IRIS
STORLAZZI, CLELIA TIZIANA
 Distribuzione geografica
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Continente #
NA - Nord America 10.420
AS - Asia 3.833
EU - Europa 3.760
SA - Sud America 1.015
AF - Africa 186
OC - Oceania 13
Continente sconosciuto - Info sul continente non disponibili 3
Totale 19.230
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Nazione #
US - Stati Uniti d'America 10.247
SG - Singapore 1.605
IT - Italia 965
CN - Cina 896
BR - Brasile 792
DE - Germania 682
SE - Svezia 559
RU - Federazione Russa 496
HK - Hong Kong 466
GB - Regno Unito 277
VN - Vietnam 245
FR - Francia 202
FI - Finlandia 198
UA - Ucraina 154
IN - India 125
BD - Bangladesh 91
AR - Argentina 82
CA - Canada 80
IQ - Iraq 65
CI - Costa d'Avorio 57
MX - Messico 53
ID - Indonesia 46
TR - Turchia 44
JP - Giappone 40
CO - Colombia 39
BE - Belgio 34
IE - Irlanda 34
ZA - Sudafrica 34
EC - Ecuador 32
PL - Polonia 31
PK - Pakistan 30
VE - Venezuela 26
NL - Olanda 25
MA - Marocco 22
UZ - Uzbekistan 22
CL - Cile 20
AT - Austria 19
ES - Italia 19
SA - Arabia Saudita 19
PH - Filippine 18
TN - Tunisia 17
IR - Iran 15
LT - Lituania 13
MY - Malesia 13
AE - Emirati Arabi Uniti 12
DZ - Algeria 12
AU - Australia 11
JM - Giamaica 10
KE - Kenya 10
PY - Paraguay 9
CZ - Repubblica Ceca 8
EG - Egitto 8
JO - Giordania 7
AZ - Azerbaigian 6
ET - Etiopia 6
IL - Israele 6
KR - Corea 6
NP - Nepal 6
PE - Perù 6
DK - Danimarca 5
HN - Honduras 5
KZ - Kazakistan 5
LY - Libia 5
OM - Oman 5
TH - Thailandia 5
AL - Albania 4
BG - Bulgaria 4
CH - Svizzera 4
CR - Costa Rica 4
DO - Repubblica Dominicana 4
HR - Croazia 4
KG - Kirghizistan 4
LB - Libano 4
NI - Nicaragua 4
PS - Palestinian Territory 4
PT - Portogallo 4
SY - Repubblica araba siriana 4
UY - Uruguay 4
AM - Armenia 3
BA - Bosnia-Erzegovina 3
BH - Bahrain 3
BN - Brunei Darussalam 3
BO - Bolivia 3
GR - Grecia 3
KH - Cambogia 3
NG - Nigeria 3
PA - Panama 3
RO - Romania 3
SN - Senegal 3
SO - Somalia 3
AO - Angola 2
BS - Bahamas 2
BY - Bielorussia 2
EU - Europa 2
GT - Guatemala 2
NZ - Nuova Zelanda 2
RS - Serbia 2
AF - Afghanistan, Repubblica islamica di 1
BB - Barbados 1
BF - Burkina Faso 1
Totale 19.207
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Città #
Ashburn 1.224
Fairfield 1.216
Singapore 821
Woodbridge 816
Chandler 679
Houston 572
Seattle 542
San Jose 505
Hong Kong 462
Cambridge 455
Nyköping 409
Ann Arbor 391
Wilmington 375
Jacksonville 371
Milan 311
Beijing 287
Los Angeles 186
Bari 171
New York 164
Lawrence 142
Roxbury 140
Lauterbourg 132
Nanjing 128
Dallas 119
Rome 107
Boardman 87
Des Moines 86
Santa Clara 86
Princeton 84
Ho Chi Minh City 81
Brooklyn 80
Moscow 79
São Paulo 76
Munich 67
Helsinki 61
Hanoi 59
Abidjan 57
Inglewood 54
Dearborn 50
San Diego 44
London 43
Columbus 42
Falkenstein 40
Nanchang 35
Buffalo 34
Council Bluffs 34
Brussels 33
Chicago 33
Dublin 33
Tokyo 33
Changsha 32
Frankfurt am Main 32
Rio de Janeiro 31
Atlanta 28
Jakarta 28
Orem 28
Figino 26
Shenyang 26
Baghdad 25
Hebei 25
Montreal 24
Warsaw 24
Denver 22
Jiaxing 22
Paris 22
Toronto 21
San Francisco 20
Bologna 19
Tashkent 19
Belo Horizonte 17
Dhaka 17
Phoenix 17
Redwood City 17
Turku 17
Curitiba 16
Guangzhou 16
Pune 16
Washington 16
Campinas 15
Chennai 15
Johannesburg 15
The Dalles 15
Medellín 14
Nuremberg 14
Tianjin 14
Turin 14
Boston 13
Brasília 13
Jinan 13
Poplar 13
Salvador 13
Caracas 12
Mexico City 12
Quito 12
Vienna 12
Amsterdam 11
Istanbul 11
Naples 11
Biên Hòa 10
Buenos Aires 10
Totale 13.041
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Nome #
A complex rearrangement involving cryptic deletion of ETV6 and CDKN1B genes in a case of childhood acute lymphoblastic leukemia 386
MYC-CONTAINING DOUBLE MINUTE CHROMOSOMES IN AML: ORIGIN, STRUCTURE AND TRANSCRIPTIONAL FEATURES 239
A fluorescence in situ hybridization study of complex t(9;22) in two chronic myelocytic leukemia cases with a masked Philadelphia chromosome 235
MYC-containing amplicons in acute myeloid leukemia: Genomic structures, evolution, and transcriptional consequences 212
Breakpoint characterization of der(9) deletions in chronic myeloid leukemia patients 210
A novel fusion 5'AFF3/3'BCL2 originated from a t(2;18)(q11.2;q21.33) translocation in follicular lymphoma 210
A novel chromosomal translocation t(3;7)(q26;q21)in myeloid leukemia resulting in overexpression of EVI1 192
A novel chromosomal translocation t(3;7)(q26;q21) in myeloid leukemia resulting in overexpression of EVI1 184
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 178
A panel of partial chromosome paints and YAC probes specific for human chromosome 2 171
t(3;12)(q26;q14) in polycythemia vera is associated with upregulation of the HMGA2 gene 167
Deregulated expression of cryptochrome genes in human colorectal cancer 166
Derivative chromosome 9 deletions in chronic myeloid leukemia are associated with loss of tumor suppressor genes 163
Novel and Rare Fusion Transcripts Involving Transcription Factors and Tumor Suppressor Genes in Acute Myeloid Leukemia 162
Similar mechanisms formed ring markers containing chromosome 12 pericentromeric region in two patients with therapy-related acute myeloid leukemia 161
CircRNAs and Fusion-circRNAs in cancer: New players in an old game 161
Characterization of a hotspot region on chromosome 12 for amplification in ring chromosomes in atypical lipomatous tumors 159
BL1391: an established cell line from a human malignant peripheral nerve sheath tumor with unique genomic features 158
Nuova linea cellulare e suoi usi. 157
Proteolysis of MOB1 by the ubiquitin ligase praja2 attenuates Hippo signalling and supports glioblastoma growth. 155
Frequent NRG1 fusions in caucasian pulmonary mucinous adenocarcinoma predicted by Phospho-ErbB3 expression 154
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 152
Upregulation of the SOX5 by promoter swapping with the P2RY8 gene in primary splenic follicular lymphoma 151
Multiple EWSR1-WT1 and WT1-EWSR1 copies in two cases of desmoplastic round cell tumor 151
circPVT1 and PVT1/AKT3 show a role in cell proliferation, apoptosis, and tumor subtype-definition in small cell lung cancer 150
MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene 150
A novel translocation t(2;9)(q14;p12) in AML-M2 with an uncommon phenotype: myeloperoxidase-positive and myeloid antigen-negative 150
NEW FUSION GENE INVOLVING EWSR1 IN ACUTE MYELOID LEUKEMIA. 149
Acute myeloblastic leukemia with minimal myeloid differentiation featuring a three-way translocation t(8;13;14) 149
High RAD51 mRNA expression characterize estrogen receptor-positive/progesteron receptor-negative breast cancer and is associated with patient's outcome 146
Genomic organization and evolution of double minutes/homogeneously staining regions with MYC amplification in human cancer 146
A New Entity of Acute Myeloid Leukemia Driven By Epigenetic and Somatic Dis-Regulation of Uncx, a Novel Homeobox Transcription Factor Gene 145
Concomitant tetrasomy 3q and trisomy 18 in CD5(-), CD13(+) chronic lymphocytic leukemia 144
Molecular cytogenetic characterization of a novel additional chromosomal aberration in blast crisis of a PH-positive chronic myeloid leukemia 143
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 140
Methylation Density Pattern of KEAP1 Gene in Lung Cancer Cell Lines Detected by Quantitative Methylation Specific PCR and Pyrosequencing 140
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. 139
A complex karyotype including a t(2;11) in a paediatric ependymoma: case report and review of the literature 139
MYC-Containing Double Minute Chromosomes: Origin, Structure and Impact upon Transcriptome in Acute Myeloid Leukemia Patients 139
ETV6 mutations and loss in AML-M0 137
Genomic deletions on other chromosomes involved in variant t(9;22) chronic myeloid leukemia cases 137
Concomitant tetrasomy 3q and trisomy 18 in CD5- CD13+ chronic lymphocytic leukemia 136
air (apoptosis-induced regulator) expression and its sequence localization in human genome 135
CBFA2T2 and C20orf112: two novel fusion partners of RUNX1 in acute myeloid leukemia 134
Molecular Cytogenetic Characterization of a Complex Rearrangement Involving Chromosomes 9 and 22 in a Case of Ph Negative Chronic Myeloid Leukemia 133
Acute promyelocytic leukemia with additional chromosome abnormalities in a renal transplant case 133
Characterization of der(9) deletions in CML patients 132
Deletions on der(9) chromosome in adult Ph-positive acute lymphoblastic leukemia occur with a frequency similar to that observed in chronic myeloid leukemia 132
FOSL1 as a candidate target gene for 11q12 rearrangements in desmoplastic fibroblastoma. 131
Alternative promoters drive the expression of the gene encoding the mouse axonal glycoprotein F3/contactin 129
Amplification of the G allele at SNP rs6983267 in 8q24 amplicons in myeloid malignancies as cause of the lack of MYC overexpression? 128
Genomic organization and evolution of double minutes/homogeneously staining regions with MYC amplification in human cancer 128
Identification of RUNX1/AML1 as a classical tumor suppressor gene 127
Inv(11)(p15q22)/NUP98-DDX10 fusion and isoforms in a new case of de novo acute myeloid leukemia 127
Molecular cytogenetic resources specific for chromosome 12 127
A t(4;13)(q21;q14) translocation in B-cell chronic lymphocytic leukemia causing concomitant homozygous DLEU2/miR15a/miR16-1 and heterozygous ARHGAP24 deletions 126
A novel t(2;10)(q31;p12) balanced translocation in acute myeloid leukemia. 126
A Novel Fusion Gene, SS18L1/SSX1, in Synovial Sarcoma 126
Myeloma cells regulate miRNA transfer from fibroblast-derived exosomes by expression of lncRNAs 126
Unraveling the internal structure of neocentromeres in ring chromosomes harboring genomic amplification in soft tissue tumors 125
Molecular analysis of the HuD gene in neuroendocrine lung cancers 124
FISH analysis reveals frequent co-occurrence of 4q24/TET2 and 5q and/or 7q deletions. 123
Gene amplification as double minutes or homogeneously staining regions in solid tumors: Origin and structure 122
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. 121
PVT1: A long non-coding RNA recurrently involved in neoplasia-associated fusion transcripts 121
Constitutional ring chromosome 11 mosaicism in a Wilms tumor patient: Cytogenetic, molecular and clinico-pathological studies 119
Double CEBPE-IGH rearrangement due to chromosome duplication and cryptic insertion in an adult with B-cell acute lymphoblastic leukemia. 119
Late-appearing pseudocentric fission event during chronic myeloid leukemia progression 119
Rearrangements of chromosome bands 15q12-q21 are secondary to HMGA2 deregulation in conventional lipoma. 119
Mechanisms of Resistance to Anti-CD38 Daratumumab in Multiple Myeloma 119
Pre-B cell receptor-mediated cell cycle arrest in Philadelphia chromosome-positive acute lymphoblastic leukemia requires IKAROS function 118
Epigenetic regulation of UNCX, a novel homeobox transcription factor gene activated in acute myeloid leukemia 118
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 117
Identification of a commonly amplified 4.3 Mb region with overexpression of C8FW, but not MYC in MYC-containing double minutes in myeloid malignancies 116
Molecular cytogenetics characterization of a novel translocation involving chromosomes 17 and 19 in a Ph+ adult acute lymphoblastic leukemia 116
Upregulation of MEL1 and FLJ42875 genes by position effect resulting from a t(1;2)(p36;p21) occurring during evolution of chronic myelomonocytic leukemia 116
Fusion of the FUS and BBF2H7 genes in low grade fibromyxoid sarcoma 116
Rare recurrent t(15;21) translocations disrupting RUNX1 in myeloid leukemia. 115
Unravelling similarities and differences in the role of circular and linear PVT1 in cancer and human disease 115
Episomal amplification of MYCN in a case of medulloblastoma 114
The chimeric FUS/CREB3l2 gene is specific for low-grade fibromyxoid sarcoma 114
1746PPrognostic role of RLF/MYCL1 and circPVT1 in SCLC 114
Molecular cytogenetic resources for chromosome 4 and comparative analysis of phylogenetic chromosome IV in great apes 111
Cytogenetic analysis of 101 giant cell tumors of bone: nonrandom patterns of telomeric associations and other structural aberrations 110
FOXP1 and TP63 involvement in the progression of myelodysplastic syndrome with 5q- and additional cytogenetic abnormalities. 110
A NOVEL FUSION 5'AFF3/3'BCL2 ORIGINATED FROM A t(2;18)(Q11.2-Q21.33) TRANSLOCATION IN FOLLICULAR LYMPHOMA 110
Evolution of Chromosome Y in primates 110
1q23.1 homozygous deletion and downregulation of Fc receptor-like family genes confer poor prognosis in chronic lymphocytic leukemia 109
Molecular cytogenetic characterization of an ins(4;X) occurring as the sole abnormality in an aggressive, poorly differentiated soft tissue sarcoma 108
Identification of a novel IGH-MMSET fusion transcript in a human myeloma cell line with the t(4;14)(p16.3;q32) chromosomal translocation 108
Gene expression deregulation by KRAS G12D and G12V in a BRAF V600E context 107
MOLECULAR CHARACTERIZATION OF FOUR MYELOID LEUKEMIA CASES WITH A t(15;21) TRANSLOCATION DISRUPTING RUNX1 107
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) 106
Linear and circular PVT1 in hematological malignancies and immune response: two faces of the same coin. 106
A novel fusion 5 ' AFF3/3 ' BCL2 originated from a t(2;18)(q11.2-q21.33) translocation in follicular lymphoma 105
t(5;6;12 ) associated with resistance to imatinib mesylate in chronic myeloid leukemia 104
Assignment to chromosome 12q24.33, gene organization and splicing of the human KRAB/FPB containing zinc finger gene ZNF84 104
Concurrent chromothripsis events in a case of TP53 depleted acute myeloid leukemia with myelodysplasia-related changes 103
RALE051: a novel established cell line of sporadic Burkitt lymphoma 103
null 102
Totale 13.856
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Categoria #
all - tutte 80.183
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 80.183
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2024/20252.779 74 42 205 79 120 270 315 282 110 185 376 721
2025/20266.056 867 312 372 652 650 356 626 170 694 542 176 639
2026/2027142 142 0 0 0 0 0 0 0 0 0 0 0
Totale 19.577