statistiche ricercatore

MASERATI, EMANUELA

Distribuzione geografica

Continente	#
NA - Nord America	11.438
EU - Europa	10.039
AS - Asia	4.428
SA - Sud America	636
AF - Africa	57
Continente sconosciuto - Info sul continente non disponibili	22
OC - Oceania	11
Totale	26.631

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Nazione	#
US - Stati Uniti d'America	11.279
IT - Italia	5.353
UA - Ucraina	1.672
SG - Singapore	1.410
CN - Cina	853
TR - Turchia	685
VN - Vietnam	665
SE - Svezia	572
BR - Brasile	548
HK - Hong Kong	526
FI - Finlandia	479
FR - Francia	405
DE - Germania	399
IE - Irlanda	372
GB - Regno Unito	320
RU - Federazione Russa	185
JP - Giappone	81
IN - India	80
CA - Canada	77
PL - Polonia	77
MX - Messico	73
AR - Argentina	33
AT - Austria	33
ES - Italia	33
BE - Belgio	31
ZA - Sudafrica	30
BD - Bangladesh	27
CH - Svizzera	27
EC - Ecuador	24
EU - Europa	22
NL - Olanda	19
IQ - Iraq	14
PK - Pakistan	11
AU - Australia	9
VE - Venezuela	9
ID - Indonesia	8
IL - Israele	8
LT - Lituania	8
UZ - Uzbekistan	8
CZ - Repubblica Ceca	7
MA - Marocco	7
PE - Perù	7
AZ - Azerbaigian	6
BG - Bulgaria	6
JO - Giordania	6
KR - Corea	6
OM - Oman	6
RO - Romania	6
RS - Serbia	6
EG - Egitto	5
PY - Paraguay	5
SA - Arabia Saudita	5
CL - Cile	4
CO - Colombia	4
PH - Filippine	4
AL - Albania	3
DZ - Algeria	3
KE - Kenya	3
LB - Libano	3
NO - Norvegia	3
BN - Brunei Darussalam	2
DK - Danimarca	2
ET - Etiopia	2
HR - Croazia	2
IM - Isola di Man	2
JM - Giamaica	2
LU - Lussemburgo	2
MC - Monaco	2
MD - Moldavia	2
MK - Macedonia	2
MY - Malesia	2
NP - Nepal	2
NZ - Nuova Zelanda	2
PA - Panama	2
SN - Senegal	2
TW - Taiwan	2
AD - Andorra	1
AE - Emirati Arabi Uniti	1
AO - Angola	1
BA - Bosnia-Erzegovina	1
BS - Bahamas	1
BY - Bielorussia	1
CG - Congo	1
CR - Costa Rica	1
DM - Dominica	1
DO - Repubblica Dominicana	1
EE - Estonia	1
GE - Georgia	1
GR - Grecia	1
HU - Ungheria	1
IR - Iran	1
KZ - Kazakistan	1
LV - Lettonia	1
ME - Montenegro	1
MN - Mongolia	1
MU - Mauritius	1
QA - Qatar	1
SK - Slovacchia (Repubblica Slovacca)	1
SR - Suriname	1
SY - Repubblica araba siriana	1
Totale	26.626

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Città	#
Milan	3.457
Jacksonville	1.252
Chandler	1.173
Fairfield	1.046
Ashburn	782
Singapore	715
Woodbridge	611
Hong Kong	526
Houston	453
Wilmington	447
Princeton	423
Seattle	399
Ann Arbor	389
Izmir	382
Dublin	371
Beijing	365
Nyköping	356
Cambridge	350
Dallas	334
Dearborn	332
Dong Ket	316
Rome	261
Boardman	246
San Mateo	176
The Dalles	146
Como	128
New York	108
Chicago	96
Los Angeles	93
San Diego	87
Santa Clara	80
Tokyo	78
Ogden	76
Helsinki	59
São Paulo	59
Munich	58
Ho Chi Minh City	49
London	47
Hefei	45
Warsaw	41
Kunming	39
Council Bluffs	37
Nanjing	37
Verona	37
Hanoi	36
Phoenix	34
Mexico City	33
Redwood City	31
Montreal	27
Brussels	26
Norwalk	26
Guangzhou	24
Turku	24
Radomsko	23
Rio de Janeiro	23
Stockholm	23
Brooklyn	22
Johannesburg	22
Poplar	22
Toronto	21
Columbus	20
Jinan	20
Nanchang	20
Washington	20
Brasília	19
Chennai	19
Atlanta	18
Nuremberg	18
Orem	18
Shanghai	18
Boston	17
Falls Church	17
Frankfurt am Main	17
Denver	16
Düsseldorf	15
San Francisco	15
Belo Horizonte	14
Catania	14
Naples	14
Quito	14
Edinburgh	13
Vienna	13
Manchester	12
Ottawa	12
Salt Lake City	12
Bologna	10
Philadelphia	10
Redmond	10
Bari	9
Brescia	9
Fuzhou	9
Kocaeli	9
Palermo	9
Zhengzhou	9
Amsterdam	8
Ankara	8
Auburn Hills	8
Berlin	8
Chengdu	8
Chiswick	8
Totale	17.516

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Nome	#
La sindrome da aneuploidia variegata a mosaico (MVA) associata a neutropenia come condizione predisponente a displasia e neoplasia ematologia	351
MOSAICISMO PIGMENTARIO CON ASPETTO FILLOIDE IN UN CASO DI TRISOMIA 13 TOTALE E PARZIALE IN MOSAICISMO INCONSUETO	298
Trisomia 8 costituzionale a mosaico nelle malattie mielodisplatiche e mieloproliferative: importanza per pratica clinica e per implicazioni teoriche	229
Shwachman-Diamond syndrome with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability	220
Sindrome di Patau con lunga sopravvivenza in un caso di trisomia 13 totale e parziale in mosaicismo inconsueto	219
Novel recurrent chromosome anomalies in Shwachman-Diamond syndrome.	215
gDNA qPCR is statistically more reliable than mRNA analysis in detecting leukemic cells to monitor CML	213
Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis	211
Parental Origin of the Deletion Del(20q) in Shwachman-Diamond Patients and Loss of the Paternally Derived Allele of the Imprinted L3MBTL1 Gene	211
CHARACTERIZATION BY MOLECULAR CYTOGENETICS, ARRAY-CGH AND WHOLE TRANSCRIPTOME ANALYSIS OF DIFFERENT BATCHES OF HeLa CELLS: GENOMIC VARIABILITY AND DIVERGENT GENE EXPRESSION	210
High variability of genomic instability and gene expression profiling in different HeLa clones	199
JUMPING TRANSLOCATIONS IN ACUTE LYMPHOBLASTIC LEUKEMIA.	195
Comparative genomic hybridization on microarray (a-CGH) in olfactory neuroblastoma: Analysis of ten cases and review of the literature	195
Establishment and characterization of a B-cell line derived from a patient with a myelodysplastic syndrome which expresses myelomonocytic and lymphoid markers	191
Improving the definition of the structure of the isochromosome i(7)(q10) in Shwachman-Diamond Syndrome	190
A homozygous contiguous gene deletion in chromosome 16p13.3 leads to autosomal recessive osteopetrosis in a Jordanian patient	190
Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells	187
Myelodysplastic syndromes: the pediatric point of view.	186
Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR	186
Chromosome anomalies in bone marrow as primarycause of aplastic or hypoplastic conditions andperipheral cytopenia: disorders due to secondaryimpairment of RUNX1 and MPL genes	186
Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms	186
Cytogenetic Monitoring in Shwachman-Diamond Syndrome: A Note on Clonal Progression and a Practical Warning	186
Clonal chromosome anomalies and propensity to myeloid malignancies in congenital amegakaryocytic thrombocytopenia (OMIM 604498)	182
A highly conserved sequence on the short arm of chromosome 7 detects multiple polymorphisms.	179
La trisomia 8 in leucemie acute e mielodisplasie e costituzionale nel 15-20% dei casi	178
Acquisizione di anomalie cromosomiche clonali nel midollo osseo di pazienti con sindrome di Shwachman Diamond in relazione all’età	177
In situ hybridization by scanning electron microscopy for painting, centromeric, and YAC localization	177
17Q21-QTER TRYSOMY IS AN INDICATOR OF POOR PROGNOSIS IN ACUTE MYELOGENOUS LEUKAEMIA	172
Acquired Chromosome change in Cholesteatoma	170
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMIM 601399)	168
Duplication of the der(14) chromosome of a translocation (8;14) in a case of Burkitt's type L3-ALL.	167
Definition of an acquired 11q deletion in a tumorigenic human monocytic cell line.	167
Sindrome di Shwachman: isocromosoma i(7)(q10), rischio di MDS/AML ed effetto da dosaggio genico della mutazione c.258+2T→C associata al gene SBDS	166
The strange case of the lost NRAS mutation in a child with juvenile myelomonocytic leukemia	166
Ring chromosome 9 with a 9p22.3-p24.3 duplication	165
Constitutional trisomy 8 mosaicism in primary myelofibrosis: relevance to clinical practice and warning for trisomy 8 studies.	165
Novel recurrent chromosome anomalies in Shwachman Diamond syndrome	165
Trisomy 8 in Philadelphia Chromosome (Ph1)- Negative Cells in the Course of Ph1-Positive Chronic Myelocytic Leukemia	163
Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15-20% of cases	163
Acute lymphoblastic leukemia and a familial balanced translocation (12;15) involving ETV6	162
CONSTITUTIONAL TRISOMY 8 MOSAICISM: MECHANISM OF ORIGIN, PHENOTYPE VARIABILITY, AND RISK OF MALIGNANCIES.	161
The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies	161
Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies	160
Comprehensive characterization of mesenchymal stromal cells from patients with Fanconi anaemia.	159
Array-based Comparative Genomic Hybridization in Shwachman-Diamond syndrome: results in 24 patients	157
Cadmium Impairs p53 Activity in HepG2 Cells	157
The isochromosome i(7)(q10) carrying c.258+2t>c mutation of the SBDS gene does not promote development of myeloid malignancies in patients with Shwachman syndrome.	156
La citogenetica interfasica dimostra che le cellule dendritiche nella Leucemia Mielomonocitica Cronica Giovanile fanno parte del clone leucemico	156
MLL-MLLT10 fusion in acute monoblastic leukemia: variant complex rearrangements and 11q proximal breakpoint heterogeneity	156
Clonal Chromosome Anomalies Affecting Fli1 Mimic Inherited Thrombocytopenia Of The Paris-Trousseau Type	156
BUSULFAN, CYCLOPHOSPHAMIDE AND MELPHALAN AS CONDITIONING REGIMEN FOR BONE MARROW TRANSPLANTATION IN CHILDREN WITH MYELODYSPLASTIC SYNDROMES.	155
Cytogenetics in autologous bone marrow transplantation.	153
DNA isolation protocol effects on nuclear DNA analysis by microarrays, droplet digital PCR, and whole genome sequencing, and on mitochondrial DNA copy number estimation	153
Transposition of c–abl oncogene in a case of masked Ph chromosome duplicated in blastic phase	152
Graft-versus-leukemia effects after allogeneic bone marrow transplantation are active also in the presence of clones with chromosomal anomalies in addition to the Ph chromosome.	151
ATAXIA WITHOUT TELANGIECTASIA IN TWO SISTERS WITH REARRANGEMENTS OF CHROMOSOMES 7 AND 14.	149
UNCOMMON ACQUIRED CHROMOSOME ANOMALIES IN SHWACHMAN-DIAMOND SYNDROME	149
Monitoring the Isochromosome i(7)(q10) in the Bone Marrow of Patients With Shwachman Syndrome by Real-time Quantitative PCR	149
Acute lymphoblastic leukemia and familial balanced translocation (12;15) involving ETV6	147
Whole exome sequencing discloses heterozygous variants in the DNAJC21 and EFL1 genes but not in SRP54 in 6 out of 16 patients with Shwachman-Diamond Syndrome carrying biallelic SBDS mutations	147
Comparative genomic hybridization su microarray (aCGH) in sindrome di Shwachman (OMIM 260400) e rischio di mielodisplasia: al di là della citogenetica standard	146
SPONTANEOUS REMISSION FROM RAEB IN A CHILD	146
Transferrin and structural anomalies of chromosome 3 in the blastic phase of chronic myelocytic leukemia	146
Evaluating chromosomal mosaicism by array-based CGH in relation to clinical issues: the proposal of a formula	146
Cytogenetics of Kaposi sarcoma: an analysis of 15 cases	145
BONE MARROW FAILURE CONDITIONS DUE TO CHROMOSOME ANOMALIES	145
Constitutional trisomy 8 mosaicism: mechanism of origin, phenotype variability, and risk of malignancies.	144
INVOLVEMENT OF 9Q22.1-31.1 REGION IN PYLORIC STENOSIS.	143
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMOM 601399)	143
Familial myelodysplastic syndromes, monosomy 7/trisomy 8, and mutator effects	143
Stimulation of DNA synthesis by endothelin-1 in primary cultures of human dental pulp	141
Sindrome di Shwachman con isocromosoma i(7q) e ruolo delle anomalie del cromosoma 7 nelle malattie mieloproliferative	139
Microarray expression studies on bone marrow of patients with Shwachman-Diamond syndrome in relation to deletion of the long arm of chromosome 20, other chromosome anomalies or normal karyotype	139
Mielodisplasia con monosomia 7 familiare: dati citogenetici e molecolari	138
Anomalie cromosomiche clonali e non-clonali in 32 casi di sindrome di Shwachman: valore prognostico e predittivo	137
Array-CGH used to monitor dysplastic/neoplastic disorders with unbalanced chromosome anomalies may detect as low as 8% abnormal cells	137
Minimal residual disease and trisomy 8	135
Molecular Mechanisms Generating and Stabilizing Terminal 22q13 Deletions in 44 Subjects with Phelan/McDermid Syndrome	135
Age related acquisition of clonal chromosome anomalies in bone marrow cells of SDS patients	134
MEIOTIC ORIGIN OF TRISOMY IN NEOPLASM: EVIDENCE IN A CASE OF ERYTROLEUKAEMIA	133
Instabilità costituzionale del cariotipo all'origine di trisomia 8 acquisita midollare	133
MONITORING SHWACHMAN-DIAMOND SYNDROME BY CYTOGENETICS AND a-CGH	133
Sindrome di Shwacham: instabilita del cromosoma 7 e rischio di patologia mielodisplastica e mieloproliferativa	132
Aplasia midollare da perdita del gene RUNX1 acquisita a causa di un riarrangiamento strutturale clonale del cromosoma 21	132
Karyotype instability evaluated by array-CGH and risk of myeloid malignancy in Shwachman Diamond syndrome	132
Acquiring an "inherited" thrombocitopenia: clonal chromosome anomalies affecting FLI1 mimic inherited thrombocitopenia of Paris-Trousseau type	132
Fenotipo di una paziente da microdelezione della regione 4q e avente di smorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di Gorge.	130
Gene dosage effect in acquired monosomy 7: distinct behaviour of β-glucuronidase and phosphoserine phosphatase.	130
The use of microarray-based comparative genomic hybridization (a-CGH) to detect and define chromosome imbalances in the bone marrow of SDS patients	129
Transposition of c-abl oncogene in a case of masked Ph chromosome duplicated in blastic phase	128
Different patterns of chromosome 20 interstitial deletion in Shwachman-Diamond syndrome and in myeloid neoplasms	128
Translocation 8/21 in two cases of refractory anaemia with excess of blasts in trasformation.	126
Cytogenetics of Kaposi Sarcoma, an analysis of 15 cases	126
Constitutional trisomy 8 as first mutation in multistep carcinogenesis: clinical, cytogenetic, and molecular data on three cases.	126
AML1-MTG16 gene rearrangement in a pediatric therapy related AML after Ewing sarcoma: a case discussion and review of literature	124
A new recurrent chromosome change in pediatric therapy-related myelodysplastic syndrome: unbalanced translocation 1/6 with cryptic duplication of the short arms of chromosome 6	124
RESTRICTED TCR REPERTOIRE AND LONG-TERM PERSISTENCE OF DONOR-DERIVED ANTIGEN-EXPERIENCED CD4+ T CELLS IN ALLOGENEIC BONE MARROW TRANSPLANTATION RECIPIENTS.	123
ANALISI DI MUTAZIONE DEL GENE SBDS IN UN GRUPPO DI PAZIENTI ITALIANI AFFETTI DALLA SINDROME DI SHWACHMAN	123
Expression studies in patients with Shwachman Diamond syndrome in relation to clonal chromosome anomalies in bone marrow	121
A case of chronic myelocytic leukaemia with five Philadelphia chromosomes.	120
Totale	16.157

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Categoria	#
all - tutte	104.215
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	104.215

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	2.092	0	0	0	0	0	361	60	280	460	136	270	525
2021/2022	1.844	177	301	188	93	40	50	66	124	108	230	176	291
2022/2023	2.968	272	168	224	338	244	628	5	391	391	93	125	89
2023/2024	5.188	881	891	906	914	957	260	35	66	117	54	18	89
2024/2025	2.942	22	43	541	60	119	177	122	204	322	240	259	833
2025/2026	3.094	568	346	330	1.012	663	175	0	0	0	0	0	0
Totale													26.768