Author network for Sverre Heim by COREMINE medical

Publications 2012

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

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

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

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

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

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

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

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

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

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

Teixeira MR, Heim S (2011)
Cytogenetic analysis of tumor clonality
Adv Cancer Res, 112, 127-49
PubMed 21925303

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

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

Aad G, Abbott B, Abdallah J, Abdelalim AA, Abdesselam A, Abdinov O, Abi B, Abolins M, Abramowicz H, Abreu H, Acerbi E, Acharya BS, Adams DL, Addy TN, Adelman J, Aderholz M, Adomeit S, Adragna P, Adye T, Aefsky S, Aguilar-Saavedra JA, Aharrouche M, Ahlen SP, Ahles F, Ahmad A et al. (2011)
Search for Dilepton Resonances in pp Collisions at sqrt[s]=7??TeV with the ATLAS Detector
Phys Rev Lett, 107 (27), 272002
PubMed 22243306

Publications 2010

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

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

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

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

Brandal P, Panagopoulos I, Bjerkehagen B, Heim S (2009)
t(19;22)(q13;q12) Translocation leading to the novel fusion gene EWSR1-ZNF444 in soft tissue myoepithelial carcinoma
Genes Chromosomes Cancer, 48 (12), 1051-6
PubMed 19760602

Dahlback HS, Brandal P, Meling TR, Gorunova L, Scheie D, Heim S (2009)
Genomic aberrations in 80 cases of primary glioblastoma multiforme: Pathogenetic heterogeneity and putative cytogenetic pathways
Genes Chromosomes Cancer, 48 (10), 908-24
PubMed 19603525

Danielsen SA, Lind GE, Biornslett M, Meling GI, Rognum TO, Heim S, Lothe RA (2009)
Novel Mutations of the Suppressor Gene PTEN in Colorectal Carcinomas Stratified by Microsatellite Instability- and TP53 Mutation- Status (vol 29, pg E252, 2008)
Hum. Mutat., 30 (6), 1023

Gorunova L, Vult von Steyern F, Storlazzi CT, Bjerkehagen B, Follerås G, Heim S, Mandahl N, Mertens F (2009)
Cytogenetic analysis of 101 giant cell tumors of bone: nonrandom patterns of telomeric associations and other structural aberrations
Genes Chromosomes Cancer, 48 (7), 583-602
PubMed 19396867

Karrman K, Forestier E, Heyman M, Andersen MK, Autio K, Blennow E, Borgström G, Ehrencrona H, Golovleva I, Heim S, Heinonen K, Hovland R, Johannsson JH, Kerndrup G, Nordgren A, Palmqvist L, Johansson B, Nordic Society of Pediatric Hematology, Oncology (NOPHO), Swedish Cytogenetic Leukemia Study Group (SCLSG), NOPHO Leukemia Cytogenetic Study Group (NLCSG) (2009)
Clinical and cytogenetic features of a population-based consecutive series of 285 pediatric T-cell acute lymphoblastic leukemias: rare T-cell receptor gene rearrangements are associated with poor outcome
Genes Chromosomes Cancer, 48 (9), 795-805
PubMed 19530250

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

Micci F, Panagopoulos I, Haugom L, Andersen HK, Tjønnfjord GE, Beiske K, Heim S (2009)
t(3;21)(q22;q22) leading to truncation of the RYK gene in atypical chronic myeloid leukemia
Cancer Lett, 277 (2), 205-11
PubMed 19168282

Micci F, Weimer J, Haugom L, Skotheim RI, Grunewald R, Abeler VM, Silins I, Lothe RA, Trope CG, Arnold N, Heim S (2009)
Reverse painting of microdissected chromosome 19 markers in ovarian carcinoma identifies a complex rearrangement map
Genes Chromosomes Cancer, 48 (2), 184-93
PubMed 18973136

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

Brandal P, Panagopoulos I, Bjerkehagen B, Gorunova L, Skjeldal S, Micci F, Heim S (2008)
Detection of a t(1;22)(q23;q12) translocation leading to an EWSR1-PBX1 fusion gene in a myoepithelioma
Genes Chromosomes Cancer, 47 (7), 558-64
PubMed 18383210

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

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

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

Forestier E, Gauffin F, Andersen MK, Autio K, Borgström G, Golovleva I, Gustafsson B, Heim S, Heinonen K, Heyman M, Hovland R, Johannsson JH, Kerndrup G, Rosenquist R, Schoumans J, Swolin B, Johansson B, Nordgren A, Nordic Society of Pediatric Hematology and Oncology, Swedish Cytogenetic Leukemia Study Group, NOPHO Leukemia Cytogenetic Study Group (2008)
Clinical and cytogenetic features of pediatric dic(9;20)(p13.2;q11.2)-positive B-cell precursor acute lymphoblastic leukemias: a Nordic series of 24 cases and review of the literature
Genes Chromosomes Cancer, 47 (2), 149-58
PubMed 17990329

Forestier E, Heyman M, 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 Paediatric Haematology, Oncology (NOPHO), Swedish Cytogenetic Leukaemia Study Group (SCLSG), NOPHO Leukaemia Cytogenetic Study Group (NLCSG) (2008)
Outcome of ETV6/RUNX1-positive childhood acute lymphoblastic leukaemia in the NOPHO-ALL-1992 protocol: frequent late relapses but good overall survival
Br J Haematol, 140 (6), 665-72
PubMed 18241254

Heim S, Mitelman F (2008)
Molecular screening for new fusion genes in cancer
Nat Genet, 40 (6), 685-6
PubMed 18509307

Micci F, Haugom L, Abeler VM, Tropé CG, Danielsen HE, Heim S (2008)
Consistent numerical chromosome aberrations in thecofibromas of the ovary
Virchows Arch, 452 (3), 269-76
PubMed 18188592

Publications 2007

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

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

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

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

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

Micci F, Heim S (2007)
Pathogenetic mechanisms in endometrial stromal sarcoma
Cytogenet Genome Res, 118 (2-4), 190-5
PubMed 18000370

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

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

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

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

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

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

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

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

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

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

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

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

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

Brandal P, Busund LT, Heim S (2005)
Chromosome abnormalities in juxtaglomerular cell tumors
Cancer, 104 (3), 504-10
PubMed 15968688

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

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

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

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

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

Brandal P, Bjerkehagen B, Heim S (2004)
Molecular cytogenetic characterization of tenosynovial giant cell tumors
Neoplasia, 6 (5), 578-83
PubMed 15548367

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Teixeira MR, Pandis N, Heim S (2002)
Cytogenetic clues to breast carcinogenesis
Genes Chromosomes Cancer, 33 (1), 1-16
PubMed 11746982

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

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

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

Heim S, Teixeira MA, Pandis N (2001)
Are some breast carcinomas polyclonal in origin?
J Pathol, 194 (4), 395-7
PubMed 11523045

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Heim S, Smeland EB (1998)
[Molecular genetic diagnosis of leukemias and lymphomas]
Tidsskr Nor Laegeforen, 118 (16), 2511-8
PubMed 9667131

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Rasmussen K, Iversen JG, Heim S (1997)
[Anders Jahre's 1997 medical awards]
Tidsskr Nor Laegeforen, 117 (24), 3554-6
PubMed 9411920

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

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

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

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

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

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

Heim S (1996)
Transient acute monoblastic leukemia with reciprocal (8;16)(p11;p13) translocation
Pediatr Hematol Oncol, 13 (3), 203-4
PubMed 8735335

Heim S (1996)
Genetic nomenclature: ISCN and ISGN
Pediatr. Hematol. Oncol., 13 (2), R3

Heim S (1996)
[Chromosome aberrations in solid tumors. Cytogenetic examinations are now available in Norway]
Tidsskr Nor Laegeforen, 116 (19), 2295-6
PubMed 8848778

Heim S (1996)
Clonal chromosome abnormalities in neoplastic cells: evidence of genetic instability?
Cancer Surv, 28, 247-60
PubMed 8977039

Heim S (1996)
Genetic nomenclature: ISCN and ISGN
Pediatr Hematol Oncol, 13 (2), iii
PubMed 8721024

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Heim S (1992)
Is cancer cytogenetics reducible to the molecular genetics of cancer cells?
Genes Chromosomes Cancer, 5 (3), 188-96
PubMed 1384669

Heim S (1992)
Cytogenetic findings in primary and secondary MDS
Leuk Res, 16 (1), 43-6
PubMed 1732669

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

Heim S, Mitelman F (1992)
Cytogenetic analysis in the diagnosis of acute leukemia
Cancer, 70 (6 Suppl), 1701-9
PubMed 1516024

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

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

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

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

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

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

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

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

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

Mitelman F, Heim S (1992)
Quantitative acute leukemia cytogenetics
Genes Chromosomes Cancer, 5 (1), 57-66
PubMed 1384663

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

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

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

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

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

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

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

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

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

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

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

Heim S (1991)
Epidemiological clues to leukaemias involving specific chromosomal abnormalities
Leukemia, 5 (9), 823-4
PubMed 1943234

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Heim S (1990)
Cytogenetics in the investigation of haematological disorders
Baillieres Clin Haematol, 3 (4), 921-48
PubMed 2271796

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

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

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

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

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

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

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

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

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

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

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

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

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

Mitelman F, Heim S (1990)
Chromosome abnormalities in cancer
Cancer Detect Prev, 14 (5), 527-37
PubMed 2224917

Mitelman F, Heim S, Mandahl N (1990)
Trisomy 21 in neoplastic cells
Am J Med Genet Suppl, 7, 262-6
PubMed 2149959

Nibert M, Heim S (1990)
Uterine leiomyoma cytogenetics
Genes Chromosomes Cancer, 2 (1), 3-13
PubMed 2278965

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Heim S, Johansson B, Mertens F (1989)
Constitutional chromosome instability and cancer risk
Mutat Res, 221 (1), 39-51
PubMed 2664494

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

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

Heim S, Mitelman F (1989)
Cytogenetically unrelated clones in hematological neoplasms
Leukemia, 3 (1), 6-8
PubMed 2909809

Heim S, Mitelman F (1989)
Primary chromosome abnormalities in human neoplasia
Adv Cancer Res, 52, 1-43
PubMed 2662710

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Heim S, Mandahl N, Mitelman F (1988)
Genetic convergence and divergence in tumor progression
Cancer Res, 48 (21), 5911-6
PubMed 3048652

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Mitelman F, Heim S (1987)
The significance of karyotypic changes in human neoplasia
Haematologica, 72 (6 Suppl), 29-33
PubMed 3127293

Publications 1986

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

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

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

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

Heim S, Mitelman F (1986)
Numerical chromosome aberrations in human neoplasia
Cancer Genet Cytogenet, 22 (2), 99-108
PubMed 3708552

Heim S, Mitelman F (1986)
Secondary chromosome aberrations in the acute leukemias
Cancer Genet Cytogenet, 22 (4), 331-8
PubMed 3460687

Heim S, Mitelman F (1986)
Chromosome abnormalities in the myelodysplastic syndromes
Clin Haematol, 15 (4), 1003-21
PubMed 3552345

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

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

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

Mitelman F, Heim S (1986)
Chromosomal segments of critical significance in human neoplasia
Prog Clin Biol Res, 209A, 583-9
PubMed 3749068

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

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

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

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

Heim S (1985)
Sister chromatid exchange with and without in vitro mutagen induction in cultured skin fibroblasts from patients with adenomatosis of the colon and rectum
Clin Genet, 27 (1), 51-8
PubMed 3978838

Heim S (1985)
Normal high resolution karyotypes in patients with adenomatosis of the colon and rectum
Hereditas, 102 (2), 171-5
PubMed 4044270

Heim S (1985)
Spontaneous and mitomycin C induced structural chromosome aberrations in lymphocyte cultures from patients with adenomatosis of the colon and rectum
Hereditas, 103 (2), 235-8
PubMed 3936823

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

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

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

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

Heim S, Mitelman F, Jerntorp P (1985)
A case of dysmyelopoietic syndrome with hypotetraploid karyotype
Cancer Genet Cytogenet, 18 (2), 179-82
PubMed 4052978

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

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

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

Heim S (1983)
In vitro growth characteristics of skin fibroblasts from patients with adenomatosis of the colon and rectum and their relatives
Clin Genet, 23 (1), 41-8
PubMed 6831763