statistiche ricercatore

LO CURTO, FRANCESCO

Distribuzione geografica

Continente	#
NA - Nord America	7.975
EU - Europa	7.182
AS - Asia	3.106
SA - Sud America	347
AF - Africa	36
Continente sconosciuto - Info sul continente non disponibili	16
OC - Oceania	3
Totale	18.665

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Nazione	#
US - Stati Uniti d'America	7.875
IT - Italia	3.847
UA - Ucraina	1.149
SG - Singapore	1.039
TR - Turchia	565
CN - Cina	538
SE - Svezia	440
VN - Vietnam	403
HK - Hong Kong	351
FI - Finlandia	330
BR - Brasile	291
DE - Germania	291
GB - Regno Unito	286
IE - Irlanda	271
FR - Francia	211
RU - Federazione Russa	128
JP - Giappone	79
PL - Polonia	68
IN - India	66
MX - Messico	50
CA - Canada	42
NL - Olanda	34
BE - Belgio	27
ES - Italia	20
AR - Argentina	19
CH - Svizzera	17
EU - Europa	16
ZA - Sudafrica	16
BD - Bangladesh	15
AT - Austria	14
EC - Ecuador	13
LT - Lituania	9
VE - Venezuela	9
IL - Israele	8
IQ - Iraq	8
PK - Pakistan	7
AL - Albania	6
CZ - Repubblica Ceca	6
MA - Marocco	6
PE - Perù	5
AE - Emirati Arabi Uniti	4
BG - Bulgaria	4
AU - Australia	3
CO - Colombia	3
DK - Danimarca	3
DO - Repubblica Dominicana	3
KE - Kenya	3
LB - Libano	3
NP - Nepal	3
OM - Oman	3
RS - Serbia	3
SN - Senegal	3
AZ - Azerbaigian	2
CL - Cile	2
DZ - Algeria	2
EE - Estonia	2
EG - Egitto	2
HU - Ungheria	2
ID - Indonesia	2
IM - Isola di Man	2
LU - Lussemburgo	2
MY - Malesia	2
NO - Norvegia	2
PA - Panama	2
PY - Paraguay	2
SA - Arabia Saudita	2
SK - Slovacchia (Repubblica Slovacca)	2
UY - Uruguay	2
UZ - Uzbekistan	2
AM - Armenia	1
AO - Angola	1
BA - Bosnia-Erzegovina	1
BO - Bolivia	1
BS - Bahamas	1
BY - Bielorussia	1
CG - Congo	1
GA - Gabon	1
GR - Grecia	1
JM - Giamaica	1
JO - Giordania	1
MC - Monaco	1
MK - Macedonia	1
MN - Mongolia	1
RO - Romania	1
TG - Togo	1
TT - Trinidad e Tobago	1
TW - Taiwan	1
Totale	18.665

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Città	#
Milan	2.312
Chandler	957
Jacksonville	851
Fairfield	599
Singapore	535
Ashburn	532
Woodbridge	368
Hong Kong	349
Izmir	293
Princeton	284
Wilmington	282
Dearborn	280
Dallas	271
Dublin	271
Houston	268
Ann Arbor	245
Seattle	241
Cambridge	232
Nyköping	229
Rome	215
Beijing	214
Dong Ket	188
Boardman	149
San Mateo	128
Como	124
New York	98
Chicago	97
The Dalles	91
Tokyo	78
Redwood City	68
San Diego	65
Ogden	61
London	60
Los Angeles	60
Munich	52
Santa Clara	51
São Paulo	44
Warsaw	36
Hefei	33
Nanjing	33
Verona	31
Helsinki	30
Kunming	28
Brussels	26
Mexico City	25
Council Bluffs	24
Hanoi	23
Phoenix	23
Radomsko	23
Philadelphia	22
Norwalk	19
Ho Chi Minh City	18
Turku	18
Düsseldorf	17
Guangzhou	16
Brooklyn	15
Nanchang	15
Toronto	15
Auburn Hills	14
Catania	14
Jinan	14
Naples	14
Frankfurt am Main	13
Pavia	13
Pune	13
Stockholm	13
Johannesburg	12
Montreal	12
Denver	11
Orem	11
Ponte Lambro	11
San Jose	11
Washington	11
Poplar	10
Rio de Janeiro	10
Atlanta	9
Boston	9
Piemonte	9
Amsterdam	8
Bangalore	8
Bari	8
Belo Horizonte	8
Brasília	8
Chennai	8
Edinburgh	8
Fuzhou	8
Miami	8
Mumbai	8
Padova	8
San Francisco	8
Shanghai	8
Istanbul	7
Manchester	7
Palermo	7
Quito	7
Turin	7
Zhengzhou	7
Baotou	6
Berlin	6
Bologna	6
Totale	12.130

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Nome	#
La sindrome da aneuploidia variegata a mosaico (MVA) associata a neutropenia come condizione predisponente a displasia e neoplasia ematologia	350
A liveborn 69,XXX triploid. Origin, X chromosome activity and gene dosage.	258
Trisomia 8 costituzionale a mosaico nelle malattie mielodisplatiche e mieloproliferative: importanza per pratica clinica e per implicazioni teoriche	228
Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis	210
Cd bands and centromeric function in dicentric chromosomes	199
A new chromosome instability disorder	199
Genomic quantitative real-time PCR proves residual disease positivity in more than 30% samples with negative mRNA-based qRT-PCR in Chronic Myeloid Leukemia	194
Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR	186
Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells	185
Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms	185
Cytogenetic Monitoring in Shwachman-Diamond Syndrome: A Note on Clonal Progression and a Practical Warning	185
Chromosome anomalies in bone marrow as primarycause of aplastic or hypoplastic conditions andperipheral cytopenia: disorders due to secondaryimpairment of RUNX1 and MPL genes	184
OTX1 and OTX2 as possible molecular markers of sinonasal carcinomas and olfactory neuroblastomas	183
Clonal chromosome anomalies and propensity to myeloid malignancies in congenital amegakaryocytic thrombocytopenia (OMIM 604498)	182
La trisomia 8 in leucemie acute e mielodisplasie e costituzionale nel 15-20% dei casi	177
Acquisizione di anomalie cromosomiche clonali nel midollo osseo di pazienti con sindrome di Shwachman Diamond in relazione all’età	176
Le basi genetiche della malattia linfoproliferativa.	174
48,XXXY/49,XXXXY Mosaicism in a month old infant.	174
The mammary gland and the homeobox gene Otx1	173
Chronic Myeloid Leukemia: Molecular Monitoring of Residual Disease by Genomic DNA Compared to Conventional mRNA Analysis in Follow-Ups up to 8 Years	171
Assessing residual disease in imatinib-treated CML patients by DNA compared to MRNA assays	169
Acquired Chromosome change in Cholesteatoma	168
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMIM 601399)	168
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	166
First trimester prenatal diagnosis of Sanfilippo disease (MPS III) type B.	165
Karyotypic variation in benign pleomorphic adenoma of the parotid and in normal salivary glands.	164
Constitutional trisomy 8 mosaicism in primary myelofibrosis: relevance to clinical practice and warning for trisomy 8 studies.	164
Acute lymphoblastic leukemia and a familial balanced translocation (12;15) involving ETV6	161
Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies	160
The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies	160
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.	156
La citogenetica interfasica dimostra che le cellule dendritiche nella Leucemia Mielomonocitica Cronica Giovanile fanno parte del clone leucemico	156
Array-based Comparative Genomic Hybridization in Shwachman-Diamond syndrome: results in 24 patients	155
Nuclear projections in tumour cells	154
Different real time PCR approaches for the fine quantification of SNP's alleles in DNA pools: assays development, characterization and pre-validation.	154
The syndrome of partial trisomy 14q.	153
Chromosome identification in a Chinese hamster pseudodiploid cell line (CHEF-125)	153
Studio molecolare del differenziamento da cellule staminali in condrociti in vivo per lo sviluppo di un protocollo di trapianti di cartilagine umana	151
Indirect immunofluorescence of inactive centromeres as indicator of centromeric function.	149
Monitoring the Isochromosome i(7)(q10) in the Bone Marrow of Patients With Shwachman Syndrome by Real-time Quantitative PCR	149
Anticentromeric antibodies and inactive centromeres.	148
Le basi genetiche della malattia linfoproliferativa legata al cromosoma X	147
Acute lymphoblastic leukemia and familial balanced translocation (12;15) involving ETV6	146
Chromosomal analysis in cultured lymphocytes and fibroblasts of psoriatic patients before and after treatment.	145
A woman carrier of two apparently unrelated reciprocal translocations: prenatal diagnosis of normal karyotype in the foetus.	145
Comparative genomic hybridization su microarray (aCGH) in sindrome di Shwachman (OMIM 260400) e rischio di mielodisplasia: al di là della citogenetica standard	144
Evaluating chromosomal mosaicism by array-based CGH in relation to clinical issues: the proposal of a formula	144
Presumptive mosaic origin of an XX/XY female with ambiguous genitalia.	143
Familial myelodysplastic syndromes, monosomy 7/trisomy 8, and mutator effects	143
Microhomologies and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia	143
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMOM 601399)	142
The role of Yp in sex determination: new evidence from X/Y translocations.	141
Establishment and study of different real-time polymerase chain reaction assays for the quantification of cells with deletions of chromosome 7.	141
Analysis of cross-contamination in established tumour cell lines.	140
Citogenetica Umana: nuove metodiche ed applicazioni in medicina.	139
Normal insulin receptors in mitochondrial myopathies with ophthalmoplegia.	139
Studio molecolare del differenziamento da cellule staminali in condrociti e osteoblasti in vivo per lo sviluppo di protocolli di trapianto	139
Criobanca automatizzata di materiale biologico: stoccaggio e monitoraggio molecolare di cellule meniscali per il trapianto autologo	139
Mielodisplasia con monosomia 7 familiare: dati citogenetici e molecolari	138
Array-CGH used to monitor dysplastic/neoplastic disorders with unbalanced chromosome anomalies may detect as low as 8% abnormal cells	136
Anomalie cromosomiche clonali e non-clonali in 32 casi di sindrome di Shwachman: valore prognostico e predittivo	135
Age related acquisition of clonal chromosome anomalies in bone marrow cells of SDS patients	133
MONITORING SHWACHMAN-DIAMOND SYNDROME BY CYTOGENETICS AND a-CGH	133
Growth Hormone and Estrogens in Patients with Turner Syndrome: in vivo and in vitro studies.	132
Microhomologiee and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia.	132
Sindrome di Shwacham: instabilita del cromosoma 7 e rischio di patologia mielodisplastica e mieloproliferativa	132
Instabilità costituzionale del cariotipo all'origine di trisomia 8 acquisita midollare	132
Aplasia midollare da perdita del gene RUNX1 acquisita a causa di un riarrangiamento strutturale clonale del cromosoma 21	131
Karyotype instability evaluated by array-CGH and risk of myeloid malignancy in Shwachman Diamond syndrome	131
Fenotipo di una paziente da microdelezione della regione 4q e avente di smorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di Gorge.	129
The use of microarray-based comparative genomic hybridization (a-CGH) to detect and define chromosome imbalances in the bone marrow of SDS patients	128
Different patterns of chromosome 20 interstitial deletion in Shwachman-Diamond syndrome and in myeloid neoplasms	127
Myotonic Dystrophy: genetic aspects ; cytochemical findings.	125
Erratum: OTX1 expression in breast cancer is regulated by p53 (Oncogene (2011) 30 (3096-3103) doi:10.1038/onc.2011.31)	124
Molecular monitoring of residual disease in chronic myeloid leukemia by genomic DNA compared with conventional mRNA analysis.	124
Protrusioni nucleari dovute a cromosomi strutturalmente alterati.	119
Variabilità cromosomica in linee cellulari derivate da melanomi.	118
Traslocazione complessa che coinvolge MLL in leucemia mielomonocitica acuta connatale	118
La linea cellulare EUE deriva da una linea HeLa.	117
Fenotipo di una paziente affetta da microdelezione subtelomerica della regione 4q e avente dimorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di George	117
Insulin receptors in psoriasis.	116
Chromosome identification and karyotypic evolution in a human melanoma cell line.	116
Chromosome size and nuclear projections	116
Distrofia miotonica: genetica e citochimica	116
Diagnostica cromosomica	116
Correlation between the numbers of sex chromosomes and the H-Y antigen titer.	115
Leucemia linfoblastica acuta e traslocazione familiare (15-15) che coinvolge ETV6	115
Different reaction of inactive centromeres to anticentromeric antibodies.	114
Studio dei fibroblasti "in vitro" nella distrofia miotonica.	114
DIFFERENTE PERDITA DI MATERIALE NELLE DELEZIONI INTERSTIZIALI DEL CROMOSOMA 20 NELLE DISPLASIE/NEOPLASIE MIELOIDI E NELLA SINDROME DI SHWACHMAN-DIAMOND	114
Familial partial monosomy 7 and myelodysplasia: different paternal origin of the monosomy 7 suggests action of a mutator gene	113
Differente reazione dei centromeri inattivi agli anticorpi anticentromero.	112
Severe aplastic anemia (SAA) due to chromosome 21 acquired chromosome anomaly and haploinsufficiency of RUNX1 gene	112
Danno cromosomico e trattamento della psoriasi.	111
Presenza di anomalie cromosomiche nelle cellule epiteliali della matrice del colesteatoma: studio citogenetico.	111
Nuclear projections and latent centromeres in primary culture and established cell lines.	111
Le basi genetiche della malattia linfoproliferativa legata al cromosoma X	110
Chromosome 7 instability and myelodysplasia in Shwachman syndrome	108
Instabilità del cariotipo e mielodisplasie nella Sindrome di Shwachman	108
Mielodisplasia familiare, monosomia 7 / trisomia 8 ed effetto mutatore	108
Totale	14.783

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Categoria	#
all - tutte	68.757
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	68.757

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	1.416	0	0	0	0	0	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	2.094	12	39	395	71	141	111	106	140	197	140	147	595
2025/2026	2.059	393	234	207	625	508	92	0	0	0	0	0	0
Totale													18.708