statistiche ricercatore

LO CURTO, FRANCESCO

Distribuzione geografica

Continente	#
NA - Nord America	6.958
EU - Europa	6.819
AS - Asia	1.458
SA - Sud America	42
Continente sconosciuto - Info sul continente non disponibili	16
OC - Oceania	3
AF - Africa	2
Totale	15.298

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Nazione	#
US - Stati Uniti d'America	6.929
IT - Italia	3.820
UA - Ucraina	1.141
TR - Turchia	557
SE - Svezia	430
VN - Vietnam	337
CN - Cina	323
FI - Finlandia	311
IE - Irlanda	270
DE - Germania	232
GB - Regno Unito	218
FR - Francia	195
SG - Singapore	122
RU - Federazione Russa	61
JP - Giappone	55
IN - India	44
PL - Polonia	36
BE - Belgio	27
BR - Brasile	26
NL - Olanda	25
EU - Europa	16
MX - Messico	14
CA - Canada	12
CH - Svizzera	8
CZ - Repubblica Ceca	5
ES - Italia	5
AL - Albania	4
AR - Argentina	4
AT - Austria	4
BG - Bulgaria	4
IL - Israele	4
PE - Perù	4
AU - Australia	3
DK - Danimarca	3
IQ - Iraq	3
LT - Lituania	3
VE - Venezuela	3
AE - Emirati Arabi Uniti	2
EC - Ecuador	2
EE - Estonia	2
ID - Indonesia	2
IM - Isola di Man	2
LU - Lussemburgo	2
NO - Norvegia	2
OM - Oman	2
PA - Panama	2
PK - Pakistan	2
RS - Serbia	2
SK - Slovacchia (Repubblica Slovacca)	2
ZA - Sudafrica	2
AM - Armenia	1
AZ - Azerbaigian	1
BD - Bangladesh	1
BS - Bahamas	1
BY - Bielorussia	1
CL - Cile	1
CO - Colombia	1
GR - Grecia	1
HU - Ungheria	1
MC - Monaco	1
MY - Malesia	1
PY - Paraguay	1
RO - Romania	1
TW - Taiwan	1
Totale	15.298

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Città	#
Milan	2.308
Chandler	957
Jacksonville	851
Fairfield	599
Ashburn	390
Woodbridge	368
Izmir	293
Princeton	284
Wilmington	282
Dearborn	280
Dublin	270
Houston	263
Ann Arbor	245
Seattle	240
Cambridge	232
Nyköping	229
Rome	209
Dong Ket	188
Boardman	149
San Mateo	128
Como	123
Singapore	107
Beijing	91
Chicago	89
Redwood City	68
San Diego	64
Ogden	61
New York	57
Tokyo	54
Hefei	32
Nanjing	32
Santa Clara	30
Helsinki	29
Verona	29
Kunming	28
Brussels	26
Dallas	26
Radomsko	23
Philadelphia	22
London	20
Norwalk	19
Düsseldorf	17
Nanchang	15
Auburn Hills	14
Guangzhou	14
Jinan	14
Naples	14
Catania	13
Pavia	13
Pune	13
Phoenix	11
Ponte Lambro	11
Washington	11
Los Angeles	10
Piemonte	9
Bangalore	8
Bari	8
Edinburgh	8
Frankfurt am Main	8
Fuzhou	8
Padova	8
Toronto	8
Palermo	7
São Paulo	7
Turin	7
Baotou	6
Bologna	6
Brescia	6
Chengdu	6
Kocaeli	6
Munich	6
Quzhou	6
Shanghai	6
Warsaw	6
Zhengzhou	6
Amsterdam	5
Berlin	5
Florence	5
Genova	5
Hebei	5
Istanbul	5
Shenyang	5
Viterbo	5
Cagliari	4
Desio	4
Foggia	4
Islington	4
Pescara	4
Prague	4
Sofia	4
Tel Aviv	4
Ancona	3
Atlanta	3
Baghdad	3
Bergamo	3
Chiswick	3
Chongqing	3
Copenhagen	3
Estrela	3
Genzano Di Roma	3
Totale	10.210

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Nome	#
La sindrome da aneuploidia variegata a mosaico (MVA) associata a neutropenia come condizione predisponente a displasia e neoplasia ematologia	311
Trisomia 8 costituzionale a mosaico nelle malattie mielodisplatiche e mieloproliferative: importanza per pratica clinica e per implicazioni teoriche	211
A liveborn 69,XXX triploid. Origin, X chromosome activity and gene dosage.	209
Genomic quantitative real-time PCR proves residual disease positivity in more than 30% samples with negative mRNA-based qRT-PCR in Chronic Myeloid Leukemia	171
Cd bands and centromeric function in dicentric chromosomes	164
Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR	161
OTX1 and OTX2 as possible molecular markers of sinonasal carcinomas and olfactory neuroblastomas	161
A new chromosome instability disorder	160
Le basi genetiche della malattia linfoproliferativa.	157
Cytogenetic Monitoring in Shwachman-Diamond Syndrome: A Note on Clonal Progression and a Practical Warning	156
Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis	155
First trimester prenatal diagnosis of Sanfilippo disease (MPS III) type B.	153
Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms	153
Clonal chromosome anomalies and propensity to myeloid malignancies in congenital amegakaryocytic thrombocytopenia (OMIM 604498)	150
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	149
La trisomia 8 in leucemie acute e mielodisplasie e costituzionale nel 15-20% dei casi	149
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMIM 601399)	149
Karyotypic variation in benign pleomorphic adenoma of the parotid and in normal salivary glands.	148
La citogenetica interfasica dimostra che le cellule dendritiche nella Leucemia Mielomonocitica Cronica Giovanile fanno parte del clone leucemico	143
The mammary gland and the homeobox gene Otx1	141
Chromosome anomalies in bone marrow as primarycause of aplastic or hypoplastic conditions andperipheral cytopenia: disorders due to secondaryimpairment of RUNX1 and MPL genes	141
Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells	140
Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies	137
The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies	137
Nuclear projections in tumour cells	136
Chromosome identification in a Chinese hamster pseudodiploid cell line (CHEF-125)	136
Assessing residual disease in imatinib-treated CML patients by DNA compared to MRNA assays	135
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.	134
Chronic Myeloid Leukemia: Molecular Monitoring of Residual Disease by Genomic DNA Compared to Conventional mRNA Analysis in Follow-Ups up to 8 Years	134
Presumptive mosaic origin of an XX/XY female with ambiguous genitalia.	131
The syndrome of partial trisomy 14q.	130
48,XXXY/49,XXXXY Mosaicism in a month old infant.	129
Normal insulin receptors in mitochondrial myopathies with ophthalmoplegia.	129
Studio molecolare del differenziamento da cellule staminali in condrociti in vivo per lo sviluppo di un protocollo di trapianti di cartilagine umana	129
Constitutional trisomy 8 mosaicism in primary myelofibrosis: relevance to clinical practice and warning for trisomy 8 studies.	129
Citogenetica Umana: nuove metodiche ed applicazioni in medicina.	127
Indirect immunofluorescence of inactive centromeres as indicator of centromeric function.	125
Microhomologies and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia	125
The role of Yp in sex determination: new evidence from X/Y translocations.	123
Le basi genetiche della malattia linfoproliferativa legata al cromosoma X	123
Mielodisplasia con monosomia 7 familiare: dati citogenetici e molecolari	122
Familial myelodysplastic syndromes, monosomy 7/trisomy 8, and mutator effects	122
Establishment and study of different real-time polymerase chain reaction assays for the quantification of cells with deletions of chromosome 7.	120
Growth Hormone and Estrogens in Patients with Turner Syndrome: in vivo and in vitro studies.	119
Monitoring the Isochromosome i(7)(q10) in the Bone Marrow of Patients With Shwachman Syndrome by Real-time Quantitative PCR	119
Different real time PCR approaches for the fine quantification of SNP's alleles in DNA pools: assays development, characterization and pre-validation.	118
Acquired Chromosome change in Cholesteatoma	116
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMOM 601399)	116
Sindrome di Shwacham: instabilita del cromosoma 7 e rischio di patologia mielodisplastica e mieloproliferativa	112
Studio molecolare del differenziamento da cellule staminali in condrociti e osteoblasti in vivo per lo sviluppo di protocolli di trapianto	112
Instabilità costituzionale del cariotipo all'origine di trisomia 8 acquisita midollare	112
Microhomologiee and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia.	111
Erratum: OTX1 expression in breast cancer is regulated by p53 (Oncogene (2011) 30 (3096-3103) doi:10.1038/onc.2011.31)	111
Anticentromeric antibodies and inactive centromeres.	110
MONITORING SHWACHMAN-DIAMOND SYNDROME BY CYTOGENETICS AND a-CGH	110
Myotonic Dystrophy: genetic aspects ; cytochemical findings.	109
Acute lymphoblastic leukemia and a familial balanced translocation (12;15) involving ETV6	108
Acquisizione di anomalie cromosomiche clonali nel midollo osseo di pazienti con sindrome di Shwachman Diamond in relazione all’età	108
Array-based Comparative Genomic Hybridization in Shwachman-Diamond syndrome: results in 24 patients	108
Comparative genomic hybridization su microarray (aCGH) in sindrome di Shwachman (OMIM 260400) e rischio di mielodisplasia: al di là della citogenetica standard	107
Molecular monitoring of residual disease in chronic myeloid leukemia by genomic DNA compared with conventional mRNA analysis.	107
Fenotipo di una paziente da microdelezione della regione 4q e avente di smorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di Gorge.	106
Karyotype instability evaluated by array-CGH and risk of myeloid malignancy in Shwachman Diamond syndrome	106
A woman carrier of two apparently unrelated reciprocal translocations: prenatal diagnosis of normal karyotype in the foetus.	105
La linea cellulare EUE deriva da una linea HeLa.	105
Acute lymphoblastic leukemia and familial balanced translocation (12;15) involving ETV6	103
Criobanca automatizzata di materiale biologico: stoccaggio e monitoraggio molecolare di cellule meniscali per il trapianto autologo	103
Fenotipo di una paziente affetta da microdelezione subtelomerica della regione 4q e avente dimorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di George	103
Evaluating chromosomal mosaicism by array-based CGH in relation to clinical issues: the proposal of a formula	103
Chromosomal analysis in cultured lymphocytes and fibroblasts of psoriatic patients before and after treatment.	102
Protrusioni nucleari dovute a cromosomi strutturalmente alterati.	102
Array-CGH used to monitor dysplastic/neoplastic disorders with unbalanced chromosome anomalies may detect as low as 8% abnormal cells	102
Danno cromosomico e trattamento della psoriasi.	101
Chromosome identification and karyotypic evolution in a human melanoma cell line.	100
Chromosome size and nuclear projections	100
Distrofia miotonica: genetica e citochimica	100
Studio dei fibroblasti "in vitro" nella distrofia miotonica.	99
Variabilità cromosomica in linee cellulari derivate da melanomi.	98
Familial partial monosomy 7 and myelodysplasia: different paternal origin of the monosomy 7 suggests action of a mutator gene	98
Analysis of cross-contamination in established tumour cell lines.	97
Leucemia linfoblastica acuta e traslocazione familiare (15-15) che coinvolge ETV6	97
The use of microarray-based comparative genomic hybridization (a-CGH) to detect and define chromosome imbalances in the bone marrow of SDS patients	96
Presenza di anomalie cromosomiche nelle cellule epiteliali della matrice del colesteatoma: studio citogenetico.	95
Insulin receptors in psoriasis.	95
Nuclear projections and latent centromeres in primary culture and established cell lines.	95
Traslocazione complessa che coinvolge MLL in leucemia mielomonocitica acuta connatale	95
Differente reazione dei centromeri inattivi agli anticorpi anticentromero.	94
Correlation between the numbers of sex chromosomes and the H-Y antigen titer.	94
Involvement of dendritic cells in juvenile chronic myelomonocytic leukaemia shown by FISH on interphase nuclei	94
Nuclear projections and latent centromeres in primary cultures and established cell lines.	93
I recettori insulinici nella distrofia miotonica: studio su fibroblasti in coltura.	92
Mielodisplasia familiare, monosomia 7 / trisomia 8 ed effetto mutatore	92
Insulin receptors in psoriasis.	91
Diagnostica cromosomica	91
Age related acquisition of clonal chromosome anomalies in bone marrow cells of SDS patients	91
Different reaction of inactive centromeres to anticentromeric antibodies.	90
The origin and phenotype of X0 males	90
Insulin receptors in Friedreich's ataxia: studies on cultured fibroblasts.	90
Anomalie cromosomiche clonali e non-clonali in 32 casi di sindrome di Shwachman: valore prognostico e predittivo	90
Le basi genetiche della malattia linfoproliferativa legata al cromosoma X	89
Totale	12.145

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Categoria	#
all - tutte	53.411
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	53.411

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	1.373	0	0	0	0	0	0	408	324	107	229	44	261
2020/2021	1.983	22	188	44	191	122	280	64	179	329	63	169	332
2021/2022	1.265	104	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	786	12	39	395	71	141	111	17	0	0	0	0	0
Totale													15.341