statistiche ricercatore

LO CURTO, FRANCESCO

Distribuzione geografica

Continente	#
NA - Nord America	9.758
EU - Europa	7.519
AS - Asia	4.008
SA - Sud America	402
AF - Africa	119
Continente sconosciuto - Info sul continente non disponibili	60
OC - Oceania	16
Totale	21.882

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Nazione	#
US - Stati Uniti d'America	9.611
IT - Italia	3.912
SG - Singapore	1.228
UA - Ucraina	1.152
CN - Cina	928
TR - Turchia	566
VN - Vietnam	566
SE - Svezia	444
HK - Hong Kong	402
FI - Finlandia	376
FR - Francia	343
BR - Brasile	323
GB - Regno Unito	312
DE - Germania	307
IE - Irlanda	271
RU - Federazione Russa	128
IN - India	103
JP - Giappone	85
PL - Polonia	73
MX - Messico	69
NG - Nigeria	69
CA - Canada	55
NL - Olanda	45
BD - Bangladesh	40
ES - Italia	31
BE - Belgio	28
AR - Argentina	20
ZA - Sudafrica	20
CH - Svizzera	17
EC - Ecuador	17
AT - Austria	16
AU - Australia	16
EU - Europa	16
IQ - Iraq	15
CO - Colombia	12
VE - Venezuela	12
IL - Israele	10
LT - Lituania	10
MA - Marocco	10
CZ - Repubblica Ceca	9
PK - Pakistan	8
DK - Danimarca	7
PH - Filippine	7
AL - Albania	6
UZ - Uzbekistan	6
AE - Emirati Arabi Uniti	5
BG - Bulgaria	5
CL - Cile	5
EG - Egitto	5
JM - Giamaica	5
JO - Giordania	5
NP - Nepal	5
OM - Oman	5
PE - Perù	5
PY - Paraguay	5
MY - Malesia	4
RS - Serbia	4
SN - Senegal	4
TT - Trinidad e Tobago	4
DO - Repubblica Dominicana	3
GR - Grecia	3
ID - Indonesia	3
KE - Kenya	3
LB - Libano	3
PA - Panama	3
SA - Arabia Saudita	3
AO - Angola	2
AZ - Azerbaigian	2
BA - Bosnia-Erzegovina	2
CR - Costa Rica	2
DZ - Algeria	2
EE - Estonia	2
HU - Ungheria	2
IM - Isola di Man	2
LU - Lussemburgo	2
MN - Mongolia	2
NO - Norvegia	2
SK - Slovacchia (Repubblica Slovacca)	2
SV - El Salvador	2
TH - Thailandia	2
TW - Taiwan	2
UY - Uruguay	2
AM - Armenia	1
BO - Bolivia	1
BS - Bahamas	1
BY - Bielorussia	1
CG - Congo	1
CW - ???statistics.table.value.countryCode.CW???	1
GA - Gabon	1
GD - Grenada	1
KG - Kirghizistan	1
KZ - Kazakistan	1
LY - Libia	1
MC - Monaco	1
MD - Moldavia	1
MK - Macedonia	1
NI - Nicaragua	1
PR - Porto Rico	1
PT - Portogallo	1
RO - Romania	1
Totale	21.838

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Città	#
Milan	2.316
Chandler	957
Jacksonville	852
San Jose	811
Ashburn	668
Singapore	650
Fairfield	599
Hong Kong	396
Woodbridge	368
Council Bluffs	307
Izmir	293
Princeton	285
Wilmington	283
Dearborn	280
Dallas	277
Houston	273
Dublin	271
Ann Arbor	245
Seattle	242
Beijing	238
Cambridge	233
Nyköping	229
Rome	220
Chicago	189
Dong Ket	188
The Dalles	162
Boardman	149
San Mateo	128
Como	124
Lauterbourg	119
New York	110
Santa Clara	88
Tokyo	84
Ho Chi Minh City	77
Helsinki	76
Los Angeles	74
Orem	72
Abuja	69
Redwood City	68
Hanoi	67
San Diego	65
London	62
Ogden	61
Guangzhou	53
Munich	52
São Paulo	46
Verona	44
Mexico City	41
Warsaw	38
Nanjing	35
Hefei	33
Chennai	31
Kunming	28
Brussels	27
Philadelphia	24
Frankfurt am Main	23
Phoenix	23
Radomsko	23
Shanghai	23
Brooklyn	20
Tianjin	20
Manchester	19
Naples	19
Norwalk	19
Turku	18
Düsseldorf	17
Montreal	17
Toronto	17
Catania	16
Jinan	16
Johannesburg	16
Shenzhen	16
Stockholm	16
Denver	15
Nanchang	15
Amsterdam	14
Atlanta	14
Auburn Hills	14
Washington	14
Mumbai	13
Pavia	13
Poplar	13
Pune	13
Da Nang	11
Ponte Lambro	11
Rio de Janeiro	11
Boston	10
Fuzhou	10
Hangzhou	10
Miami	10
San Francisco	10
Zhengzhou	10
Bari	9
Belo Horizonte	9
Brasília	9
Palermo	9
Piemonte	9
Turin	9
Bangalore	8
Bologna	8
Totale	14.416

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Nome	#
La sindrome da aneuploidia variegata a mosaico (MVA) associata a neutropenia come condizione predisponente a displasia e neoplasia ematologia	379
A liveborn 69,XXX triploid. Origin, X chromosome activity and gene dosage.	288
Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis	278
Trisomia 8 costituzionale a mosaico nelle malattie mielodisplatiche e mieloproliferative: importanza per pratica clinica e per implicazioni teoriche	248
The mammary gland and the homeobox gene Otx1	233
Cd bands and centromeric function in dicentric chromosomes	225
A new chromosome instability disorder	223
Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells	221
Chromosome anomalies in bone marrow as primarycause of aplastic or hypoplastic conditions andperipheral cytopenia: disorders due to secondaryimpairment of RUNX1 and MPL genes	215
OTX1 and OTX2 as possible molecular markers of sinonasal carcinomas and olfactory neuroblastomas	215
Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms	214
Genomic quantitative real-time PCR proves residual disease positivity in more than 30% samples with negative mRNA-based qRT-PCR in Chronic Myeloid Leukemia	213
Cytogenetic Monitoring in Shwachman-Diamond Syndrome: A Note on Clonal Progression and a Practical Warning	212
Array-based Comparative Genomic Hybridization in Shwachman-Diamond syndrome: results in 24 patients	206
Clonal chromosome anomalies and propensity to myeloid malignancies in congenital amegakaryocytic thrombocytopenia (OMIM 604498)	205
Chronic Myeloid Leukemia: Molecular Monitoring of Residual Disease by Genomic DNA Compared to Conventional mRNA Analysis in Follow-Ups up to 8 Years	205
Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR	201
La trisomia 8 in leucemie acute e mielodisplasie e costituzionale nel 15-20% dei casi	199
48,XXXY/49,XXXXY Mosaicism in a month old infant.	198
Acquisizione di anomalie cromosomiche clonali nel midollo osseo di pazienti con sindrome di Shwachman Diamond in relazione all’età	198
Acquired Chromosome change in Cholesteatoma	197
Assessing residual disease in imatinib-treated CML patients by DNA compared to MRNA assays	192
Evaluating chromosomal mosaicism by array-based CGH in relation to clinical issues: the proposal of a formula	192
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.	190
Different real time PCR approaches for the fine quantification of SNP's alleles in DNA pools: assays development, characterization and pre-validation.	190
Constitutional trisomy 8 mosaicism in primary myelofibrosis: relevance to clinical practice and warning for trisomy 8 studies.	189
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMIM 601399)	188
Acute lymphoblastic leukemia and a familial balanced translocation (12;15) involving ETV6	185
Le basi genetiche della malattia linfoproliferativa.	184
First trimester prenatal diagnosis of Sanfilippo disease (MPS III) type B.	184
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	183
Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies	183
The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies	183
Karyotypic variation in benign pleomorphic adenoma of the parotid and in normal salivary glands.	181
The syndrome of partial trisomy 14q.	180
Analysis of cross-contamination in established tumour cell lines.	177
La citogenetica interfasica dimostra che le cellule dendritiche nella Leucemia Mielomonocitica Cronica Giovanile fanno parte del clone leucemico	174
Monitoring the Isochromosome i(7)(q10) in the Bone Marrow of Patients With Shwachman Syndrome by Real-time Quantitative PCR	172
Comparative genomic hybridization su microarray (aCGH) in sindrome di Shwachman (OMIM 260400) e rischio di mielodisplasia: al di là della citogenetica standard	171
Nuclear projections in tumour cells	171
Studio molecolare del differenziamento da cellule staminali in condrociti in vivo per lo sviluppo di un protocollo di trapianti di cartilagine umana	171
Anticentromeric antibodies and inactive centromeres.	170
The role of Yp in sex determination: new evidence from X/Y translocations.	169
Indirect immunofluorescence of inactive centromeres as indicator of centromeric function.	169
Le basi genetiche della malattia linfoproliferativa legata al cromosoma X	169
Chromosomal analysis in cultured lymphocytes and fibroblasts of psoriatic patients before and after treatment.	168
Chromosome identification in a Chinese hamster pseudodiploid cell line (CHEF-125)	168
Microhomologies and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia	168
A woman carrier of two apparently unrelated reciprocal translocations: prenatal diagnosis of normal karyotype in the foetus.	167
Acute lymphoblastic leukemia and familial balanced translocation (12;15) involving ETV6	167
Studio molecolare del differenziamento da cellule staminali in condrociti e osteoblasti in vivo per lo sviluppo di protocolli di trapianto	167
Familial myelodysplastic syndromes, monosomy 7/trisomy 8, and mutator effects	165
Mielodisplasia con monosomia 7 familiare: dati citogenetici e molecolari	164
Different patterns of chromosome 20 interstitial deletion in Shwachman-Diamond syndrome and in myeloid neoplasms	163
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMOM 601399)	160
Criobanca automatizzata di materiale biologico: stoccaggio e monitoraggio molecolare di cellule meniscali per il trapianto autologo	160
Establishment and study of different real-time polymerase chain reaction assays for the quantification of cells with deletions of chromosome 7.	160
Microhomologiee and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia.	158
Normal insulin receptors in mitochondrial myopathies with ophthalmoplegia.	158
Age related acquisition of clonal chromosome anomalies in bone marrow cells of SDS patients	157
Array-CGH used to monitor dysplastic/neoplastic disorders with unbalanced chromosome anomalies may detect as low as 8% abnormal cells	157
Presumptive mosaic origin of an XX/XY female with ambiguous genitalia.	156
Anomalie cromosomiche clonali e non-clonali in 32 casi di sindrome di Shwachman: valore prognostico e predittivo	156
Aplasia midollare da perdita del gene RUNX1 acquisita a causa di un riarrangiamento strutturale clonale del cromosoma 21	154
MONITORING SHWACHMAN-DIAMOND SYNDROME BY CYTOGENETICS AND a-CGH	154
Myotonic Dystrophy: genetic aspects ; cytochemical findings.	152
The use of microarray-based comparative genomic hybridization (a-CGH) to detect and define chromosome imbalances in the bone marrow of SDS patients	151
Citogenetica Umana: nuove metodiche ed applicazioni in medicina.	150
Instabilità costituzionale del cariotipo all'origine di trisomia 8 acquisita midollare	150
Sindrome di Shwacham: instabilita del cromosoma 7 e rischio di patologia mielodisplastica e mieloproliferativa	149
Fenotipo di una paziente da microdelezione della regione 4q e avente di smorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di Gorge.	149
Erratum: OTX1 expression in breast cancer is regulated by p53 (Oncogene (2011) 30 (3096-3103) doi:10.1038/onc.2011.31)	147
Molecular monitoring of residual disease in chronic myeloid leukemia by genomic DNA compared with conventional mRNA analysis.	145
Growth Hormone and Estrogens in Patients with Turner Syndrome: in vivo and in vitro studies.	144
Karyotype instability evaluated by array-CGH and risk of myeloid malignancy in Shwachman Diamond syndrome	144
La linea cellulare EUE deriva da una linea HeLa.	141
Chromosome size and nuclear projections	141
Nuclear projections and latent centromeres in primary culture and established cell lines.	141
Variabilità cromosomica in linee cellulari derivate da melanomi.	139
Different reaction of inactive centromeres to anticentromeric antibodies.	138
Distrofia miotonica: genetica e citochimica	138
Traslocazione complessa che coinvolge MLL in leucemia mielomonocitica acuta connatale	138
Studio dei fibroblasti "in vitro" nella distrofia miotonica.	137
Leucemia linfoblastica acuta e traslocazione familiare (15-15) che coinvolge ETV6	137
Diagnostica cromosomica	136
Le anomalie cromosomiche nel midollo come causa primaria di aplasia o ipoplasia a rischio di mielodisplasia e leucemia acuta: coinvolgimento dei geni FLI1 e MPL	136
Insulin receptors in psoriasis.	135
Fenotipo di una paziente affetta da microdelezione subtelomerica della regione 4q e avente dimorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di George	135
Instabilità del cariotipo e mielodisplasie nella Sindrome di Shwachman	134
DIFFERENTE PERDITA DI MATERIALE NELLE DELEZIONI INTERSTIZIALI DEL CROMOSOMA 20 NELLE DISPLASIE/NEOPLASIE MIELOIDI E NELLA SINDROME DI SHWACHMAN-DIAMOND	134
Chromosome identification and karyotypic evolution in a human melanoma cell line.	133
Correlation between the numbers of sex chromosomes and the H-Y antigen titer.	132
Le basi genetiche della malattia linfoproliferativa legata al cromosoma X	132
Differente reazione dei centromeri inattivi agli anticorpi anticentromero.	131
Familial partial monosomy 7 and myelodysplasia: different paternal origin of the monosomy 7 suggests action of a mutator gene	131
Protrusioni nucleari dovute a cromosomi strutturalmente alterati.	130
MONITORAGGIO CITOGENETICO E MEDIANTE a-CGH DELLA SINDROME DI SHWACHMAN-DIAMOND	130
Mielodisplasia familiare, monosomia 7 / trisomia 8 ed effetto mutatore	129
Severe aplastic anemia (SAA) due to chromosome 21 acquired chromosome anomaly and haploinsufficiency of RUNX1 gene	129
Chromosome 7 instability and myelodysplasia in Shwachman syndrome	127
Totale	17.162

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Categoria	#
all - tutte	80.224
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	80.224

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2021/2022	1.161	0	177	137	76	38	26	44	77	70	194	98	224
2022/2023	2.356	186	143	200	279	156	472	2	336	322	90	101	69
2023/2024	3.566	594	611	591	636	630	189	23	74	94	26	11	87
2024/2025	2.094	12	39	395	71	141	111	106	140	197	140	147	595
2025/2026	4.957	393	234	207	625	508	376	1.062	277	602	307	215	151
2026/2027	276	84	192	0	0	0	0	0	0	0	0	0	0
Totale													21.882