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

LA STARZA, Roberta
 Distribuzione geografica
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Continente #
NA - Nord America 5.279
EU - Europa 3.704
AS - Asia 3.502
SA - Sud America 549
AF - Africa 102
Continente sconosciuto - Info sul continente non disponibili 9
OC - Oceania 5
Totale 13.150
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Nazione #
US - Stati Uniti d'America 5.143
SG - Singapore 1.647
IE - Irlanda 683
UA - Ucraina 581
IT - Italia 517
HK - Hong Kong 487
RU - Federazione Russa 446
CN - Cina 444
BR - Brasile 423
SE - Svezia 422
VN - Vietnam 319
DE - Germania 280
FI - Finlandia 223
FR - Francia 189
KR - Corea 162
GB - Regno Unito 103
IN - India 87
BD - Bangladesh 80
CA - Canada 67
PL - Polonia 46
AR - Argentina 45
TR - Turchia 40
MX - Messico 39
IQ - Iraq 38
CZ - Repubblica Ceca 35
NL - Olanda 35
AT - Austria 31
ES - Italia 27
PK - Pakistan 27
JP - Giappone 26
UZ - Uzbekistan 26
ZA - Sudafrica 25
BE - Belgio 19
CH - Svizzera 18
EC - Ecuador 17
CO - Colombia 16
ID - Indonesia 16
SA - Arabia Saudita 15
MA - Marocco 14
CL - Cile 13
PH - Filippine 13
DZ - Algeria 12
KE - Kenya 11
LT - Lituania 11
VE - Venezuela 11
LB - Libano 9
PY - Paraguay 9
TN - Tunisia 9
AE - Emirati Arabi Uniti 8
EG - Egitto 8
ET - Etiopia 8
JM - Giamaica 8
JO - Giordania 8
UY - Uruguay 8
GR - Grecia 7
NP - Nepal 7
EU - Europa 6
RO - Romania 6
CR - Costa Rica 5
IL - Israele 5
MY - Malesia 5
AZ - Azerbaigian 4
PA - Panama 4
AL - Albania 3
BG - Bulgaria 3
KG - Kirghizistan 3
KZ - Kazakistan 3
NI - Nicaragua 3
OM - Oman 3
PE - Perù 3
SK - Slovacchia (Repubblica Slovacca) 3
AM - Armenia 2
AO - Angola 2
AU - Australia 2
BB - Barbados 2
BH - Bahrain 2
BN - Brunei Darussalam 2
BO - Bolivia 2
CG - Congo 2
DK - Danimarca 2
GE - Georgia 2
HN - Honduras 2
HU - Ungheria 2
MN - Mongolia 2
MU - Mauritius 2
NG - Nigeria 2
NZ - Nuova Zelanda 2
PS - Palestinian Territory 2
PT - Portogallo 2
SI - Slovenia 2
SY - Repubblica araba siriana 2
XK - ???statistics.table.value.countryCode.XK??? 2
A1 - Anonimo 1
AF - Afghanistan, Repubblica islamica di 1
BA - Bosnia-Erzegovina 1
BJ - Benin 1
BY - Bielorussia 1
CY - Cipro 1
DM - Dominica 1
DO - Repubblica Dominicana 1
Totale 13.127
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Città #
Singapore 1.161
Chandler 718
Dublin 680
San Jose 489
Hong Kong 486
San Mateo 331
Jacksonville 307
Ashburn 299
Boardman 209
Perugia 200
Santa Clara 190
Seoul 160
Moscow 157
Medford 140
Princeton 138
Lauterbourg 130
Altamura 117
Beijing 115
Dong Ket 110
Lawrence 107
Munich 107
Los Angeles 102
Wilmington 101
The Dalles 100
Ann Arbor 96
New York 86
Ho Chi Minh City 80
Andover 78
Piscataway 69
Helsinki 58
Redmond 56
Dearborn 46
Orem 46
Turku 43
São Paulo 37
Hanoi 36
San Paolo di Civitate 35
Saint Petersburg 32
Warsaw 31
Frankfurt am Main 29
Montreal 29
Norwalk 28
Dallas 26
Des Moines 26
Amsterdam 24
Tokyo 24
Brooklyn 23
Chennai 22
Stockholm 22
Woodbridge 21
Atlanta 20
Chicago 20
London 20
Rome 19
Brno 18
Brussels 18
Denver 18
Houston 18
Baghdad 17
Mexico City 17
Council Bluffs 16
Toronto 16
Johannesburg 15
Nuremberg 15
Shanghai 15
Falkenstein 13
Falls Church 13
Izmir 12
San Diego 12
San Francisco 12
Ankara 11
Auburn Hills 11
Boston 11
Haiphong 11
Phoenix 11
Tashkent 11
Vienna 11
Mumbai 10
Nairobi 10
Redwood City 10
Rio de Janeiro 10
Brasília 8
Lahore 8
Manchester 8
Milan 8
Wroclaw 8
Belo Horizonte 7
Campinas 7
Changsha 7
Columbus 7
Da Nang 7
Hefei 7
Joinville 7
Medellín 7
Olomouc 7
Prague 7
Quito 7
Addis Ababa 6
Amman 6
Charlotte 6
Totale 8.333
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Nome #
Design of a Comprehensive Fluorescence in Situ Hybridization Assay for Genetic Classification of T-Cell Acute Lymphoblastic Leukemia 162
NPM1 deletion is associated with gross chromosomal rearrangements in leukemia 147
Combined interphase fluorescence in situ hybridization elucidates the genetic heterogeneity of T-cell acute lymphoblastic leukemia in adults 145
A common 93-kb duplicated DNA sequence at 1q21.2 in acute lymphoblastic leukemia and Burkitt lymphoma 144
14q+ chromosome marker in a T-cell-rich B-cell lymphoma. 143
New somatic TERT promoter variants enhance the Telomerase activity in Glioblastoma 140
Acute lymphoblastic leukaemia in Noonan syndrome 129
14q32 rearrangements deregulating BCL11B mark a distinct subgroup of T and myeloid immature acute leukemia 127
Constitutive phosphorylation of Janus kinase2 in the GL15 glioblastoma derived human cell line 126
Comparison between Sickle Cell Disease Patients and Healthy Donors: Untargeted Lipidomic Study of Erythrocytes 124
3q aberration and monosomy 7 in ANLL presenting with high platelet count and diabetes insipidus. 124
A NUP98-positive acute myeloid leukemia with a t(11;12)(p15;q13) without HOXC cluster gene involvement 124
Genetic profile of acute myeloid leukemia 123
Inv(11)(p15q22)/NUP98-DDX10 fusion and isoforms in a new case of de novo acute myeloid leukemia. 122
DDX3X-MLLT10 fusion in adults with NOTCH1 positive T-cell acute lymphoblastic leukemia. 121
Deletions of the long arm of chromosome 5 define subgroups of T-cell acute lymphoblastic leukemia 119
Blockade of Oncogenic NOTCH1 With the SERCA Inhibitor CAD204520 in T Cell Acute Lymphoblastic Leukemia 118
t(3;11)(q12;p15)/NUP98-LOC348801 fusion transcript in acute myeloid leukemia 117
Alterazioni strutturali del cromosoma 12p dei disordini mieloidi 116
Chromothripsis is a frequent event and underlies typical genetic changes in early T-cell precursor lymphoblastic leukemia in adults 115
Regions of juxtaposition in unbalanced 1q rearrangements of malignant hemopathies 115
Rescue of genomic information in adult acute lymphoblastic leukaemia (ALL) with normal/failed cytogenetics: a GIMEMA centralized biological study 115
Cryptic insertion producing two NUP98/NSD1 chimeric transcripts in adult refractory anemia with an excess of blasts 114
The hypereosinophilic syndrome: fluorescence in situ hybridization detects the del(4)(q12)-FIP1L1/PDGFRA but not genomic rearrangements of other tyrosine kinases 114
Molecular cytogenetic analysis of the 5Q-chromosome in the HL60 cell-line and in the 5Q-Syndrome 112
Interstitial insertion of AF10 into the ALL1 gene in a case of infant acute lymphoblastic leukemia 112
MYB rearrangements and over-expression in T-cell acute lymphoblastic leukemia 111
Comprehensive analysis of mitochondrial and nuclear DNA variations in patients affected by hemoglobinopathies: A pilot study 110
A PDGFRB-positive acute myeloid malignancy with a new t(5;12)(q33;p13.3) involving the ERC1 gene 109
Cytogenetic/mutation profile of chronic lymphocytic leukemia/malignant melanoma collision tumors of the skin 109
4q12 translocations with GSX2 expression identify a CD7(+) acute myeloid leukaemia subset 108
Cytoplasmic nucleophosmin in acute myelogenous leukemia with a normal karyotype 108
A new NDE1/PDGFRB fusion transcript underlying chronic myelomonocytic leukaemia in Noonan Syndrome 107
Targeting Cytokine- And Therapy-Induced PIM1 Activation in Preclinical Models of T-cell Acute Lymphoblastic Leukemia and Lymphoma 107
Detection and monitoring of trisomy 8 by fluorescence in situ hybridization in acute myeloid leukemia: a multicentric study. 106
Myeloid cell differentiation arrest by miR-125b-1 in myelodysplastic syndrome and acute myeloid leukemia with the t(2;11)(p21;q23) translocation 105
AML1/MTG16 fusion gene from a t(16;21)(q24;q22) translocation in treatment-induced leukemia after breast cancer 105
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. 104
e6a2 BCR/ABL1 fusion with cryptic der(9)t(9;22) deletions in a patient with chronic myeloid leukemia 104
The hereditary hyperferritinemia-cataract syndrome in 2 italian families 104
FIP1L1-PDGFRA in chronic eosinophilic leukemia and BCR-ABL1 in chronic myeloid leukemia affect different leukemic cells 103
Leukemic recombinations involving heterochromatin in myeloproliferative disorders with t(1;9) 103
Cryptic chromosome 9q34 deletion generates TAF-Ialpha/CAN and TAF-Ibeta/CAN fusion transcripts in acute myeloid leukemia. 103
Metachronous cardiac and cerebral sarcomas: case report with focus on molecular findings and review of the literature 103
Extramedullary molecular evidence of the 5'KIAA1509/3'PDGFRB fusion gene in chronic eosinophilic leukemia 102
The ETV6,CDKN1B and D12S178 loci are involved in a segment commonly deleted in various 12p aberrations in different hematological malignancies. 101
A novel germline variant in PIK3R1 results in SHORT syndrome associated with TAL/LMO T-cell acute lymphoblastic leukemia 101
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 100
Aberrant subcellular expression of nucleophosmin and NPM-MLF1 fusion protein in acute myeloid leukaemia carrying t(3;5): a comparison with NPMc+ AML. 100
Submicroscopic deletions in 5q- associated malignancies 100
Genetic pathways in low-and high-grade HCV-related lymphomas are different 98
Targeted sequencing identifies associations between IL7R-JAK mutations and epigenetic modulators in T-cell acute lymphoblastic leukemia 98
Different genomic imbalances in low- and high-grade HCV-related lymphomas 97
Acute myeloid leukemia 97
Genomic gain at 6p21: a new cryptic molecular rearrangement in secondary myelodysplastic syndrome and acute myeloid leukemia 96
RNA sequencing unravels the genetics of refractory/relapsed T-cell acute lymphoblastic leukemia. Prognostic and therapeutic implications 96
Clonal eosinophils are a morphologic hallmark of ETV6/ABL1 positive acute myeloid leukemia 95
Totipotent stem cells bearing del(20q) maintain multipotential differentiation in Shwachman Diamond syndrome 94
A novel dic(1;10) in a patient with myelodysplastic syndrome 94
T-Cell Acute Lymphoblastic Leukemia: Biomarkers and Their Clinical Usefulness 94
A Novel t(5;7)(q31;q21)/CDK6::IL3 in Immature T-cell Acute Lymphoblastic Leukemia With IL3 Expression and Eosinophilia 93
Combined translocation with ZNF198-FGFR1 gene fusion and deletion of potential tumor suppressors in a myeloproliferative disorder 93
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 93
Cytogenetic and FISH investigations on Tetrasomy 8 in ALL. 92
Genomic and clinical findings in myeloid neoplasms with PDGFRB rearrangement 92
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 91
MN1-ETV6 fusion gene arising from MDS With 5q- 91
MYB deregulation from a EWSR1-MYB fusion at leukemic evolution of a JAK2 V617F positive primary myelofibrosis 91
A novel germline mutation in CDK4 codon 24 associated to familial melanoma 90
t(4;11) translocation involving NUP98 and RAP1GDS1 genes. Characterisation of a new subset of T acute lymphoblastc leukaemia 89
CIZ gene rearrangements in acute leukemia: report of a diagnostic FISH assay and clinical features of nine patients 89
Genetic profile of T-cell acute lymphoblastic leukemias with MYC translocations. 89
Involvement of a member of the histone cluster 1 at 6p21 in NUP98-positive MDS/AML 89
TPM3/PDGFRB fusion transcript and its reciprocal in chronic eosinophilic leukemia 88
Le sindromi mielodisplastiche: citogenetica e biologia molecolare 87
Double CEBPE-IGH rearrangement due to chromosome duplication and cryptic insertion in an adult with B-cell acute lymphoblastic leukemia. 87
Succeful use of the same slide for consecutive fluorescence in situ hybridization (FISH) experiments. 86
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 86
Case report: Ponatinib as a bridge to CAR-T cells and subsequent maintenance in a patient with relapsed/refractory Philadelphia-like acute lymphoblastic leukemia 85
NUP98/11p15 translocations affect CD34+ cells in myeloid and T lymphoid leukemias 85
Different mechanisms lead to a karyotypically identical t(20;21) in myelodysplastic syndrome and in acute myelocytic leukemia 85
NUP98 is fused to the NSD3 gene in acute myeloid leukemia associated with (8;11) (p11,2;p15) 85
Trisomy 8 in PDGFRB-negative cells in a patient with imatinib-sensitive chronic myelomonocytic leukemia and t(5;16)(q33;p13), PDGFRB-NDE1 fusion 84
Optimizing the risk stratification of astrocytic tumors by applying the cIMPACT-NOW Update 3 signature: real-word single center experience 83
Human homeobox gene HOXC13 is the partner of NUP98 in adult acute myeloid leukemia with t(11;12)(p15;q13) 83
T-lymphoid/myeloid biphenotypic leukemia morphologically resembling malignant histiocytosis. Immunological, cytogenetic and molecular studies. 82
Rapid reversion of Loeffler's endocarditis by imatinib in early stage clonal hypereosinophilic syndrome 80
SQSTM1-NUP214: a new gene fusion in adult T-cell acute lymphoblastic leukemia 80
New MLLT10 gene recombinations in pediatric T-acute lymphoblastic leukemia. 80
High PIM1 expression is a biomarker of T-cell acute lymphoblastic leukemia with JAK/STAT activation or t(6;7)(p21;q34)/TRB@-PIM1 rearrangement 80
FISH analysis reveals frequent co-occurrence of 4q24/TET2 and 5q and/or 7q deletions. 79
Trisomy 6 is the hallmark of a dysplastic clone in bone marrow aplasia. 78
Molecular Cytogenetics Detect an Unbalanced t(2;13)(q36;q14) and PAX3-FOXO1 Fusion in Rhabdomyosarcoma With Mixed Embryonal/Alveolar Features 78
Chronic lymphocytic leukaemia Is terminal del(14)(q24) a new marker for prognostic stratification? 78
Distinct genomic events in the myeloid and lymphoid lineages in simultaneous presentation of chronic myeloid leukemia and B-chronic lymphocytic leukemia 77
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 77
Orthogonal proteogenomic analysis identifies the druggable PA2G4-MYC axis in 3q26 AML 76
Haplo-identical haematopoietic stem cell transplantation for secondary leukaemia 76
Involvement of MLL gene in a t(10;11)(q22;q23) and a t(8;11)(q24;q23) identified by fluorescence in situ hybridization. 76
Incidence and significance of cryptic chromosome aberrations detected by fluorescence in situ hybridization in acute myeloid leukemia with normal karyotype 75
Totale 10.118
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Categoria #
all - tutte 60.316
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 60.316
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021129 0 0 0 0 0 0 0 0 0 0 0 129
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
2024/20252.039 35 218 112 69 284 101 81 162 376 113 309 179
2025/20264.740 331 334 186 601 728 450 813 235 456 384 186 36
Totale 13.527