statistiche ricercatore

LO CURTO, FRANCESCO

Distribuzione geografica

Continente	#
EU - Europa	6.607
NA - Nord America	6.545
AS - Asia	1.317
SA - Sud America	24
Continente sconosciuto - Info sul continente non disponibili	16
OC - Oceania	3
Totale	14.512

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Nazione	#
US - Stati Uniti d'America	6.522
IT - Italia	3.704
UA - Ucraina	1.141
TR - Turchia	557
SE - Svezia	430
VN - Vietnam	337
CN - Cina	307
FI - Finlandia	305
IE - Irlanda	270
DE - Germania	225
GB - Regno Unito	216
FR - Francia	195
JP - Giappone	55
IN - India	43
PL - Polonia	35
BE - Belgio	26
EU - Europa	16
BR - Brasile	12
CA - Canada	11
MX - Messico	9
NL - Olanda	9
CH - Svizzera	8
CZ - Repubblica Ceca	5
ES - Italia	5
AL - Albania	4
AR - Argentina	4
BG - Bulgaria	4
IL - Israele	4
SG - Singapore	4
AT - Austria	3
AU - Australia	3
DK - Danimarca	3
VE - Venezuela	3
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
AE - Emirati Arabi Uniti	1
BD - Bangladesh	1
BS - Bahamas	1
BY - Bielorussia	1
CL - Cile	1
CO - Colombia	1
GR - Grecia	1
HU - Ungheria	1
LT - Lituania	1
MC - Monaco	1
MY - Malesia	1
PY - Paraguay	1
RO - Romania	1
RU - Federazione Russa	1
TW - Taiwan	1
Totale	14.512

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Città	#
Milan	2.299
Chandler	957
Jacksonville	851
Fairfield	599
Woodbridge	368
Ashburn	348
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
San Mateo	128
Como	123
Beijing	91
Redwood City	68
San Diego	64
Ogden	61
New York	57
Tokyo	54
Hefei	32
Nanjing	32
Verona	29
Kunming	28
Brussels	25
Helsinki	23
Radomsko	23
Philadelphia	22
London	19
Norwalk	19
Düsseldorf	17
Nanchang	15
Auburn Hills	14
Jinan	13
Pavia	13
Pune	13
Guangzhou	12
Catania	11
Phoenix	11
Ponte Lambro	11
Washington	11
Los Angeles	10
Piemonte	9
Bangalore	8
Edinburgh	8
Fuzhou	8
Boardman	7
Naples	7
Palermo	7
Toronto	7
Baotou	6
Bologna	6
Chengdu	6
Frankfurt am Main	6
Kocaeli	6
Padova	6
Quzhou	6
Shanghai	6
Zhengzhou	6
Bari	5
Brescia	5
Genova	5
Hebei	5
Istanbul	5
Shenyang	5
Viterbo	5
Warsaw	5
Amsterdam	4
Berlin	4
Cagliari	4
Dallas	4
Foggia	4
Islington	4
Pescara	4
Prague	4
Sofia	4
Tel Aviv	4
Turin	4
Ancona	3
Atlanta	3
Bergamo	3
Chiswick	3
Chongqing	3
Copenhagen	3
Estrela	3
Genzano Di Roma	3
Guwahati	3
Kilburn	3
Lissone	3
Mexico	3
Miami	3
Mountain View	3
Napoli	3
Paris	3
Totale	9.726

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Nome	#
La sindrome da aneuploidia variegata a mosaico (MVA) associata a neutropenia come condizione predisponente a displasia e neoplasia ematologia	293
Trisomia 8 costituzionale a mosaico nelle malattie mielodisplatiche e mieloproliferative: importanza per pratica clinica e per implicazioni teoriche	208
Genomic quantitative real-time PCR proves residual disease positivity in more than 30% samples with negative mRNA-based qRT-PCR in Chronic Myeloid Leukemia	166
Cd bands and centromeric function in dicentric chromosomes	157
Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR	156
OTX1 and OTX2 as possible molecular markers of sinonasal carcinomas and olfactory neuroblastomas	155
Le basi genetiche della malattia linfoproliferativa.	152
A new chromosome instability disorder	152
First trimester prenatal diagnosis of Sanfilippo disease (MPS III) type B.	149
Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis	149
Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms	148
Karyotypic variation in benign pleomorphic adenoma of the parotid and in normal salivary glands.	145
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMIM 601399)	144
Clonal chromosome anomalies and propensity to myeloid malignancies in congenital amegakaryocytic thrombocytopenia (OMIM 604498)	144
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	140
La citogenetica interfasica dimostra che le cellule dendritiche nella Leucemia Mielomonocitica Cronica Giovanile fanno parte del clone leucemico	139
La trisomia 8 in leucemie acute e mielodisplasie e costituzionale nel 15-20% dei casi	138
The mammary gland and the homeobox gene Otx1	137
Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells	135
Chromosome anomalies in bone marrow as primarycause of aplastic or hypoplastic conditions andperipheral cytopenia: disorders due to secondaryimpairment of RUNX1 and MPL genes	135
Nuclear projections in tumour cells	133
Chromosome identification in a Chinese hamster pseudodiploid cell line (CHEF-125)	133
The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies	133
Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies	131
Cytogenetic Monitoring in Shwachman-Diamond Syndrome: A Note on Clonal Progression and a Practical Warning	130
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.	128
Assessing residual disease in imatinib-treated CML patients by DNA compared to MRNA assays	127
Presumptive mosaic origin of an XX/XY female with ambiguous genitalia.	127
Chronic Myeloid Leukemia: Molecular Monitoring of Residual Disease by Genomic DNA Compared to Conventional mRNA Analysis in Follow-Ups up to 8 Years	127
Normal insulin receptors in mitochondrial myopathies with ophthalmoplegia.	126
Constitutional trisomy 8 mosaicism in primary myelofibrosis: relevance to clinical practice and warning for trisomy 8 studies.	126
The syndrome of partial trisomy 14q.	125
Studio molecolare del differenziamento da cellule staminali in condrociti in vivo per lo sviluppo di un protocollo di trapianti di cartilagine umana	123
48,XXXY/49,XXXXY Mosaicism in a month old infant.	122
Microhomologies and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia	122
Citogenetica Umana: nuove metodiche ed applicazioni in medicina.	121
Indirect immunofluorescence of inactive centromeres as indicator of centromeric function.	121
The role of Yp in sex determination: new evidence from X/Y translocations.	120
Le basi genetiche della malattia linfoproliferativa legata al cromosoma X	119
Mielodisplasia con monosomia 7 familiare: dati citogenetici e molecolari	118
Familial myelodysplastic syndromes, monosomy 7/trisomy 8, and mutator effects	118
Growth Hormone and Estrogens in Patients with Turner Syndrome: in vivo and in vitro studies.	116
Establishment and study of different real-time polymerase chain reaction assays for the quantification of cells with deletions of chromosome 7.	115
Monitoring the Isochromosome i(7)(q10) in the Bone Marrow of Patients With Shwachman Syndrome by Real-time Quantitative PCR	113
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMOM 601399)	112
Different real time PCR approaches for the fine quantification of SNP's alleles in DNA pools: assays development, characterization and pre-validation.	112
Sindrome di Shwacham: instabilita del cromosoma 7 e rischio di patologia mielodisplastica e mieloproliferativa	108
Erratum: OTX1 expression in breast cancer is regulated by p53 (Oncogene (2011) 30 (3096-3103) doi:10.1038/onc.2011.31)	108
Acquired Chromosome change in Cholesteatoma	107
Microhomologiee and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia.	107
Studio molecolare del differenziamento da cellule staminali in condrociti e osteoblasti in vivo per lo sviluppo di protocolli di trapianto	107
Instabilità costituzionale del cariotipo all'origine di trisomia 8 acquisita midollare	107
Myotonic Dystrophy: genetic aspects ; cytochemical findings.	106
MONITORING SHWACHMAN-DIAMOND SYNDROME BY CYTOGENETICS AND a-CGH	105
Molecular monitoring of residual disease in chronic myeloid leukemia by genomic DNA compared with conventional mRNA analysis.	104
Anticentromeric antibodies and inactive centromeres.	103
Acute lymphoblastic leukemia and a familial balanced translocation (12;15) involving ETV6	102
Karyotype instability evaluated by array-CGH and risk of myeloid malignancy in Shwachman Diamond syndrome	102
Acquisizione di anomalie cromosomiche clonali nel midollo osseo di pazienti con sindrome di Shwachman Diamond in relazione all’età	102
Array-based Comparative Genomic Hybridization in Shwachman-Diamond syndrome: results in 24 patients	102
Comparative genomic hybridization su microarray (aCGH) in sindrome di Shwachman (OMIM 260400) e rischio di mielodisplasia: al di là della citogenetica standard	101
La linea cellulare EUE deriva da una linea HeLa.	100
Evaluating chromosomal mosaicism by array-based CGH in relation to clinical issues: the proposal of a formula	100
Criobanca automatizzata di materiale biologico: stoccaggio e monitoraggio molecolare di cellule meniscali per il trapianto autologo	99
A woman carrier of two apparently unrelated reciprocal translocations: prenatal diagnosis of normal karyotype in the foetus.	98
Protrusioni nucleari dovute a cromosomi strutturalmente alterati.	98
Fenotipo di una paziente da microdelezione della regione 4q e avente di smorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di Gorge.	98
Danno cromosomico e trattamento della psoriasi.	97
A liveborn 69,XXX triploid. Origin, X chromosome activity and gene dosage.	97
Acute lymphoblastic leukemia and familial balanced translocation (12;15) involving ETV6	97
Distrofia miotonica: genetica e citochimica	97
Chromosomal analysis in cultured lymphocytes and fibroblasts of psoriatic patients before and after treatment.	95
Studio dei fibroblasti "in vitro" nella distrofia miotonica.	95
Chromosome identification and karyotypic evolution in a human melanoma cell line.	95
Chromosome size and nuclear projections	95
Array-CGH used to monitor dysplastic/neoplastic disorders with unbalanced chromosome anomalies may detect as low as 8% abnormal cells	95
Variabilità cromosomica in linee cellulari derivate da melanomi.	94
Leucemia linfoblastica acuta e traslocazione familiare (15-15) che coinvolge ETV6	94
Familial partial monosomy 7 and myelodysplasia: different paternal origin of the monosomy 7 suggests action of a mutator gene	92
Traslocazione complessa che coinvolge MLL in leucemia mielomonocitica acuta connatale	92
Fenotipo di una paziente affetta da microdelezione subtelomerica della regione 4q e avente dimorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di George	92
The use of microarray-based comparative genomic hybridization (a-CGH) to detect and define chromosome imbalances in the bone marrow of SDS patients	92
Correlation between the numbers of sex chromosomes and the H-Y antigen titer.	91
Insulin receptors in psoriasis.	91
Nuclear projections and latent centromeres in primary culture and established cell lines.	91
Analysis of cross-contamination in established tumour cell lines.	90
Involvement of dendritic cells in juvenile chronic myelomonocytic leukaemia shown by FISH on interphase nuclei	90
Mielodisplasia familiare, monosomia 7 / trisomia 8 ed effetto mutatore	90
Differente reazione dei centromeri inattivi agli anticorpi anticentromero.	89
Presenza di anomalie cromosomiche nelle cellule epiteliali della matrice del colesteatoma: studio citogenetico.	89
Nuclear projections and latent centromeres in primary cultures and established cell lines.	89
Insulin receptors in psoriasis.	88
I recettori insulinici nella distrofia miotonica: studio su fibroblasti in coltura.	88
Diagnostica cromosomica	88
The origin and phenotype of X0 males	87
Insulin receptors in Friedreich's ataxia: studies on cultured fibroblasts.	87
Le basi genetiche della malattia linfoproliferativa legata al cromosoma X	87
Different reaction of inactive centromeres to anticentromeric antibodies.	86
Anomalie cromosomiche clonali e non-clonali in 32 casi di sindrome di Shwachman: valore prognostico e predittivo	86
Age related acquisition of clonal chromosome anomalies in bone marrow cells of SDS patients	86
Totale	11.516

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Categoria	#
all - tutte	42.974
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	42.974

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2018/2019	429	0	0	0	0	0	0	0	0	0	0	0	429
2019/2020	2.257	76	72	66	342	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
Totale													14.555