statistiche ricercatore

LO CURTO, FRANCESCO

Distribuzione geografica

Continente	#
NA - Nord America	6.953
EU - Europa	6.714
AS - Asia	1.424
SA - Sud America	35
Continente sconosciuto - Info sul continente non disponibili	16
OC - Oceania	3
Totale	15.145

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Nazione	#
US - Stati Uniti d'America	6.924
IT - Italia	3.787
UA - Ucraina	1.141
TR - Turchia	557
SE - Svezia	430
VN - Vietnam	337
CN - Cina	312
FI - Finlandia	308
IE - Irlanda	270
DE - Germania	231
GB - Regno Unito	218
FR - Francia	195
SG - Singapore	102
JP - Giappone	55
IN - India	44
PL - Polonia	36
BE - Belgio	26
BR - Brasile	20
NL - Olanda	18
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
BG - Bulgaria	4
IL - Israele	4
AT - Austria	3
AU - Australia	3
DK - Danimarca	3
LT - Lituania	3
PE - Perù	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
RU - Federazione Russa	2
SK - Slovacchia (Repubblica Slovacca)	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	15.145

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Città	#
Milan	2.306
Chandler	957
Jacksonville	851
Fairfield	599
Ashburn	386
Woodbridge	368
Izmir	293
Princeton	284
Wilmington	282
Dearborn	280
Dublin	270
Houston	263
Ann Arbor	245
Seattle	240
Cambridge	232
Nyköping	229
Rome	202
Dong Ket	188
Boardman	149
San Mateo	128
Como	123
Beijing	91
Chicago	89
Singapore	87
Redwood City	68
San Diego	64
Ogden	61
New York	57
Tokyo	54
Hefei	32
Nanjing	32
Santa Clara	30
Verona	29
Kunming	28
Dallas	26
Helsinki	26
Brussels	25
Radomsko	23
Philadelphia	22
London	20
Norwalk	19
Düsseldorf	17
Nanchang	15
Auburn Hills	14
Catania	13
Jinan	13
Pavia	13
Pune	13
Guangzhou	12
Naples	11
Phoenix	11
Ponte Lambro	11
Washington	11
Los Angeles	10
Piemonte	9
Bangalore	8
Bari	8
Edinburgh	8
Fuzhou	8
Padova	8
Toronto	8
Frankfurt am Main	7
Palermo	7
Baotou	6
Bologna	6
Brescia	6
Chengdu	6
Kocaeli	6
Munich	6
Quzhou	6
Shanghai	6
São Paulo	6
Turin	6
Warsaw	6
Zhengzhou	6
Amsterdam	5
Berlin	5
Florence	5
Genova	5
Hebei	5
Istanbul	5
Shenyang	5
Viterbo	5
Cagliari	4
Foggia	4
Islington	4
Pescara	4
Prague	4
Sofia	4
Tel Aviv	4
Ancona	3
Atlanta	3
Bergamo	3
Chiswick	3
Chongqing	3
Copenhagen	3
Estrela	3
Genzano Di Roma	3
Guwahati	3
Kilburn	3
Totale	10.163

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Nome	#
La sindrome da aneuploidia variegata a mosaico (MVA) associata a neutropenia come condizione predisponente a displasia e neoplasia ematologia	308
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.	174
Genomic quantitative real-time PCR proves residual disease positivity in more than 30% samples with negative mRNA-based qRT-PCR in Chronic Myeloid Leukemia	170
Cd bands and centromeric function in dicentric chromosomes	163
A new chromosome instability disorder	160
Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR	160
OTX1 and OTX2 as possible molecular markers of sinonasal carcinomas and olfactory neuroblastomas	160
Le basi genetiche della malattia linfoproliferativa.	156
First trimester prenatal diagnosis of Sanfilippo disease (MPS III) type B.	153
Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis	152
Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms	150
Karyotypic variation in benign pleomorphic adenoma of the parotid and in normal salivary glands.	148
La trisomia 8 in leucemie acute e mielodisplasie e costituzionale nel 15-20% dei casi	148
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMIM 601399)	148
Clonal chromosome anomalies and propensity to myeloid malignancies in congenital amegakaryocytic thrombocytopenia (OMIM 604498)	148
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	146
Cytogenetic Monitoring in Shwachman-Diamond Syndrome: A Note on Clonal Progression and a Practical Warning	146
La citogenetica interfasica dimostra che le cellule dendritiche nella Leucemia Mielomonocitica Cronica Giovanile fanno parte del clone leucemico	142
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	140
Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells	138
Nuclear projections in tumour cells	136
Chromosome identification in a Chinese hamster pseudodiploid cell line (CHEF-125)	136
Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies	136
The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies	136
Assessing residual disease in imatinib-treated CML patients by DNA compared to MRNA assays	134
Chronic Myeloid Leukemia: Molecular Monitoring of Residual Disease by Genomic DNA Compared to Conventional mRNA Analysis in Follow-Ups up to 8 Years	132
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.	131
Presumptive mosaic origin of an XX/XY female with ambiguous genitalia.	131
The syndrome of partial trisomy 14q.	129
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	128
Constitutional trisomy 8 mosaicism in primary myelofibrosis: relevance to clinical practice and warning for trisomy 8 studies.	128
Citogenetica Umana: nuove metodiche ed applicazioni in medicina.	126
Indirect immunofluorescence of inactive centromeres as indicator of centromeric function.	124
Microhomologies and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia	124
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
Familial myelodysplastic syndromes, monosomy 7/trisomy 8, and mutator effects	122
Mielodisplasia con monosomia 7 familiare: dati citogenetici e molecolari	121
Growth Hormone and Estrogens in Patients with Turner Syndrome: in vivo and in vitro studies.	119
Establishment and study of different real-time polymerase chain reaction assays for the quantification of cells with deletions of chromosome 7.	119
Different real time PCR approaches for the fine quantification of SNP's alleles in DNA pools: assays development, characterization and pre-validation.	118
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMOM 601399)	116
Monitoring the Isochromosome i(7)(q10) in the Bone Marrow of Patients With Shwachman Syndrome by Real-time Quantitative PCR	116
Acquired Chromosome change in Cholesteatoma	115
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
Anticentromeric antibodies and inactive centromeres.	110
Microhomologiee and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia.	110
Instabilità costituzionale del cariotipo all'origine di trisomia 8 acquisita midollare	110
Erratum: OTX1 expression in breast cancer is regulated by p53 (Oncogene (2011) 30 (3096-3103) doi:10.1038/onc.2011.31)	110
Myotonic Dystrophy: genetic aspects ; cytochemical findings.	109
MONITORING SHWACHMAN-DIAMOND SYNDROME BY CYTOGENETICS AND a-CGH	109
Array-based Comparative Genomic Hybridization in Shwachman-Diamond syndrome: results in 24 patients	108
Acute lymphoblastic leukemia and a familial balanced translocation (12;15) involving ETV6	107
Acquisizione di anomalie cromosomiche clonali nel midollo osseo di pazienti con sindrome di Shwachman Diamond in relazione all’età	107
Molecular monitoring of residual disease in chronic myeloid leukemia by genomic DNA compared with conventional mRNA analysis.	107
Comparative genomic hybridization su microarray (aCGH) in sindrome di Shwachman (OMIM 260400) e rischio di mielodisplasia: al di là della citogenetica standard	105
La linea cellulare EUE deriva da una linea HeLa.	105
A woman carrier of two apparently unrelated reciprocal translocations: prenatal diagnosis of normal karyotype in the foetus.	104
Fenotipo di una paziente da microdelezione della regione 4q e avente di smorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di Gorge.	104
Karyotype instability evaluated by array-CGH and risk of myeloid malignancy in Shwachman Diamond syndrome	104
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
Protrusioni nucleari dovute a cromosomi strutturalmente alterati.	102
Evaluating chromosomal mosaicism by array-based CGH in relation to clinical issues: the proposal of a formula	102
Chromosomal analysis in cultured lymphocytes and fibroblasts of psoriatic patients before and after treatment.	101
Danno cromosomico e trattamento della psoriasi.	100
Chromosome identification and karyotypic evolution in a human melanoma cell line.	100
Chromosome size and nuclear projections	100
Distrofia miotonica: genetica e citochimica	100
Array-CGH used to monitor dysplastic/neoplastic disorders with unbalanced chromosome anomalies may detect as low as 8% abnormal cells	100
Studio dei fibroblasti "in vitro" nella distrofia miotonica.	99
Variabilità cromosomica in linee cellulari derivate da melanomi.	97
Analysis of cross-contamination in established tumour cell lines.	96
Leucemia linfoblastica acuta e traslocazione familiare (15-15) che coinvolge ETV6	96
Insulin receptors in psoriasis.	95
Nuclear projections and latent centromeres in primary culture and established cell lines.	95
Familial partial monosomy 7 and myelodysplasia: different paternal origin of the monosomy 7 suggests action of a mutator gene	95
Fenotipo di una paziente affetta da microdelezione subtelomerica della regione 4q e avente dimorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di George	95
The use of microarray-based comparative genomic hybridization (a-CGH) to detect and define chromosome imbalances in the bone marrow of SDS patients	95
Presenza di anomalie cromosomiche nelle cellule epiteliali della matrice del colesteatoma: studio citogenetico.	94
Correlation between the numbers of sex chromosomes and the H-Y antigen titer.	94
Traslocazione complessa che coinvolge MLL in leucemia mielomonocitica acuta connatale	94
Differente reazione dei centromeri inattivi agli anticorpi anticentromero.	93
Nuclear projections and latent centromeres in primary cultures and established cell lines.	93
Involvement of dendritic cells in juvenile chronic myelomonocytic leukaemia shown by FISH on interphase nuclei	93
Mielodisplasia familiare, monosomia 7 / trisomia 8 ed effetto mutatore	92
Insulin receptors in psoriasis.	91
I recettori insulinici nella distrofia miotonica: studio su fibroblasti in coltura.	91
Diagnostica cromosomica	91
The origin and phenotype of X0 males	90
Insulin receptors in Friedreich's ataxia: studies on cultured fibroblasts.	90
Age related acquisition of clonal chromosome anomalies in bone marrow cells of SDS patients	90
Different reaction of inactive centromeres to anticentromeric antibodies.	89
Le basi genetiche della malattia linfoproliferativa legata al cromosoma X	89
Anomalie cromosomiche clonali e non-clonali in 32 casi di sindrome di Shwachman: valore prognostico e predittivo	89
Totale	12.013

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Categoria	#
all - tutte	50.921
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	50.921

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	1.701	0	0	0	0	80	248	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	633	12	39	395	71	116	0	0	0	0	0	0	0
Totale													15.188