CATALOGO DEI PRODOTTI DELLA RICERCA

TRABETTI, Elisabetta
 Distribuzione geografica
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Continente #
NA - Nord America 13.716
EU - Europa 11.412
AS - Asia 7.565
SA - Sud America 952
AF - Africa 194
OC - Oceania 22
Continente sconosciuto - Info sul continente non disponibili 9
Totale 33.870
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Nazione #
US - Stati Uniti d'America 13.524
RU - Federazione Russa 4.042
SG - Singapore 3.083
GB - Regno Unito 2.762
CN - Cina 2.256
IT - Italia 969
BR - Brasile 758
SE - Svezia 721
VN - Vietnam 708
DE - Germania 664
FI - Finlandia 624
HK - Hong Kong 562
FR - Francia 559
IE - Irlanda 510
KR - Corea 236
UA - Ucraina 177
IN - India 140
CA - Canada 101
BD - Bangladesh 97
JP - Giappone 94
TR - Turchia 74
BE - Belgio 67
AR - Argentina 65
NL - Olanda 64
PL - Polonia 52
ZA - Sudafrica 52
MX - Messico 50
NG - Nigeria 50
PK - Pakistan 47
ID - Indonesia 46
IQ - Iraq 46
ES - Italia 44
AT - Austria 36
CO - Colombia 24
VE - Venezuela 21
EC - Ecuador 20
AU - Australia 19
UZ - Uzbekistan 19
LT - Lituania 18
MA - Marocco 18
SA - Arabia Saudita 18
CL - Cile 17
PY - Paraguay 16
JO - Giordania 15
CZ - Repubblica Ceca 14
PE - Perù 14
AE - Emirati Arabi Uniti 13
PH - Filippine 13
CR - Costa Rica 12
UY - Uruguay 12
AZ - Azerbaigian 11
EG - Egitto 11
IR - Iran 11
CH - Svizzera 10
NP - Nepal 10
TN - Tunisia 10
BJ - Benin 9
KG - Kirghizistan 9
AL - Albania 8
DZ - Algeria 8
GR - Grecia 8
KE - Kenya 8
HN - Honduras 7
RS - Serbia 7
GE - Georgia 6
JM - Giamaica 6
KZ - Kazakistan 6
TG - Togo 6
BG - Bulgaria 5
EE - Estonia 5
EU - Europa 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
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 33.836
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Città #
Southend 2.359
Ashburn 1.854
Singapore 1.710
Jacksonville 1.494
Dallas 1.433
Moscow 1.325
Chandler 1.295
San Jose 1.026
Woodbridge 906
Ann Arbor 679
Hong Kong 554
Dublin 510
Verona 493
Houston 364
Beijing 353
The Dalles 325
New York 309
Ho Chi Minh City 223
Wilmington 222
Los Angeles 202
Lawrence 199
Princeton 199
Council Bluffs 176
Nanjing 166
Munich 165
Helsinki 163
Hanoi 141
Jinan 141
Boardman 126
Shenyang 109
Buffalo 107
Dong Ket 93
Tokyo 90
Sindelfingen 89
Tianjin 85
Santa Clara 82
São Paulo 81
Turku 81
Hebei 77
Columbus 68
Brussels 64
Zhengzhou 61
Milan 60
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
Chennai 37
Montreal 36
San Francisco 36
Taiyuan 35
Johannesburg 34
Redmond 33
Taizhou 33
Washington 32
Brooklyn 31
Norwalk 31
Phoenix 30
Toronto 29
Nuremberg 28
Vienna 28
Chicago 27
Denver 27
Falkenstein 27
Amsterdam 26
Lanzhou 26
Atlanta 25
Dearborn 25
Rome 25
Da Nang 24
Jakarta 24
Rio de Janeiro 24
Manchester 23
Stockholm 23
Haiphong 22
Brasília 21
Redwood City 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 22.069
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Nome #
A preliminary microRNA analysis of non syndromic thoracic aortic aneurysms 527
Common Variants Associated to Type 2 Diabetes in the Italian Population 492
MALAT1 Expression Is Deregulated in miR-34a Knockout Cell Lines 364
Ability of different flow rates of fractional exaled nitric oxide (FeNO) to discriminate between asthmatic and no asthamatic subject 267
1059G/C polymorphism within the exon 2 of the C-reactive protein gene: relationship to C-reactive protein levels and prognosis in unstable angina. 258
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 257
A genome scan for allergic asthma and related phenotypes in an Italian population sample 241
ALOX5AP gene variants and risk of coronary artery disease: an angiography-based study 239
Detection of allele-specific gene expression on next generation sequencing data 234
A1298C methylentetrahydrofolate reductase mutation and coronary artery disease:relationship with C677T polymorphysm and homocystein/folate metabolism 233
Associazione di polimorfismi del cluster dei geni FADS1 e FADS2 con i livelli di acidi grassi polinsaturi in malattie coronariche 230
Affected sib-pair and mutation analyses of the high affinity IgE receptor beta chain locus in Italian families with atopic asthmatic children 228
Association of a Lymphotoxin alpha gene polymorphism and atopy in Italian families. 228
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 227
A renal genetic risk score (GRS) is associated with kidney dysfunction in people with type 2 diabetes 227
Novel serum paraoxonase activity assays are associated with coronary artery disease 223
Gene Environment Interactions in Respiratory Diseases – Protocol, Standard Operative Procedures and Questionnaires 222
A novel synonymous substitution in the GCK gene causes aberrant splicing in an Italian patient with GCK-MODY phenotype 221
Analisi multilocus per l’identificazione di un genotipo di rischio in Malattie Cardiovascolari 221
CACNA1E variants affect beta cell function in patients with newly diagnosed type 2 diabetes. the Verona newly diagnosed type 2 diabetes study (VNDS) 3. 219
Candidate genes and a genome-wide search in Italian families with atopic asthmatic children 210
Allele frequencies of six highly polymorphic DNA loci in the Croatian population 207
Analisi di 51 polimorfismi in 35 geni dell’infiammazione per la valutazione del rischio di coronaropatia e di infarto del miocardio 207
Studiare la regione HLA negli esomi 207
The Gene-Environment Interactions in Respiratory Diseases (GEIRD) Project 206
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. 204
Combined effect of hemostatic gene polymorphisms and the risk of myocardial infarction in patients with advanced coronary atherosclerosis. 203
The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families 203
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
Frequency distribution of the alleles of several variable number of tandem repeat DNA polymorphisms in the Italian population 201
Renovascular disease: effect of ACE gene deletion polymorphism and endovascular revascularization. 201
Acquired and genetic determinants of homocysteine in atheromatous renel artery stenosis with mild renal insufficiency 200
Analisi di espressione genica in aneurismi non sindromici dell’aorta ascendente 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
Biochemical and genetic markers of iron status and the risk of coronary disease 195
Association of the IL33 gene region with childhood allergic asthma 195
Genetic variability of G6PC2 influences beta cell function and insulin sensitivity in patients with newly diagnosed type 2 diabetes 195
Forensic applications of molecular genetic analysis: an Italian collaborative study on paternity testing by the determination of variable number of tandem repeat DNA polymorphisms 193
Genomic and proteomic investigation into non-syndromic aneurysms of the human ascending aorta. 193
Studies on sporadic non-syndromic thoracic aortic aneurysms: II. Alterations of extra-cellular matrix components and focal adhesion proteins 193
Analyzing BioRad-Illumina Single Cell RNA-Seq data with open source tools 192
Proteomic investigation into nonsyndromic aneurysm of the human ascenging aorta 191
Chromosome 14 linkage analysis and mutation study of two serpin genes in allergic asthmatic families 190
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
Dissection of HLA-C gene region to investigate its association with complex traits 189
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) 188
Bone marrow transplantation monitoring by DNA analysis 187
Advanced cellular models for rare disease study: exploring neural, muscle and skeletal organoids 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. 186
Association of childhood allergic asthma with markers flanking the IL33 gene in Italian families. 186
Hyperhomocysteinemia and Mortality after Coronary Artery Bypass Grafting 185
Association of FcER1A and RAD50 polymorphisms with serum IgE levels, asthma and rhinitis 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
Cromosoma 19 e asma atopica in famiglie Italiane 184
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically proven coronary artery disease. 184
807 C/T polymorphism of the glycoprotein IA gene and pharmacogenetic modulation of platelet response to dual antiplatelet treatment 183
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 182
Hyperhomocysteinemia and mortality after coronary artery by-pass grafing. 182
Reconstruction and functional analysis of altered molecular pathways in human atherosclerotic arteries 182
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 182
Expression profiles of non syndromic thoracic aortic aneurysms 180
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically confirmed coronary artery disease. 179
Hyperhomocysteinemia in relation to total and cardiovascular death after coronary bypass grafting. 178
Single and multilocus analyses for the identification of at risk genotypes in cardiovascular disease 178
Analisi di associazione del cluster genico degli interferoni nella regione 9p21 in famiglie italiane con asma allergico 177
A1298C methylenetetrahydrofolate reductase mutation and coronary artery disease: Relationships with C677T polymorphism and homocysteine/folate metabolism 177
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
Allele and genotype frequencies of eight DNA polymorphisms in the Italian population 176
Interaction between metabolic syndrome and PON 1 polymorphism as a determinant of the risk of coronary artery disease 175
Early detection of bone marrow engraftment by amplification of hypervariable DNA regions 174
Asthma and atopy in Italian families: a genome-wide linkage analysis 174
Studies on sporadic non-syndromic thoracic aortic aneurysms: 1. Deregulation of Jagged/Notch 1 homeostasis and selection of synthetic/secretor phenotype smooth muscle cells 174
Analisi multilocus su scala genomica in famiglie con asma allergico 173
Variants in CACNA1E affect beta cell function and glucose homeostasis in newly diagnosed type 2 diabetes patients 173
Interaction between folate and MTHFR1298 A/C polymorphism on Genomic DNA Methylation 170
Valutazione del software Defuse per la rilevazione di fusioni geniche da esperimenti di Next Generation Sequencing 170
Association analysis of 65 genetic polymorphisms in coronary artery disease patients 169
Association between genetic polymorphisms of the insulin receptor substrate-1 (IRS1) gene and cardiovascular events in type 2 diabetes mellitus patients 169
Detection of a large deletion in the P-selectin (SELP) gene 169
Family based association study of the 9p22 chromosomal region in Italian subjects with allergic asthma 169
Whole Genome microarray and Real-time PcR to detect genes involved in non-syndromic ascending aortic aneurysms 169
Tipizzazione della proteina Gc (Componente Gruppo-specifica) mediante isoelettrofocalizzazione su gel di poliacrilamide con range di pH ristretto 168
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically confirmed coronary artery disease. 168
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) 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
Interaction between PON 2 polymorphism Ser-Cys and smoking as a determinant of myocardial infarction risk 167
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. 167
Impact of insulin receptor substrate-1 genotypes on platelet reactivity and cardiovascular outcomes in patients with type 2 diabetes mellitus and coronary artery disease 167
High levels of homocysteine are associated with small number of traditional cardiovascular risk factors in patients with similar degree of coronary atherosclerosis. 166
Interaction between smoking and PON2 Ser311 Cys polymorphism as a determinant of the risk of myocardial infarction 164
ORMDL3 haplotype is associated with asthma in an italian familial collection 164
ApoE epsilon 2/epsilon 3/epsilon 4 polymorphism, ApoC-III/ApoE ratio and metabolic syndrome 163
Apolipoprotein C-III, metabolic syndrome, and risk of coronary artery disease 162
Associazione di due snp sul cromosoma 9p24.1 con Asma Allergico Pediatrico in famiglie Italiane 162
BIOCHEMICAL AND GENETIC MARKERS OF IRON STATUS AND RISK OF CORONARY ARTERY DISEASE: AN ANGIOGRAPHIC-BASED STUDY. 161
SNPs of the FADS gene cluster are associated with polyunsaturated fatty acids in a cohort of patients with cardiovascular disease 161
Multilocus analysis for the identification of at risk genotype in cardiovascular disease 161
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
Totale 19.919
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Categoria #
all - tutte 104.599
article - articoli 59.972
book - libri 678
conference - conferenze 42.738
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.211
Totale 209.198
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021155 0 0 0 0 0 0 0 0 0 0 0 155
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
2025/202613.388 902 690 1.381 2.134 3.451 904 1.159 612 982 755 152 266
Totale 33.995