F. Micci

发表

NDRG1-PLAG1 and TRPS1-PLAG1 Fusion Genes in Chondroid Syringoma

L. Gorunova, I. Panagopoulos, S. Heim, 2020, Cancer Genomics & Proteomics.

Deregulation of HMGA2 in an aggressive angiomyxoma with t(11;12)(q23;q15)

B. Bjerkehagen, I. Panagopoulos, S. Heim, 2006, Virchows Archiv.

Fusion genes in angiomatoid fibrous histiocytoma.

F. Mertens, P. Bacchini, N. Mandahl, 2007, Cancer letters.

Trisomy 7 in postoperative spindle cell nodules.

V. Abeler, B. Bjerkehagen, S. Heim, 2007, Cancer genetics and cytogenetics.

Soft Tissue Tumors: Aggressive angiomyxoma

F. Micci, P. Brandal, 2008 .

Detection of a t(1;22)(q23;q12) translocation leading to an EWSR1‐PBX1 fusion gene in a myoepithelioma

S. Skjeldal, B. Bjerkehagen, L. Gorunova, 2008, Genes, chromosomes & cancer.

Molecular Genetics of Uterine Sarcomas

B. Davidson, F. Micci, 2019, eLS.

RNA‐sequencing identifies novel GREB1‐NCOA2 fusion gene in a uterine sarcoma with the chromosomal translocation t(2;8)(p25;q13)

L. Gorunova, B. Davidson, I. Panagopoulos, 2017, Genes, chromosomes & cancer.

The EPH Receptor Bs (EPHBs) Promoters are Unmethylated in Colon and Ovarian Cancers

R. Lothe, G. Lind, J. Nesland, 2007, Epigenetics.

Upregulation of INS-IGF2 read-through expression and identification of a novel INS-IGF2 splice variant in insulinomas.

L. E. Johannessen, I. Panagopoulos, I. Gladhaug, 2016, Oncology reports.

DNA methylation profiling of ovarian carcinomas and their in vitro models identifies HOXA9, HOXB5, SCGB3A1, and CRABP1 as novel targets

Qinghua Wu, R. Lothe, J. Nesland, 2007, Molecular Cancer.

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

L. Gorunova, I. Panagopoulos, S. Heim, 2020, Cancer Genomics & Proteomics.

Fusion of the COL4A5 Gene With NR2F2-AS1 in a Hemangioma Carrying a t(X;15)(q22;q26) Chromosomal Translocation

L. Gorunova, I. Panagopoulos, S. Heim, 2020, Cancer Genomics & Proteomics.

Genetic Characterization of Myoid Hamartoma of the Breast

L. Gorunova, I. Panagopoulos, S. Heim, 2019, Cancer Genomics & Proteomics.

PAN3–PSMA2 fusion resulting from a novel t(7;13)(p14;q12) chromosome translocation in a myelodysplastic syndrome that evolved into acute myeloid leukemia

L. Gorunova, I. Panagopoulos, S. Heim, 2018, Experimental Hematology & Oncology.

A novel truncated form of HMGA2 in tumors of the ovaries.

B. Davidson, C. Tropé, I. Panagopoulos, 2016, Oncology letters.

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).

B. Bjerkehagen, I. Panagopoulos, M. Teixeira, 2003, Cancer genetics and cytogenetics.

Expression and clinical role of the dipeptidyl peptidases DPP8 and DPP9 in ovarian carcinoma

B. Davidson, I. Panagopoulos, A. Staff, 2018, Virchows Archiv.

Genomic imbalances in endometrial adenocarcinomas — Comparison of DNA ploidy, karyotyping and comparative genomic hybridization

V. Abeler, H. Danielsen, G. Kristensen, 2012, Molecular oncology.

Diagnostic utility of Restriction Spectrum Imaging in the characterization of the peritumoral brain zone in glioblastoma: Analysis of overall and progression-free survival.

O. Geier, A. Server, E. Vik-Mo, 2020, European journal of radiology.

Transcriptomic Profiling of Tumor Aggressiveness in Sporadic Nonfunctioning Pancreatic Neuroendocrine Neoplasms

E. Hovig, D. Vodák, I. Gladhaug, 2016, Pancreas.

ZC3H7B-BCOR high-grade endometrial stromal sarcomas: a report of 17 cases of a newly defined entity

M. Ladanyi, C. Antonescu, E. Oliva, 2017, Modern Pathology.

G‐banding and molecular cytogenetic analyses of marginal zone lymphoma

J. Delabie, H. Holte, S. Heim, 2005, British journal of haematology.

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

L. Gorunova, I. Panagopoulos, S. Heim, 2022, Cancer Genomics & Proteomics.

Fusion of the genes BRD8 and PHF1 in endometrial stromal sarcoma

M. Nucci, L. Gorunova, I. Panagopoulos, 2017, Genes, chromosomes & cancer.

Molecular characteristics of uterine sarcomas

B. Davidson, F. Micci, 2017, Expert review of molecular diagnostics.

MEAF6/PHF1 is a recurrent gene fusion in endometrial stromal sarcoma.

X. Matías-Guiu, L. Gorunova, B. Davidson, 2014, Cancer letters.

Cytogenetic and molecular analyses of 291 gastrointestinal stromal tumors: site-specific cytogenetic evolution as evidence of pathogenetic heterogeneity

B. Bjerkehagen, L. Gorunova, J. Berner, 2022, Oncotarget.

[The lived experience of family member caring for a person affected by Alzheimer's disease: preliminary results].

J. Sansoni, E. Vellone, F. Micci, 2000, Professioni infermieristiche.

An Unbalanced Chromosome Translocation Between 7p22 and 12q13 Leads to ACTB-GLI1 Fusion in Pericytoma

L. Gorunova, I. Panagopoulos, S. Heim, 2020, AntiCancer Research.

Acute Myeloid Leukemia with inv(8)(p11q13)

B. Johansson, F. Mitelman, I. Panagopoulos, 2000, Leukemia & lymphoma.

High-throughput sequencing identifies an NFIA/CBFA2T3 fusion gene in acute erythroid leukemia with t(1;16)(p31;q24)

I. Panagopoulos, S. Heim, F. Micci, 2012, Leukemia.

An Adult Patient with Early Pre-B Acute Lymphoblastic Leukemia with t(12;17)(p13;q21)/ZNF384-TAF15

F. Micci, N. Viniou, P. Diamantopoulos, 2018, In Vivo.

Endometrial Carcinoma: Molecular Cytogenetics and Transcriptomic Profile

V. Vitelli, B. Davidson, A.G.Z. Eriksson, 2022, Cancers.

Fusion of ZMYND8 and RELA Genes in Acute Erythroid Leukemia

I. Panagopoulos, J. Buechner, S. Heim, 2013, PloS one.

M-FISH cytogenetic Analysis of Non-Hodgkin Lymphomas with t(14;18)(q32;q21) and add(1)(p36) as a Secondary Abnormality Shows that the Extra Material Often Comes from Chromosome Arm 17q

J. Delabie, H. Holte, S. Heim, 2002, Leukemia & lymphoma.

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

L. Gorunova, B. Davidson, I. Panagopoulos, 2022, Cancer Genomics & Proteomics.

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

L. Gorunova, I. Panagopoulos, S. Heim, 2022, Cancer Genomics & Proteomics.

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

L. Gorunova, I. Panagopoulos, S. Heim, 2022, Cancer Genomics & Proteomics.

Fusion of the HMGA2 and BNC2 Genes in Uterine Leiomyoma With t(9;12)(p22;q14)

L. Gorunova, I. Panagopoulos, S. Heim, 2022, In Vivo.

Extraskeletal myxoid chondrosarcoma: multimodal diagnosis and identification of a new cytogenetic subgroup characterized by t(9;17)(q22;q11)

J. Nesland, A. Berner, B. Bjerkehagen, 1999, Virchows Archiv.

Translocation t(1;16)(p31;q24) rearranging CBFA2T3 is specific for acute erythroid leukemia

S. Heim, F. Micci, L. Haugom, 2011, Leukemia.

Cytogenetic and Molecular Study of an Adult Sclerosing Rhabdomyosarcoma of the Extremity: MYOD1-mutation and Clonal Evolution

B. Bjerkehagen, L. Gorunova, I. Panagopoulos, 2020, Cancer Genomics & Proteomics.

Identification of an EPC2-PHF1 fusion transcript in low-grade endometrial stromal sarcoma

L. Gorunova, B. Davidson, I. Panagopoulos, 2018, Oncotarget.

FAM53B truncation caused by t(10;19)(q26;q13) chromosome translocation in acute lymphoblastic leukemia

L. Gorunova, I. Panagopoulos, S. Heim, 2017, Oncology letters.

Molecular cytogenetic characterization of t(14;19)(q32;p13), a new recurrent translocation in B cell malignancies

J. Delabie, K. Beiske, I. Panagopoulos, 2007, Virchows Archiv.

Cytogenetic follow-up in a case with a primary cutaneous melanoma and five metastatic lesions.

P. Grammatico, G. del Porto, C. Catricalà, 1998, Pigment cell research.

Functional temozolomide sensitivity testing of patient-specific glioblastoma stem cell cultures is predictive of clinical outcome

I. Panagopoulos, E. Vik-Mo, I. Langmoen, 2022, Translational oncology.

ZRF4, a combi-molecule with increased efficacy as compared with the individual components in chronic lymphocytic leukemia lymphocytes in vitro

S. Heim, F. Micci, L. Haugom, 2011 .

Determination of gross α-activity in urine by microprecipitation with LaF3 and α-spectrometry

F. Micci, C. Testa, G. Jia, 1994 .

Are keratoacanthomas variants of squamous cell carcinomas? A comparison of chromosomal aberrations by comparative genomic hybridization.

L. Bolund, M. Mattingsdal, C. Proby, 2006, The Journal of investigative dermatology.

Reverse painting of microdissected chromosome 19 markers in ovarian carcinoma identifies a complex rearrangement map

R. Lothe, R. Skotheim, V. Abeler, 2009, Genes, chromosomes & cancer.

Differential propagation of stroma and cancer stem cells dictates tumorigenesis and multipotency

J. Behnan, M. Joel, B. Stangeland, 2016, Oncogene.

Fusion of the Paired Box 3 (PAX3) and Myocardin (MYOCD) Genes in Pediatric Rhabdomyosarcoma

L. Gorunova, I. Panagopoulos, S. Heim, 2021, Cancer Genomics & Proteomics.

Characterization of supernumerary rings and giant marker chromosomes in well-differentiated lipomatous tumors by a combination of G-banding, CGH, M-FISH, and chromosome- and locus-specific FISH

B. Bjerkehagen, M. Teixeira, S. Heim, 2002, Cytogenetic and Genome Research.

t(12;13)(q14;q31) leading to HMGA2 upregulation in acute myeloid leukaemia

R. Roberto, I. Panagopoulos, S. Heim, 2012, British journal of haematology.

The study was approved by the Regional Ethics Committee and the Norwegian Directorate of Health.

R. Roberto, I. Panagopoulos, S. Heim, 2012 .

Replication-induced DNA damage after PARP inhibition causes G2 delay, and cell line-dependent apoptosis, necrosis and multinucleation

T. Stokke, Idun Dale Rein, S. Patzke, 2015, Cell cycle.

Tumors of the Female Genital Organs

S. Heim, F. Micci, 2015 .

Genomic aberrations in borderline ovarian tumors

R. Lothe, V. Abeler, T. Ahlquist, 2010, Journal of Translational Medicine.

Chromosome 19 rearrangements in ovarian carcinomas: Zinc finger genes are particularly targeted

R. Lothe, R. Skotheim, B. Davidson, 2014, Genes, chromosomes & cancer.

Fusion genes with ALK as recurrent partner in ependymoma-like gliomas: a new brain tumor entity?

L. Gorunova, D. Scheie, I. Panagopoulos, 2015, Neuro-oncology.

Genomic imbalances are involved in miR-30c and let-7a deregulation in ovarian tumors: implications for HMGA2 expression

B. Davidson, C. Tropé, I. Panagopoulos, 2017, Oncotarget.

Molecular characterization of carcinosarcomas arising in the uterus and ovaries

B. Davidson, S. Heim, F. Micci, 2019, Oncotarget.

HMGA2 expression pattern and TERT mutations in tumors of the vulva

B. Davidson, C. Tropé, I. Panagopoulos, 2015, Oncology reports.

Rare KMT2A-ELL and Novel ZNF56-KMT2A Fusion Genes in Pediatric T-cell Acute Lymphoblastic Leukemia

I. Panagopoulos, S. Heim, K. Andersen, 2021, Cancer Genomics & Proteomics.

Loss of 11p11 is a frequent and early event in sporadic nonfunctioning pancreatic neuroendocrine neoplasms

L. Gorunova, I. Gladhaug, S. Heim, 2014, Oncology reports.

Recurrent Fusion of the GRB2 Associated Binding Protein 1 (GAB1) Gene With ABL Proto-oncogene 1 (ABL1) in Benign Pediatric Soft Tissue Tumors

L. Gorunova, I. Panagopoulos, S. Heim, 2020, Cancer Genomics & Proteomics.

Genomic aberration patterns and expression profiles of squamous cell carcinomas of the vulva

V. Abeler, H. Danielsen, B. Davidson, 2013, Genes, chromosomes & cancer.

Novel fusion genes and chimeric transcripts in ependymal tumors

Ioannis Panagopoulos, David Scheie, Torstein R Meling, 2016, Genes, chromosomes & cancer.

Sequential combination of karyotyping and RNA-sequencing in the search for cancer-specific fusion genes.

L. Gorunova, I. Panagopoulos, S. Heim, 2014, The international journal of biochemistry & cell biology.

Identification of novel cyclin gene fusion transcripts in endometrioid ovarian carcinomas

B. Davidson, I. Panagopoulos, S. Heim, 2018, International journal of cancer.

Frequent translocations of 11q13.2 and 19p13.2 in ovarian cancer

Amke Caliebe, A. Caliebe, N. Maass, 2014, Genes, chromosomes & cancer.

Molecular pathogenesis and prognostication of "low‐grade'' and "high‐grade" endometrial stromal sarcoma

I. Panagopoulos, S. Heim, F. Micci, 2020, Genes, chromosomes & cancer.

Whole-Transcriptome Sequencing Identifies Novel IRF2BP2-CDX1 Fusion Gene Brought about by Translocation t(1;5)(q42;q32) in Mesenchymal Chondrosarcoma

R. Lothe, R. Skotheim, B. Bjerkehagen, 2012, PloS one.

Identification of chromosomal breakpoints of cancer-specific translocations by rolling circle amplification and long-distance inverse PCR.

S. Heim, F. Micci, J. Thorsen, 2011, Cancer genetics.

Molecular Cytogenetic Analysis of a Gliosarcoma with Osseous Metaplasia

L. Gorunova, D. Scheie, T. Meling, 2011, Cytogenetic and Genome Research.

Myelodysplastic syndrome with a t(2;11)(p21;q23-24) and translocation breakpoint close to miR-125b-1.

R. Roberto, G. Tjønnfjord, S. Heim, 2012, Cancer genetics.

Genomic aberrations in carcinomas of the uterine corpus

V. Abeler, G. Kristensen, M. Teixeira, 2004, Genes, chromosomes & cancer.

MGMT Gene Promoter Methylation Status – Assessment of Two Pyrosequencing Kits and Three Methylation-specific PCR Methods for their Predictive Capacity in Glioblastomas

L. E. Johannessen, T. Myklebust, I. Panagopoulos, 2018, Cancer Genomics & Proteomics.

Identification of the TAF15-ZNF384 fusion gene in two new cases of acute lymphoblastic leukemia with a t(12;17)(p13;q12).

G. Trøen, S. Heim, F. Micci, 2011, Cancer genetics.

Cytogenetic and molecular profile of endometrial stromal sarcoma

L. Gorunova, L. E. Johannessen, B. Davidson, 2016, Genes, chromosomes & cancer.

RNA sequencing identifies fusion of the EWSR1 and YY1 genes in mesothelioma with t(14;22)(q32;q12)

L. Gorunova, B. Davidson, I. Panagopoulos, 2013, Genes, chromosomes & cancer.

Tumor Spreading to the Contralateral Ovary in Bilateral Ovarian Carcinoma Is a Late Event in Clonal Evolution

R. Lothe, V. Abeler, T. Ahlquist, 2009, Journal of oncology.

Breakpoint characterization of the der(19)t(11;19)(q13;p13) in the ovarian cancer cell line SKOV‐3

R. Siebert, O. Janssen, R. Ullmann, 2013, Genes, chromosomes & cancer.

Consistent numerical chromosome aberrations in thecofibromas of the ovary

V. Abeler, H. Danielsen, C. Tropé, 2008, Virchows Archiv.

Molecular cytogenetic characterization of desmoid tumors.

R. Lothe, S. Knuutila, B. Bjerkehagen, 2003, Cancer genetics and cytogenetics.

Brief Gene Mapping Reports A / B / C / D / E / F / G

C. Auffray, A. Zinn, K. Kratochwil, 2002, Cytogenetic and Genome Research.

High-resolution analysis of genetic stability of human adipose tissue stem cells cultured to senescence

O. Myklebost, L. Meza-Zepeda, P. Collas, 2007, Journal of cellular and molecular medicine.

Low Frequency of ESRRA–C11orf20 Fusion Gene in Ovarian Carcinomas

B. Davidson, C. Tropé, I. Panagopoulos, 2014, PLoS biology.

Pyrosequencing Analysis of MGMT Promoter Methylation in Meningioma

L. Gorunova, L. E. Johannessen, I. Panagopoulos, 2018, Cancer Genomics & Proteomics.

Unrestrained ESCRT-III drives micronuclear catastrophe and chromosome fragmentation

S. Grellscheid, P. Collas, E. Skarpen, 2020, Nature Cell Biology.

Unrestrained ESCRT-III drives chromosome fragmentation and micronuclear catastrophe

S. Grellscheid, P. Collas, E. Skarpen, 2019, bioRxiv.

A novel TCF3-HLF fusion transcript in acute lymphoblastic leukemia with a t(17;19)(q22;p13).

I. Panagopoulos, S. Heim, F. Micci, 2012, Cancer genetics.

Fusion of the ZC3H7B and BCOR genes in endometrial stromal sarcomas carrying an X;22‐translocation

B. Bjerkehagen, L. Gorunova, B. Davidson, 2013, Genes, chromosomes & cancer.

Mutation analysis and genomic imbalances of cells found in effusion fluids from patients with ovarian cancer

B. Davidson, I. Panagopoulos, S. Heim, 2020, Oncology letters.

The microRNA miR-192/215 family is upregulated in mucinous ovarian carcinomas

B. Davidson, C. Tropé, I. Panagopoulos, 2018, Scientific Reports.

Pairwise comparison of genomic imbalances between primary and recurrent well differentiated liposarcomas.

B. Bjerkehagen, S. Heim, F. Micci, 2007, Cancer genetics and cytogenetics.

Consistent rearrangement of chromosomal band 6p21 with generation of fusion genes JAZF1/PHF1 and EPC1/PHF1 in endometrial stromal sarcoma.

B. Bjerkehagen, I. Panagopoulos, S. Heim, 2006, Cancer research.

Novel Fusion of MYST/Esa1-Associated Factor 6 and PHF1 in Endometrial Stromal Sarcoma

B. Bjerkehagen, L. Gorunova, B. Davidson, 2012, PloS one.

Recurrent fusion transcripts in squamous cell carcinomas of the vulva

B. Davidson, C. Tropé, I. Panagopoulos, 2017, Oncotarget.

Genomic profile of ovarian carcinomas

V. Abeler, B. Davidson, C. Tropé, 2014, BMC Cancer.

MGMT promoter methylation is a rare epigenetic change in malignant effusions

B. Davidson, I. Panagopoulos, F. Micci, 2019, Cytopathology : official journal of the British Society for Clinical Cytology.

Cross‐species color banding characterization of chromosomal rearrangements in leukemias with incomplete G‐band karyotypes

M. Teixeira, S. Heim, F. Micci, 1999, Genes, chromosomes & cancer.

Combined RxFISH/G-banding allows refined karyotyping of solid tumors

B. Bjerkehagen, M. Teixeira, S. Heim, 1999, Human Genetics.

Molecular characterization of the MLL-SEPT6 fusion gene in acute myeloid leukemia: identification of novel fusion transcripts and cloning of genomic breakpoint junctions

M. Teixeira, S. Heim, F. Micci, 2008, Haematologica.

Lymphoplasmacytic lymphoma and marginal zone lymphoma in the bone marrow: paratrabecular involvement as an important distinguishing feature.

J. Delabie, G. Trøen, F. Micci, 2014, American journal of clinical pathology.

Involvement of DPP9 in gene fusions in serous ovarian carcinoma

R. Skotheim, B. Davidson, C. Tropé, 2017, BMC Cancer.

Expression pattern of the septin gene family in acute myeloid leukemias with and without MLL-SEPT fusion genes.

L. Shih, M. Teixeira, C. Mellink, 2010, Leukemia research.

Bilateral ovarian carcinomas differ in the expression of metastasis-related genes

R. Skotheim, B. Davidson, C. Tropé, 2016, Oncology letters.

t(3;21)(q22;q22) leading to truncation of the RYK gene in atypical chronic myeloid leukemia.

K. Beiske, I. Panagopoulos, G. Tjønnfjord, 2009, Cancer letters.

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

L. Osnes, I. Panagopoulos, J. Buechner, 2021, Cancer Genomics & Proteomics.

Werner Schmid, 1930–2002

C. Auffray, A. Zinn, K. Kratochwil, 2002, Cytogenetic and Genome Research.

Array‐CGH analysis of microdissected chromosome 19 markers in ovarian carcinoma identifies candidate target genes

R. Lothe, R. Skotheim, V. Abeler, 2010, Genes, chromosomes & cancer.

I. Panagopoulos, S. Heim, K. Andersen, 2021, AntiCancer Research.

Primary mediastinal choriocarcinoma in a female patient: Case report and review of the literature

T. Morgan, M. Moffitt, F. Micci, 2018, Gynecologic oncology reports.

Pathogenetic mechanisms in endometrial stromal sarcoma

S. Heim, F. Micci, 2007, Cytogenetic and Genome Research.

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

L. Gorunova, I. Panagopoulos, S. Heim, 2023, In Vivo.

Generation and characterization of an immortalized human mesenchymal stromal cell line.

Stine H. Kresse, O. Myklebost, S. Lorenz, 2014, Stem cells and development.

A universal assay for detection of oncogenic fusion transcripts by oligo microarray analysis

Torbjørn Rognes, R. Lothe, R. Skotheim, 2009, Molecular Cancer.

Fusion of the genes ataxin 2 like, ATXN2L, and Janus kinase 2, JAK2, in cutaneous CD4 positive T-cell lymphoma

L. Gorunova, K. Beiske, I. Panagopoulos, 2017, Oncotarget.

VOLIN and KJON—Two novel hyperdiploid myeloma cell lines

L. Meza-Zepeda, E. Tian, A. Waage, 2016, Genes, chromosomes & cancer.

Unrestrained ESCRT-III drives micronuclear catastrophe and chromosome fragmentation

S. Grellscheid, P. Collas, E. Skarpen, 2020, Nature Cell Biology.

TYRO3 Truncation Resulting From a t(10;15)(p11;q15) Chromosomal Translocation in Pediatric Acute Myeloid Leukemia

I. Panagopoulos, S. Heim, F. Micci, 2020, AntiCancer Research.

Novel GTF2I–PDGFRB and IKZF1–TYW1 fusions in pediatric leukemia with normal karyotype

S. Lorenz, I. Panagopoulos, T. Hveem, 2019, Experimental Hematology & Oncology.

RUNX1-PDCD6 fusion resulting from a novel t(5;21)(p15;q22) chromosome translocation in myelodysplastic syndrome secondary to chronic lymphocytic leukemia

L. Gorunova, I. Panagopoulos, S. Heim, 2018, PloS one.

Cytogenetic characterization of tumors of the vulva and vagina

V. Abeler, M. Teixeira, S. Heim, 2003, Genes, chromosomes & cancer.

Genetic Pathways in Peritoneal Mesothelioma Tumorigenesis

L. Gorunova, B. Davidson, I. Panagopoulos, 2023, Cancer Genomics & Proteomics.

Recurrent 8q11-13 Aberrations Leading to PLAG1 Rearrangements, Including Novel Chimeras HNRNPA2B1::PLAG1 and SDCBP::PLAG1, in Lipomatous Tumors

L. Gorunova, I. Panagopoulos, S. Heim, 2023, Cancer Genomics & Proteomics.

Acute Undifferentiated Leukemia With a Balanced t(5;10)(q35;p12) Resulting in Fusion of HNRNPH1 With MLLT10

I. Panagopoulos, S. Heim, K. Andersen, 2023, Cancer Genomics & Proteomics.

Genomic characterization of ependymomas reveals 6q loss as the most common aberration

L. Gorunova, D. Scheie, T. Meling, 2014, Oncology reports.

DEK-NUP214-Fusion Identified by RNA-Sequencing of an Acute Myeloid Leukemia with t(9;12)(q34;q15).

L. Gorunova, I. Panagopoulos, G. Tjønnfjord, 2017, Cancer genomics & proteomics.

Complete cytogenetic characterization of the human breast cancer cell line MA11 combining G-banding, comparative genomic hybridization, multicolor fluorescence in situ hybridization, RxFISH, and chromosome-specific painting.

M. Teixeira, S. Heim, F. Micci, 2001, Cancer genetics and cytogenetics.

Expressions of miR-30c and let-7a are inversely correlated with HMGA2 expression in squamous cell carcinoma of the vulva

B. Davidson, C. Tropé, I. Panagopoulos, 2016, Oncotarget.

Detailed genome-wide screening for inter- and intrachromosomal abnormalities by sequential G-banding and RxFISH color banding of the same metaphase cells.

M. Teixeira, S. Heim, F. Micci, 2000, Cancer genetics and cytogenetics.

Novel insights into the pathogenesis of follicular lymphoma by molecular profiling of localized and systemic disease forms.

A. Rosenwald, W. Klapper, E. Hoster, 2023, Leukemia.

t(3;21)(q22;q22) leading to truncation of the RYK gene in atypical chronic myeloid leukemia.

K. Beiske, I. Panagopoulos, G. Tjønnfjord, 2009, Cancer letters.

Molecular characteristics of uterine sarcomas

B. Davidson, F. Micci, 2017, Expert review of molecular diagnostics.

Pathogenetic Dichotomy in Angioleiomyoma

L. Gorunova, I. Panagopoulos, W. Kildal, 2023, Cancer Genomics & Proteomics.

Novel MYCBP::EHD2 and RUNX1::ZNF780A Fusion Genes in T-cell Acute Lymphoblastic Leukemia

I. Panagopoulos, S. Heim, K. Andersen, 2022, Cancer Genomics & Proteomics.

Chromosome Translocation t(10;19)(q26;q13) in a CIC-sarcoma

L. Gorunova, I. Panagopoulos, S. Heim, 2023, In Vivo.

Genetic characterization of intramuscular myxomas

I. Panagopoulos, M. Lund-Iversen, K. Andersen, 2024, Pathology oncology research : POR.

NUP214 fusion genes in acute leukemias: genetic characterization of rare cases

K. Andersen, F. Micci, S. Spetalen, 2024, Frontiers in Oncology.