Ludmila Gorunova
Position: research
Phone: 22934467
Email:
 

Author network for Ludmila Gorunova by COREMINE medical


Publications 2017

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
PubMed 28193293

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
PubMed 28476785

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
PubMed 28160572

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 (in press)
PubMed 28498454

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
PubMed 28454383

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
PubMed 28179318

Publications 2016

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
PubMed 27588119

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
PubMed 27219024

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
PubMed 27401149

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
PubMed 26857357

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
PubMed 27469327

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
PubMed 27633981

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
PubMed 27667292

Publications 2015

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
PubMed 25795305

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
PubMed 26043835

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
PubMed 25875009

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
PubMed 25621995

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
PubMed 26202160

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
PubMed 26432191

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
PubMed 26708416

Panagopoulos I, Gorunova L, Kerndrup G, Spetalen S, Tierens A, Osnes LT, Andersen K, Müller LS, Hellebostad M, Zeller B, Heim S (2015)
Rare MLL-ELL fusion transcripts in childhood acute myeloid leukemia-association with young age and myeloid sarcomas?
Exp Hematol Oncol, 5, 8
PubMed 26949571

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
PubMed 26170993

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
PubMed 26186352

Publications 2014

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
PubMed 25018013

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
PubMed 24530230

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
PubMed 24939246

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
PubMed 25176350

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
PubMed 24604026

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
PubMed 24839999

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
PubMed 24950227

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
PubMed 25484136

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
PubMed 24863361

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
PubMed 24798186

Publications 2013

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
PubMed 23877199

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
PubMed 24068373

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
PubMed 23580382

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
PubMed 23630070

Publications 2012

Gorunova L (2012)
Psychological determinants of information searching activity
Work, 41 Suppl 1, 2882-6
PubMed 22317156

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
PubMed 23185413

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
PubMed 22761769

Publications 2011

Dahlback HS, Brandal P, Gorunova L, Widing E, Meling TR, Krossnes BK, Heim S (2011)
Genomic aberrations in pediatric gliomas and embryonal tumors
Genes Chromosomes Cancer, 50 (10), 788-99
PubMed 21717527

Dahlback HS, Gorunova L, Brandal P, Scheie D, Helseth E, Meling TR, Heim S (2011)
Genomic aberrations in diffuse low-grade gliomas
Genes Chromosomes Cancer, 50 (6), 409-20
PubMed 21412929

Dahlback HS, Gorunova L, Micci F, Scheie D, Brandal P, Meling TR, Heim S (2011)
Molecular cytogenetic analysis of a gliosarcoma with osseous metaplasia
Cytogenet Genome Res, 134 (2), 88-95
PubMed 21555877

Gorunova L, Bjerkehagen B, Heim S (2011)
Paratesticular leiomyoma with a der(14)t(12;14)(q15;q24)
Cancer Genet, 204 (8), 465-8
PubMed 21962898

Publications 2009

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

Gebre-Medhin S, Broberg K, Jonson T, Gorunova L, von Steyern FV, Brosjö O, Jin Y, Gisselsson D, Panagopoulos I, Mandahl N, Mertens F (2009)
Telomeric associations correlate with telomere length reduction and clonal chromosome aberrations in giant cell tumor of bone
Cytogenet Genome Res, 124 (2), 121-7
PubMed 19420923

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

Norum OJ, Bruland ØS, Gorunova L, Berg K (2009)
Photochemical internalization of bleomycin before external-beam radiotherapy improves locoregional control in a human sarcoma model
Int J Radiat Oncol Biol Phys, 75 (3), 878-85
PubMed 19665318

Publications 2008

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

Publications 2005

Behboudi A, Winnes M, Gorunova L, van den Oord JJ, Mertens F, Enlund F, Stenman G (2005)
Clear cell hidradenoma of the skin-a third tumor type with a t(11;19)--associated TORC1-MAML2 gene fusion
Genes Chromosomes Cancer, 43 (2), 202-5
PubMed 15729701

Heidenblad M, Lindgren D, Veltman JA, Jonson T, Mahlamäki EH, Gorunova L, van Kessel AG, Schoenmakers EF, Höglund M (2005)
Microarray analyses reveal strong influence of DNA copy number alterations on the transcriptional patterns in pancreatic cancer: implications for the interpretation of genomic amplifications
Oncogene, 24 (10), 1794-801
PubMed 15688027

Stewénius Y, Gorunova L, Jonson T, Larsson N, Höglund M, Mandahl N, Mertens F, Mitelman F, Gisselsson D (2005)
Structural and numerical chromosome changes in colon cancer develop through telomere-mediated anaphase bridges, not through mitotic multipolarity
Proc Natl Acad Sci U S A, 102 (15), 5541-6
PubMed 15809428

Publications 2004

Gisselsson D, Gorunova L, Höglund M, Mandahl N, Elfving P (2004)
Telomere shortening and mitotic dysfunction generate cytogenetic heterogeneity in a subgroup of renal cell carcinomas
Br J Cancer, 91 (2), 327-32
PubMed 15162157

Heidenblad M, Schoenmakers EF, Jonson T, Gorunova L, Veltman JA, van Kessel AG, Höglund M (2004)
Genome-wide array-based comparative genomic hybridization reveals multiple amplification targets and novel homozygous deletions in pancreatic carcinoma cell lines
Cancer Res, 64 (9), 3052-9
PubMed 15126341

Publications 2003

Fadl-Elmula I, Gorunova L, Mandahl N, Heim S (2003)
Chromosomal abnormalities in inflammatory pseudotumor of the urinary bladder
Cancer Genet Cytogenet, 143 (2), 169-71
PubMed 12781452

Jonson T, Heidenblad M, Håkansson P, Gorunova L, Johansson B, Fioretos T, Höglund M (2003)
Pancreatic carcinoma cell lines with SMAD4 inactivation show distinct expression responses to TGFB1
Genes Chromosomes Cancer, 36 (4), 340-52
PubMed 12619158

Publications 2002

Hallén M, Parada LA, Gorunova L, Pålsson B, Dictor M, Johansson B (2002)
Cytogenetic abnormalities in a hemangiopericytoma of the spleen
Cancer Genet Cytogenet, 136 (1), 62-5
PubMed 12165454

Heidenblad M, Jonson T, Mahlamäki EH, Gorunova L, Karhu R, Johansson B, Höglund M (2002)
Detailed genomic mapping and expression analyses of 12p amplifications in pancreatic carcinomas reveal a 3.5-Mb target region for amplification
Genes Chromosomes Cancer, 34 (2), 211-23
PubMed 11979555

Mahlamäki EH, Bärlund M, Tanner M, Gorunova L, Höglund M, Karhu R, Kallioniemi A (2002)
Frequent amplification of 8q24, 11q, 17q, and 20q-specific genes in pancreatic cancer
Genes Chromosomes Cancer, 35 (4), 353-8
PubMed 12378529

Publications 2001

Fadl-Elmula I, Kytölä S, Pan Y, Lui WO, Derienzo G, Forsberg L, Mandahl N, Gorunova L, Bergerheim US, Heim S, Larsson C (2001)
Characterization of chromosomal abnormalities in uroepithelial carcinomas by G-banding, spectral karyotyping and FISH analysis
Int J Cancer, 92 (6), 824-31
PubMed 11351302

Gorunova L, Dawiskiba S, Andrén-Sandberg A, Höglund M, Johansson B (2001)
Extensive cytogenetic heterogeneity in a benign retroperitoneal schwannoma
Cancer Genet Cytogenet, 127 (2), 148-54
PubMed 11425455

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

Fadl-Elmula I, Gorunova L, Mandahl N, Elfving P, Lundgren R, Mitelman F, Heim S (2000)
Karyotypic characterization of urinary bladder transitional cell carcinomas
Genes Chromosomes Cancer, 29 (3), 256-65
PubMed 10992300

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

Gisselsson D, Pettersson L, Höglund M, Heidenblad M, Gorunova L, Wiegant J, Mertens F, Dal Cin P, Mitelman F, Mandahl N (2000)
Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity
Proc Natl Acad Sci U S A, 97 (10), 5357-62
PubMed 10805796

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

Fadl-Elmula I, Gorunova L, Mandahl N, Elfving P, Lundgren R, Mitelman F, Heim S (1999)
Cytogenetic monoclonality in multifocal uroepithelial carcinomas: evidence of intraluminal tumour seeding
Br J Cancer, 81 (1), 6-12
PubMed 10487605

Fadl-Elmula I, Gorunova L, Mandahl N, Elfving P, Lundgren R, Rademark C, Heim S (1999)
Cytogenetic analysis of upper urinary tract transitional cell carcinomas
Cancer Genet Cytogenet, 115 (2), 123-7
PubMed 10598145

Gorunova L, Parada LA, Limon J, Jin Y, Hallén M, Hägerstrand I, Iliszko M, Wajda Z, Johansson B (1999)
Nonrandom chromosomal aberrations and cytogenetic heterogeneity in gallbladder carcinomas
Genes Chromosomes Cancer, 26 (4), 312-21
PubMed 10534766

Jonson T, Gorunova L, Dawiskiba S, Andrén-Sandberg A, Stenman G, ten Dijke P, Johansson B, Höglund M (1999)
Molecular analyses of the 15q and 18q SMAD genes in pancreatic cancer
Genes Chromosomes Cancer, 24 (1), 62-71
PubMed 9892110

Publications 1998

Fadl-Elmula I, Bonaldi L, Gorunova L, Mandahl N, Elfving P, Heim S (1998)
Cytogenetic heterogeneity in a second primary radiation-induced bladder carcinoma: ten karyotypically unrelated clones
Cancer Genet Cytogenet, 105 (2), 134-7
PubMed 9723030

Fadl-Elmula I, Gorunova L, Lundgren R, Mandahl N, Forsby N, Mitelman F, Heim S (1998)
Chromosomal abnormalities in two bladder carcinomas with secondary squamous cell differentiation
Cancer Genet Cytogenet, 102 (2), 125-30
PubMed 9546064

Fadl-Elmula I, Gorunova L, Mandahl N, Elfving P, Heim S (1998)
Chromosome abnormalities in squamous cell carcinoma of the urethra
Genes Chromosomes Cancer, 23 (1), 72-3
PubMed 9714000

Gorunova L, Höglund M, Andrén-Sandberg A, Dawiskiba S, Jin Y, Mitelman F, Johansson B (1998)
Cytogenetic analysis of pancreatic carcinomas: intratumor heterogeneity and nonrandom pattern of chromosome aberrations
Genes Chromosomes Cancer, 23 (2), 81-99
PubMed 9739011

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

Höglund M, Gorunova L, Jonson T, Dawiskiba S, Andrén-Sandberg A, Stenman G, Johansson B (1998)
Cytogenetic and FISH analyses of pancreatic carcinoma reveal breaks in 18q11 with consistent loss of 18q12-qter and frequent gain of 18p
Br J Cancer, 77 (11), 1893-9
PubMed 9667665

Publications 1997

Mahlamäki EH, Höglund M, Gorunova L, Karhu R, Dawiskiba S, Andrén-Sandberg A, Kallioniemi OP, Johansson B (1997)
Comparative genomic hybridization reveals frequent gains of 20q, 8q, 11q, 12p, and 17q, and losses of 18q, 9p, and 15q in pancreatic cancer
Genes Chromosomes Cancer, 20 (4), 383-91
PubMed 9408755

Publications 1996

Pandis N, Idvall I, Bardi G, Jin Y, Gorunova L, Mertens F, Olsson H, Ingvar C, Beroukas K, Mitelman F, Heim S (1996)
Correlation between karyotypic pattern and clincopathologic features in 125 breast cancer cases
Int J Cancer, 66 (2), 191-6
PubMed 8603810

Publications 1995

Gorunova L, Johansson B, Dawiskiba S, Andrén-Sandberg A, Jin Y, Mandahl N, Heim S, Mitelman F (1995)
Massive cytogenetic heterogeneity in a pancreatic carcinoma: fifty-four karyotypically unrelated clones
Genes Chromosomes Cancer, 14 (4), 259-66
PubMed 8605114

Gorunova L, Johansson B, Dawiskiba S, Andrén-Sandberg A, Mandahl N, Heim S, Mitelman F (1995)
Cytogenetically detected clonal heterogeneity in a duodenal adenocarcinoma
Cancer Genet Cytogenet, 82 (2), 146-50
PubMed 7664244

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

Pandis N, Jin Y, Gorunova L, Petersson C, Bardi G, Idvall I, Johansson B, Ingvar C, Mandahl N, Mitelman F (1995)
Chromosome analysis of 97 primary breast carcinomas: identification of eight karyotypic subgroups
Genes Chromosomes Cancer, 12 (3), 173-85
PubMed 7536456

Publications 1994

Bardi G, Gorunova L, Limon J, Nedoszytko B, Johansson B, Pandis N, Mandahl N, Bak-Jensen E, Andrén-Sandberg A, Rys J (1994)
Abnormal karyotypes in three carcinomas of the gallbladder
Cancer Genet Cytogenet, 76 (1), 15-8
PubMed 8076343

Gorunova L, Mertens F, Mandahl N, Jonsson N, Persson B, Heim S, Mitelman F (1994)
Cytogenetic heterogeneity in a clear cell hidradenoma of the skin
Cancer Genet Cytogenet, 77 (1), 26-32
PubMed 7923079

Johansson B, Bardi G, Pandis N, Gorunova L, Bäckman PL, Mandahl N, Dawiskiba S, Andrén-Sandberg A, Heim S, Mitelman F (1994)
Karyotypic pattern of pancreatic adenocarcinomas correlates with survival and tumour grade
Int J Cancer, 58 (1), 8-13
PubMed 8014018

Petersson C, Johansson B, Pandis N, Gorunova L, Ingvar C, Idvall I, Mandahl N, Mitelman F (1994)
Clonal chromosome-aberrations in fibrocystic breast disease-associated with increased risk of cancer
Int J Oncol, 5 (6), 1207-10
PubMed 21559699