CATALOGO DEI PRODOTTI DELLA RICERCA

TRABETTI, Elisabetta
 Distribuzione geografica
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Continente #
NA - Nord America 14.109
EU - Europa 11.448
AS - Asia 7.601
SA - Sud America 959
AF - Africa 197
Continente sconosciuto - Info sul continente non disponibili 135
OC - Oceania 22
Totale 34.471
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Nazione #
US - Stati Uniti d'America 13.895
RU - Federazione Russa 4.042
SG - Singapore 3.097
GB - Regno Unito 2.763
CN - Cina 2.266
IT - Italia 996
BR - Brasile 764
SE - Svezia 721
VN - Vietnam 708
DE - Germania 664
FI - Finlandia 624
HK - Hong Kong 566
FR - Francia 561
IE - Irlanda 511
KR - Corea 236
UA - Ucraina 177
IN - India 140
CA - Canada 108
BD - Bangladesh 103
JP - Giappone 94
TR - Turchia 74
BE - Belgio 69
AR - Argentina 65
NL - Olanda 65
MX - Messico 52
PL - Polonia 52
ZA - Sudafrica 52
NG - Nigeria 50
ID - Indonesia 47
PK - Pakistan 47
ES - Italia 46
IQ - Iraq 46
AT - Austria 36
CO - Colombia 24
EC - Ecuador 21
VE - Venezuela 21
AU - Australia 19
MA - Marocco 19
UZ - Uzbekistan 19
LT - Lituania 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
CR - Costa Rica 13
PH - Filippine 13
IR - Iran 12
UY - Uruguay 12
AZ - Azerbaigian 11
EG - Egitto 11
TN - Tunisia 11
CH - Svizzera 10
NP - Nepal 10
BJ - Benin 9
JM - Giamaica 9
KG - Kirghizistan 9
AL - Albania 8
DZ - Algeria 8
GR - Grecia 8
HN - Honduras 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
GT - Guatemala 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
SC - Seychelles 3
TT - Trinidad e Tobago 3
BA - Bosnia-Erzegovina 2
Totale 34.307
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Città #
Southend 2.359
Ashburn 1.877
Singapore 1.715
Jacksonville 1.495
Dallas 1.435
Moscow 1.325
Chandler 1.295
San Jose 1.032
Woodbridge 907
Ann Arbor 679
Hong Kong 558
Dublin 510
Verona 495
Council Bluffs 365
Houston 364
Beijing 359
The Dalles 325
New York 313
Wilmington 225
Ho Chi Minh City 223
Los Angeles 215
Lawrence 199
Princeton 199
Nanjing 167
Munich 165
Helsinki 163
Hanoi 141
Jinan 141
Boardman 126
Buffalo 111
Shenyang 109
Santa Clara 94
Dong Ket 93
Tokyo 90
Sindelfingen 89
Tianjin 85
São Paulo 81
Turku 81
Hebei 77
Columbus 68
Brussels 65
Zhengzhou 61
Milan 60
Nanchang 57
Hangzhou 53
Lancaster 53
Orem 52
Redondo Beach 51
Seattle 51
Jiaxing 50
Changsha 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
Phoenix 34
Rome 34
Redmond 33
Taizhou 33
Washington 33
Brooklyn 31
Norwalk 31
Toronto 30
Chicago 29
Denver 28
Nuremberg 28
Vienna 28
Atlanta 27
Falkenstein 27
Amsterdam 26
Lanzhou 26
Dearborn 25
Rio de Janeiro 25
Da Nang 24
Jakarta 24
Manchester 23
Stockholm 23
Haiphong 22
Boston 21
Brasília 21
Redwood City 21
Baghdad 20
Falls Church 20
Fuzhou 20
Kent 20
Poplar 20
Shanghai 20
Fairfield 19
Tashkent 18
Mianwali 17
Düsseldorf 16
Totale 22.374
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Nome #
A preliminary microRNA analysis of non syndromic thoracic aortic aneurysms 530
Common Variants Associated to Type 2 Diabetes in the Italian Population 497
MALAT1 Expression Is Deregulated in miR-34a Knockout Cell Lines 368
Ability of different flow rates of fractional exaled nitric oxide (FeNO) to discriminate between asthmatic and no asthamatic subject 272
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 261
1059G/C polymorphism within the exon 2 of the C-reactive protein gene: relationship to C-reactive protein levels and prognosis in unstable angina. 260
A genome scan for allergic asthma and related phenotypes in an Italian population sample 243
ALOX5AP gene variants and risk of coronary artery disease: an angiography-based study 240
A1298C methylentetrahydrofolate reductase mutation and coronary artery disease:relationship with C677T polymorphysm and homocystein/folate metabolism 236
Detection of allele-specific gene expression on next generation sequencing data 235
Associazione di polimorfismi del cluster dei geni FADS1 e FADS2 con i livelli di acidi grassi polinsaturi in malattie coronariche 232
A renal genetic risk score (GRS) is associated with kidney dysfunction in people with type 2 diabetes 232
Affected sib-pair and mutation analyses of the high affinity IgE receptor beta chain locus in Italian families with atopic asthmatic children 230
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 230
Association of a Lymphotoxin alpha gene polymorphism and atopy in Italian families. 229
Gene Environment Interactions in Respiratory Diseases – Protocol, Standard Operative Procedures and Questionnaires 227
Novel serum paraoxonase activity assays are associated with coronary artery disease 226
A novel synonymous substitution in the GCK gene causes aberrant splicing in an Italian patient with GCK-MODY phenotype 224
Analisi multilocus per l’identificazione di un genotipo di rischio in Malattie Cardiovascolari 223
CACNA1E variants affect beta cell function in patients with newly diagnosed type 2 diabetes. the Verona newly diagnosed type 2 diabetes study (VNDS) 3. 222
Candidate genes and a genome-wide search in Italian families with atopic asthmatic children 212
Analisi di 51 polimorfismi in 35 geni dell’infiammazione per la valutazione del rischio di coronaropatia e di infarto del miocardio 211
Allele frequencies of six highly polymorphic DNA loci in the Croatian population 210
Studiare la regione HLA negli esomi 210
The Gene-Environment Interactions in Respiratory Diseases (GEIRD) Project 207
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. 207
The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families 206
Combined effect of hemostatic gene polymorphisms and the risk of myocardial infarction in patients with advanced coronary atherosclerosis. 205
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
Analisi di espressione genica in aneurismi non sindromici dell’aorta ascendente 203
Impact of insulin receptor substrate-1 genotypes on platelet reactivity and cardiovascular outcomes in patients with type 2 diabetes mellitus and coronary artery disease 203
Frequency distribution of the alleles of several variable number of tandem repeat DNA polymorphisms in the Italian population 202
Forensic applications of molecular genetic analysis: an Italian collaborative study on paternity testing by the determination of variable number of tandem repeat DNA polymorphisms 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 201
Association of the IL33 gene region with childhood allergic asthma 199
Linkage to atopy on chromosome 19 in north-eastern Italian families with allergic asthma 198
Biochemical and genetic markers of iron status and the risk of coronary disease 197
Studies on sporadic non-syndromic thoracic aortic aneurysms: II. Alterations of extra-cellular matrix components and focal adhesion proteins 197
ApoC-III gene polymorphisms and risk of coronary artery disease 196
Genetic variability of G6PC2 influences beta cell function and insulin sensitivity in patients with newly diagnosed type 2 diabetes 196
Genomic and proteomic investigation into non-syndromic aneurysms of the human ascending aorta. 194
Analyzing BioRad-Illumina Single Cell RNA-Seq data with open source tools 194
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) 192
Proteomic investigation into nonsyndromic aneurysm of the human ascenging aorta 192
Reply to Novelli 191
Chromosome 14 linkage analysis and mutation study of two serpin genes in allergic asthmatic families 191
Potential role of MTNR1B locus in regulating beta cell function and glucose levels in patients with newly diagnosed type 2 diabetes 191
Dissection of HLA-C gene region to investigate its association with complex traits 191
Association of childhood allergic asthma with markers flanking the IL33 gene in Italian families. 190
Advanced cellular models for rare disease study: exploring neural, muscle and skeletal organoids 188
Bone marrow transplantation monitoring by DNA analysis 188
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. 187
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically proven coronary artery disease. 187
Association of FcER1A and RAD50 polymorphisms with serum IgE levels, asthma and rhinitis 187
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 187
Hyperhomocysteinemia and Mortality after Coronary Artery Bypass Grafting 186
Cromosoma 19 e asma atopica in famiglie Italiane 186
807 C/T polymorphism of the glycoprotein IA gene and pharmacogenetic modulation of platelet response to dual antiplatelet treatment 185
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 184
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 183
Hyperhomocysteinemia and mortality after coronary artery by-pass grafing. 183
Reconstruction and functional analysis of altered molecular pathways in human atherosclerotic arteries 183
Expression profiles of non syndromic thoracic aortic aneurysms 182
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically confirmed coronary artery disease. 181
Single and multilocus analyses for the identification of at risk genotypes in cardiovascular disease 180
Hyperhomocysteinemia in relation to total and cardiovascular death after coronary bypass grafting. 179
Analisi di associazione del cluster genico degli interferoni nella regione 9p21 in famiglie italiane con asma allergico 179
A1298C methylenetetrahydrofolate reductase mutation and coronary artery disease: Relationships with C677T polymorphism and homocysteine/folate metabolism 179
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 178
Asthma and atopy in Italian families: a genome-wide linkage analysis 177
Interaction between metabolic syndrome and PON 1 polymorphism as a determinant of the risk of coronary artery disease 176
Early detection of bone marrow engraftment by amplification of hypervariable DNA regions 176
Allele and genotype frequencies of eight DNA polymorphisms in the Italian population 176
Studies on sporadic non-syndromic thoracic aortic aneurysms: 1. Deregulation of Jagged/Notch 1 homeostasis and selection of synthetic/secretor phenotype smooth muscle cells 176
Interaction between folate and MTHFR1298 A/C polymorphism on Genomic DNA Methylation 174
Analisi multilocus su scala genomica in famiglie con asma allergico 174
Variants in CACNA1E affect beta cell function and glucose homeostasis in newly diagnosed type 2 diabetes patients 174
Family based association study of the 9p22 chromosomal region in Italian subjects with allergic asthma 172
Valutazione del software Defuse per la rilevazione di fusioni geniche da esperimenti di Next Generation Sequencing 172
Tipizzazione della proteina Gc (Componente Gruppo-specifica) mediante isoelettrofocalizzazione su gel di poliacrilamide con range di pH ristretto 171
Association analysis of 65 genetic polymorphisms in coronary artery disease patients 171
Circular RNA circ_0001591 Contributes to Melanoma Cell Migration Through AXL and FRA1 Proteins by Targeting miR-20a-3p and miR-34a-5p 170
Association between genetic polymorphisms of the insulin receptor substrate-1 (IRS1) gene and cardiovascular events in type 2 diabetes mellitus patients 170
Detection of a large deletion in the P-selectin (SELP) gene 170
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically confirmed coronary artery disease. 170
Whole Genome microarray and Real-time PcR to detect genes involved in non-syndromic ascending aortic aneurysms 170
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. 169
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) 169
Interaction between PON 2 polymorphism Ser-Cys and smoking as a determinant of myocardial infarction risk 168
High levels of homocysteine are associated with small number of traditional cardiovascular risk factors in patients with similar degree of coronary atherosclerosis. 168
Interaction between smoking and PON2 Ser311 Cys polymorphism as a determinant of the risk of myocardial infarction 166
ORMDL3 haplotype is associated with asthma in an italian familial collection 166
Associazione di due snp sul cromosoma 9p24.1 con Asma Allergico Pediatrico in famiglie Italiane 165
ApoE epsilon 2/epsilon 3/epsilon 4 polymorphism, ApoC-III/ApoE ratio and metabolic syndrome 164
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 162
BIOCHEMICAL AND GENETIC MARKERS OF IRON STATUS AND RISK OF CORONARY ARTERY DISEASE: AN ANGIOGRAPHIC-BASED STUDY. 162
Apolipoprotein C-III, metabolic syndrome, and risk of coronary artery disease 162
SNPs of the FADS gene cluster are associated with polyunsaturated fatty acids in a cohort of patients with cardiovascular disease 162
Multilocus analysis for the identification of at risk genotype in cardiovascular disease 162
Totale 20.165
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Categoria #
all - tutte 109.230
article - articoli 62.918
book - libri 703
conference - conferenze 44.354
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.255
Totale 218.460
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.360 0 319 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
2025/202613.435 902 690 1.381 2.134 3.451 904 1.159 612 982 755 152 313
2026/2027429 146 283 0 0 0 0 0 0 0 0 0 0
Totale 34.471