TORRICELLI, FRANCESCA
 Distribuzione geografica
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Continente #
NA - Nord America 4.272
EU - Europa 3.092
AS - Asia 1.548
SA - Sud America 188
Continente sconosciuto - Info sul continente non disponibili 57
AF - Africa 47
OC - Oceania 32
Totale 9.236
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Nazione #
US - Stati Uniti d'America 4.216
RU - Federazione Russa 865
PL - Polonia 850
IT - Italia 484
SG - Singapore 449
CN - Cina 356
HK - Hong Kong 226
IE - Irlanda 226
SE - Svezia 212
VN - Vietnam 183
BR - Brasile 151
KR - Corea 108
DE - Germania 107
FI - Finlandia 73
FR - Francia 62
IN - India 61
GB - Regno Unito 58
UA - Ucraina 57
JO - Giordania 39
CA - Canada 37
AU - Australia 30
TR - Turchia 26
CH - Svizzera 25
ES - Italia 24
ID - Indonesia 18
JP - Giappone 16
AR - Argentina 15
BD - Bangladesh 13
NL - Olanda 13
BE - Belgio 11
MX - Messico 11
CI - Costa d'Avorio 10
CO - Colombia 8
IQ - Iraq 8
AT - Austria 7
PH - Filippine 7
IL - Israele 6
MA - Marocco 6
NG - Nigeria 6
SA - Arabia Saudita 6
EC - Ecuador 5
PK - Pakistan 5
ZA - Sudafrica 5
LT - Lituania 4
SN - Senegal 4
VE - Venezuela 4
SC - Seychelles 3
TH - Thailandia 3
AO - Angola 2
AZ - Azerbaigian 2
BY - Bielorussia 2
DZ - Algeria 2
EE - Estonia 2
GT - Guatemala 2
HN - Honduras 2
IR - Iran 2
KE - Kenya 2
LK - Sri Lanka 2
PE - Perù 2
RO - Romania 2
SV - El Salvador 2
SY - Repubblica araba siriana 2
TN - Tunisia 2
UY - Uruguay 2
UZ - Uzbekistan 2
AF - Afghanistan, Repubblica islamica di 1
BG - Bulgaria 1
BJ - Benin 1
CG - Congo 1
CR - Costa Rica 1
EG - Egitto 1
ET - Etiopia 1
GI - Gibilterra 1
HU - Ungheria 1
KG - Kirghizistan 1
KZ - Kazakistan 1
LB - Libano 1
LV - Lettonia 1
ME - Montenegro 1
MU - Mauritius 1
NC - Nuova Caledonia 1
NR - Nauru 1
OM - Oman 1
PA - Panama 1
PS - Palestinian Territory 1
PT - Portogallo 1
PY - Paraguay 1
SI - Slovenia 1
SK - Slovacchia (Repubblica Slovacca) 1
TM - Turkmenistan 1
TW - Taiwan 1
Totale 9.179
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Città #
Warsaw 850
Santa Clara 759
Ashburn 500
Fairfield 431
Singapore 318
Chandler 252
Dublin 225
Hong Kong 186
Woodbridge 181
Seattle 161
Cambridge 153
Wilmington 145
Houston 141
Seoul 108
San Jose 107
Beijing 104
Jacksonville 93
Milan 79
Ann Arbor 74
Los Angeles 66
Buffalo 62
Altamura 58
Princeton 57
Lawrence 54
Boardman 53
Rome 48
The Dalles 44
Lauterbourg 43
Florence 42
Ho Chi Minh City 40
Munich 39
Boston 38
Council Bluffs 37
Hanoi 37
New York 37
Hefei 33
Shanghai 33
Mumbai 31
Melbourne 28
Bern 24
São Paulo 20
San Diego 19
Dallas 18
Helsinki 18
Kent 18
Moscow 18
Bologna 17
Clifton 17
Dong Ket 16
Izmir 16
Jakarta 15
Turku 15
Medford 14
Barcelona 12
Brooklyn 12
Montreal 12
Brussels 11
Naples 11
Phoenix 11
Turin 11
Abidjan 10
Da Nang 10
Paris 10
Orem 9
Tokyo 9
Verona 9
London 8
Norwalk 8
Rio de Janeiro 8
Venice 8
Chennai 7
Columbus 7
Toronto 7
Abuja 6
Falls Church 6
Frankfurt am Main 6
Salerno 6
San Francisco 6
Tianjin 6
Vienna 6
Amman 5
Andover 5
Belo Horizonte 5
Bogotá 5
Chicago 5
Curitiba 5
Haiphong 5
Hillsboro 5
New Delhi 5
Redondo Beach 5
Stockholm 5
Tel Aviv 5
Yubileyny 5
Bari 4
Brescia 4
Can Tho 4
Catania 4
Charlotte 4
Dakar 4
Dammam 4
Totale 6.317
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Nome #
Detecting common copy number variants in high-throughput sequencing data by using JointSLM algorithm. 373
Microvascular function is selectively impaired in patients with hypertrophic cardiomyopathy and sarcomere myofilament gene mutations. 350
Sphingosine 1-phosphate induces differentiation of mesoangioblasts towards smooth muscle. A role for GATA6. 333
Use of donor bone marrow mesenchymal stem cells for treatment of skin allograft rejection in a preclinical rat model 327
Using a calibration experiment to assess gene-specific information: full Bayesian and empirical Bayesian models for two-channel microarray data. 310
Clinical Features and Outcome of Hypertrophic Cardiomyopathy Associated With Triple Sarcomere Protein Gene Mutations 310
Improvement of low-density microelectronic array technology to characterize 14 mutations/single-nucleotide polymorphisms from several human genes on a large scale. 292
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 274
[Y chromosome abnormalities and azoospermia. Description of 2 cases] 231
CFH Y402H polymorphism in Italian patients with age-related macular degeneration, retinitis pigmentosa, and Stargardt disease 215
Th2-oriented profile of male offspring T cells present in women with systemic sclerosis and reactive with maternal major histocompatibility complex antigens. 214
372 kb microdeletion in 18q12.3 causing SETBP1 haploinsufficiency associated with mild mental retardation and expressive speech impairment. 213
A very fast and accurate method for calling aberrations in array-CGH data. 201
Impact of Genotype on the Occurrence of Atrial Fibrillation in Patients With Hypertrophic Cardiomyopathy. 199
Utility of droplet digital PCR for the quantitative detection of polyomavirus JC in clinical samples 194
A new ATTR Phe64Ile mutation with late-onset multiorgan involvement. 190
Read count approach for DNA copy number variants detection. 189
Draft genome sequence of the first hypermucoviscous Klebsiella quasipneumoniae subsp. quasipneumoniae isolate from a bloodstream infection 188
Draft genome sequence of Clostridium difficile belonging to ribotype 018 and sequence type 17 187
Coronary microvascular dysfunction is an early feature of cardiac involvement in patients with Anderson-Fabry disease. 186
P53 and DPC4 alterations in the bile of patients with pancreatic carcinoma 184
A large-scale association study to assess the impact of known variants of the human INHA gene on premature ovarian failure 184
EX-HOM (EXome HOMozygosity): A Proof of Principle. 179
Genetic identification of burned corpses as a part of disaster victim identification effort 176
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. 168
A shifting level model algorithm that identifies aberrations in array-CGH data 167
A novel mutation in the VMD2 gene in an Italian family with Best maculopathy. 166
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 166
RELEVANCE OF CORONARY MICROVASCULAR FLOW IMPAIRMENT TO LONG TERM REMODELING AND SYSTOLIC DYSFUNCTION IN HYPERTROPHIC CARDIOMYOPATHY 164
A NEW CASE OF TERMINAL DELETION 14Q32.3 IN A NEWBORN WITH PLURIMALFORMATIONS 163
Blood cell mitochondrial DNA content and premature ovarian aging 163
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 162
Evaluation of maternal serum alpha-fetoprotein and ultrasound examination to screen fetal chromosomal abnormalities. 159
MYO7A and USH2A gene sequence variants in Italian patients with Usher syndrome 153
Myofilament protein gene mutation screening and outcome of patients with hypertrophic cardiomyopathy. 152
Different patterns of fundus autofluorescence related to ABCA4 gene mutations in Stargardt disease. 148
Clinical phenotype and outcome of hypertrophic cardiomyopathy associated with thin-filament gene mutations. 147
Le anomalie genetiche del carcinoma pancreatico e le applicazioni cliniche [Genetic anomalies of pancreatic carcinoma and clinical applications] 146
ESTROGEN RECEPTORS IN THE SECRETORY ENDOMETRIUM AND FIRST TRIMESTER DECIDUA. BIOCHEMICAL AND IMMUNOCYTOCHEMICAL ASSAY. 142
DEMONSTARTION OF P29, AN ESTROGEN RECEPTOR-ASSOCIATED TUMOR MARKER, IN THE DECIDUA FROM THE FIRST TRIMESTER OF PREGNANCY 142
Identification of hematopoietic progenitor cells in human amniotic fluid before the 12th week of gestation. 140
[Multiple malformations in infants born to drug-addicted parents. Report of 2 cases of which was accompanied by chromosome aberration] 138
IMPLICATIONS OF IL28-B GENE SINGLE NUCLEOTIDE POLYMORPHISMS IN PHARMACOLOGIC TREATMENT OF HCV+ PATIENTS: AN ITALIAN STUDY 131
Retinal astrocytic hamartoma and Stargardt's disease: unusual association in a patient with ABCR mutation without phacomatosis. 129
Newborn bacteraemia caused by an Aeromonas caviae producing the VIM-1 and SHV-12 β-lactamases, encoded by a transferable plasmid 126
Techniques of dental DNA extraction: some operative experiences 125
Microsatellite analysis of chromosome 3p region in sporadic renal cell carcinomas. 125
Genetic alteration in the duodenal juice of patients with pancreatic carcinoma 115
Totale 9.236
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Categoria #
all - tutte 24.424
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 24.424
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022359 0 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
2025/20262.479 312 334 132 189 306 95 272 111 156 176 53 343
2026/202780 68 12 0 0 0 0 0 0 0 0 0 0
Totale 9.236