CATALOGO DEI PRODOTTI DELLA RICERCA

PIGNATTI, Pierfranco
 Distribuzione geografica
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Continente #
NA - Nord America 25.794
EU - Europa 21.590
AS - Asia 14.906
SA - Sud America 1.713
AF - Africa 318
OC - Oceania 64
Continente sconosciuto - Info sul continente non disponibili 13
AN - Antartide 1
Totale 64.399
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Nazione #
US - Stati Uniti d'America 25.454
RU - Federazione Russa 7.365
SG - Singapore 6.124
GB - Regno Unito 5.609
CN - Cina 4.826
SE - Svezia 1.605
BR - Brasile 1.407
FI - Finlandia 1.280
DE - Germania 1.239
VN - Vietnam 1.218
IT - Italia 1.195
IE - Irlanda 1.101
FR - Francia 1.074
HK - Hong Kong 1.073
KR - Corea 494
UA - Ucraina 392
IN - India 216
CA - Canada 182
JP - Giappone 171
TR - Turchia 141
BE - Belgio 139
AR - Argentina 124
NL - Olanda 120
BD - Bangladesh 108
PL - Polonia 105
ZA - Sudafrica 90
MX - Messico 87
IQ - Iraq 83
NG - Nigeria 81
ES - Italia 70
ID - Indonesia 70
AU - Australia 56
PK - Pakistan 45
LT - Lituania 42
AT - Austria 39
VE - Venezuela 34
CH - Svizzera 33
CL - Cile 31
MA - Marocco 30
UZ - Uzbekistan 30
EC - Ecuador 29
IR - Iran 29
SA - Arabia Saudita 29
IL - Israele 26
PH - Filippine 26
CO - Colombia 25
JO - Giordania 25
PY - Paraguay 25
AE - Emirati Arabi Uniti 23
CZ - Repubblica Ceca 23
EG - Egitto 21
CM - Camerun 20
PE - Perù 20
AZ - Azerbaigian 17
LV - Lettonia 17
NP - Nepal 17
KE - Kenya 16
MY - Malesia 16
TN - Tunisia 16
KZ - Kazakistan 15
PA - Panama 15
KG - Kirghizistan 14
AL - Albania 13
CR - Costa Rica 13
BG - Bulgaria 12
HR - Croazia 12
RO - Romania 12
GR - Grecia 11
TW - Taiwan 11
DZ - Algeria 10
ET - Etiopia 10
HN - Honduras 10
JM - Giamaica 10
PT - Portogallo 10
EU - Europa 9
RS - Serbia 9
UY - Uruguay 9
BO - Bolivia 8
NZ - Nuova Zelanda 8
EE - Estonia 7
LB - Libano 7
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
BJ - Benin 4
KH - Cambogia 4
LA - Repubblica Popolare Democratica del Laos 4
LU - Lussemburgo 4
MD - Moldavia 4
MK - Macedonia 4
NI - Nicaragua 4
SK - Slovacchia (Repubblica Slovacca) 4
SN - Senegal 4
Totale 64.330
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Città #
Southend 4.703
Jacksonville 3.513
Singapore 3.491
Ashburn 2.818
Chandler 2.745
Moscow 2.322
Dallas 2.097
Woodbridge 1.902
San Jose 1.855
Ann Arbor 1.383
Dublin 1.101
Hong Kong 1.055
Houston 933
Beijing 676
Verona 655
The Dalles 653
New York 521
Wilmington 439
Lawrence 412
Princeton 412
Ho Chi Minh City 409
Nanjing 396
Jinan 392
Los Angeles 372
Helsinki 327
Boardman 288
Munich 286
Shenyang 263
Hanoi 262
Tianjin 223
Buffalo 219
Hebei 217
Sindelfingen 183
São Paulo 171
Changsha 160
Tokyo 153
Zhengzhou 145
Santa Clara 140
Nanchang 136
Turku 136
Ningbo 123
Milan 121
Brussels 119
Hangzhou 119
Haikou 117
Dong Ket 109
Orem 103
Jiaxing 100
Warsaw 98
Guangzhou 93
Columbus 90
Seoul 90
Redondo Beach 89
Lancaster 88
Taizhou 87
Taiyuan 83
Dearborn 78
Council Bluffs 76
San Francisco 75
Seattle 72
Abuja 71
London 67
Chennai 66
Montreal 66
Frankfurt am Main 62
Toronto 62
Chicago 60
Norwalk 57
Stockholm 57
Philadelphia 56
Washington 56
Johannesburg 54
Brooklyn 53
Rio de Janeiro 51
Kent 50
Denver 47
Fuzhou 47
Lanzhou 45
Amsterdam 44
Atlanta 43
Auburn Hills 43
Da Nang 40
Poplar 40
Falls Church 39
Baghdad 37
Phoenix 36
Belo Horizonte 35
Falkenstein 34
Haiphong 34
Manchester 34
Rome 34
Boston 33
Fairfield 32
Redwood City 32
Tashkent 30
Brasília 28
Mumbai 28
Düsseldorf 27
Ankara 26
Mexico City 26
Totale 42.276
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Nome #
A preliminary microRNA analysis of non syndromic thoracic aortic aneurysms 526
Effects of Duplex-specific nuclease on human cells expression profiling using RNA-seq 314
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 291
A 48-bp insertion between exon 13 and 14 of the HEXB gene causes infantile-onset Sandhoff disease 283
α1-Antitrypsin TAQ I polymorphism and α1-antichymotrypsin mutations in patients with obstructive pulmonary disease 283
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 268
ASSOCIATION ANALYSIS OF CANDIDATE GENE POLYMORPHISMS WITH ASTHMA SEVERITY: RESULTS FROM THE GEIRD STUDY 266
Ability of different flow rates of fractional exaled nitric oxide (FeNO) to discriminate between asthmatic and no asthamatic subject 265
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 261
1059G/C polymorphism within the exon 2 of the C-reactive protein gene: relationship to C-reactive protein levels and prognosis in unstable angina. 256
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 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 247
A bioinformatic framework to build junction databases for the detection of alternative splicing isoforms from Next Generation Sequencing data 245
Cationic trypsinogen and pancreatic secretory trypsin inhibitor gene mutations in neonatal hypertrypsinaemia 244
SNP detection by RNA-seq 243
A genome scan for allergic asthma and related phenotypes in an Italian population sample 238
ALOX5AP gene variants and risk of coronary artery disease: an angiography-based study 235
Cyclooxygenase 2, toll-like receptor 4 and interleukin 1beta mRNA expression in atherosclerotic plaques of type 2 diabetic patients. 232
A1298C methylentetrahydrofolate reductase mutation and coronary artery disease:relationship with C677T polymorphysm and homocystein/folate metabolism 231
Detection of allele-specific gene expression on next generation sequencing data 231
Analisi del riarrangiamento bcr-abl in alcuni pazienti affetti da leucemia mieloide cronica 230
An assessment of chimeric transcript detection in CML patients after bone marrow transplantation 229
Associazione di polimorfismi del cluster dei geni FADS1 e FADS2 con i livelli di acidi grassi polinsaturi in malattie coronariche 229
Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in idiopathic pancreatitis. 228
Association of a Lymphotoxin alpha gene polymorphism and atopy in Italian families. 227
Family based association analysis of TGFB1 as modifier gene in Cystic Fibrosis 227
Affected sib-pair and mutation analyses of the high affinity IgE receptor beta chain locus in Italian families with atopic asthmatic children 226
A genetic risk factor for vascular disease which leads to mild hyperhomocysteinemia is common in northern Italy. 225
Imputation reliability on DNA biallelic markers for drug metabolism studies 224
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 222
A 931 +2T-C transition in one COL1A2 allele causes exon 16 skipping in pro alpha 2(I) mRNA and produces moderately severe OI 221
Analisi multilocus per l’identificazione di un genotipo di rischio in Malattie Cardiovascolari 221
A novel synonymous substitution in the GCK gene causes aberrant splicing in an Italian patient with GCK-MODY phenotype 219
A method to detect individuals with different genetic background in case-control studies 218
CACNA1E variants affect beta cell function in patients with newly diagnosed type 2 diabetes. the Verona newly diagnosed type 2 diabetes study (VNDS) 3. 218
Novel serum paraoxonase activity assays are associated with coronary artery disease 217
Association analysis of candidate gene polymorphisms in Asthma, Rhinitis and Chronic Bronchitis: preliminary results from the GEIRD study 216
Gene Environment Interactions in Respiratory Diseases – Protocol, Standard Operative Procedures and Questionnaires 214
A method to target individuals with an unusual genetic background and to tag SNPs for linkage disequilibrium (LD) mapping 214
Family based association analysis of TGFB1 as modifier gene in Cystic Fibrosis 214
A computational method to test for genetic relatedness in unrelated individuals 213
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 212
Analisi del gene TGFb1 quale possibile modificatore del fenotipo in fibrosi cistica 211
Candidate genes and a genome-wide search in Italian families with atopic asthmatic children 208
Association of IL4Ra gene with severity of lung disease in Cystic Fibrosis 208
Analisi di 51 polimorfismi in 35 geni dell’infiammazione per la valutazione del rischio di coronaropatia e di infarto del miocardio 206
The Gene-Environment Interactions in Respiratory Diseases (GEIRD) Project 204
IFRD1 gene polymorphisms are associated with nasal polyposis in cystic fibrosis patients 204
Different suppression of Ph1 positive hemopoiesis induced by intensive chemotherapy in lymphoid and myeloid blast crisis of CML 203
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. 203
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 203
The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families 201
Frequency distribution of the alleles of several variable number of tandem repeat DNA polymorphisms in the Italian population 200
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. 200
Polymorphism -2604G>A variants in TLR4 promoter are associated with different gene expression level in peripheral blood of atherosclerotic patients. 200
Haplotype analysis of collagen type I genes in the general population and in osteogenesis imperfecta families. 199
Combined effect of hemostatic gene polymorphisms and the risk of myocardial infarction in patients with advanced coronary atherosclerosis. 199
Analisi funzionale di polimorfismi nel promotore del gene PLA2G7. 198
A new approach to identify non-pathogenic mutations. An analysis of the cystic fibrosis transmembrane regulator gene in normal individuals. 198
CFTR and cationic trypsinogen gene mutations in idiopathic pancreatitis and neonatal hypertrypsinemia 197
Linkage to atopy on chromosome 19 in north-eastern Italian families with allergic asthma 197
Analisi di linkage in famiglie con carcinoma mammario ereditario. 197
doRNA-seq: uno script per automatizzare l’analisi RNA-seq 197
ApoC-III gene polymorphisms and risk of coronary artery disease 196
Acquired and genetic determinants of homocysteine in atheromatous renel artery stenosis with mild renal insufficiency 196
Analisi di espressione genica in aneurismi non sindromici dell’aorta ascendente 196
High levels of COX-2 gene expression in peripheral blood of cardioembolic and atherothrombotic stroke patients 196
Biochemical and genetic markers of iron status and the risk of coronary disease 195
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations 194
Allelic frequencies of FBN1 gene polymorphisms and genetic analysis of Italian families with Marfan syndrome 194
A large-scale study of the random variability of a coding sequence: a study on the CFTR gene 194
Association of the IL33 gene region with childhood allergic asthma 194
Allele frequencies of six highly polymorphic DNA loci in the Croatian population 193
COX-2 promoter region polymorphisms in multiple sclerosis: lack of association of -765G>C with disease risk 193
Forensic applications of molecular genetic analysis: an Italian collaborative study on paternity testing by the determination of variable number of tandem repeat DNA polymorphisms 192
Genomic and proteomic investigation into non-syndromic aneurysms of the human ascending aorta. 192
Espressione dei geni COX-2 e TLR4 nel sangue periferico di pazienti con ictus ischemico. 192
Upregulated expression of toll-like receptor 4 in peripheral blood of ischaemic stroke patients correlates with cyclooxygenase 2 expression. 192
Candidate gene polymorphisms in cardiovascular disease: A comparative study of frequencies between a French and an Italian population 191
Genetic variability of G6PC2 influences beta cell function and insulin sensitivity in patients with newly diagnosed type 2 diabetes 191
Potential role of MTNR1B locus in regulating beta cell function and glucose levels in patients with newly diagnosed type 2 diabetes 190
Reply to Novelli 189
Proteomic investigation into nonsyndromic aneurysm of the human ascenging aorta 189
Studies on sporadic non-syndromic thoracic aortic aneurysms: II. Alterations of extra-cellular matrix components and focal adhesion proteins 189
CD45 and multiple sclerosis: the exon 4 C77G polymorphism (additional studies and meta-analysis) and new markers 188
Case-control association analysis of candidate genes in asthma, rhinitis and COPD: A preliminary report 188
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 187
Chromosome 14 linkage analysis and mutation study of two serpin genes in allergic asthmatic families 187
Complete mutational screening of the CFTR gene in 120 patients with pulmonary disease. 187
Bone marrow transplantation monitoring by DNA analysis 186
La placca carotidea sintomatica: caratterizzazionegenetica, istopatologica e per immagini 185
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. 185
Association of childhood allergic asthma with markers flanking the IL33 gene in Italian families. 185
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 185
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically proven coronary artery disease. 184
Hyperhomocysteinemia and Mortality after Coronary Artery Bypass Grafting 183
807 C/T polymorphism of the glycoprotein IA gene and pharmacogenetic modulation of platelet response to dual antiplatelet treatment 183
A computational test for biological relatedness in genetic association studies using probabilistically inferred haplotypes 183
A common polymorphism in exon 46 of the human autosomal dominant polycystic kidney disease 1 gene (PKD1) 182
Cromosoma 19 e asma atopica in famiglie Italiane 182
Totale 21.520
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Categoria #
all - tutte 191.032
article - articoli 118.806
book - libri 642
conference - conferenze 70.314
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.270
Totale 382.064
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021776 0 0 0 0 0 0 0 0 0 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
2025/202623.338 1.718 1.270 1.984 3.917 6.375 1.745 2.244 1.101 1.709 1.275 0 0
Totale 64.522