ArTS Archivio della ricerca di Trieste

GIROTTO, GIORGIA
 Distribuzione geografica
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Continente #
NA - Nord America 12.445
EU - Europa 8.057
AS - Asia 7.484
SA - Sud America 1.113
Continente sconosciuto - Info sul continente non disponibili 729
AF - Africa 315
OC - Oceania 41
Totale 30.184
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Nazione #
US - Stati Uniti d'America 12.085
SG - Singapore 2.404
IT - Italia 2.256
PL - Polonia 2.140
CN - Cina 1.712
BR - Brasile 854
VN - Vietnam 798
HK - Hong Kong 770
BD - Bangladesh 582
DE - Germania 545
SE - Svezia 542
FR - Francia 394
KR - Corea 350
GB - Regno Unito 313
RU - Federazione Russa 295
FI - Finlandia 290
NL - Olanda 287
UA - Ucraina 245
IN - India 191
CA - Canada 169
TR - Turchia 160
BG - Bulgaria 145
IE - Irlanda 136
MA - Marocco 96
MX - Messico 91
JP - Giappone 90
AT - Austria 84
AR - Argentina 81
CH - Svizzera 80
ZA - Sudafrica 69
BE - Belgio 66
ES - Italia 65
IQ - Iraq 64
SN - Senegal 50
ID - Indonesia 41
PK - Pakistan 40
SA - Arabia Saudita 40
AU - Australia 38
CO - Colombia 36
CZ - Repubblica Ceca 36
EC - Ecuador 36
CL - Cile 31
UZ - Uzbekistan 29
VE - Venezuela 28
IL - Israele 22
JO - Giordania 21
AE - Emirati Arabi Uniti 20
EG - Egitto 20
PH - Filippine 20
LT - Lituania 19
NO - Norvegia 18
PY - Paraguay 18
AZ - Azerbaigian 15
DZ - Algeria 14
KE - Kenya 14
PE - Perù 14
CR - Costa Rica 13
HN - Honduras 11
IR - Iran 11
PT - Portogallo 11
DK - Danimarca 10
DO - Repubblica Dominicana 10
GR - Grecia 10
GT - Guatemala 10
HR - Croazia 10
NP - Nepal 10
TH - Thailandia 10
TT - Trinidad e Tobago 10
MY - Malesia 9
TW - Taiwan 9
JM - Giamaica 8
KZ - Kazakistan 8
PS - Palestinian Territory 8
RO - Romania 8
TN - Tunisia 7
AM - Armenia 6
BO - Bolivia 6
BY - Bielorussia 6
CI - Costa d'Avorio 6
EE - Estonia 6
HU - Ungheria 6
NI - Nicaragua 6
PA - Panama 6
UY - Uruguay 6
AL - Albania 5
BB - Barbados 5
ET - Etiopia 5
EU - Europa 5
KG - Kirghizistan 5
LK - Sri Lanka 5
LU - Lussemburgo 5
PR - Porto Rico 5
SK - Slovacchia (Repubblica Slovacca) 5
CY - Cipro 4
LB - Libano 4
LV - Lettonia 4
LY - Libia 4
OM - Oman 4
RS - Serbia 4
XK - ???statistics.table.value.countryCode.XK??? 4
Totale 29.379
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Città #
Warsaw 1.989
Ashburn 1.656
Singapore 1.452
San Jose 793
Hong Kong 726
Chandler 661
Houston 614
Fairfield 611
Woodbridge 567
Trieste 490
Ann Arbor 456
Council Bluffs 380
Hefei 378
Wilmington 344
Beijing 337
Seoul 336
Seattle 333
Los Angeles 293
Jacksonville 250
Chicago 249
Cambridge 245
Ho Chi Minh City 245
Boardman 228
Milan 220
Dallas 215
Columbus 202
Santa Clara 184
Hanoi 181
Princeton 177
New York 163
Lauterbourg 150
Sofia 140
Dublin 135
Zgierz 132
Munich 131
Helsinki 128
Frankfurt am Main 119
Moscow 111
The Dalles 98
London 96
Izmir 95
Rome 94
Buffalo 91
São Paulo 86
Nuremberg 76
Casablanca 75
Phoenix 75
Bern 62
Dearborn 62
Tokyo 55
Turin 55
Düsseldorf 54
Lappeenranta 54
Atlanta 52
Brussels 51
Dakar 50
Dong Ket 50
Montreal 48
Orem 47
Nanjing 45
Shanghai 45
San Diego 44
Bremen 42
Denver 42
Vienna 41
Amsterdam 39
Johannesburg 38
Brooklyn 37
Da Nang 37
Redondo Beach 37
Toronto 37
Guangzhou 36
Bologna 35
Haiphong 33
Stockholm 33
Mexico City 31
Turku 31
Mumbai 29
Naples 28
Saint Petersburg 28
Tashkent 28
Chennai 27
Florence 27
Rio de Janeiro 27
Tianjin 27
Des Moines 26
Salt Lake City 26
Paris 25
San Francisco 25
Bari 24
Boston 24
Baghdad 23
Brno 22
Amman 21
Philadelphia 21
Brasília 20
Barletta 19
Belo Horizonte 19
Madrid 19
Poplar 19
Totale 18.684
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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
Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus 579
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
Usher syndrome: An effective sequencing approach to establish a genetic and clinical diagnosis 416
Association of SNPs in LCP1 and CTIF with hearing in 11 year old children: Findings from the Avon Longitudinal Study of Parents and Children (ALSPAC) birth cohort and the G-EAR consortium 398
Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals 398
The p.Cys169Tyr variant of connexin 26 is not a polymorphism 386
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
Cx26 partial loss causes accelerated presbycusis by redox imbalance and dysregulation of Nfr2 pathway 359
Pharmacogenetics driving personalized medicine: Analysis of genetic polymorphisms related to breast cancer medications in Italian isolated populations 346
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
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels 322
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 312
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
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 292
Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability 275
Evidence of Inbreeding Depression on Human Height 270
A novel P2RX2 mutation in an Italian family affected by autosomal dominant nonsyndromic hearing loss 262
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
Associations of autozygosity with a broad range of human phenotypes 258
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 252
Linkage Study and Exome Sequencing Identify a BDP1 Mutation Associated with Hereditary Hearing Loss 251
Consanguinity and Hereditary Hearing Loss in Qatar 250
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
Estrogen-related receptor gamma and hearing function: evidence of a role in humans and mice 242
Age-related hearing loss and level of education: an epidemiological study on a large cohort of isolated popu-lations 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
Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations. 235
Effects of Calcium, Magnesium, and Potassium Concentrations on Ventricular Repolarization in Unselected Individuals. 234
Genetic and Phenotypic Characterization of Nexilin (NEXN)-Related Cardiomyopathy: Results From a Multicentric Study 234
Genome-wide association study identifies 74 loci associated with educational attainment 233
Targeted sequencing identifies novel variants involved in autosomal recessive hereditary hearing loss in Qatari families 229
MYH9 related disease: four novel mutations of the tail domain of myosin-9 correlating with a mild clinical phenotype 227
Frequency of hearing loss in a series of rural communities of five developing countries located along the Silk Road 227
Hereditary hearing loss: a 96 gene targeted sequencing protocol reveals novel alleles in a series of Italian and Qatari patients 225
Directional dominance on stature and cognition in diverse human populations 221
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals 220
Salt-inducible kinase 3, SIK3, is a new gene associated with hearing. 220
Odontostomatological Traits in North-Eastern Italy's Isolated Populations: An Epidemiological Cross-Sectional Study 218
New age-related hearing loss candidate genes in humans: an ongoing challenge 218
Genome-wide meta-analysis of common variant differences between men and women 216
Erratum to: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (Nature Genetics, (2018), 50, 10, (1412-1425), 10.1038/s41588-018-0205-x) 215
Increased rate of deleterious variants in long runs of homozygosity of an inbred population from Qatar 209
Challenging Occam's Razor: Dual Molecular Diagnoses Explain Entangled Clinical Pictures 208
A novel founder MYO15A frameshift duplication is the major cause of genetic hearing loss in Oman 207
Lights and shadows in the genetics of syndromic and non-syndromic hearing loss in the Italian population 196
Maps of open chromatin highlight cell type-restricted patterns of regulatory sequence variation at hematological trait loci. 195
Expression and Replication Studies to Identify New Candidate Genes Involved in Normal Hearing Function 195
Lifestyle and normal hearing function in Italy and Central Asia: The potential role of coffee 193
Genetic variants linked to education predict longevity. 192
Seventy-five genetic loci influencing the human red blood cell. 192
Genetics, odor perception and food liking: The intriguing role of cinnamon 191
A saturated map of common genetic variants associated with human height 187
The power of genetic diversity in genome-wide association studies of lipids 187
Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity 184
A bird’s-eye view of Italian genomic variation through whole-genome sequencing 181
Hearing function and thresholds: a genome-wide association study in European isolated populations identifies new loci and pathways. 179
Proangiogenic properties of complement protein C1q can contribute to endometriosis 178
Rare and low-frequency coding variants alter human adult height 178
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits 176
Prognostic Prediction of Genotype vs Phenotype in Genetic Cardiomyopathies 174
Puzzling Out the Genetic Architecture of Endometriosis: Whole-Exome Sequencing and Novel Candidate Gene Identification in a Deeply Clinically Characterised Cohort 172
Pendred syndrome, or not pendred syndrome? That is the question 171
Cardiovascular Risk Factors and MRI Markers of Cerebral Small Vessel Disease 169
Lactobacillus iners dominates the vaginal microbiota of healthy Italian women of reproductive age 167
Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function 167
TTC5 syndrome: Clinical and molecular spectrum of a severe and recognizable condition 164
Natural human knockouts and Mendelian disorders: deep phenotyping in Italian isolates 163
Long QT syndrome and left ventricular non-compaction in a family with KCNH2 mutation: A case report 160
The Enigmatic Genetic Landscape of Hereditary Hearing Loss: A Multistep Diagnostic Strategy in the Italian Population 159
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences 158
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways 157
There Is More Than Meets the Eye: Identification of Dual Molecular Diagnosis in Patients Affected by Hearing Loss 155
Uncovering a Novel Pathogenic Mechanism of BCS1L in Mitochondrial Disorders: Insights from Functional Studies on the c.38A>G Variant 154
Genetic dissection of temperament personality traits in Italian isolates 154
A possible association between low MBL/lectin pathway functionality and microbiota dysbiosis in endometriosis patients 154
Hidden in the Genome: The First Italian Family with North Carolina Macular Dystrophy Carrying a Novel PRDM13 and CCNC Duplication 153
Haploinsufficiency as a Foreground Pathomechanism of Poirer-Bienvenu Syndrome and Novel Insights Underlying the Phenotypic Continuum of CSNK2B-Associated Disorders 150
Genetics of hearing loss (from congenital forms to presbycusis) 150
Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color 150
Ancestry-related distribution of Runs of homozygosity and functional variants in Qatari population 149
The role of knockout olfactory receptor genes in odor discrimination 149
Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour 148
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution 147
Chromoanagenesis of chromosome 22 in a subject with obesity and borderline cognitive performance 146
The Bittersweet Symphony of COVID-19: Associations between TAS1Rs and TAS2R38 Genetic Variations and COVID-19 Symptoms 145
Primary Ciliary Dyskinesia: The Impact of Taste Receptor (TAS2R38) Gene Polymorphisms on Disease Outcome and Severity 144
Mutations in PLS1, encoding fimbrin, cause autosomal dominant nonsyndromic hearing loss 143
Totale 23.975
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Categoria #
all - tutte 87.672
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 87.672
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.034 0 0 83 54 84 84 67 37 146 104 58 317
2022/20232.209 176 250 128 308 216 331 39 299 249 51 112 50
2023/20241.832 130 122 98 160 121 169 358 304 24 62 138 146
2024/20254.674 168 228 452 367 384 481 278 290 459 594 577 396
2025/202611.613 1.032 710 906 1.016 924 925 1.567 392 1.210 1.395 924 612
2026/20271.661 471 796 394 0 0 0 0 0 0 0 0 0
Totale 30.184