CATALOGO DEI PRODOTTI DELLA RICERCA

PIGNATTI, Pierfranco
 Distribuzione geografica
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Continente #
NA - Nord America 17.095
EU - Europa 13.440
AS - Asia 7.046
SA - Sud America 524
AF - Africa 59
OC - Oceania 46
Continente sconosciuto - Info sul continente non disponibili 10
Totale 38.220
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Nazione #
US - Stati Uniti d'America 17.002
GB - Regno Unito 5.389
CN - Cina 3.659
SG - Singapore 2.739
SE - Svezia 1.550
IE - Irlanda 1.091
FI - Finlandia 1.089
FR - Francia 1.027
RU - Federazione Russa 995
DE - Germania 884
IT - Italia 689
BR - Brasile 460
UA - Ucraina 357
BE - Belgio 137
VN - Vietnam 120
KR - Corea 88
TR - Turchia 84
HK - Hong Kong 70
JP - Giappone 61
NL - Olanda 61
CA - Canada 54
AU - Australia 38
IN - India 35
IR - Iran 24
CM - Camerun 20
AT - Austria 18
AR - Argentina 17
CH - Svizzera 15
IL - Israele 14
LV - Lettonia 14
MX - Messico 13
PH - Filippine 13
ES - Italia 12
ID - Indonesia 12
PA - Panama 12
UZ - Uzbekistan 12
BD - Bangladesh 11
CZ - Repubblica Ceca 11
KG - Kirghizistan 11
MA - Marocco 11
TW - Taiwan 11
VE - Venezuela 11
PK - Pakistan 10
PL - Polonia 10
RO - Romania 10
BG - Bulgaria 9
CL - Cile 9
EU - Europa 9
IQ - Iraq 9
LT - Lituania 9
ZA - Sudafrica 9
AZ - Azerbaigian 8
HR - Croazia 8
NZ - Nuova Zelanda 8
SA - Arabia Saudita 8
AE - Emirati Arabi Uniti 7
EC - Ecuador 7
EE - Estonia 7
PE - Perù 7
CO - Colombia 6
JO - Giordania 6
MY - Malesia 6
DZ - Algeria 5
NO - Norvegia 5
PT - Portogallo 5
CR - Costa Rica 4
DK - Danimarca 4
EG - Egitto 4
HU - Ungheria 4
TN - Tunisia 4
BA - Bosnia-Erzegovina 3
BO - Bolivia 3
GR - Grecia 3
HN - Honduras 3
JM - Giamaica 3
LA - Repubblica Popolare Democratica del Laos 3
LK - Sri Lanka 3
LU - Lussemburgo 3
ME - Montenegro 3
MT - Malta 3
NP - Nepal 3
PY - Paraguay 3
SK - Slovacchia (Repubblica Slovacca) 3
AL - Albania 2
KH - Cambogia 2
KZ - Kazakistan 2
LI - Liechtenstein 2
MD - Moldavia 2
MK - Macedonia 2
PS - Palestinian Territory 2
SI - Slovenia 2
SY - Repubblica araba siriana 2
BH - Bahrain 1
BN - Brunei Darussalam 1
BY - Bielorussia 1
CI - Costa d'Avorio 1
CY - Cipro 1
DO - Repubblica Dominicana 1
GA - Gabon 1
GE - Georgia 1
Totale 38.203
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Città #
Southend 4.703
Jacksonville 3.508
Chandler 2.745
Woodbridge 1.902
Singapore 1.781
Ann Arbor 1.383
Ashburn 1.308
Dublin 1.091
Houston 905
Beijing 496
Wilmington 439
Lawrence 412
Princeton 412
Nanjing 392
Jinan 384
New York 360
Boardman 286
Helsinki 275
Shenyang 255
Verona 241
Hebei 217
Tianjin 184
Sindelfingen 183
Changsha 147
Zhengzhou 138
Nanchang 135
Ningbo 123
Brussels 118
Haikou 117
Hangzhou 112
Dong Ket 109
Milan 109
Jiaxing 97
Lancaster 88
Taizhou 87
Taiyuan 82
Seoul 81
Dearborn 78
Guangzhou 69
Hong Kong 64
Santa Clara 63
Los Angeles 61
Norwalk 57
Seattle 57
Washington 55
Tokyo 51
Kent 50
Philadelphia 49
Fuzhou 44
Moscow 44
Auburn Hills 43
Lanzhou 42
São Paulo 40
Falls Church 39
San Francisco 38
Toronto 37
Dallas 36
Fairfield 32
Redwood City 32
Düsseldorf 27
Chicago 22
Rio de Janeiro 22
Council Bluffs 20
Waanrode 19
London 18
Munich 18
Rome 17
Nuremberg 16
Riva 16
Vienna 16
Detroit 15
Leawood 14
Clearwater 13
Falkenstein 13
Augusta 12
Belo Horizonte 12
Brasília 12
Dongguan 12
Tashkent 12
Bishkek 11
Cambridge 11
Edinburgh 11
Melbourne 11
Riga 11
Romola 11
Canberra 10
Manila 10
Mehlingen 10
San Mateo 10
Tappahannock 10
Amsterdam 9
San Diego 9
Ardabil 8
Baku 8
Frankfurt am Main 8
Malmo 8
New Taipei 8
Redmond 8
Sofia 8
Torino 8
Totale 27.010
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Nome #
A preliminary microRNA analysis of non syndromic thoracic aortic aneurysms 396
α1-Antitrypsin TAQ I polymorphism and α1-antichymotrypsin mutations in patients with obstructive pulmonary disease 236
Effects of Duplex-specific nuclease on human cells expression profiling using RNA-seq 218
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 169
Analisi del riarrangiamento bcr-abl in alcuni pazienti affetti da leucemia mieloide cronica 168
A 48-bp insertion between exon 13 and 14 of the HEXB gene causes infantile-onset Sandhoff disease 165
1059G/C polymorphism within the exon 2 of the C-reactive protein gene: relationship to C-reactive protein levels and prognosis in unstable angina. 148
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 146
Novel serum paraoxonase activity assays are associated with coronary artery disease 143
CACNA1E variants affect beta cell function in patients with newly diagnosed type 2 diabetes. the Verona newly diagnosed type 2 diabetes study (VNDS) 3. 143
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 142
Associazione di polimorfismi del cluster dei geni FADS1 e FADS2 con i livelli di acidi grassi polinsaturi in malattie coronariche 140
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. 137
An assessment of chimeric transcript detection in CML patients after bone marrow transplantation 136
Family based association analysis of TGFB1 as modifier gene in Cystic Fibrosis 136
Detection of allele-specific gene expression on next generation sequencing data 136
Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in idiopathic pancreatitis. 134
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 134
Family based association analysis of TGFB1 as modifier gene in Cystic Fibrosis 134
The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families 134
Cyclooxygenase 2, toll-like receptor 4 and interleukin 1beta mRNA expression in atherosclerotic plaques of type 2 diabetic patients. 132
Ability of different flow rates of fractional exaled nitric oxide (FeNO) to discriminate between asthmatic and no asthamatic subject 132
Imputation reliability on DNA biallelic markers for drug metabolism studies 130
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 128
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically proven coronary artery disease. 127
Association analysis of candidate gene polymorphisms in Asthma, Rhinitis and Chronic Bronchitis: preliminary results from the GEIRD study 127
A1298C methylentetrahydrofolate reductase mutation and coronary artery disease:relationship with C677T polymorphysm and homocystein/folate metabolism 126
Gene Environment Interactions in Respiratory Diseases – Protocol, Standard Operative Procedures and Questionnaires 126
Linkage to atopy on chromosome 19 in north-eastern Italian families with allergic asthma 125
SNP detection by RNA-seq 125
Cationic trypsinogen and pancreatic secretory trypsin inhibitor gene mutations in neonatal hypertrypsinaemia 124
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 124
Genetic testing for adult-type hypolactasia in Italian families 124
Analisi del gene TGFb1 quale possibile modificatore del fenotipo in fibrosi cistica 124
Analisi multilocus per l’identificazione di un genotipo di rischio in Malattie Cardiovascolari 123
Potential role of MTNR1B locus in regulating beta cell function and glucose levels in patients with newly diagnosed type 2 diabetes 122
The Gene-Environment Interactions in Respiratory Diseases (GEIRD) Project 121
A genetic risk factor for vascular disease which leads to mild hyperhomocysteinemia is common in northern Italy. 120
Different suppression of Ph1 positive hemopoiesis induced by intensive chemotherapy in lymphoid and myeloid blast crisis of CML 119
Interaction between metabolic syndrome and PON 1 polymorphism as a determinant of the risk of coronary artery disease 119
Interaction between folate and MTHFR1298 A/C polymorphism on Genomic DNA Methylation 118
A 931 +2T-C transition in one COL1A2 allele causes exon 16 skipping in pro alpha 2(I) mRNA and produces moderately severe OI 118
Haplotype analysis of collagen type I genes in the general population and in osteogenesis imperfecta families. 118
Association of a Lymphotoxin alpha gene polymorphism and atopy in Italian families. 118
Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patients 117
Chromosome 14 linkage analysis and mutation study of two serpin genes in allergic asthmatic families 117
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 116
Splicing mutation causes infantile Sandhoff disease 116
Association of IL4Ra gene with severity of lung disease in Cystic Fibrosis 116
Polymorphism -2604G>A variants in TLR4 promoter are associated with different gene expression level in peripheral blood of atherosclerotic patients. 116
Allelic frequencies of FBN1 gene polymorphisms and genetic analysis of Italian families with Marfan syndrome 115
doRNA-seq: uno script per automatizzare l’analisi RNA-seq 115
IFRD1 gene polymorphisms are associated with nasal polyposis in cystic fibrosis patients 115
Studies on sporadic non-syndromic thoracic aortic aneurysms: II. Alterations of extra-cellular matrix components and focal adhesion proteins 115
Frequency distribution of the alleles of several variable number of tandem repeat DNA polymorphisms in the Italian population 114
Hyperhomocysteinemia and Mortality after Coronary Artery Bypass Grafting 114
Reconstruction and functional analysis of altered molecular pathways in human atherosclerotic arteries 114
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. 114
Case-control association analysis of candidate genes in asthma, rhinitis and COPD: A preliminary report 114
Candidate gene polymorphisms in cardiovascular disease: A comparative study of frequencies between a French and an Italian population 113
Effect of inhibitors of cellular polymerase alpha on the replication of TK- Herpes simplex virus. 113
Reply to Novelli 113
A genome scan for allergic asthma and related phenotypes in an Italian population sample 113
Bone marrow transplantation monitoring by DNA analysis 112
Post-methionine loading hyperhomocysteinemia in patients with angiographically documented coronary artery disease 112
Candidate genes and a genome-wide search in Italian families with atopic asthmatic children 112
Proteomic investigation into nonsyndromic aneurysm of the human ascenging aorta 112
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically confirmed coronary artery disease. 112
Homocysteine and atheromatous renal artery stenosis 111
A new approach to identify non-pathogenic mutations. An analysis of the cystic fibrosis transmembrane regulator gene in normal individuals. 111
Single and multilocus analyses for the identification of at risk genotypes in cardiovascular disease 111
ASSOCIATION ANALYSIS OF CANDIDATE GENE POLYMORPHISMS WITH ASTHMA SEVERITY: RESULTS FROM THE GEIRD STUDY 111
Forensic applications of molecular genetic analysis: an Italian collaborative study on paternity testing by the determination of variable number of tandem repeat DNA polymorphisms 110
X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene 110
Studio su sette polimorfismi VNTR nella popolazione veronese. 110
A large-scale study of the random variability of a coding sequence: a study on the CFTR gene 110
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 110
“Fingerprinting” of HLA-DQA by polymerase chain reaction and heteroduplex analysis 109
Hyperhomocysteinemia and mortality after coronary artery by-pass grafing. 109
Upregulated expression of toll-like receptor 4 in peripheral blood of ischaemic stroke patients correlates with cyclooxygenase 2 expression. 109
Herpes simplex virus DNA synthesis in a partially purified soluble extract from infected cells 108
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations 108
Combined effect of hemostatic gene polymorphisms and the risk of myocardial infarction in patients with advanced coronary atherosclerosis. 108
Analisi di 51 polimorfismi in 35 geni dell’infiammazione per la valutazione del rischio di coronaropatia e di infarto del miocardio 108
A bioinformatic framework to build junction databases for the detection of alternative splicing isoforms from Next Generation Sequencing data 108
Tracking disease genes by reverse genetics 107
CFTR and cationic trypsinogen gene mutations in idiopathic pancreatitis and neonatal hypertrypsinemia 107
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically confirmed coronary artery disease. 107
Family based association study of the 9p22 chromosomal region in Italian subjects with allergic asthma 107
Viral and cellular deoxyribonucleases are associated with herpes simplex virus replicative intermediates 106
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 106
Delta F508 gene deletion in cystic fibrosis in southern Europe [letter] 105
A common polymorphism in exon 46 of the human autosomal dominant polycystic kidney disease 1 gene (PKD1) 105
Hyperhomocysteinemia in relation to total and cardiovascular death after coronary bypass grafting. 104
Chromosome 7p linkage and GPR154 gene association in Italian families with asthma 104
CD45 and multiple sclerosis: the exon 4 C77G polymorphism (additional studies and meta-analysis) and new markers 104
Genomic and proteomic investigation into non-syndromic aneurysms of the human ascending aorta. 104
ALOX5AP gene variants and risk of coronary artery disease: an angiography-based study 104
Cromosoma 19 e asma atopica in famiglie Italiane 104
Variants in CACNA1E affect beta cell function and glucose homeostasis in newly diagnosed type 2 diabetes patients 104
Totale 12.444
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Categoria #
all - tutte 125.634
article - articoli 78.441
book - libri 404
conference - conferenze 45.919
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 870
Totale 251.268
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.481 0 0 0 0 0 0 0 0 166 525 244 546
2020/20214.196 419 702 195 437 444 465 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
2024/20255.273 575 648 298 1.342 400 150 420 296 1.144 0 0 0
Totale 38.343