ArTS Archivio della ricerca di Trieste

GASPARINI, PAOLO
 Distribuzione geografica
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Continente #
NA - Nord America 37.626
EU - Europa 21.744
AS - Asia 19.840
SA - Sud America 2.369
AF - Africa 516
OC - Oceania 82
Continente sconosciuto - Info sul continente non disponibili 40
Totale 82.217
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Nazione #
US - Stati Uniti d'America 37.203
SG - Singapore 7.453
PL - Polonia 6.421
CN - Cina 4.536
IT - Italia 3.223
UA - Ucraina 2.403
SE - Svezia 2.176
HK - Hong Kong 2.107
VN - Vietnam 1.953
BR - Brasile 1.860
KR - Corea 1.240
DE - Germania 1.207
FR - Francia 1.103
TR - Turchia 913
GB - Regno Unito 908
FI - Finlandia 866
RU - Federazione Russa 753
NL - Olanda 535
IE - Irlanda 527
BG - Bulgaria 521
CH - Svizzera 424
IN - India 372
JP - Giappone 185
AR - Argentina 178
CA - Canada 175
MX - Messico 153
BD - Bangladesh 151
AT - Austria 147
BE - Belgio 139
MA - Marocco 130
PH - Filippine 118
ZA - Sudafrica 111
IQ - Iraq 99
ES - Italia 94
ID - Indonesia 88
EC - Ecuador 86
PK - Pakistan 74
SA - Arabia Saudita 74
CZ - Repubblica Ceca 70
SN - Senegal 69
AU - Australia 65
UZ - Uzbekistan 58
CL - Cile 53
VE - Venezuela 52
TH - Thailandia 50
IL - Israele 48
CO - Colombia 45
JO - Giordania 41
DZ - Algeria 37
KE - Kenya 35
EG - Egitto 34
PE - Perù 34
AE - Emirati Arabi Uniti 31
MY - Malesia 30
PY - Paraguay 30
LT - Lituania 28
EU - Europa 27
GR - Grecia 26
AZ - Azerbaigian 23
TW - Taiwan 23
IR - Iran 20
RO - Romania 20
OM - Oman 19
PT - Portogallo 19
HU - Ungheria 18
JM - Giamaica 18
TN - Tunisia 18
BO - Bolivia 17
PS - Palestinian Territory 16
AL - Albania 15
DK - Danimarca 15
KZ - Kazakistan 15
CI - Costa d'Avorio 14
NP - Nepal 14
NZ - Nuova Zelanda 14
CR - Costa Rica 13
DO - Repubblica Dominicana 13
LB - Libano 13
KG - Kirghizistan 12
BY - Bielorussia 11
HR - Croazia 11
NG - Nigeria 11
SK - Slovacchia (Repubblica Slovacca) 11
LK - Sri Lanka 10
NO - Norvegia 10
QA - Qatar 10
TT - Trinidad e Tobago 10
NI - Nicaragua 9
UY - Uruguay 9
XK - ???statistics.table.value.countryCode.XK??? 9
GA - Gabon 8
GE - Georgia 8
LV - Lettonia 8
AO - Angola 7
ET - Etiopia 7
RS - Serbia 7
HN - Honduras 6
PA - Panama 6
AM - Armenia 5
BH - Bahrain 5
Totale 82.096
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Città #
Warsaw 5.918
Singapore 4.105
Fairfield 3.713
Ashburn 3.600
Woodbridge 3.012
Chandler 2.442
Houston 2.213
Jacksonville 2.198
Ann Arbor 2.008
Hong Kong 2.004
Wilmington 1.902
Seattle 1.622
San Jose 1.575
Hefei 1.318
Cambridge 1.236
Seoul 1.212
Beijing 968
Princeton 926
Boardman 886
Izmir 769
Chicago 681
Trieste 640
Ho Chi Minh City 577
Dublin 517
Sofia 514
Lauterbourg 480
Los Angeles 466
Columbus 465
Hanoi 443
Zgierz 440
Bern 404
Moscow 396
The Dalles 395
Dearborn 354
Dallas 351
Milan 327
Santa Clara 302
Buffalo 301
Helsinki 279
Munich 256
Frankfurt am Main 235
San Diego 226
Düsseldorf 225
Amsterdam 205
Des Moines 177
New York 166
São Paulo 158
Council Bluffs 154
Tokyo 139
London 130
Verona 121
Brussels 118
Nuremberg 116
Dong Ket 110
Nanjing 103
Orem 94
Bremen 93
Phoenix 92
Casablanca 89
Falls Church 89
Haiphong 84
Rome 83
Da Nang 82
Guangzhou 81
Norwalk 81
Shanghai 73
Redondo Beach 71
Redwood City 70
Rio de Janeiro 70
Vienna 70
Dakar 69
Turku 62
Brno 61
Johannesburg 57
Tashkent 57
Montreal 54
Lappeenranta 53
Chennai 52
Tianjin 52
Stockholm 50
Washington 50
Kocaeli 48
Kunming 48
Brooklyn 47
Denver 47
Jinan 47
Atlanta 46
Redmond 45
Toronto 44
Mexico City 42
Turin 42
Nanchang 39
Amman 38
Baghdad 38
Fremont 38
Paris 38
Pune 38
San Francisco 38
Torino 37
Hải Dương 36
Totale 57.233
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Nome #
Il Registro Regionale delle Morti Cardiache Improvvise in età giovanile del Friuli Venezia Giulia. Protocolli operativi e risultati di un progetto multidisciplinare 612
1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function 465
PSIP1/LEDGF: A new gene likely involved in sensorineural progressive hearing loss 448
Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss 442
Brain-derived neurotrophic factor serum levels in genetically isolated populations: Gender-specific association with anxiety disorder subtypes but not with anxiety levels or Val66Met polymorphism 411
Assessment of the olfactory function in Italian patients with type 3 von Willebrand disease caused by a homozygous 253 Kb deletion involving VWF and TMEM16B/ANO2 398
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel 397
Genetic evidence for an origin of the Armenians from Bronze Age mixing of multiple populations 391
Y chromosome variation and complex traits: the Ygen consortium 388
The Role Of Personality Traits On Taste Perception and Food Preferences. 381
Global diversity in the TAS2R38 bitter taste receptor: Revisiting a classic evolutionary PROPosal 377
The p.Cys169Tyr variant of connexin 26 is not a polymorphism 367
Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals 365
Clinical and Molecular Cytogenetic Characterisation of Children with Developmental Delay and Dysmorphic Features = Klinična in Molekularna Citogenetska Obravnava Otrok Z Razvojnim Zaostankom in Displastičnimi Znaki 360
Non-additive genome-wide association scan reveals a new gene associated with habitual coffee consumption 357
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function 356
A catalog of genetic loci associated with kidney function from analyses of a million individuals. 353
Enrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populations 351
Genomic Studies in a Large Cohort of Hearing Impaired Italian Patients Revealed Several New Alleles, a Rare Case of Uniparental Disomy (UPD) and the Importance to Search for Copy Number Variations 351
Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss 348
Cx26 partial loss causes accelerated presbycusis by redox imbalance and dysregulation of Nfr2 pathway 348
The UK10K project identifies rare variants in health and disease 347
Multicohort analysis of the maternal age effect on recombination 347
Genetic structure in the Sherpa and neighboring Nepalese populations 345
Pharmacogenetics driving personalized medicine: Analysis of genetic polymorphisms related to breast cancer medications in Italian isolated populations 338
Modulation of genetic associations with serum urate levels by body-mass-index in humans 334
Genetic testing and genomic analysis: A debate on ethical, social and legal issues in the Arab world with a focus on Qatar 330
Mutations in L-type amino acid transporter-2 support SLC7A8 as a novel gene involved in age-related hearing loss 329
Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss 326
Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers 315
Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversity. 314
PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity 311
Genetic Landscape of Slovenians: Past Admixture and Natural Selection Pattern 310
Whole-genome sequencing reveals new insights into age-related hearing loss: cumulative effects, pleiotropy and the role of selection 308
A genome-wide association study identifies an association between variants in EFCAB4B gene and periodontal disease in an Italian isolated population 305
Variation in the bitter-taste receptor gene TAS2R38, and adiposity in a genetically isolated population in Southern Italy. 302
Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6 300
Next Generation Sequencing and Animal Models Reveal SLC9A3R1 as a New Gene Involved in Human Age-Related Hearing Loss 298
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity 288
Common variants in CLDN14 are associated with differential excretion of magnesium over calcium in urine 284
Factors influencing the phenotypic characterization of the oral marker, PROP 283
Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment 281
Joint data analysis in nutritional epidemiology: Identification of observational studies and minimal requirements 281
Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits 280
Association of a variant in the CHRNA5-A3-B4 gene cluster region to heavy smoking in the Italian population. 278
A Novel CRYBB2 Missense Mutation Causing Congenital Autosomal Dominant Cataract in an Italian Family. 278
Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits 278
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels 274
A polymorphism in the 5' UTR of the DEFB1 gene is associated with the lung phenotype in F508del homozygous Italian cystic fibrosis patients 273
Common Variants in UMOD Associate with Urinary Uromodulin Levels: A Meta-Analysis. 272
A Brief Review of Genetic Approaches to the Study of Food Preferences: Current Knowledge and Future Directions. 272
TAS2R38 bitter taste genotype is associated with complementary feeding behavior in infants 272
Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries 271
Analysis of functional variants reveals new candidate genes associated with alexithymia 270
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk 268
19p13 microduplications encompassing NFIX are responsible for intellectual disability, short stature and small head circumference 267
Genetics of Food Preferences: A First View from Silk Road Populations 260
A general approach for haplotype phasing across the full spectrum of relatedness. 258
TBL1Y: a new gene involved in syndromic hearing loss 257
Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability 256
Evidence of Inbreeding Depression on Human Height 254
Understanding the role of personality and alexithymia in food preferences and PROP taste perception 254
A novel P2RX2 mutation in an Italian family affected by autosomal dominant nonsyndromic hearing loss 251
Functional analysis of mutations in SLC7A9, and genotype-phenotype correlation in non-Type I cystinuria. 248
Genetic landscape of populations along the Silk Road: admixture and migration patterns 248
Heterogeneity in Circulating Tumor Cells: The Relevance of the Stem-Cell Subset 248
Genome-wide meta-analysis unravels interactions between magnesium homeostasis and metabolic phenotypes 247
A Meta-Analysis of Genome-Wide Association Studies of the Electrocardiographic Early Repolarization Pattern. 246
Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation 244
Associations of autozygosity with a broad range of human phenotypes 244
A case of lymphedema-distichiasis syndrome carrying a new de novo frameshift FOXC2 mutation 243
Congenital hyperinsulinism: clinical and molecular analysis of a large Italian cohort. 241
Consanguinity and Hereditary Hearing Loss in Qatar 241
Linkage Study and Exome Sequencing Identify a BDP1 Mutation Associated with Hereditary Hearing Loss 240
A “population-based approach” to study the link between TAS2R genes, taste perception and food liking. 240
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair 240
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney 240
Age- And Sex-Related Variations in Platelet Count in Italy: A Proposal of Reference Ranges Based on 40987 Subjects' Data 239
Contribution of SNP arrays in diagnosis of deletion 2p11.2-p12 239
Association analysis of bitter receptor genes in five isolated populations identifies a significant correlation between TAS2R43 variants and coffee liking. 238
A novel deletion mutation involving TMEM38B in a patient with autosomal recessive osteogenesis imperfecta 236
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals 236
A Genome-Wide Association Study in isolated populations reveals new genes associated to common food likings 233
Estrogen-related receptor gamma and hearing function: evidence of a role in humans and mice 229
Genome-wide analysis identifies 12 loci influencing human reproductive behavior. 228
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure 228
Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity 227
"A novel mutation in the Mitochondrial tRNAval gene associated with a complex neurological presentation" 226
Age-related hearing loss and level of education: an epidemiological study on a large cohort of isolated popu-lations 226
Autosomal recessive stickler syndrome due to a loss of function mutation in theCOL9A3gene 226
GJB2 and GJB6 genes and the A1555G mitochondrial mutation are only minor causes of nonsyndromic hearing loss in the Qatari population 223
The Meaning of Food Preferences in the Human Behaviour and Personalities. 222
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits 220
"A benign form of thalassemia intermedia may be determined by the interaction of triplicated alfa locus and heterozygous beta thalassemia" 217
Association of LTA gene haploblock with periodontal disease in Italian adults. 217
Factors associated with food liking and their relationship with metabolic traits in Italian cohorts 217
Next generation sequencing study in a cohort of Italian patients with syndromic hearing loss 217
"A tetranucleotide repeat polymorphism in the cystic fibrosis gene" 216
Connexin 26 variant carriers have a better gastrointestinal health: is this the heterozygote advantage? 216
Genome-wide association analysis on five isolated populations identifies variants of the HLA-DOA gene associated with white wine liking 215
Totale 29.086
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Categoria #
all - tutte 242.648
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 242.648
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.790 0 0 0 0 0 0 0 0 0 892 222 676
2021/20224.892 203 355 279 419 195 394 227 182 651 550 380 1.057
2022/20237.664 762 737 436 1.046 864 1.453 77 740 871 92 446 140
2023/20244.955 624 310 316 397 539 407 783 847 69 134 247 282
2024/202510.013 152 423 989 777 890 1.385 438 722 1.179 1.031 1.003 1.024
2025/202623.017 2.251 1.835 1.904 1.963 2.132 2.650 3.732 836 2.839 2.875 0 0
Totale 83.523