CATALOGO DEI PRODOTTI DELLA RICERCA

PIGNATTI, Pierfranco
 Distribuzione geografica
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Continente #
NA - Nord America 22.293
EU - Europa 20.773
AS - Asia 12.951
SA - Sud America 1.593
AF - Africa 176
OC - Oceania 55
Continente sconosciuto - Info sul continente non disponibili 12
AN - Antartide 1
Totale 57.854
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Nazione #
US - Stati Uniti d'America 22.009
RU - Federazione Russa 7.357
GB - Regno Unito 5.524
SG - Singapore 5.275
CN - Cina 4.637
SE - Svezia 1.600
BR - Brasile 1.331
FI - Finlandia 1.230
DE - Germania 1.193
IE - Irlanda 1.093
FR - Francia 1.043
HK - Hong Kong 1.000
VN - Vietnam 752
IT - Italia 735
KR - Corea 455
UA - Ucraina 372
CA - Canada 156
BE - Belgio 138
JP - Giappone 135
IN - India 131
TR - Turchia 117
AR - Argentina 113
PL - Polonia 96
NL - Olanda 94
BD - Bangladesh 74
MX - Messico 74
ZA - Sudafrica 68
ID - Indonesia 64
ES - Italia 56
AU - Australia 47
IQ - Iraq 47
LT - Lituania 38
AT - Austria 37
IR - Iran 29
EC - Ecuador 27
VE - Venezuela 27
CL - Cile 25
PK - Pakistan 25
CH - Svizzera 24
MA - Marocco 23
CZ - Repubblica Ceca 22
IL - Israele 22
PY - Paraguay 22
CM - Camerun 20
UZ - Uzbekistan 20
AE - Emirati Arabi Uniti 19
CO - Colombia 17
LV - Lettonia 16
AZ - Azerbaigian 15
EG - Egitto 14
PA - Panama 14
PE - Perù 14
PH - Filippine 14
SA - Arabia Saudita 14
KG - Kirghizistan 13
TN - Tunisia 13
BG - Bulgaria 11
JO - Giordania 11
RO - Romania 11
TW - Taiwan 11
NP - Nepal 10
EU - Europa 9
HN - Honduras 9
HR - Croazia 9
KZ - Kazakistan 9
UY - Uruguay 9
CR - Costa Rica 8
DZ - Algeria 8
KE - Kenya 8
MY - Malesia 8
NZ - Nuova Zelanda 8
PT - Portogallo 8
BO - Bolivia 7
EE - Estonia 7
AL - Albania 6
NO - Norvegia 6
DO - Repubblica Dominicana 5
GR - Grecia 5
JM - Giamaica 5
LB - Libano 5
BJ - Benin 4
DK - Danimarca 4
GE - Georgia 4
HU - Ungheria 4
LU - Lussemburgo 4
MD - Moldavia 4
MK - Macedonia 4
SY - Repubblica araba siriana 4
BA - Bosnia-Erzegovina 3
BB - Barbados 3
CI - Costa d'Avorio 3
CY - Cipro 3
KH - Cambogia 3
LA - Repubblica Popolare Democratica del Laos 3
LK - Sri Lanka 3
ME - Montenegro 3
MT - Malta 3
NG - Nigeria 3
PS - Palestinian Territory 3
RS - Serbia 3
Totale 57.801
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Città #
Southend 4.703
Jacksonville 3.508
Singapore 2.785
Chandler 2.745
Moscow 2.318
Dallas 2.084
Ashburn 1.964
Woodbridge 1.902
Ann Arbor 1.383
Dublin 1.093
Hong Kong 993
Houston 928
Beijing 673
New York 492
Wilmington 439
Lawrence 412
Princeton 412
Nanjing 396
Jinan 392
The Dalles 356
Los Angeles 345
Boardman 288
Munich 286
Helsinki 277
Shenyang 263
Ho Chi Minh City 245
Verona 243
Tianjin 220
Hebei 217
Buffalo 209
Sindelfingen 183
Changsha 159
São Paulo 156
Zhengzhou 145
Hanoi 137
Nanchang 136
Turku 136
Ningbo 123
Tokyo 123
Brussels 118
Haikou 117
Hangzhou 117
Milan 114
Santa Clara 111
Dong Ket 109
Jiaxing 100
Columbus 90
Seoul 90
Redondo Beach 89
Warsaw 89
Guangzhou 88
Lancaster 88
Taizhou 87
Taiyuan 83
Dearborn 78
Seattle 72
San Francisco 71
Norwalk 57
Chicago 56
Washington 55
Toronto 54
Montreal 53
Philadelphia 53
Stockholm 52
London 51
Kent 50
Council Bluffs 49
Rio de Janeiro 49
Brooklyn 47
Fuzhou 47
Lanzhou 45
San Jose 45
Auburn Hills 43
Denver 41
Johannesburg 41
Poplar 40
Falls Church 39
Chennai 35
Orem 35
Atlanta 34
Falkenstein 34
Belo Horizonte 33
Fairfield 32
Redwood City 32
Boston 31
Phoenix 31
Amsterdam 27
Brasília 27
Düsseldorf 27
Haiphong 26
Rome 26
Nuremberg 25
Vienna 23
Ankara 22
Jakarta 22
Mexico City 21
Baghdad 20
Manchester 20
Tashkent 20
Frankfurt am Main 19
Totale 37.169
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Nome #
A preliminary microRNA analysis of non syndromic thoracic aortic aneurysms 508
Effects of Duplex-specific nuclease on human cells expression profiling using RNA-seq 291
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 269
α1-Antitrypsin TAQ I polymorphism and α1-antichymotrypsin mutations in patients with obstructive pulmonary disease 264
A 48-bp insertion between exon 13 and 14 of the HEXB gene causes infantile-onset Sandhoff disease 261
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 253
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 239
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 239
1059G/C polymorphism within the exon 2 of the C-reactive protein gene: relationship to C-reactive protein levels and prognosis in unstable angina. 238
ASSOCIATION ANALYSIS OF CANDIDATE GENE POLYMORPHISMS WITH ASTHMA SEVERITY: RESULTS FROM THE GEIRD STUDY 236
Ability of different flow rates of fractional exaled nitric oxide (FeNO) to discriminate between asthmatic and no asthamatic subject 236
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 225
Cationic trypsinogen and pancreatic secretory trypsin inhibitor gene mutations in neonatal hypertrypsinaemia 221
A genome scan for allergic asthma and related phenotypes in an Italian population sample 219
A bioinformatic framework to build junction databases for the detection of alternative splicing isoforms from Next Generation Sequencing data 219
Analisi del riarrangiamento bcr-abl in alcuni pazienti affetti da leucemia mieloide cronica 214
Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in idiopathic pancreatitis. 213
SNP detection by RNA-seq 213
Detection of allele-specific gene expression on next generation sequencing data 212
ALOX5AP gene variants and risk of coronary artery disease: an angiography-based study 209
An assessment of chimeric transcript detection in CML patients after bone marrow transplantation 207
A1298C methylentetrahydrofolate reductase mutation and coronary artery disease:relationship with C677T polymorphysm and homocystein/folate metabolism 205
Cyclooxygenase 2, toll-like receptor 4 and interleukin 1beta mRNA expression in atherosclerotic plaques of type 2 diabetic patients. 205
Associazione di polimorfismi del cluster dei geni FADS1 e FADS2 con i livelli di acidi grassi polinsaturi in malattie coronariche 204
Family based association analysis of TGFB1 as modifier gene in Cystic Fibrosis 204
CACNA1E variants affect beta cell function in patients with newly diagnosed type 2 diabetes. the Verona newly diagnosed type 2 diabetes study (VNDS) 3. 203
Imputation reliability on DNA biallelic markers for drug metabolism studies 203
A 931 +2T-C transition in one COL1A2 allele causes exon 16 skipping in pro alpha 2(I) mRNA and produces moderately severe OI 202
A genetic risk factor for vascular disease which leads to mild hyperhomocysteinemia is common in northern Italy. 202
Analisi multilocus per l’identificazione di un genotipo di rischio in Malattie Cardiovascolari 202
A computational method to test for genetic relatedness in unrelated individuals 200
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 199
Association analysis of candidate gene polymorphisms in Asthma, Rhinitis and Chronic Bronchitis: preliminary results from the GEIRD study 197
A novel synonymous substitution in the GCK gene causes aberrant splicing in an Italian patient with GCK-MODY phenotype 196
Affected sib-pair and mutation analyses of the high affinity IgE receptor beta chain locus in Italian families with atopic asthmatic children 195
A method to target individuals with an unusual genetic background and to tag SNPs for linkage disequilibrium (LD) mapping 195
A method to detect individuals with different genetic background in case-control studies 194
Novel serum paraoxonase activity assays are associated with coronary artery disease 193
Analisi del gene TGFb1 quale possibile modificatore del fenotipo in fibrosi cistica 193
Gene Environment Interactions in Respiratory Diseases – Protocol, Standard Operative Procedures and Questionnaires 192
Family based association analysis of TGFB1 as modifier gene in Cystic Fibrosis 192
IFRD1 gene polymorphisms are associated with nasal polyposis in cystic fibrosis patients 191
Association of a Lymphotoxin alpha gene polymorphism and atopy in Italian families. 190
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 189
The Gene-Environment Interactions in Respiratory Diseases (GEIRD) Project 188
Association of IL4Ra gene with severity of lung disease in Cystic Fibrosis 188
Candidate genes and a genome-wide search in Italian families with atopic asthmatic children 185
Analisi di 51 polimorfismi in 35 geni dell’infiammazione per la valutazione del rischio di coronaropatia e di infarto del miocardio 185
The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families 184
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. 183
doRNA-seq: uno script per automatizzare l’analisi RNA-seq 182
COX-2 promoter region polymorphisms in multiple sclerosis: lack of association of -765G>C with disease risk 181
Polymorphism -2604G>A variants in TLR4 promoter are associated with different gene expression level in peripheral blood of atherosclerotic patients. 181
ApoC-III gene polymorphisms and risk of coronary artery disease 180
Biochemical and genetic markers of iron status and the risk of coronary disease 180
A new approach to identify non-pathogenic mutations. An analysis of the cystic fibrosis transmembrane regulator gene in normal individuals. 179
Different suppression of Ph1 positive hemopoiesis induced by intensive chemotherapy in lymphoid and myeloid blast crisis of CML 178
A large-scale study of the random variability of a coding sequence: a study on the CFTR gene 178
Association of the IL33 gene region with childhood allergic asthma 178
Genetic variability of G6PC2 influences beta cell function and insulin sensitivity in patients with newly diagnosed type 2 diabetes 178
Upregulated expression of toll-like receptor 4 in peripheral blood of ischaemic stroke patients correlates with cyclooxygenase 2 expression. 178
Analisi funzionale di polimorfismi nel promotore del gene PLA2G7. 177
Acquired and genetic determinants of homocysteine in atheromatous renel artery stenosis with mild renal insufficiency 177
CFTR and cationic trypsinogen gene mutations in idiopathic pancreatitis and neonatal hypertrypsinemia 176
Haplotype analysis of collagen type I genes in the general population and in osteogenesis imperfecta families. 175
Genomic and proteomic investigation into non-syndromic aneurysms of the human ascending aorta. 175
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations 174
Allelic frequencies of FBN1 gene polymorphisms and genetic analysis of Italian families with Marfan syndrome 174
Analisi di espressione genica in aneurismi non sindromici dell’aorta ascendente 174
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 174
High levels of COX-2 gene expression in peripheral blood of cardioembolic and atherothrombotic stroke patients 173
Case-control association analysis of candidate genes in asthma, rhinitis and COPD: A preliminary report 173
Potential role of MTNR1B locus in regulating beta cell function and glucose levels in patients with newly diagnosed type 2 diabetes 173
Frequency distribution of the alleles of several variable number of tandem repeat DNA polymorphisms in the Italian population 172
Reply to Novelli 172
Complete mutational screening of the CFTR gene in 120 patients with pulmonary disease. 172
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. 172
Proteomic investigation into nonsyndromic aneurysm of the human ascenging aorta 171
Linkage to atopy on chromosome 19 in north-eastern Italian families with allergic asthma 170
Analisi di linkage in famiglie con carcinoma mammario ereditario. 170
Combined effect of hemostatic gene polymorphisms and the risk of myocardial infarction in patients with advanced coronary atherosclerosis. 170
Candidate gene polymorphisms in cardiovascular disease: A comparative study of frequencies between a French and an Italian population 169
CD45 and multiple sclerosis: the exon 4 C77G polymorphism (additional studies and meta-analysis) and new markers 169
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. 169
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically proven coronary artery disease. 169
Espressione dei geni COX-2 e TLR4 nel sangue periferico di pazienti con ictus ischemico. 169
Hyperhomocysteinemia and Mortality after Coronary Artery Bypass Grafting 168
Reconstruction and functional analysis of altered molecular pathways in human atherosclerotic arteries 168
Hyperhomocysteinemia and mortality after coronary artery by-pass grafing. 167
Body mass index is a potential modifier of the influence on beta cell function exerted by SLC30A8 and KCNJ11 diabetes risk variants in patients with newly diagnosed type 2 diabetes 167
Studies on sporadic non-syndromic thoracic aortic aneurysms: II. Alterations of extra-cellular matrix components and focal adhesion proteins 167
Forensic applications of molecular genetic analysis: an Italian collaborative study on paternity testing by the determination of variable number of tandem repeat DNA polymorphisms 166
Chromosome 14 linkage analysis and mutation study of two serpin genes in allergic asthmatic families 165
La placca carotidea sintomatica: caratterizzazionegenetica, istopatologica e per immagini 165
Association of childhood allergic asthma with markers flanking the IL33 gene in Italian families. 165
A computational test for biological relatedness in genetic association studies using probabilistically inferred haplotypes 164
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 163
Allele frequencies of six highly polymorphic DNA loci in the Croatian population 163
Cromosoma 19 e asma atopica in famiglie Italiane 163
A novel nonsense mutation in the PKD1 gene (C3817T) is associated with autosomal dominant polycystic kidney disease (ADPKD) in a large three-generation Italian family 162
Totale 19.440
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Categoria #
all - tutte 178.103
article - articoli 110.615
book - libri 598
conference - conferenze 65.688
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.202
Totale 356.206
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.999 0 0 0 0 0 465 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
2025/202616.793 1.718 1.270 1.984 3.917 6.375 1.529 0 0 0 0 0 0
Totale 57.977