CATALOGO DEI PRODOTTI DELLA RICERCA

PIGNATTI, Pierfranco
 Distribuzione geografica
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Continente #
NA - Nord America 27.094
EU - Europa 21.698
AS - Asia 15.016
SA - Sud America 1.746
AF - Africa 319
Continente sconosciuto - Info sul continente non disponibili 136
OC - Oceania 64
AN - Antartide 1
Totale 66.074
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Nazione #
US - Stati Uniti d'America 26.701
RU - Federazione Russa 7.365
SG - Singapore 6.153
GB - Regno Unito 5.610
CN - Cina 4.848
SE - Svezia 1.606
BR - Brasile 1.424
FI - Finlandia 1.280
IT - Italia 1.276
DE - Germania 1.239
VN - Vietnam 1.218
IE - Irlanda 1.104
FR - Francia 1.078
HK - Hong Kong 1.078
KR - Corea 494
UA - Ucraina 392
IN - India 219
CA - Canada 206
JP - Giappone 171
BD - Bangladesh 156
TR - Turchia 142
BE - Belgio 141
AR - Argentina 129
NL - Olanda 124
PL - Polonia 106
MX - Messico 91
ZA - Sudafrica 90
IQ - Iraq 83
NG - Nigeria 81
ES - Italia 77
ID - Indonesia 71
AU - Australia 56
PK - Pakistan 46
LT - Lituania 42
AT - Austria 39
CL - Cile 35
VE - Venezuela 34
CH - Svizzera 33
EC - Ecuador 31
MA - Marocco 30
UZ - Uzbekistan 30
CO - Colombia 29
IR - Iran 29
SA - Arabia Saudita 29
IL - Israele 26
PH - Filippine 26
JO - Giordania 25
PY - Paraguay 25
AE - Emirati Arabi Uniti 23
CZ - Repubblica Ceca 23
CR - Costa Rica 22
EG - Egitto 21
PE - Perù 21
CM - Camerun 20
AZ - Azerbaigian 17
LV - Lettonia 17
NP - Nepal 17
TN - Tunisia 17
KE - Kenya 16
MY - Malesia 16
KZ - Kazakistan 15
PA - Panama 15
KG - Kirghizistan 14
RO - Romania 14
AL - Albania 13
BG - Bulgaria 12
HN - Honduras 12
HR - Croazia 12
JM - Giamaica 12
PT - Portogallo 12
GR - Grecia 11
TW - Taiwan 11
DZ - Algeria 10
ET - Etiopia 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
GT - Guatemala 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
BB - Barbados 4
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
Totale 65.872
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Città #
Southend 4.703
Jacksonville 3.515
Singapore 3.496
Ashburn 2.893
Chandler 2.745
Moscow 2.322
Dallas 2.108
San Jose 2.003
Woodbridge 1.903
Ann Arbor 1.383
Dublin 1.101
Hong Kong 1.060
Houston 934
Beijing 688
Verona 655
The Dalles 653
Council Bluffs 639
New York 550
Wilmington 440
Lawrence 412
Princeton 412
Ho Chi Minh City 409
Los Angeles 399
Nanjing 396
Jinan 392
Helsinki 327
Boardman 288
Munich 286
Shenyang 263
Hanoi 262
Buffalo 230
Tianjin 223
Hebei 217
Sindelfingen 183
Santa Clara 181
São Paulo 173
Changsha 161
Tokyo 153
Zhengzhou 145
Milan 136
Nanchang 136
Turku 136
Ningbo 123
Brussels 120
Hangzhou 119
Haikou 117
Dong Ket 109
Orem 103
Jiaxing 100
Warsaw 98
Guangzhou 93
Columbus 90
Seoul 90
Lancaster 89
Redondo Beach 89
Taizhou 87
Taiyuan 83
Dearborn 78
San Francisco 76
Seattle 74
Abuja 71
Montreal 71
Chicago 67
London 67
Chennai 66
Toronto 66
Frankfurt am Main 62
Brooklyn 60
Philadelphia 60
Norwalk 57
Stockholm 57
Washington 56
Johannesburg 54
Rio de Janeiro 52
Denver 50
Kent 50
Atlanta 49
Fuzhou 47
Phoenix 46
Rome 46
Lanzhou 45
Amsterdam 44
Auburn Hills 43
Da Nang 40
Poplar 40
Falls Church 39
Baghdad 37
Belo Horizonte 35
Boston 34
Falkenstein 34
Haiphong 34
Manchester 34
Fairfield 32
Redwood City 32
Tashkent 30
Brasília 28
Mexico City 28
Mumbai 28
Düsseldorf 27
Ankara 26
Totale 43.293
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Nome #
A preliminary microRNA analysis of non syndromic thoracic aortic aneurysms 530
Effects of Duplex-specific nuclease on human cells expression profiling using RNA-seq 316
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 296
A 48-bp insertion between exon 13 and 14 of the HEXB gene causes infantile-onset Sandhoff disease 286
α1-Antitrypsin TAQ I polymorphism and α1-antichymotrypsin mutations in patients with obstructive pulmonary disease 284
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 272
Ability of different flow rates of fractional exaled nitric oxide (FeNO) to discriminate between asthmatic and no asthamatic subject 271
ASSOCIATION ANALYSIS OF CANDIDATE GENE POLYMORPHISMS WITH ASTHMA SEVERITY: RESULTS FROM THE GEIRD STUDY 270
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 262
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 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. 260
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 251
Cationic trypsinogen and pancreatic secretory trypsin inhibitor gene mutations in neonatal hypertrypsinaemia 249
SNP detection by RNA-seq 248
A bioinformatic framework to build junction databases for the detection of alternative splicing isoforms from Next Generation Sequencing data 247
A genome scan for allergic asthma and related phenotypes in an Italian population sample 243
ALOX5AP gene variants and risk of coronary artery disease: an angiography-based study 240
A1298C methylentetrahydrofolate reductase mutation and coronary artery disease:relationship with C677T polymorphysm and homocystein/folate metabolism 236
Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in idiopathic pancreatitis. 236
Cyclooxygenase 2, toll-like receptor 4 and interleukin 1beta mRNA expression in atherosclerotic plaques of type 2 diabetic patients. 236
Detection of allele-specific gene expression on next generation sequencing data 235
An assessment of chimeric transcript detection in CML patients after bone marrow transplantation 232
Associazione di polimorfismi del cluster dei geni FADS1 e FADS2 con i livelli di acidi grassi polinsaturi in malattie coronariche 232
Analisi del riarrangiamento bcr-abl in alcuni pazienti affetti da leucemia mieloide cronica 231
Family based association analysis of TGFB1 as modifier gene in Cystic Fibrosis 231
A genetic risk factor for vascular disease which leads to mild hyperhomocysteinemia is common in northern Italy. 230
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 230
Affected sib-pair and mutation analyses of the high affinity IgE receptor beta chain locus in Italian families with atopic asthmatic children 229
Association of a Lymphotoxin alpha gene polymorphism and atopy in Italian families. 229
Imputation reliability on DNA biallelic markers for drug metabolism studies 229
Novel serum paraoxonase activity assays are associated with coronary artery disease 226
Gene Environment Interactions in Respiratory Diseases – Protocol, Standard Operative Procedures and Questionnaires 226
Association analysis of candidate gene polymorphisms in Asthma, Rhinitis and Chronic Bronchitis: preliminary results from the GEIRD study 224
A 931 +2T-C transition in one COL1A2 allele causes exon 16 skipping in pro alpha 2(I) mRNA and produces moderately severe OI 223
A novel synonymous substitution in the GCK gene causes aberrant splicing in an Italian patient with GCK-MODY phenotype 223
Analisi multilocus per l’identificazione di un genotipo di rischio in Malattie Cardiovascolari 223
CACNA1E variants affect beta cell function in patients with newly diagnosed type 2 diabetes. the Verona newly diagnosed type 2 diabetes study (VNDS) 3. 222
A method to detect individuals with different genetic background in case-control studies 220
A computational method to test for genetic relatedness in unrelated individuals 218
Family based association analysis of TGFB1 as modifier gene in Cystic Fibrosis 217
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 216
A method to target individuals with an unusual genetic background and to tag SNPs for linkage disequilibrium (LD) mapping 215
Analisi del gene TGFb1 quale possibile modificatore del fenotipo in fibrosi cistica 214
Candidate genes and a genome-wide search in Italian families with atopic asthmatic children 212
Association of IL4Ra gene with severity of lung disease in Cystic Fibrosis 211
Analisi di 51 polimorfismi in 35 geni dell’infiammazione per la valutazione del rischio di coronaropatia e di infarto del miocardio 211
Allele frequencies of six highly polymorphic DNA loci in the Croatian population 209
The Gene-Environment Interactions in Respiratory Diseases (GEIRD) Project 207
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. 207
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 207
The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families 206
Different suppression of Ph1 positive hemopoiesis induced by intensive chemotherapy in lymphoid and myeloid blast crisis of CML 205
A new approach to identify non-pathogenic mutations. An analysis of the cystic fibrosis transmembrane regulator gene in normal individuals. 205
Combined effect of hemostatic gene polymorphisms and the risk of myocardial infarction in patients with advanced coronary atherosclerosis. 205
IFRD1 gene polymorphisms are associated with nasal polyposis in cystic fibrosis patients 205
Analisi di linkage in famiglie con carcinoma mammario ereditario. 204
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. 204
Analisi di espressione genica in aneurismi non sindromici dell’aorta ascendente 203
Polymorphism -2604G>A variants in TLR4 promoter are associated with different gene expression level in peripheral blood of atherosclerotic patients. 203
Frequency distribution of the alleles of several variable number of tandem repeat DNA polymorphisms in the Italian population 202
Analisi funzionale di polimorfismi nel promotore del gene PLA2G7. 202
Haplotype analysis of collagen type I genes in the general population and in osteogenesis imperfecta families. 202
Impact of insulin receptor substrate-1 genotypes on platelet reactivity and cardiovascular outcomes in patients with type 2 diabetes mellitus and coronary artery disease 202
Acquired and genetic determinants of homocysteine in atheromatous renel artery stenosis with mild renal insufficiency 201
doRNA-seq: uno script per automatizzare l’analisi RNA-seq 201
CFTR and cationic trypsinogen gene mutations in idiopathic pancreatitis and neonatal hypertrypsinemia 200
Association of the IL33 gene region with childhood allergic asthma 199
High levels of COX-2 gene expression in peripheral blood of cardioembolic and atherothrombotic stroke patients 199
Linkage to atopy on chromosome 19 in north-eastern Italian families with allergic asthma 198
COX-2 promoter region polymorphisms in multiple sclerosis: lack of association of -765G>C with disease risk 198
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations 197
Biochemical and genetic markers of iron status and the risk of coronary disease 197
Studies on sporadic non-syndromic thoracic aortic aneurysms: II. Alterations of extra-cellular matrix components and focal adhesion proteins 197
ApoC-III gene polymorphisms and risk of coronary artery disease 196
A large-scale study of the random variability of a coding sequence: a study on the CFTR gene 196
Genetic variability of G6PC2 influences beta cell function and insulin sensitivity in patients with newly diagnosed type 2 diabetes 196
Forensic applications of molecular genetic analysis: an Italian collaborative study on paternity testing by the determination of variable number of tandem repeat DNA polymorphisms 195
Candidate gene polymorphisms in cardiovascular disease: A comparative study of frequencies between a French and an Italian population 195
Allelic frequencies of FBN1 gene polymorphisms and genetic analysis of Italian families with Marfan syndrome 195
Genomic and proteomic investigation into non-syndromic aneurysms of the human ascending aorta. 194
Espressione dei geni COX-2 e TLR4 nel sangue periferico di pazienti con ictus ischemico. 194
Upregulated expression of toll-like receptor 4 in peripheral blood of ischaemic stroke patients correlates with cyclooxygenase 2 expression. 193
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 192
Proteomic investigation into nonsyndromic aneurysm of the human ascenging aorta 192
Reply to Novelli 191
Chromosome 14 linkage analysis and mutation study of two serpin genes in allergic asthmatic families 191
Case-control association analysis of candidate genes in asthma, rhinitis and COPD: A preliminary report 191
Potential role of MTNR1B locus in regulating beta cell function and glucose levels in patients with newly diagnosed type 2 diabetes 191
CD45 and multiple sclerosis: the exon 4 C77G polymorphism (additional studies and meta-analysis) and new markers 190
Complete mutational screening of the CFTR gene in 120 patients with pulmonary disease. 190
Association of childhood allergic asthma with markers flanking the IL33 gene in Italian families. 190
La placca carotidea sintomatica: caratterizzazionegenetica, istopatologica e per immagini 189
Bone marrow transplantation monitoring by DNA analysis 188
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. 187
A computational test for biological relatedness in genetic association studies using probabilistically inferred haplotypes 187
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically proven coronary artery disease. 187
Association of FcER1A and RAD50 polymorphisms with serum IgE levels, asthma and rhinitis 187
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 187
Hyperhomocysteinemia and Mortality after Coronary Artery Bypass Grafting 186
Cromosoma 19 e asma atopica in famiglie Italiane 186
Totale 21.924
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Categoria #
all - tutte 209.283
article - articoli 131.040
book - libri 698
conference - conferenze 76.159
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.386
Totale 418.566
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20222.956 0 841 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
2025/202624.136 1.718 1.270 1.984 3.917 6.375 1.745 2.244 1.101 1.709 1.377 227 469
2026/2027754 233 521 0 0 0 0 0 0 0 0 0 0
Totale 66.074