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

MATTEUCCI, Caterina
 Distribuzione geografica
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Continente #
NA - Nord America 2.838
AS - Asia 1.684
EU - Europa 1.625
SA - Sud America 255
Continente sconosciuto - Info sul continente non disponibili 172
AF - Africa 52
OC - Oceania 3
Totale 6.629
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Nazione #
US - Stati Uniti d'America 2.725
SG - Singapore 736
IT - Italia 329
IE - Irlanda 275
CN - Cina 246
HK - Hong Kong 218
BR - Brasile 199
RU - Federazione Russa 194
UA - Ucraina 181
VN - Vietnam 166
DE - Germania 154
SE - Svezia 98
FI - Finlandia 88
FR - Francia 80
BD - Bangladesh 79
KR - Corea 59
CA - Canada 58
GB - Regno Unito 55
IN - India 37
CZ - Repubblica Ceca 32
PL - Polonia 31
JP - Giappone 22
NL - Olanda 22
TR - Turchia 22
IQ - Iraq 20
MX - Messico 20
PK - Pakistan 19
AR - Argentina 18
AT - Austria 17
BE - Belgio 16
ES - Italia 15
ZA - Sudafrica 13
CO - Colombia 11
UZ - Uzbekistan 11
ID - Indonesia 10
CL - Cile 8
EC - Ecuador 8
JM - Giamaica 8
LT - Lituania 8
CR - Costa Rica 7
EG - Egitto 7
SA - Arabia Saudita 7
DZ - Algeria 6
GR - Grecia 6
KE - Kenya 6
PH - Filippine 6
CH - Svizzera 5
EE - Estonia 5
MA - Marocco 5
ET - Etiopia 4
HN - Honduras 4
LB - Libano 4
PY - Paraguay 4
VE - Venezuela 4
AM - Armenia 3
EU - Europa 3
MY - Malesia 3
NI - Nicaragua 3
SV - El Salvador 3
TN - Tunisia 3
AE - Emirati Arabi Uniti 2
AL - Albania 2
AU - Australia 2
BG - Bulgaria 2
BO - Bolivia 2
CW - ???statistics.table.value.countryCode.CW??? 2
IL - Israele 2
JO - Giordania 2
MU - Mauritius 2
NP - Nepal 2
PR - Porto Rico 2
PT - Portogallo 2
RO - Romania 2
TT - Trinidad e Tobago 2
AO - Angola 1
BA - Bosnia-Erzegovina 1
BN - Brunei Darussalam 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
GD - Grenada 1
GE - Georgia 1
GT - Guatemala 1
HT - Haiti 1
IR - Iran 1
KG - Kirghizistan 1
KY - Cayman, isole 1
LK - Sri Lanka 1
LY - Libia 1
MD - Moldavia 1
MK - Macedonia 1
ML - Mali 1
MN - Mongolia 1
MZ - Mozambico 1
NZ - Nuova Zelanda 1
PA - Panama 1
PS - Palestinian Territory 1
QA - Qatar 1
RE - Reunion 1
SC - Seychelles 1
SI - Slovenia 1
Totale 6.460
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Città #
Singapore 529
Chandler 343
San Jose 289
Dublin 275
Hong Kong 217
Ashburn 205
San Mateo 134
Perugia 104
Santa Clara 103
Jacksonville 99
Council Bluffs 90
Beijing 80
Boardman 78
Munich 76
Moscow 66
New York 64
Ann Arbor 61
Los Angeles 60
Seoul 58
Lauterbourg 52
Medford 52
Princeton 52
Altamura 46
Lawrence 43
Ho Chi Minh City 42
Dong Ket 41
The Dalles 37
Wilmington 37
Andover 27
Dallas 27
Piscataway 27
Redmond 27
Hanoi 26
Helsinki 25
Montreal 25
Dearborn 24
São Paulo 24
Saint Petersburg 22
Turku 22
Chicago 21
Tokyo 20
Rome 18
Warsaw 18
Brno 17
Phoenix 17
Brussels 16
Frankfurt am Main 16
Orem 16
Amsterdam 14
Atlanta 14
Mexico City 13
Norwalk 13
San Paolo di Civitate 12
Brooklyn 11
Falkenstein 11
Toronto 11
London 10
North Bergen 10
Stockholm 10
Woodbridge 10
Charlotte 9
Chennai 9
Johannesburg 9
Lahore 9
Milan 9
Denver 8
Falls Church 8
Poplar 8
Brasília 7
Buffalo 7
Florence 7
Gualdo Cattaneo 7
Haiphong 7
Izmir 7
Naples 7
Prague 7
Rio de Janeiro 7
San José 7
Vienna 7
Baghdad 6
Changsha 6
Houston 6
Nairobi 6
Nuremberg 6
San Francisco 6
Shanghai 6
Tashkent 6
Cairo 5
Columbus 5
Lucca 5
Mumbai 5
Olomouc 5
Philadelphia 5
San Diego 5
Santiago 5
Seattle 5
Wroclaw 5
Ankara 4
Basra 4
Boston 4
Totale 4.163
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Nome #
Design of a Comprehensive Fluorescence in Situ Hybridization Assay for Genetic Classification of T-Cell Acute Lymphoblastic Leukemia 176
Role of BCL2L10 methylation and TET2 mutations in higher risk myelodysplastic syndromes treated with 5-Azacytidine 162
Activating somatic and germline TERT promoter variants in myeloid malignancies 159
NPM1 deletion is associated with gross chromosomal rearrangements in leukemia 158
A novel mutation of indoleamine 2,3-dioxygenase 1 causes a rapid proteasomal degradation and compromises protein function 157
Combined interphase fluorescence in situ hybridization elucidates the genetic heterogeneity of T-cell acute lymphoblastic leukemia in adults 154
A common 93-kb duplicated DNA sequence at 1q21.2 in acute lymphoblastic leukemia and Burkitt lymphoma 153
Comparison between Sickle Cell Disease Patients and Healthy Donors: Untargeted Lipidomic Study of Erythrocytes 142
14q32 rearrangements deregulating BCL11B mark a distinct subgroup of T and myeloid immature acute leukemia 140
Deletions of the long arm of chromosome 5 define subgroups of T-cell acute lymphoblastic leukemia 132
A NUP98-positive acute myeloid leukemia with a t(11;12)(p15;q13) without HOXC cluster gene involvement 129
Germline GATA2 variant disrupting endothelial eNOS cell function and angiogenesis can be restored by c-Jun/AP-1 upregulation 128
Inv(11)(p15q22)/NUP98-DDX10 fusion and isoforms in a new case of de novo acute myeloid leukemia. 127
Chromothripsis is a frequent event and underlies typical genetic changes in early T-cell precursor lymphoblastic leukemia in adults 126
DDX3X-MLLT10 fusion in adults with NOTCH1 positive T-cell acute lymphoblastic leukemia. 126
Comprehensive analysis of mitochondrial and nuclear DNA variations in patients affected by hemoglobinopathies: A pilot study 123
Rescue of genomic information in adult acute lymphoblastic leukaemia (ALL) with normal/failed cytogenetics: a GIMEMA centralized biological study 121
Cytogenetic/mutation profile of chronic lymphocytic leukemia/malignant melanoma collision tumors of the skin 121
Interstitial insertion of AF10 into the ALL1 gene in a case of infant acute lymphoblastic leukemia 119
Detection and monitoring of trisomy 8 by fluorescence in situ hybridization in acute myeloid leukemia: a multicentric study. 113
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 110
Cryptic chromosome 9q34 deletion generates TAF-Ialpha/CAN and TAF-Ibeta/CAN fusion transcripts in acute myeloid leukemia. 110
AML1/MTG16 fusion gene from a t(16;21)(q24;q22) translocation in treatment-induced leukemia after breast cancer 109
Submicroscopic deletions in 5q- associated malignancies 107
Detection of the NUP214-ABL rearrangement in T-ALL by high-density oligonucleotide arrays: Evidence of the value of this approach in the identification of gene amplifications 105
Genomic gain at 6p21: a new cryptic molecular rearrangement in secondary myelodysplastic syndrome and acute myeloid leukemia 103
Different genomic imbalances in low- and high-grade HCV-related lymphomas 102
Totipotent stem cells bearing del(20q) maintain multipotential differentiation in Shwachman Diamond syndrome 101
A Novel t(5;7)(q31;q21)/CDK6::IL3 in Immature T-cell Acute Lymphoblastic Leukemia With IL3 Expression and Eosinophilia 100
Characterization of ABL1 expression in adult T-cell acute lymphoblastic leukemia by oligonucleotide array analysis 100
Genetic profile of T-cell acute lymphoblastic leukemias with MYC translocations. 100
Genomic and clinical findings in myeloid neoplasms with PDGFRB rearrangement 100
Comparative genomic hybridization identifies 17q11.2 approximately q12 duplication as an early event in cutaneous T-cell lymphomas 98
MN1-ETV6 fusion gene arising from MDS With 5q- 97
A novel t(X;21)(p11.4;q22.12) translocation adds to the role of BCOR and RUNX1 in myelodysplastic syndromes and acute myeloid leukemias 94
Different mechanisms lead to a karyotypically identical t(20;21) in myelodysplastic syndrome and in acute myelocytic leukemia 94
Highly aggressive T-cell acute lymphoblastic leukemia with t(8;14)(q24;q11): extensive genetic characterization and achievement of early molecular remission and long-term survival in an adult patient. 93
Double CEBPE-IGH rearrangement due to chromosome duplication and cryptic insertion in an adult with B-cell acute lymphoblastic leukemia. 92
NUP98/11p15 translocations affect CD34+ cells in myeloid and T lymphoid leukemias 91
The GNAS1 gene in myelodysplastic syndromes (MDS). 91
TPM3/PDGFRB fusion transcript and its reciprocal in chronic eosinophilic leukemia 90
Venetoclax plus azacitidine as genetic-driven bridge-to-transplant therapy for IDH2-mutated acute myeloid leukaemia (AML) refractory to intensive chemotherapy: proof-of-concept case reports 89
Human homeobox gene HOXC13 is the partner of NUP98 in adult acute myeloid leukemia with t(11;12)(p15;q13) 89
Sensitivity of cutaneous chronic myelomonocytic leukaemia lesions to hypomethylating treatment 88
One disease, two faces: clonally-related AML and MPDCP with skin involvement 87
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 87
FISH analysis reveals frequent co-occurrence of 4q24/TET2 and 5q and/or 7q deletions. 87
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 85
Distinct genomic events in the myeloid and lymphoid lineages in simultaneous presentation of chronic myeloid leukemia and B-chronic lymphocytic leukemia 84
Chronic lymphocytic leukaemia Is terminal del(14)(q24) a new marker for prognostic stratification? 83
Multiple EWSR1-WT1 and WT1-EWSR1 copies in two cases of desmoplastic round cell tumor. 82
New dead/H-box helicase gene (ddx41) mutation in an Italian family with recurrent leukemia 82
Typical genomic imbalances in primary MALT lymphoma of the orbit 80
Epigenetic Modeling of Jumping Translocations of 1q Heterochromatin in Acute Myeloid Leukemia After 5'-Azacytidine Treatment 79
Correction to: One disease, two faces: clonally-related AML and MPDCP with skin involvement 70
Regression of lymphoproliferative disorder after treatment for hepatitis C virus infection in a patient with partial trisomy 3, Bcl-2 overexpression, and type II cryoglobulinemia 70
Microdissection and FISH investigations in acute myeloid leukemia: a step forward to full identification of complex karyotypic changes. 67
The EMT transcription factor Zeb2 controls adult murine hematopoietic differentiation by regulating cytokine signaling 67
Interphase FISH for Y chromosome, VNTR polymorphisms, and RT-PCR for BCR-ABL in the monitoring of HLA-matched and mismatched transplants. 66
MN1-ETV6 fusion gene arising from MDS With 5q- 61
Repurposing the Whole Expression Transcriptome Assay for the Genetic Diagnosis of T-Cell Acute Lymphoblastic Leukemia and Lymphoma 53
The c.2031–2A>C MPO gene variant and the predisposition to myeloid neoplasms 35
BIALLELIC LOSS OF RB1 AND LPAR6 AT 13Q14 DRIVES KEY CELL CYCLE ABNORMALITIES IN T-CELL ACUTE LYMPHOBLASTIC LEUKEMIA 32
Screening for gene variants causing inherited platelet disorders: are the cons always cons? 30
CPX-351 Induces High Rate of Complete Remission in the New ICC/ELN 2022 Adverse-Risk Entity ‘AML with MDS-Related Gene Mutations’: Evidence from a Large Real-World Italian Study 27
A specific stem cell program and CD112 immunological axis dysfunctions underpinning monosomy 7-associated myeloid neoplasms 21
Durable remission despite transplantation with active disease in therapy-related NUP98::TOP1-rearranged acute myeloid leukemia 19
Deregulation of FOXF1/FENDRR from t(14;16)(q32;q24) defines a subtype of high-risk lineage ambiguous leukemia 18
COMBINED NF1/SUZ12 HAPLOINSUFFICIENCY DRIVES ABERRANT ACTIVATION OF THE RAS SIGNALING CASCADE IN IMMATURE HOXA-POSITIVE T-ALL 15
Ex vivo drug response profiling guides therapy in a case of high-risk acute undifferentiated leukemia with PICALM::MLLT10 12
null 11
Totale 6.629
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Categoria #
all - tutte 30.610
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 30.610
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022322 0 0 0 19 13 8 3 138 14 14 57 56
2022/2023982 56 188 15 105 88 89 0 44 370 2 20 5
2023/2024450 37 37 23 9 8 1 110 2 70 8 72 73
2024/2025924 31 85 48 39 89 72 49 62 144 59 152 94
2025/20262.361 145 149 88 291 397 186 363 122 236 194 150 40
2026/2027640 51 94 165 330 0 0 0 0 0 0 0 0
Totale 6.629