statistiche ricercatore

LO CURTO, FRANCESCO

Distribuzione geografica

Continente	#
NA - Nord America	11.373
EU - Europa	7.593
AS - Asia	4.018
SA - Sud America	451
AF - Africa	119
Continente sconosciuto - Info sul continente non disponibili	65
OC - Oceania	16
Totale	23.635

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Nazione	#
US - Stati Uniti d'America	11.165
IT - Italia	3.978
SG - Singapore	1.229
UA - Ucraina	1.152
CN - Cina	930
TR - Turchia	566
VN - Vietnam	566
SE - Svezia	445
HK - Hong Kong	402
FI - Finlandia	376
BR - Brasile	368
FR - Francia	343
GB - Regno Unito	315
DE - Germania	308
IE - Irlanda	271
RU - Federazione Russa	128
IN - India	104
CA - Canada	91
JP - Giappone	85
PL - Polonia	73
MX - Messico	70
NG - Nigeria	69
NL - Olanda	45
BD - Bangladesh	42
ES - Italia	31
BE - Belgio	29
AR - Argentina	21
ZA - Sudafrica	20
CH - Svizzera	17
EC - Ecuador	17
AT - Austria	16
AU - Australia	16
EU - Europa	16
IQ - Iraq	15
CO - Colombia	13
IL - Israele	12
VE - Venezuela	12
LT - Lituania	10
MA - Marocco	10
PK - Pakistan	10
CZ - Repubblica Ceca	9
HN - Honduras	9
JM - Giamaica	8
DK - Danimarca	7
PH - Filippine	7
AL - Albania	6
CL - Cile	6
CR - Costa Rica	6
CW - ???statistics.table.value.countryCode.CW???	6
UZ - Uzbekistan	6
AE - Emirati Arabi Uniti	5
BG - Bulgaria	5
EG - Egitto	5
JO - Giordania	5
NP - Nepal	5
OM - Oman	5
PE - Perù	5
PR - Porto Rico	5
PY - Paraguay	5
TT - Trinidad e Tobago	5
EE - Estonia	4
MY - Malesia	4
RS - Serbia	4
SN - Senegal	4
DO - Repubblica Dominicana	3
GR - Grecia	3
ID - Indonesia	3
KE - Kenya	3
LB - Libano	3
PA - Panama	3
SA - Arabia Saudita	3
SV - El Salvador	3
AO - Angola	2
AZ - Azerbaigian	2
BA - Bosnia-Erzegovina	2
BO - Bolivia	2
DZ - Algeria	2
HU - Ungheria	2
IM - Isola di Man	2
LU - Lussemburgo	2
MN - Mongolia	2
NO - Norvegia	2
SK - Slovacchia (Repubblica Slovacca)	2
TH - Thailandia	2
TW - Taiwan	2
UY - Uruguay	2
AM - Armenia	1
BS - Bahamas	1
BY - Bielorussia	1
CG - Congo	1
GA - Gabon	1
GD - Grenada	1
GP - Guadalupe	1
GT - Guatemala	1
KG - Kirghizistan	1
KZ - Kazakistan	1
LY - Libia	1
MC - Monaco	1
MD - Moldavia	1
MK - Macedonia	1
Totale	23.588

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Città	#
Milan	2.320
Ashburn	1.465
Chandler	957
San Jose	949
Jacksonville	854
Singapore	651
Fairfield	599
Council Bluffs	463
Hong Kong	396
Woodbridge	368
Izmir	293
Princeton	285
Dallas	284
Wilmington	283
Dearborn	280
Houston	275
Dublin	271
Ann Arbor	245
Seattle	244
Beijing	239
Cambridge	233
Nyköping	229
Rome	227
Chicago	192
Dong Ket	188
The Dalles	164
Boardman	152
San Mateo	128
Como	124
New York	122
Lauterbourg	119
Santa Clara	108
Los Angeles	91
São Paulo	91
Tokyo	84
Ho Chi Minh City	77
Helsinki	76
Orem	72
Abuja	69
Redwood City	68
Hanoi	67
San Diego	66
London	62
Ogden	61
Guangzhou	53
Munich	52
Verona	44
Mexico City	41
Warsaw	38
Nanjing	35
Hefei	33
Chennai	31
Toronto	31
Phoenix	30
Philadelphia	29
Brussels	28
Kunming	28
Brooklyn	24
Naples	24
Frankfurt am Main	23
Radomsko	23
Shanghai	23
Norwalk	21
Atlanta	20
Montreal	20
Tianjin	20
Manchester	19
Turku	18
Bologna	17
Catania	17
Düsseldorf	17
Stockholm	17
Jinan	16
Johannesburg	16
Shenzhen	16
Denver	15
Nanchang	15
Amsterdam	14
Auburn Hills	14
Washington	14
Buffalo	13
Miami	13
Mumbai	13
Pavia	13
Poplar	13
Pune	13
Boston	12
Turin	12
Da Nang	11
Ponte Lambro	11
Rio de Janeiro	11
San Francisco	11
Charlotte	10
Fuzhou	10
Hangzhou	10
Palermo	10
Zhengzhou	10
Bari	9
Belo Horizonte	9
Brasília	9
Totale	15.710

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Nome	#
La sindrome da aneuploidia variegata a mosaico (MVA) associata a neutropenia come condizione predisponente a displasia e neoplasia ematologia	394
A liveborn 69,XXX triploid. Origin, X chromosome activity and gene dosage.	299
Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis	290
Trisomia 8 costituzionale a mosaico nelle malattie mielodisplatiche e mieloproliferative: importanza per pratica clinica e per implicazioni teoriche	254
The mammary gland and the homeobox gene Otx1	244
Cd bands and centromeric function in dicentric chromosomes	233
Acute lymphoblastic leukemia and a familial balanced translocation (12;15) involving ETV6	233
A new chromosome instability disorder	228
Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells	227
Acquired Chromosome change in Cholesteatoma	225
Assessing residual disease in imatinib-treated CML patients by DNA compared to MRNA assays	223
OTX1 and OTX2 as possible molecular markers of sinonasal carcinomas and olfactory neuroblastomas	223
Array-based Comparative Genomic Hybridization in Shwachman-Diamond syndrome: results in 24 patients	222
Chromosome anomalies in bone marrow as primarycause of aplastic or hypoplastic conditions andperipheral cytopenia: disorders due to secondaryimpairment of RUNX1 and MPL genes	221
Genomic quantitative real-time PCR proves residual disease positivity in more than 30% samples with negative mRNA-based qRT-PCR in Chronic Myeloid Leukemia	220
Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms	218
Cytogenetic Monitoring in Shwachman-Diamond Syndrome: A Note on Clonal Progression and a Practical Warning	217
Clonal chromosome anomalies and propensity to myeloid malignancies in congenital amegakaryocytic thrombocytopenia (OMIM 604498)	215
Acquisizione di anomalie cromosomiche clonali nel midollo osseo di pazienti con sindrome di Shwachman Diamond in relazione all’età	214
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	213
Chronic Myeloid Leukemia: Molecular Monitoring of Residual Disease by Genomic DNA Compared to Conventional mRNA Analysis in Follow-Ups up to 8 Years	211
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.	209
Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR	207
48,XXXY/49,XXXXY Mosaicism in a month old infant.	205
Analysis of cross-contamination in established tumour cell lines.	203
La trisomia 8 in leucemie acute e mielodisplasie e costituzionale nel 15-20% dei casi	203
Chromosomal analysis in cultured lymphocytes and fibroblasts of psoriatic patients before and after treatment.	201
Evaluating chromosomal mosaicism by array-based CGH in relation to clinical issues: the proposal of a formula	201
Le basi genetiche della malattia linfoproliferativa.	197
First trimester prenatal diagnosis of Sanfilippo disease (MPS III) type B.	197
Different real time PCR approaches for the fine quantification of SNP's alleles in DNA pools: assays development, characterization and pre-validation.	197
Array-CGH used to monitor dysplastic/neoplastic disorders with unbalanced chromosome anomalies may detect as low as 8% abnormal cells	196
Constitutional trisomy 8 mosaicism in primary myelofibrosis: relevance to clinical practice and warning for trisomy 8 studies.	195
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMIM 601399)	193
Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies	193
Studio molecolare del differenziamento da cellule staminali in condrociti in vivo per lo sviluppo di un protocollo di trapianti di cartilagine umana	192
The syndrome of partial trisomy 14q.	191
Karyotypic variation in benign pleomorphic adenoma of the parotid and in normal salivary glands.	191
Criobanca automatizzata di materiale biologico: stoccaggio e monitoraggio molecolare di cellule meniscali per il trapianto autologo	189
The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies	189
La citogenetica interfasica dimostra che le cellule dendritiche nella Leucemia Mielomonocitica Cronica Giovanile fanno parte del clone leucemico	186
Le basi genetiche della malattia linfoproliferativa legata al cromosoma X	184
Anticentromeric antibodies and inactive centromeres.	183
Mielodisplasia con monosomia 7 familiare: dati citogenetici e molecolari	180
Nuclear projections in tumour cells	177
Indirect immunofluorescence of inactive centromeres as indicator of centromeric function.	177
Comparative genomic hybridization su microarray (aCGH) in sindrome di Shwachman (OMIM 260400) e rischio di mielodisplasia: al di là della citogenetica standard	176
A woman carrier of two apparently unrelated reciprocal translocations: prenatal diagnosis of normal karyotype in the foetus.	176
The role of Yp in sex determination: new evidence from X/Y translocations.	176
Chromosome identification and karyotypic evolution in a human melanoma cell line.	176
Monitoring the Isochromosome i(7)(q10) in the Bone Marrow of Patients With Shwachman Syndrome by Real-time Quantitative PCR	176
Chromosome identification in a Chinese hamster pseudodiploid cell line (CHEF-125)	175
Instabilità costituzionale del cariotipo all'origine di trisomia 8 acquisita midollare	175
Acute lymphoblastic leukemia and familial balanced translocation (12;15) involving ETV6	173
Microhomologies and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia	173
i(7)(q10) carring c.258+2T>C mutazion and risk of myeloid malignancies in patients with SDS	173
Studio molecolare del differenziamento da cellule staminali in condrociti e osteoblasti in vivo per lo sviluppo di protocolli di trapianto	172
Anomalie cromosomiche clonali e non-clonali in 32 casi di sindrome di Shwachman: valore prognostico e predittivo	172
Different reaction of inactive centromeres to anticentromeric antibodies.	171
Different patterns of chromosome 20 interstitial deletion in Shwachman-Diamond syndrome and in myeloid neoplasms	171
Normal insulin receptors in mitochondrial myopathies with ophthalmoplegia.	170
Microhomologiee and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia.	169
La linea cellulare EUE deriva da una linea HeLa.	169
Familial myelodysplastic syndromes, monosomy 7/trisomy 8, and mutator effects	169
Aplasia midollare da perdita del gene RUNX1 acquisita a causa di un riarrangiamento strutturale clonale del cromosoma 21	169
Chromosome size and nuclear projections	166
Establishment and study of different real-time polymerase chain reaction assays for the quantification of cells with deletions of chromosome 7.	165
Age related acquisition of clonal chromosome anomalies in bone marrow cells of SDS patients	165
Citogenetica Umana: nuove metodiche ed applicazioni in medicina.	164
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMOM 601399)	164
Karyotype instability evaluated by array-CGH and risk of myeloid malignancy in Shwachman Diamond syndrome	164
Differente reazione dei centromeri inattivi agli anticorpi anticentromero.	161
Presumptive mosaic origin of an XX/XY female with ambiguous genitalia.	161
MONITORING SHWACHMAN-DIAMOND SYNDROME BY CYTOGENETICS AND a-CGH	160
Mielodisplasia familiare, monosomia 7 / trisomia 8 ed effetto mutatore	159
The use of microarray-based comparative genomic hybridization (a-CGH) to detect and define chromosome imbalances in the bone marrow of SDS patients	158
Myotonic Dystrophy: genetic aspects ; cytochemical findings.	155
Sindrome di Shwacham: instabilita del cromosoma 7 e rischio di patologia mielodisplastica e mieloproliferativa	154
Traslocazione complessa che coinvolge MLL in leucemia mielomonocitica acuta connatale	154
Fenotipo di una paziente da microdelezione della regione 4q e avente di smorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di Gorge.	153
MONITORAGGIO CITOGENETICO E MEDIANTE a-CGH DELLA SINDROME DI SHWACHMAN-DIAMOND	153
Erratum: OTX1 expression in breast cancer is regulated by p53 (Oncogene (2011) 30 (3096-3103) doi:10.1038/onc.2011.31)	153
Severe aplastic anemia (SAA) due to chromosome 21 acquired chromosome anomaly and haploinsufficiency of RUNX1 gene	150
Growth Hormone and Estrogens in Patients with Turner Syndrome: in vivo and in vitro studies.	149
Molecular monitoring of residual disease in chronic myeloid leukemia by genomic DNA compared with conventional mRNA analysis.	149
Fenotipo di una paziente affetta da microdelezione subtelomerica della regione 4q e avente dimorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di George	148
DIFFERENTE PERDITA DI MATERIALE NELLE DELEZIONI INTERSTIZIALI DEL CROMOSOMA 20 NELLE DISPLASIE/NEOPLASIE MIELOIDI E NELLA SINDROME DI SHWACHMAN-DIAMOND	148
Instabilità del cariotipo e mielodisplasie nella Sindrome di Shwachman	147
Nuclear projections and latent centromeres in primary culture and established cell lines.	145
Variabilità cromosomica in linee cellulari derivate da melanomi.	144
Correlation between the numbers of sex chromosomes and the H-Y antigen titer.	144
Distrofia miotonica: genetica e citochimica	143
Shwachman sindrome as mutator phenotype responsible for myeloid dysplasia/neoplasia through karyotype instability and chromosomes 7 and 20 anomalies	143
Leucemia linfoblastica acuta e traslocazione familiare (15-15) che coinvolge ETV6	142
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	142
Metodo di studio per accertare eventuali contaminazioni tra linee cellulari.	141
Studio dei fibroblasti "in vitro" nella distrofia miotonica.	141
Familial partial monosomy 7 and myelodysplasia: different paternal origin of the monosomy 7 suggests action of a mutator gene	141
Insulin receptors in Friedreich's ataxia: studies on cultured fibroblasts.	140
Insulin receptors in psoriasis.	140
Totale	18.447

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Categoria	#
all - tutte	85.257
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	85.257

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2021/2022	847	0	0	0	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	2.029	84	238	936	771	0	0	0	0	0	0	0	0
Totale													23.635