ArTS Archivio della ricerca di Trieste

GASPARINI, PAOLO
 Distribuzione geografica
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Continente #
NA - Nord America 28.102
EU - Europa 16.763
AS - Asia 4.331
SA - Sud America 75
AF - Africa 61
OC - Oceania 54
Continente sconosciuto - Info sul continente non disponibili 30
Totale 49.416
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Nazione #
US - Stati Uniti d'America 28.045
PL - Polonia 5.825
IT - Italia 2.568
UA - Ucraina 2.349
SE - Svezia 2.128
CN - Cina 1.651
HK - Hong Kong 1.001
TR - Turchia 828
FI - Finlandia 601
GB - Regno Unito 577
DE - Germania 518
BG - Bulgaria 507
IE - Irlanda 501
SG - Singapore 469
CH - Svizzera 412
FR - Francia 233
NL - Olanda 166
BE - Belgio 125
VN - Vietnam 114
CZ - Repubblica Ceca 65
KR - Corea 64
RU - Federazione Russa 56
SN - Senegal 53
CA - Canada 44
PH - Filippine 44
IN - India 43
AU - Australia 41
BR - Brasile 41
JP - Giappone 41
ES - Italia 29
EU - Europa 27
AT - Austria 26
GR - Grecia 18
IL - Israele 15
CL - Cile 13
MX - Messico 13
NZ - Nuova Zelanda 13
RO - Romania 10
MY - Malesia 9
PT - Portogallo 9
AE - Emirati Arabi Uniti 8
DK - Danimarca 8
IR - Iran 8
HU - Ungheria 7
TW - Taiwan 7
EC - Ecuador 6
LK - Sri Lanka 5
NO - Norvegia 5
PK - Pakistan 5
QA - Qatar 5
HR - Croazia 4
PE - Perù 4
A2 - ???statistics.table.value.countryCode.A2??? 3
AR - Argentina 3
LU - Lussemburgo 3
PY - Paraguay 3
SI - Slovenia 3
BO - Bolivia 2
EG - Egitto 2
IM - Isola di Man 2
JO - Giordania 2
LB - Libano 2
NG - Nigeria 2
RS - Serbia 2
TH - Thailandia 2
ZA - Sudafrica 2
AL - Albania 1
BD - Bangladesh 1
BN - Brunei Darussalam 1
BT - Bhutan 1
CO - Colombia 1
DZ - Algeria 1
FK - Isole Falkland (Malvinas) 1
IS - Islanda 1
KG - Kirghizistan 1
KZ - Kazakistan 1
LV - Lettonia 1
MC - Monaco 1
MK - Macedonia 1
MO - Macao, regione amministrativa speciale della Cina 1
OM - Oman 1
SA - Arabia Saudita 1
SC - Seychelles 1
SK - Slovacchia (Repubblica Slovacca) 1
VE - Venezuela 1
Totale 49.416
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Città #
Warsaw 5.796
Fairfield 3.710
Woodbridge 3.012
Chandler 2.442
Jacksonville 2.195
Houston 2.175
Ashburn 2.024
Ann Arbor 2.008
Wilmington 1.898
Seattle 1.603
Cambridge 1.235
Hong Kong 959
Princeton 926
Izmir 765
Beijing 554
Trieste 526
Sofia 507
Dublin 496
Bern 403
Boardman 385
Dearborn 354
Singapore 281
Milan 226
San Diego 221
Des Moines 168
Düsseldorf 131
Verona 117
Dong Ket 110
Brussels 109
Chicago 108
Helsinki 107
Amsterdam 101
Bremen 93
Falls Church 89
Nanjing 88
Norwalk 81
Munich 79
Hefei 76
Redwood City 70
Buffalo 66
Phoenix 64
Brno 61
Los Angeles 56
Dakar 53
Seoul 50
Rome 49
Kocaeli 48
Kunming 45
Redmond 45
Washington 45
Jinan 43
Turin 42
Fremont 37
Nanchang 37
Torino 37
London 36
Guangzhou 33
Edinburgh 32
Shanghai 32
Saint Petersburg 31
Shenyang 31
Pune 29
Mestre 27
Lappeenranta 25
Pignone 25
Central 24
Barletta 22
Toronto 21
Fuzhou 20
Dongguan 18
Udine 18
Auburn Hills 17
Bagumbayan 17
Boydton 17
Hebei 17
Tappahannock 17
Scuola 16
São Paulo 16
Tokyo 16
Vienna 16
Florence 15
Grafing 15
Hangzhou 15
Madrid 15
New York 15
Xian 15
Columbus 14
Naaldwijk 14
Paris 14
Bologna 13
Provo 13
Tulsa 13
Waanrode 13
Campo Grande 12
Dallas 12
Zhengzhou 12
Changsha 11
Kraków 11
Berlin 10
Brisbane 10
Totale 37.841
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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 417
PSIP1/LEDGF: A new gene likely involved in sensorineural progressive hearing loss 347
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel 339
1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function 334
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 331
Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss 321
Genetic evidence for an origin of the Armenians from Bronze Age mixing of multiple populations 312
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 311
The p.Cys169Tyr variant of connexin 26 is not a polymorphism 308
Non-additive genome-wide association scan reveals a new gene associated with habitual coffee consumption 304
Multicohort analysis of the maternal age effect on recombination 303
Pharmacogenetics driving personalized medicine: Analysis of genetic polymorphisms related to breast cancer medications in Italian isolated populations 301
Genetic structure in the Sherpa and neighboring Nepalese populations 296
Global diversity in the TAS2R38 bitter taste receptor: Revisiting a classic evolutionary PROPosal 293
Y chromosome variation and complex traits: the Ygen consortium 292
Genetic testing and genomic analysis: A debate on ethical, social and legal issues in the Arab world with a focus on Qatar 292
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function 290
Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss 289
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 281
Mutations in L-type amino acid transporter-2 support SLC7A8 as a novel gene involved in age-related hearing loss 274
Cx26 partial loss causes accelerated presbycusis by redox imbalance and dysregulation of Nfr2 pathway 272
The UK10K project identifies rare variants in health and disease 269
Enrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populations 265
Modulation of genetic associations with serum urate levels by body-mass-index in humans 264
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 258
Whole-genome sequencing reveals new insights into age-related hearing loss: cumulative effects, pleiotropy and the role of selection 256
Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits 242
Factors influencing the phenotypic characterization of the oral marker, PROP 240
Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss 240
A catalog of genetic loci associated with kidney function from analyses of a million individuals. 231
Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversity. 228
Genetic Landscape of Slovenians: Past Admixture and Natural Selection Pattern 227
PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity 226
Joint data analysis in nutritional epidemiology: Identification of observational studies and minimal requirements 226
Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6 224
Next Generation Sequencing and Animal Models Reveal SLC9A3R1 as a New Gene Involved in Human Age-Related Hearing Loss 219
The Role Of Personality Traits On Taste Perception and Food Preferences. 214
Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits 213
Variation in the bitter-taste receptor gene TAS2R38, and adiposity in a genetically isolated population in Southern Italy. 211
Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries 209
A genome-wide association study identifies an association between variants in EFCAB4B gene and periodontal disease in an Italian isolated population 206
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity 203
Common variants in CLDN14 are associated with differential excretion of magnesium over calcium in urine 203
Heterogeneity in Circulating Tumor Cells: The Relevance of the Stem-Cell Subset 202
A Meta-Analysis of Genome-Wide Association Studies of the Electrocardiographic Early Repolarization Pattern. 197
A Brief Review of Genetic Approaches to the Study of Food Preferences: Current Knowledge and Future Directions. 189
Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment 189
Association of a variant in the CHRNA5-A3-B4 gene cluster region to heavy smoking in the Italian population. 186
Genetics of Food Preferences: A First View from Silk Road Populations 184
Understanding the role of personality and alexithymia in food preferences and PROP taste perception 180
Functional analysis of mutations in SLC7A9, and genotype-phenotype correlation in non-Type I cystinuria. 179
TAS2R38 bitter taste genotype is associated with complementary feeding behavior in infants 179
Evidence of Inbreeding Depression on Human Height 174
TBL1Y: a new gene involved in syndromic hearing loss 172
A Novel CRYBB2 Missense Mutation Causing Congenital Autosomal Dominant Cataract in an Italian Family. 171
Analysis of functional variants reveals new candidate genes associated with alexithymia 170
19p13 microduplications encompassing NFIX are responsible for intellectual disability, short stature and small head circumference 164
A novel deletion mutation involving TMEM38B in a patient with autosomal recessive osteogenesis imperfecta 162
Genome-wide meta-analysis unravels interactions between magnesium homeostasis and metabolic phenotypes 162
A novel P2RX2 mutation in an Italian family affected by autosomal dominant nonsyndromic hearing loss 161
Targeted sequencing identifies novel variants involved in autosomal recessive hereditary hearing loss in Qatari families 161
Congenital hyperinsulinism: clinical and molecular analysis of a large Italian cohort. 160
Frequency of hearing loss in a series of rural communities of five developing countries located along the Silk Road 160
Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability 158
Autosomal recessive stickler syndrome due to a loss of function mutation in theCOL9A3gene 156
Linkage Study and Exome Sequencing Identify a BDP1 Mutation Associated with Hereditary Hearing Loss 155
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair 155
New gene functions in megakaryopoiesis and platelet formation 154
Age and origin of major Smith-Lemli-Opitz Syndrome (SLOS) mutations in European populations. 153
Genetic landscape of populations along the Silk Road: admixture and migration patterns 151
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney 151
Contribution of SNP arrays in diagnosis of deletion 2p11.2-p12 151
Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation 150
Factors associated with food liking and their relationship with metabolic traits in Italian cohorts 150
Association analysis of bitter receptor genes in five isolated populations identifies a significant correlation between TAS2R43 variants and coffee liking. 149
A “population-based approach” to study the link between TAS2R genes, taste perception and food liking. 147
Consanguinity and Hereditary Hearing Loss in Qatar 146
Salt-inducible kinase 3, SIK3, is a new gene associated with hearing. 146
Connexin 26 variant carriers have a better gastrointestinal health: is this the heterozygote advantage? 146
Co-inheritance of two ABCC8 mutations causing an unresponsive congenital hyperinsulinism: Clinical and functional characterization of two novel ABCC8 mutations 145
A general approach for haplotype phasing across the full spectrum of relatedness. 145
Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity 145
Vezatin, an integral membrane protein of adherens junctions, is required for the sound resilience of cochlear hair cells 144
Estrogen-related receptor gamma and hearing function: evidence of a role in humans and mice 143
Common Variants in UMOD Associate with Urinary Uromodulin Levels: A Meta-Analysis. 143
Identification of a Novel Mutation in the Myosin VIIA Motor Domain in a Family with Autosomal Dominant Hearing Loss (DFNA11) 143
Heritability and demographic analyses in the large isolated population of val borbera suggest advantages in mapping complex traits genes. 141
Next generation sequencing in nonsyndromic intellectual disability: From a negative molecular karyotype to a possible causative mutation detection 141
Lifestyle and normal hearing function in Italy and Central Asia: The potential role of coffee 141
Phospholipase C-β3 is a key modulator of IL-8 expression in cystic fibrosis bronchial epithelial cells. 140
GJB2 and GJB6 genes and the A1555G mitochondrial mutation are only minor causes of nonsyndromic hearing loss in the Qatari population 140
Genome Wide Association Analysis of a Founder Population Identified TAF3 as a Gene for MCHC in Humans. 139
The Meaning of Food Preferences in the Human Behaviour and Personalities. 138
A case of lymphedema-distichiasis syndrome carrying a new de novo frameshift FOXC2 mutation 138
Age- And Sex-Related Variations in Platelet Count in Italy: A Proposal of Reference Ranges Based on 40987 Subjects' Data 137
Association of LTA gene haploblock with periodontal disease in Italian adults. 137
Severe infantile encephalomyopathy caused by a mutation in COX6B1, a nucleus-encoded subunit of cytochrome c oxidase 136
A polymorphism in the 5' UTR of the DEFB1 gene is associated with the lung phenotype in F508del homozygous Italian cystic fibrosis patients 135
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk 135
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits 135
Totale 20.442
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Categoria #
all - tutte 140.147
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 140.147
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202010.896 0 557 561 1.919 824 1.617 1.140 1.260 1.016 599 856 547
2020/20218.022 751 587 779 895 722 819 509 683 487 892 222 676
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
2024/2025173 152 21 0 0 0 0 0 0 0 0 0 0
Totale 50.666