statistiche ricercatore

MASERATI, EMANUELA

Distribuzione geografica

Continente	#
NA - Nord America	13.620
EU - Europa	10.509
AS - Asia	5.812
SA - Sud America	713
AF - Africa	116
OC - Oceania	25
Continente sconosciuto - Info sul continente non disponibili	22
Totale	30.817

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Nazione	#
US - Stati Uniti d'America	13.420
IT - Italia	5.426
SG - Singapore	1.765
UA - Ucraina	1.674
CN - Cina	1.419
VN - Vietnam	905
TR - Turchia	690
FR - Francia	612
HK - Hong Kong	604
BR - Brasile	587
SE - Svezia	574
FI - Finlandia	571
DE - Germania	419
IE - Irlanda	374
GB - Regno Unito	357
RU - Federazione Russa	189
IN - India	115
MX - Messico	96
CA - Canada	89
JP - Giappone	86
PL - Polonia	82
BD - Bangladesh	62
AR - Argentina	40
AT - Austria	37
ES - Italia	37
ZA - Sudafrica	36
EC - Ecuador	32
NG - Nigeria	32
BE - Belgio	31
NL - Olanda	29
CH - Svizzera	27
IQ - Iraq	26
AU - Australia	23
EU - Europa	22
PK - Pakistan	18
VE - Venezuela	14
SA - Arabia Saudita	12
ID - Indonesia	11
PH - Filippine	11
UZ - Uzbekistan	11
MA - Marocco	10
PY - Paraguay	10
CO - Colombia	9
IL - Israele	9
JO - Giordania	9
PE - Perù	9
CL - Cile	8
EG - Egitto	8
LT - Lituania	8
MY - Malesia	8
OM - Oman	8
BG - Bulgaria	7
CZ - Repubblica Ceca	7
AZ - Azerbaigian	6
DZ - Algeria	6
KE - Kenya	6
KR - Corea	6
NP - Nepal	6
RO - Romania	6
RS - Serbia	6
MD - Moldavia	5
JM - Giamaica	4
SC - Seychelles	4
AE - Emirati Arabi Uniti	3
AL - Albania	3
BY - Bielorussia	3
KZ - Kazakistan	3
LB - Libano	3
NO - Norvegia	3
PA - Panama	3
TW - Taiwan	3
AO - Angola	2
BN - Brunei Darussalam	2
BS - Bahamas	2
DK - Danimarca	2
DO - Repubblica Dominicana	2
ET - Etiopia	2
GE - Georgia	2
GR - Grecia	2
HR - Croazia	2
HU - Ungheria	2
IM - Isola di Man	2
IR - Iran	2
LU - Lussemburgo	2
MC - Monaco	2
MK - Macedonia	2
NZ - Nuova Zelanda	2
SN - Senegal	2
SR - Suriname	2
AD - Andorra	1
BA - Bosnia-Erzegovina	1
BF - Burkina Faso	1
BO - Bolivia	1
CG - Congo	1
CR - Costa Rica	1
DM - Dominica	1
EE - Estonia	1
GA - Gabon	1
GT - Guatemala	1
KW - Kuwait	1
Totale	30.801

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Città	#
Milan	3.465
Jacksonville	1.254
San Jose	1.197
Chandler	1.173
Fairfield	1.046
Singapore	939
Ashburn	938
Woodbridge	611
Hong Kong	598
Houston	455
Wilmington	447
Princeton	423
Beijing	416
Seattle	401
Ann Arbor	389
Izmir	382
Dublin	371
Nyköping	356
Cambridge	352
Dallas	344
Dearborn	332
Dong Ket	316
Rome	265
Council Bluffs	260
Boardman	246
The Dalles	245
Lauterbourg	183
San Mateo	176
Chicago	166
Helsinki	151
New York	133
Ho Chi Minh City	132
Como	128
Los Angeles	105
Hanoi	99
Santa Clara	95
San Diego	87
Tokyo	83
Ogden	76
Orem	74
Guangzhou	67
São Paulo	63
Munich	58
Mexico City	51
London	50
Hefei	45
Warsaw	45
Shanghai	41
Kunming	40
Nanjing	40
Phoenix	39
Verona	37
Chennai	36
Abuja	31
Frankfurt am Main	31
Redwood City	31
Montreal	30
Brooklyn	27
Johannesburg	27
Brussels	26
Norwalk	26
Manchester	25
Stockholm	24
Turku	24
Atlanta	23
Poplar	23
Radomsko	23
Rio de Janeiro	23
Tianjin	23
Columbus	22
Toronto	22
Brasília	21
Nanchang	21
Shenzhen	21
Washington	21
Boston	20
Jinan	20
Denver	19
Nuremberg	19
Zhengzhou	19
Amsterdam	17
Da Nang	17
Falls Church	17
Naples	16
Catania	15
Düsseldorf	15
Miami	15
San Francisco	15
Belo Horizonte	14
Biên Hòa	14
Quito	14
Vienna	14
Edinburgh	13
Hangzhou	13
Mumbai	13
Bologna	12
Ottawa	12
Philadelphia	12
Salt Lake City	12
Brescia	11
Totale	20.444

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Nome	#
La sindrome da aneuploidia variegata a mosaico (MVA) associata a neutropenia come condizione predisponente a displasia e neoplasia ematologia	375
MOSAICISMO PIGMENTARIO CON ASPETTO FILLOIDE IN UN CASO DI TRISOMIA 13 TOTALE E PARZIALE IN MOSAICISMO INCONSUETO	339
Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis	272
Trisomia 8 costituzionale a mosaico nelle malattie mielodisplatiche e mieloproliferative: importanza per pratica clinica e per implicazioni teoriche	247
CHARACTERIZATION BY MOLECULAR CYTOGENETICS, ARRAY-CGH AND WHOLE TRANSCRIPTOME ANALYSIS OF DIFFERENT BATCHES OF HeLa CELLS: GENOMIC VARIABILITY AND DIVERGENT GENE EXPRESSION	238
Shwachman-Diamond syndrome with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability	237
High variability of genomic instability and gene expression profiling in different HeLa clones	235
Sindrome di Patau con lunga sopravvivenza in un caso di trisomia 13 totale e parziale in mosaicismo inconsueto	231
gDNA qPCR is statistically more reliable than mRNA analysis in detecting leukemic cells to monitor CML	231
A homozygous contiguous gene deletion in chromosome 16p13.3 leads to autosomal recessive osteopetrosis in a Jordanian patient	230
Establishment and characterization of a B-cell line derived from a patient with a myelodysplastic syndrome which expresses myelomonocytic and lymphoid markers	228
Myelodysplastic syndromes: the pediatric point of view.	227
Novel recurrent chromosome anomalies in Shwachman-Diamond syndrome.	225
Parental Origin of the Deletion Del(20q) in Shwachman-Diamond Patients and Loss of the Paternally Derived Allele of the Imprinted L3MBTL1 Gene	224
Comparative genomic hybridization on microarray (a-CGH) in olfactory neuroblastoma: Analysis of ten cases and review of the literature	219
MLL-MLLT10 fusion in acute monoblastic leukemia: variant complex rearrangements and 11q proximal breakpoint heterogeneity	218
Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells	218
JUMPING TRANSLOCATIONS IN ACUTE LYMPHOBLASTIC LEUKEMIA.	217
Chromosome anomalies in bone marrow as primarycause of aplastic or hypoplastic conditions andperipheral cytopenia: disorders due to secondaryimpairment of RUNX1 and MPL genes	211
Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms	211
Cytogenetic Monitoring in Shwachman-Diamond Syndrome: A Note on Clonal Progression and a Practical Warning	209
Clonal chromosome anomalies and propensity to myeloid malignancies in congenital amegakaryocytic thrombocytopenia (OMIM 604498)	203
Array-based Comparative Genomic Hybridization in Shwachman-Diamond syndrome: results in 24 patients	203
Improving the definition of the structure of the isochromosome i(7)(q10) in Shwachman-Diamond Syndrome	201
Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR	200
BUSULFAN, CYCLOPHOSPHAMIDE AND MELPHALAN AS CONDITIONING REGIMEN FOR BONE MARROW TRANSPLANTATION IN CHILDREN WITH MYELODYSPLASTIC SYNDROMES.	199
La trisomia 8 in leucemie acute e mielodisplasie e costituzionale nel 15-20% dei casi	197
Acquired Chromosome change in Cholesteatoma	196
A highly conserved sequence on the short arm of chromosome 7 detects multiple polymorphisms.	196
Acquisizione di anomalie cromosomiche clonali nel midollo osseo di pazienti con sindrome di Shwachman Diamond in relazione all’età	196
In situ hybridization by scanning electron microscopy for painting, centromeric, and YAC localization	191
17Q21-QTER TRYSOMY IS AN INDICATOR OF POOR PROGNOSIS IN ACUTE MYELOGENOUS LEUKAEMIA	190
Novel recurrent chromosome anomalies in Shwachman Diamond syndrome	190
Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15-20% of cases	188
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.	187
Duplication of the der(14) chromosome of a translocation (8;14) in a case of Burkitt's type L3-ALL.	186
Constitutional trisomy 8 mosaicism in primary myelofibrosis: relevance to clinical practice and warning for trisomy 8 studies.	186
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMIM 601399)	185
Cadmium Impairs p53 Activity in HepG2 Cells	184
Acute lymphoblastic leukemia and a familial balanced translocation (12;15) involving ETV6	183
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	181
Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies	181
The strange case of the lost NRAS mutation in a child with juvenile myelomonocytic leukemia	181
CONSTITUTIONAL TRISOMY 8 MOSAICISM: MECHANISM OF ORIGIN, PHENOTYPE VARIABILITY, AND RISK OF MALIGNANCIES.	180
Definition of an acquired 11q deletion in a tumorigenic human monocytic cell line.	180
Ring chromosome 9 with a 9p22.3-p24.3 duplication	180
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	179
The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies	179
Trisomy 8 in Philadelphia Chromosome (Ph1)- Negative Cells in the Course of Ph1-Positive Chronic Myelocytic Leukemia	178
Clonal Chromosome Anomalies Affecting Fli1 Mimic Inherited Thrombocytopenia Of The Paris-Trousseau Type	177
Comprehensive characterization of mesenchymal stromal cells from patients with Fanconi anaemia.	176
Evaluating chromosomal mosaicism by array-based CGH in relation to clinical issues: the proposal of a formula	175
Transposition of c–abl oncogene in a case of masked Ph chromosome duplicated in blastic phase	172
BONE MARROW FAILURE CONDITIONS DUE TO CHROMOSOME ANOMALIES	172
La citogenetica interfasica dimostra che le cellule dendritiche nella Leucemia Mielomonocitica Cronica Giovanile fanno parte del clone leucemico	170
DNA isolation protocol effects on nuclear DNA analysis by microarrays, droplet digital PCR, and whole genome sequencing, and on mitochondrial DNA copy number estimation	170
Comparative genomic hybridization su microarray (aCGH) in sindrome di Shwachman (OMIM 260400) e rischio di mielodisplasia: al di là della citogenetica standard	169
Constitutional trisomy 8 mosaicism: mechanism of origin, phenotype variability, and risk of malignancies.	169
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.	169
Monitoring the Isochromosome i(7)(q10) in the Bone Marrow of Patients With Shwachman Syndrome by Real-time Quantitative PCR	168
Cytogenetics in autologous bone marrow transplantation.	167
Acute lymphoblastic leukemia and familial balanced translocation (12;15) involving ETV6	165
UNCOMMON ACQUIRED CHROMOSOME ANOMALIES IN SHWACHMAN-DIAMOND SYNDROME	164
Familial myelodysplastic syndromes, monosomy 7/trisomy 8, and mutator effects	163
MEIOTIC ORIGIN OF TRISOMY IN NEOPLASM: EVIDENCE IN A CASE OF ERYTROLEUKAEMIA	162
Mielodisplasia con monosomia 7 familiare: dati citogenetici e molecolari	161
Molecular Mechanisms Generating and Stabilizing Terminal 22q13 Deletions in 44 Subjects with Phelan/McDermid Syndrome	161
Different patterns of chromosome 20 interstitial deletion in Shwachman-Diamond syndrome and in myeloid neoplasms	161
ATAXIA WITHOUT TELANGIECTASIA IN TWO SISTERS WITH REARRANGEMENTS OF CHROMOSOMES 7 AND 14.	160
Cytogenetics of Kaposi sarcoma: an analysis of 15 cases	160
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	158
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMOM 601399)	157
SPONTANEOUS REMISSION FROM RAEB IN A CHILD	157
Age related acquisition of clonal chromosome anomalies in bone marrow cells of SDS patients	156
Array-CGH used to monitor dysplastic/neoplastic disorders with unbalanced chromosome anomalies may detect as low as 8% abnormal cells	156
Stimulation of DNA synthesis by endothelin-1 in primary cultures of human dental pulp	156
INVOLVEMENT OF 9Q22.1-31.1 REGION IN PYLORIC STENOSIS.	155
Sindrome di Shwachman con isocromosoma i(7q) e ruolo delle anomalie del cromosoma 7 nelle malattie mieloproliferative	155
Transferrin and structural anomalies of chromosome 3 in the blastic phase of chronic myelocytic leukemia	155
Anomalie cromosomiche clonali e non-clonali in 32 casi di sindrome di Shwachman: valore prognostico e predittivo	154
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	154
Expression studies in patients with Shwachman Diamond syndrome in relation to clonal chromosome anomalies in bone marrow	154
Aplasia midollare da perdita del gene RUNX1 acquisita a causa di un riarrangiamento strutturale clonale del cromosoma 21	153
AML1-MTG16 gene rearrangement in a pediatric therapy related AML after Ewing sarcoma: a case discussion and review of literature	152
MONITORING SHWACHMAN-DIAMOND SYNDROME BY CYTOGENETICS AND a-CGH	152
Minimal residual disease and trisomy 8	149
Gene dosage effect in acquired monosomy 7: distinct behaviour of β-glucuronidase and phosphoserine phosphatase.	149
Acquiring an "inherited" thrombocitopenia: clonal chromosome anomalies affecting FLI1 mimic inherited thrombocitopenia of Paris-Trousseau type	149
Translocation 8/21 in two cases of refractory anaemia with excess of blasts in trasformation.	148
Sindrome di Shwacham: instabilita del cromosoma 7 e rischio di patologia mielodisplastica e mieloproliferativa	148
Instabilità costituzionale del cariotipo all'origine di trisomia 8 acquisita midollare	148
ANALISI DI MUTAZIONE DEL GENE SBDS IN UN GRUPPO DI PAZIENTI ITALIANI AFFETTI DALLA SINDROME DI SHWACHMAN	147
The use of microarray-based comparative genomic hybridization (a-CGH) to detect and define chromosome imbalances in the bone marrow of SDS patients	147
Fenotipo di una paziente da microdelezione della regione 4q e avente di smorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di Gorge.	146
A 45, X male with a Yp/18 translocation.	146
CYTOGENETIC AND MOLECULAR DETERMINANTS OF TRASFORMATION IN SCHWACHMAN DIAMOND SYNDROME	144
RESTRICTED TCR REPERTOIRE AND LONG-TERM PERSISTENCE OF DONOR-DERIVED ANTIGEN-EXPERIENCED CD4+ T CELLS IN ALLOGENEIC BONE MARROW TRANSPLANTATION RECIPIENTS.	142
Cytogenetics in Shwachmann Syndrome: Chromosom changes and haematological implications	142
Karyotype instability evaluated by array-CGH and risk of myeloid malignancy in Shwachman Diamond syndrome	142
Cytogenetic and a-CGH monitoring in Shwachman-Diamond syndrome.	142
Totale	18.346

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Categoria	#
all - tutte	115.517
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	115.517

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	525	0	0	0	0	0	0	0	0	0	0	0	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	7.280	568	346	330	1.012	663	501	1.630	491	758	512	344	125
Totale													30.954