MALERBA, Giovanni
 Distribuzione geografica
Continente #
EU - Europa 16.757
NA - Nord America 16.086
AS - Asia 9.311
SA - Sud America 1.442
AF - Africa 214
OC - Oceania 66
Continente sconosciuto - Info sul continente non disponibili 8
AN - Antartide 1
Totale 43.885
Nazione #
US - Stati Uniti d'America 15.785
RU - Federazione Russa 6.274
SG - Singapore 3.363
CN - Cina 3.239
GB - Regno Unito 3.062
IT - Italia 1.942
DE - Germania 1.195
BR - Brasile 1.160
SE - Svezia 1.069
HK - Hong Kong 853
FI - Finlandia 817
IE - Irlanda 761
FR - Francia 749
VN - Vietnam 575
KR - Corea 307
IN - India 186
CA - Canada 184
UA - Ucraina 165
JP - Giappone 140
BE - Belgio 122
NL - Olanda 118
ID - Indonesia 115
AR - Argentina 111
TR - Turchia 106
ES - Italia 100
PL - Polonia 97
MX - Messico 82
BD - Bangladesh 69
AT - Austria 65
ZA - Sudafrica 58
PK - Pakistan 53
AU - Australia 49
IR - Iran 46
TW - Taiwan 40
EC - Ecuador 37
CH - Svizzera 36
CL - Cile 32
IQ - Iraq 27
LT - Lituania 26
PE - Perù 26
TG - Togo 25
VE - Venezuela 25
BJ - Benin 23
CZ - Repubblica Ceca 21
CM - Camerun 20
GR - Grecia 20
SA - Arabia Saudita 20
CO - Colombia 19
UZ - Uzbekistan 18
NZ - Nuova Zelanda 17
AE - Emirati Arabi Uniti 16
IL - Israele 16
MA - Marocco 16
MY - Malesia 16
JO - Giordania 14
PY - Paraguay 13
TH - Thailandia 13
CI - Costa d'Avorio 12
UY - Uruguay 12
KE - Kenya 11
KZ - Kazakistan 11
DK - Danimarca 10
RO - Romania 10
AZ - Azerbaigian 9
BG - Bulgaria 9
HR - Croazia 9
LV - Lettonia 9
PH - Filippine 9
DZ - Algeria 8
HU - Ungheria 8
NG - Nigeria 8
NP - Nepal 8
PT - Portogallo 8
TN - Tunisia 8
CR - Costa Rica 7
KG - Kirghizistan 7
PA - Panama 7
BO - Bolivia 6
EE - Estonia 6
EG - Egitto 6
RS - Serbia 6
SK - Slovacchia (Repubblica Slovacca) 6
SN - Senegal 6
EU - Europa 5
HN - Honduras 5
MK - Macedonia 5
AL - Albania 4
BA - Bosnia-Erzegovina 4
BY - Bielorussia 4
LB - Libano 4
MO - Macao, regione amministrativa speciale della Cina 4
NO - Norvegia 4
OM - Oman 4
DO - Repubblica Dominicana 3
GE - Georgia 3
IS - Islanda 3
KH - Cambogia 3
MT - Malta 3
PS - Palestinian Territory 3
SC - Seychelles 3
Totale 43.833
Città #
Southend 2.425
Moscow 2.125
Ashburn 2.120
Dallas 2.069
Chandler 1.874
Singapore 1.440
Jacksonville 1.324
Verona 899
Woodbridge 864
Ann Arbor 841
Hong Kong 810
Dublin 756
Beijing 665
New York 493
Houston 461
Wilmington 299
Los Angeles 288
Munich 276
Lawrence 264
Princeton 261
Helsinki 240
The Dalles 222
Jinan 210
Nanjing 196
Boardman 172
Ho Chi Minh City 160
Shenyang 152
Dong Ket 136
Turku 134
São Paulo 131
Tianjin 129
Milan 121
Hebei 116
Brussels 110
Tokyo 110
Redondo Beach 105
Buffalo 103
Sindelfingen 103
Columbus 101
Santa Clara 99
Redmond 86
Hanoi 85
Changsha 81
Jakarta 81
London 80
Seattle 80
Seoul 77
Warsaw 76
Montreal 74
Zhengzhou 72
Haikou 68
Nanchang 68
Ningbo 67
Guangzhou 63
Chicago 56
Nuremberg 55
Taizhou 55
Washington 55
San Francisco 54
Hangzhou 53
Denver 51
Taiyuan 51
Jiaxing 49
Brooklyn 48
Atlanta 47
Falls Church 47
Lancaster 46
Phoenix 45
Stockholm 45
Dearborn 44
Redwood City 44
Chennai 43
Kent 43
Norwalk 43
Toronto 42
Council Bluffs 41
Poplar 41
Amsterdam 40
Lappeenranta 40
Düsseldorf 39
Vienna 38
Boston 36
Rio de Janeiro 34
Johannesburg 32
Oxford 32
Padova 32
Madrid 31
Belo Horizonte 30
Orem 30
Falkenstein 29
Frankfurt am Main 29
Auburn Hills 28
Fuzhou 27
Parma 26
Lanzhou 25
Lomé 25
Melbourne 25
Mexico City 25
Shanghai 25
Manchester 24
Totale 26.262
Nome #
A broad overview of genotype imputation: Standard guidelines, approaches, and future investigations in genomic association studies 617
A preliminary microRNA analysis of non syndromic thoracic aortic aneurysms 502
Common Variants Associated to Type 2 Diabetes in the Italian Population 454
Identification of granulocytic myeloid-derived suppressor cells (G-MDSCs) in the peripheral blood of Hodgkin and non-Hodgkin lymphoma patients 424
Resistome, mobilome and virulome analysis of shewanella algae and vibrio spp. Strains isolated in italian aquaculture centers 369
SNPs in FAM13A and IL2RB genes are associated with FeNO in adult subjects with asthma 345
16S rRNA gene amplicons and taxonomic classification of oral microbiome 287
Effects of Duplex-specific nuclease on human cells expression profiling using RNA-seq 286
A study to find sequence motifs that affect splicing of exons regulated by RBM20 273
α1-Antitrypsin TAQ I polymorphism and α1-antichymotrypsin mutations in patients with obstructive pulmonary disease 261
An Interleukin 13 polymorphism is associated with symptom severity in adult subjects with ever asthma 259
Biopsychosocial model of resilience in young adults with multiple sclerosis (BPS-ARMS): an observational study protocol exploring psychological reactions early after diagnosis 258
An integrated approach identifies new oncotargets in melanoma 253
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 232
ASSOCIATION ANALYSIS OF CANDIDATE GENE POLYMORPHISMS WITH ASTHMA SEVERITY: RESULTS FROM THE GEIRD STUDY 232
Virulence and antibiotic resistance of Achromobacter spp. isolates from chronic and occasional lung infection in cystic fibrosis patients 226
Empowering bulk RNA-seq deconvolution algorithms by integrating multiple transcriptomics datasets 222
Association of functional gene variants in the regulatory regions of COX-2 gene (PTGS2) with nonmelanoma skin cancer after organ transplantation. 219
STUDIO PILOTA SULL’ANALISI DEL MICROBIOTA E DEL MICROBIOMA ORALE PRIMA E DOPO L’ESTRAZIONE DEGLI OTTAVI INFERIORI CON L’UTILIZZO DEL PROBIOTICO CURASEPT PREVENT 215
A bioinformatic framework to build junction databases for the detection of alternative splicing isoforms from Next Generation Sequencing data 214
A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans. 213
A genome scan for allergic asthma and related phenotypes in an Italian population sample 213
PTCH1 gene haplotype association with basal cell carcinoma after transplantation. 211
Association of CTR and COLIA1 alleles with BMD values in peri and postmenopausal women 210
AUMENTATA ESPRESSIONE DEL GENE COX-2 NEL SANGUE PERIFERICO DI PAZIENTI CON ICTUS ISCHEMICO 209
Detection of allele-specific gene expression on next generation sequencing data 208
SNP detection by RNA-seq 207
Genetic and bioinformatics analysis of four novel GCK missense variants detected in Caucasian families with GCK-MODY phenotype. 206
Identification of granulocytic myeloid-derived suppressor cells (G-MDSCs) in the peripheral blood of Hodgkin and non-Hodgkin lymphoma patients. 204
Testing the performance of the imputation of MHC region in large datasets when using different reference panels 203
ALOX5AP gene variants and risk of coronary artery disease: an angiography-based study 203
Analysis of the 3'UTR of the prostaglandin synthetase-2 (PTGS-2/COX-2) gene in non-melanoma skin cancer after organ transplantation 202
Associazione di polimorfismi del cluster dei geni FADS1 e FADS2 con i livelli di acidi grassi polinsaturi in malattie coronariche 201
Cyclooxygenase 2, toll-like receptor 4 and interleukin 1beta mRNA expression in atherosclerotic plaques of type 2 diabetic patients. 201
Family based association analysis of TGFB1 as modifier gene in Cystic Fibrosis 200
P139 Hypermutation as an evolutionary mechanism for Achromobacter spp. in cystic fibrosis lung infection 200
Gα15 in early onset of pancreatic ductal adenocarcinoma 200
CACNA1E variants affect beta cell function in patients with newly diagnosed type 2 diabetes. the Verona newly diagnosed type 2 diabetes study (VNDS) 3. 198
Analisi multilocus per l’identificazione di un genotipo di rischio in Malattie Cardiovascolari 197
A computational method to test for genetic relatedness in unrelated individuals 195
Association analysis of candidate gene polymorphisms in Asthma, Rhinitis and Chronic Bronchitis: preliminary results from the GEIRD study 195
Imputation reliability on DNA biallelic markers for drug metabolism studies 194
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 194
Application of the whole-transcriptome shotgun sequencing approach to the study of Philadelphia-positive acute lymphoblastic leukemia 192
A method to target individuals with an unusual genetic background and to tag SNPs for linkage disequilibrium (LD) mapping 190
Indagine sul coinvolgimento di gene LRP5 nella densità minerale ossea 189
Glutathione S-transferase and CYP1A1 gene polymorphisms and non-melanoma skin cancer risk in Italian transplanted patients. 188
Family based association analysis of TGFB1 as modifier gene in Cystic Fibrosis 188
A method to detect individuals with different genetic background in case-control studies 187
Erectile Dysfunction after Allogeneic Hematopoietic Stem Cell Transplant: Results from a Single Center Experience 187
Association of microRNA 146a polymorphism rs2910164 and the risk of melanoma in an Italian population 187
Microbial genomes metadata on public repositories: friends or foes? 187
Charcot-Marie-Tooth disease type 2E, a disorder of the cytoskeleton. 186
IFRD1 gene polymorphisms are associated with nasal polyposis in cystic fibrosis patients 186
A renal genetic risk score (GRS) is associated with kidney dysfunction in people with type 2 diabetes 186
Analisi del gene TGFb1 quale possibile modificatore del fenotipo in fibrosi cistica 185
Chronic graft versus host disease is associated with erectile dysfunction in allogeneic hematopoietic stem cell transplant patients: a single-center experience 184
Association of a Lymphotoxin alpha gene polymorphism and atopy in Italian families. 183
Association of IL4Ra gene with severity of lung disease in Cystic Fibrosis 183
Analisi di linkage di geni candidati per densità minerale 182
Candidate genes and a genome-wide search in Italian families with atopic asthmatic children 181
Analisi di 51 polimorfismi in 35 geni dell’infiammazione per la valutazione del rischio di coronaropatia e di infarto del miocardio 181
GATK hard filtering: tunable parameters to improve variant calling for next generation sequencing targeted gene panel data 181
COX-2 promoter region polymorphisms in multiple sclerosis: lack of association of -765G>C with disease risk 179
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. 179
The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families 178
Association of variant -765G>C in the PTGS2 gene promoter with melanoma in Italian patients and its relation to gene expression in dermal fibroblasts. 178
doRNA-seq: uno script per automatizzare l’analisi RNA-seq 176
The genetic background of osteoporosis in cystic fibrosis: association analysis with polymorphic markers in four candidate genes 175
Polymorphism -2604G>A variants in TLR4 promoter are associated with different gene expression level in peripheral blood of atherosclerotic patients. 175
Genetic variability of G6PC2 influences beta cell function and insulin sensitivity in patients with newly diagnosed type 2 diabetes 175
HIV-1-associated neurocognitive disorders: is HLA-C binding stability to β2-microglobulin a missing piece of the pathogenetic puzzle? 175
Characterization of transcriptional complexity during berry development in Vitis vinifera using RNA-Seq 174
Association of the IL33 gene region with childhood allergic asthma 173
Mutational and haplotype map of NOTCH3 in a cohort of Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). 173
Upregulated expression of toll-like receptor 4 in peripheral blood of ischaemic stroke patients correlates with cyclooxygenase 2 expression. 173
Association of candidate genes with FeNO in asthma: preliminary results from the Gene Environment Interactions in Respiratory Diseases (GEIRD) study 173
Towards pocket-sized genomic analyses: cross-platform benchmark of multi-organism genomic data indexing and alignment 172
PERFORMANCE ASSESSMENT OF DIFFERENT MICROARRAY GRAPE DESIGNS 171
The Runt domain of RUNX2 induces the migration of melanoma cells to bone 171
Studiare la regione HLA negli esomi 170
Pocket-sized genomics and transcriptomics analyses: a look at the newborn BioVRPi project 170
Case-control association analysis of candidate genes in asthma, rhinitis and COPD: A preliminary report 169
Potential role of MTNR1B locus in regulating beta cell function and glucose levels in patients with newly diagnosed type 2 diabetes 169
HDAC9, TWIST1 and FERD3L gene expression in asymptomatic stable and unstable carotid plaques 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. 168
Correlations between gene expression highlight a different activation of ACE/TLR4/PTGS2 signaling in symptomatic and asymptomatic plaques in atherosclerotic patients 168
Reply to Novelli 167
Espressione dei geni COX-2 e TLR4 nel sangue periferico di pazienti con ictus ischemico. 166
Linkage to atopy on chromosome 19 in north-eastern Italian families with allergic asthma 165
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically proven coronary artery disease. 164
Association of childhood allergic asthma with markers flanking the IL33 gene in Italian families. 163
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 163
Chromosome 14 linkage analysis and mutation study of two serpin genes in allergic asthmatic families 161
Association of promoter polymorphism -765G>C in the PTGS2 gene with malignant melanoma in Italian patients and its correlation to gene expression in dermal fibroblasts. 161
Enhancer of zeste 2 polycomb repressive complex 2 subunit polymorphisms in melanoma skin cancer risk 161
Identification of granulocytic myeloid-derived suppressor cells (G-MDSCs) in the peripheral blood of Hodgkin and non-Hodgkin lymphoma patients 161
Association analysis of 65 genetic polymorphisms in coronary artery disease patients 160
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 160
Family based association analysis of TGFB1 as modifier gene in Cystic Fibrosis 158
Totale 20.788
Categoria #
all - tutte 139.542
article - articoli 82.290
book - libri 0
conference - conferenze 56.706
curatela - curatele 0
other - altro 546
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 279.084


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.146 0 0 0 0 0 210 62 179 123 50 257 265
2021/20222.211 247 479 20 215 105 59 93 144 75 115 155 504
2022/20235.433 350 624 414 1.021 431 1.254 59 347 606 57 140 130
2023/20244.430 133 240 311 364 381 685 237 1.052 55 231 460 281
2024/20257.731 481 542 394 1.235 382 296 479 411 999 467 681 1.364
2025/202613.995 1.477 1.287 1.852 3.581 5.626 172 0 0 0 0 0 0
Totale 44.226