CATALOGO DEI PRODOTTI DELLA RICERCA

PIGNATTI, Pierfranco
 Distribuzione geografica
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Continente #
NA - Nord America 20.319
EU - Europa 14.084
AS - Asia 9.938
SA - Sud America 1.194
AF - Africa 106
OC - Oceania 53
Continente sconosciuto - Info sul continente non disponibili 11
AN - Antartide 1
Totale 45.706
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Nazione #
US - Stati Uniti d'America 20.142
GB - Regno Unito 5.430
SG - Singapore 3.971
CN - Cina 3.907
SE - Svezia 1.562
FI - Finlandia 1.228
DE - Germania 1.170
IE - Irlanda 1.093
BR - Brasile 1.065
FR - Francia 1.042
RU - Federazione Russa 1.004
HK - Hong Kong 984
IT - Italia 709
UA - Ucraina 361
KR - Corea 290
VN - Vietnam 228
BE - Belgio 138
TR - Turchia 100
CA - Canada 99
JP - Giappone 82
NL - Olanda 77
IN - India 72
BD - Bangladesh 49
AR - Argentina 46
AU - Australia 45
PL - Polonia 41
MX - Messico 37
AT - Austria 35
IQ - Iraq 29
IR - Iran 28
ZA - Sudafrica 27
ES - Italia 26
CH - Svizzera 23
CZ - Repubblica Ceca 22
CM - Camerun 20
UZ - Uzbekistan 19
VE - Venezuela 19
IL - Israele 17
LT - Lituania 17
PK - Pakistan 17
MA - Marocco 16
EC - Ecuador 14
ID - Indonesia 14
LV - Lettonia 14
SA - Arabia Saudita 14
KG - Kirghizistan 13
PA - Panama 13
PH - Filippine 13
AE - Emirati Arabi Uniti 12
CL - Cile 12
PY - Paraguay 11
RO - Romania 11
TW - Taiwan 11
AZ - Azerbaigian 10
BG - Bulgaria 10
TN - Tunisia 10
CO - Colombia 9
EU - Europa 9
PE - Perù 9
HR - Croazia 8
NZ - Nuova Zelanda 8
BO - Bolivia 7
CR - Costa Rica 7
EE - Estonia 7
EG - Egitto 7
JO - Giordania 7
KZ - Kazakistan 7
MY - Malesia 7
DZ - Algeria 6
KE - Kenya 6
NO - Norvegia 6
PT - Portogallo 6
HN - Honduras 5
JM - Giamaica 5
NP - Nepal 5
DK - Danimarca 4
HU - Ungheria 4
LU - Lussemburgo 4
MK - Macedonia 4
AL - Albania 3
BA - Bosnia-Erzegovina 3
GR - Grecia 3
KH - Cambogia 3
LA - Repubblica Popolare Democratica del Laos 3
LB - Libano 3
LK - Sri Lanka 3
ME - Montenegro 3
MT - Malta 3
SK - Slovacchia (Repubblica Slovacca) 3
SY - Repubblica araba siriana 3
BB - Barbados 2
BH - Bahrain 2
BY - Bielorussia 2
CI - Costa d'Avorio 2
GE - Georgia 2
LI - Liechtenstein 2
MD - Moldavia 2
PS - Palestinian Territory 2
SI - Slovenia 2
SN - Senegal 2
Totale 45.669
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Città #
Southend 4.703
Jacksonville 3.508
Chandler 2.745
Singapore 2.081
Woodbridge 1.902
Dallas 1.873
Ashburn 1.429
Ann Arbor 1.383
Dublin 1.093
Hong Kong 978
Houston 907
Beijing 537
Wilmington 439
Lawrence 412
Princeton 412
New York 396
Nanjing 393
Jinan 387
Boardman 286
Munich 285
Helsinki 277
Shenyang 260
Verona 241
Los Angeles 229
Hebei 217
Buffalo 187
Tianjin 185
Sindelfingen 183
Changsha 150
Zhengzhou 142
Nanchang 136
Turku 135
The Dalles 126
Ningbo 123
Brussels 118
Haikou 117
Hangzhou 115
Milan 111
Dong Ket 109
Jiaxing 97
São Paulo 92
Columbus 90
Santa Clara 90
Lancaster 88
Taizhou 87
Seoul 84
Taiyuan 83
Dearborn 78
Guangzhou 75
Tokyo 72
San Francisco 67
Seattle 67
Norwalk 57
Redondo Beach 57
Washington 55
Philadelphia 53
Kent 50
Council Bluffs 47
Ho Chi Minh City 47
Fuzhou 46
Moscow 45
Rio de Janeiro 45
Toronto 45
Auburn Hills 43
Lanzhou 43
Chicago 42
Falls Church 39
Warsaw 36
Brooklyn 33
Fairfield 32
Redwood City 32
Belo Horizonte 29
London 28
Düsseldorf 27
Brasília 25
Nuremberg 25
Vienna 23
Atlanta 21
Hanoi 20
Rome 20
Tashkent 19
Waanrode 19
Frankfurt am Main 18
Boston 17
Campinas 16
Detroit 16
Riva 16
Stockholm 16
Curitiba 15
Montreal 15
Amsterdam 14
Johannesburg 14
Leawood 14
Bishkek 13
Canberra 13
Clearwater 13
Dongguan 13
Falkenstein 13
Melbourne 13
Augusta 12
Totale 31.744
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Nome #
A preliminary microRNA analysis of non syndromic thoracic aortic aneurysms 446
Effects of Duplex-specific nuclease on human cells expression profiling using RNA-seq 251
α1-Antitrypsin TAQ I polymorphism and α1-antichymotrypsin mutations in patients with obstructive pulmonary disease 249
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 212
A 48-bp insertion between exon 13 and 14 of the HEXB gene causes infantile-onset Sandhoff disease 208
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 197
Analisi del riarrangiamento bcr-abl in alcuni pazienti affetti da leucemia mieloide cronica 186
Ability of different flow rates of fractional exaled nitric oxide (FeNO) to discriminate between asthmatic and no asthamatic subject 184
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 179
1059G/C polymorphism within the exon 2 of the C-reactive protein gene: relationship to C-reactive protein levels and prognosis in unstable angina. 175
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 172
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 171
Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in idiopathic pancreatitis. 167
A genetic risk factor for vascular disease which leads to mild hyperhomocysteinemia is common in northern Italy. 163
Novel serum paraoxonase activity assays are associated with coronary artery disease 163
Associazione di polimorfismi del cluster dei geni FADS1 e FADS2 con i livelli di acidi grassi polinsaturi in malattie coronariche 163
CACNA1E variants affect beta cell function in patients with newly diagnosed type 2 diabetes. the Verona newly diagnosed type 2 diabetes study (VNDS) 3. 163
A1298C methylentetrahydrofolate reductase mutation and coronary artery disease:relationship with C677T polymorphysm and homocystein/folate metabolism 161
ASSOCIATION ANALYSIS OF CANDIDATE GENE POLYMORPHISMS WITH ASTHMA SEVERITY: RESULTS FROM THE GEIRD STUDY 161
SNP detection by RNA-seq 161
A genome scan for allergic asthma and related phenotypes in an Italian population sample 160
Family based association analysis of TGFB1 as modifier gene in Cystic Fibrosis 160
Cyclooxygenase 2, toll-like receptor 4 and interleukin 1beta mRNA expression in atherosclerotic plaques of type 2 diabetic patients. 160
Detection of allele-specific gene expression on next generation sequencing data 160
Association analysis of candidate gene polymorphisms in Asthma, Rhinitis and Chronic Bronchitis: preliminary results from the GEIRD study 160
Cationic trypsinogen and pancreatic secretory trypsin inhibitor gene mutations in neonatal hypertrypsinaemia 159
An assessment of chimeric transcript detection in CML patients after bone marrow transplantation 158
A bioinformatic framework to build junction databases for the detection of alternative splicing isoforms from Next Generation Sequencing data 155
Analisi multilocus per l’identificazione di un genotipo di rischio in Malattie Cardiovascolari 154
A 931 +2T-C transition in one COL1A2 allele causes exon 16 skipping in pro alpha 2(I) mRNA and produces moderately severe OI 153
Gene Environment Interactions in Respiratory Diseases – Protocol, Standard Operative Procedures and Questionnaires 153
The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families 152
Family based association analysis of TGFB1 as modifier gene in Cystic Fibrosis 151
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. 150
A novel synonymous substitution in the GCK gene causes aberrant splicing in an Italian patient with GCK-MODY phenotype 148
Analisi del gene TGFb1 quale possibile modificatore del fenotipo in fibrosi cistica 148
Imputation reliability on DNA biallelic markers for drug metabolism studies 147
ALOX5AP gene variants and risk of coronary artery disease: an angiography-based study 146
Different suppression of Ph1 positive hemopoiesis induced by intensive chemotherapy in lymphoid and myeloid blast crisis of CML 145
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 145
The Gene-Environment Interactions in Respiratory Diseases (GEIRD) Project 144
Polymorphism -2604G>A variants in TLR4 promoter are associated with different gene expression level in peripheral blood of atherosclerotic patients. 144
IFRD1 gene polymorphisms are associated with nasal polyposis in cystic fibrosis patients 144
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 144
Association of a Lymphotoxin alpha gene polymorphism and atopy in Italian families. 143
Analisi di 51 polimorfismi in 35 geni dell’infiammazione per la valutazione del rischio di coronaropatia e di infarto del miocardio 142
Association of IL4Ra gene with severity of lung disease in Cystic Fibrosis 141
Potential role of MTNR1B locus in regulating beta cell function and glucose levels in patients with newly diagnosed type 2 diabetes 141
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 141
Linkage to atopy on chromosome 19 in north-eastern Italian families with allergic asthma 140
Affected sib-pair and mutation analyses of the high affinity IgE receptor beta chain locus in Italian families with atopic asthmatic children 140
Haplotype analysis of collagen type I genes in the general population and in osteogenesis imperfecta families. 139
A large-scale study of the random variability of a coding sequence: a study on the CFTR gene 139
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically proven coronary artery disease. 139
Frequency distribution of the alleles of several variable number of tandem repeat DNA polymorphisms in the Italian population 138
Interaction between folate and MTHFR1298 A/C polymorphism on Genomic DNA Methylation 138
Analisi funzionale di polimorfismi nel promotore del gene PLA2G7. 138
Case-control association analysis of candidate genes in asthma, rhinitis and COPD: A preliminary report 138
Reply to Novelli 137
doRNA-seq: uno script per automatizzare l’analisi RNA-seq 137
Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patients 136
Allelic frequencies of FBN1 gene polymorphisms and genetic analysis of Italian families with Marfan syndrome 136
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. 136
A computational method to test for genetic relatedness in unrelated individuals 136
Splicing mutation causes infantile Sandhoff disease 135
Interaction between metabolic syndrome and PON 1 polymorphism as a determinant of the risk of coronary artery disease 135
A new approach to identify non-pathogenic mutations. An analysis of the cystic fibrosis transmembrane regulator gene in normal individuals. 135
Proteomic investigation into nonsyndromic aneurysm of the human ascenging aorta 135
Forensic applications of molecular genetic analysis: an Italian collaborative study on paternity testing by the determination of variable number of tandem repeat DNA polymorphisms 134
Combined effect of hemostatic gene polymorphisms and the risk of myocardial infarction in patients with advanced coronary atherosclerosis. 134
Studies on sporadic non-syndromic thoracic aortic aneurysms: II. Alterations of extra-cellular matrix components and focal adhesion proteins 134
Bone marrow transplantation monitoring by DNA analysis 133
Candidate genes and a genome-wide search in Italian families with atopic asthmatic children 133
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 133
Candidate gene polymorphisms in cardiovascular disease: A comparative study of frequencies between a French and an Italian population 132
CFTR and cationic trypsinogen gene mutations in idiopathic pancreatitis and neonatal hypertrypsinemia 132
Reconstruction and functional analysis of altered molecular pathways in human atherosclerotic arteries 132
Genetic testing for adult-type hypolactasia in Italian families 132
Hyperhomocysteinemia and Mortality after Coronary Artery Bypass Grafting 131
Chromosome 14 linkage analysis and mutation study of two serpin genes in allergic asthmatic families 131
Hyperhomocysteinemia and mortality after coronary artery by-pass grafing. 131
COX-2 promoter region polymorphisms in multiple sclerosis: lack of association of -765G>C with disease risk 131
Genetic variability of G6PC2 influences beta cell function and insulin sensitivity in patients with newly diagnosed type 2 diabetes 131
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. 130
Homocysteine and atheromatous renal artery stenosis 129
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations 129
CD45 and multiple sclerosis: the exon 4 C77G polymorphism (additional studies and meta-analysis) and new markers 129
Analisi di espressione genica in aneurismi non sindromici dell’aorta ascendente 129
Upregulated expression of toll-like receptor 4 in peripheral blood of ischaemic stroke patients correlates with cyclooxygenase 2 expression. 129
Acquired and genetic determinants of homocysteine in atheromatous renel artery stenosis with mild renal insufficiency 128
Single and multilocus analyses for the identification of at risk genotypes in cardiovascular disease 127
Mild dominant osteogenesis imperfecta with intrafamilial variability: the cause is a serine for glycine alpha 1(I) 901 substitution in a type-I collagen gene 126
Effect of inhibitors of cellular polymerase alpha on the replication of TK- Herpes simplex virus. 126
Best practice guidelines for molecular genetic diagnosis of cystic fibrosis and CFTR-related disorders-updated European recommandations 126
La placca carotidea sintomatica: caratterizzazionegenetica, istopatologica e per immagini 126
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically confirmed coronary artery disease. 126
Herpes simplex virus DNA synthesis in a partially purified soluble extract from infected cells 125
Delta F508 gene deletion in cystic fibrosis in southern Europe [letter] 125
ApoC-III gene polymorphisms and risk of coronary artery disease 125
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 125
Totale 15.031
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Categoria #
all - tutte 154.169
article - articoli 96.400
book - libri 510
conference - conferenze 56.211
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.048
Totale 308.338
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20213.075 0 0 195 437 444 465 47 404 307 27 526 223
2021/20223.247 291 841 26 338 136 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
2025/20264.645 1.718 1.270 1.657 0 0 0 0 0 0 0 0 0
Totale 45.829