ArTS Archivio della ricerca di Trieste

GASPARINI, PAOLO
 Distribuzione geografica
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Continente #
NA - Nord America 42.618
EU - Europa 22.576
AS - Asia 20.636
SA - Sud America 2.447
Continente sconosciuto - Info sul continente non disponibili 1.346
AF - Africa 518
OC - Oceania 88
Totale 90.229
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Nazione #
US - Stati Uniti d'America 41.943
SG - Singapore 7.490
PL - Polonia 6.430
CN - Cina 4.628
IT - Italia 3.954
UA - Ucraina 2.406
SE - Svezia 2.179
HK - Hong Kong 2.137
VN - Vietnam 1.954
BR - Brasile 1.903
KR - Corea 1.241
DE - Germania 1.215
FR - Francia 1.110
GB - Regno Unito 925
TR - Turchia 913
FI - Finlandia 867
BD - Bangladesh 761
RU - Federazione Russa 752
NL - Olanda 549
IE - Irlanda 526
BG - Bulgaria 521
CH - Svizzera 429
IN - India 377
CA - Canada 318
AR - Argentina 189
JP - Giappone 189
MX - Messico 165
AT - Austria 150
BE - Belgio 140
MA - Marocco 130
PH - Filippine 119
ZA - Sudafrica 112
ES - Italia 107
IQ - Iraq 99
ID - Indonesia 96
EC - Ecuador 93
SA - Arabia Saudita 76
PK - Pakistan 75
AU - Australia 71
CZ - Repubblica Ceca 71
SN - Senegal 68
UZ - Uzbekistan 58
CL - Cile 57
VE - Venezuela 54
CO - Colombia 52
TH - Thailandia 52
IL - Israele 50
JO - Giordania 42
DZ - Algeria 37
PE - Perù 36
KE - Kenya 35
EG - Egitto 34
JM - Giamaica 34
AE - Emirati Arabi Uniti 32
PY - Paraguay 30
MY - Malesia 29
LT - Lituania 28
EU - Europa 27
GR - Grecia 26
TT - Trinidad e Tobago 25
AZ - Azerbaigian 23
CR - Costa Rica 23
PT - Portogallo 23
TW - Taiwan 23
RO - Romania 22
IR - Iran 20
OM - Oman 19
AL - Albania 18
HN - Honduras 18
HU - Ungheria 18
TN - Tunisia 18
BO - Bolivia 17
GT - Guatemala 17
PS - Palestinian Territory 16
DK - Danimarca 15
KZ - Kazakistan 15
NI - Nicaragua 15
CI - Costa d'Avorio 14
HR - Croazia 14
NP - Nepal 14
NZ - Nuova Zelanda 14
DO - Repubblica Dominicana 13
LB - Libano 13
KG - Kirghizistan 12
BY - Bielorussia 11
NG - Nigeria 11
SK - Slovacchia (Repubblica Slovacca) 11
LK - Sri Lanka 10
NO - Norvegia 10
QA - Qatar 10
RS - Serbia 10
SV - El Salvador 10
UY - Uruguay 10
LV - Lettonia 9
XK - ???statistics.table.value.countryCode.XK??? 9
GA - Gabon 8
GE - Georgia 8
PR - Porto Rico 8
AO - Angola 7
ET - Etiopia 7
Totale 88.779
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Città #
Warsaw 5.920
Ashburn 4.222
Singapore 4.122
Fairfield 3.713
Woodbridge 3.015
Chandler 2.432
Houston 2.241
Jacksonville 2.206
San Jose 2.127
Hong Kong 2.031
Ann Arbor 2.008
Wilmington 1.907
Seattle 1.639
Hefei 1.318
Cambridge 1.237
Seoul 1.211
Beijing 1.006
Council Bluffs 1.000
Princeton 928
Boardman 884
Izmir 769
Columbus 739
Chicago 719
Trieste 649
Ho Chi Minh City 577
Los Angeles 575
Dublin 518
Sofia 514
Milan 491
Lauterbourg 479
Hanoi 443
Zgierz 439
Dallas 428
Santa Clara 408
Bern 404
The Dalles 399
Moscow 396
Dearborn 354
Buffalo 353
New York 282
Helsinki 279
Munich 256
Frankfurt am Main 236
San Diego 230
Düsseldorf 225
Amsterdam 207
Des Moines 178
São Paulo 161
Phoenix 159
Rome 145
Tokyo 142
London 140
Verona 123
Brussels 119
Nuremberg 116
Dong Ket 110
Nanjing 104
Orem 103
Bremen 93
Casablanca 89
Falls Church 89
Haiphong 84
Toronto 84
Shanghai 83
Da Nang 82
Guangzhou 82
Norwalk 82
Atlanta 79
Montreal 77
Redondo Beach 71
Rio de Janeiro 71
Redwood City 70
Vienna 70
Brooklyn 69
Dakar 68
Washington 63
Turku 62
Brno 61
Denver 58
Turin 58
Johannesburg 57
San Francisco 57
Tashkent 57
Miano 56
Chennai 53
Lappeenranta 53
Stockholm 53
Tianjin 52
Kocaeli 48
Kunming 48
Mexico City 48
Jinan 47
Redmond 45
Miami 42
Philadelphia 42
Naples 41
Amman 39
Bologna 39
Nanchang 39
Baghdad 38
Totale 60.735
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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 646
Genetic evidence for an origin of the Armenians from Bronze Age mixing of multiple populations 476
1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function 474
Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss 459
PSIP1/LEDGF: A new gene likely involved in sensorineural progressive hearing loss 455
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 423
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel 421
Y chromosome variation and complex traits: the Ygen consortium 414
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 411
The Role Of Personality Traits On Taste Perception and Food Preferences. 407
The p.Cys169Tyr variant of connexin 26 is not a polymorphism 401
Global diversity in the TAS2R38 bitter taste receptor: Revisiting a classic evolutionary PROPosal 399
Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals 399
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function 384
Non-additive genome-wide association scan reveals a new gene associated with habitual coffee consumption 372
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 366
Genetic testing and genomic analysis: A debate on ethical, social and legal issues in the Arab world with a focus on Qatar 363
Genetic structure in the Sherpa and neighboring Nepalese populations 363
The UK10K project identifies rare variants in health and disease 362
Enrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populations 362
A catalog of genetic loci associated with kidney function from analyses of a million individuals. 362
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 362
Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss 360
Cx26 partial loss causes accelerated presbycusis by redox imbalance and dysregulation of Nfr2 pathway 359
Multicohort analysis of the maternal age effect on recombination 358
Modulation of genetic associations with serum urate levels by body-mass-index in humans 350
Genetic Landscape of Slovenians: Past Admixture and Natural Selection Pattern 349
Pharmacogenetics driving personalized medicine: Analysis of genetic polymorphisms related to breast cancer medications in Italian isolated populations 346
Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers 343
Mutations in L-type amino acid transporter-2 support SLC7A8 as a novel gene involved in age-related hearing loss 339
Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss 335
A genome-wide association study identifies an association between variants in EFCAB4B gene and periodontal disease in an Italian isolated population 333
Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversity. 329
PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity 325
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels 322
Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries 319
Variation in the bitter-taste receptor gene TAS2R38, and adiposity in a genetically isolated population in Southern Italy. 317
Whole-genome sequencing reveals new insights into age-related hearing loss: cumulative effects, pleiotropy and the role of selection 314
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk 313
Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6 313
A general approach for haplotype phasing across the full spectrum of relatedness. 312
Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits 311
TBL1Y: a new gene involved in syndromic hearing loss 309
Next Generation Sequencing and Animal Models Reveal SLC9A3R1 as a New Gene Involved in Human Age-Related Hearing Loss 306
Common variants in CLDN14 are associated with differential excretion of magnesium over calcium in urine 303
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity 301
Association of a variant in the CHRNA5-A3-B4 gene cluster region to heavy smoking in the Italian population. 298
Factors influencing the phenotypic characterization of the oral marker, PROP 297
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals 296
Common Variants in UMOD Associate with Urinary Uromodulin Levels: A Meta-Analysis. 295
Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment 293
Joint data analysis in nutritional epidemiology: Identification of observational studies and minimal requirements 290
Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits 288
A Novel CRYBB2 Missense Mutation Causing Congenital Autosomal Dominant Cataract in an Italian Family. 287
A polymorphism in the 5' UTR of the DEFB1 gene is associated with the lung phenotype in F508del homozygous Italian cystic fibrosis patients 284
TAS2R38 bitter taste genotype is associated with complementary feeding behavior in infants 283
Analysis of functional variants reveals new candidate genes associated with alexithymia 282
A Brief Review of Genetic Approaches to the Study of Food Preferences: Current Knowledge and Future Directions. 279
Understanding the role of personality and alexithymia in food preferences and PROP taste perception 277
Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability 275
19p13 microduplications encompassing NFIX are responsible for intellectual disability, short stature and small head circumference 274
A case of lymphedema-distichiasis syndrome carrying a new de novo frameshift FOXC2 mutation 272
Heterogeneity in Circulating Tumor Cells: The Relevance of the Stem-Cell Subset 272
Evidence of Inbreeding Depression on Human Height 270
Functional analysis of mutations in SLC7A9, and genotype-phenotype correlation in non-Type I cystinuria. 268
Genetics of Food Preferences: A First View from Silk Road Populations 266
Genome-wide meta-analysis unravels interactions between magnesium homeostasis and metabolic phenotypes 263
A novel P2RX2 mutation in an Italian family affected by autosomal dominant nonsyndromic hearing loss 262
Age- And Sex-Related Variations in Platelet Count in Italy: A Proposal of Reference Ranges Based on 40987 Subjects' Data 259
Genetic landscape of populations along the Silk Road: admixture and migration patterns 259
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits 259
Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation 258
Associations of autozygosity with a broad range of human phenotypes 258
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure 257
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney 255
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair 254
A Meta-Analysis of Genome-Wide Association Studies of the Electrocardiographic Early Repolarization Pattern. 253
Congenital hyperinsulinism: clinical and molecular analysis of a large Italian cohort. 252
A “population-based approach” to study the link between TAS2R genes, taste perception and food liking. 252
Association analysis of bitter receptor genes in five isolated populations identifies a significant correlation between TAS2R43 variants and coffee liking. 251
Linkage Study and Exome Sequencing Identify a BDP1 Mutation Associated with Hereditary Hearing Loss 251
Consanguinity and Hereditary Hearing Loss in Qatar 250
Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity 247
Contribution of SNP arrays in diagnosis of deletion 2p11.2-p12 247
Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci 247
GJB2 and GJB6 genes and the A1555G mitochondrial mutation are only minor causes of nonsyndromic hearing loss in the Qatari population 246
A Genome-Wide Association Study in isolated populations reveals new genes associated to common food likings 244
Positive predictive values and outcomes for uninformative cell-free DNA tests: An Italian multicentric Cytogenetic and cytogenomic Audit of diagnOstic testing (ICARO Study) 244
Estrogen-related receptor gamma and hearing function: evidence of a role in humans and mice 242
Autosomal recessive stickler syndrome due to a loss of function mutation in theCOL9A3gene 242
Age-related hearing loss and level of education: an epidemiological study on a large cohort of isolated popu-lations 241
A novel deletion mutation involving TMEM38B in a patient with autosomal recessive osteogenesis imperfecta 240
Next generation sequencing study in a cohort of Italian patients with syndromic hearing loss 239
Genome-wide analysis identifies 12 loci influencing human reproductive behavior. 238
"A benign form of thalassemia intermedia may be determined by the interaction of triplicated alfa locus and heterozygous beta thalassemia" 236
"A novel mutation in the Mitochondrial tRNAval gene associated with a complex neurological presentation" 236
Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations. 235
Genetic and Phenotypic Characterization of Nexilin (NEXN)-Related Cardiomyopathy: Results From a Multicentric Study 235
The Meaning of Food Preferences in the Human Behaviour and Personalities. 234
Genome-wide association study identifies 74 loci associated with educational attainment 234
Totale 31.013
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Categoria #
all - tutte 273.148
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 273.148
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20224.334 0 0 279 419 195 394 227 182 651 550 380 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
2025/202626.017 2.251 1.835 1.903 1.963 2.128 2.643 3.724 833 2.829 3.449 1.572 887
2026/20273.761 1.155 1.436 1.170 0 0 0 0 0 0 0 0 0
Totale 90.229