersen NT (1992)
    Acute myelomonocytic leukemia with inv(16)(p13q22) complicating Philadelphia chromosome positive chronic myeloid leukemia
    Cancer Genet Cytogenet, 59 (1), 35-8
    PubMed 1555189
12. Heim S, Mitelman F (1992)
    Cytogenetic analysis in the diagnosis of acute leukemia
    Cancer, 70 (6 Suppl), 1701-9
    PubMed 1516024
13. Heim S, Sørensen AG, Christensen BE, Pedersen NT (1992)
    Re-emergence in remission of primary clone in acute myelogenous leukaemias with multiple chromosomal aberrations at diagnosis
    Br J Haematol, 82 (2), 332-6
    PubMed 1419815
14. Higashi K, Sarashina N, Okamoto T, Matsuki C, Heim S (1992)
    Supernumerary ring marker chromosome as a secondary rearrangement in a parapharyngeal lipoma with t(10;12)(q25;q15) as the primary karyotypic abnormality
    Cancer Genet Cytogenet, 64 (2), 163-5
    PubMed 1486566
15. Johansson B, Bardi G, Heim S, Mandahl N, Mertens F, Bak-Jensen E, Andrén-Sandberg A, Mitelman F (1992)
    Nonrandom chromosomal rearrangements in pancreatic carcinomas
    Cancer, 69 (7), 1674-81
    PubMed 1551052
16. Johansson M, Heim S, Mandahl N, Johansson L, Hambraeus G, Mitelman F (1992)
    t(3;6;14)(p21;p21;q24) as the sole clonal chromosome abnormality in a hamartoma of the lung
    Cancer Genet Cytogenet, 60 (2), 219-20
    PubMed 1606572
17. Johansson M, Jin Y, Heim S, Mandahl N, Hambraeus G, Johansson L, Mitelman F (1992)
    Pseudodiploid karyotypes in adenosquamous carcinomas of the lung
    Cancer Genet Cytogenet, 63 (2), 95-6
    PubMed 1423237
18. Lang T, Heim S (1992)
    [A case from practice (241). Ischemic insult in the left thalamus region in the framework of an accompanying migraine. Hysterical personality]
    Schweiz Rundsch Med Prax, 81 (16), 529-31
    PubMed 1574673
19. Lundgren R, Heim S, Mandahl N, Anderson H, Mitelman F (1992)
    Chromosome abnormalities are associated with unfavorable outcome in prostatic cancer patients
    J Urol, 147 (3 Pt 2), 784-8
    PubMed 1538480
20. Lundgren R, Mandahl N, Heim S, Limon J, Henrikson H, Mitelman F (1992)
    Cytogenetic analysis of 57 primary prostatic adenocarcinomas
    Genes Chromosomes Cancer, 4 (1), 16-24
    PubMed 1377005
21. Mertens F, Jin Y, Heim S, Mandahl N, Jonsson N, Mertens O, Persson B, Salemark L, Wennerberg J, Mitelman F (1992)
    Clonal structural chromosome aberrations in nonneoplastic cells of the skin and upper aerodigestive tract
    Genes Chromosomes Cancer, 4 (3), 235-40
    PubMed 1382565
22. Mitelman F, Heim S (1992)
    Quantitative acute leukemia cytogenetics
    Genes Chromosomes Cancer, 5 (1), 57-66
    PubMed 1384663
23. Olegård C, Mandahl N, Heim S, Willén H, Leifsson B, Mitelman F (1992)
    Embryonal rhabdomyosarcoma with 100 chromosomes but no structural aberrations
    Cancer Genet Cytogenet, 60 (2), 198-201
    PubMed 1606566
24. Orndal C, Mandahl N, Carlén B, Willén H, Wennerberg J, Heim S, Mitelman F (1992)
    Near-haploid clones in a malignant fibrous histiocytoma
    Cancer Genet Cytogenet, 60 (2), 147-51
    PubMed 1318780
25. Orndal C, Mandahl N, Rydholm A, Willén H, Brosjö O, Heim S, Mitelman F (1992)
    Supernumerary ring chromosomes in five bone and soft tissue tumors of low or borderline malignancy
    Cancer Genet Cytogenet, 60 (2), 170-5
    PubMed 1318782
26. Pandis N, Heim S, Bardi G, Idvall I, Mandahl N, Mitelman F (1992)
    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, 5 (3), 235-8
    PubMed 1384676
27. Pandis N, Heim S, Bardi G, Limon J, Mandahl N, Mitelman F (1992)
    Improved technique for short-term culture and cytogenetic analysis of human breast cancer
    Genes Chromosomes Cancer, 5 (1), 14-20
    PubMed 1384657
28. Pejovic T, Heim S, Mandahl N, Baldetorp B, Elmfors B, Flodérus UM, Furgyik S, Helm G, Himmelmann A, Willén H (1992)
    Chromosome aberrations in 35 primary ovarian carcinomas
    Genes Chromosomes Cancer, 4 (1), 58-68
    PubMed 1377010
29. Pejovic T, Himmelmann A, Heim S, Mandahl N, Flodérus UM, Furgyik S, Elmfors B, Helm G, Willén H, Mitelman F (1992)
    Prognostic impact of chromosome aberrations in ovarian cancer
    Br J Cancer, 65 (2), 282-6
    PubMed 1739630

Publications 1991

1. Bardi G, Johansson B, Pandis N, Békássy AN, Kullendorff CM, Hägerstrand I, Heim S (1991)
   i(8q) as the primary structural chromosome abnormality in a hepatoblastoma
   Cancer Genet Cytogenet, 51 (2), 281-3
   PubMed 1847091
2. Bardi G, Johansson B, Pandis N, Heim S, Mandahl N, Andrén-Sandberg A, Hägerstrand I, Mitelman F (1991)
   Trisomy 7 in short-term cultures of colorectal adenocarcinomas
   Genes Chromosomes Cancer, 3 (2), 149-52
   PubMed 2069912
3. Bardi G, Pandis N, Mandahl N, Heim S, Sfikas K, Willén H, Panagiotopoulos G, Rydholm A, Mitelman F (1991)
   Chromosomal abnormalities in giant cell tumors of bone
   Cancer Genet Cytogenet, 57 (2), 161-7
   PubMed 1756493
4. Callen DF, Hull YJ, Toogood IR, Fioretos T, Heim S, Mandahl N, Mitelman F (1991)
   New chromosomal rearrangement, t(12;22)(p13;q12), in acute nonlymphocytic leukemia
   Cancer Genet Cytogenet, 51 (2), 255-8
   PubMed 1993309
5. Heim S (1991)
   Epidemiological clues to leukaemias involving specific chromosomal abnormalities
   Leukemia, 5 (9), 823-4
   PubMed 1943234
6. Higashi K, Jin Y, Heim S, Mandahl N, Biörklund A, Wennerberg J, Dictor M, Mitelman F (1991)
   Chromosome abnormalities in a carcinoma in pleomorphic adenoma of the lacrimal gland
   Cancer Genet Cytogenet, 55 (1), 125-8
   PubMed 1655240
7. Higashi K, Jin Y, Johansson M, Heim S, Mandahl N, Biörklund A, Wennerberg J, Hambraeus G, Johansson L, Mitelman F (1991)
   Rearrangement of 9p13 as the primary chromosomal aberration in adenoid cystic carcinoma of the respiratory tract
   Genes Chromosomes Cancer, 3 (1), 21-3
   PubMed 1648955
8. Johansson B, Mertens F, Heim S, Kristoffersson U, Mitelman F (1991)
   Cytogenetics of secondary myelodysplasia (sMDS) and acute nonlymphocytic leukemia (sANLL)
   Eur J Haematol, 47 (1), 17-27
   PubMed 1868912
9. Lindström E, Salford LG, Heim S, Mandahl N, Strömblad S, Brun A, Mitelman F (1991)
   Trisomy 7 and sex chromosome loss need not be representative of tumor parenchyma cells in malignant glioma
   Genes Chromosomes Cancer, 3 (6), 474-9
   PubMed 1663782
10. Mamaeva S, Lundgren R, Elfving P, Limon J, Mandahl N, Mamaev N, Henrikson H, Heim S, Mitelman F (1991)
    AgNOR staining in benign hyperplasia and carcinoma of the prostate
    Prostate, 18 (2), 155-62
    PubMed 1706512
11. Mertens F, Heim S, Mandahl N, Johansson B, Mertens O, Persson B, Salemark L, Wennerberg J, Jonsson N, Mitelman F (1991)
    Cytogenetic analysis of 33 basal cell carcinomas
    Cancer Res, 51 (3), 954-7
    PubMed 1988137
12. Mertens F, Johansson B, Heim S, Kristoffersson U, Mitelman F (1991)
    Karyotypic patterns in chronic myeloproliferative disorders: report on 74 cases and review of the literature
    Leukemia, 5 (3), 214-20
    PubMed 2013980
13. Mertens F, Sallerfors B, Heim S, Johansson B, Kristoffersson U, Malm C, Mitelman F (1991)
    Trisomy 13 as a primary chromosome aberration in acute leukemia
    Cancer Genet Cytogenet, 56 (1), 39-44
    PubMed 1747868
14. Orndal C, Carlén B, Akerman M, Willén H, Mandahl N, Heim S, Rydholm A, Mitelman F (1991)
    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, 2 (5), 261-70
    PubMed 1782363
15. Pandis N, Heim S, Bardi G, Flodérus UM, Willén H, Mandahl N, Mitelman F (1991)
    Chromosome analysis of 96 uterine leiomyomas
    Cancer Genet Cytogenet, 55 (1), 11-8
    PubMed 1913597
16. Pejovic T, Heim S, Mandahl N, Elmfors B, Furgyik S, Flodérus UM, Helm G, Willén H, Mitelman F (1991)
    Bilateral ovarian carcinoma: cytogenetic evidence of unicentric origin
    Int J Cancer, 47 (3), 358-61
    PubMed 1993543

Publications 1990

1. Billström R, Heim S, Kristoffersson U, Mandahl N, Mitelman F (1990)
   Structural chromosomal abnormalities of 3q in myelodysplastic syndrome/acute myeloid leukaemia with Sweet's syndrome
   Eur J Haematol, 45 (3), 150-2
   PubMed 2226727
2. Brøgger A, Hagmar L, Hansteen IL, Heim S, Högstedt B, Knudsen L, Lambert B, Linnainmaa K, Mitelman F, Nordenson I (1990)
   An inter-Nordic prospective study on cytogenetic endpoints and cancer risk. Nordic Study Group on the Health Risk of Chromosome Damage
   Cancer Genet Cytogenet, 45 (1), 85-92
   PubMed 2302690
3. Elfving P, Cigudosa JC, Lundgren R, Limon J, Mandahl N, Kristoffersson U, Heim S, Mitelman F (1990)
   Trisomy 7, trisomy 10, and loss of the Y chromosome in short-term cultures of normal kidney tissue
   Cytogenet Cell Genet, 53 (2-3), 123-5
   PubMed 2369838
4. Eneroth M, Mandahl N, Heim S, Willén H, Rydholm A, Alberts KA, Mitelman F (1990)
   Localization of the chromosomal breakpoints of the t(12;16) in liposarcoma to subbands 12q13.3 and 16p11.2
   Cancer Genet Cytogenet, 48 (1), 101-7
   PubMed 2372777
5. Heim S (1990)
   Cytogenetics in the investigation of haematological disorders
   Baillieres Clin Haematol, 3 (4), 921-48
   PubMed 2271796
6. Heim S, Békàssy AN, Garwicz S, Heldrup J, Kristoffersson U, Mandahl N, Wiebe T, Mitelman F (1990)
   Bone marrow karyotypes in 94 children with acute leukemia
   Eur J Haematol, 44 (4), 227-33
   PubMed 2344885
7. Jin YS, Heim S, Mandahl N, Biörklund A, Wennerberg J, Mitelman F (1990)
   Unrelated clonal chromosomal aberrations in carcinomas of the oral cavity
   Genes Chromosomes Cancer, 1 (3), 209-15
   PubMed 2083216
8. Jin YS, Heim S, Mandahl N, Biörklund A, Wennerberg J, Mitelman F (1990)
   Multiple clonal chromosome aberrations in squamous cell carcinomas of the larynx
   Cancer Genet Cytogenet, 44 (2), 209-16
   PubMed 2297681
9. Jin YS, Higashi K, Mandahl N, Heim S, Wennerberg J, Biörklund A, Dictor M, Mitelman F (1990)
   Frequent rearrangement of chromosomal bands 1p22 and 11q13 in squamous cell carcinomas of the head and neck
   Genes Chromosomes Cancer, 2 (3), 198-204
   PubMed 2078510
10. Johansson B, Mertens F, Fioretos T, Heim S, Kristoffersson U, Mandahl N, Bartram CR, Mitelman F (1990)
    Remarkably long survival of a patient with Ph1-positive chronic myeloid leukemia and 5' bcr rearrangement
    Leukemia, 4 (6), 448-9
    PubMed 2359344
11. Johansson B, Mertens F, Heim S, Kristoffersson U, Mandahl N, Nilsson PG, Mitelman F (1990)
    Cytogenetic findings in acute megakaryoblastic leukemia (ANLL-M7)
    Cancer Genet Cytogenet, 48 (1), 119-23
    PubMed 2372779
12. Kristoffersson U, Heim S, Johnsson A, Mandahl N, Olsson H, Akerman M, Mitelman F (1990)
    Deletion of 14q in non-Hodgkin's lymphoma
    Eur J Haematol, 44 (4), 261-4
    PubMed 2344888
13. Limon J, Lundgren R, Elfving P, Heim S, Kristoffersson U, Mandahl N, Mitelman F (1990)
    An improved technique for short-term culturing of human prostatic adenocarcinoma tissue for cytogenetic analysis
    Cancer Genet Cytogenet, 46 (2), 191-9
    PubMed 2340490
14. Limon J, Mrózek K, Heim S, Elfving P, Nedoszytko B, Babi?ska M, Mandahl N, Lundgren R, Mitelman F (1990)
    On the significance of trisomy 7 and sex chromosome loss in renal cell carcinoma
    Cancer Genet Cytogenet, 49 (2), 259-63
    PubMed 2208062
15. Mandahl N, Heim S, Arheden K, Rydholm A, Willén H, Mitelman F (1990)
    Chromosomal rearrangements in chondromatous tumors
    Cancer, 65 (2), 242-8
    PubMed 2295046
16. Mandahl N, Heim S, Willén H, Rydholm A, Mitelman F (1990)
    Supernumerary ring chromosome as the sole cytogenetic abnormality in a dermatofibrosarcoma protuberans
    Cancer Genet Cytogenet, 49 (2), 273-5
    PubMed 2208065
17. Mandahl N, Jin YS, Heim S, Willén H, Wennerberg J, Biörklund A, Mitelman F (1990)
    Trisomy 5 and loss of the Y chromosome as the sole cytogenetic anomalies in a cavernous hemangioma/angiosarcoma
    Genes Chromosomes Cancer, 1 (4), 315-6
    PubMed 2278963
18. Mertens F, Johansson B, Heim S, Kristoffersson U, Mandahl N, Turesson I, Malm C, Othzén A, Bartram CR, Catovsky D (1990)
    Trisomy 14 in atypical chronic myeloid leukemia
    Leukemia, 4 (2), 117-20
    PubMed 2406515
19. Mitelman F, Heim S (1990)
    Chromosome abnormalities in cancer
    Cancer Detect Prev, 14 (5), 527-37
    PubMed 2224917
20. Mitelman F, Heim S, Mandahl N (1990)
    Trisomy 21 in neoplastic cells
    Am J Med Genet Suppl, 7, 262-6
    PubMed 2149959
21. Nibert M, Heim S (1990)
    Uterine leiomyoma cytogenetics
    Genes Chromosomes Cancer, 2 (1), 3-13
    PubMed 2278965
22. Nilbert M, Heim S, Mandahl N, Flodérus UM, Willén H, Mitelman F (1990)
    Trisomy 12 in uterine leiomyomas. A new cytogenetic subgroup
    Cancer Genet Cytogenet, 45 (1), 63-6
    PubMed 2302686
23. Nilbert M, Heim S, Mandahl N, Flodérus UM, Willén H, Mitelman F (1990)
    Characteristic chromosome abnormalities, including rearrangements of 6p, del(7q), +12, and t(12;14), in 44 uterine leiomyomas
    Hum Genet, 85 (6), 605-11
    PubMed 2227952
24. Nilbert M, Jin YS, Heim S, Mandahl N, Flodérus UM, Willén H, Mitelman F (1990)
    Chromosome rearrangements in two uterine sarcomas
    Cancer Genet Cytogenet, 44 (1), 27-35
    PubMed 2152853
25. Nilbert M, Mandahl N, Heim S, Rydholm A, Helm G, Willén H, Baldetorp B, Mitelman F (1990)
    Complex karyotypic changes, including rearrangements of 12q13 and 14q24, in two leiomyosarcomas
    Cancer Genet Cytogenet, 48 (2), 217-23
    PubMed 2397453
26. Orndal C, Johansson M, Heim S, Mandahl N, Månsson B, Alumets J, Mitelman F (1990)
    Parathyroid adenoma with t(1;5)(p22;q32) as the sole clonal chromosome abnormality
    Cancer Genet Cytogenet, 48 (2), 225-8
    PubMed 2397454
27. Orndal C, Mandahl N, Rydholm A, Nilbert M, Heim S, Akerman M, Mitelman F (1990)
    Chromosomal evolution and tumor progression in a myxoid liposarcoma
    Acta Orthop Scand, 61 (2), 99-105
    PubMed 2193480
28. Pandis N, Heim S, Bardi G, Flodérus UM, Willén H, Mandahl N, Mitelman F (1990)
    Parallel karyotypic evolution and tumor progression in uterine leiomyoma
    Genes Chromosomes Cancer, 2 (4), 311-7
    PubMed 2268579
29. Pandis N, Heim S, Bardi G, Mandahl N, Mitelman F (1990)
    High resolution mapping of consistent leiomyoma breakpoints in chromosomes 12 and 14 to 12q15 and 14q24.1
    Genes Chromosomes Cancer, 2 (3), 227-30
    PubMed 2078514
30. Pejovic T, Heim S, Mandahl N, Elmfors B, Flodérus UM, Furgyik S, Helm G, Willén H, Mitelman F (1990)
    Trisomy 12 is a consistent chromosomal aberration in benign ovarian tumors
    Genes Chromosomes Cancer, 2 (1), 48-52
    PubMed 2177641
31. Pejovic T, Heim S, Mandahl N, Flodérus UM, Willén H, Mitelman F (1990)
    Complex karyotypic anomalies, including an i(5p) marker chromosome, in malignant mixed mesodermal tumor of the ovary
    Cancer Genet Cytogenet, 46 (1), 65-9
    PubMed 2331684
32. Pejovic T, Heim S, Orndal C, Jin YS, Mandahl N, Willén H, Mitelman F (1990)
    Simple numerical chromosome aberrations in well-differentiated malignant epithelial tumors
    Cancer Genet Cytogenet, 49 (1), 95-101
    PubMed 2397477
33. Rydholm A, Mandahl N, Heim S, Kreicbergs A, Willén H, Mitelman F (1990)
    Malignant fibrous histiocytomas with a 19p+ marker chromosome have increased relapse rate
    Genes Chromosomes Cancer, 2 (4), 296-9
    PubMed 2176542

Publications 1989

1. Arheden K, Mandahl N, Heim S, Mitelman F (1989)
   In situ hybridization localizes the human type II alpha 1 collagen gene (COL2A1) to 12q13
   Hereditas, 110 (2), 165-7
   PubMed 2745153
2. Arheden K, Mandahl N, Heim S, Mitelman F (1989)
   The INT1 oncogene is not rearranged or amplified in lipomas with structural chromosomal abnormalities of 12q13-15
   Cancer Genet Cytogenet, 42 (1), 143-6
   PubMed 2790742
3. Arheden K, Nilbert M, Heim S, Mandahl N, Mitelman F (1989)
   No amplification or rearrangement of INT1, GLI, or COL2A1 in uterine leiomyomas with t(12;14)(q14-15;q23-24)
   Cancer Genet Cytogenet, 39 (2), 195-201
   PubMed 2752373
4. Arheden K, Rønne M, Mandahl N, Heim S, Kinzler KW, Vogelstein B, Mitelman F (1989)
   In situ hybridization localizes the human putative oncogene GLI to chromosome subbands 12q13.3-14.1
   Hum Genet, 82 (1), 1-2
   PubMed 2497059
5. Gedde-Dahl T, Heim S, Lothe R, Bye R, Geitvik GA, Kyrkjebø HT, Hognestad J, Nygaard K, Bergan A, Olaisen B (1989)
   [The polyposis project]
   Nord Med, 104 (1), 12-5
   PubMed 2536147
6. Heim S, Caron M, Jin Y, Mandahl N, Mitelman F (1989)
   Genetic convergence during serial in vitro passage of a polyclonal squamous cell carcinoma
   Cytogenet Cell Genet, 52 (3-4), 133-5
   PubMed 2630184
7. Heim S, Johansson B, Mertens F (1989)
   Constitutional chromosome instability and cancer risk
   Mutat Res, 221 (1), 39-51
   PubMed 2664494
8. Heim S, Mandahl N, Jin Y, Strömblad S, Lindström E, Salford LG, Mitelman F (1989)
   Trisomy 7 and sex chromosome loss in human brain tissue
   Cytogenet Cell Genet, 52 (3-4), 136-8
   PubMed 2630185
9. Heim S, Mertens F, Jin YS, Mandahl N, Johansson B, Biörklund A, Wennerberg J, Jonsson N, Mitelman F (1989)
   Diverse chromosome abnormalities in squamous cell carcinomas of the skin
   Cancer Genet Cytogenet, 39 (1), 69-76
   PubMed 2731150
10. Heim S, Mitelman F (1989)
    Cytogenetically unrelated clones in hematological neoplasms
    Leukemia, 3 (1), 6-8
    PubMed 2909809
11. Heim S, Mitelman F (1989)
    Primary chromosome abnormalities in human neoplasia
    Adv Cancer Res, 52, 1-43
    PubMed 2662710
12. Jin YS, Heim S, Mandahl N, Biörklund A, Wennerberg J, Willén R, Mitelman F (1989)
    Two unrelated clonal chromosome rearrangements in a nasal papilloma
    Cancer Genet Cytogenet, 39 (1), 29-34
    PubMed 2731145
13. Johansson B, Mandahl N, Heim S, Mertens F, Andrén-Sandberg A, Mitelam F (1989)
    Chromosome abnormalities in a pancreatic adenocarcinoma
    Cancer Genet Cytogenet, 37 (2), 209-13
    PubMed 2702620
14. Kristoffersson U, Berger R, Bernheim A, Desatnik P, Heim S, Mandahl N, Olsson H, Mitelman F (1989)
    No abnormal C-band polymorphism in lung cancer patients
    Hereditas, 110 (3), 201-2
    PubMed 2753740
15. Kristoffersson U, Bernheim A, Berger R, Nilsson B, Heim S, Mandahl N, Mitelman F (1989)
    Constitutional C-band polymorphism in lymphocytes from patients with chronic myeloid leukemia
    Hereditas, 110 (2), 145-8
    PubMed 2745151
16. Kristoffersson U, Heim S, Mandahl N, Akerman M, Mitelman F (1989)
    Multiple clonal chromosome aberrations in two thymomas
    Cancer Genet Cytogenet, 41 (1), 93-8
    PubMed 2766255
17. Limon J, Lundgren R, Elfving P, Heim S, Kristoffersson U, Mandahl N, Mitelman F (1989)
    Double minutes in two primary adenocarcinomas of the prostate
    Cancer Genet Cytogenet, 39 (2), 191-4
    PubMed 2752372
18. Lundgren R, Elfving P, Heim S, Kristoffersson U, Mandahl N, Mitelman F (1989)
    A squamous cell bladder carcinoma with karyotypic abnormalities reminiscent of transitional cell carcinoma
    J Urol, 142 (2 Pt 1), 374-6
    PubMed 2746756
19. Mandahl N, Heim S, Arheden K, Rydholm A, Willén H, Mitelman F (1989)
    Separate karyotypic features in a local recurrence and a metastasis of a fibrosarcoma
    Cancer Genet Cytogenet, 37 (1), 139-40
    PubMed 2917329
20. Mandahl N, Heim S, Brosjö O, Bauer HC, Tribukait B, Rydholm A, Mitelman F (1989)
    Cytogenetic and quantitative DNA analysis of primary and xenografted human osteosarcomas
    Cancer Genet Cytogenet, 42 (1), 27-34
    PubMed 2790744
21. Mandahl N, Heim S, Rydholm A, Willén H, Mitelman F (1989)
    Structural chromosome aberrations in an adamantinoma
    Cancer Genet Cytogenet, 42 (2), 187-90
    PubMed 2790753
22. Mandahl N, Heim S, Rydholm A, Willen H, Mitelman F (1989)
    Nonrandom numerical chromosome aberrations (+8, +11, +17, +20) in infantile fibrosarcoma
    Cancer Genet Cytogenet, 40 (1), 137-9
    PubMed 2758397
23. Mandahl N, Heim S, Willén H, Rydholm A, Eneroth M, Nilbert M, Kreicbergs A, Mitelman F (1989)
    Characteristic karyotypic anomalies identify subtypes of malignant fibrous histiocytoma
    Genes Chromosomes Cancer, 1 (1), 9-14
    PubMed 2562116
24. Mertens F, Heim S, Jin YS, Johansson B, Mandahl N, Biörklund A, Wennerberg J, Jonsson N, Mitelman F (1989)
    Basosquamous papilloma. A benign epithelial skin tumor with multiple cytogenetic clones
    Cancer Genet Cytogenet, 37 (2), 235-9
    PubMed 2702623
25. Mertens F, Heim S, Mandahl N, Johansson B, Rydholm A, Biörklund A, Wennerberg J, Jonsson N, Mitelman F (1989)
    Clonal chromosome aberrations in a keratoacanthoma and a basal cell papilloma
    Cancer Genet Cytogenet, 39 (2), 227-32
    PubMed 2752375
26. Myklebost O, Arheden K, Rogne S, Geurts van Kessel A, Mandahl N, Herz J, Stanley K, Heim S, Mitelman F (1989)
    The gene for the human putative apoE receptor is on chromosome 12 in the segment q13-14
    Genomics, 5 (1), 65-9
    PubMed 2548950
27. Nilbert M, Heim S, Mandahl N, Flodérus UM, Willén H, Baldetorp B, Mitelman F (1989)
    Complex karyotypic anomalies in a bizarre leiomyoma of the uterus
    Genes Chromosomes Cancer, 1 (2), 131-4
    PubMed 2487152
28. Nilbert M, Heim S, Mandahl N, Flodérus UM, Willén H, Mitelman F (1989)
    Different karyotypic abnormalities, t(1;6) and del(7), in two uterine leiomyomas from the same patient
    Cancer Genet Cytogenet, 42 (1), 51-3
    PubMed 2790746
29. Nilbert M, Mandahl N, Heim S, Rydholm A, Willén H, Mitelman F (1989)
    Cytogenetic abnormalities in an angioleiomyoma
    Cancer Genet Cytogenet, 37 (1), 61-4
    PubMed 2917333
30. Pejovic T, Heim S, Mandahl N, Elmfors B, Flodérus UM, Furgyik S, Helm G, Willén H, Mitelman F (1989)
    Consistent occurrence of a 19p+ marker chromosome and loss of 11p material in ovarian seropapillary cystadenocarcinomas
    Genes Chromosomes Cancer, 1 (2), 167-71
    PubMed 2487157
31. Wissing J, Heim S, Wagner KG (1989)
    Diacylglycerol kinase from suspension cultured plant cells : purification and properties
    Plant Physiol, 90 (4), 1546-51
    PubMed 16666963

Publications 1988

1. Arheden K, Tommerup N, Mandahl N, Heim S, Winther J, Jensen OA, Prause JU, Mitelman F (1988)
   Amplification of the human putative oncogene INT1 in primary retinoblastoma tumors
   Cytogenet Cell Genet, 48 (3), 174-7
   PubMed 3069341
2. Billström R, Thiede T, Hansen S, Heim S, Kristoffersson U, Mandahl N, Mitelman F (1988)
   Bone marrow karyotype and prognosis in primary myelodysplastic syndromes
   Eur J Haematol, 41 (4), 341-6
   PubMed 3197821
3. Gedde-Dahl T, Heim S, Lothe R, Bye R, Brevik K, Geitvik GA, Kyrkjebø HT, Hognestad J, Nygaard K, Bergan A (1988)
   [The polyposis project]
   Tidsskr Nor Laegeforen, 108 (29), 2465-8
   PubMed 2905084
4. Heim S, Jin Y, Mandahl N, Biörklund A, Wennerberg J, Jonsson N, Mitelman F (1988)
   Multiple unrelated clonal chromosome abnormalities in an in situ squamous cell carcinoma of the skin
   Cancer Genet Cytogenet, 36 (2), 149-53
   PubMed 3203301
5. Heim S, Kristoffersson U, Mandahl N, Malm C, Mitelman F (1988)
   Variant translocation t(3;15)(q21;q22) in a patient with acute promyelocytic leukemia
   Leukemia, 2 (1), 65-7
   PubMed 3422330
6. Heim S, Mandahl N, Arheden K, Giovanella BC, Yim SO, Stehlin JS, Mitelman F (1988)
   Multiple karyotypic abnormalities, including structural rearrangements of 11p, in cell lines from malignant melanomas
   Cancer Genet Cytogenet, 35 (1), 5-20
   PubMed 3180009
7. Heim S, Mandahl N, Mitelman F (1988)
   Genetic convergence and divergence in tumor progression
   Cancer Res, 48 (21), 5911-6
   PubMed 3048652
8. Heim S, Mandahl N, Rydholm A, Willén H, Mitelman F (1988)
   Different karyotypic features characterize different clinico-pathologic subgroups of benign lipogenic tumors
   Int J Cancer, 42 (6), 863-7
   PubMed 3192332
9. Heim S, Nilbert M, Vanni R, Floderus UM, Mandahl N, Liedgren S, Lecca U, Mitelman F (1988)
   A specific translocation, t(12;14)(q14-15;q23-24), characterizes a subgroup of uterine leiomyomas
   Cancer Genet Cytogenet, 32 (1), 13-7
   PubMed 3355995
10. Jin YS, Heim S, Mandahl N, Biörklund A, Wennerberg J, Mitelman F (1988)
    Multiple apparently unrelated clonal chromosome abnormalities in a squamous cell carcinoma of the tongue
    Cancer Genet Cytogenet, 32 (1), 93-100
    PubMed 3162710
11. Jin YS, Mandahl N, Heim S, Biörklund A, Wennerberg J, Mitelman F (1988)
    t(6;7)(q23;p22) as the sole chromosomal anomaly in a vocal cord carcinoma
    Cancer Genet Cytogenet, 32 (2), 305-7
    PubMed 3365684
12. Jin YS, Mandahl N, Heim S, Biörklund A, Wennerberg J, Mitelman F (1988)
    Unique karyotypic abnormalities in a squamous cell carcinoma of the larynx
    Cancer Genet Cytogenet, 30 (1), 177-9
    PubMed 3422045
13. Jin YS, Mandahl N, Heim S, Schüller H, Mitelman F (1988)
    Isochromosomes i(8q) or i(9q) in three adenocarcinomas of the lung
    Cancer Genet Cytogenet, 33 (1), 11-7
    PubMed 3164233
14. Johansson B, Mertens F, Heim S, Kristoffersson U, Mandahl N, Olsson H, Mitelman F (1988)
    Breakprone chromosome bands in fibroblasts from patients with non-Hodgkin's lymphoma do not coincide with bands involved in primary rearrangements in non-Hodgkin's lymphomas
    Hereditas, 109 (1), 131-7
    PubMed 3192422
15. Johansson B, Mertens F, Heim S, Kristoffersson U, Mandahl N, Olsson H, Mitelman F (1988)
    Normal frequency of structural chromosome aberrations in fibroblasts from patients with non-Hodgkin's lymphoma
    Hereditas, 109 (2), 277-80
    PubMed 3230028
16. Karlsson I, Mandahl N, Heim S, Rydholm A, Willén H, Mitelman F (1988)
    Complex chromosome rearrangements in an extraabdominal desmoid tumor
    Cancer Genet Cytogenet, 34 (2), 241-5
    PubMed 3165696
17. Kristoffersson U, Heim S, Mandahl N, Mitelman F, Olsson H, Akerman M (1988)
    Do clonal chromosome abnormalities prognosticate early relapse in Hodgkin's disease?
    Cancer Genet Cytogenet, 31 (2), 299
    PubMed 3349444
18. Kristoffersson U, Heim S, Mandahl N, Olsson H, Akerman M, Mitelman F (1988)
    Trisomy 5 and t(5;14)(q11;q32) as the sole abnormalities in two different clones from a centroblastic non-Hodgkin's lymphoma
    Cancer Genet Cytogenet, 36 (2), 173-6
    PubMed 3203305
19. Kristoffersson U, Lagergren J, Heim S, Mandahl N (1988)
    Four copies of 8p in a mentally retarded boy with the mosaic karyotype 47,XY, + i(8p)/46,XY
    Clin Genet, 34 (3), 201-3
    PubMed 3180507
20. Lundgren R, Kristoffersson U, Heim S, Mandahl N, Mitelman F (1988)
    Multiple structural chromosome rearrangements, including del(7q) and del(10q), in an adenocarcinoma of the prostate
    Cancer Genet Cytogenet, 35 (1), 103-8
    PubMed 3180000
21. Mandahl N, Heim S, Arheden K, Rydholm A, Willén H, Mitelman F (1988)
    Rings, dicentrics, and telomeric association in histiocytomas
    Cancer Genet Cytogenet, 30 (1), 23-33
    PubMed 2825965
22. Mandahl N, Heim S, Arheden K, Rydholm A, Willén H, Mitelman F (1988)
    Multiple karyotypic rearrangements, including t(X;18)(p11;q11), in a fibrosarcoma
    Cancer Genet Cytogenet, 30 (2), 323-7
    PubMed 3342387
23. Mandahl N, Heim S, Arheden K, Rydholm A, Willén H, Mitelman F (1988)
    Three major cytogenetic subgroups can be identified among chromosomally abnormal solitary lipomas
    Hum Genet, 79 (3), 203-8
    PubMed 3402992
24. Mertens F, Johansson B, Heim S, Mandahl N, Rydholm A, Mitelman F (1988)
    Bands involved in primary chromosome rearrangements in sarcomas are not constitutionally liable to breakage in sarcoma patients
    Hum Genet, 79 (4), 309-14
    PubMed 3410455
25. Mertens F, Johansson B, Heim S, Mandahl N, Rydholm A, Mitelman F (1988)
    Normal frequency of chromosome breakage in lymphocytes from patients with musculoskeletal sarcoma
    Cancer Genet Cytogenet, 33 (2), 299-304
    PubMed 3383170
26. Mitelman F, Heim S (1988)
    Consistent involvement of only 71 of the 329 chromosomal bands of the human genome in primary neoplasia-associated rearrangements
    Cancer Res, 48 (24 Pt 1), 7115-9
    PubMed 3191487
27. Mitelman F, Prigogina EL, Fleischman EW, Frenkel MA, Garwicz S, Heim S, Ilyinskaya GW, Kristoffersson U, Mandahl N, Volkova MA (1988)
    A new specific chromosomal rearrangement, t(11;20)(p15;q11), in myeloblastic leukemia with maturation
    Leukemia, 2 (7), 430-2
    PubMed 3164800
28. Nilbert M, Heim S, Mandahl N, Flodérus UM, Willén H, Akerman M, Mitelman F (1988)
    Ring formation and structural rearrangements of chromosome 1 as secondary changes in uterine leiomyomas with t(12;14)(q14-15;q23-24)
    Cancer Genet Cytogenet, 36 (2), 183-90
    PubMed 3203307
29. Nilbert M, Heim S, Mandahl N, Flodérus UM, Willén H, Mitelman F (1988)
    Karyotypic rearrangements in 20 uterine leiomyomas
    Cytogenet Cell Genet, 49 (4), 300-4
    PubMed 3248388
30. Nilbert M, Mandahl N, Heim S, Rydholm A, Willén H, Akerman M, Mitelman F (1988)
    Chromosome abnormalities in leiomyosarcomas
    Cancer Genet Cytogenet, 34 (2), 209-18
    PubMed 3409201
31. Toor MA, Heim S, Mandahl N, Högstedt B, Mitelman F (1988)
    Admixture of intact or lysed platelets to lymphocyte cultures results in higher chromosome aberration frequencies
    Hereditas, 108 (2), 219-21
    PubMed 3209419

Publications 1987

1. Heim S, Alimena G, Billström R, Diverio D, Kristoffersson U, Mandahl N, Nanni M, Mitelman F (1987)
   Tetraploid karyotype (92,XXYY) in two patients with acute lymphoblastic leukemia
   Cancer Genet Cytogenet, 29 (1), 129-33
   PubMed 3478124
2. Heim S, Avanzi GC, Billström R, Kristoffersson U, Mandahl N, Bekassy AN, Garwicz S, Wiebe T, Pegoraro L, Falda M (1987)
   A new specific chromosomal rearrangement, t(8;16) (p11;p13), in acute monocytic leukaemia
   Br J Haematol, 66 (3), 323-6
   PubMed 3476150
3. Heim S, Békàssy AN, Garwicz S, Heldrup J, Wiebe T, Kristoffersson U, Mandahl N, Mitelman F (1987)
   New structural chromosomal rearrangements in congenital leukemia
   Leukemia, 1 (1), 16-23
   PubMed 3312830
4. Heim S, Billström R, Kristoffersson U, Mandahl N, Mitelman F (1987)
   Late appearing 5q--marker in refractory anemia
   Cancer Genet Cytogenet, 24 (1), 159-62
   PubMed 3466668
5. Heim S, Mandahl N, Kristoffersson U, Mitelman F, Rööser B, Rydholm A, Willén H (1987)
   Marker ring chromosome--a new cytogenetic abnormality characterizing lipogenic tumors?
   Cancer Genet Cytogenet, 24 (2), 319-26
   PubMed 3466681
6. Heim S, Mitelman F (1987)
   Nineteen of 26 cellular oncogenes precisely localized in the human genome map to one of the 83 bands involved in primary cancer-specific rearrangements
   Hum Genet, 75 (1), 70-2
   PubMed 3468057
7. Kristoffersson U, Heim S, Mandahl N, Olsson H, Akerman M, Mitelman F (1987)
   Cytogenetic studies in Hodgkin's disease
   Acta Pathol Microbiol Immunol Scand A, 95 (5), 289-95
   PubMed 3630709
8. Kristoffersson U, Heim S, Mandahl N, Olsson H, Ranstam J, Akerman M, Mitelman F (1987)
   Prognostic implication of cytogenetic findings in 106 patients with non-Hodgkin lymphoma
   Cancer Genet Cytogenet, 25 (1), 55-64
   PubMed 3467832
9. Kristoffersson U, Heim S, Mandahl N, Sundkvist L, Szelest J, Hägerstrand I (1987)
   Monosomy and trisomy of 15q24----qter in a family with a translocation t(6;15)(p25;q24)
   Clin Genet, 32 (3), 169-71
   PubMed 3621663
10. Kristoffersson U, Heim S, Olsson H, Akerman M, Mitelman F (1987)
    Relationship between cytogenetic findings and histopathology in non-Hodgkin lymphoma
    Acta Pathol Microbiol Immunol Scand A, 95 (1), 1-5
    PubMed 3825539
11. Kristoffersson U, Mineur A, Heim S, Mandahl N, Mitelman F (1987)
    Normal high-resolution karyotypes in three patients with the Holt-Oram syndrome
    Am J Med Genet, 28 (1), 229-31
    PubMed 3674114
12. Mandahl N, Heim S, Johansson B, Bennet K, Mertens F, Olsson G, Rööser B, Rydholm A, Willén H, Mitelman F (1987)
    Lipomas have characteristic structural chromosomal rearrangements of 12q13-q14
    Int J Cancer, 39 (6), 685-8
    PubMed 3473046
13. Mertens F, Johansson B, Mandahl N, Heim S, Bennet K, Rydholm A, Willén H, Mitelman F (1987)
    Clonal chromosome abnormalities in two liposarcomas
    Cancer Genet Cytogenet, 28 (1), 137-44
    PubMed 3607734
14. Mitelman F, Heim S (1987)
    The significance of karyotypic changes in human neoplasia
    Haematologica, 72 (6 Suppl), 29-33
    PubMed 3127293

Publications 1986

1. Heim S, Kristoffersson U, Mandahl N, Mitelman F, Bekassy AN, Garwicz S, Heldrup J, Wiebe T (1986)
   Reciprocal translocation (11;19)(q23;p13) in congenital acute lymphoblastic leukemia
   Cancer Genet Cytogenet, 23 (3), 239-44
   PubMed 3464343
2. Heim S, Kristoffersson U, Mandahl N, Mitelman F, Bekassy AN, Garwicz S, Wiebe T (1986)
   High resolution banding analysis of the reciprocal translocation t(6;9) in acute nonlymphocytic leukemia
   Cancer Genet Cytogenet, 22 (3), 195-201
   PubMed 3458523
3. Heim S, Mandahl N, Kristoffersson U, Mitelman F, Rööser B, Rydholm A, Willén H (1986)
   Reciprocal translocation t(3;12)(q27;q13) in lipoma
   Cancer Genet Cytogenet, 23 (4), 301-4
   PubMed 3779626
4. Heim S, Mandahl N, Kristoffersson U, Mitelman F, Rööser B, Rydholm A, Willén H (1986)
   Structural chromosome aberrations in a case of angioleiomyoma
   Cancer Genet Cytogenet, 20 (3-4), 325-30
   PubMed 3943070
5. Heim S, Mitelman F (1986)
   Numerical chromosome aberrations in human neoplasia
   Cancer Genet Cytogenet, 22 (2), 99-108
   PubMed 3708552
6. Heim S, Mitelman F (1986)
   Secondary chromosome aberrations in the acute leukemias
   Cancer Genet Cytogenet, 22 (4), 331-8
   PubMed 3460687
7. Heim S, Mitelman F (1986)
   Chromosome abnormalities in the myelodysplastic syndromes
   Clin Haematol, 15 (4), 1003-21
   PubMed 3552345
8. Heim S, Mitelman F (1986)
   Proliferation-specific and differentiation-associated chromosomal breakpoints in human neoplasia--a unifying model
   Hereditas, 104 (2), 307-12
   PubMed 3771268
9. Kristoffersson U, Heim S, Olsson H, Akerman M, Mitelman F (1986)
   Cytogenetic studies in non-Hodgkin lymphomas--results from surgical biopsies
   Hereditas, 104 (1), 1-13
   PubMed 3710822
10. Mandahl N, Heim S, Kristoffersson U, Mitelman F, Rydholm A, Rööser B, Willén H (1986)
    Multiple cytogenetic abnormalities in a case of osteosarcoma
    Cancer Genet Cytogenet, 23 (3), 257-60
    PubMed 3464346
11. Mitelman F, Heim S (1986)
    Chromosomal segments of critical significance in human neoplasia
    Prog Clin Biol Res, 209A, 583-9
    PubMed 3749068
12. Mitelman F, Manolov G, Manolova Y, Billström R, Heim S, Kristoffersson U, Mandahl N, Ferro MT, San Roman C (1986)
    High resolution chromosome analysis of constitutional and acquired t(15;17) maps c-erbA to subband 17q11.2
    Cancer Genet Cytogenet, 22 (2), 95-8
    PubMed 3458521
13. Mitelman F, Manolova Y, Manolov G, Billström R, Heim S, Kristoffersson U, Mandahl N (1986)
    High resolution analysis of the 5q-marker chromosome in refractory anemia
    Hereditas, 105 (1), 49-54
    PubMed 3793519
14. Pero RW, Heim S, Bryngelsson C (1986)
    Lower rates of thymidine incorporation into DNA of skin fibroblasts from patients with adenomatosis of the colon and rectum
    Carcinogenesis, 7 (4), 541-5
    PubMed 2870819

Publications 1985

1. Gustavii B, Edvall H, Mineur A, Heim S, Mandahl N, Kristoffersson U, Mitelman F (1985)
   Trophoblast samples suitable for long-term culture
   Acta Obstet Gynecol Scand, 64 (8), 661-2
   PubMed 3832757
2. Heim S, Berger R, Bernheim A, Mitelman F (1985)
   Constitutional C-band pattern in patients with adenomatosis of the colon and rectum
   Cancer Genet Cytogenet, 18 (1), 31-5
   PubMed 4027948
3. Heim S, Billström R, Kristoffersson U, Mandahl N, Strömbeck B, Mitelman F (1985)
   Variant Ph translocations in chronic myeloid leukemia
   Cancer Genet Cytogenet, 18 (3), 215-27
   PubMed 3863698
4. Heim S, Johansen SG, Kolnig AM, Strömbeck B (1985)
   Increased levels of spontaneous and mutagen-induced chromosome aberrations in skin fibroblasts from patients with adenomatosis of the colon and rectum
   Cancer Genet Cytogenet, 17 (4), 333-46
   PubMed 4016717
5. Heim S, Kristoffersson U, Mandahl N, Mineur A, Mitelman F, Edvall H, Gustavii B (1985)
   Chromosome analysis in 100 cases of first trimester trophoblast sampling
   Clin Genet, 27 (5), 451-7
   PubMed 4006268
6. Heim S, Mitelman F, Jerntorp P (1985)
   A case of dysmyelopoietic syndrome with hypotetraploid karyotype
   Cancer Genet Cytogenet, 18 (2), 179-82
   PubMed 4052978
7. Kristoffersson U, Heim S, Heldrup J, Akerman M, Garwicz S, Mitelman F (1985)
   Cytogenetic studies of childhood non-Hodgkin lymphomas
   Hereditas, 103 (1), 77-84
   PubMed 3877035
8. Mandahl N, Heim S, Kristoffersson U, Mitelman F, Rööser B, Rydholm A, Willén H (1985)
   Telomeric association in a malignant fibrous histiocytoma
   Hum Genet, 71 (4), 321-4
   PubMed 3000915

Publications 1983

1. Heim S (1983)
   [Chromosome aberrations in cancer]
   Tidsskr Nor Laegeforen, 103 (34-36), 2320-4
   PubMed 6665780