IRIS
STORLAZZI, CLELIA TIZIANA
 Distribuzione geografica
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Continente #
NA - Nord America 7.921
EU - Europa 2.049
AS - Asia 919
SA - Sud America 46
AF - Africa 10
OC - Oceania 9
Continente sconosciuto - Info sul continente non disponibili 2
Totale 10.956
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Nazione #
US - Stati Uniti d'America 7.900
CN - Cina 557
SE - Svezia 548
DE - Germania 527
SG - Singapore 300
IT - Italia 262
GB - Regno Unito 210
UA - Ucraina 141
FI - Finlandia 138
RU - Federazione Russa 100
BE - Belgio 33
BR - Brasile 33
FR - Francia 32
IE - Irlanda 27
IN - India 19
CA - Canada 12
MX - Messico 9
VN - Vietnam 9
AU - Australia 7
IR - Iran 7
CZ - Repubblica Ceca 5
CO - Colombia 4
JP - Giappone 4
KZ - Kazakistan 4
MA - Marocco 4
TR - Turchia 4
BG - Bulgaria 3
EC - Ecuador 3
HR - Croazia 3
LT - Lituania 3
NL - Olanda 3
AR - Argentina 2
AT - Austria 2
CL - Cile 2
DK - Danimarca 2
EU - Europa 2
IL - Israele 2
IQ - Iraq 2
NG - Nigeria 2
NZ - Nuova Zelanda 2
OM - Oman 2
PT - Portogallo 2
RO - Romania 2
AL - Albania 1
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
CH - Svizzera 1
DZ - Algeria 1
EG - Egitto 1
HK - Hong Kong 1
HU - Ungheria 1
KR - Corea 1
LA - Repubblica Popolare Democratica del Laos 1
LV - Lettonia 1
LY - Libia 1
PH - Filippine 1
PK - Pakistan 1
PY - Paraguay 1
SA - Arabia Saudita 1
SI - Slovenia 1
SY - Repubblica araba siriana 1
TH - Thailandia 1
TN - Tunisia 1
VE - Venezuela 1
Totale 10.956
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Città #
Fairfield 1.216
Woodbridge 816
Ashburn 760
Chandler 679
Houston 554
Seattle 534
Cambridge 455
Nyköping 409
Ann Arbor 391
Wilmington 374
Jacksonville 370
Singapore 233
Bari 149
Lawrence 142
Roxbury 140
Nanjing 126
Beijing 118
New York 101
Des Moines 85
Princeton 84
Boardman 79
Los Angeles 78
Brooklyn 61
Inglewood 54
Dearborn 50
San Diego 43
Santa Clara 37
Nanchang 35
Brussels 33
Changsha 32
London 32
Dublin 27
Hebei 25
Shenyang 24
Jiaxing 22
Helsinki 18
Redwood City 17
Guangzhou 16
Tianjin 13
Jinan 12
Paris 12
Washington 12
Pune 11
Hefei 8
Toronto 8
Acton 7
Munich 7
Ningbo 7
Dong Ket 6
San Francisco 6
Suri 6
Wuhan 6
Zhengzhou 6
Boydton 5
Corigliano Calabro 5
Edinburgh 5
Frankfurt am Main 5
Grottaglie 5
Kilburn 5
Kunming 5
Norwalk 5
Shanghai 5
Belo Horizonte 4
Brescia 4
Brno 4
Falls Church 4
Milan 4
São Paulo 4
Tappahannock 4
Almaty 3
Auburn Hills 3
Avigliano 3
Bologna 3
Catania 3
Downham Market 3
Hanoi 3
Indiana 3
Ottawa 3
Perugia 3
Prescot 3
Rome 3
Seelze 3
Serrenti 3
Sofia 3
Taizhou 3
Triggiano 3
Yiwu 3
Zagreb 3
Aarhus 2
Adelaide 2
Baotou 2
Berlin 2
Capurso 2
Chengdu 2
Chiswick 2
Falkenstein 2
Foggia 2
Jinhua 2
Lisbon 2
Marseille 2
Totale 8.700
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Nome #
A complex rearrangement involving cryptic deletion of ETV6 and CDKN1B genes in a case of childhood acute lymphoblastic leukemia 337
A fluorescence in situ hybridization study of complex t(9;22) in two chronic myelocytic leukemia cases with a masked Philadelphia chromosome 154
Breakpoint characterization of der(9) deletions in chronic myeloid leukemia patients 141
A novel fusion 5'AFF3/3'BCL2 originated from a t(2;18)(q11.2;q21.33) translocation in follicular lymphoma 137
MYC-containing amplicons in acute myeloid leukemia: Genomic structures, evolution, and transcriptional consequences 133
t(3;12)(q26;q14) in polycythemia vera is associated with upregulation of the HMGA2 gene 127
Similar mechanisms formed ring markers containing chromosome 12 pericentromeric region in two patients with therapy-related acute myeloid leukemia 120
A novel chromosomal translocation t(3;7)(q26;q21)in myeloid leukemia resulting in overexpression of EVI1 120
Upregulation of the SOX5 by promoter swapping with the P2RY8 gene in primary splenic follicular lymphoma 117
Proteolysis of MOB1 by the ubiquitin ligase praja2 attenuates Hippo signalling and supports glioblastoma growth. 115
MYC-CONTAINING DOUBLE MINUTE CHROMOSOMES IN AML: ORIGIN, STRUCTURE AND TRANSCRIPTIONAL FEATURES 114
A novel chromosomal translocation t(3;7)(q26;q21) in myeloid leukemia resulting in overexpression of EVI1 113
Derivative chromosome 9 deletions in chronic myeloid leukemia are associated with loss of tumor suppressor genes 110
High RAD51 mRNA expression characterize estrogen receptor-positive/progesteron receptor-negative breast cancer and is associated with patient's outcome 108
Characterization of a hotspot region on chromosome 12 for amplification in ring chromosomes in atypical lipomatous tumors 107
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 104
Molecular cytogenetic characterization of a novel additional chromosomal aberration in blast crisis of a PH-positive chronic myeloid leukemia 102
Concomitant tetrasomy 3q and trisomy 18 in CD5(-), CD13(+) chronic lymphocytic leukemia 102
null 102
Deregulated expression of cryptochrome genes in human colorectal cancer 102
Novel and Rare Fusion Transcripts Involving Transcription Factors and Tumor Suppressor Genes in Acute Myeloid Leukemia 102
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. 101
A panel of partial chromosome paints and YAC probes specific for human chromosome 2 101
MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene 101
null 99
Genomic deletions on other chromosomes involved in variant t(9;22) chronic myeloid leukemia cases 98
ETV6 mutations and loss in AML-M0 97
Concomitant tetrasomy 3q and trisomy 18 in CD5- CD13+ chronic lymphocytic leukemia 97
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 96
Frequent NRG1 fusions in caucasian pulmonary mucinous adenocarcinoma predicted by Phospho-ErbB3 expression 94
Molecular Cytogenetic Characterization of a Complex Rearrangement Involving Chromosomes 9 and 22 in a Case of Ph Negative Chronic Myeloid Leukemia 93
null 93
Identification of RUNX1/AML1 as a classical tumor suppressor gene 92
CBFA2T2 and C20orf112: two novel fusion partners of RUNX1 in acute myeloid leukemia 91
Characterization of der(9) deletions in CML patients 90
NEW FUSION GENE INVOLVING EWSR1 IN ACUTE MYELOID LEUKEMIA. 89
Multiple EWSR1-WT1 and WT1-EWSR1 copies in two cases of desmoplastic round cell tumor 89
null 89
null 88
Inv(11)(p15q22)/NUP98-DDX10 fusion and isoforms in a new case of de novo acute myeloid leukemia 88
BL1391: an established cell line from a human malignant peripheral nerve sheath tumor with unique genomic features 88
Pre-B cell receptor-mediated cell cycle arrest in Philadelphia chromosome-positive acute lymphoblastic leukemia requires IKAROS function 87
Molecular cytogenetics characterization of a novel translocation involving chromosomes 17 and 19 in a Ph+ adult acute lymphoblastic leukemia 85
Amplification of the G allele at SNP rs6983267 in 8q24 amplicons in myeloid malignancies as cause of the lack of MYC overexpression? 85
A novel translocation t(2;9)(q14;p12) in AML-M2 with an uncommon phenotype: myeloperoxidase-positive and myeloid antigen-negative 85
null 85
Genomic organization and evolution of double minutes/homogeneously staining regions with MYC amplification in human cancer 85
Molecular analysis of the HuD gene in neuroendocrine lung cancers 84
Acute myeloblastic leukemia with minimal myeloid differentiation featuring a three-way translocation t(8;13;14) 84
Molecular cytogenetic resources specific for chromosome 12 84
Deletions on der(9) chromosome in adult Ph-positive acute lymphoblastic leukemia occur with a frequency similar to that observed in chronic myeloid leukemia 84
Late-appearing pseudocentric fission event during chronic myeloid leukemia progression 84
FISH analysis reveals frequent co-occurrence of 4q24/TET2 and 5q and/or 7q deletions. 82
Upregulation of MEL1 and FLJ42875 genes by position effect resulting from a t(1;2)(p36;p21) occurring during evolution of chronic myelomonocytic leukemia 82
The chimeric FUS/CREB3l2 gene is specific for low-grade fibromyxoid sarcoma 82
null 82
Constitutional ring chromosome 11 mosaicism in a Wilms tumor patient: Cytogenetic, molecular and clinico-pathological studies 81
Nuova linea cellulare e suoi usi. 81
Acute promyelocytic leukemia with additional chromosome abnormalities in a renal transplant case 80
FOSL1 as a candidate target gene for 11q12 rearrangements in desmoplastic fibroblastoma. 80
Episomal amplification of MYCN in a case of medulloblastoma 79
Methylation Density Pattern of KEAP1 Gene in Lung Cancer Cell Lines Detected by Quantitative Methylation Specific PCR and Pyrosequencing 79
FOXP1 and TP63 involvement in the progression of myelodysplastic syndrome with 5q- and additional cytogenetic abnormalities. 78
null 78
A Novel Fusion Gene, SS18L1/SSX1, in Synovial Sarcoma 78
A New Entity of Acute Myeloid Leukemia Driven By Epigenetic and Somatic Dis-Regulation of Uncx, a Novel Homeobox Transcription Factor Gene 77
Rearrangements of chromosome bands 15q12-q21 are secondary to HMGA2 deregulation in conventional lipoma. 77
A complex karyotype including a t(2;11) in a paediatric ependymoma: case report and review of the literature 77
Identification of a novel IGH-MMSET fusion transcript in a human myeloma cell line with the t(4;14)(p16.3;q32) chromosomal translocation 77
Cytogenetic analysis of 101 giant cell tumors of bone: nonrandom patterns of telomeric associations and other structural aberrations 75
Molecular cytogenetic resources for chromosome 4 and comparative analysis of phylogenetic chromosome IV in great apes 75
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. 75
Double CEBPE-IGH rearrangement due to chromosome duplication and cryptic insertion in an adult with B-cell acute lymphoblastic leukemia. 74
Alternative promoters drive the expression of the gene encoding the mouse axonal glycoprotein F3/contactin 74
MYC-Containing Double Minute Chromosomes: Origin, Structure and Impact upon Transcriptome in Acute Myeloid Leukemia Patients 74
Evolution of Chromosome Y in primates 74
null 74
Identification of a commonly amplified 4.3 Mb region with overexpression of C8FW, but not MYC in MYC-containing double minutes in myeloid malignancies 73
t(5;6;12 ) associated with resistance to imatinib mesylate in chronic myeloid leukemia 73
Genomic organization and evolution of double minutes/homogeneously staining regions with MYC amplification in human cancer 73
Assignment to chromosome 12q24.33, gene organization and splicing of the human KRAB/FPB containing zinc finger gene ZNF84 73
Gene expression deregulation by KRAS G12D and G12V in a BRAF V600E context 71
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 71
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 71
Molecular cytogenetic characterization of an ins(4;X) occurring as the sole abnormality in an aggressive, poorly differentiated soft tissue sarcoma 71
A novel t(2;10)(q31;p12) balanced translocation in acute myeloid leukemia. 70
null 70
IKAROS Deletions Dictate a Unique Gene Expression Signature in Patients with Adult B-Cell Acute Lymphoblastic Leukemia. 70
Fusion of the FUS and BBF2H7 genes in low grade fibromyxoid sarcoma 69
Gene amplification as double minutes or homogeneously staining regions in solid tumors: Origin and structure 68
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) 66
Rearrangement of the COL12A1 and COL4A5 genes in subungual exostosis: molecular cytogenetic delineation of the tumor-specific translocationt(X;6)(q13-14;q22) 66
Rare recurrent t(15;21) translocations disrupting RUNX1 in myeloid leukemia. 64
Ring Chromosomes and Low-grade Gene Amplification in an Atypical Lipomatous Tumor with Minimal Nuclear Atypia 63
Linear and circular PVT1 in hematological malignancies and immune response: two faces of the same coin. 63
Identification and characterization of mouse orthologs of the AMMECR1 and FACL4 genes deleted in AMME syndrome: orthology of Xq22.3 and MmuXF1-F3 62
Novel rearrangement of chromosome band 22q11.2 causing 22q11 microdeletion syndrome-like phenotype and rhabdoid tumor of the kidney 62
Molecular characterization of a complex karyotype revealed cryptic dletion of the ETV6 and CDKN1B genes on 12p in the case of childood B-ALL. 61
air (apoptosis-induced regulator) expression and its sequence localization in human genome 61
CDKN2A/B Alterations Impair Prognosis in Adult BCR-ABL1-Positive Acute Lymphoblastic Leukemia Patients. 59
Totale 8.968
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Categoria #
all - tutte 49.532
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 49.532
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.777 0 0 0 0 0 199 377 390 357 187 178 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
2022/20231.790 276 208 125 159 216 235 20 195 262 11 47 36
2023/2024835 42 105 39 53 48 154 13 260 15 13 9 84
2024/2025665 74 42 205 79 120 145 0 0 0 0 0 0
Totale 11.265