TRABETTI, Elisabetta
 Distribuzione geografica
Continente #
NA - Nord America 11.455
EU - Europa 10.889
AS - Asia 6.564
SA - Sud America 853
AF - Africa 102
OC - Oceania 15
Continente sconosciuto - Info sul continente non disponibili 8
Totale 29.886
Nazione #
US - Stati Uniti d'America 11.315
RU - Federazione Russa 4.041
SG - Singapore 2.730
GB - Regno Unito 2.706
CN - Cina 2.143
SE - Svezia 719
BR - Brasile 698
IT - Italia 681
DE - Germania 632
FI - Finlandia 592
FR - Francia 541
HK - Hong Kong 531
IE - Irlanda 507
VN - Vietnam 473
KR - Corea 208
UA - Ucraina 160
IN - India 86
CA - Canada 78
JP - Giappone 75
BE - Belgio 65
TR - Turchia 61
AR - Argentina 58
NL - Olanda 46
PL - Polonia 46
BD - Bangladesh 43
ZA - Sudafrica 42
ID - Indonesia 41
MX - Messico 38
PK - Pakistan 37
AT - Austria 36
ES - Italia 28
IQ - Iraq 22
EC - Ecuador 19
LT - Lituania 16
VE - Venezuela 15
CO - Colombia 13
CZ - Repubblica Ceca 13
PY - Paraguay 13
AE - Emirati Arabi Uniti 12
AU - Australia 12
MA - Marocco 12
PE - Perù 12
UZ - Uzbekistan 12
CL - Cile 11
IR - Iran 11
UY - Uruguay 11
AZ - Azerbaigian 10
BJ - Benin 9
JO - Giordania 9
CH - Svizzera 8
KG - Kirghizistan 8
DZ - Algeria 7
EG - Egitto 7
TN - Tunisia 6
CR - Costa Rica 5
EE - Estonia 5
EU - Europa 5
GE - Georgia 5
IL - Israele 5
KZ - Kazakistan 5
LV - Lettonia 5
PA - Panama 5
PH - Filippine 5
RO - Romania 5
TG - Togo 5
GR - Grecia 4
HN - Honduras 4
SA - Arabia Saudita 4
BG - Bulgaria 3
BH - Bahrain 3
HR - Croazia 3
JM - Giamaica 3
KE - Kenya 3
KH - Cambogia 3
LK - Sri Lanka 3
LU - Lussemburgo 3
MT - Malta 3
NP - Nepal 3
NZ - Nuova Zelanda 3
RS - Serbia 3
SI - Slovenia 3
XK - ???statistics.table.value.countryCode.XK??? 3
AL - Albania 2
BA - Bosnia-Erzegovina 2
BN - Brunei Darussalam 2
BO - Bolivia 2
CI - Costa d'Avorio 2
CY - Cipro 2
DK - Danimarca 2
HU - Ungheria 2
LA - Repubblica Popolare Democratica del Laos 2
LB - Libano 2
MK - Macedonia 2
NO - Norvegia 2
SC - Seychelles 2
SN - Senegal 2
TJ - Tagikistan 2
AM - Armenia 1
BB - Barbados 1
BS - Bahamas 1
Totale 29.867
Città #
Southend 2.359
Jacksonville 1.491
Singapore 1.431
Dallas 1.418
Ashburn 1.390
Moscow 1.325
Chandler 1.295
Woodbridge 906
Ann Arbor 679
Hong Kong 530
Dublin 507
Houston 362
Beijing 350
New York 279
Verona 275
Wilmington 222
Lawrence 199
Princeton 199
The Dalles 177
Los Angeles 176
Nanjing 166
Munich 165
Ho Chi Minh City 144
Jinan 141
Helsinki 132
Boardman 126
Shenyang 109
Buffalo 93
Dong Ket 93
Sindelfingen 89
Tianjin 82
Turku 81
Hebei 77
Hanoi 75
Tokyo 72
São Paulo 69
Columbus 68
Brussels 62
Zhengzhou 60
Santa Clara 58
Nanchang 57
Milan 55
Hangzhou 52
Lancaster 52
Redondo Beach 51
Jiaxing 50
Changsha 49
Seattle 49
Haikou 43
Ningbo 42
Warsaw 42
Guangzhou 41
Seoul 40
Taiyuan 35
London 34
Redmond 33
Taizhou 33
San Francisco 32
Norwalk 31
Washington 31
Nuremberg 28
Vienna 28
Falkenstein 27
Johannesburg 27
Montreal 27
Lanzhou 26
Phoenix 26
Brooklyn 25
Council Bluffs 25
Dearborn 25
Jakarta 23
Chicago 22
Denver 22
Toronto 22
Redwood City 21
Rio de Janeiro 21
Stockholm 21
Brasília 20
Falls Church 20
Fuzhou 20
Kent 20
Poplar 20
Fairfield 19
Rome 18
Boston 17
Chennai 17
Haiphong 17
Mianwali 17
Atlanta 16
Düsseldorf 16
Amsterdam 15
Auburn Hills 15
Lappeenranta 15
Shanghai 15
Frankfurt am Main 14
Manchester 13
San Jose 13
Belo Horizonte 12
Hyderabad 12
Orem 12
Totale 19.173
Nome #
A preliminary microRNA analysis of non syndromic thoracic aortic aneurysms 508
Common Variants Associated to Type 2 Diabetes in the Italian Population 462
MALAT1 Expression Is Deregulated in miR-34a Knockout Cell Lines 337
Analisi di linkage e associazione di un polimorfismo del promotore del gene UGRP1 che mappa nella regione 5q31, una regione ricca di geni candidati potenzialmente implicati in asma allergico 239
1059G/C polymorphism within the exon 2 of the C-reactive protein gene: relationship to C-reactive protein levels and prognosis in unstable angina. 238
Ability of different flow rates of fractional exaled nitric oxide (FeNO) to discriminate between asthmatic and no asthamatic subject 236
A genome scan for allergic asthma and related phenotypes in an Italian population sample 219
Detection of allele-specific gene expression on next generation sequencing data 213
ALOX5AP gene variants and risk of coronary artery disease: an angiography-based study 209
A1298C methylentetrahydrofolate reductase mutation and coronary artery disease:relationship with C677T polymorphysm and homocystein/folate metabolism 206
Associazione di polimorfismi del cluster dei geni FADS1 e FADS2 con i livelli di acidi grassi polinsaturi in malattie coronariche 204
CACNA1E variants affect beta cell function in patients with newly diagnosed type 2 diabetes. the Verona newly diagnosed type 2 diabetes study (VNDS) 3. 204
Analisi multilocus per l’identificazione di un genotipo di rischio in Malattie Cardiovascolari 203
A low "genetic load" of risk variants for type 2 diabetes is associated to better beta cell function in patients with newly diagnosed type 2 diabetes 199
A novel synonymous substitution in the GCK gene causes aberrant splicing in an Italian patient with GCK-MODY phenotype 196
Affected sib-pair and mutation analyses of the high affinity IgE receptor beta chain locus in Italian families with atopic asthmatic children 195
Novel serum paraoxonase activity assays are associated with coronary artery disease 193
A renal genetic risk score (GRS) is associated with kidney dysfunction in people with type 2 diabetes 193
Gene Environment Interactions in Respiratory Diseases – Protocol, Standard Operative Procedures and Questionnaires 192
Association of a Lymphotoxin alpha gene polymorphism and atopy in Italian families. 190
Renovascular disease: effect of ACE gene deletion polymorphism and endovascular revascularization. 188
The Gene-Environment Interactions in Respiratory Diseases (GEIRD) Project 188
Candidate genes and a genome-wide search in Italian families with atopic asthmatic children 186
Analisi di 51 polimorfismi in 35 geni dell’infiammazione per la valutazione del rischio di coronaropatia e di infarto del miocardio 185
The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families 184
PPARG2 Pro12Ala and ADAMTS9 rs4607103 as "insulin resistance loci" and "insulin secretion loci" in Italian individuals. The GENFIEV study and the Verona Newly Diagnosed Type 2 Diabetes Study (VNDS) 4. 184
ApoC-III gene polymorphisms and risk of coronary artery disease 180
Biochemical and genetic markers of iron status and the risk of coronary disease 180
Association of the IL33 gene region with childhood allergic asthma 179
Genetic variability of G6PC2 influences beta cell function and insulin sensitivity in patients with newly diagnosed type 2 diabetes 178
Acquired and genetic determinants of homocysteine in atheromatous renel artery stenosis with mild renal insufficiency 177
Studiare la regione HLA negli esomi 176
Genomic and proteomic investigation into non-syndromic aneurysms of the human ascending aorta. 175
Analisi di espressione genica in aneurismi non sindromici dell’aorta ascendente 175
Frequency distribution of the alleles of several variable number of tandem repeat DNA polymorphisms in the Italian population 173
Potential role of MTNR1B locus in regulating beta cell function and glucose levels in patients with newly diagnosed type 2 diabetes 173
Reply to Novelli 172
Additive effect of LRP8/APOER2 R952Q variant to APOE epsilon2/epsilon3/epsilon4 genotype in modulating apolipoprotein E concentration and the risk of myocardial infarction: a case-control study. 172
Linkage to atopy on chromosome 19 in north-eastern Italian families with allergic asthma 171
Proteomic investigation into nonsyndromic aneurysm of the human ascenging aorta 171
Combined effect of hemostatic gene polymorphisms and the risk of myocardial infarction in patients with advanced coronary atherosclerosis. 171
Variants and haplotypes of TCF7L2 are associated with beta cell function in patients with newly diagnosed type 2 diabetes. The Verona Newly Diagnosed Type 2 Diabetes Study (VNDS).1. 170
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically proven coronary artery disease. 169
Hyperhomocysteinemia and Mortality after Coronary Artery Bypass Grafting 168
Reconstruction and functional analysis of altered molecular pathways in human atherosclerotic arteries 168
Hyperhomocysteinemia and mortality after coronary artery by-pass grafing. 167
Body mass index is a potential modifier of the influence on beta cell function exerted by SLC30A8 and KCNJ11 diabetes risk variants in patients with newly diagnosed type 2 diabetes 167
Studies on sporadic non-syndromic thoracic aortic aneurysms: II. Alterations of extra-cellular matrix components and focal adhesion proteins 167
Forensic applications of molecular genetic analysis: an Italian collaborative study on paternity testing by the determination of variable number of tandem repeat DNA polymorphisms 166
Chromosome 14 linkage analysis and mutation study of two serpin genes in allergic asthmatic families 165
Accertamento preliminare della possibile mescolanza di tracce ematiche: descrizione di un caso peritale di recente osaservazione indagato con la tecnica della amplificazione del DNA (PCR) 165
Association of childhood allergic asthma with markers flanking the IL33 gene in Italian families. 165
Allele frequencies of six highly polymorphic DNA loci in the Croatian population 163
Cromosoma 19 e asma atopica in famiglie Italiane 163
Single and multilocus analyses for the identification of at risk genotypes in cardiovascular disease 163
Homozygosity for APOCIII variant at position 455 of insulin responsive element promoter region is associated with increased APOC-III levels and risk of coronary artery disease 162
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically confirmed coronary artery disease. 162
Bone marrow transplantation monitoring by DNA analysis 161
Association analysis of 65 genetic polymorphisms in coronary artery disease patients 161
The -1131 T > C and S19W APOA5 gene polymorphisms are associated with high levels of triglycerides and apolipoprotein C-III, but not with coronary artery disease: an angiographic study 161
Interaction between folate and MTHFR1298 A/C polymorphism on Genomic DNA Methylation 160
Variants in CACNA1E affect beta cell function and glucose homeostasis in newly diagnosed type 2 diabetes patients 160
Association of FcER1A and RAD50 polymorphisms with serum IgE levels, asthma and rhinitis 160
Hyperhomocysteinemia in relation to total and cardiovascular death after coronary bypass grafting. 159
Asthma and atopy in Italian families: a genome-wide linkage analysis 159
Valutazione del software Defuse per la rilevazione di fusioni geniche da esperimenti di Next Generation Sequencing 158
Interaction between metabolic syndrome and PON 1 polymorphism as a determinant of the risk of coronary artery disease 157
Apolipoprotein C-III, n-3 Polyunsaturated Fatty Acids, and “Insulin-Resistant” T-455C APOC3 gene polymorphism in heart disease patients: example of gene-diet interaction 157
807 C/T polymorphism of the glycoprotein IA gene and pharmacogenetic modulation of platelet response to dual antiplatelet treatment 157
Expression profiles of non syndromic thoracic aortic aneurysms 157
Dissection of HLA-C gene region to investigate its association with complex traits 156
Allele and genotype frequencies of eight DNA polymorphisms in the Italian population 155
Polymorphisms in the Hemostatic Pathway Genes and the Risk of Myocardial infarction in Patients with Advanced Coronary Artery Disease. Results from the Verona Heart Project. 154
Analyzing BioRad-Illumina Single Cell RNA-Seq data with open source tools 154
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically confirmed coronary artery disease. 153
Analisi di associazione del cluster genico degli interferoni nella regione 9p21 in famiglie italiane con asma allergico 153
Advanced cellular models for rare disease study: exploring neural, muscle and skeletal organoids 152
Whole Genome microarray and Real-time PcR to detect genes involved in non-syndromic ascending aortic aneurysms 152
A1298C methylenetetrahydrofolate reductase mutation and coronary artery disease: Relationships with C677T polymorphism and homocysteine/folate metabolism 151
Haplotypes of the genes (GCK and G6PC2) underlying the glucose/glucose-6-phosphate cycle are associated with pancreatic beta cell glucose sensitivity in patients with newly diagnosed type 2 diabetes from the VNDS study (VNDS 11) 151
High levels of homocysteine are associated with small number of traditional cardiovascular risk factors in patients with similar degree of coronary atherosclerosis. 150
Family based association study of the 9p22 chromosomal region in Italian subjects with allergic asthma 150
Studies on sporadic non-syndromic thoracic aortic aneurysms: 1. Deregulation of Jagged/Notch 1 homeostasis and selection of synthetic/secretor phenotype smooth muscle cells 150
Tipizzazione della proteina Gc (Componente Gruppo-specifica) mediante isoelettrofocalizzazione su gel di poliacrilamide con range di pH ristretto 149
Interaction between PON 2 polymorphism Ser-Cys and smoking as a determinant of myocardial infarction risk 149
Associazione di due snp sul cromosoma 9p24.1 con Asma Allergico Pediatrico in famiglie Italiane 148
Delation variant of ACE gene is associated wwith atherosclerotic renal artery stenosis not with coronary artery disease 147
Delation variant of ACE gene is associated with atherosclerotic renal stenosis not with coronary artery disease 147
Detection of a large deletion in the P-selectin (SELP) gene 147
Analisi multilocus su scala genomica in famiglie con asma allergico 147
Circular RNA circ_0001591 Contributes to Melanoma Cell Migration Through AXL and FRA1 Proteins by Targeting miR-20a-3p and miR-34a-5p 146
ApoE epsilon 2/epsilon 3/epsilon 4 polymorphism, ApoC-III/ApoE ratio and metabolic syndrome 146
ORMDL3 haplotype is associated with asthma in an italian familial collection 146
Clinical value of PCR in diagnosis and follow-up of leukaemia and lymphoma: report of the Third Workshop of the Molecular Biology/BMT Study Group 144
Chromosome 7p linkage and GPR154 gene association in Italian families with asthma 143
BIOCHEMICAL AND GENETIC MARKERS OF IRON STATUS AND RISK OF CORONARY ARTERY DISEASE: AN ANGIOGRAPHIC-BASED STUDY. 143
No linkage or association of five polymorphisms in the interleukin-4 receptor α gene with atopic asthma in Italian families 143
Apolipoprotein C-III, metabolic syndrome, and risk of coronary artery disease 143
Impact of insulin receptor substrate-1 genotypes on platelet reactivity and cardiovascular outcomes in patients with type 2 diabetes mellitus and coronary artery disease 143
Role of monogenic diabetes genes on beta cell function in Italian patients with newly diagnosed type 2 diabetes. The Verona Newly Diagnosed Type 2 Diabetes Study (VNDS) 13 143
Totale 17.746
Categoria #
all - tutte 92.458
article - articoli 52.486
book - libri 603
conference - conferenze 38.306
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.063
Totale 184.916


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021965 0 0 0 0 0 192 37 180 156 24 221 155
2021/20221.488 128 319 18 150 90 39 56 101 53 45 130 359
2022/20233.625 252 422 327 678 348 821 37 197 405 28 71 39
2023/20242.432 80 128 147 199 232 378 66 634 22 101 277 168
2024/20254.401 236 355 187 754 179 123 235 190 594 244 393 911
2025/20269.402 902 690 1.381 2.134 3.451 844 0 0 0 0 0 0
Totale 30.009