CATALOGO DEI PRODOTTI DELLA RICERCA

PIGNATTI, Pierfranco
 Distribuzione geografica
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Continente #
NA - Nord America 16.418
EU - Europa 12.851
AS - Asia 4.368
OC - Oceania 41
AF - Africa 28
SA - Sud America 28
Continente sconosciuto - Info sul continente non disponibili 9
Totale 33.743
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Nazione #
US - Stati Uniti d'America 16.369
GB - Regno Unito 5.367
CN - Cina 3.410
SE - Svezia 1.540
IE - Irlanda 1.085
FI - Finlandia 1.026
FR - Francia 1.025
DE - Germania 821
RU - Federazione Russa 688
IT - Italia 637
SG - Singapore 499
UA - Ucraina 351
BE - Belgio 129
VN - Vietnam 118
KR - Corea 85
TR - Turchia 62
JP - Giappone 54
NL - Olanda 49
CA - Canada 34
AU - Australia 33
IN - India 31
CM - Camerun 20
IR - Iran 16
BR - Brasile 13
HK - Hong Kong 13
ES - Italia 12
AT - Austria 11
CH - Svizzera 11
IL - Israele 11
CZ - Repubblica Ceca 10
LV - Lettonia 10
PH - Filippine 10
EU - Europa 9
RO - Romania 9
CL - Cile 8
HR - Croazia 8
NZ - Nuova Zelanda 8
PL - Polonia 8
TW - Taiwan 8
BG - Bulgaria 6
EE - Estonia 6
ID - Indonesia 6
KG - Kirghizistan 6
MX - Messico 6
SA - Arabia Saudita 6
MY - Malesia 5
NO - Norvegia 5
PA - Panama 5
AE - Emirati Arabi Uniti 4
AZ - Azerbaigian 4
DK - Danimarca 4
MA - Marocco 4
AR - Argentina 3
GR - Grecia 3
HU - Ungheria 3
LU - Lussemburgo 3
ME - Montenegro 3
MT - Malta 3
PK - Pakistan 3
AL - Albania 2
BD - Bangladesh 2
CR - Costa Rica 2
IQ - Iraq 2
KH - Cambogia 2
LA - Repubblica Popolare Democratica del Laos 2
LI - Liechtenstein 2
LT - Lituania 2
MD - Moldavia 2
MK - Macedonia 2
PE - Perù 2
PT - Portogallo 2
SI - Slovenia 2
UZ - Uzbekistan 2
BA - Bosnia-Erzegovina 1
BN - Brunei Darussalam 1
BY - Bielorussia 1
CO - Colombia 1
EC - Ecuador 1
EG - Egitto 1
IS - Islanda 1
JM - Giamaica 1
KW - Kuwait 1
LK - Sri Lanka 1
MN - Mongolia 1
MO - Macao, regione amministrativa speciale della Cina 1
MS - Montserrat 1
NG - Nigeria 1
NP - Nepal 1
SC - Seychelles 1
SK - Slovacchia (Repubblica Slovacca) 1
TH - Thailandia 1
ZA - Sudafrica 1
Totale 33.743
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Città #
Southend 4.703
Jacksonville 3.508
Chandler 2.745
Woodbridge 1.902
Ann Arbor 1.383
Ashburn 1.140
Dublin 1.085
Houston 905
Beijing 494
Wilmington 439
Lawrence 412
Princeton 412
Nanjing 391
Jinan 383
New York 360
Singapore 359
Boardman 286
Shenyang 254
Verona 238
Hebei 217
Helsinki 217
Tianjin 184
Sindelfingen 183
Changsha 147
Zhengzhou 135
Nanchang 134
Ningbo 123
Haikou 117
Hangzhou 111
Brussels 110
Dong Ket 109
Milan 108
Jiaxing 97
Lancaster 88
Taizhou 86
Taiyuan 82
Seoul 81
Dearborn 78
Guangzhou 64
Norwalk 57
Seattle 57
Washington 55
Kent 50
Tokyo 50
Los Angeles 49
Philadelphia 49
Auburn Hills 43
Fuzhou 42
Lanzhou 42
Falls Church 39
San Francisco 38
Fairfield 32
Redwood City 32
Toronto 29
Düsseldorf 27
Moscow 26
Chicago 20
Waanrode 19
Riva 16
Detroit 15
Leawood 14
Clearwater 13
Rome 13
Augusta 12
Cambridge 11
Edinburgh 11
Melbourne 11
Canberra 10
Dongguan 10
Mehlingen 10
San Mateo 10
Tappahannock 10
Vienna 10
Ardabil 8
London 8
Manila 8
New Taipei 8
Redmond 8
San Diego 8
Torino 8
Zagreb 8
Amsterdam 7
Groningen 7
Hong Kong 7
Riga 7
Warsaw 7
Bishkek 6
Florence 6
Madrid 6
Sofia 6
São Paulo 6
Tallinn 6
Zurich 6
Bangalore 5
Bologna 5
Changle 5
Kochi 5
North Bergen 5
Oslo 5
Padova 5
Totale 24.978
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Nome #
A preliminary microRNA analysis of non syndromic thoracic aortic aneurysms 380
α1-Antitrypsin TAQ I polymorphism and α1-antichymotrypsin mutations in patients with obstructive pulmonary disease 225
Effects of Duplex-specific nuclease on human cells expression profiling using RNA-seq 169
Analisi del riarrangiamento bcr-abl in alcuni pazienti affetti da leucemia mieloide cronica 153
A 48-bp insertion between exon 13 and 14 of the HEXB gene causes infantile-onset Sandhoff disease 148
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 148
1059G/C polymorphism within the exon 2 of the C-reactive protein gene: relationship to C-reactive protein levels and prognosis in unstable angina. 135
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 131
Novel serum paraoxonase activity assays are associated with coronary artery disease 131
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 130
Associazione di polimorfismi del cluster dei geni FADS1 e FADS2 con i livelli di acidi grassi polinsaturi in malattie coronariche 125
CACNA1E variants affect beta cell function in patients with newly diagnosed type 2 diabetes. the Verona newly diagnosed type 2 diabetes study (VNDS) 3. 124
Family based association analysis of TGFB1 as modifier gene in Cystic Fibrosis 123
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 121
Cyclooxygenase 2, toll-like receptor 4 and interleukin 1beta mRNA expression in atherosclerotic plaques of type 2 diabetic patients. 121
The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families 120
Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in idiopathic pancreatitis. 118
Ability of different flow rates of fractional exaled nitric oxide (FeNO) to discriminate between asthmatic and no asthamatic subject 117
Family based association analysis of TGFB1 as modifier gene in Cystic Fibrosis 115
Detection of allele-specific gene expression on next generation sequencing data 115
Gene Environment Interactions in Respiratory Diseases – Protocol, Standard Operative Procedures and Questionnaires 114
Genetic testing for adult-type hypolactasia in Italian families 113
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 113
Linkage to atopy on chromosome 19 in north-eastern Italian families with allergic asthma 112
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 112
Analisi multilocus per l’identificazione di un genotipo di rischio in Malattie Cardiovascolari 112
Splicing mutation causes infantile Sandhoff disease 111
A1298C methylentetrahydrofolate reductase mutation and coronary artery disease:relationship with C677T polymorphysm and homocystein/folate metabolism 111
Interaction between folate and MTHFR1298 A/C polymorphism on Genomic DNA Methylation 111
Cationic trypsinogen and pancreatic secretory trypsin inhibitor gene mutations in neonatal hypertrypsinaemia 111
The Gene-Environment Interactions in Respiratory Diseases (GEIRD) Project 111
Interaction between metabolic syndrome and PON 1 polymorphism as a determinant of the risk of coronary artery disease 110
A 931 +2T-C transition in one COL1A2 allele causes exon 16 skipping in pro alpha 2(I) mRNA and produces moderately severe OI 110
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically proven coronary artery disease. 110
Imputation reliability on DNA biallelic markers for drug metabolism studies 110
Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patients 109
Chromosome 14 linkage analysis and mutation study of two serpin genes in allergic asthmatic families 109
Association of a Lymphotoxin alpha gene polymorphism and atopy in Italian families. 109
Association analysis of candidate gene polymorphisms in Asthma, Rhinitis and Chronic Bronchitis: preliminary results from the GEIRD study 109
Haplotype analysis of collagen type I genes in the general population and in osteogenesis imperfecta families. 106
Analisi del gene TGFb1 quale possibile modificatore del fenotipo in fibrosi cistica 106
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 105
Association of IL4Ra gene with severity of lung disease in Cystic Fibrosis 105
Effect of inhibitors of cellular polymerase alpha on the replication of TK- Herpes simplex virus. 104
Post-methionine loading hyperhomocysteinemia in patients with angiographically documented coronary artery disease 104
Candidate gene polymorphisms in cardiovascular disease: A comparative study of frequencies between a French and an Italian population 103
Reconstruction and functional analysis of altered molecular pathways in human atherosclerotic arteries 103
A genome scan for allergic asthma and related phenotypes in an Italian population sample 103
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically confirmed coronary artery disease. 103
Potential role of MTNR1B locus in regulating beta cell function and glucose levels in patients with newly diagnosed type 2 diabetes 103
Different suppression of Ph1 positive hemopoiesis induced by intensive chemotherapy in lymphoid and myeloid blast crisis of CML 102
Homocysteine and atheromatous renal artery stenosis 102
X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene 101
“Fingerprinting” of HLA-DQA by polymerase chain reaction and heteroduplex analysis 101
Allelic frequencies of FBN1 gene polymorphisms and genetic analysis of Italian families with Marfan syndrome 101
Candidate genes and a genome-wide search in Italian families with atopic asthmatic children 101
A new approach to identify non-pathogenic mutations. An analysis of the cystic fibrosis transmembrane regulator gene in normal individuals. 101
A genetic risk factor for vascular disease which leads to mild hyperhomocysteinemia is common in northern Italy. 101
Polymorphism -2604G>A variants in TLR4 promoter are associated with different gene expression level in peripheral blood of atherosclerotic patients. 101
Upregulated expression of toll-like receptor 4 in peripheral blood of ischaemic stroke patients correlates with cyclooxygenase 2 expression. 101
Frequency distribution of the alleles of several variable number of tandem repeat DNA polymorphisms in the Italian population 100
Reply to Novelli 100
Hyperhomocysteinemia and mortality after coronary artery by-pass grafing. 100
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 100
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. 100
Forensic applications of molecular genetic analysis: an Italian collaborative study on paternity testing by the determination of variable number of tandem repeat DNA polymorphisms 99
Herpes simplex virus DNA synthesis in a partially purified soluble extract from infected cells 99
CFTR and cationic trypsinogen gene mutations in idiopathic pancreatitis and neonatal hypertrypsinemia 99
Studio su sette polimorfismi VNTR nella popolazione veronese. 99
Proteomic investigation into nonsyndromic aneurysm of the human ascenging aorta 99
Case-control association analysis of candidate genes in asthma, rhinitis and COPD: A preliminary report 99
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations 98
Combined effect of hemostatic gene polymorphisms and the risk of myocardial infarction in patients with advanced coronary atherosclerosis. 98
Single and multilocus analyses for the identification of at risk genotypes in cardiovascular disease 98
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. 98
Bone marrow transplantation monitoring by DNA analysis 97
Tracking disease genes by reverse genetics 97
Viral and cellular deoxyribonucleases are associated with herpes simplex virus replicative intermediates 97
Hyperhomocysteinemia and Mortality after Coronary Artery Bypass Grafting 97
ASSOCIATION ANALYSIS OF CANDIDATE GENE POLYMORPHISMS WITH ASTHMA SEVERITY: RESULTS FROM THE GEIRD STUDY 96
Studies on sporadic non-syndromic thoracic aortic aneurysms: II. Alterations of extra-cellular matrix components and focal adhesion proteins 96
Herpes simplex virus replication in the presence of DNA polymerase alpha inhibitors 95
Family based association study of the 9p22 chromosomal region in Italian subjects with allergic asthma 95
The characterization of the alpha-subunits of 7S nerve growth factor 94
Segregation analysis of dominant osteogenesis imperfecta in Italy 94
Intarfamilial variable expressivity of osteogenesis imperfecta due to mosaicism for a lethal G382R substitution in the COL1A1 gene 94
A large-scale study of the random variability of a coding sequence: a study on the CFTR gene 94
Genetic and environmental determinants of hyperhomocysteinemia in subjects with angiographically proven coronary artery disease 94
Analisi di 51 polimorfismi in 35 geni dell’infiammazione per la valutazione del rischio di coronaropatia e di infarto del miocardio 94
doRNA-seq: uno script per automatizzare l’analisi RNA-seq 94
Discussion of "Recent application of DNA analysis to issues of paternity" [letter; comment] 93
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. 93
Increased incidence of Cystic Fibrosis gene mutations in adults with disseminated bronchiectasis. 93
Association of the FcεRIβ gene with bronchial hyper-responsiveness in an Italian population 93
Complete mutational screening of the CFTR gene in 120 patients with pulmonary disease. 93
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. 93
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically confirmed coronary artery disease. 93
Cromosoma 19 e asma atopica in famiglie Italiane 93
Association of FcER1A and RAD50 polymorphisms with serum IgE levels, asthma and rhinitis 93
Physical mapping of three Syn loci simultaneously mutated in a syncytial mutant of Herpes simplex virus type 1 93
Totale 11.057
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Categoria #
all - tutte 99.165
article - articoli 62.202
book - libri 310
conference - conferenze 35.934
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 719
Totale 198.330
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20203.835 0 45 30 447 367 528 489 448 166 525 244 546
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
2024/2025796 575 221 0 0 0 0 0 0 0 0 0 0
Totale 33.866