CATALOGO DEI PRODOTTI DELLA RICERCA

TRABETTI, Elisabetta
 Distribuzione geografica
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Continente #
NA - Nord America 13.326
EU - Europa 11.386
AS - Asia 7.515
SA - Sud America 945
AF - Africa 194
OC - Oceania 21
Continente sconosciuto - Info sul continente non disponibili 9
Totale 33.396
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Nazione #
US - Stati Uniti d'America 13.151
RU - Federazione Russa 4.042
SG - Singapore 3.075
GB - Regno Unito 2.762
CN - Cina 2.252
IT - Italia 946
BR - Brasile 755
SE - Svezia 721
VN - Vietnam 708
DE - Germania 664
FI - Finlandia 624
FR - Francia 559
HK - Hong Kong 559
IE - Irlanda 510
KR - Corea 236
UA - Ucraina 177
IN - India 139
JP - Giappone 94
CA - Canada 93
TR - Turchia 74
BE - Belgio 67
AR - Argentina 65
BD - Bangladesh 64
NL - Olanda 62
PL - Polonia 52
ZA - Sudafrica 52
NG - Nigeria 50
MX - Messico 49
ID - Indonesia 46
IQ - Iraq 46
PK - Pakistan 46
ES - Italia 43
AT - Austria 36
CO - Colombia 21
VE - Venezuela 21
EC - Ecuador 20
UZ - Uzbekistan 19
AU - Australia 18
LT - Lituania 18
MA - Marocco 18
SA - Arabia Saudita 18
CL - Cile 16
PY - Paraguay 16
JO - Giordania 15
CZ - Repubblica Ceca 14
PE - Perù 14
AE - Emirati Arabi Uniti 13
PH - Filippine 13
UY - Uruguay 12
AZ - Azerbaigian 11
EG - Egitto 11
IR - Iran 11
CH - Svizzera 10
NP - Nepal 10
TN - Tunisia 10
BJ - Benin 9
CR - Costa Rica 9
KG - Kirghizistan 9
AL - Albania 8
DZ - Algeria 8
GR - Grecia 8
KE - Kenya 8
RS - Serbia 7
GE - Georgia 6
KZ - Kazakistan 6
TG - Togo 6
BG - Bulgaria 5
EE - Estonia 5
EU - Europa 5
HN - Honduras 5
IL - Israele 5
LB - Libano 5
LV - Lettonia 5
MT - Malta 5
MY - Malesia 5
PA - Panama 5
RO - Romania 5
SI - Slovenia 5
SN - Senegal 5
BO - Bolivia 4
ET - Etiopia 4
HR - Croazia 4
JM - Giamaica 4
KH - Cambogia 4
NO - Norvegia 4
XK - ???statistics.table.value.countryCode.XK??? 4
BH - Bahrain 3
CI - Costa d'Avorio 3
CY - Cipro 3
DK - Danimarca 3
HU - Ungheria 3
LA - Repubblica Popolare Democratica del Laos 3
LK - Sri Lanka 3
LU - Lussemburgo 3
NI - Nicaragua 3
NZ - Nuova Zelanda 3
BA - Bosnia-Erzegovina 2
BN - Brunei Darussalam 2
MK - Macedonia 2
OM - Oman 2
Totale 33.363
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Città #
Southend 2.359
Ashburn 1.823
Singapore 1.707
Jacksonville 1.494
Dallas 1.427
Moscow 1.325
Chandler 1.295
San Jose 958
Woodbridge 906
Ann Arbor 679
Hong Kong 551
Dublin 510
Verona 491
Houston 364
Beijing 352
The Dalles 325
New York 294
Ho Chi Minh City 223
Wilmington 222
Lawrence 199
Princeton 199
Los Angeles 193
Nanjing 166
Munich 165
Helsinki 163
Hanoi 141
Jinan 141
Boardman 126
Shenyang 109
Buffalo 103
Dong Ket 93
Tokyo 90
Sindelfingen 89
Tianjin 85
São Paulo 81
Turku 81
Hebei 77
Santa Clara 76
Columbus 68
Brussels 64
Zhengzhou 61
Milan 59
Nanchang 57
Hangzhou 53
Lancaster 52
Orem 52
Redondo Beach 51
Jiaxing 50
Changsha 49
Seattle 49
Warsaw 48
Guangzhou 44
London 44
Abuja 43
Frankfurt am Main 43
Haikou 43
Ningbo 42
Seoul 40
Council Bluffs 39
Chennai 37
Montreal 35
Taiyuan 35
Johannesburg 34
San Francisco 34
Redmond 33
Taizhou 33
Washington 32
Norwalk 31
Phoenix 29
Brooklyn 28
Nuremberg 28
Toronto 28
Vienna 28
Falkenstein 27
Amsterdam 26
Chicago 26
Denver 26
Lanzhou 26
Dearborn 25
Da Nang 24
Jakarta 24
Rio de Janeiro 24
Manchester 23
Stockholm 23
Atlanta 22
Haiphong 22
Brasília 21
Redwood City 21
Rome 21
Baghdad 20
Falls Church 20
Fuzhou 20
Kent 20
Poplar 20
Fairfield 19
Shanghai 19
Boston 18
Tashkent 18
Mianwali 17
Düsseldorf 16
Totale 21.766
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Nome #
A preliminary microRNA analysis of non syndromic thoracic aortic aneurysms 526
Common Variants Associated to Type 2 Diabetes in the Italian Population 491
MALAT1 Expression Is Deregulated in miR-34a Knockout Cell Lines 361
Ability of different flow rates of fractional exaled nitric oxide (FeNO) to discriminate between asthmatic and no asthamatic subject 265
1059G/C polymorphism within the exon 2 of the C-reactive protein gene: relationship to C-reactive protein levels and prognosis in unstable angina. 256
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 256
A genome scan for allergic asthma and related phenotypes in an Italian population sample 238
ALOX5AP gene variants and risk of coronary artery disease: an angiography-based study 234
A1298C methylentetrahydrofolate reductase mutation and coronary artery disease:relationship with C677T polymorphysm and homocystein/folate metabolism 231
Detection of allele-specific gene expression on next generation sequencing data 231
Associazione di polimorfismi del cluster dei geni FADS1 e FADS2 con i livelli di acidi grassi polinsaturi in malattie coronariche 229
Association of a Lymphotoxin alpha gene polymorphism and atopy in Italian families. 227
Affected sib-pair and mutation analyses of the high affinity IgE receptor beta chain locus in Italian families with atopic asthmatic children 225
A renal genetic risk score (GRS) is associated with kidney dysfunction in people with type 2 diabetes 225
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 222
Analisi multilocus per l’identificazione di un genotipo di rischio in Malattie Cardiovascolari 221
A novel synonymous substitution in the GCK gene causes aberrant splicing in an Italian patient with GCK-MODY phenotype 219
CACNA1E variants affect beta cell function in patients with newly diagnosed type 2 diabetes. the Verona newly diagnosed type 2 diabetes study (VNDS) 3. 218
Novel serum paraoxonase activity assays are associated with coronary artery disease 217
Gene Environment Interactions in Respiratory Diseases – Protocol, Standard Operative Procedures and Questionnaires 214
Candidate genes and a genome-wide search in Italian families with atopic asthmatic children 208
Analisi di 51 polimorfismi in 35 geni dell’infiammazione per la valutazione del rischio di coronaropatia e di infarto del miocardio 206
The Gene-Environment Interactions in Respiratory Diseases (GEIRD) Project 204
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. 203
Renovascular disease: effect of ACE gene deletion polymorphism and endovascular revascularization. 201
The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families 201
Frequency distribution of the alleles of several variable number of tandem repeat DNA polymorphisms in the Italian population 200
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. 200
Combined effect of hemostatic gene polymorphisms and the risk of myocardial infarction in patients with advanced coronary atherosclerosis. 199
Studiare la regione HLA negli esomi 199
Linkage to atopy on chromosome 19 in north-eastern Italian families with allergic asthma 197
ApoC-III gene polymorphisms and risk of coronary artery disease 196
Acquired and genetic determinants of homocysteine in atheromatous renel artery stenosis with mild renal insufficiency 196
Analisi di espressione genica in aneurismi non sindromici dell’aorta ascendente 196
Biochemical and genetic markers of iron status and the risk of coronary disease 195
Association of the IL33 gene region with childhood allergic asthma 194
Allele frequencies of six highly polymorphic DNA loci in the Croatian population 193
Forensic applications of molecular genetic analysis: an Italian collaborative study on paternity testing by the determination of variable number of tandem repeat DNA polymorphisms 192
Genomic and proteomic investigation into non-syndromic aneurysms of the human ascending aorta. 192
Genetic variability of G6PC2 influences beta cell function and insulin sensitivity in patients with newly diagnosed type 2 diabetes 191
Potential role of MTNR1B locus in regulating beta cell function and glucose levels in patients with newly diagnosed type 2 diabetes 190
Reply to Novelli 189
Proteomic investigation into nonsyndromic aneurysm of the human ascenging aorta 189
Studies on sporadic non-syndromic thoracic aortic aneurysms: II. Alterations of extra-cellular matrix components and focal adhesion proteins 189
Chromosome 14 linkage analysis and mutation study of two serpin genes in allergic asthmatic families 187
Bone marrow transplantation monitoring by DNA analysis 186
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) 186
Analyzing BioRad-Illumina Single Cell RNA-Seq data with open source tools 186
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. 185
Association of childhood allergic asthma with markers flanking the IL33 gene in Italian families. 185
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 185
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically proven coronary artery disease. 184
Dissection of HLA-C gene region to investigate its association with complex traits 184
Hyperhomocysteinemia and Mortality after Coronary Artery Bypass Grafting 183
807 C/T polymorphism of the glycoprotein IA gene and pharmacogenetic modulation of platelet response to dual antiplatelet treatment 183
Cromosoma 19 e asma atopica in famiglie Italiane 182
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 180
Hyperhomocysteinemia and mortality after coronary artery by-pass grafing. 180
Reconstruction and functional analysis of altered molecular pathways in human atherosclerotic arteries 179
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 179
Association of FcER1A and RAD50 polymorphisms with serum IgE levels, asthma and rhinitis 179
Advanced cellular models for rare disease study: exploring neural, muscle and skeletal organoids 178
Single and multilocus analyses for the identification of at risk genotypes in cardiovascular disease 178
Hyperhomocysteinemia in relation to total and cardiovascular death after coronary bypass grafting. 176
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 176
Expression profiles of non syndromic thoracic aortic aneurysms 176
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically confirmed coronary artery disease. 176
Allele and genotype frequencies of eight DNA polymorphisms in the Italian population 174
Analisi di associazione del cluster genico degli interferoni nella regione 9p21 in famiglie italiane con asma allergico 174
A1298C methylenetetrahydrofolate reductase mutation and coronary artery disease: Relationships with C677T polymorphism and homocysteine/folate metabolism 174
Interaction between metabolic syndrome and PON 1 polymorphism as a determinant of the risk of coronary artery disease 173
Asthma and atopy in Italian families: a genome-wide linkage analysis 173
Variants in CACNA1E affect beta cell function and glucose homeostasis in newly diagnosed type 2 diabetes patients 173
Studies on sporadic non-syndromic thoracic aortic aneurysms: 1. Deregulation of Jagged/Notch 1 homeostasis and selection of synthetic/secretor phenotype smooth muscle cells 172
Analisi multilocus su scala genomica in famiglie con asma allergico 171
Interaction between folate and MTHFR1298 A/C polymorphism on Genomic DNA Methylation 170
Association analysis of 65 genetic polymorphisms in coronary artery disease patients 169
Family based association study of the 9p22 chromosomal region in Italian subjects with allergic asthma 169
Tipizzazione della proteina Gc (Componente Gruppo-specifica) mediante isoelettrofocalizzazione su gel di poliacrilamide con range di pH ristretto 168
Valutazione del software Defuse per la rilevazione di fusioni geniche da esperimenti di Next Generation Sequencing 168
Whole Genome microarray and Real-time PcR to detect genes involved in non-syndromic ascending aortic aneurysms 168
Circular RNA circ_0001591 Contributes to Melanoma Cell Migration Through AXL and FRA1 Proteins by Targeting miR-20a-3p and miR-34a-5p 167
Association between genetic polymorphisms of the insulin receptor substrate-1 (IRS1) gene and cardiovascular events in type 2 diabetes mellitus patients 167
Interaction between PON 2 polymorphism Ser-Cys and smoking as a determinant of myocardial infarction risk 166
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically confirmed coronary artery disease. 166
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) 166
Detection of a large deletion in the P-selectin (SELP) gene 165
Interaction between smoking and PON2 Ser311 Cys polymorphism as a determinant of the risk of myocardial infarction 164
High levels of homocysteine are associated with small number of traditional cardiovascular risk factors in patients with similar degree of coronary atherosclerosis. 164
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. 164
ORMDL3 haplotype is associated with asthma in an italian familial collection 163
Associazione di due snp sul cromosoma 9p24.1 con Asma Allergico Pediatrico in famiglie Italiane 162
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 160
Apolipoprotein C-III, metabolic syndrome, and risk of coronary artery disease 160
Association of the FADS gene cluster with polyunsaturated fatty acids in serum and erythrocytes 160
Chromosome 7p linkage and GPR154 gene association in Italian families with asthma 159
ApoE epsilon 2/epsilon 3/epsilon 4 polymorphism, ApoC-III/ApoE ratio and metabolic syndrome 159
Delation variant of ACE gene is associated with atherosclerotic renal stenosis not with coronary artery disease 158
SNPs of the FADS gene cluster are associated with polyunsaturated fatty acids in a cohort of patients with cardiovascular disease 158
Homocysteine and atheromatous renal artery stenosis 157
Totale 19.680
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Categoria #
all - tutte 99.018
article - articoli 56.462
book - libri 642
conference - conferenze 40.787
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.127
Totale 198.036
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021400 0 0 0 0 0 0 0 0 0 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
2025/202612.912 902 690 1.381 2.134 3.451 904 1.159 612 982 697 0 0
Totale 33.519