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

MATTEUCCI, Caterina
 Distribuzione geografica
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Continente #
NA - Nord America 2.218
AS - Asia 1.579
EU - Europa 1.518
SA - Sud America 245
AF - Africa 49
Continente sconosciuto - Info sul continente non disponibili 4
OC - Oceania 3
Totale 5.616
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Nazione #
US - Stati Uniti d'America 2.166
SG - Singapore 719
IE - Irlanda 275
IT - Italia 245
CN - Cina 229
HK - Hong Kong 216
BR - Brasile 193
RU - Federazione Russa 193
UA - Ucraina 180
VN - Vietnam 164
DE - Germania 153
SE - Svezia 98
FI - Finlandia 88
FR - Francia 78
KR - Corea 58
GB - Regno Unito 48
IN - India 36
CZ - Repubblica Ceca 32
PL - Polonia 30
CA - Canada 26
TR - Turchia 22
BD - Bangladesh 21
IQ - Iraq 20
JP - Giappone 20
NL - Olanda 20
AR - Argentina 18
PK - Pakistan 18
AT - Austria 17
MX - Messico 17
BE - Belgio 16
ES - Italia 15
ZA - Sudafrica 12
UZ - Uzbekistan 11
CO - Colombia 10
ID - Indonesia 10
CL - Cile 8
EG - Egitto 7
LT - Lituania 7
SA - Arabia Saudita 7
DZ - Algeria 6
EC - Ecuador 6
GR - Grecia 6
KE - Kenya 6
CH - Svizzera 5
PH - Filippine 5
CR - Costa Rica 4
ET - Etiopia 4
MA - Marocco 4
VE - Venezuela 4
EU - Europa 3
LB - Libano 3
MY - Malesia 3
PY - Paraguay 3
TN - Tunisia 3
AE - Emirati Arabi Uniti 2
AL - Albania 2
AM - Armenia 2
AU - Australia 2
BO - Bolivia 2
HN - Honduras 2
IL - Israele 2
JM - Giamaica 2
JO - Giordania 2
MU - Mauritius 2
NP - Nepal 2
PT - Portogallo 2
RO - Romania 2
AO - Angola 1
BA - Bosnia-Erzegovina 1
BG - Bulgaria 1
BN - Brunei Darussalam 1
DK - Danimarca 1
EE - Estonia 1
GE - Georgia 1
IR - Iran 1
KG - Kirghizistan 1
LK - Sri Lanka 1
LY - Libia 1
MD - Moldavia 1
ML - Mali 1
MN - Mongolia 1
MZ - Mozambico 1
NZ - Nuova Zelanda 1
PA - Panama 1
PS - Palestinian Territory 1
RE - Reunion 1
SI - Slovenia 1
UY - Uruguay 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 5.616
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Città #
Singapore 525
Chandler 343
Dublin 275
Hong Kong 215
San Jose 209
Ashburn 156
San Mateo 134
Perugia 100
Jacksonville 97
Boardman 78
Munich 76
Santa Clara 74
Beijing 71
Moscow 66
Ann Arbor 61
Seoul 57
Lauterbourg 52
Medford 52
Princeton 51
Altamura 46
New York 46
Lawrence 43
Los Angeles 43
Ho Chi Minh City 42
Dong Ket 41
The Dalles 37
Wilmington 37
Andover 27
Redmond 27
Hanoi 25
Helsinki 25
Piscataway 25
Dearborn 23
Saint Petersburg 22
São Paulo 22
Turku 22
Tokyo 18
Warsaw 18
Brno 17
Brussels 16
Chicago 15
Frankfurt am Main 15
Orem 15
Amsterdam 14
Montreal 14
Norwalk 13
Rome 13
San Paolo di Civitate 12
Atlanta 11
Brooklyn 11
Falkenstein 11
Mexico City 11
Dallas 10
Stockholm 10
Woodbridge 10
Chennai 9
Johannesburg 9
Falls Church 8
Lahore 8
London 8
Poplar 8
Denver 7
Haiphong 7
Izmir 7
Prague 7
Rio de Janeiro 7
Vienna 7
Baghdad 6
Changsha 6
Houston 6
Nairobi 6
Nuremberg 6
Phoenix 6
San Francisco 6
Shanghai 6
Tashkent 6
Brasília 5
Cairo 5
Florence 5
Olomouc 5
San Diego 5
Santiago 5
Wroclaw 5
Ankara 4
Basra 4
Boston 4
Buenos Aires 4
Columbus 4
Como 4
Hải Dương 4
Istanbul 4
Lucca 4
Mumbai 4
New Delhi 4
San José 4
Addis Ababa 3
Bexley 3
Can Tho 3
Caracas 3
Chengdu 3
Totale 3.743
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Nome #
Design of a Comprehensive Fluorescence in Situ Hybridization Assay for Genetic Classification of T-Cell Acute Lymphoblastic Leukemia 161
Role of BCL2L10 methylation and TET2 mutations in higher risk myelodysplastic syndromes treated with 5-Azacytidine 151
Activating somatic and germline TERT promoter variants in myeloid malignancies 147
Combined interphase fluorescence in situ hybridization elucidates the genetic heterogeneity of T-cell acute lymphoblastic leukemia in adults 144
A common 93-kb duplicated DNA sequence at 1q21.2 in acute lymphoblastic leukemia and Burkitt lymphoma 142
A novel mutation of indoleamine 2,3-dioxygenase 1 causes a rapid proteasomal degradation and compromises protein function 141
14q32 rearrangements deregulating BCL11B mark a distinct subgroup of T and myeloid immature acute leukemia 127
NPM1 deletion is associated with gross chromosomal rearrangements in leukemia 125
Inv(11)(p15q22)/NUP98-DDX10 fusion and isoforms in a new case of de novo acute myeloid leukemia. 121
A NUP98-positive acute myeloid leukemia with a t(11;12)(p15;q13) without HOXC cluster gene involvement 120
Deletions of the long arm of chromosome 5 define subgroups of T-cell acute lymphoblastic leukemia 117
Rescue of genomic information in adult acute lymphoblastic leukaemia (ALL) with normal/failed cytogenetics: a GIMEMA centralized biological study 115
Germline GATA2 variant disrupting endothelial eNOS cell function and angiogenesis can be restored by c-Jun/AP-1 upregulation 114
Chromothripsis is a frequent event and underlies typical genetic changes in early T-cell precursor lymphoblastic leukemia in adults 113
Interstitial insertion of AF10 into the ALL1 gene in a case of infant acute lymphoblastic leukemia 111
Comprehensive analysis of mitochondrial and nuclear DNA variations in patients affected by hemoglobinopathies: A pilot study 110
DDX3X-MLLT10 fusion in adults with NOTCH1 positive T-cell acute lymphoblastic leukemia. 109
Cytogenetic/mutation profile of chronic lymphocytic leukemia/malignant melanoma collision tumors of the skin 109
AML1/MTG16 fusion gene from a t(16;21)(q24;q22) translocation in treatment-induced leukemia after breast cancer 105
Detection and monitoring of trisomy 8 by fluorescence in situ hybridization in acute myeloid leukemia: a multicentric study. 104
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 101
Cryptic chromosome 9q34 deletion generates TAF-Ialpha/CAN and TAF-Ibeta/CAN fusion transcripts in acute myeloid leukemia. 101
Submicroscopic deletions in 5q- associated malignancies 100
Comparison between Sickle Cell Disease Patients and Healthy Donors: Untargeted Lipidomic Study of Erythrocytes 99
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 99
Different genomic imbalances in low- and high-grade HCV-related lymphomas 96
Genomic gain at 6p21: a new cryptic molecular rearrangement in secondary myelodysplastic syndrome and acute myeloid leukemia 94
Comparative genomic hybridization identifies 17q11.2 approximately q12 duplication as an early event in cutaneous T-cell lymphomas 94
Characterization of ABL1 expression in adult T-cell acute lymphoblastic leukemia by oligonucleotide array analysis 92
A Novel t(5;7)(q31;q21)/CDK6::IL3 in Immature T-cell Acute Lymphoblastic Leukemia With IL3 Expression and Eosinophilia 91
Totipotent stem cells bearing del(20q) maintain multipotential differentiation in Shwachman Diamond syndrome 91
MN1-ETV6 fusion gene arising from MDS With 5q- 91
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. 89
Genetic profile of T-cell acute lymphoblastic leukemias with MYC translocations. 87
TPM3/PDGFRB fusion transcript and its reciprocal in chronic eosinophilic leukemia 87
Genomic and clinical findings in myeloid neoplasms with PDGFRB rearrangement 87
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 85
The GNAS1 gene in myelodysplastic syndromes (MDS). 85
Different mechanisms lead to a karyotypically identical t(20;21) in myelodysplastic syndrome and in acute myelocytic leukemia 85
NUP98/11p15 translocations affect CD34+ cells in myeloid and T lymphoid leukemias 84
Human homeobox gene HOXC13 is the partner of NUP98 in adult acute myeloid leukemia with t(11;12)(p15;q13) 83
Double CEBPE-IGH rearrangement due to chromosome duplication and cryptic insertion in an adult with B-cell acute lymphoblastic leukemia. 81
Sensitivity of cutaneous chronic myelomonocytic leukaemia lesions to hypomethylating treatment 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 79
One disease, two faces: clonally-related AML and MPDCP with skin involvement 78
Chronic lymphocytic leukaemia Is terminal del(14)(q24) a new marker for prognostic stratification? 78
FISH analysis reveals frequent co-occurrence of 4q24/TET2 and 5q and/or 7q deletions. 76
Distinct genomic events in the myeloid and lymphoid lineages in simultaneous presentation of chronic myeloid leukemia and B-chronic lymphocytic leukemia 75
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 75
Multiple EWSR1-WT1 and WT1-EWSR1 copies in two cases of desmoplastic round cell tumor. 73
New dead/H-box helicase gene (ddx41) mutation in an Italian family with recurrent leukemia 73
Typical genomic imbalances in primary MALT lymphoma of the orbit 72
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 64
Correction to: One disease, two faces: clonally-related AML and MPDCP with skin involvement 62
The EMT transcription factor Zeb2 controls adult murine hematopoietic differentiation by regulating cytokine signaling 62
Microdissection and FISH investigations in acute myeloid leukemia: a step forward to full identification of complex karyotypic changes. 60
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 58
Interphase FISH for Y chromosome, VNTR polymorphisms, and RT-PCR for BCR-ABL in the monitoring of HLA-matched and mismatched transplants. 54
Epigenetic Modeling of Jumping Translocations of 1q Heterochromatin in Acute Myeloid Leukemia After 5'-Azacytidine Treatment 53
MN1-ETV6 fusion gene arising from MDS With 5q- 47
Repurposing the Whole Expression Transcriptome Assay for the Genetic Diagnosis of T-Cell Acute Lymphoblastic Leukemia and Lymphoma 23
Screening for gene variants causing inherited platelet disorders: are the cons always cons? 20
The c.2031–2A>C MPO gene variant and the predisposition to myeloid neoplasms 12
null 11
Totale 5.773
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Categoria #
all - tutte 24.328
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 24.328
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021102 0 0 0 0 0 0 0 0 0 22 33 47
2021/2022448 19 99 8 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
2025/20262.145 145 149 88 291 397 186 363 122 236 168 0 0
Totale 5.773