ArTS Archivio della ricerca di Trieste

GASPARINI, PAOLO
 Distribuzione geografica
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Continente #
NA - Nord America 39.318
EU - Europa 22.246
AS - Asia 20.439
SA - Sud America 2.364
AF - Africa 515
OC - Oceania 84
Continente sconosciuto - Info sul continente non disponibili 40
Totale 85.006
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Nazione #
US - Stati Uniti d'America 38.808
SG - Singapore 7.465
PL - Polonia 6.425
CN - Cina 4.566
IT - Italia 3.700
UA - Ucraina 2.403
SE - Svezia 2.171
HK - Hong Kong 2.107
VN - Vietnam 1.951
BR - Brasile 1.856
KR - Corea 1.240
DE - Germania 1.214
FR - Francia 1.102
GB - Regno Unito 912
TR - Turchia 912
FI - Finlandia 866
RU - Federazione Russa 752
BD - Bangladesh 707
NL - Olanda 539
IE - Irlanda 526
BG - Bulgaria 521
CH - Svizzera 429
IN - India 372
CA - Canada 239
JP - Giappone 188
AR - Argentina 179
MX - Messico 155
AT - Austria 149
BE - Belgio 139
MA - Marocco 130
PH - Filippine 118
ZA - Sudafrica 111
IQ - Iraq 98
ES - Italia 96
ID - Indonesia 90
EC - Ecuador 85
PK - Pakistan 75
SA - Arabia Saudita 73
CZ - Repubblica Ceca 70
SN - Senegal 68
AU - Australia 67
UZ - Uzbekistan 58
CL - Cile 53
VE - Venezuela 52
TH - Thailandia 50
IL - Israele 49
CO - Colombia 44
JO - Giordania 42
DZ - Algeria 37
KE - Kenya 35
EG - Egitto 34
PE - Perù 34
AE - Emirati Arabi Uniti 31
PY - Paraguay 30
MY - Malesia 29
LT - Lituania 28
EU - Europa 27
GR - Grecia 26
AZ - Azerbaigian 23
TW - Taiwan 23
JM - Giamaica 21
RO - Romania 21
IR - Iran 20
OM - Oman 19
PT - Portogallo 19
HU - Ungheria 18
TN - Tunisia 18
BO - Bolivia 17
CR - Costa Rica 16
PS - Palestinian Territory 16
AL - Albania 15
DK - Danimarca 15
KZ - Kazakistan 15
TT - Trinidad e Tobago 15
CI - Costa d'Avorio 14
NP - Nepal 14
NZ - Nuova Zelanda 14
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
RS - Serbia 10
NI - Nicaragua 9
UY - Uruguay 9
XK - ???statistics.table.value.countryCode.XK??? 9
GA - Gabon 8
GE - Georgia 8
HN - Honduras 8
LV - Lettonia 8
AO - Angola 7
ET - Etiopia 7
GT - Guatemala 7
PA - Panama 6
AM - Armenia 5
Totale 84.879
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Città #
Warsaw 5.918
Singapore 4.105
Ashburn 3.923
Fairfield 3.713
Woodbridge 3.012
Chandler 2.431
Houston 2.224
Jacksonville 2.199
Ann Arbor 2.008
Hong Kong 2.004
San Jose 1.909
Wilmington 1.903
Seattle 1.625
Hefei 1.318
Cambridge 1.236
Seoul 1.211
Beijing 983
Princeton 925
Boardman 884
Izmir 769
Chicago 691
Trieste 648
Ho Chi Minh City 577
Los Angeles 529
Dublin 517
Sofia 514
Lauterbourg 479
Columbus 464
Hanoi 441
Zgierz 439
Milan 437
Bern 404
The Dalles 397
Moscow 396
Dallas 379
Dearborn 354
Buffalo 345
Santa Clara 331
Helsinki 279
Munich 256
New York 249
Frankfurt am Main 235
San Diego 227
Düsseldorf 225
Council Bluffs 221
Amsterdam 205
Des Moines 177
São Paulo 159
Tokyo 141
London 135
Verona 120
Brussels 118
Nuremberg 116
Rome 114
Dong Ket 110
Nanjing 103
Phoenix 100
Orem 99
Bremen 93
Casablanca 89
Falls Church 89
Haiphong 84
Da Nang 82
Guangzhou 82
Norwalk 81
Shanghai 77
Redondo Beach 71
Redwood City 70
Rio de Janeiro 70
Toronto 70
Vienna 69
Dakar 68
Montreal 66
Atlanta 63
Turku 62
Brno 61
Johannesburg 57
Tashkent 57
Brooklyn 54
Washington 54
Lappeenranta 53
Chennai 52
Denver 52
Miano 52
Tianjin 52
Stockholm 50
Turin 50
Kocaeli 48
Kunming 48
Jinan 47
Redmond 45
Mexico City 43
San Francisco 43
Amman 39
Nanchang 39
Baghdad 38
Fremont 38
Paris 38
Pune 38
Bologna 37
Totale 58.502
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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 631
1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function 469
PSIP1/LEDGF: A new gene likely involved in sensorineural progressive hearing loss 452
Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss 452
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 419
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 405
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel 404
Genetic evidence for an origin of the Armenians from Bronze Age mixing of multiple populations 399
Global diversity in the TAS2R38 bitter taste receptor: Revisiting a classic evolutionary PROPosal 394
The Role Of Personality Traits On Taste Perception and Food Preferences. 391
Y chromosome variation and complex traits: the Ygen consortium 390
Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals 376
The p.Cys169Tyr variant of connexin 26 is not a polymorphism 374
Non-additive genome-wide association scan reveals a new gene associated with habitual coffee consumption 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 364
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function 363
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 358
The UK10K project identifies rare variants in health and disease 355
Enrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populations 355
A catalog of genetic loci associated with kidney function from analyses of a million individuals. 353
Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss 353
Cx26 partial loss causes accelerated presbycusis by redox imbalance and dysregulation of Nfr2 pathway 353
Multicohort analysis of the maternal age effect on recombination 351
Genetic structure in the Sherpa and neighboring Nepalese populations 350
Pharmacogenetics driving personalized medicine: Analysis of genetic polymorphisms related to breast cancer medications in Italian isolated populations 342
Genetic Landscape of Slovenians: Past Admixture and Natural Selection Pattern 339
Modulation of genetic associations with serum urate levels by body-mass-index in humans 337
Genetic testing and genomic analysis: A debate on ethical, social and legal issues in the Arab world with a focus on Qatar 337
Mutations in L-type amino acid transporter-2 support SLC7A8 as a novel gene involved in age-related hearing loss 333
Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss 331
Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers 328
A genome-wide association study identifies an association between variants in EFCAB4B gene and periodontal disease in an Italian isolated population 328
Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversity. 322
PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity 318
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels 313
Whole-genome sequencing reveals new insights into age-related hearing loss: cumulative effects, pleiotropy and the role of selection 310
Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits 308
Variation in the bitter-taste receptor gene TAS2R38, and adiposity in a genetically isolated population in Southern Italy. 305
TBL1Y: a new gene involved in syndromic hearing loss 305
A general approach for haplotype phasing across the full spectrum of relatedness. 304
Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6 303
Next Generation Sequencing and Animal Models Reveal SLC9A3R1 as a New Gene Involved in Human Age-Related Hearing Loss 300
Common variants in CLDN14 are associated with differential excretion of magnesium over calcium in urine 295
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity 294
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk 293
Association of a variant in the CHRNA5-A3-B4 gene cluster region to heavy smoking in the Italian population. 288
Common Variants in UMOD Associate with Urinary Uromodulin Levels: A Meta-Analysis. 288
Factors influencing the phenotypic characterization of the oral marker, PROP 288
Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment 288
Joint data analysis in nutritional epidemiology: Identification of observational studies and minimal requirements 287
A Novel CRYBB2 Missense Mutation Causing Congenital Autosomal Dominant Cataract in an Italian Family. 284
Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits 282
Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries 281
A polymorphism in the 5' UTR of the DEFB1 gene is associated with the lung phenotype in F508del homozygous Italian cystic fibrosis patients 277
A Brief Review of Genetic Approaches to the Study of Food Preferences: Current Knowledge and Future Directions. 275
Analysis of functional variants reveals new candidate genes associated with alexithymia 275
TAS2R38 bitter taste genotype is associated with complementary feeding behavior in infants 274
19p13 microduplications encompassing NFIX are responsible for intellectual disability, short stature and small head circumference 271
Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability 267
Genetics of Food Preferences: A First View from Silk Road Populations 264
Heterogeneity in Circulating Tumor Cells: The Relevance of the Stem-Cell Subset 263
Evidence of Inbreeding Depression on Human Height 259
Understanding the role of personality and alexithymia in food preferences and PROP taste perception 258
Genome-wide meta-analysis unravels interactions between magnesium homeostasis and metabolic phenotypes 258
A novel P2RX2 mutation in an Italian family affected by autosomal dominant nonsyndromic hearing loss 256
Genetic landscape of populations along the Silk Road: admixture and migration patterns 255
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals 254
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney 253
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure 251
Associations of autozygosity with a broad range of human phenotypes 251
Functional analysis of mutations in SLC7A9, and genotype-phenotype correlation in non-Type I cystinuria. 250
Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation 250
A case of lymphedema-distichiasis syndrome carrying a new de novo frameshift FOXC2 mutation 250
Linkage Study and Exome Sequencing Identify a BDP1 Mutation Associated with Hereditary Hearing Loss 248
A Meta-Analysis of Genome-Wide Association Studies of the Electrocardiographic Early Repolarization Pattern. 247
Age- And Sex-Related Variations in Platelet Count in Italy: A Proposal of Reference Ranges Based on 40987 Subjects' Data 247
Association analysis of bitter receptor genes in five isolated populations identifies a significant correlation between TAS2R43 variants and coffee liking. 246
Congenital hyperinsulinism: clinical and molecular analysis of a large Italian cohort. 245
Consanguinity and Hereditary Hearing Loss in Qatar 245
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits 244
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair 243
Contribution of SNP arrays in diagnosis of deletion 2p11.2-p12 243
A “population-based approach” to study the link between TAS2R genes, taste perception and food liking. 241
Estrogen-related receptor gamma and hearing function: evidence of a role in humans and mice 239
A Genome-Wide Association Study in isolated populations reveals new genes associated to common food likings 238
GJB2 and GJB6 genes and the A1555G mitochondrial mutation are only minor causes of nonsyndromic hearing loss in the Qatari population 238
A novel deletion mutation involving TMEM38B in a patient with autosomal recessive osteogenesis imperfecta 237
Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity 237
Genome-wide analysis identifies 12 loci influencing human reproductive behavior. 233
Positive predictive values and outcomes for uninformative cell-free DNA tests: An Italian multicentric Cytogenetic and cytogenomic Audit of diagnOstic testing (ICARO Study) 233
Age-related hearing loss and level of education: an epidemiological study on a large cohort of isolated popu-lations 231
Autosomal recessive stickler syndrome due to a loss of function mutation in theCOL9A3gene 229
"A novel mutation in the Mitochondrial tRNAval gene associated with a complex neurological presentation" 228
The Meaning of Food Preferences in the Human Behaviour and Personalities. 227
Genome-wide association study identifies 74 loci associated with educational attainment 226
Next generation sequencing study in a cohort of Italian patients with syndromic hearing loss 224
"A benign form of thalassemia intermedia may be determined by the interaction of triplicated alfa locus and heterozygous beta thalassemia" 223
Co-inheritance of two ABCC8 mutations causing an unresponsive congenital hyperinsulinism: Clinical and functional characterization of two novel ABCC8 mutations 223
Connexin 26 variant carriers have a better gastrointestinal health: is this the heterozygote advantage? 222
Association of LTA gene haploblock with periodontal disease in Italian adults. 222
Totale 29.977
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Categoria #
all - tutte 255.726
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 255.726
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021676 0 0 0 0 0 0 0 0 0 0 0 676
2021/20224.892 203 355 279 419 195 394 227 182 651 550 380 1.057
2022/20237.639 760 734 432 1.042 863 1.448 77 737 870 92 444 140
2023/20244.942 624 309 315 397 534 406 783 845 67 134 247 281
2024/20259.996 152 423 989 776 889 1.380 438 721 1.175 1.029 1.003 1.021
2025/202625.861 2.251 1.835 1.903 1.963 2.128 2.643 3.724 833 2.829 3.449 1.572 731
Totale 86.312