CATALOGO DEI PRODOTTI DELLA RICERCA

PIGNATTI, Pierfranco
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 29.470
EU - Europa 21.832
AS - Asia 15.076
SA - Sud America 1.841
AF - Africa 321
Continente sconosciuto - Info sul continente non disponibili 136
OC - Oceania 64
AN - Antartide 1
Totale 68.741
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 28.974
RU - Federazione Russa 7.366
SG - Singapore 6.163
GB - Regno Unito 5.626
CN - Cina 4.853
SE - Svezia 1.606
BR - Brasile 1.499
IT - Italia 1.388
FI - Finlandia 1.280
DE - Germania 1.239
VN - Vietnam 1.222
IE - Irlanda 1.104
HK - Hong Kong 1.081
FR - Francia 1.079
KR - Corea 494
UA - Ucraina 392
CA - Canada 267
IN - India 220
BD - Bangladesh 179
JP - Giappone 174
TR - Turchia 144
BE - Belgio 141
AR - Argentina 129
NL - Olanda 124
PL - Polonia 106
MX - Messico 96
ZA - Sudafrica 90
IQ - Iraq 83
NG - Nigeria 81
ES - Italia 77
ID - Indonesia 74
AU - Australia 56
PK - Pakistan 46
LT - Lituania 42
VE - Venezuela 41
AT - Austria 39
CO - Colombia 36
CL - Cile 35
EC - Ecuador 35
CH - Svizzera 33
MA - Marocco 31
CR - Costa Rica 30
SA - Arabia Saudita 30
UZ - Uzbekistan 30
IR - Iran 29
IL - Israele 26
PH - Filippine 26
JO - Giordania 25
PY - Paraguay 25
AE - Emirati Arabi Uniti 23
CZ - Repubblica Ceca 23
EG - Egitto 21
PE - Perù 21
CM - Camerun 20
AZ - Azerbaigian 17
JM - Giamaica 17
LV - Lettonia 17
MY - Malesia 17
NP - Nepal 17
TN - Tunisia 17
HN - Honduras 16
KE - Kenya 16
KZ - Kazakistan 16
PA - Panama 15
AL - Albania 14
KG - Kirghizistan 14
NI - Nicaragua 14
RO - Romania 14
BG - Bulgaria 12
HR - Croazia 12
PT - Portogallo 12
TW - Taiwan 12
GR - Grecia 11
BO - Bolivia 10
DZ - Algeria 10
ET - Etiopia 10
EE - Estonia 9
EU - Europa 9
RS - Serbia 9
UY - Uruguay 9
GT - Guatemala 8
LB - Libano 8
NZ - Nuova Zelanda 8
NO - Norvegia 7
DK - Danimarca 6
MT - Malta 6
PS - Palestinian Territory 6
SY - Repubblica araba siriana 6
CY - Cipro 5
DO - Repubblica Dominicana 5
GE - Georgia 5
HU - Ungheria 5
SI - Slovenia 5
TT - Trinidad e Tobago 5
BA - Bosnia-Erzegovina 4
BB - Barbados 4
BJ - Benin 4
KH - Cambogia 4
LA - Repubblica Popolare Democratica del Laos 4
LU - Lussemburgo 4
Totale 68.529
Salva come PNG Salva come JPEG
Città #
Southend 4.703
Ashburn 3.597
Jacksonville 3.519
Singapore 3.501
Chandler 2.745
Moscow 2.322
San Jose 2.261
Dallas 2.208
Woodbridge 1.904
Ann Arbor 1.383
Dublin 1.101
Hong Kong 1.063
Houston 938
Beijing 692
Verona 657
The Dalles 654
Council Bluffs 641
New York 561
Wilmington 440
Los Angeles 423
Lawrence 413
Princeton 412
Ho Chi Minh City 411
Nanjing 396
Jinan 392
Helsinki 327
Boardman 288
Munich 286
Hanoi 263
Shenyang 263
Buffalo 240
São Paulo 232
Tianjin 223
Hebei 217
Santa Clara 207
Sindelfingen 183
Changsha 161
Tokyo 155
Zhengzhou 145
Milan 142
Nanchang 136
Turku 136
Ningbo 123
Brussels 120
Hangzhou 119
Haikou 117
Dong Ket 109
Orem 104
Jiaxing 100
Warsaw 98
Toronto 97
Columbus 95
Guangzhou 93
Annandale 92
Seoul 90
Lancaster 89
Redondo Beach 89
Taizhou 87
Taiyuan 83
Dearborn 79
San Francisco 79
Seattle 79
Philadelphia 77
Chicago 74
Brooklyn 72
Abuja 71
Montreal 71
London 68
Chennai 66
Denver 65
Rome 63
Frankfurt am Main 62
Washington 60
Norwalk 58
Stockholm 57
Johannesburg 54
Las Vegas 54
Phoenix 53
Atlanta 52
Rio de Janeiro 52
Kent 51
Fuzhou 47
Amsterdam 45
Lanzhou 45
Auburn Hills 43
Da Nang 40
Falls Church 40
Poplar 40
Boston 39
Manchester 38
Baghdad 37
Providence 37
Belo Horizonte 36
Haiphong 35
Falkenstein 34
Fairfield 32
Redwood City 32
Tashkent 30
Brasília 28
Mexico City 28
Totale 44.769
Salva come PNG Salva come JPEG
Nome #
A preliminary microRNA analysis of non syndromic thoracic aortic aneurysms 534
Effects of Duplex-specific nuclease on human cells expression profiling using RNA-seq 326
A base substitution at IVS-19 3'-end splice junction causes exon 20 skipping in pro alpha 2(I) collagen mRNA and produces mild osteogenesis imperfecta 314
α1-Antitrypsin TAQ I polymorphism and α1-antichymotrypsin mutations in patients with obstructive pulmonary disease 293
A 48-bp insertion between exon 13 and 14 of the HEXB gene causes infantile-onset Sandhoff disease 291
Ability of different flow rates of fractional exaled nitric oxide (FeNO) to discriminate between asthmatic and no asthamatic subject 287
ASSOCIATION ANALYSIS OF CANDIDATE GENE POLYMORPHISMS WITH ASTHMA SEVERITY: RESULTS FROM THE GEIRD STUDY 280
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 277
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 273
A de novo G to T transversion in a pro-alpha 1(I) collagen gene for a moderate case of osteogenesis imperfecta. Substitution of cysteine for glycine 178 in the triple helical domain 267
A bioinformatic framework to build junction databases for the detection of alternative splicing isoforms from Next Generation Sequencing data 264
1059G/C polymorphism within the exon 2 of the C-reactive protein gene: relationship to C-reactive protein levels and prognosis in unstable angina. 262
SNP detection by RNA-seq 259
Homozygosity for a novel splice site mutation (2790-2 A/G) preceding exon 15 of the CFTR gene in a cystic fibrosis patient of North-East Italian descendent. 256
A base substitution at IVS-19 3' splice junction causes exon 20 skipping in pro alpha 2(I) collagen mRNA and produces mild osteogenesis imperfecta 256
Cationic trypsinogen and pancreatic secretory trypsin inhibitor gene mutations in neonatal hypertrypsinaemia 256
A genome scan for allergic asthma and related phenotypes in an Italian population sample 252
Associazione di polimorfismi del cluster dei geni FADS1 e FADS2 con i livelli di acidi grassi polinsaturi in malattie coronariche 248
ALOX5AP gene variants and risk of coronary artery disease: an angiography-based study 247
Cyclooxygenase 2, toll-like receptor 4 and interleukin 1beta mRNA expression in atherosclerotic plaques of type 2 diabetic patients. 243
Association analysis of candidate gene polymorphisms in Asthma, Rhinitis and Chronic Bronchitis: preliminary results from the GEIRD study 243
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 243
Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in idiopathic pancreatitis. 242
Analisi del riarrangiamento bcr-abl in alcuni pazienti affetti da leucemia mieloide cronica 240
Detection of allele-specific gene expression on next generation sequencing data 240
A1298C methylentetrahydrofolate reductase mutation and coronary artery disease:relationship with C677T polymorphysm and homocystein/folate metabolism 239
Gene Environment Interactions in Respiratory Diseases – Protocol, Standard Operative Procedures and Questionnaires 239
An assessment of chimeric transcript detection in CML patients after bone marrow transplantation 238
Affected sib-pair and mutation analyses of the high affinity IgE receptor beta chain locus in Italian families with atopic asthmatic children 238
A genetic risk factor for vascular disease which leads to mild hyperhomocysteinemia is common in northern Italy. 237
Imputation reliability on DNA biallelic markers for drug metabolism studies 236
Association of a Lymphotoxin alpha gene polymorphism and atopy in Italian families. 235
Family based association analysis of TGFB1 as modifier gene in Cystic Fibrosis 234
Novel serum paraoxonase activity assays are associated with coronary artery disease 231
A 931 +2T-C transition in one COL1A2 allele causes exon 16 skipping in pro alpha 2(I) mRNA and produces moderately severe OI 230
A novel synonymous substitution in the GCK gene causes aberrant splicing in an Italian patient with GCK-MODY phenotype 230
Analisi multilocus per l’identificazione di un genotipo di rischio in Malattie Cardiovascolari 230
CACNA1E variants affect beta cell function in patients with newly diagnosed type 2 diabetes. the Verona newly diagnosed type 2 diabetes study (VNDS) 3. 228
A method to detect individuals with different genetic background in case-control studies 226
A method to target individuals with an unusual genetic background and to tag SNPs for linkage disequilibrium (LD) mapping 225
Analisi del gene TGFb1 quale possibile modificatore del fenotipo in fibrosi cistica 223
Family based association analysis of TGFB1 as modifier gene in Cystic Fibrosis 222
A computational method to test for genetic relatedness in unrelated individuals 221
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 220
Association of IL4Ra gene with severity of lung disease in Cystic Fibrosis 220
Allele frequencies of six highly polymorphic DNA loci in the Croatian population 218
Candidate genes and a genome-wide search in Italian families with atopic asthmatic children 218
Analisi di 51 polimorfismi in 35 geni dell’infiammazione per la valutazione del rischio di coronaropatia e di infarto del miocardio 217
Different suppression of Ph1 positive hemopoiesis induced by intensive chemotherapy in lymphoid and myeloid blast crisis of CML 215
Analisi di espressione genica in aneurismi non sindromici dell’aorta ascendente 215
The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families 215
Analysis of the complete coding region of the CFTR gene in a cohort of patients from North-Eastern Italy: identification of 90% of the mutations 213
Analisi funzionale di polimorfismi nel promotore del gene PLA2G7. 212
A new approach to identify non-pathogenic mutations. An analysis of the cystic fibrosis transmembrane regulator gene in normal individuals. 212
Analisi di linkage in famiglie con carcinoma mammario ereditario. 212
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. 212
High levels of COX-2 gene expression in peripheral blood of cardioembolic and atherothrombotic stroke patients 212
Frequency distribution of the alleles of several variable number of tandem repeat DNA polymorphisms in the Italian population 211
Genomic and proteomic investigation into non-syndromic aneurysms of the human ascending aorta. 211
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. 211
The Gene-Environment Interactions in Respiratory Diseases (GEIRD) Project 211
Genetic variability of G6PC2 influences beta cell function and insulin sensitivity in patients with newly diagnosed type 2 diabetes 211
IFRD1 gene polymorphisms are associated with nasal polyposis in cystic fibrosis patients 211
Combined effect of hemostatic gene polymorphisms and the risk of myocardial infarction in patients with advanced coronary atherosclerosis. 210
Impact of insulin receptor substrate-1 genotypes on platelet reactivity and cardiovascular outcomes in patients with type 2 diabetes mellitus and coronary artery disease 209
Espressione dei geni COX-2 e TLR4 nel sangue periferico di pazienti con ictus ischemico. 209
Haplotype analysis of collagen type I genes in the general population and in osteogenesis imperfecta families. 208
doRNA-seq: uno script per automatizzare l’analisi RNA-seq 207
Association of the IL33 gene region with childhood allergic asthma 207
Polymorphism -2604G>A variants in TLR4 promoter are associated with different gene expression level in peripheral blood of atherosclerotic patients. 207
Forensic applications of molecular genetic analysis: an Italian collaborative study on paternity testing by the determination of variable number of tandem repeat DNA polymorphisms 206
Biochemical and genetic markers of iron status and the risk of coronary disease 206
Studies on sporadic non-syndromic thoracic aortic aneurysms: II. Alterations of extra-cellular matrix components and focal adhesion proteins 205
Linkage to atopy on chromosome 19 in north-eastern Italian families with allergic asthma 204
A large-scale study of the random variability of a coding sequence: a study on the CFTR gene 204
Candidate gene polymorphisms in cardiovascular disease: A comparative study of frequencies between a French and an Italian population 203
CFTR and cationic trypsinogen gene mutations in idiopathic pancreatitis and neonatal hypertrypsinemia 203
ApoC-III gene polymorphisms and risk of coronary artery disease 203
Acquired and genetic determinants of homocysteine in atheromatous renel artery stenosis with mild renal insufficiency 203
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations 202
COX-2 promoter region polymorphisms in multiple sclerosis: lack of association of -765G>C with disease risk 202
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 202
Allelic frequencies of FBN1 gene polymorphisms and genetic analysis of Italian families with Marfan syndrome 200
Upregulated expression of toll-like receptor 4 in peripheral blood of ischaemic stroke patients correlates with cyclooxygenase 2 expression. 199
Proteomic investigation into nonsyndromic aneurysm of the human ascenging aorta 198
Determination of a new collagen type I alpha 2 gene point mutation which causes a Gly640 Cys substitution in osteogenesis imperfecta and prenatal diagnosis by DNA hybridisation 197
Chromosome 14 linkage analysis and mutation study of two serpin genes in allergic asthmatic families 197
Potential role of MTNR1B locus in regulating beta cell function and glucose levels in patients with newly diagnosed type 2 diabetes 197
Reply to Novelli 196
Complete mutational screening of the CFTR gene in 120 patients with pulmonary disease. 196
CD45 and multiple sclerosis: the exon 4 C77G polymorphism (additional studies and meta-analysis) and new markers 195
Case-control association analysis of candidate genes in asthma, rhinitis and COPD: A preliminary report 195
Associazione di varianti geniche nei geni FCER1A e STAT6 con le IgE Seriche totali nei panificatori 194
Association of childhood allergic asthma with markers flanking the IL33 gene in Italian families. 194
Association of FcER1A and RAD50 polymorphisms with serum IgE levels, asthma and rhinitis 194
Bone marrow transplantation monitoring by DNA analysis 193
La placca carotidea sintomatica: caratterizzazionegenetica, istopatologica e per immagini 193
Broncopneumopatia Cronica Ostruttiva e Bronchiettasie Disseminate. 192
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. 192
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 192
Totale 22.746
Salva come PNG Salva come JPEG
Categoria #
all - tutte 217.807
article - articoli 136.388
book - libri 736
conference - conferenze 79.239
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.444
Totale 435.614
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20222.089 0 0 0 338 136 97 53 201 118 91 271 784
2022/20237.652 534 814 680 1.330 769 1.780 81 509 843 48 180 84
2023/20243.777 145 297 292 405 461 615 135 471 28 165 491 272
2024/20258.114 575 648 298 1.342 400 150 420 296 1.148 410 704 1.723
2025/202624.136 1.718 1.270 1.984 3.917 6.375 1.745 2.244 1.101 1.709 1.377 227 469
2026/20273.421 233 621 1.406 1.161 0 0 0 0 0 0 0 0
Totale 68.741