CATALOGO DEI PRODOTTI DELLA RICERCA

PIGNATTI, Pierfranco
 Distribuzione geografica
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Continente #
NA - Nord America 16.940
EU - Europa 13.266
AS - Asia 5.782
OC - Oceania 46
SA - Sud America 42
AF - Africa 31
Continente sconosciuto - Info sul continente non disponibili 9
Totale 36.116
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Nazione #
US - Stati Uniti d'America 16.873
GB - Regno Unito 5.373
CN - Cina 3.618
SG - Singapore 1.658
SE - Svezia 1.541
IE - Irlanda 1.090
FI - Finlandia 1.057
FR - Francia 1.025
RU - Federazione Russa 980
DE - Germania 837
IT - Italia 675
UA - Ucraina 352
BE - Belgio 130
VN - Vietnam 119
KR - Corea 85
TR - Turchia 64
JP - Giappone 58
NL - Olanda 55
CA - Canada 43
AU - Australia 38
IN - India 33
IR - Iran 23
CM - Camerun 20
BR - Brasile 19
CH - Svizzera 14
HK - Hong Kong 14
IL - Israele 13
LV - Lettonia 13
ES - Italia 12
PH - Filippine 12
AT - Austria 11
CZ - Repubblica Ceca 11
ID - Indonesia 11
PA - Panama 11
PL - Polonia 10
RO - Romania 10
TW - Taiwan 10
CL - Cile 9
EU - Europa 9
KG - Kirghizistan 9
HR - Croazia 8
NZ - Nuova Zelanda 8
SA - Arabia Saudita 8
BG - Bulgaria 7
EE - Estonia 7
MX - Messico 7
AE - Emirati Arabi Uniti 6
AR - Argentina 6
AZ - Azerbaigian 6
MA - Marocco 5
MY - Malesia 5
NO - Norvegia 5
PT - Portogallo 5
DK - Danimarca 4
PK - Pakistan 4
CO - Colombia 3
CR - Costa Rica 3
GR - Grecia 3
HU - Ungheria 3
LA - Repubblica Popolare Democratica del Laos 3
LK - Sri Lanka 3
LT - Lituania 3
LU - Lussemburgo 3
ME - Montenegro 3
MT - Malta 3
PE - Perù 3
SK - Slovacchia (Repubblica Slovacca) 3
UZ - Uzbekistan 3
AL - Albania 2
BD - Bangladesh 2
EG - Egitto 2
IQ - Iraq 2
KH - Cambogia 2
LI - Liechtenstein 2
MD - Moldavia 2
MK - Macedonia 2
NP - Nepal 2
SI - Slovenia 2
BA - Bosnia-Erzegovina 1
BN - Brunei Darussalam 1
BO - Bolivia 1
BY - Bielorussia 1
CY - Cipro 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
EC - Ecuador 1
IS - Islanda 1
JM - Giamaica 1
JO - Giordania 1
KW - Kuwait 1
KZ - Kazakistan 1
MN - Mongolia 1
MO - Macao, regione amministrativa speciale della Cina 1
MS - Montserrat 1
NG - Nigeria 1
SC - Seychelles 1
SY - Repubblica araba siriana 1
TH - Thailandia 1
ZA - Sudafrica 1
Totale 36.116
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Città #
Southend 4.703
Jacksonville 3.508
Chandler 2.745
Woodbridge 1.902
Singapore 1.388
Ann Arbor 1.383
Ashburn 1.306
Dublin 1.090
Houston 905
Beijing 495
Wilmington 439
Lawrence 412
Princeton 412
Nanjing 392
Jinan 384
New York 360
Boardman 286
Shenyang 255
Helsinki 243
Verona 240
Hebei 217
Tianjin 184
Sindelfingen 183
Changsha 147
Zhengzhou 135
Nanchang 134
Ningbo 123
Haikou 117
Brussels 111
Hangzhou 111
Dong Ket 109
Milan 108
Jiaxing 97
Lancaster 88
Taizhou 87
Taiyuan 82
Seoul 81
Dearborn 78
Guangzhou 67
Santa Clara 63
Los Angeles 59
Norwalk 57
Seattle 57
Washington 55
Tokyo 51
Kent 50
Philadelphia 49
Auburn Hills 43
Fuzhou 43
Lanzhou 42
Moscow 42
Falls Church 39
San Francisco 38
Dallas 36
Toronto 33
Fairfield 32
Redwood City 32
Düsseldorf 27
Chicago 21
Waanrode 19
Munich 18
Riva 16
Detroit 15
Rome 15
Leawood 14
Clearwater 13
Augusta 12
Dongguan 12
Cambridge 11
Edinburgh 11
Melbourne 11
Romola 11
Canberra 10
London 10
Manila 10
Mehlingen 10
Riga 10
San Mateo 10
Tappahannock 10
Vienna 10
Bishkek 9
San Diego 9
Amsterdam 8
Ardabil 8
Hong Kong 8
New Taipei 8
Redmond 8
Torino 8
Zagreb 8
Zurich 8
Groningen 7
Newark 7
Sofia 7
São Paulo 7
Tallinn 7
Warsaw 7
Baku 6
Florence 6
Irvine 6
Madrid 6
Totale 26.382
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Nome #
A preliminary microRNA analysis of non syndromic thoracic aortic aneurysms 389
α1-Antitrypsin TAQ I polymorphism and α1-antichymotrypsin mutations in patients with obstructive pulmonary disease 232
Effects of Duplex-specific nuclease on human cells expression profiling using RNA-seq 197
Analisi del riarrangiamento bcr-abl in alcuni pazienti affetti da leucemia mieloide cronica 159
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 155
A 48-bp insertion between exon 13 and 14 of the HEXB gene causes infantile-onset Sandhoff disease 154
1059G/C polymorphism within the exon 2 of the C-reactive protein gene: relationship to C-reactive protein levels and prognosis in unstable angina. 144
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 140
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 140
Novel serum paraoxonase activity assays are associated with coronary artery disease 139
Associazione di polimorfismi del cluster dei geni FADS1 e FADS2 con i livelli di acidi grassi polinsaturi in malattie coronariche 133
CACNA1E variants affect beta cell function in patients with newly diagnosed type 2 diabetes. the Verona newly diagnosed type 2 diabetes study (VNDS) 3. 132
Family based association analysis of TGFB1 as modifier gene in Cystic Fibrosis 131
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 128
The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families 126
Cyclooxygenase 2, toll-like receptor 4 and interleukin 1beta mRNA expression in atherosclerotic plaques of type 2 diabetic patients. 126
Ability of different flow rates of fractional exaled nitric oxide (FeNO) to discriminate between asthmatic and no asthamatic subject 126
Detection of allele-specific gene expression on next generation sequencing data 124
Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in idiopathic pancreatitis. 123
Linkage to atopy on chromosome 19 in north-eastern Italian families with allergic asthma 122
Genetic testing for adult-type hypolactasia in Italian families 122
Analisi multilocus per l’identificazione di un genotipo di rischio in Malattie Cardiovascolari 122
Family based association analysis of TGFB1 as modifier gene in Cystic Fibrosis 122
Gene Environment Interactions in Respiratory Diseases – Protocol, Standard Operative Procedures and Questionnaires 121
Imputation reliability on DNA biallelic markers for drug metabolism studies 121
A1298C methylentetrahydrofolate reductase mutation and coronary artery disease:relationship with C677T polymorphysm and homocystein/folate metabolism 120
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 120
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 119
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. 118
Interaction between metabolic syndrome and PON 1 polymorphism as a determinant of the risk of coronary artery disease 117
A 931 +2T-C transition in one COL1A2 allele causes exon 16 skipping in pro alpha 2(I) mRNA and produces moderately severe OI 117
The Gene-Environment Interactions in Respiratory Diseases (GEIRD) Project 117
Association analysis of candidate gene polymorphisms in Asthma, Rhinitis and Chronic Bronchitis: preliminary results from the GEIRD study 117
Interaction between folate and MTHFR1298 A/C polymorphism on Genomic DNA Methylation 116
Cationic trypsinogen and pancreatic secretory trypsin inhibitor gene mutations in neonatal hypertrypsinaemia 116
Association of a Lymphotoxin alpha gene polymorphism and atopy in Italian families. 116
Analisi del gene TGFb1 quale possibile modificatore del fenotipo in fibrosi cistica 116
Chromosome 14 linkage analysis and mutation study of two serpin genes in allergic asthmatic families 115
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically proven coronary artery disease. 115
Splicing mutation causes infantile Sandhoff disease 114
Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patients 113
Potential role of MTNR1B locus in regulating beta cell function and glucose levels in patients with newly diagnosed type 2 diabetes 113
Allelic frequencies of FBN1 gene polymorphisms and genetic analysis of Italian families with Marfan syndrome 112
Association of IL4Ra gene with severity of lung disease in Cystic Fibrosis 112
Different suppression of Ph1 positive hemopoiesis induced by intensive chemotherapy in lymphoid and myeloid blast crisis of CML 111
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 111
Haplotype analysis of collagen type I genes in the general population and in osteogenesis imperfecta families. 111
A genetic risk factor for vascular disease which leads to mild hyperhomocysteinemia is common in northern Italy. 111
Candidate gene polymorphisms in cardiovascular disease: A comparative study of frequencies between a French and an Italian population 110
Candidate genes and a genome-wide search in Italian families with atopic asthmatic children 110
A new approach to identify non-pathogenic mutations. An analysis of the cystic fibrosis transmembrane regulator gene in normal individuals. 110
Reconstruction and functional analysis of altered molecular pathways in human atherosclerotic arteries 110
A genome scan for allergic asthma and related phenotypes in an Italian population sample 110
Frequency distribution of the alleles of several variable number of tandem repeat DNA polymorphisms in the Italian population 109
Homocysteine and atheromatous renal artery stenosis 108
Effect of inhibitors of cellular polymerase alpha on the replication of TK- Herpes simplex virus. 108
Post-methionine loading hyperhomocysteinemia in patients with angiographically documented coronary artery disease 108
Polymorphism -2604G>A variants in TLR4 promoter are associated with different gene expression level in peripheral blood of atherosclerotic patients. 108
Upregulated expression of toll-like receptor 4 in peripheral blood of ischaemic stroke patients correlates with cyclooxygenase 2 expression. 108
Hyperhomocysteinemia and mortality after coronary artery by-pass grafing. 107
Proteomic investigation into nonsyndromic aneurysm of the human ascenging aorta 107
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. 107
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically confirmed coronary artery disease. 107
Reply to Novelli 106
Hyperhomocysteinemia and Mortality after Coronary Artery Bypass Grafting 106
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 106
Case-control association analysis of candidate genes in asthma, rhinitis and COPD: A preliminary report 106
IFRD1 gene polymorphisms are associated with nasal polyposis in cystic fibrosis patients 106
An assessment of chimeric transcript detection in CML patients after bone marrow transplantation 105
Bone marrow transplantation monitoring by DNA analysis 105
CFTR and cationic trypsinogen gene mutations in idiopathic pancreatitis and neonatal hypertrypsinemia 105
“Fingerprinting” of HLA-DQA by polymerase chain reaction and heteroduplex analysis 105
Combined effect of hemostatic gene polymorphisms and the risk of myocardial infarction in patients with advanced coronary atherosclerosis. 105
Single and multilocus analyses for the identification of at risk genotypes in cardiovascular disease 105
Analisi di 51 polimorfismi in 35 geni dell’infiammazione per la valutazione del rischio di coronaropatia e di infarto del miocardio 105
Herpes simplex virus DNA synthesis in a partially purified soluble extract from infected cells 104
X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene 104
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations 104
Studio su sette polimorfismi VNTR nella popolazione veronese. 104
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically confirmed coronary artery disease. 103
doRNA-seq: uno script per automatizzare l’analisi RNA-seq 103
Studies on sporadic non-syndromic thoracic aortic aneurysms: II. Alterations of extra-cellular matrix components and focal adhesion proteins 103
Forensic applications of molecular genetic analysis: an Italian collaborative study on paternity testing by the determination of variable number of tandem repeat DNA polymorphisms 102
Tracking disease genes by reverse genetics 102
Viral and cellular deoxyribonucleases are associated with herpes simplex virus replicative intermediates 102
A bioinformatic framework to build junction databases for the detection of alternative splicing isoforms from Next Generation Sequencing data 102
ASSOCIATION ANALYSIS OF CANDIDATE GENE POLYMORPHISMS WITH ASTHMA SEVERITY: RESULTS FROM THE GEIRD STUDY 102
A large-scale study of the random variability of a coding sequence: a study on the CFTR gene 101
Genetic and environmental determinants of hyperhomocysteinemia in subjects with angiographically proven coronary artery disease 101
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. 101
Family based association study of the 9p22 chromosomal region in Italian subjects with allergic asthma 101
SNP detection by RNA-seq 101
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 100
Delta F508 gene deletion in cystic fibrosis in southern Europe [letter] 99
Herpes simplex virus replication in the presence of DNA polymerase alpha inhibitors 99
Cromosoma 19 e asma atopica in famiglie Italiane 99
Espressione dei geni COX-2 e TLR4 nel sangue periferico di pazienti con ictus ischemico. 99
The characterization of the alpha-subunits of 7S nerve growth factor 98
Segregation analysis of dominant osteogenesis imperfecta in Italy 98
Intarfamilial variable expressivity of osteogenesis imperfecta due to mosaicism for a lethal G382R substitution in the COL1A1 gene 98
Totale 11.797
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Categoria #
all - tutte 112.512
article - articoli 70.325
book - libri 348
conference - conferenze 41.043
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 796
Totale 225.024
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20203.313 0 0 0 0 367 528 489 448 166 525 244 546
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
2024/20253.169 575 648 298 1.342 306 0 0 0 0 0 0 0
Totale 36.239