Publications published since 1983 from OUS - Section for Cancer Cytogenetics

141 publications found

Publications 2020

  1. 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
    DOI 10.1007/s00428-020-02842-4, PubMed 32533344
  2. 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
  3. 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
  4. 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
  5. 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
  6. 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
  7. 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
  8. 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
  9. 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
  10. 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, 1-26 (in press)
    DOI 10.1080/13854046.2020.1794045, PubMed 32729777
  11. 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
    DOI 10.1111/apa.15188, PubMed 31977119
  12. 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)
    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
  7. 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
  8. 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
  9. 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
  10. 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
  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. 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
  2. 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
  3. 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
  4. 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
  5. 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
  6. 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
  7. 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
  8. 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
  9. 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

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. 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
  7. 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
  8. 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
  9. 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
  10. Nyquist KB, Thorsen J, Zeller B, Haaland A, Trøen G, Heim S, Micci F (2011)
    Identification of the TAF15-ZNF384 fusion gene in two new cases of acute lymphoblastic leukemia with a t(12;17)(p13;q12)
    Cancer Genet, 204 (3), 147-52
    DOI 10.1016/j.cancergen.2011.01.003, PubMed 21504714
  11. 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
  12. 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
  13. 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
  14. 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. 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

Publications 2003

  1. 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. 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

Publications 1995

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