IRIS
STORLAZZI, CLELIA TIZIANA
 Distribuzione geografica
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Continente #
NA - Nord America 7.788
EU - Europa 1.989
AS - Asia 622
OC - Oceania 7
AF - Africa 6
SA - Sud America 6
Continente sconosciuto - Info sul continente non disponibili 2
Totale 10.420
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Nazione #
US - Stati Uniti d'America 7.774
SE - Svezia 551
CN - Cina 525
DE - Germania 519
IT - Italia 248
GB - Regno Unito 206
UA - Ucraina 141
FI - Finlandia 130
RU - Federazione Russa 90
SG - Singapore 51
FR - Francia 30
BE - Belgio 27
IE - Irlanda 27
IN - India 19
MX - Messico 9
VN - Vietnam 9
AU - Australia 6
CA - Canada 5
CZ - Repubblica Ceca 5
TR - Turchia 4
BG - Bulgaria 3
HR - Croazia 3
IR - Iran 3
JP - Giappone 3
CL - Cile 2
CO - Colombia 2
EU - Europa 2
KZ - Kazakistan 2
NG - Nigeria 2
RO - Romania 2
AL - Albania 1
AR - Argentina 1
AT - Austria 1
BA - Bosnia-Erzegovina 1
BR - Brasile 1
DZ - Algeria 1
EG - Egitto 1
IL - Israele 1
LA - Repubblica Popolare Democratica del Laos 1
LU - Lussemburgo 1
LY - Libia 1
NL - Olanda 1
NZ - Nuova Zelanda 1
OM - Oman 1
PH - Filippine 1
PT - Portogallo 1
SA - Arabia Saudita 1
SI - Slovenia 1
TH - Thailandia 1
TN - Tunisia 1
Totale 10.420
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Città #
Fairfield 1.216
Woodbridge 816
Ashburn 760
Chandler 686
Houston 554
Seattle 534
Cambridge 455
Nyköping 412
Ann Arbor 391
Wilmington 374
Jacksonville 370
Bari 149
Lawrence 143
Roxbury 140
Nanjing 125
Beijing 116
New York 101
Des Moines 85
Princeton 84
Boardman 71
Los Angeles 66
Brooklyn 61
Inglewood 54
Dearborn 50
San Diego 43
Nanchang 35
Changsha 32
Singapore 31
London 30
Brussels 27
Dublin 27
Hebei 25
Shenyang 23
Jiaxing 22
Redwood City 17
Guangzhou 13
Tianjin 13
Jinan 12
Paris 12
Washington 12
Pune 11
Helsinki 10
Hefei 8
Acton 7
Ningbo 7
Dong Ket 6
San Francisco 6
Suri 6
Wuhan 6
Zhengzhou 6
Boydton 5
Brno 5
Corigliano Calabro 5
Edinburgh 5
Kilburn 5
Kunming 5
Norwalk 5
Shanghai 5
Brescia 4
Falls Church 4
Munich 4
Tappahannock 4
Auburn Hills 3
Avigliano 3
Bologna 3
Downham Market 3
Hanoi 3
Indiana 3
Milan 3
Perugia 3
Prescot 3
Rome 3
Seelze 3
Serrenti 3
Sofia 3
Taizhou 3
Toronto 3
Triggiano 3
Yiwu 3
Zagreb 3
Baotou 2
Berlin 2
Chengdu 2
Chiswick 2
Foggia 2
Frankfurt am Main 2
Jinhua 2
Marseille 2
Medellín 2
Melbourne 2
Palermo 2
Pisa 2
Reggio Calabria 2
Romainville 2
San Antonio 2
Santiago 2
Shenzhen 2
Sydney 2
Tokyo 2
Wandsworth 2
Totale 8.410
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Nome #
A complex rearrangement involving cryptic deletion of ETV6 and CDKN1B genes in a case of childhood acute lymphoblastic leukemia 336
A fluorescence in situ hybridization study of complex t(9;22) in two chronic myelocytic leukemia cases with a masked Philadelphia chromosome 147
Breakpoint characterization of der(9) deletions in chronic myeloid leukemia patients 136
A novel fusion 5'AFF3/3'BCL2 originated from a t(2;18)(q11.2;q21.33) translocation in follicular lymphoma 132
MYC-containing amplicons in acute myeloid leukemia: Genomic structures, evolution, and transcriptional consequences 128
t(3;12)(q26;q14) in polycythemia vera is associated with upregulation of the HMGA2 gene 126
Similar mechanisms formed ring markers containing chromosome 12 pericentromeric region in two patients with therapy-related acute myeloid leukemia 117
Upregulation of the SOX5 by promoter swapping with the P2RY8 gene in primary splenic follicular lymphoma 115
A novel chromosomal translocation t(3;7)(q26;q21)in myeloid leukemia resulting in overexpression of EVI1 115
Proteolysis of MOB1 by the ubiquitin ligase praja2 attenuates Hippo signalling and supports glioblastoma growth. 113
A novel chromosomal translocation t(3;7)(q26;q21) in myeloid leukemia resulting in overexpression of EVI1 111
High RAD51 mRNA expression characterize estrogen receptor-positive/progesteron receptor-negative breast cancer and is associated with patient's outcome 107
Derivative chromosome 9 deletions in chronic myeloid leukemia are associated with loss of tumor suppressor genes 107
Characterization of a hotspot region on chromosome 12 for amplification in ring chromosomes in atypical lipomatous tumors 105
Bone marrow ectopic expression of a non-coding RNA in childhood T-cell acute lymphoblastic leukemia with a novel t(2;11)(q11.2;p15.1) translocation 102
null 102
Concomitant tetrasomy 3q and trisomy 18 in CD5(-), CD13(+) chronic lymphocytic leukemia 101
MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene 100
Deregulated expression of cryptochrome genes in human colorectal cancer 100
Two alternatively spliced 5'BCR/3'JAK2 fusion transcripts in a myeloproliferative neoplasm with a three-way t(9;18;22)(p23;p11.3;q11.2) translocation. 99
Molecular cytogenetic characterization of a novel additional chromosomal aberration in blast crisis of a PH-positive chronic myeloid leukemia 99
null 99
A panel of partial chromosome paints and YAC probes specific for human chromosome 2 98
Concomitant tetrasomy 3q and trisomy 18 in CD5- CD13+ chronic lymphocytic leukemia 95
Genomic deletions on other chromosomes involved in variant t(9;22) chronic myeloid leukemia cases 95
ETV6 mutations and loss in AML-M0 93
null 93
Frequent NRG1 fusions in caucasian pulmonary mucinous adenocarcinoma predicted by Phospho-ErbB3 expression 92
Identification of RUNX1/AML1 as a classical tumor suppressor gene 90
CBFA2T2 and C20orf112: two novel fusion partners of RUNX1 in acute myeloid leukemia 90
A 76-kb duplicon maps close to the BCR gene on chromosome 22 and the ABL gene on chromosome 9: possible involvement in the genesis of the Philadelphia chromosome translocation 90
Molecular Cytogenetic Characterization of a Complex Rearrangement Involving Chromosomes 9 and 22 in a Case of Ph Negative Chronic Myeloid Leukemia 89
null 89
null 88
Pre-B cell receptor-mediated cell cycle arrest in Philadelphia chromosome-positive acute lymphoblastic leukemia requires IKAROS function 86
Multiple EWSR1-WT1 and WT1-EWSR1 copies in two cases of desmoplastic round cell tumor 86
NEW FUSION GENE INVOLVING EWSR1 IN ACUTE MYELOID LEUKEMIA. 85
Inv(11)(p15q22)/NUP98-DDX10 fusion and isoforms in a new case of de novo acute myeloid leukemia 85
null 85
Characterization of der(9) deletions in CML patients 84
Molecular analysis of the HuD gene in neuroendocrine lung cancers 83
Molecular cytogenetics characterization of a novel translocation involving chromosomes 17 and 19 in a Ph+ adult acute lymphoblastic leukemia 83
Late-appearing pseudocentric fission event during chronic myeloid leukemia progression 83
Amplification of the G allele at SNP rs6983267 in 8q24 amplicons in myeloid malignancies as cause of the lack of MYC overexpression? 82
null 82
Molecular cytogenetic resources specific for chromosome 12 81
Upregulation of MEL1 and FLJ42875 genes by position effect resulting from a t(1;2)(p36;p21) occurring during evolution of chronic myelomonocytic leukemia 81
The chimeric FUS/CREB3l2 gene is specific for low-grade fibromyxoid sarcoma 81
FISH analysis reveals frequent co-occurrence of 4q24/TET2 and 5q and/or 7q deletions. 80
Constitutional ring chromosome 11 mosaicism in a Wilms tumor patient: Cytogenetic, molecular and clinico-pathological studies 80
Acute myeloblastic leukemia with minimal myeloid differentiation featuring a three-way translocation t(8;13;14) 80
Genomic organization and evolution of double minutes/homogeneously staining regions with MYC amplification in human cancer 80
Deletions on der(9) chromosome in adult Ph-positive acute lymphoblastic leukemia occur with a frequency similar to that observed in chronic myeloid leukemia 79
BL1391: an established cell line from a human malignant peripheral nerve sheath tumor with unique genomic features 79
null 78
A novel translocation t(2;9)(q14;p12) in AML-M2 with an uncommon phenotype: myeloperoxidase-positive and myeloid antigen-negative 78
Acute promyelocytic leukemia with additional chromosome abnormalities in a renal transplant case 77
MYC-CONTAINING DOUBLE MINUTE CHROMOSOMES IN AML: ORIGIN, STRUCTURE AND TRANSCRIPTIONAL FEATURES 77
FOXP1 and TP63 involvement in the progression of myelodysplastic syndrome with 5q- and additional cytogenetic abnormalities. 76
Episomal amplification of MYCN in a case of medulloblastoma 76
FOSL1 as a candidate target gene for 11q12 rearrangements in desmoplastic fibroblastoma. 76
Nuova linea cellulare e suoi usi. 75
A Novel Fusion Gene, SS18L1/SSX1, in Synovial Sarcoma 75
Methylation Density Pattern of KEAP1 Gene in Lung Cancer Cell Lines Detected by Quantitative Methylation Specific PCR and Pyrosequencing 75
Cytogenetic analysis of 101 giant cell tumors of bone: nonrandom patterns of telomeric associations and other structural aberrations 74
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. 74
null 74
A New Entity of Acute Myeloid Leukemia Driven By Epigenetic and Somatic Dis-Regulation of Uncx, a Novel Homeobox Transcription Factor Gene 73
Identification of a novel IGH-MMSET fusion transcript in a human myeloma cell line with the t(4;14)(p16.3;q32) chromosomal translocation 73
Molecular cytogenetic resources for chromosome 4 and comparative analysis of phylogenetic chromosome IV in great apes 72
Identification of a commonly amplified 4.3 Mb region with overexpression of C8FW, but not MYC in MYC-containing double minutes in myeloid malignancies 72
Rearrangements of chromosome bands 15q12-q21 are secondary to HMGA2 deregulation in conventional lipoma. 72
A complex karyotype including a t(2;11) in a paediatric ependymoma: case report and review of the literature 72
t(5;6;12 ) associated with resistance to imatinib mesylate in chronic myeloid leukemia 71
Assignment to chromosome 12q24.33, gene organization and splicing of the human KRAB/FPB containing zinc finger gene ZNF84 71
Alternative promoters drive the expression of the gene encoding the mouse axonal glycoprotein F3/contactin 71
Gene expression deregulation by KRAS G12D and G12V in a BRAF V600E context 70
Double CEBPE-IGH rearrangement due to chromosome duplication and cryptic insertion in an adult with B-cell acute lymphoblastic leukemia. 70
null 70
Genomic organization and evolution of double minutes/homogeneously staining regions with MYC amplification in human cancer 70
MYC-Containing Double Minute Chromosomes: Origin, Structure and Impact upon Transcriptome in Acute Myeloid Leukemia Patients 70
The PAX5 gene is frequently rearranged in BCR-ABL1-positive acute lymphoblastic leukemia but is not associated with outcome. a report on behalf of the GIMEMA acute leukemia working party 69
IKAROS Deletions Dictate a Unique Gene Expression Signature in Patients with Adult B-Cell Acute Lymphoblastic Leukemia. 69
Novel and Rare Fusion Transcripts Involving Transcription Factors and Tumor Suppressor Genes in Acute Myeloid Leukemia 69
Fusion of the FUS and BBF2H7 genes in low grade fibromyxoid sarcoma 68
Evolution of Chromosome Y in primates 68
Molecular cytogenetic characterization of an ins(4;X) occurring as the sole abnormality in an aggressive, poorly differentiated soft tissue sarcoma 67
A novel t(2;10)(q31;p12) balanced translocation in acute myeloid leukemia. 66
Gene amplification as double minutes or homogeneously staining regions in solid tumors: Origin and structure 65
A 76kb interchromosomal duplicon maps close to BCR gene on chromosome 22 and to ABL gene on chromosome 9: possible involvement in the genesis of the Philadelphia-chromosome translocation 65
Rearrangement of the COL12A1 and COL4A5 genes in subungual exostosis: molecular cytogenetic delineation of the tumor-specific translocationt(X;6)(q13-14;q22) 65
Identification and molecular characterization of recurrent genomic deletions on 7p12 in the IKZF1 gene in a large cohort of BCR-ABL1-positive acute lymphoblastic leukemia patients: on behalf of Gruppo Italiano Malattie Ematologiche dell'Adulto Acute Leukemia Working Party (GIMEMA AL WP) 64
Ring Chromosomes and Low-grade Gene Amplification in an Atypical Lipomatous Tumor with Minimal Nuclear Atypia 62
Novel rearrangement of chromosome band 22q11.2 causing 22q11 microdeletion syndrome-like phenotype and rhabdoid tumor of the kidney 62
Identification and characterization of mouse orthologs of the AMMECR1 and FACL4 genes deleted in AMME syndrome: orthology of Xq22.3 and MmuXF1-F3 60
Rare recurrent t(15;21) translocations disrupting RUNX1 in myeloid leukemia. 59
Novel chromosomal translocation (17;22)(q12;q12) in a case of myelodisplastic syndrome characterized with signs of hemolytic anemia at presentation. 57
air (apoptosis-induced regulator) expression and its sequence localization in human genome 57
null 57
A NOVEL FUSION 5'AFF3/3'BCL2 ORIGINATED FROM A t(2;18)(Q11.2-Q21.33) TRANSLOCATION IN FOLLICULAR LYMPHOMA 55
Totale 8.630
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Categoria #
all - tutte 43.821
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 43.821
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20203.030 429 127 94 327 276 199 377 390 357 187 178 89
2020/20211.409 129 132 125 113 157 82 106 125 100 181 66 93
2021/20221.246 45 199 8 41 87 101 95 50 65 81 189 285
2022/20231.805 277 210 126 160 219 237 20 197 264 11 48 36
2023/2024842 43 105 39 53 48 155 13 264 15 13 9 85
2024/202574 74 0 0 0 0 0 0 0 0 0 0 0
Totale 10.696