CATALOGO DEI PRODOTTI DELLA RICERCA

TRABETTI, Elisabetta
 Distribuzione geografica
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Continente #
NA - Nord America 16.419
EU - Europa 11.621
AS - Asia 7.650
SA - Sud America 1.026
AF - Africa 200
Continente sconosciuto - Info sul continente non disponibili 149
OC - Oceania 22
Totale 37.087
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Nazione #
US - Stati Uniti d'America 15.990
RU - Federazione Russa 4.048
SG - Singapore 3.108
GB - Regno Unito 2.780
CN - Cina 2.266
IT - Italia 1.124
BR - Brasile 822
SE - Svezia 721
VN - Vietnam 708
DE - Germania 668
FI - Finlandia 624
HK - Hong Kong 567
FR - Francia 566
IE - Irlanda 513
KR - Corea 236
CA - Canada 222
UA - Ucraina 178
IN - India 141
BD - Bangladesh 122
JP - Giappone 96
TR - Turchia 74
BE - Belgio 70
NL - Olanda 68
AR - Argentina 65
MX - Messico 54
ZA - Sudafrica 54
PL - Polonia 52
NG - Nigeria 50
ID - Indonesia 49
PK - Pakistan 47
ES - Italia 46
IQ - Iraq 46
AT - Austria 36
CO - Colombia 28
CR - Costa Rica 27
VE - Venezuela 24
EC - Ecuador 22
LT - Lituania 21
AU - Australia 19
GT - Guatemala 19
MA - Marocco 19
SA - Arabia Saudita 19
UZ - Uzbekistan 19
HN - Honduras 18
CL - Cile 17
NI - Nicaragua 17
SV - El Salvador 17
PY - Paraguay 16
JO - Giordania 15
CZ - Repubblica Ceca 14
PE - Perù 14
AE - Emirati Arabi Uniti 13
JM - Giamaica 13
PH - Filippine 13
AZ - Azerbaigian 12
CW - ???statistics.table.value.countryCode.CW??? 12
IR - Iran 12
UY - Uruguay 12
EG - Egitto 11
TN - Tunisia 11
CH - Svizzera 10
NP - Nepal 10
PR - Porto Rico 10
AL - Albania 9
BJ - Benin 9
IL - Israele 9
KG - Kirghizistan 9
DZ - Algeria 8
GP - Guadalupe 8
GR - Grecia 8
KE - Kenya 8
TT - Trinidad e Tobago 8
EE - Estonia 7
KZ - Kazakistan 7
MY - Malesia 7
RS - Serbia 7
GE - Georgia 6
TG - Togo 6
BB - Barbados 5
BG - Bulgaria 5
BO - Bolivia 5
EU - Europa 5
LB - Libano 5
LV - Lettonia 5
MT - Malta 5
PA - Panama 5
RO - Romania 5
SI - Slovenia 5
SN - Senegal 5
ET - Etiopia 4
HR - Croazia 4
KH - Cambogia 4
NO - Norvegia 4
SC - Seychelles 4
XK - ???statistics.table.value.countryCode.XK??? 4
AM - Armenia 3
BH - Bahrain 3
CI - Costa d'Avorio 3
CY - Cipro 3
DK - Danimarca 3
Totale 36.905
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Città #
Ashburn 2.969
Southend 2.359
Singapore 1.718
Dallas 1.504
Jacksonville 1.496
Moscow 1.325
Chandler 1.295
San Jose 1.171
Woodbridge 908
Ann Arbor 679
Hong Kong 559
Dublin 510
Verona 500
Houston 370
Council Bluffs 368
Beijing 359
The Dalles 325
New York 324
Los Angeles 235
Wilmington 225
Ho Chi Minh City 223
Lawrence 200
Princeton 200
Nanjing 167
Munich 165
Helsinki 163
Hanoi 141
Jinan 141
São Paulo 134
Boardman 128
Santa Clara 121
Buffalo 117
Shenyang 109
Dong Ket 93
Tokyo 92
Sindelfingen 89
Tianjin 85
Turku 81
Hebei 77
Columbus 69
Milan 69
Brussels 65
Toronto 62
Zhengzhou 61
Nanchang 57
Lancaster 54
Orem 54
Seattle 54
Hangzhou 53
Redondo Beach 51
Rome 51
Jiaxing 50
Changsha 49
Warsaw 48
London 45
Frankfurt am Main 44
Guangzhou 44
Montreal 44
Abuja 43
Haikou 43
Ningbo 42
Phoenix 42
Seoul 40
San Francisco 38
Chennai 37
Washington 36
Chicago 35
Johannesburg 35
Taiyuan 35
Brooklyn 34
Atlanta 33
Denver 33
Las Vegas 33
Redmond 33
Taizhou 33
Norwalk 31
Amsterdam 28
Nuremberg 28
Vienna 28
Falkenstein 27
Lanzhou 26
Dearborn 25
Manchester 25
Rio de Janeiro 25
Da Nang 24
Jakarta 24
Boston 23
Stockholm 23
Haiphong 22
Brasília 21
Redwood City 21
Baghdad 20
Falls Church 20
Fuzhou 20
Kent 20
Philadelphia 20
Poplar 20
Shanghai 20
Fairfield 19
San Diego 18
Totale 23.952
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Nome #
A preliminary microRNA analysis of non syndromic thoracic aortic aneurysms 537
Common Variants Associated to Type 2 Diabetes in the Italian Population 508
MALAT1 Expression Is Deregulated in miR-34a Knockout Cell Lines 381
Ability of different flow rates of fractional exaled nitric oxide (FeNO) to discriminate between asthmatic and no asthamatic subject 304
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 280
1059G/C polymorphism within the exon 2 of the C-reactive protein gene: relationship to C-reactive protein levels and prognosis in unstable angina. 265
A genome scan for allergic asthma and related phenotypes in an Italian population sample 265
Associazione di polimorfismi del cluster dei geni FADS1 e FADS2 con i livelli di acidi grassi polinsaturi in malattie coronariche 258
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 254
ALOX5AP gene variants and risk of coronary artery disease: an angiography-based study 250
Gene Environment Interactions in Respiratory Diseases – Protocol, Standard Operative Procedures and Questionnaires 245
Analisi multilocus per l’identificazione di un genotipo di rischio in Malattie Cardiovascolari 244
Detection of allele-specific gene expression on next generation sequencing data 243
A renal genetic risk score (GRS) is associated with kidney dysfunction in people with type 2 diabetes 242
A1298C methylentetrahydrofolate reductase mutation and coronary artery disease:relationship with C677T polymorphysm and homocystein/folate metabolism 241
Affected sib-pair and mutation analyses of the high affinity IgE receptor beta chain locus in Italian families with atopic asthmatic children 241
Association of a Lymphotoxin alpha gene polymorphism and atopy in Italian families. 236
Novel serum paraoxonase activity assays are associated with coronary artery disease 234
A novel synonymous substitution in the GCK gene causes aberrant splicing in an Italian patient with GCK-MODY phenotype 234
CACNA1E variants affect beta cell function in patients with newly diagnosed type 2 diabetes. the Verona newly diagnosed type 2 diabetes study (VNDS) 3. 233
Studiare la regione HLA negli esomi 229
Analisi di 51 polimorfismi in 35 geni dell’infiammazione per la valutazione del rischio di coronaropatia e di infarto del miocardio 228
Analisi di espressione genica in aneurismi non sindromici dell’aorta ascendente 227
Genomic and proteomic investigation into non-syndromic aneurysms of the human ascending aorta. 224
Candidate genes and a genome-wide search in Italian families with atopic asthmatic children 223
Genetic variability of G6PC2 influences beta cell function and insulin sensitivity in patients with newly diagnosed type 2 diabetes 223
Allele frequencies of six highly polymorphic DNA loci in the Croatian population 220
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. 220
Biochemical and genetic markers of iron status and the risk of coronary disease 217
The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families 217
Association of the IL33 gene region with childhood allergic asthma 216
Analyzing BioRad-Illumina Single Cell RNA-Seq data with open source tools 216
Proteomic investigation into nonsyndromic aneurysm of the human ascenging aorta 215
The Gene-Environment Interactions in Respiratory Diseases (GEIRD) Project 214
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. 214
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 214
Renovascular disease: effect of ACE gene deletion polymorphism and endovascular revascularization. 213
Frequency distribution of the alleles of several variable number of tandem repeat DNA polymorphisms in the Italian population 212
Combined effect of hemostatic gene polymorphisms and the risk of myocardial infarction in patients with advanced coronary atherosclerosis. 212
Potential role of MTNR1B locus in regulating beta cell function and glucose levels in patients with newly diagnosed type 2 diabetes 212
Impact of insulin receptor substrate-1 genotypes on platelet reactivity and cardiovascular outcomes in patients with type 2 diabetes mellitus and coronary artery disease 210
Forensic applications of molecular genetic analysis: an Italian collaborative study on paternity testing by the determination of variable number of tandem repeat DNA polymorphisms 208
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) 207
Studies on sporadic non-syndromic thoracic aortic aneurysms: II. Alterations of extra-cellular matrix components and focal adhesion proteins 207
Association of FcER1A and RAD50 polymorphisms with serum IgE levels, asthma and rhinitis 206
Linkage to atopy on chromosome 19 in north-eastern Italian families with allergic asthma 205
ApoC-III gene polymorphisms and risk of coronary artery disease 205
Acquired and genetic determinants of homocysteine in atheromatous renel artery stenosis with mild renal insufficiency 204
Cromosoma 19 e asma atopica in famiglie Italiane 203
Family based association study of the 9p22 chromosomal region in Italian subjects with allergic asthma 203
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically proven coronary artery disease. 201
Dissection of HLA-C gene region to investigate its association with complex traits 201
Hyperhomocysteinemia in relation to total and cardiovascular death after coronary bypass grafting. 200
Association of childhood allergic asthma with markers flanking the IL33 gene in Italian families. 199
Variants in CACNA1E affect beta cell function and glucose homeostasis in newly diagnosed type 2 diabetes patients 199
Reply to Novelli 198
Chromosome 14 linkage analysis and mutation study of two serpin genes in allergic asthmatic families 198
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 197
Hyperhomocysteinemia and Mortality after Coronary Artery Bypass Grafting 196
Expression profiles of non syndromic thoracic aortic aneurysms 196
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically confirmed coronary artery disease. 196
Bone marrow transplantation monitoring by DNA analysis 195
Advanced cellular models for rare disease study: exploring neural, muscle and skeletal organoids 194
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 194
Analisi di associazione del cluster genico degli interferoni nella regione 9p21 in famiglie italiane con asma allergico 194
Tipizzazione della proteina Gc (Componente Gruppo-specifica) mediante isoelettrofocalizzazione su gel di poliacrilamide con range di pH ristretto 193
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 193
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. 193
807 C/T polymorphism of the glycoprotein IA gene and pharmacogenetic modulation of platelet response to dual antiplatelet treatment 192
Analisi multilocus su scala genomica in famiglie con asma allergico 192
ORMDL3 haplotype is associated with asthma in an italian familial collection 192
Reconstruction and functional analysis of altered molecular pathways in human atherosclerotic arteries 191
Single and multilocus analyses for the identification of at risk genotypes in cardiovascular disease 191
Interaction between folate and MTHFR1298 A/C polymorphism on Genomic DNA Methylation 189
Association between genetic polymorphisms of the insulin receptor substrate-1 (IRS1) gene and cardiovascular events in type 2 diabetes mellitus patients 189
Hyperhomocysteinemia and mortality after coronary artery by-pass grafing. 188
Whole Genome microarray and Real-time PcR to detect genes involved in non-syndromic ascending aortic aneurysms 188
Studies on sporadic non-syndromic thoracic aortic aneurysms: 1. Deregulation of Jagged/Notch 1 homeostasis and selection of synthetic/secretor phenotype smooth muscle cells 188
Association analysis of 65 genetic polymorphisms in coronary artery disease patients 186
High levels of homocysteine are associated with small number of traditional cardiovascular risk factors in patients with similar degree of coronary atherosclerosis. 186
A1298C methylenetetrahydrofolate reductase mutation and coronary artery disease: Relationships with C677T polymorphism and homocysteine/folate metabolism 185
Interaction between metabolic syndrome and PON 1 polymorphism as a determinant of the risk of coronary artery disease 184
Early detection of bone marrow engraftment by amplification of hypervariable DNA regions 184
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. 184
Asthma and atopy in Italian families: a genome-wide linkage analysis 183
Interaction between PON 2 polymorphism Ser-Cys and smoking as a determinant of myocardial infarction risk 182
Detection of a large deletion in the P-selectin (SELP) gene 182
Delation variant of ACE gene is associated with atherosclerotic renal stenosis not with coronary artery disease 181
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) 181
Expression profile study of atherosclerosis: microarray analysis in human coronaries with atheromas 180
Allele and genotype frequencies of eight DNA polymorphisms in the Italian population 180
Associazione di due snp sul cromosoma 9p24.1 con Asma Allergico Pediatrico in famiglie Italiane 180
Interaction between smoking and PON2 Ser311 Cys polymorphism as a determinant of the risk of myocardial infarction 179
Valutazione del software Defuse per la rilevazione di fusioni geniche da esperimenti di Next Generation Sequencing 179
Circular RNA circ_0001591 Contributes to Melanoma Cell Migration Through AXL and FRA1 Proteins by Targeting miR-20a-3p and miR-34a-5p 178
Multilocus analysis for the identification of at risk genotype in cardiovascular disease 178
Carriership of apolipoprotein CIII –455C gene variant strongly increases the coronary artery disease risk associated with the metabolic sindrome. 177
Apolipoprotein C-III, metabolic syndrome, and risk of coronary artery disease 176
Omocisteina, polimorfismi del gene MTHFR e rischio cardiocerebrovascolare 176
PPARgamma Pro12Ala and ADAMTS9 rs4607103 are determinants of insulin sensitivity in both non-diabetic and type 2 diabetic Italian subjects 175
Totale 21.532
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Categoria #
all - tutte 116.490
article - articoli 66.910
book - libri 754
conference - conferenze 47.465
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.361
Totale 232.980
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.023 0 0 0 150 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
2025/202613.435 902 690 1.381 2.134 3.451 904 1.159 612 982 755 152 313
2026/20273.045 146 320 698 1.881 0 0 0 0 0 0 0 0
Totale 37.087