IRIS - Res&Arch Institutional Research Information System - Research & Archive

LA STARZA, Roberta
 Distribuzione geografica
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Continente #
NA - Nord America 3.498
EU - Europa 2.668
AS - Asia 1.119
SA - Sud America 19
Continente sconosciuto - Info sul continente non disponibili 7
OC - Oceania 2
Totale 7.313
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Nazione #
US - Stati Uniti d'America 3.486
IE - Irlanda 678
UA - Ucraina 565
SG - Singapore 472
IT - Italia 421
SE - Svezia 400
HK - Hong Kong 329
FI - Finlandia 165
DE - Germania 150
CN - Cina 148
VN - Vietnam 110
RU - Federazione Russa 109
GB - Regno Unito 49
AT - Austria 22
CZ - Repubblica Ceca 22
BR - Brasile 17
CH - Svizzera 17
FR - Francia 16
KR - Corea 16
BE - Belgio 14
NL - Olanda 14
TR - Turchia 13
UZ - Uzbekistan 11
GR - Grecia 7
CA - Canada 6
EU - Europa 6
LB - Libano 6
PL - Polonia 5
MX - Messico 4
ES - Italia 3
IL - Israele 3
SK - Slovacchia (Repubblica Slovacca) 3
BG - Bulgaria 2
DK - Danimarca 2
KG - Kirghizistan 2
NZ - Nuova Zelanda 2
RO - Romania 2
A1 - Anonimo 1
AE - Emirati Arabi Uniti 1
AM - Armenia 1
AZ - Azerbaigian 1
BD - Bangladesh 1
BO - Bolivia 1
GE - Georgia 1
IN - India 1
IQ - Iraq 1
JP - Giappone 1
LK - Sri Lanka 1
NI - Nicaragua 1
NO - Norvegia 1
PA - Panama 1
PE - Perù 1
PT - Portogallo 1
Totale 7.313
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Città #
Chandler 718
Dublin 675
Singapore 376
San Mateo 331
Hong Kong 329
Jacksonville 305
Boardman 209
Perugia 178
Santa Clara 168
Medford 140
Princeton 138
Altamura 117
Dong Ket 110
Lawrence 107
Wilmington 101
Ann Arbor 96
Andover 78
Beijing 61
Redmond 56
Dearborn 46
Helsinki 43
San Paolo di Civitate 35
Munich 33
Saint Petersburg 32
Ashburn 28
Norwalk 28
Des Moines 26
Los Angeles 25
New York 22
Woodbridge 20
Brno 18
Seoul 15
Brussels 14
Moscow 14
Falls Church 13
Dallas 12
Houston 12
Izmir 12
San Diego 12
Auburn Hills 11
Rome 11
Redwood City 10
Vienna 9
Nuremberg 7
Amsterdam 6
Shanghai 6
Chicago 5
Forlì 5
Bologna 4
Chengdu 4
Boston 3
Bratislava 3
Den Haag 3
Lappeenranta 3
London 3
Madrid 3
Milan 3
Ottawa 3
Ponte 3
Salerno 3
Simi Valley 3
Bishkek 2
Deruta 2
Edinburgh 2
Florence 2
Frankfurt Am Main 2
Fremont 2
Gualdo Tadino 2
Guangzhou 2
Hadera 2
Indianapolis 2
Memphis 2
Mexico City 2
Nanjing 2
Naples 2
New Haven 2
Philadelphia 2
Piraeus 2
Prague 2
Santarcangelo di Romagna 2
São Paulo 2
Toronto 2
Agronômica 1
Aprilia 1
Athens 1
Auckland 1
Baghdad 1
Baku 1
Belo Horizonte 1
Birmingham 1
Bucharest 1
Cambridge 1
Carapicuíba 1
Cariacica 1
Castiglione del Lago 1
Changsha 1
Chelyabinsk 1
Colombo 1
Coroatá 1
Dnipro 1
Totale 4.924
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Nome #
Design of a Comprehensive Fluorescence in Situ Hybridization Assay for Genetic Classification of T-Cell Acute Lymphoblastic Leukemia 98
14q+ chromosome marker in a T-cell-rich B-cell lymphoma. 91
Regions of juxtaposition in unbalanced 1q rearrangements of malignant hemopathies 89
Molecular cytogenetic analysis of the 5Q-chromosome in the HL60 cell-line and in the 5Q-Syndrome 87
e6a2 BCR/ABL1 fusion with cryptic der(9)t(9;22) deletions in a patient with chronic myeloid leukemia 86
Acute lymphoblastic leukaemia in Noonan syndrome 84
NPM1 deletion is associated with gross chromosomal rearrangements in leukemia 80
t(3;11)(q12;p15)/NUP98-LOC348801 fusion transcript in acute myeloid leukemia 79
Myeloid cell differentiation arrest by miR-125b-1 in myelodysplastic syndrome and acute myeloid leukemia with the t(2;11)(p21;q23) translocation 79
Leukemic recombinations involving heterochromatin in myeloproliferative disorders with t(1;9) 77
3q aberration and monosomy 7 in ANLL presenting with high platelet count and diabetes insipidus. 77
Interstitial insertion of AF10 into the ALL1 gene in a case of infant acute lymphoblastic leukemia 76
Constitutive phosphorylation of Janus kinase2 in the GL15 glioblastoma derived human cell line 76
FIP1L1-PDGFRA in chronic eosinophilic leukemia and BCR-ABL1 in chronic myeloid leukemia affect different leukemic cells 76
A common 93-kb duplicated DNA sequence at 1q21.2 in acute lymphoblastic leukemia and Burkitt lymphoma 76
Extramedullary molecular evidence of the 5'KIAA1509/3'PDGFRB fusion gene in chronic eosinophilic leukemia 75
Alterazioni strutturali del cromosoma 12p dei disordini mieloidi 74
Genetic profile of acute myeloid leukemia 73
Inv(11)(p15q22)/NUP98-DDX10 fusion and isoforms in a new case of de novo acute myeloid leukemia. 73
Genetic pathways in low-and high-grade HCV-related lymphomas are different 69
The hypereosinophilic syndrome: fluorescence in situ hybridization detects the del(4)(q12)-FIP1L1/PDGFRA but not genomic rearrangements of other tyrosine kinases 69
14q32 rearrangements deregulating BCL11B mark a distinct subgroup of T and myeloid immature acute leukemia 69
RNA sequencing unravels the genetics of refractory/relapsed T-cell acute lymphoblastic leukemia. Prognostic and therapeutic implications 68
AML1/MTG16 fusion gene from a t(16;21)(q24;q22) translocation in treatment-induced leukemia after breast cancer 68
t(4;11) translocation involving NUP98 and RAP1GDS1 genes. Characterisation of a new subset of T acute lymphoblastc leukaemia 67
Succeful use of the same slide for consecutive fluorescence in situ hybridization (FISH) experiments. 67
Cytogenetic and FISH investigations on Tetrasomy 8 in ALL. 66
Blockade of Oncogenic NOTCH1 With the SERCA Inhibitor CAD204520 in T Cell Acute Lymphoblastic Leukemia 66
New somatic TERT promoter variants enhance the Telomerase activity in Glioblastoma 66
A NUP98-positive acute myeloid leukemia with a t(11;12)(p15;q13) without HOXC cluster gene involvement 65
Dual-color split signal fluorescence in situ hybridization assays for the detection of CALM/AF10 in t(10;11)(p13;q14-q21)-positive acute leukemia 64
Combined interphase fluorescence in situ hybridization elucidates the genetic heterogeneity of T-cell acute lymphoblastic leukemia in adults 64
The ETV6,CDKN1B and D12S178 loci are involved in a segment commonly deleted in various 12p aberrations in different hematological malignancies. 64
4q12 translocations with GSX2 expression identify a CD7(+) acute myeloid leukaemia subset 64
Detection and monitoring of trisomy 8 by fluorescence in situ hybridization in acute myeloid leukemia: a multicentric study. 64
Prognostic impact of genetic characterization in the GIMEMA LAM99P study for newly diagnosed adult AML. Relevance of combined analysis of conventional karyotyping, FLT3 and NPM mutational status 63
MYB rearrangements and over-expression in T-cell acute lymphoblastic leukemia 63
Combined translocation with ZNF198-FGFR1 gene fusion and deletion of potential tumor suppressors in a myeloproliferative disorder 62
Cryptic insertion producing two NUP98/NSD1 chimeric transcripts in adult refractory anemia with an excess of blasts 62
Rescue of genomic information in adult acute lymphoblastic leukaemia (ALL) with normal/failed cytogenetics: a GIMEMA centralized biological study 62
MN1-ETV6 fusion gene arising from MDS With 5q- 62
Comprehensive analysis of mitochondrial and nuclear DNA variations in patients affected by hemoglobinopathies: A pilot study 62
Molecular cytogenetic findings in a four-way t(1;12;5;12)(p36;p13;q33;q24) underlying the ETV6-PDGFRB fusion gene in chronic myelomonocytic leukemia 61
Deletions of the long arm of chromosome 5 define subgroups of T-cell acute lymphoblastic leukemia 61
Totipotent stem cells bearing del(20q) maintain multipotential differentiation in Shwachman Diamond syndrome 60
Aberrant subcellular expression of nucleophosmin and NPM-MLF1 fusion protein in acute myeloid leukaemia carrying t(3;5): a comparison with NPMc+ AML. 60
Targeted sequencing identifies associations between IL7R-JAK mutations and epigenetic modulators in T-cell acute lymphoblastic leukemia 60
CALM/AF10-positive leukemias show upregulation of genes involved in chromatin assembly and DNA repair processes and of genes adjacent to the breakpoint at 10p12. 59
DDX3X-MLLT10 fusion in adults with NOTCH1 positive T-cell acute lymphoblastic leukemia. 59
Acute myeloid leukemia 59
Trisomy 8 in PDGFRB-negative cells in a patient with imatinib-sensitive chronic myelomonocytic leukemia and t(5;16)(q33;p13), PDGFRB-NDE1 fusion 58
Different genomic imbalances in low- and high-grade HCV-related lymphomas 58
A PDGFRB-positive acute myeloid malignancy with a new t(5;12)(q33;p13.3) involving the ERC1 gene 58
Submicroscopic deletions in 5q- associated malignancies 58
The hereditary hyperferritinemia-cataract syndrome in 2 italian families 58
NUP98/11p15 translocations affect CD34+ cells in myeloid and T lymphoid leukemias 57
Trisomy 6 is the hallmark of a dysplastic clone in bone marrow aplasia. 56
Genomic gain at 6p21: a new cryptic molecular rearrangement in secondary myelodysplastic syndrome and acute myeloid leukemia 56
Metachronous cardiac and cerebral sarcomas: case report with focus on molecular findings and review of the literature 56
MYB deregulation from a EWSR1-MYB fusion at leukemic evolution of a JAK2 V617F positive primary myelofibrosis 56
A novel germline variant in PIK3R1 results in SHORT syndrome associated with TAL/LMO T-cell acute lymphoblastic leukemia 55
Haplo-identical haematopoietic stem cell transplantation for secondary leukaemia 54
Rapid reversion of Loeffler's endocarditis by imatinib in early stage clonal hypereosinophilic syndrome 54
Distinct genomic events in the myeloid and lymphoid lineages in simultaneous presentation of chronic myeloid leukemia and B-chronic lymphocytic leukemia 54
The Italian external quality assessment scheme in classical cytogenetics: four years of activity. 54
Le sindromi mielodisplastiche: citogenetica e biologia molecolare 53
Cryptic chromosome 9q34 deletion generates TAF-Ialpha/CAN and TAF-Ibeta/CAN fusion transcripts in acute myeloid leukemia. 53
Genetic profile of T-cell acute lymphoblastic leukemias with MYC translocations. 53
Cytogenetic/mutation profile of chronic lymphocytic leukemia/malignant melanoma collision tumors of the skin 53
CIZ gene rearrangements in acute leukemia: report of a diagnostic FISH assay and clinical features of nine patients 52
New MLLT10 gene recombinations in pediatric T-acute lymphoblastic leukemia. 52
Different mechanisms lead to a karyotypically identical t(20;21) in myelodysplastic syndrome and in acute myelocytic leukemia 52
NUP98 is fused to the NSD3 gene in acute myeloid leukemia associated with (8;11) (p11,2;p15) 52
T-lymphoid/myeloid biphenotypic leukemia morphologically resembling malignant histiocytosis. Immunological, cytogenetic and molecular studies. 51
TPM3/PDGFRB fusion transcript and its reciprocal in chronic eosinophilic leukemia 51
Philadelphia-like acute lymphoblastic leukemia is associated with minimal residual disease persistence and poor outcome. First report of the minimal residual disease-oriented GIMEMA LAL1913 51
Chromothripsis is a frequent event and underlies typical genetic changes in early T-cell precursor lymphoblastic leukemia in adults 50
Recurrent rearrangement of the Ewing's sarcoma gene, EWSR1, or its homologue, TAF15, with the transcription factor CIZ/NMP4 in acute leukemia 50
A new NDE1/PDGFRB fusion transcript underlying chronic myelomonocytic leukaemia in Noonan Syndrome 50
Clonal eosinophils are a morphologic hallmark of ETV6/ABL1 positive acute myeloid leukemia 50
Prognostic impact of genetic characterization in the GIMEMA LAM99P multicenter study for newly diagnosed acute myeloid leukemia 49
Human homeobox gene HOXC13 is the partner of NUP98 in adult acute myeloid leukemia with t(11;12)(p15;q13) 49
Insertions generating the 5'RUNX1/3'CBFA2T1 gene in acute myeloid leukemia cases show variable breakpoints. 49
Partial duplication of the MLL oncogene in patients with aggressive aute myeloid leukemia 48
Characterization of 12p molecular events outside ETV6 in complex karyotypes of acute myeloid malignancies 48
Cytoplasmic nucleophosmin in acute myelogenous leukemia with a normal karyotype 48
Targeting Cytokine- And Therapy-Induced PIM1 Activation in Preclinical Models of T-cell Acute Lymphoblastic Leukemia and Lymphoma 48
Philadelphia-positive acute lymphoblastic leukemia with multiple subclones including duplication of the Philadelphia chromosome and Abelson oncogene 48
A novel germline mutation in CDK4 codon 24 associated to familial melanoma 47
Fluorescence In Situ Hybridization characterization of new translocation involving TEL (ETV6) in a wide spectrum of hematologic malignancies. 46
MLL tandem duplication in two cases of acute myelocytic leukemia with unbalanced translocations: der(16)t(11;16)(q23;p13) and der(18)t(11;18)(q22;p11.2) 46
Interpretation of the complex karyotipe and identification of a new 6p amplicon by integrated comparative genomic hybridization and fluorescence in situ hybridization on the U937-I cell line 45
Rearrangement between the MYH11 gene at 16p13 and D12S158 at 12p13 in a case of acute myeloid leukemia M1 (AML-M1) 44
H4(D10S170), a gene frequently rearranged in papillary thyroid carcinoma, is fused to the platelet-derived growth factor receptor beta gene in atypical chronic myeloid leukemia with t(5;10)(q33;q22) 44
Double CEBPE-IGH rearrangement due to chromosome duplication and cryptic insertion in an adult with B-cell acute lymphoblastic leukemia. 44
Multiple EWSR1-WT1 and WT1-EWSR1 copies in two cases of desmoplastic round cell tumor. 44
Leukemogenic mechanisms and targets of a NUP98/HHEX fusion in acute myeloid leukemia 43
Different boundaries characterize isolated and non-isolated 5q deletions in myelodysplastic syndromes and acute myeloid leukemias. 43
Involvement of a member of the histone cluster 1 at 6p21 in NUP98-positive MDS/AML 43
Insights Into Genetic Susceptibility to Melanoma by Gene Panel Testing: Potential Pathogenic Variants in ACD, ATM, BAP1, and POT1 43
Totale 6.035
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Categoria #
all - tutte 35.878
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 35.878
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020286 0 0 0 0 0 0 0 11 90 70 33 82
2020/20211.206 3 85 47 110 335 73 90 20 130 73 111 129
2021/20221.170 25 236 15 76 35 10 14 367 11 47 161 173
2022/20232.261 147 398 18 206 182 210 3 125 883 1 71 17
2023/2024940 79 93 48 14 9 1 199 10 163 23 118 183
2024/2025932 35 218 112 69 284 101 81 32 0 0 0 0
Totale 7.680