TORRICELLI, FRANCESCA
 Distribuzione geografica
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Continente #
NA - Nord America 3.752
EU - Europa 2.712
AS - Asia 1.212
SA - Sud America 165
AF - Africa 33
OC - Oceania 32
Totale 7.906
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Nazione #
US - Stati Uniti d'America 3.728
RU - Federazione Russa 865
PL - Polonia 849
SG - Singapore 357
CN - Cina 284
IE - Irlanda 225
HK - Hong Kong 220
SE - Svezia 212
IT - Italia 192
BR - Brasile 139
KR - Corea 108
DE - Germania 106
VN - Vietnam 72
FI - Finlandia 65
UA - Ucraina 57
IN - India 46
GB - Regno Unito 44
JO - Giordania 37
AU - Australia 30
CH - Svizzera 24
TR - Turchia 23
ES - Italia 20
ID - Indonesia 18
FR - Francia 14
CA - Canada 12
JP - Giappone 12
NL - Olanda 12
AR - Argentina 11
BE - Belgio 11
CI - Costa d'Avorio 10
BD - Bangladesh 9
MX - Messico 9
CO - Colombia 7
MA - Marocco 5
LT - Lituania 4
PH - Filippine 4
IQ - Iraq 3
SA - Arabia Saudita 3
SC - Seychelles 3
ZA - Sudafrica 3
AO - Angola 2
AT - Austria 2
BY - Bielorussia 2
DZ - Algeria 2
EC - Ecuador 2
EE - Estonia 2
IR - Iran 2
KE - Kenya 2
LK - Sri Lanka 2
PE - Perù 2
PK - Pakistan 2
RO - Romania 2
TN - Tunisia 2
UZ - Uzbekistan 2
VE - Venezuela 2
AF - Afghanistan, Repubblica islamica di 1
AZ - Azerbaigian 1
BJ - Benin 1
CR - Costa Rica 1
EG - Egitto 1
GI - Gibilterra 1
GT - Guatemala 1
HU - Ungheria 1
IL - Israele 1
KG - Kirghizistan 1
KZ - Kazakistan 1
LB - Libano 1
ME - Montenegro 1
MU - Mauritius 1
NC - Nuova Caledonia 1
NR - Nauru 1
PA - Panama 1
PY - Paraguay 1
SK - Slovacchia (Repubblica Slovacca) 1
SN - Senegal 1
TH - Thailandia 1
TM - Turkmenistan 1
UY - Uruguay 1
Totale 7.906
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Città #
Warsaw 849
Santa Clara 741
Fairfield 431
Ashburn 356
Chandler 252
Singapore 239
Dublin 224
Hong Kong 183
Woodbridge 181
Seattle 160
Cambridge 152
Wilmington 145
Houston 140
Seoul 108
Beijing 102
Jacksonville 93
Ann Arbor 74
Buffalo 61
Altamura 58
Princeton 57
Lawrence 54
Boardman 52
Los Angeles 48
Munich 39
Boston 38
Florence 37
New York 35
Hefei 33
Shanghai 32
Mumbai 31
Melbourne 28
Bern 24
Ho Chi Minh City 21
San Diego 19
Kent 18
Moscow 18
São Paulo 18
Clifton 17
Dallas 17
Dong Ket 16
Izmir 16
Jakarta 15
Turku 15
Medford 14
Barcelona 12
Brussels 11
Hanoi 11
Milan 11
Abidjan 10
Brooklyn 10
Helsinki 10
Paris 10
Norwalk 8
Phoenix 8
Rio de Janeiro 8
The Dalles 8
Bologna 7
Rome 7
Falls Church 6
London 6
Montreal 6
Tokyo 6
Toronto 6
Andover 5
Belo Horizonte 5
Curitiba 5
Frankfurt am Main 5
Hillsboro 5
Redondo Beach 5
Stockholm 5
Yubileyny 5
Bogotá 4
Chicago 4
Council Bluffs 4
Hangzhou 4
New Delhi 4
Salerno 4
Verona 4
Amman 3
Auburn Hills 3
Bremen 3
Buenos Aires 3
Colombo 3
Dhaka 3
Johannesburg 3
Niterói 3
Poplar 3
Pune 3
Quezon City 3
Tianjin 3
Bengaluru 2
Beni Mellal 2
Botucatu 2
Castelnuovo Berardenga 2
Charlotte 2
Contagem 2
Da Nang 2
Dammam 2
Dearborn 2
Denver 2
Totale 5.546
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Nome #
Detecting common copy number variants in high-throughput sequencing data by using JointSLM algorithm. 344
Sphingosine 1-phosphate induces differentiation of mesoangioblasts towards smooth muscle. A role for GATA6. 310
Microvascular function is selectively impaired in patients with hypertrophic cardiomyopathy and sarcomere myofilament gene mutations. 303
Use of donor bone marrow mesenchymal stem cells for treatment of skin allograft rejection in a preclinical rat model 292
Using a calibration experiment to assess gene-specific information: full Bayesian and empirical Bayesian models for two-channel microarray data. 273
Improvement of low-density microelectronic array technology to characterize 14 mutations/single-nucleotide polymorphisms from several human genes on a large scale. 269
Clinical Features and Outcome of Hypertrophic Cardiomyopathy Associated With Triple Sarcomere Protein Gene Mutations 238
Defining the diagnostic effectiveness of genes for inclusion in panels: the experience of two decades of genetic testing for hypertrophic cardiomyopathy at a single center 238
[Y chromosome abnormalities and azoospermia. Description of 2 cases] 190
Th2-oriented profile of male offspring T cells present in women with systemic sclerosis and reactive with maternal major histocompatibility complex antigens. 185
372 kb microdeletion in 18q12.3 causing SETBP1 haploinsufficiency associated with mild mental retardation and expressive speech impairment. 182
CFH Y402H polymorphism in Italian patients with age-related macular degeneration, retinitis pigmentosa, and Stargardt disease 179
A very fast and accurate method for calling aberrations in array-CGH data. 178
Impact of Genotype on the Occurrence of Atrial Fibrillation in Patients With Hypertrophic Cardiomyopathy. 172
A new ATTR Phe64Ile mutation with late-onset multiorgan involvement. 171
Utility of droplet digital PCR for the quantitative detection of polyomavirus JC in clinical samples 167
Read count approach for DNA copy number variants detection. 166
Draft genome sequence of Clostridium difficile belonging to ribotype 018 and sequence type 17 164
Draft genome sequence of the first hypermucoviscous Klebsiella quasipneumoniae subsp. quasipneumoniae isolate from a bloodstream infection 162
Coronary microvascular dysfunction is an early feature of cardiac involvement in patients with Anderson-Fabry disease. 159
EX-HOM (EXome HOMozygosity): A Proof of Principle. 158
Genetic Epidemiology of Paget's Disease of Bone in Italy: sequestosome1/p62 Gene Mutational Test and Haplotype Analysis at 5q35 in a Large Representative Series of Sporadic and Familial Italian Cases of Paget's Disease of Bone. 152
Genetic identification of burned corpses as a part of disaster victim identification effort 151
P53 and DPC4 alterations in the bile of patients with pancreatic carcinoma 149
A novel mutation in the VMD2 gene in an Italian family with Best maculopathy. 149
Blood cell mitochondrial DNA content and premature ovarian aging 145
Draft genome sequence of Proteus mirabilis NO-051/ 03, representative of a multidrug-resistant clone spreading in Europe and expressing the CMY-16 AmpC-type β-lactamase 144
Characterization of a novel putative Xer-dependent integrative mobile element carrying the blaNMC-A carbapenemase gene, inserted into the chromosome of members of the Enterobacter cloacae complex 144
A large-scale association study to assess the impact of known variants of the human INHA gene on premature ovarian failure 142
A shifting level model algorithm that identifies aberrations in array-CGH data 140
A NEW CASE OF TERMINAL DELETION 14Q32.3 IN A NEWBORN WITH PLURIMALFORMATIONS 140
RELEVANCE OF CORONARY MICROVASCULAR FLOW IMPAIRMENT TO LONG TERM REMODELING AND SYSTOLIC DYSFUNCTION IN HYPERTROPHIC CARDIOMYOPATHY 136
Different patterns of fundus autofluorescence related to ABCA4 gene mutations in Stargardt disease. 136
MYO7A and USH2A gene sequence variants in Italian patients with Usher syndrome 136
Evaluation of maternal serum alpha-fetoprotein and ultrasound examination to screen fetal chromosomal abnormalities. 135
Myofilament protein gene mutation screening and outcome of patients with hypertrophic cardiomyopathy. 132
Identification of hematopoietic progenitor cells in human amniotic fluid before the 12th week of gestation. 124
ESTROGEN RECEPTORS IN THE SECRETORY ENDOMETRIUM AND FIRST TRIMESTER DECIDUA. BIOCHEMICAL AND IMMUNOCYTOCHEMICAL ASSAY. 120
Le anomalie genetiche del carcinoma pancreatico e le applicazioni cliniche [Genetic anomalies of pancreatic carcinoma and clinical applications] 118
Clinical phenotype and outcome of hypertrophic cardiomyopathy associated with thin-filament gene mutations. 114
Newborn bacteraemia caused by an Aeromonas caviae producing the VIM-1 and SHV-12 β-lactamases, encoded by a transferable plasmid 113
DEMONSTARTION OF P29, AN ESTROGEN RECEPTOR-ASSOCIATED TUMOR MARKER, IN THE DECIDUA FROM THE FIRST TRIMESTER OF PREGNANCY 112
Retinal astrocytic hamartoma and Stargardt's disease: unusual association in a patient with ABCR mutation without phacomatosis. 111
IMPLICATIONS OF IL28-B GENE SINGLE NUCLEOTIDE POLYMORPHISMS IN PHARMACOLOGIC TREATMENT OF HCV+ PATIENTS: AN ITALIAN STUDY 111
Techniques of dental DNA extraction: some operative experiences 109
[Multiple malformations in infants born to drug-addicted parents. Report of 2 cases of which was accompanied by chromosome aberration] 103
Microsatellite analysis of chromosome 3p region in sporadic renal cell carcinomas. 101
Genetic alteration in the duodenal juice of patients with pancreatic carcinoma 96
Totale 7.963
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Categoria #
all - tutte 20.631
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 20.631
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021350 0 0 0 0 0 52 31 44 57 78 34 54
2021/2022368 9 39 26 13 15 17 16 27 14 15 91 86
2022/20231.035 90 192 67 64 85 164 129 62 115 5 29 33
2023/2024329 19 37 47 10 16 67 15 52 4 5 22 35
2024/20252.227 77 254 159 370 652 289 20 116 92 55 82 61
2025/20261.286 312 334 132 189 306 13 0 0 0 0 0 0
Totale 7.963