Publications published since 1983 from OUS - Section for Cancer Cytogenetics

256 publications found

Publications 2023

  1. Blakstad H, Brekke J, Rahman MA, Arnesen VS, Miletic H, Brandal P, Lie SA, Chekenya M, Goplen D (2023)
    Survival in a consecutive series of 467 glioblastoma patients: Association with prognostic factors and treatment at recurrence at two independent institutions
    PLoS One, 18 (2), e0281166
    DOI 10.1371/journal.pone.0281166, PubMed 36730349
  2. Boye K, Gorunova L, Gunawan B, Hompland I, Sander B, Panagopoulos I, Langer C, Golas M, Heim S, Füzesi L, Hølmebakk T, Micci F (2023)
    Genomic Complexity as a Biomarker to De-Escalate Adjuvant Imatinib Treatment in High-Risk Gastrointestinal Stromal Tumor
    JCO Precis Oncol, 7, e2200351
    DOI 10.1200/PO.22.00351, PubMed 36724411
  3. Heggebø LC, Borgen IMH, Rylander H, Kiserud C, Nordenmark TH, Hellebust TP, Evensen ME, Gustavsson M, Ramberg C, Sprauten M, Magelssen H, Blakstad H, Moorthy J, Andersson K, Raunert I, Henry T, Moe C, Granlund C, Goplen D, Brekke J, Johannessen TA, Solheim TS, Marienhagen K, Humberset Ø, Bergström P et al. (2023)
    Investigating survival, quality of life and cognition in PROton versus photon therapy for IDH-mutated diffuse grade 2 and 3 GLIOmas (PRO-GLIO): a randomised controlled trial in Norway and Sweden
    BMJ Open, 13 (3), e070071
    DOI 10.1136/bmjopen-2022-070071, PubMed 36940951
  4. Leske H, Blakstad H, Lund-Iversen M, Skovholt EK, Niehusmann P, Ramm-Pettersen JT, Skogen K, Kongelf G, Sprauten M, Magelssen H, Brandal P (2023)
    Astrocytoma (CNS WHO grade 4), IDH-mutant with co-occurrence of BRAF p.V600E mutation, and homozygous loss of CDKN2A
    Neuropathology (in press)
    DOI 10.1111/neup.12895, PubMed 36754566
  5. Panagopoulos I, Andersen K, Brunetti M, Gorunova L, Lund-Iversen M, Micci F, Heim S (2023)
    Fusion of the High-mobility Group AT-Hook 2 (HMGA2) and the Gelsolin (GSN) Genes in Lipomas With t(9;12)(q33;q14) Chromosomal Translocation
    In Vivo, 37 (2), 524-530
    DOI 10.21873/invivo.13110, PubMed 36881074
  6. Panagopoulos I, Andersen K, Gorunova L, Hognestad HR, Pedersen TD, Lobmaier I, Micci F, Heim S (2023)
    Chromosome Translocation t(10;19)(q26;q13) in a CIC-sarcoma
    In Vivo, 37 (1), 57-69
    DOI 10.21873/invivo.13054, PubMed 36593014
  7. Panagopoulos I, Andersen K, Gorunova L, Lund-Iversen M, Lobmaier I, Micci F, Heim S (2023)
    Recurrent 8q11-13 Aberrations Leading to PLAG1 Rearrangements, Including Novel Chimeras HNRNPA2B1::PLAG1 and SDCBP::PLAG1, in Lipomatous Tumors
    Cancer Genomics Proteomics, 20 (2), 171-181
    DOI 10.21873/cgp.20372, PubMed 36870688
  8. Panagopoulos I, Andersen K, Rinvoll Johannsdottir IM, Micci F, Heim S (2023)
    Novel MYCBP::EHD2 and RUNX1::ZNF780A Fusion Genes in T-cell Acute Lymphoblastic Leukemia
    Cancer Genomics Proteomics, 20 (1), 51-63
    DOI 10.21873/cgp.20364, PubMed 36581344
  9. Schipmann-Miletic S, Sivakanesan S, Rath DS, Brandal P, Vik-Mo E, Bjørås M, Solheim O, Ingebrigtsen T, Sund F, Bjerkvig R, Miletic H, Johannessen TA, Sundstrøm T (2023)
    [Not Available]
    Tidsskr Nor Laegeforen, 143 (2)
    DOI 10.4045/tidsskr.22.0314, PubMed 36718891

Publications 2022

  1. Blakstad H, Wohlleben C, Saxhaug C, Brandal P (2022)
    SMART syndrome: two cases highlighting a complex and rare complication of brain irradiation
    BMJ Case Rep, 15 (9)
    DOI 10.1136/bcr-2022-249599, PubMed 36167430
  2. Brunetti M, Panagopoulos I, Vitelli V, Andersen K, Hveem TS, Davidson B, Eriksson AGZ, Trent PKB, Heim S, Micci F (2022)
    Endometrial Carcinoma: Molecular Cytogenetics and Transcriptomic Profile
    Cancers (Basel), 14 (14)
    DOI 10.3390/cancers14143536, PubMed 35884597
  3. Gorunova L, Boye K, Panagopoulos I, Berner JM, Bjerkehagen B, Hompland I, Lobmaier I, Hølmebakk T, Hveem TS, Heim S, Micci F (2022)
    Cytogenetic and molecular analyses of 291 gastrointestinal stromal tumors: site-specific cytogenetic evolution as evidence of pathogenetic heterogeneity
    Oncotarget, 13, 508-517
    DOI 10.18632/oncotarget.28209, PubMed 35284037
  4. Kvammen JA, Stensvold E, Godang K, Bollerslev J, Myklebust TÅ, Brandal P, Henriksen C, Bechensteen AG (2022)
    Bone mineral density and nutrition in long-term survivors of childhood brain tumors
    Clin Nutr ESPEN, 50, 162-169
    DOI 10.1016/j.clnesp.2022.05.025, PubMed 35871919
  5. Panagopoulos I, Andersen K, Gorunova L, Davidson B, Micci F, Heim S (2022)
    A Novel Cryptic t(2;3)(p21;q25) Translocation Fuses the WWTR1 and PRKCE Genes in Uterine Leiomyoma With 3q- as the Sole Visible Chromosome Abnormality
    Cancer Genomics Proteomics, 19 (5), 636-646
    DOI 10.21873/cgp.20348, PubMed 35985686
  6. Panagopoulos I, Andersen K, Gorunova L, Davidson B, Micci F, Heim S (2022)
    Fusion of the HMGA2 and BNC2 Genes in Uterine Leiomyoma With t(9;12)(p22;q14)
    In Vivo, 36 (6), 2654-2661
    DOI 10.21873/invivo.13000, PubMed 36309352
  7. Panagopoulos I, Andersen K, Gorunova L, Eilert-Olsen M, Lund-Iversen M, Wessel-Aas T, Lloret I, Micci F, Heim S (2022)
    Presence of a t(12;18)(q14;q21) Chromosome Translocation and Fusion of the Genes for High-mobility Group AT-Hook 2 (HMGA2) and WNT Inhibitory Factor 1 (WIF1) in Infrapatellar Fat Pad Cells from a Patient With Hoffa's Disease
    Cancer Genomics Proteomics, 19 (5), 584-590
    DOI 10.21873/cgp.20343, PubMed 35985683
  8. Panagopoulos I, Andersen K, Gorunova L, Lund-Iversen M, Lobmaier I, Heim S (2022)
    Recurrent Fusion of the Genes for High-mobility Group AT-hook 2 (HMGA2) and Nuclear Receptor Co-repressor 2 (NCOR2) in Osteoclastic Giant Cell-rich Tumors of Bone
    Cancer Genomics Proteomics, 19 (2), 163-177
    DOI 10.21873/cgp.20312, PubMed 35181586
  9. Panagopoulos I, Gorunova L, Andersen K, Lobmaier I, Micci F, Heim S (2022)
    Fusion of High Mobility Group AT-hook 2 Gene (HMGA2) With the Chromosome 12 Open Reading Frame 42 Gene (C12orf42) in an Aggressive Angiomyxoma With del(12)(q14q23) as the Sole Cytogenetic Anomaly
    Cancer Genomics Proteomics, 19 (5), 576-583
    DOI 10.21873/cgp.20342, PubMed 35985684
  10. Panagopoulos I, Gorunova L, Andersen K, Lund-Iversen M, Hognestad HR, Lobmaier I, Micci F, Heim S (2022)
    Chromosomal Translocation t(5;12)(p13;q14) Leading to Fusion of High-mobility Group AT-hook 2 Gene With Intergenic Sequences From Chromosome Sub-Band 5p13.2 in Benign Myoid Neoplasms of the Breast: A Second Case
    Cancer Genomics Proteomics, 19 (4), 445-455
    DOI 10.21873/cgp.20331, PubMed 35732319
  11. Panagopoulos I, Heim S (2022)
    Neoplasia-associated Chromosome Translocations Resulting in Gene Truncation
    Cancer Genomics Proteomics, 19 (6), 647-672
    DOI 10.21873/cgp.20349, PubMed 36316036
  12. Skaga E, Kulesskiy E, Potdar S, Panagopoulos I, Micci F, Langmoen IA, Sandberg CJ, Vik-Mo EO (2022)
    Functional temozolomide sensitivity testing of patient-specific glioblastoma stem cell cultures is predictive of clinical outcome
    Transl Oncol, 26, 101535 (in press)
    DOI 10.1016/j.tranon.2022.101535, PubMed 36115076
  13. Tanem KE, Stensvold E, Wilberg P, Skaare AB, Brandal P, Herlofson BB (2022)
    Oral and dental late effects in long-term survivors of childhood embryonal brain tumors
    Support Care Cancer, 30 (12), 10233-10241
    DOI 10.1007/s00520-022-07405-8, PubMed 36307656
  14. Tanem KE, Stensvold E, Wilberg P, Skaare AB, Singh PB, Brandal P, Herlofson BB (2022)
    Taste and smell function in long-term survivors after childhood medulloblastoma/CNS-PNET
    Support Care Cancer, 30 (7), 6155-6162
    DOI 10.1007/s00520-022-07048-9, PubMed 35426047

Publications 2021

  1. Husum YS, Skogen K, Brandal P, Rønning PA, Wigers AR, Evang JA, Jørstad ØK (2021)
    Bilateral calcification of the optic nerve sheath: A diagnostic dilemma
    Am J Ophthalmol Case Rep, 22, 101106
    DOI 10.1016/j.ajoc.2021.101106, PubMed 33997471
  2. Panagopoulos I, Andersen K, Eilert-Olsen M, Rognlien AG, Munthe-Kaas MC, Micci F, Heim S (2021)
    Rare KMT2A-ELL and Novel ZNF56-KMT2A Fusion Genes in Pediatric T-cell Acute Lymphoblastic Leukemia
    Cancer Genomics Proteomics, 18 (2), 121-131
    DOI 10.21873/cgp.20247, PubMed 33608309
  3. Panagopoulos I, Andersen K, Eilert-Olsen M, Zeller B, Munthe-Kaas MC, Buechner J, Osnes LTN, Micci F, Heim S (2021)
    Therapy-induced Deletion in 11q23 Leading to Fusion of KMT2A With ARHGEF12 and Development of B Lineage Acute Lymphoplastic Leukemia in a Child Treated for Acute Myeloid Leukemia Caused by t(9;11)(p21;q23)/KMT2A-MLLT3
    Cancer Genomics Proteomics, 18 (1), 67-81
    DOI 10.21873/cgp.20242, PubMed 33419897
  4. Panagopoulos I, Andersen K, Ramslien LF, Ikonomou IM, Micci F, Heim S (2021)
    Therapy-related Myeloid Leukemia With the Translocation t(8;19)(p11;q13) Leading to a KAT6A-LEUTX Fusion Gene
    Anticancer Res, 41 (4), 1753-1760
    DOI 10.21873/anticanres.14940, PubMed 33813379
  5. Panagopoulos I, Gorunova L, Andersen K, Lobmaier I, Heim S (2021)
    Several Fusion Genes Identified in a Spermatic Cord Leiomyoma With Rearrangements of Chromosome Arms 3p and 21q
    Cancer Genomics Proteomics, 18 (4), 531-542
    DOI 10.21873/cgp.20278, PubMed 34183386
  6. Panagopoulos I, Gorunova L, Andersen K, Lund-Iversen M, Tafjord S, Micci F, Heim S (2021)
    Fusion of the Paired Box 3 (PAX3) and Myocardin (MYOCD) Genes in Pediatric Rhabdomyosarcoma
    Cancer Genomics Proteomics, 18 (6), 723-734
    DOI 10.21873/cgp.20293, PubMed 34697065
  7. Panagopoulos I, Gorunova L, Lund-Iversen M, Heim S (2021)
    Monosomy 13 in Mammary Myofibroblastoma
    Anticancer Res, 41 (8), 3747-3751
    DOI 10.21873/anticanres.15166, PubMed 34281833
  8. Panagopoulos I, Heim S (2021)
    Interstitial Deletions Generating Fusion Genes
    Cancer Genomics Proteomics, 18 (3), 167-196
    DOI 10.21873/cgp.20251, PubMed 33893073
  9. Toussaint L, Brandal P, Embring A, Engellau J, Evensen ME, Griskeviskius R, Hansen J, Hietala H, Wickart Johansson G, Jørgensen M, Kramer PH, Kristensen I, Lehtio K, Magelssen H, Maraldo MV, Marienhagen K, Martinsson U, Nilsson K, Peters S, Plaude S, Seiersen K, Sendiuliene D, Smulders B, Edvardsen T, Søbstad JM et al. (2021)
    Inter-observer variation in target delineation and dose trade-off for radiotherapy of paediatric ependymoma
    Acta Oncol, 61 (2), 235-238
    DOI 10.1080/0284186X.2021.2022202, PubMed 34970940

Publications 2020

  1. Brandal P, Bergfeldt K, Aggerholm-Pedersen N, Bäckström G, Kerna I, Gubanski M, Björnlinger K, Evensen ME, Kuddu M, Pettersson E, Brydøy M, Hellebust TP, Dale E, Valdman A, Weber L, Høyer M (2020)
    A Nordic-Baltic perspective on indications for proton therapy with strategies for identification of proper patients
    Acta Oncol, 59 (10), 1157-1163
    DOI 10.1080/0284186X.2020.1817977, PubMed 32902341
  2. Brunetti M, Panagopoulos I, Kostolomov I, Davidson B, Heim S, Micci F (2020)
    Mutation analysis and genomic imbalances of cells found in effusion fluids from patients with ovarian cancer
    Oncol Lett, 20 (3), 2273-2279
    DOI 10.3892/ol.2020.11782, PubMed 32782545
  3. Brunetti M, Zeller B, Tierens A, Heim S, Micci F, Panagopoulos I (2020)
    TYRO3 Truncation Resulting From a t(10;15)(p11;q15) Chromosomal Translocation in Pediatric Acute Myeloid Leukemia
    Anticancer Res, 40 (11), 6115-6121
    DOI 10.21873/anticanres.14632, PubMed 33109549
  4. Davidson B, McFadden E, Holth A, Brunetti M, Flørenes VA (2020)
    Death domain-associated protein (DAXX) expression is associated with poor survival in metastatic high-grade serous carcinoma
    Virchows Arch, 477 (6), 857-864
    DOI 10.1007/s00428-020-02842-4, PubMed 32533344
  5. Gorunova L, Bjerkehagen B, Micci F, Heim S, Panagopoulos I (2020)
    Cytogenetic and Molecular Study of an Adult Sclerosing Rhabdomyosarcoma of the Extremity: MYOD1-mutation and Clonal Evolution
    Cancer Genomics Proteomics, 17 (5), 563-569
    DOI 10.21873/cgp.20212, PubMed 32859634
  6. Jeanmougin M, Håvik AB, Cekaite L, Brandal P, Sveen A, Meling TR, Ågesen TH, Scheie D, Heim S, Lothe RA, Lind GE (2020)
    Improved prognostication of glioblastoma beyond molecular subtyping by transcriptional profiling of the tumor microenvironment
    Mol Oncol, 14 (5), 1016-1027
    DOI 10.1002/1878-0261.12668, PubMed 32171051
  7. Kierulf-Vieira KS, Sandberg CJ, Waaler J, Lund K, Skaga E, Saberniak BM, Panagopoulos I, Brandal P, Krauss S, Langmoen IA, Vik-Mo EO (2020)
    A Small-Molecule Tankyrase Inhibitor Reduces Glioma Stem Cell Proliferation and Sphere Formation
    Cancers (Basel), 12 (6)
    DOI 10.3390/cancers12061630, PubMed 32575464
  8. Latysheva A, Geier OM, Hope TR, Brunetti M, Micci F, Vik-Mo EO, Emblem KE, Server A (2020)
    Diagnostic utility of Restriction Spectrum Imaging in the characterization of the peritumoral brain zone in glioblastoma: Analysis of overall and progression-free survival
    Eur J Radiol, 132, 109289
    DOI 10.1016/j.ejrad.2020.109289, PubMed 33002815
  9. Panagopoulos I, Gorunova L, Andersen K, Lobmaier I, Lund-Iversen M, Micci F, Heim S (2020)
    Fusion of the Lumican (LUM) Gene With the Ubiquitin Specific Peptidase 6 (USP6) Gene in an Aneurysmal Bone Cyst Carrying a t(12;17)(q21;p13) Chromosome Translocation
    Cancer Genomics Proteomics, 17 (5), 555-561
    DOI 10.21873/cgp.20211, PubMed 32859633
  10. Panagopoulos I, Gorunova L, Andersen K, Lund-Iversen M, Lobmaier I, Micci F, Heim S (2020)
    NDRG1-PLAG1 and TRPS1-PLAG1 Fusion Genes in Chondroid Syringoma
    Cancer Genomics Proteomics, 17 (3), 237-248
    DOI 10.21873/cgp.20184, PubMed 32345665
  11. Panagopoulos I, Gorunova L, Andersen K, Tafjord S, Lund-Iversen M, Lobmaier I, Micci F, Heim S (2020)
    Recurrent Fusion of the GRB2 Associated Binding Protein 1 (GAB1) Gene With ABL Proto-oncogene 1 (ABL1) in Benign Pediatric Soft Tissue Tumors
    Cancer Genomics Proteomics, 17 (5), 499-508
    DOI 10.21873/cgp.20206, PubMed 32859628
  12. Panagopoulos I, Gorunova L, Johannsdottir IMR, Andersen K, Holth A, Beiske K, Heim S (2020)
    Chromosome Translocation t(14;21)(q11;q22) Activates Both OLIG1 and OLIG2 in Pediatric T-cell Lymphoblastic Malignancies and May Signify Adverse Prognosis
    Cancer Genomics Proteomics, 17 (1), 41-48
    DOI 10.21873/cgp.20166, PubMed 31882550
  13. Panagopoulos I, Gorunova L, Kostolomov I, Lobmaier I, Bjerkehagen B, Heim S (2020)
    Chronic Expanding Hematoma with a t(11;19)(q13;q13) Chromosomal Translocation
    Anticancer Res, 40 (1), 97-100
    DOI 10.21873/anticanres.13930, PubMed 31892557
  14. Panagopoulos I, Gorunova L, Lobmaier I, Andersen K, Kostolomov I, Lund-Iversen M, Bjerkehagen B, Heim S (2020)
    FOS-ANKH and FOS-RUNX2 Fusion Genes in Osteoblastoma
    Cancer Genomics Proteomics, 17 (2), 161-168
    DOI 10.21873/cgp.20176, PubMed 32108038
  15. Panagopoulos I, Gorunova L, Lobmaier I, Andersen K, Lund-Iversen M, Micci F, Heim S (2020)
    Fusion of the COL4A5 Gene With NR2F2-AS1 in a Hemangioma Carrying a t(X;15)(q22;q26) Chromosomal Translocation
    Cancer Genomics Proteomics, 17 (4), 383-390
    DOI 10.21873/cgp.20197, PubMed 32576583
  16. Panagopoulos I, Gorunova L, Rise TV, Andersen K, Micci F, Heim S (2020)
    An Unbalanced Chromosome Translocation Between 7p22 and 12q13 Leads to ACTB-GLI1 Fusion in Pericytoma
    Anticancer Res, 40 (3), 1239-1245
    DOI 10.21873/anticanres.14065, PubMed 32132020
  17. Stadskleiv K, Stensvold E, Stokka K, Bechensteen AG, Brandal P (2020)
    Neuropsychological functioning in survivors of childhood medulloblastoma/CNS-PNET: The role of secondary medical complications
    Clin Neuropsychol, 36 (3), 600-625
    DOI 10.1080/13854046.2020.1794045, PubMed 32729777
  18. Stensvold E, Stadskleiv K, Myklebust TÅ, Wesenberg F, Helseth E, Bechensteen AG, Brandal P (2020)
    Unmet rehabilitation needs in 86% of Norwegian paediatric embryonal brain tumour survivors
    Acta Paediatr, 109 (9), 1875-1886
    DOI 10.1111/apa.15188, PubMed 31977119
  19. Vietri M, Schultz SW, Bellanger A, Jones CM, Petersen LI, Raiborg C, Skarpen E, Pedurupillay CRJ, Kjos I, Kip E, Timmer R, Jain A, Collas P, Knorr RL, Grellscheid SN, Kusumaatmaja H, Brech A, Micci F, Stenmark H, Campsteijn C (2020)
    Unrestrained ESCRT-III drives micronuclear catastrophe and chromosome fragmentation
    Nat Cell Biol, 22 (7), 856-867
    DOI 10.1038/s41556-020-0537-5, PubMed 32601372

Publications 2019

  1. Bogsrud TV, Londalen A, Brandal P, Leske H, Panagopoulos I, Borghammer P, Bach-Gansmo T (2019)
    18F-Fluciclovine PET/CT in Suspected Residual or Recurrent High-Grade Glioma
    Clin Nucl Med, 44 (8), 605-611
    DOI 10.1097/RLU.0000000000002641, PubMed 31274605
  2. Brunetti M, Agostini A, Staurseth J, Davidson B, Heim S, Micci F (2019)
    Molecular characterization of carcinosarcomas arising in the uterus and ovaries
    Oncotarget, 10 (38), 3614-3624
    DOI 10.18632/oncotarget.26942, PubMed 31217897
  3. Brunetti M, Panagopoulos I, Micci F, Davidson B (2019)
    MGMT promoter methylation is a rare epigenetic change in malignant effusions
    Cytopathology, 31 (1), 12-15
    DOI 10.1111/cyt.12782, PubMed 31808217
  4. Panagopoulos I, Gorunova L, Andersen HK, Pedersen TD, Lømo J, Lund-Iversen M, Micci F, Heim S (2019)
    Genetic Characterization of Myoid Hamartoma of the Breast
    Cancer Genomics Proteomics, 16 (6), 563-568
    DOI 10.21873/cgp.20158, PubMed 31659109
  5. Panagopoulos I, Gorunova L, Lobmaier I, Lund-Iversen M, Andersen K, Holth A, Bjerkehagen B, Heim S (2019)
    Fusion of the COL1A1 and FYN Genes in Epithelioid Osteoblastoma
    Cancer Genomics Proteomics, 16 (5), 361-368
    DOI 10.21873/cgp.20141, PubMed 31467230
  6. Panagopoulos I, Gorunova L, Lund-Iversen M, Bassarova A, Heim S (2019)
    Fusion of the Genes PHF1 and TFE3 in Malignant Chondroid Syringoma
    Cancer Genomics Proteomics, 16 (5), 345-351
    DOI 10.21873/cgp.20139, PubMed 31467228
  7. Panagopoulos I, Lobmaier I, Gorunova L, Heim S (2019)
    Fusion of the Genes WWTR1 and FOSB in Pseudomyogenic Hemangioendothelioma
    Cancer Genomics Proteomics, 16 (4), 293-298
    DOI 10.21873/cgp.20134, PubMed 31243110
  8. Stensvold E, Myklebust TÅ, Cappelen J, Due-Tønnessen BJ, Due-Tønnessen P, Kepka A, Johannesen TB, Krossnes B, Lundar T, Maric S, Miletic H, Moholdt V, Myrmel KS, Nordberg T, Rydland J, Stokland T, Solem K, Solheim O, Torsvik I, Wikran GC, Zeller B, Wesenberg F, Bechensteen AG, Brandal P (2019)
    Children treated for medulloblastoma and supratentorial primitive neuroectodermal tumor in Norway from 1974 through 2013: Unexplainable regional differences in survival
    Pediatr Blood Cancer, 66 (10), e27910
    DOI 10.1002/pbc.27910, PubMed 31264356
  9. Torkildsen S, Gorunova L, Heim S, Tjønnfjord GE, Spetalen S, Risberg B, Tran HTT, Panagopoulos I (2019)
    Molecular Genetic Characterization of Acute Myeloid Leukemia With Trisomy 4 as the Sole Chromosome Abnormality
    Cancer Genomics Proteomics, 16 (3), 175-178
    DOI 10.21873/cgp.20123, PubMed 31018948

Publications 2018

  1. Agostini A, Brunetti M, Davidson B, Göran Tropé C, Heim S, Panagopoulos I, Micci F (2018)
    Identification of novel cyclin gene fusion transcripts in endometrioid ovarian carcinomas
    Int J Cancer, 143 (6), 1379-1387
    DOI 10.1002/ijc.31418, PubMed 29633253
  2. Agostini A, Brunetti M, Davidson B, Tropé CG, Eriksson AGZ, Heim S, Panagopoulos I, Micci F (2018)
    The microRNA miR-192/215 family is upregulated in mucinous ovarian carcinomas
    Sci Rep, 8 (1), 11069
    DOI 10.1038/s41598-018-29332-7, PubMed 30038317
  3. Batman S, Morgan T, Brunetti M, Strandabø RAU, Micci F, Moffitt M, Pejovic T (2018)
    Primary mediastinal choriocarcinoma in a female patient: Case report and review of the literature
    Gynecol Oncol Rep, 26, 99-101
    DOI 10.1016/j.gore.2018.10.013, PubMed 30456287
  4. Brunetti M, Gorunova L, Davidson B, Heim S, Panagopoulos I, Micci F (2018)
    Identification of an EPC2-PHF1 fusion transcript in low-grade endometrial stromal sarcoma
    Oncotarget, 9 (27), 19203-19208
    DOI 10.18632/oncotarget.24969, PubMed 29721194
  5. Brunetti M, Holth A, Panagopoulos I, Staff AC, Micci F, Davidson B (2018)
    Expression and clinical role of the dipeptidyl peptidases DPP8 and DPP9 in ovarian carcinoma
    Virchows Arch, 474 (2), 177-185
    DOI 10.1007/s00428-018-2487-x, PubMed 30467600
  6. Georgakopoulos N, Diamantopoulos P, Micci F, Giannakopoulou N, Zervakis K, Dimitrakopoulou A, Viniou NA (2018)
    An Adult Patient with Early Pre-B Acute Lymphoblastic Leukemia with t(12;17)(p13;q21)/ZNF384-TAF15
    In Vivo, 32 (5), 1241-1245
    DOI 10.21873/invivo.11371, PubMed 30150451
  7. Johannessen LE, Brandal P, Myklebust TÅ, Heim S, Micci F, Panagopoulos I (2018)
    MGMT Gene Promoter Methylation Status - Assessment of Two Pyrosequencing Kits and Three Methylation-specific PCR Methods for their Predictive Capacity in Glioblastomas
    Cancer Genomics Proteomics, 15 (6), 437-446
    DOI 10.21873/cgp.20102, PubMed 30343277
  8. Leske H, Rushing E, Budka H, Niehusmann P, Pahnke J, Panagopoulos I (2018)
    K27/G34 versus K28/G35 in histone H3-mutant gliomas: A note of caution
    Acta Neuropathol, 136 (1), 175-176
    DOI 10.1007/s00401-018-1867-2, PubMed 29766298
  9. Panagopoulos I, Gorunova L, Andersen HK, Bergrem A, Dahm A, Andersen K, Micci F, Heim S (2018)
    PAN3-PSMA2 fusion resulting from a novel t(7;13)(p14;q12) chromosome translocation in a myelodysplastic syndrome that evolved into acute myeloid leukemia
    Exp Hematol Oncol, 7, 7
    DOI 10.1186/s40164-018-0099-4, PubMed 29560286
  10. Panagopoulos I, Gorunova L, Andersen K, Lobmaier I, Bjerkehagen B, Heim S (2018)
    Consistent Involvement of Chromosome 13 in Angiolipoma
    Cancer Genomics Proteomics, 15 (1), 61-65
    DOI 10.21873/cgp.20065, PubMed 29275363
  11. Panagopoulos I, Gorunova L, Jacobsen EM, Andersen K, Micci F, Heim S (2018)
    RUNX1-PDCD6 fusion resulting from a novel t(5;21)(p15;q22) chromosome translocation in myelodysplastic syndrome secondary to chronic lymphocytic leukemia
    PLoS One, 13 (4), e0196181
    DOI 10.1371/journal.pone.0196181, PubMed 29672642
  12. Panagopoulos I, Gorunova L, Leske H, Niehusmann P, Johannessen LE, Staurseth J, Øino N, Meling TR, Heim S, Micci F, Brandal P (2018)
    Pyrosequencing Analysis of MGMT Promoter Methylation in Meningioma
    Cancer Genomics Proteomics, 15 (5), 379-385
    DOI 10.21873/cgp.20096, PubMed 30194078
  13. Panagopoulos I, Gorunova L, Lund-Iversen M, Andersen K, Andersen HK, Lobmaier I, Bjerkehagen B, Heim S (2018)
    Cytogenetics of Spindle Cell/Pleomorphic Lipomas: Karyotyping and FISH Analysis of 31 Tumors
    Cancer Genomics Proteomics, 15 (3), 193-200
    DOI 10.21873/cgp.20077, PubMed 29695401

Publications 2017

  1. Agostini A, Brunetti M, Davidson B, Tropé CG, Heim S, Panagopoulos I, Micci F (2017)
    Genomic imbalances are involved in miR-30c and let-7a deregulation in ovarian tumors: implications for HMGA2 expression
    Oncotarget, 8 (13), 21554-21560
    DOI 10.18632/oncotarget.15795, PubMed 28423547
  2. Brunetti M, Agostini A, Davidson B, Tropé CG, Heim S, Panagopoulos I, Micci F (2017)
    Recurrent fusion transcripts in squamous cell carcinomas of the vulva
    Oncotarget, 8 (10), 16843-16850
    DOI 10.18632/oncotarget.15167, PubMed 28186972
  3. Brunetti M, Panagopoulos I, Gorunova L, Davidson B, Heim S, Micci F (2017)
    RNA-sequencing identifies novel GREB1-NCOA2 fusion gene in a uterine sarcoma with the chromosomal translocation t(2;8)(p25;q13)
    Genes Chromosomes Cancer, 57 (4), 176-181
    DOI 10.1002/gcc.22518, PubMed 29218853
  4. Davidson B, Micci F (2017)
    Molecular characteristics of uterine sarcomas
    Expert Rev Mol Diagn, 17 (5), 515-522
    DOI 10.1080/14737159.2017.1311790, PubMed 28335657
  5. Leske H, Brandal P, Rushing EJ, Niehusmann P (2017)
    IDH-mutant giant cell glioblastoma: A neglected tumor variant?
    Clin Neuropathol, 36 (6), 293-295
    DOI 10.5414/NP301054, PubMed 29035191
  6. Lewis N, Soslow RA, Delair DF, Park KJ, Murali R, Hollmann TJ, Davidson B, Micci F, Panagopoulos I, Hoang LN, Arias-Stella JA, Oliva E, Young RH, Hensley ML, Leitao MM, Hameed M, Benayed R, Ladanyi M, Frosina D, Jungbluth AA, Antonescu CR, Chiang S (2017)
    ZC3H7B-BCOR high-grade endometrial stromal sarcomas: a report of 17 cases of a newly defined entity
    Mod Pathol, 31 (4), 674-684
    DOI 10.1038/modpathol.2017.162, PubMed 29192652
  7. Micci F, Brunetti M, Dal Cin P, Nucci MR, Gorunova L, Heim S, Panagopoulos I (2017)
    Fusion of the genes BRD8 and PHF1 in endometrial stromal sarcoma
    Genes Chromosomes Cancer, 56 (12), 841-845
    DOI 10.1002/gcc.22485, PubMed 28758277
  8. Panagopoulos I, Gorunova L, Bjerkehagen B, Andersen K, Lund-Iversen M, Heim S (2017)
    Loss of chromosome 13 material in cellular angiofibromas indicates pathogenetic similarity with spindle cell lipomas
    Diagn Pathol, 12 (1), 17
    DOI 10.1186/s13000-017-0607-6, PubMed 28193293
  9. Panagopoulos I, Gorunova L, Brunetti M, Agostini A, Andersen HK, Lobmaier I, Bjerkehagen B, Heim S (2017)
    Genetic heterogeneity in leiomyomas of deep soft tissue
    Oncotarget, 8 (30), 48769-48781
    DOI 10.18632/oncotarget.17953, PubMed 28591699
  10. Panagopoulos I, Gorunova L, Lobmaier I, Andersen HK, Bjerkehagen B, Heim S (2017)
    Cytogenetic Analysis of a Pseudoangiomatous Pleomorphic/Spindle Cell Lipoma
    Anticancer Res, 37 (5), 2219-2223
    DOI 10.21873/anticanres.11557, PubMed 28476785
  11. Panagopoulos I, Gorunova L, Lobmaier I, Bjerkehagen B, Heim S (2017)
    Karyotyping and analysis of GNAS locus in intramuscular myxomas
    Oncotarget, 8 (13), 22086-22094
    DOI 10.18632/oncotarget.14986, PubMed 28160572
  12. Panagopoulos I, Gorunova L, Lobmaier I, Bjerkehagen B, Heim S (2017)
    Identification of SETD2-NF1 fusion gene in a pediatric spindle cell tumor with the chromosomal translocation t(3;17)(p21;q12)
    Oncol Rep, 37 (6), 3181-3188
    DOI 10.3892/or.2017.5628, PubMed 28498454
  13. Panagopoulos I, Gorunova L, Spetalen S, Bassarova A, Beiske K, Micci F, Heim S (2017)
    Fusion of the genes ataxin 2 like, ATXN2L, and Janus kinase 2, JAK2, in cutaneous CD4 positive T-cell lymphoma
    Oncotarget, 8 (61), 103775-103784
    DOI 10.18632/oncotarget.21790, PubMed 29262599
  14. Panagopoulos I, Gorunova L, Torkildsen S, Tierens A, Heim S, Micci F (2017)
    FAM53B truncation caused by t(10;19)(q26;q13) chromosome translocation in acute lymphoblastic leukemia
    Oncol Lett, 13 (4), 2216-2220
    DOI 10.3892/ol.2017.5705, PubMed 28454383
  15. Panagopoulos I, Gorunova L, Torkildsen S, Tjønnfjord GE, Micci F, Heim S (2017)
    DEK-NUP214-Fusion Identified by RNA-Sequencing of an Acute Myeloid Leukemia with t(9;12)(q34;q15)
    Cancer Genomics Proteomics, 14 (6), 437-443
    DOI 10.21873/cgp.20053, PubMed 29109093
  16. Smebye ML, Agostini A, Johannessen B, Thorsen J, Davidson B, Tropé CG, Heim S, Skotheim RI, Micci F (2017)
    Involvement of DPP9 in gene fusions in serous ovarian carcinoma
    BMC Cancer, 17 (1), 642
    DOI 10.1186/s12885-017-3625-6, PubMed 28893231
  17. Torkildsen S, Brunetti M, Gorunova L, Spetalen S, Beiske K, Heim S, Panagopoulos I (2017)
    Rearrangement of the Chromatin Organizer Special AT-rich Binding Protein 1 Gene, SATB1, Resulting from a t(3;5)(p24;q14) Chromosomal Translocation in Acute Myeloid Leukemia
    Anticancer Res, 37 (2), 693-698
    DOI 10.21873/anticanres.11365, PubMed 28179318

Publications 2016

  1. Agostini A, Brunetti M, Davidson B, Trope CG, Heim S, Panagopoulos I, Micci F (2016)
    Expressions of miR-30c and let-7a are inversely correlated with HMGA2 expression in squamous cell carcinoma of the vulva
    Oncotarget, 7 (51), 85058-85062
    DOI 10.18632/oncotarget.13187, PubMed 27835588
  2. Agostini A, Gorunova L, Bjerkehagen B, Lobmaier I, Heim S, Panagopoulos I (2016)
    Molecular characterization of the t(4;12)(q27~28;q14~15) chromosomal rearrangement in lipoma
    Oncol Lett, 12 (3), 1701-1704
    DOI 10.3892/ol.2016.4834, PubMed 27588119
  3. Agostini A, Panagopoulos I, Davidson B, Trope CG, Heim S, Micci F (2016)
    A novel truncated form of HMGA2 in tumors of the ovaries
    Oncol Lett, 12 (2), 1559-1563
    DOI 10.3892/ol.2016.4805, PubMed 27446471
  4. Behnan J, Stangeland B, Hosainey SA, Joel M, Olsen TK, Micci F, Glover JC, Isakson P, Brinchmann JE (2016)
    Differential propagation of stroma and cancer stem cells dictates tumorigenesis and multipotency
    Oncogene, 36 (4), 570-584
    DOI 10.1038/onc.2016.230, PubMed 27345406
  5. Haugvik SP, Vodák D, Haugom L, Hovig E, Gladhaug IP, Heim S, Micci F (2016)
    Transcriptomic Profiling of Tumor Aggressiveness in Sporadic Nonfunctioning Pancreatic Neuroendocrine Neoplasms
    Pancreas, 45 (8), 1196-203
    DOI 10.1097/MPA.0000000000000610, PubMed 26918873
  6. Johannessen LE, Panagopoulos I, Haugvik SP, Gladhaug IP, Heim S, Micci F (2016)
    Upregulation of INS-IGF2 read-through expression and identification of a novel INS-IGF2 splice variant in insulinomas
    Oncol Rep, 36 (5), 2653-2662
    DOI 10.3892/or.2016.5132, PubMed 27667266
  7. Micci F, Gorunova L, Agostini A, Johannessen LE, Brunetti M, Davidson B, Heim S, Panagopoulos I (2016)
    Cytogenetic and molecular profile of endometrial stromal sarcoma
    Genes Chromosomes Cancer, 55 (11), 834-46
    DOI 10.1002/gcc.22380, PubMed 27219024
  8. Olsen TK, Panagopoulos I, Gorunova L, Micci F, Andersen K, Kilen Andersen H, Meling TR, Due-Tønnessen B, Scheie D, Heim S, Brandal P (2016)
    Novel fusion genes and chimeric transcripts in ependymal tumors
    Genes Chromosomes Cancer, 55 (12), 944-953
    DOI 10.1002/gcc.22392, PubMed 27401149
  9. Panagopoulos I, Gorunova L, Agostini A, Lobmaier I, Bjerkehagen B, Heim S (2016)
    Fusion of the HMGA2 and C9orf92 genes in myolipoma with t(9;12)(p22;q14)
    Diagn Pathol, 11, 22
    DOI 10.1186/s13000-016-0472-8, PubMed 26857357
  10. Panagopoulos I, Gorunova L, Kerndrup G, Spetalen S, Tierens A, Osnes LT, Andersen K, Müller LS, Hellebostad M, Zeller B, Heim S (2016)
    Rare MLL-ELL fusion transcripts in childhood acute myeloid leukemia-association with young age and myeloid sarcomas?
    Exp Hematol Oncol, 5, 8
    DOI 10.1186/s40164-016-0037-2, PubMed 26949571
  11. Panagopoulos I, Gorunova L, Lund-Iversen M, Lobmaier I, Bjerkehagen B, Heim S (2016)
    Recurrent fusion of the genes FN1 and ALK in gastrointestinal leiomyomas
    Mod Pathol, 29 (11), 1415-1423
    DOI 10.1038/modpathol.2016.129, PubMed 27469327
  12. Panagopoulos I, Gorunova L, Viset T, Heim S (2016)
    Gene fusions AHRR-NCOA2, NCOA2-ETV4, ETV4-AHRR, P4HA2-TBCK, and TBCK-P4HA2 resulting from the translocations t(5;8;17)(p15;q13;q21) and t(4;5)(q24;q31) in a soft tissue angiofibroma
    Oncol Rep, 36 (5), 2455-2462
    DOI 10.3892/or.2016.5096, PubMed 27633981
  13. Panagopoulos I, Torkildsen S, Gorunova L, Ulvmoen A, Tierens A, Zeller B, Heim S (2016)
    RUNX1 truncation resulting from a cryptic and novel t(6;21)(q25;q22) chromosome translocation in acute myeloid leukemia: A case report
    Oncol Rep, 36 (5), 2481-2488
    DOI 10.3892/or.2016.5119, PubMed 27667292
  14. Smebye ML, Haugom L, Davidson B, Trope CG, Heim S, Skotheim RI, Micci F (2016)
    Bilateral ovarian carcinomas differ in the expression of metastasis-related genes
    Oncol Lett, 13 (1), 184-190
    DOI 10.3892/ol.2016.5384, PubMed 28123539
  15. Vandraas K, Tjønnfjord GE, Johannesen TB, Brandal P (2016)
    Persistent bone marrow depression following short-term treatment with temozolomide
    BMJ Case Rep, 2016
    DOI 10.1136/bcr-2016-215797, PubMed 27130558
  16. Våtsveen TK, Børset M, Dikic A, Tian E, Micci F, Lid AH, Meza-Zepeda LA, Coward E, Waage A, Sundan A, Kuehl WM, Holien T (2016)
    VOLIN and KJON-Two novel hyperdiploid myeloma cell lines
    Genes Chromosomes Cancer, 55 (11), 890-901
    DOI 10.1002/gcc.22388, PubMed 27311012

Publications 2015

  1. Agostini A, Panagopoulos I, Andersen HK, Johannesen LE, Davidson B, Tropé CG, Heim S, Micci F (2015)
    HMGA2 expression pattern and TERT mutations in tumors of the vulva
    Oncol Rep, 33 (6), 2675-80
    DOI 10.3892/or.2015.3882, PubMed 25823555
  2. Bassarova A, Trøen G, Spetalen S, Micci F, Tierens A, Delabie J (2015)
    Lymphoplasmacytic lymphoma and marginal zone lymphoma in the bone marrow: paratrabecular involvement as an important distinguishing feature
    Am J Clin Pathol, 143 (6), 797-806
    DOI 10.1309/AJCP6ZODWV1CIDME, PubMed 25972321
  3. Dale Rein I, Solberg Landsverk K, Micci F, Patzke S, Stokke T (2015)
    Replication-induced DNA damage after PARP inhibition causes G2 delay, and cell line-dependent apoptosis, necrosis and multinucleation
    Cell Cycle, 14 (20), 3248-60
    DOI 10.1080/15384101.2015.1085137, PubMed 26312527
  4. Olsen TK, Panagopoulos I, Meling TR, Micci F, Gorunova L, Thorsen J, Due-Tønnessen B, Scheie D, Lund-Iversen M, Krossnes B, Saxhaug C, Heim S, Brandal P (2015)
    Fusion genes with ALK as recurrent partner in ependymoma-like gliomas: a new brain tumor entity?
    Neuro Oncol, 17 (10), 1365-73
    DOI 10.1093/neuonc/nov039, PubMed 25795305
  5. Panagopoulos I, Bjerkehagen B, Gorunova L, Taksdal I, Heim S (2015)
    Rearrangement of chromosome bands 12q14~15 causing HMGA2-SOX5 gene fusion and HMGA2 expression in extraskeletal osteochondroma
    Oncol Rep, 34 (2), 577-84
    DOI 10.3892/or.2015.4035, PubMed 26043835
  6. Panagopoulos I, Gorunova L, Bjerkehagen B, Heim S (2015)
    Novel KAT6B-KANSL1 fusion gene identified by RNA sequencing in retroperitoneal leiomyoma with t(10;17)(q22;q21)
    PLoS One, 10 (1), e0117010
    DOI 10.1371/journal.pone.0117010, PubMed 25621995
  7. Panagopoulos I, Gorunova L, Bjerkehagen B, Heim S (2015)
    Fusion of the genes EWSR1 and PBX3 in retroperitoneal leiomyoma with t(9;22)(q33;q12)
    PLoS One, 10 (4), e0124288
    DOI 10.1371/journal.pone.0124288, PubMed 25875009
  8. Panagopoulos I, Gorunova L, Bjerkehagen B, Lobmaier I, Heim S (2015)
    The recurrent chromosomal translocation t(12;18)(q14~15;q12~21) causes the fusion gene HMGA2-SETBP1 and HMGA2 expression in lipoma and osteochondrolipoma
    Int J Oncol, 47 (3), 884-90
    DOI 10.3892/ijo.2015.3099, PubMed 26202160
  9. Panagopoulos I, Gorunova L, Bjerkehagen B, Lobmaier I, Heim S (2015)
    LAMTOR1-PRKCD and NUMA1-SFMBT1 fusion genes identified by RNA sequencing in aneurysmal benign fibrous histiocytoma with t(3;11)(p21;q13)
    Cancer Genet, 208 (11), 545-51
    DOI 10.1016/j.cancergen.2015.07.007, PubMed 26432191
  10. Panagopoulos I, Gorunova L, Bjerkehagen B, Lobmaier I, Heim S (2015)
    Fusion of the TBL1XR1 and HMGA1 genes in splenic hemangioma with t(3;6)(q26;p21)
    Int J Oncol, 48 (3), 1242-50
    DOI 10.3892/ijo.2015.3310, PubMed 26708416
  11. Panagopoulos I, Gorunova L, Taksdal I, Bjerkehagen B, Heim S (2015)
    Recurrent 12q13-15 chromosomal aberrations, high frequency of isocitrate dehydrogenase 1 mutations, and absence of high mobility group AT-hook 2 expression in periosteal chondromas
    Oncol Lett, 10 (1), 163-167
    DOI 10.3892/ol.2015.3197, PubMed 26170993
  12. Torkildsen S, Gorunova L, Beiske K, Tjønnfjord GE, Heim S, Panagopoulos I (2015)
    Novel ZEB2-BCL11B Fusion Gene Identified by RNA-Sequencing in Acute Myeloid Leukemia with t(2;14)(q22;q32)
    PLoS One, 10 (7), e0132736
    DOI 10.1371/journal.pone.0132736, PubMed 26186352

Publications 2014

  1. Haugvik SP, Gorunova L, Haugom L, Eibak AM, Gladhaug IP, Heim S, Micci F (2014)
    Loss of 11p11 is a frequent and early event in sporadic nonfunctioning pancreatic neuroendocrine neoplasms
    Oncol Rep, 32 (3), 906-12
    DOI 10.3892/or.2014.3328, PubMed 25018013
  2. Heim S (2014)
    Boveri at 100: Boveri, chromosomes and cancer
    J Pathol, 234 (2), 138-41
    DOI 10.1002/path.4406, PubMed 25043504
  3. Lundin C, Forestier E, Klarskov Andersen M, Autio K, Barbany G, Cavelier L, Golovleva I, Heim S, Heinonen K, Hovland R, Johannsson JH, Kjeldsen E, 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) (2014)
    Clinical and genetic features of pediatric acute lymphoblastic leukemia in Down syndrome in the Nordic countries
    J Hematol Oncol, 7, 32
    DOI 10.1186/1756-8722-7-32, PubMed 24726034
  4. Micci F, Gorunova L, Gatius S, Matias-Guiu X, Davidson B, Heim S, Panagopoulos I (2014)
    MEAF6/PHF1 is a recurrent gene fusion in endometrial stromal sarcoma
    Cancer Lett, 347 (1), 75-8
    DOI 10.1016/j.canlet.2014.01.030, PubMed 24530230
  5. Micci F, Haugom L, Abeler VM, Davidson B, Tropé CG, Heim S (2014)
    Genomic profile of ovarian carcinomas
    BMC Cancer, 14, 315
    DOI 10.1186/1471-2407-14-315, PubMed 24886194
  6. Micci F, Panagopoulos I, Thorsen J, Davidson B, Tropé CG, Heim S (2014)
    Low frequency of ESRRA-C11orf20 fusion gene in ovarian carcinomas
    PLoS Biol, 12 (2), e1001784
    DOI 10.1371/journal.pbio.1001784, PubMed 24504521
  7. Olsen TK, Gorunova L, Meling TR, Micci F, Scheie D, Due-Tønnessen B, Heim S, Brandal P (2014)
    Genomic characterization of ependymomas reveals 6q loss as the most common aberration
    Oncol Rep, 32 (2), 483-90
    DOI 10.3892/or.2014.3271, PubMed 24939246
  8. Panagopoulos I, Bjerkehagen B, Gorunova L, Berner JM, Boye K, Heim S (2014)
    Several fusion genes identified by whole transcriptome sequencing in a spindle cell sarcoma with rearrangements of chromosome arm 12q and MDM2 amplification
    Int J Oncol, 45 (5), 1829-36
    DOI 10.3892/ijo.2014.2605, PubMed 25176350
  9. Panagopoulos I, Brandal P, Gorunova L, Bjerkehagen B, Heim S (2014)
    Novel CSF1-S100A10 fusion gene and CSF1 transcript identified by RNA sequencing in tenosynovial giant cell tumors
    Int J Oncol, 44 (5), 1425-32
    DOI 10.3892/ijo.2014.2326, PubMed 24604026
  10. Panagopoulos I, Gorunova L, Bjerkehagen B, Boye K, Heim S (2014)
    Chromosome aberrations and HEY1-NCOA2 fusion gene in a mesenchymal chondrosarcoma
    Oncol Rep, 32 (1), 40-4
    DOI 10.3892/or.2014.3180, PubMed 24839999
  11. Panagopoulos I, Gorunova L, Bjerkehagen B, Heim S (2014)
    The "grep" command but not FusionMap, FusionFinder or ChimeraScan captures the CIC-DUX4 fusion gene from whole transcriptome sequencing data on a small round cell tumor with t(4;19)(q35;q13)
    PLoS One, 9 (6), e99439
    DOI 10.1371/journal.pone.0099439, PubMed 24950227
  12. Panagopoulos I, Gorunova L, Davidson B, Heim S (2014)
    Novel TNS3-MAP3K3 and ZFPM2-ELF5 fusion genes identified by RNA sequencing in multicystic mesothelioma with t(7;17)(p12;q23) and t(8;11)(q23;p13)
    Cancer Lett, 357 (2), 502-9
    DOI 10.1016/j.canlet.2014.12.002, PubMed 25484136
  13. Panagopoulos I, Thorsen J, Gorunova L, Micci F, Heim S (2014)
    Sequential combination of karyotyping and RNA-sequencing in the search for cancer-specific fusion genes
    Int J Biochem Cell Biol, 53, 462-5
    DOI 10.1016/j.biocel.2014.05.018, PubMed 24863361
  14. Panagopoulos I, Torkildsen S, Gorunova L, Tierens A, Tjønnfjord GE, Heim S (2014)
    Comparison between karyotyping-FISH-reverse transcription PCR and RNA-sequencing-fusion gene identification programs in the detection of KAT6A-CREBBP in acute myeloid leukemia
    PLoS One, 9 (5), e96570
    DOI 10.1371/journal.pone.0096570, PubMed 24798186
  15. Skårn M, Noordhuis P, Wang MY, Veuger M, Kresse SH, Egeland EV, Micci F, Namløs HM, Håkelien AM, Olafsrud SM, Lorenz S, Haraldsen G, Kvalheim G, Meza-Zepeda LA, Myklebost O (2014)
    Generation and characterization of an immortalized human mesenchymal stromal cell line
    Stem Cells Dev, 23 (19), 2377-89
    DOI 10.1089/scd.2013.0599, PubMed 24857590
  16. Smebye ML, Sveen A, Haugom L, Davidson B, Tropé CG, Lothe RA, Heim S, Skotheim RI, Micci F (2014)
    Chromosome 19 rearrangements in ovarian carcinomas: zinc finger genes are particularly targeted
    Genes Chromosomes Cancer, 53 (7), 558-67
    DOI 10.1002/gcc.22166, PubMed 24634323
  17. Torsvik A, Stieber D, Enger PØ, Golebiewska A, Molven A, Svendsen A, Westermark B, Niclou SP, Olsen TK, Chekenya Enger M, Bjerkvig R (2014)
    U-251 revisited: genetic drift and phenotypic consequences of long-term cultures of glioblastoma cells
    Cancer Med, 3 (4), 812-24
    DOI 10.1002/cam4.219, PubMed 24810477
  18. Wang L, Wenners A, Hilpert F, Fredrik R, Micci F, Onkes W, Caliebe A, Maass N, Weimer J, Arnold N (2014)
    Frequent translocations of 11q13.2 and 19p13.2 in ovarian cancer
    Genes Chromosomes Cancer, 53 (6), 447-53
    DOI 10.1002/gcc.22152, PubMed 24615723

Publications 2013

  1. Ellingsen T, Hansen I, Thorsen J, Møller BK, Tarp U, Lottenburger T, Andersen LS, Skjødt H, Pedersen JK, Lauridsen UB, Svendsen A, Lindegaard H, Jacobsen S, Østergaard M, Vestergaard A, Jurik AG, Junker P, Christensen AF, Hetland ML, Hørslev-Petersen K, Stengaard-Pedersen K (2013)
    Upregulated baseline plasma CCL19 and CCR7 cell-surface expression on monocytes in early rheumatoid arthritis normalized during treatment and CCL19 correlated with radiographic progression
    Scand J Rheumatol, 43 (2), 91-100
    DOI 10.3109/03009742.2013.803149, PubMed 23980529
  2. Fiskvik I, Aamot HV, Delabie J, Smeland EB, Stokke T, Heim S, Holte H (2013)
    Karyotyping of diffuse large B-cell lymphomas: loss of 17p is associated with poor patient outcome
    Eur J Haematol, 91 (4), 332-8
    DOI 10.1111/ejh.12171, PubMed 23859481
  3. Håvik AB, Lind GE, Honne H, Meling TR, Scheie D, Hall KS, van den Berg E, Mertens F, Picci P, Lothe RA, Heim S, Brandal P (2013)
    Sequencing IDH1/2 glioma mutation hotspots in gliomas and malignant peripheral nerve sheath tumors
    Neuro Oncol, 16 (2), 320-2
    DOI 10.1093/neuonc/not230, PubMed 24311631
  4. Micci F, Panagopoulos I, Haugom L, Dahlback HS, Pretorius ME, Davidson B, Abeler VM, Tropé CG, Danielsen HE, Heim S (2013)
    Genomic aberration patterns and expression profiles of squamous cell carcinomas of the vulva
    Genes Chromosomes Cancer, 52 (6), 551-63
    DOI 10.1002/gcc.22053, PubMed 23404381
  5. Onkes W, Fredrik R, Micci F, Schönbeck BJ, Martin-Subero JI, Ullmann R, Hilpert F, Bräutigam K, Janssen O, Maass N, Siebert R, Heim S, Arnold N, Weimer J (2013)
    Breakpoint characterization of the der(19)t(11;19)(q13;p13) in the ovarian cancer cell line SKOV-3
    Genes Chromosomes Cancer, 52 (5), 512-22
    DOI 10.1002/gcc.22048, PubMed 23362175
  6. Panagopoulos I, Gorunova L, Brandal P, Garnes M, Tierens A, Heim S (2013)
    Myeloid leukemia with t(7;21)(p22;q22) and 5q deletion
    Oncol Rep, 30 (4), 1549-52
    DOI 10.3892/or.2013.2623, PubMed 23877199
  7. Panagopoulos I, Gorunova L, Zeller B, Tierens A, Heim S (2013)
    Cryptic FUS-ERG fusion identified by RNA-sequencing in childhood acute myeloid leukemia
    Oncol Rep, 30 (6), 2587-92
    DOI 10.3892/or.2013.2751, PubMed 24068373
  8. Panagopoulos I, Micci F, Thorsen J, Haugom L, Buechner J, Kerndrup G, Tierens A, Zeller B, Heim S (2013)
    Fusion of ZMYND8 and RELA genes in acute erythroid leukemia
    PLoS One, 8 (5), e63663
    DOI 10.1371/journal.pone.0063663, PubMed 23667654
  9. Panagopoulos I, Thorsen J, Gorunova L, Haugom L, Bjerkehagen B, Davidson B, Heim S, Micci F (2013)
    Fusion of the ZC3H7B and BCOR genes in endometrial stromal sarcomas carrying an X;22-translocation
    Genes Chromosomes Cancer, 52 (7), 610-8
    DOI 10.1002/gcc.22057, PubMed 23580382
  10. Panagopoulos I, Thorsen J, Gorunova L, Micci F, Haugom L, Davidson B, Heim S (2013)
    RNA sequencing identifies fusion of the EWSR1 and YY1 genes in mesothelioma with t(14;22)(q32;q12)
    Genes Chromosomes Cancer, 52 (8), 733-40
    DOI 10.1002/gcc.22068, PubMed 23630070

Publications 2012

  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, Nordic Society of Paediatric Haematology and Oncology, Swedish Cytogenetic Leukaemia Study Group, NOPHO Leukaemia Cytogenetic Study Group (2012)
    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, 36 (7), 936-8
    DOI 10.1016/j.leukres.2012.03.024, PubMed 22521551
  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
    DOI 10.1186/1479-5876-10-36, PubMed 22390413
  3. Larsen HA, Austbø L, Mørkøre T, Thorsen J, Hordvik I, Fischer U, Jirillo E, Rimstad E, Koppang EO (2012)
    Pigment-producing granulomatous myopathy in Atlantic salmon: a novel inflammatory response
    Fish Shellfish Immunol, 33 (2), 277-85
    DOI 10.1016/j.fsi.2012.05.012, PubMed 22634154
  4. Micci F, Thorsen J, Panagopoulos I, Nyquist KB, Zeller B, Tierens A, Heim S (2012)
    High-throughput sequencing identifies an NFIA/CBFA2T3 fusion gene in acute erythroid leukemia with t(1;16)(p31;q24)
    Leukemia, 27 (4), 980-2
    DOI 10.1038/leu.2012.266, PubMed 23032695
  5. Nyquist KB, Panagopoulos I, Thorsen J, Haugom L, Gorunova L, Bjerkehagen B, Fosså A, Guriby M, Nome T, Lothe RA, Skotheim RI, Heim S, Micci F (2012)
    Whole-transcriptome sequencing identifies novel IRF2BP2-CDX1 fusion gene brought about by translocation t(1;5)(q42;q32) in mesenchymal chondrosarcoma
    PLoS One, 7 (11), e49705
    DOI 10.1371/journal.pone.0049705, PubMed 23185413
  6. Nyquist KB, Panagopoulos I, Thorsen J, Roberto R, Wik HS, Tierens A, Heim S, Micci F (2012)
    t(12;13)(q14;q31) leading to HMGA2 upregulation in acute myeloid leukaemia
    Br J Haematol, 157 (6), 769-71
    DOI 10.1111/j.1365-2141.2012.09081.x, PubMed 22404713
  7. Panagopoulos I, Micci F, Thorsen J, Gorunova L, Eibak AM, Bjerkehagen B, Davidson B, Heim S (2012)
    Novel fusion of MYST/Esa1-associated factor 6 and PHF1 in endometrial stromal sarcoma
    PLoS One, 7 (6), e39354
    DOI 10.1371/journal.pone.0039354, PubMed 22761769
  8. Panagopoulos I, Micci F, Thorsen J, Haugom L, Tierens A, Ulvmoen A, Heim S (2012)
    A novel TCF3-HLF fusion transcript in acute lymphoblastic leukemia with a t(17;19)(q22;p13)
    Cancer Genet, 205 (12), 669-72
    DOI 10.1016/j.cancergen.2012.10.004, PubMed 23181981
  9. Thorsen J, Aamot HV, Roberto R, Tjønnfjord GE, Micci F, Heim S (2012)
    Myelodysplastic syndrome with a t(2;11)(p21;q23-24) and translocation breakpoint close to miR-125b-1
    Cancer Genet, 205 (10), 528-32
    DOI 10.1016/j.cancergen.2012.06.003, PubMed 22944560
  10. Tjønnfjord GE, Ly BE, Johannesen TB, Tierens A, Beiske K, Heim S, Jønsson V (2012)
    Chronic lymphocytic leukaemia in Norway--incidence and prognostic markers at diagnosis
    Tidsskr Nor Laegeforen, 132 (18), 2056-9
    DOI 10.4045/tidsskr.11.1349, PubMed 23038195

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
    DOI 10.1111/j.1365-2141.2011.08824.x, 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
    DOI 10.1002/gcc.20898, 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
    DOI 10.1016/j.humpath.2011.02.012, 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
    DOI 10.1002/gcc.20866, 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
    DOI 10.1159/000326804, PubMed 21555877
  6. Giampetruzzi A, Roumi V, Roberto R, Malossini U, Yoshikawa N, La Notte P, Terlizzi F, Credi R, Saldarelli P (2011)
    A new grapevine virus discovered by deep sequencing of virus- and viroid-derived small RNAs in Cv Pinot gris
    Virus Res, 163 (1), 262-8
    DOI 10.1016/j.virusres.2011.10.010, PubMed 22036729
  7. Gorunova L, Bjerkehagen B, Heim S (2011)
    Paratesticular leiomyoma with a der(14)t(12;14)(q15;q24)
    Cancer Genet, 204 (8), 465-8
    DOI 10.1016/j.cancergen.2011.06.005, PubMed 21962898
  8. Guastadisegni MC, Roberto R, L'Abbate A, Palumbo O, Carella M, Giordani L, Cecinati V, Giordano P, Storlazzi CT (2011)
    Thrombocytopenia-absent-radius syndrome in a child showing a larger 1q21.1 deletion than the one in his healthy mother, and a significant downregulation of the commonly deleted genes
    Eur J Med Genet, 55 (2), 120-3
    DOI 10.1016/j.ejmg.2011.11.007, PubMed 22201559
  9. Kildal W, Micci F, Risberg B, Abeler VM, Kristensen GB, Heim S, Danielsen HE (2011)
    Genomic imbalances in endometrial adenocarcinomas - comparison of DNA ploidy, karyotyping and comparative genomic hybridization
    Mol Oncol, 6 (1), 98-107
    DOI 10.1016/j.molonc.2011.10.002, PubMed 22062770
  10. 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
    DOI 10.1016/j.cancergen.2011.10.013, PubMed 22285020
  11. 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
    DOI 10.1038/leu.2011.100, PubMed 21606959
  12. 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
    DOI 10.1016/j.cancergen.2011.01.003, PubMed 21504714
  13. Randen U, Yri OE, Tierens A, Heim S, Beiske K, Delabie J (2011)
    Mantle cell lymphoma with features of marginal-zone lymphoma
    J Hematop, 4 (1), 7-11
    DOI 10.1007/s12308-011-0084-x, PubMed 25089161
  14. Teixeira MR, Heim S (2011)
    Cytogenetic analysis of tumor clonality
    Adv Cancer Res, 112, 127-49
    DOI 10.1016/B978-0-12-387688-1.00005-3, PubMed 21925303
  15. 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
    DOI 10.1016/j.cancergen.2011.07.007, PubMed 21962896
  16. 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
    DOI 10.1182/blood-2011-03-341651, 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
    DOI 10.1002/gcc.20792, PubMed 20607708
  2. Eide MB, Liestøl K, Lingjaerde OC, Hystad ME, Kresse SH, Meza-Zepeda L, Myklebost O, Trøen G, Aamot HV, Holte H, Smeland EB, Delabie J (2010)
    Genomic alterations reveal potential for higher grade transformation in follicular lymphoma and confirm parallel evolution of tumor cell clones
    Blood, 116 (9), 1489-97
    DOI 10.1182/blood-2010-03-272278, PubMed 20505157
  3. 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
    DOI 10.1186/1479-5876-8-21, PubMed 20184781
  4. 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
    DOI 10.1002/gcc.20813, PubMed 20725991

Publications 2009

  1. 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 (2009)
    Expression pattern of the septin gene family in acute myeloid leukemias with and without MLL-SEPT fusion genes
    Leuk Res, 34 (5), 615-21
    DOI 10.1016/j.leukres.2009.08.018, PubMed 19748670

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
    DOI 10.3324/haematol.12594, PubMed 18492691

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
    DOI 10.1002/gcc.20423, PubMed 17285576
  2. 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
    DOI 10.1097/PAS.0b013e31803071a4, PubMed 17460466
  3. 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
    DOI 10.1016/j.cancergencyto.2007.06.019, PubMed 17954275
  4. 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
    DOI 10.1016/j.cancergencyto.2006.12.003, PubMed 17452257
  5. Micci F, Heim S (2007)
    Pathogenetic mechanisms in endometrial stromal sarcoma
    Cytogenet Genome Res, 118 (2-4), 190-5
    DOI 10.1159/000108300, PubMed 18000370
  6. 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
    DOI 10.1007/s00428-007-0407-6, PubMed 17406891
  7. 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
    DOI 10.1186/1476-4598-6-45, PubMed 17623056
  8. 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
    DOI 10.1007/s00432-006-0188-3, 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
    DOI 10.1002/path.1879, 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
    DOI 10.1038/modpathol.3800499, 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
    DOI 10.1038/sj.jid.5700375, PubMed 16728973
  4. Hallor KH, Micci F, Meis-Kindblom JM, Kindblom LG, Bacchini P, Mandahl N, Mertens F, Panagopoulos I (2006)
    Fusion genes in angiomatoid fibrous histiocytoma
    Cancer Lett, 251 (1), 158-63
    DOI 10.1016/j.canlet.2006.11.014, PubMed 17188428
  5. 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
    DOI 10.1007/s00428-005-0123-z, PubMed 16633785
  6. 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
    DOI 10.1111/j.1365-2141.2006.06286.x, PubMed 16965388
  7. 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
    DOI 10.1158/0008-5472.CAN-05-2485, PubMed 16397222
  8. 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
    DOI 10.1007/s00428-006-0186-5, PubMed 16568309
  9. Torres L, Ribeiro FR, Pandis N, Andersen JA, Heim S, Teixeira MR (2006)
    Intratumor genomic heterogeneity in breast cancer with clonal divergence between primary carcinomas and lymph node metastases
    Breast Cancer Res Treat, 102 (2), 143-55
    DOI 10.1007/s10549-006-9317-6, PubMed 16906480
  10. 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
    DOI 10.1016/j.cancergencyto.2005.08.012, 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
    DOI 10.1002/gcc.20168, 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
    DOI 10.1016/j.cancergencyto.2004.11.016, PubMed 15949565
  3. Brandal P, Busund LT, Heim S (2005)
    Chromosome abnormalities in juxtaglomerular cell tumors
    Cancer, 104 (3), 504-10
    DOI 10.1002/cncr.21205, PubMed 15968688
  4. 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
    DOI 10.1038/sj.onc.1208383, PubMed 15688027
  5. 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
    DOI 10.1002/path.1812, PubMed 16007576
  6. 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
    DOI 10.1073/pnas.0408454102, PubMed 15809428
  7. 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
    DOI 10.1016/j.semcancer.2004.09.006, PubMed 15613283
  8. 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
    DOI 10.1111/j.1365-2141.2005.05688.x, PubMed 16156854
  9. 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
    DOI 10.1111/j.1365-2141.2005.05706.x, 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
    DOI 10.1200/JCO.2004.11.014, PubMed 15226330
  2. Brandal P, Bjerkehagen B, Heim S (2004)
    Molecular cytogenetic characterization of tenosynovial giant cell tumors
    Neoplasia, 6 (5), 578-83
    DOI 10.1593/neo.04202, 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
    DOI 10.1038/sj.bjc.6601803, 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
    DOI 10.1158/0008-5472.can-03-3159, PubMed 15126341
  5. 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
    DOI 10.1002/gcc.20038, PubMed 15139002
  6. 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
    DOI 10.1002/cncr.20527, PubMed 15386312

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
    DOI 10.1016/s0165-4608(03)00190-0, 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
    DOI 10.2174/1566523034578302, 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
    DOI 10.1016/s0165-4608(03)00122-5, 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
    DOI 10.1016/s0165-4608(02)00846-4, 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
    DOI 10.1046/j.1365-2141.2003.04349.x, PubMed 12752097
  6. 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
    DOI 10.1002/ijc.10794, PubMed 12532419
  7. 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
    DOI 10.1002/gcc.10179, PubMed 12619158
  8. 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
    DOI 10.1016/s0046-8177(03)00345-9, PubMed 14562293
  9. 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
    DOI 10.1002/gcc.10263, PubMed 12939741
  10. 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
    DOI 10.1016/s0165-4608(03)00025-6, PubMed 12850374
  11. 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
    DOI 10.1034/j.1600-0609.2003.00133.x, PubMed 12950236
  12. 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
    DOI 10.1016/s1476-5586(03)80009-x, PubMed 12659690
  13. Teixeira MR, Pandis N, Heim S (2003)
    Multicentric mammary carcinoma: evidence of monoclonal proliferation
    Cancer, 97 (3), 715-7; author reply 717
    DOI 10.1002/cncr.11109, 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
    DOI 10.1186/1471-2407-2-5, 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
    DOI 10.1016/s0165-4608(01)00664-1, 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
    DOI 10.1002/gcc.10063, PubMed 11979555
  4. Ikonomou IM, Nesland JM, Schjølseth SA, Heim S, Delabie J (2002)
    Mantle cell lymphoma with Homer-Wright rosettes
    Virchows Arch, 442 (2), 179-82
    DOI 10.1007/s00428-002-0739-1, PubMed 12596071
  5. 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
    DOI 10.1002/gcc.10032, PubMed 11807988
  6. 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
    DOI 10.1002/gcc.10122, PubMed 12378529
  7. 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
    DOI 10.1002/gcc.10127, PubMed 12378528
  8. Teixeira MR, Pandis N, Heim S (2002)
    Cytogenetic clues to breast carcinogenesis
    Genes Chromosomes Cancer, 33 (1), 1-16
    DOI 10.1002/gcc.1206, PubMed 11746982

Publications 2001

  1. 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
    DOI 10.1002/ijc.1267, PubMed 11351302
  2. 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

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
    DOI 10.1002/1098-2264(2000)9999:9999<::AID-GCC1034>3.0.CO;2-O, PubMed 10992300
  2. 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
  3. 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
    DOI 10.1073/pnas.090013497, PubMed 10805796
  4. 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

Publications 1999

  1. 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
    DOI 10.1038/sj.bjc.6690643, PubMed 10487605
  2. 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
    DOI 10.1016/s0165-4608(99)00075-8, PubMed 10598145
  3. 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
    DOI 10.1002/(sici)1098-2264(199901)24:1<62::aid-gcc9>3.0.co;2-4, PubMed 9892110

Publications 1998

  1. 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
    DOI 10.1016/s0165-4608(98)00028-4, PubMed 9723030
  2. 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
    DOI 10.1016/s0165-4608(97)00363-4, PubMed 9546064
  3. 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
  4. 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
  5. 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
    DOI 10.1038/bjc.1998.315, PubMed 9667665

Publications 1997

  1. 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
    DOI 10.1002/(sici)1098-2264(199712)20:4<383::aid-gcc10>3.0.co;2-o, PubMed 9408755

Publications 1996

  1. 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
    DOI 10.1002/(SICI)1097-0215(19960410)66:2<191::AID-IJC9>3.0.CO;2-Y, PubMed 8603810

Publications 1995

  1. HAUGOM L (1995)
    AVENUES OF PARTICIPATION - FAMILY, POLITICS, AND NETWORKS IN URBAN QUARTERS OF CAIRO - SINGERMAN,D
    J. Peace Res., 32 (4), 500
    DOI 10.1177/0022343395032004042
  2. HAUGOM L (1995)
    DEMOCRACY WITHOUT DEMOCRATS - THE RENEWAL OF POLITICS IN THE MUSLIM WORLD - SALAME,G
    J. Peace Res., 32 (3), 377-378
    DOI 10.1177/0022343395032003021
  3. HAUGOM L (1995)
    DEMOCRACY AND ARAB POLITICAL-CULTURE - KEDOURIE,E
    J. Peace Res., 32 (3), 377-378
    DOI 10.1177/0022343395032003021
  4. 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
  5. 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
    DOI 10.1002/gcc.2870120304, PubMed 7536456

Publications 1994

  1. 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
    DOI 10.1016/0165-4608(94)90062-0, PubMed 8076343
  2. 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
    DOI 10.1002/ijc.2910580103, PubMed 8014018
  3. 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
    DOI 10.3892/ijo.5.6.1207, PubMed 21559699
 
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