MALERBA, Giovanni
 Distribuzione geografica
Continente #
NA - Nord America 19.322
EU - Europa 17.679
AS - Asia 11.807
SA - Sud America 1.660
AF - Africa 367
OC - Oceania 80
Continente sconosciuto - Info sul continente non disponibili 9
AN - Antartide 1
Totale 50.925
Nazione #
US - Stati Uniti d'America 18.950
RU - Federazione Russa 6.287
SG - Singapore 4.560
CN - Cina 3.431
GB - Regno Unito 3.186
IT - Italia 2.389
BR - Brasile 1.294
DE - Germania 1.236
VN - Vietnam 1.105
SE - Svezia 1.079
HK - Hong Kong 903
FI - Finlandia 857
FR - Francia 787
IE - Irlanda 771
KR - Corea 405
IN - India 279
CA - Canada 225
UA - Ucraina 184
JP - Giappone 174
NL - Olanda 146
AR - Argentina 133
TR - Turchia 132
ES - Italia 131
ID - Indonesia 130
BD - Bangladesh 128
BE - Belgio 126
PL - Polonia 122
MX - Messico 92
ZA - Sudafrica 83
PK - Pakistan 82
IQ - Iraq 77
NG - Nigeria 73
AT - Austria 71
AU - Australia 62
CH - Svizzera 50
EC - Ecuador 50
IR - Iran 47
CL - Cile 42
TW - Taiwan 42
SA - Arabia Saudita 36
VE - Venezuela 36
UZ - Uzbekistan 34
LT - Lituania 33
CO - Colombia 30
MY - Malesia 27
PE - Perù 27
TG - Togo 26
JO - Giordania 24
MA - Marocco 24
BJ - Benin 23
CI - Costa d'Avorio 23
CZ - Repubblica Ceca 23
GR - Grecia 22
PY - Paraguay 22
PH - Filippine 21
CM - Camerun 20
IL - Israele 19
KE - Kenya 19
TH - Thailandia 19
AE - Emirati Arabi Uniti 18
NZ - Nuova Zelanda 18
TN - Tunisia 18
AZ - Azerbaigian 17
KZ - Kazakistan 16
NP - Nepal 16
UY - Uruguay 16
HR - Croazia 15
AL - Albania 14
EG - Egitto 14
PT - Portogallo 14
RO - Romania 14
CR - Costa Rica 13
LV - Lettonia 13
DK - Danimarca 12
RS - Serbia 12
DZ - Algeria 11
HU - Ungheria 11
BG - Bulgaria 10
SI - Slovenia 10
SN - Senegal 10
BO - Bolivia 9
PA - Panama 9
KG - Kirghizistan 8
NO - Norvegia 8
EE - Estonia 7
LB - Libano 7
MK - Macedonia 7
MT - Malta 7
OM - Oman 7
HN - Honduras 6
JM - Giamaica 6
PS - Palestinian Territory 6
SK - Slovacchia (Repubblica Slovacca) 6
CY - Cipro 5
DO - Repubblica Dominicana 5
EU - Europa 5
GE - Georgia 5
KH - Cambogia 5
BA - Bosnia-Erzegovina 4
BY - Bielorussia 4
Totale 50.847
Città #
Ashburn 2.843
Singapore 2.504
Southend 2.425
Moscow 2.129
Dallas 2.082
Chandler 1.874
San Jose 1.504
Jacksonville 1.329
Verona 1.223
Woodbridge 864
Hong Kong 848
Ann Arbor 841
Dublin 766
Beijing 672
New York 543
Houston 471
The Dalles 471
Ho Chi Minh City 349
Los Angeles 333
Wilmington 299
Helsinki 278
Munich 276
Lawrence 264
Princeton 261
Hanoi 222
Jinan 210
Nanjing 196
Boardman 174
Shenyang 152
São Paulo 150
Tokyo 140
Santa Clara 138
Dong Ket 136
Tianjin 136
Turku 134
Milan 128
Buffalo 123
Hebei 116
Brussels 114
Council Bluffs 109
Orem 107
London 106
Redondo Beach 105
Sindelfingen 103
Columbus 101
Warsaw 98
Montreal 95
Redmond 86
Jakarta 85
Seattle 84
Changsha 81
Seoul 78
Zhengzhou 72
Chennai 69
Haikou 68
Nanchang 68
Guangzhou 67
Ningbo 67
Frankfurt am Main 64
Chicago 62
Abuja 59
Phoenix 59
San Francisco 57
Toronto 57
Denver 56
Nuremberg 56
Washington 56
Amsterdam 55
Atlanta 55
Stockholm 55
Taizhou 55
Hangzhou 54
Brooklyn 53
Taiyuan 51
Jiaxing 49
Falls Church 47
Johannesburg 46
Lancaster 46
Poplar 46
Dearborn 44
Madrid 44
Redwood City 44
Kent 43
Norwalk 43
Lappeenranta 42
Rio de Janeiro 42
Boston 41
Manchester 41
Vienna 40
Düsseldorf 39
Rome 36
Shanghai 35
Da Nang 33
Haiphong 33
Istanbul 33
Paris 33
Oxford 32
Padova 32
Ankara 31
Belo Horizonte 31
Totale 31.297
Nome #
A broad overview of genotype imputation: Standard guidelines, approaches, and future investigations in genomic association studies 709
A preliminary microRNA analysis of non syndromic thoracic aortic aneurysms 526
Common Variants Associated to Type 2 Diabetes in the Italian Population 491
Identification of granulocytic myeloid-derived suppressor cells (G-MDSCs) in the peripheral blood of Hodgkin and non-Hodgkin lymphoma patients 457
Resistome, mobilome and virulome analysis of shewanella algae and vibrio spp. Strains isolated in italian aquaculture centers 387
SNPs in FAM13A and IL2RB genes are associated with FeNO in adult subjects with asthma 376
16S rRNA gene amplicons and taxonomic classification of oral microbiome 329
Effects of Duplex-specific nuclease on human cells expression profiling using RNA-seq 314
A study to find sequence motifs that affect splicing of exons regulated by RBM20 306
An Interleukin 13 polymorphism is associated with symptom severity in adult subjects with ever asthma 304
Biopsychosocial model of resilience in young adults with multiple sclerosis (BPS-ARMS): an observational study protocol exploring psychological reactions early after diagnosis 301
An integrated approach identifies new oncotargets in melanoma 287
α1-Antitrypsin TAQ I polymorphism and α1-antichymotrypsin mutations in patients with obstructive pulmonary disease 283
Empowering bulk RNA-seq deconvolution algorithms by integrating multiple transcriptomics datasets 280
ASSOCIATION ANALYSIS OF CANDIDATE GENE POLYMORPHISMS WITH ASTHMA SEVERITY: RESULTS FROM THE GEIRD STUDY 266
Virulence and antibiotic resistance of Achromobacter spp. isolates from chronic and occasional lung infection in cystic fibrosis patients 258
Association of functional gene variants in the regulatory regions of COX-2 gene (PTGS2) with nonmelanoma skin cancer after organ transplantation. 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
PTCH1 gene haplotype association with basal cell carcinoma after transplantation. 246
A bioinformatic framework to build junction databases for the detection of alternative splicing isoforms from Next Generation Sequencing data 245
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 244
SNP detection by RNA-seq 243
A genome scan for allergic asthma and related phenotypes in an Italian population sample 238
Association of CTR and COLIA1 alleles with BMD values in peri and postmenopausal women 237
A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans. 235
ALOX5AP gene variants and risk of coronary artery disease: an angiography-based study 235
Identification of granulocytic myeloid-derived suppressor cells (G-MDSCs) in the peripheral blood of Hodgkin and non-Hodgkin lymphoma patients. 234
AUMENTATA ESPRESSIONE DEL GENE COX-2 NEL SANGUE PERIFERICO DI PAZIENTI CON ICTUS ISCHEMICO 233
Application of the whole-transcriptome shotgun sequencing approach to the study of Philadelphia-positive acute lymphoblastic leukemia 232
Cyclooxygenase 2, toll-like receptor 4 and interleukin 1beta mRNA expression in atherosclerotic plaques of type 2 diabetic patients. 232
Gα15 in early onset of pancreatic ductal adenocarcinoma 232
Genetic and bioinformatics analysis of four novel GCK missense variants detected in Caucasian families with GCK-MODY phenotype. 231
Detection of allele-specific gene expression on next generation sequencing data 231
Testing the performance of the imputation of MHC region in large datasets when using different reference panels 230
Associazione di polimorfismi del cluster dei geni FADS1 e FADS2 con i livelli di acidi grassi polinsaturi in malattie coronariche 229
Association of a Lymphotoxin alpha gene polymorphism and atopy in Italian families. 227
Analysis of the 3'UTR of the prostaglandin synthetase-2 (PTGS-2/COX-2) gene in non-melanoma skin cancer after organ transplantation 227
Family based association analysis of TGFB1 as modifier gene in Cystic Fibrosis 227
A renal genetic risk score (GRS) is associated with kidney dysfunction in people with type 2 diabetes 226
Glutathione S-transferase and CYP1A1 gene polymorphisms and non-melanoma skin cancer risk in Italian transplanted patients. 224
Imputation reliability on DNA biallelic markers for drug metabolism studies 224
P139 Hypermutation as an evolutionary mechanism for Achromobacter spp. in cystic fibrosis lung infection 224
Towards pocket-sized genomic analyses: cross-platform benchmark of multi-organism genomic data indexing and alignment 222
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
Analisi multilocus per l’identificazione di un genotipo di rischio in Malattie Cardiovascolari 221
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
Association analysis of candidate gene polymorphisms in Asthma, Rhinitis and Chronic Bronchitis: preliminary results from the GEIRD study 216
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
GATK hard filtering: tunable parameters to improve variant calling for next generation sequencing targeted gene panel data 214
Erectile Dysfunction after Allogeneic Hematopoietic Stem Cell Transplant: Results from a Single Center Experience 214
A computational method to test for genetic relatedness in unrelated individuals 213
Chronic graft versus host disease is associated with erectile dysfunction in allogeneic hematopoietic stem cell transplant patients: a single-center experience 212
Association of microRNA 146a polymorphism rs2910164 and the risk of melanoma in an Italian population 212
Analisi del gene TGFb1 quale possibile modificatore del fenotipo in fibrosi cistica 211
HIV-1-associated neurocognitive disorders: is HLA-C binding stability to β2-microglobulin a missing piece of the pathogenetic puzzle? 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 linkage di geni candidati per densità minerale 207
Indagine sul coinvolgimento di gene LRP5 nella densità minerale ossea 206
Analisi di 51 polimorfismi in 35 geni dell’infiammazione per la valutazione del rischio di coronaropatia e di infarto del miocardio 206
Microbial genomes metadata on public repositories: friends or foes? 206
Charcot-Marie-Tooth disease type 2E, a disorder of the cytoskeleton. 204
IFRD1 gene polymorphisms are associated with nasal polyposis in cystic fibrosis patients 204
Pocket-sized genomics and transcriptomics analyses: a look at the newborn BioVRPi project 204
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
The genetic background of osteoporosis in cystic fibrosis: association analysis with polymorphic markers in four candidate genes 201
The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families 201
Association of variant -765G>C in the PTGS2 gene promoter with melanoma in Italian patients and its relation to gene expression in dermal fibroblasts. 201
Association of candidate genes with FeNO in asthma: preliminary results from the Gene Environment Interactions in Respiratory Diseases (GEIRD) study 201
Polymorphism -2604G>A variants in TLR4 promoter are associated with different gene expression level in peripheral blood of atherosclerotic patients. 200
Correlations between gene expression highlight a different activation of ACE/TLR4/PTGS2 signaling in symptomatic and asymptomatic plaques in atherosclerotic patients 200
PERFORMANCE ASSESSMENT OF DIFFERENT MICROARRAY GRAPE DESIGNS 199
Studiare la regione HLA negli esomi 199
HDAC9, TWIST1 and FERD3L gene expression in asymptomatic stable and unstable carotid plaques 198
Linkage to atopy on chromosome 19 in north-eastern Italian families with allergic asthma 197
doRNA-seq: uno script per automatizzare l’analisi RNA-seq 197
Association of the IL33 gene region with childhood allergic asthma 194
Mutational and haplotype map of NOTCH3 in a cohort of Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). 194
COX-2 promoter region polymorphisms in multiple sclerosis: lack of association of -765G>C with disease risk 193
Characterization of transcriptional complexity during berry development in Vitis vinifera using RNA-Seq 193
The Runt domain of RUNX2 induces the migration of melanoma cells to bone 193
Identification of granulocytic myeloid-derived suppressor cells (G-MDSCs) in the peripheral blood of Hodgkin and non-Hodgkin lymphoma patients 193
Interleukin-28B polymorphisms, IP-10 and viral load predict virological response to therapy in chronic hepatitis C under real-life conditions 192
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. 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
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
Case-control association analysis of candidate genes in asthma, rhinitis and COPD: A preliminary report 189
Identification of granulocytic myeloid-derived suppressor cells (G-MDSCs) in the peripheral blood of Hodgkin and non-Hodgkin lymphoma patients 188
Adaptive Interactions of Achromobacter spp. with Pseudomonas aeruginosa in Cystic Fibrosis Chronic Lung Co-Infection 188
Chromosome 14 linkage analysis and mutation study of two serpin genes in allergic asthmatic families 187
Enhancer of zeste 2 polycomb repressive complex 2 subunit polymorphisms in melanoma skin cancer risk 187
Analyzing BioRad-Illumina Single Cell RNA-Seq data with open source tools 186
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
Totale 23.632
Categoria #
all - tutte 153.287
article - articoli 90.703
book - libri 0
conference - conferenze 61.996
curatela - curatele 0
other - altro 588
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 306.574


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021572 0 0 0 0 0 0 0 0 0 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
2025/202621.041 1.477 1.287 1.852 3.581 5.626 1.493 1.922 1.046 1.549 1.208 0 0
Totale 51.272