TORRICELLI, FRANCESCA
 Distribuzione geografica
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Continente #
NA - Nord America 2.453
EU - Europa 1.943
AS - Asia 354
AF - Africa 7
SA - Sud America 5
Totale 4.762
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Nazione #
US - Stati Uniti d'America 2.448
PL - Polonia 844
RU - Federazione Russa 254
IE - Irlanda 224
SE - Svezia 209
IT - Italia 167
CN - Cina 94
HK - Hong Kong 84
DE - Germania 58
UA - Ucraina 56
SG - Singapore 52
FI - Finlandia 40
IN - India 40
JO - Giordania 34
GB - Regno Unito 26
CH - Svizzera 24
VN - Vietnam 22
TR - Turchia 20
ES - Italia 15
BE - Belgio 10
CA - Canada 5
NL - Olanda 5
BR - Brasile 3
PH - Filippine 3
SC - Seychelles 3
AO - Angola 2
AR - Argentina 2
AT - Austria 2
EE - Estonia 2
FR - Francia 2
IR - Iran 2
JP - Giappone 2
LT - Lituania 2
RO - Romania 2
KR - Corea 1
ME - Montenegro 1
MU - Mauritius 1
TN - Tunisia 1
Totale 4.762
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Città #
Warsaw 844
Fairfield 431
Chandler 252
Dublin 224
Ashburn 198
Woodbridge 181
Seattle 159
Cambridge 152
Wilmington 145
Houston 138
Jacksonville 92
Ann Arbor 74
Altamura 58
Princeton 57
Lawrence 54
Boardman 52
Hong Kong 48
Buffalo 39
Boston 36
Singapore 36
Beijing 35
Florence 34
Mumbai 31
Shanghai 30
Bern 24
New York 24
San Diego 19
Dong Ket 16
Izmir 16
Medford 14
Kent 13
Barcelona 12
Brussels 10
Norwalk 8
Los Angeles 7
Milan 7
Phoenix 7
Falls Church 6
Andover 5
Hillsboro 5
Toronto 5
Bologna 4
Rome 4
Salerno 4
Verona 4
Auburn Hills 3
Bremen 3
Pune 3
Quezon City 3
Buenos Aires 2
Castelnuovo Berardenga 2
Dearborn 2
Guangzhou 2
Kiel 2
London 2
Luanda 2
Montespertoli 2
Munich 2
New Delhi 2
Redwood City 2
San Mateo 2
Stockholm 2
Tappahannock 2
Timisoara 2
Venice 2
Vienna 2
West Jordan 2
Americana 1
Arnsberg 1
Attimis 1
Bari 1
Chiswick 1
Duncan 1
Frankfurt Am Main 1
Genova 1
Grafing 1
Gävle 1
Heze 1
Jinan 1
Legnago 1
Loughborough 1
Lund 1
Madrid 1
Margherita Di Savoia 1
Marlborough 1
Moscow 1
Nagoya 1
Nanjing 1
Nanning 1
North Dartmouth 1
Nuremberg 1
Pavia 1
Pignataro Maggiore 1
Pirna 1
Podgorica 1
Prescot 1
Reggio Nell'emilia 1
Sabz 1
Santa Clara 1
Scuola 1
Totale 3.695
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Nome #
Detecting common copy number variants in high-throughput sequencing data by using JointSLM algorithm. 273
Sphingosine 1-phosphate induces differentiation of mesoangioblasts towards smooth muscle. A role for GATA6. 255
Use of donor bone marrow mesenchymal stem cells for treatment of skin allograft rejection in a preclinical rat model 236
Microvascular function is selectively impaired in patients with hypertrophic cardiomyopathy and sarcomere myofilament gene mutations. 231
Improvement of low-density microelectronic array technology to characterize 14 mutations/single-nucleotide polymorphisms from several human genes on a large scale. 211
Using a calibration experiment to assess gene-specific information: full Bayesian and empirical Bayesian models for two-channel microarray data. 211
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 166
Clinical Features and Outcome of Hypertrophic Cardiomyopathy Associated With Triple Sarcomere Protein Gene Mutations 155
Read count approach for DNA copy number variants detection. 130
EX-HOM (EXome HOMozygosity): A Proof of Principle. 118
A very fast and accurate method for calling aberrations in array-CGH data. 114
372 kb microdeletion in 18q12.3 causing SETBP1 haploinsufficiency associated with mild mental retardation and expressive speech impairment. 110
CFH Y402H polymorphism in Italian patients with age-related macular degeneration, retinitis pigmentosa, and Stargardt disease 105
A new ATTR Phe64Ile mutation with late-onset multiorgan involvement. 103
Th2-oriented profile of male offspring T cells present in women with systemic sclerosis and reactive with maternal major histocompatibility complex antigens. 101
Coronary microvascular dysfunction is an early feature of cardiac involvement in patients with Anderson-Fabry disease. 101
Impact of Genotype on the Occurrence of Atrial Fibrillation in Patients With Hypertrophic Cardiomyopathy. 97
P53 and DPC4 alterations in the bile of patients with pancreatic carcinoma 95
Draft genome sequence of the first hypermucoviscous Klebsiella quasipneumoniae subsp. quasipneumoniae isolate from a bloodstream infection 95
Utility of droplet digital PCR for the quantitative detection of polyomavirus JC in clinical samples 93
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. 88
Myofilament protein gene mutation screening and outcome of patients with hypertrophic cardiomyopathy. 86
Draft genome sequence of Clostridium difficile belonging to ribotype 018 and sequence type 17 86
[Y chromosome abnormalities and azoospermia. Description of 2 cases] 82
RELEVANCE OF CORONARY MICROVASCULAR FLOW IMPAIRMENT TO LONG TERM REMODELING AND SYSTOLIC DYSFUNCTION IN HYPERTROPHIC CARDIOMYOPATHY 81
Genetic identification of burned corpses as a part of disaster victim identification effort 81
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 80
A novel mutation in the VMD2 gene in an Italian family with Best maculopathy. 79
A shifting level model algorithm that identifies aberrations in array-CGH data 76
A large-scale association study to assess the impact of known variants of the human INHA gene on premature ovarian failure 73
Retinal astrocytic hamartoma and Stargardt's disease: unusual association in a patient with ABCR mutation without phacomatosis. 71
Techniques of dental DNA extraction: some operative experiences 70
A NEW CASE OF TERMINAL DELETION 14Q32.3 IN A NEWBORN WITH PLURIMALFORMATIONS 67
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 67
Newborn bacteraemia caused by an Aeromonas caviae producing the VIM-1 and SHV-12 β-lactamases, encoded by a transferable plasmid 67
Blood cell mitochondrial DNA content and premature ovarian aging 66
ESTROGEN RECEPTORS IN THE SECRETORY ENDOMETRIUM AND FIRST TRIMESTER DECIDUA. BIOCHEMICAL AND IMMUNOCYTOCHEMICAL ASSAY. 64
Microsatellite analysis of chromosome 3p region in sporadic renal cell carcinomas. 63
Different patterns of fundus autofluorescence related to ABCA4 gene mutations in Stargardt disease. 62
Evaluation of maternal serum alpha-fetoprotein and ultrasound examination to screen fetal chromosomal abnormalities. 60
Identification of hematopoietic progenitor cells in human amniotic fluid before the 12th week of gestation. 60
Le anomalie genetiche del carcinoma pancreatico e le applicazioni cliniche [Genetic anomalies of pancreatic carcinoma and clinical applications] 58
DEMONSTARTION OF P29, AN ESTROGEN RECEPTOR-ASSOCIATED TUMOR MARKER, IN THE DECIDUA FROM THE FIRST TRIMESTER OF PREGNANCY 53
Genetic alteration in the duodenal juice of patients with pancreatic carcinoma 46
MYO7A and USH2A gene sequence variants in Italian patients with Usher syndrome 43
IMPLICATIONS OF IL28-B GENE SINGLE NUCLEOTIDE POLYMORPHISMS IN PHARMACOLOGIC TREATMENT OF HCV+ PATIENTS: AN ITALIAN STUDY 42
[Multiple malformations in infants born to drug-addicted parents. Report of 2 cases of which was accompanied by chromosome aberration] 40
Clinical phenotype and outcome of hypertrophic cardiomyopathy associated with thin-filament gene mutations. 8
Totale 4.819
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Categoria #
all - tutte 13.104
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 13.104
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020915 0 0 25 83 130 135 114 137 112 73 87 19
2020/2021600 65 49 31 72 33 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
2024/2025369 77 254 38 0 0 0 0 0 0 0 0 0
Totale 4.819