ArTS Archivio della ricerca di Trieste

GIROTTO, GIORGIA
 Distribuzione geografica
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Continente #
NA - Nord America 10.408
EU - Europa 7.546
AS - Asia 6.859
SA - Sud America 1.078
AF - Africa 310
OC - Oceania 34
Continente sconosciuto - Info sul continente non disponibili 10
Totale 26.245
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Nazione #
US - Stati Uniti d'America 10.181
SG - Singapore 2.382
PL - Polonia 2.138
IT - Italia 1.825
CN - Cina 1.669
BR - Brasile 826
VN - Vietnam 796
HK - Hong Kong 760
DE - Germania 537
SE - Svezia 537
FR - Francia 388
KR - Corea 347
GB - Regno Unito 296
RU - Federazione Russa 295
FI - Finlandia 288
NL - Olanda 272
UA - Ucraina 245
IN - India 188
TR - Turchia 156
BG - Bulgaria 145
IE - Irlanda 135
MA - Marocco 96
CA - Canada 93
MX - Messico 87
AT - Austria 82
JP - Giappone 80
AR - Argentina 78
CH - Svizzera 76
ZA - Sudafrica 68
BD - Bangladesh 67
BE - Belgio 65
IQ - Iraq 64
ES - Italia 60
SN - Senegal 50
SA - Arabia Saudita 38
ID - Indonesia 37
EC - Ecuador 35
PK - Pakistan 35
CO - Colombia 34
CZ - Repubblica Ceca 34
AU - Australia 32
CL - Cile 30
UZ - Uzbekistan 29
VE - Venezuela 28
IL - Israele 21
JO - Giordania 21
AE - Emirati Arabi Uniti 20
EG - Egitto 20
LT - Lituania 19
PH - Filippine 19
NO - Norvegia 18
PY - Paraguay 18
AZ - Azerbaigian 15
DZ - Algeria 14
PE - Perù 14
KE - Kenya 13
IR - Iran 11
PT - Portogallo 11
DO - Repubblica Dominicana 10
GR - Grecia 10
NP - Nepal 10
TH - Thailandia 10
MY - Malesia 9
TW - Taiwan 9
DK - Danimarca 8
KZ - Kazakistan 8
PS - Palestinian Territory 8
RO - Romania 7
TN - Tunisia 7
AM - Armenia 6
BO - Bolivia 6
BY - Bielorussia 6
CI - Costa d'Avorio 6
CR - Costa Rica 6
EE - Estonia 6
HR - Croazia 6
HU - Ungheria 6
PA - Panama 6
UY - Uruguay 6
ET - Etiopia 5
EU - Europa 5
KG - Kirghizistan 5
LK - Sri Lanka 5
LU - Lussemburgo 5
SK - Slovacchia (Repubblica Slovacca) 5
TT - Trinidad e Tobago 5
AL - Albania 4
CY - Cipro 4
GT - Guatemala 4
LB - Libano 4
LV - Lettonia 4
LY - Libia 4
OM - Oman 4
XK - ???statistics.table.value.countryCode.XK??? 4
BH - Bahrain 3
CG - Congo 3
GE - Georgia 3
NI - Nicaragua 3
PR - Porto Rico 3
RS - Serbia 3
Totale 26.179
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Città #
Warsaw 1.988
Singapore 1.442
Ashburn 1.381
Hong Kong 718
San Jose 712
Chandler 661
Fairfield 611
Houston 606
Woodbridge 567
Trieste 480
Ann Arbor 456
Hefei 378
Wilmington 339
Seoul 336
Seattle 326
Beijing 325
Jacksonville 248
Ho Chi Minh City 245
Cambridge 242
Chicago 229
Los Angeles 228
Boardman 226
Dallas 180
Hanoi 179
Princeton 176
Milan 161
Lauterbourg 150
Santa Clara 146
Sofia 140
Dublin 134
Zgierz 132
Columbus 131
Munich 131
Helsinki 128
Council Bluffs 120
Frankfurt am Main 119
Moscow 111
The Dalles 98
Izmir 95
London 91
New York 87
São Paulo 86
Nuremberg 76
Casablanca 75
Bern 62
Buffalo 61
Dearborn 61
Düsseldorf 54
Lappeenranta 54
Tokyo 52
Brussels 51
Dakar 50
Dong Ket 50
Orem 45
Nanjing 43
Rome 43
Bremen 42
San Diego 42
Turin 40
Vienna 40
Shanghai 39
Johannesburg 38
Amsterdam 37
Atlanta 37
Da Nang 37
Redondo Beach 37
Guangzhou 36
Denver 34
Haiphong 33
Montreal 32
Bologna 31
Turku 31
Phoenix 30
Stockholm 30
Mexico City 29
Mumbai 28
Saint Petersburg 28
Tashkent 28
Tianjin 27
Chennai 26
Des Moines 25
Paris 25
Rio de Janeiro 25
Brooklyn 24
Salt Lake City 24
Baghdad 23
Brno 22
Amman 21
Florence 20
Barletta 19
Belo Horizonte 19
Poplar 19
Redwood City 19
Toronto 19
Boston 18
Boydton 18
Falls Church 18
Jinan 18
Kunming 18
Madrid 18
Totale 17.340
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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 617
Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus 523
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 444
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 390
The p.Cys169Tyr variant of connexin 26 is not a polymorphism 370
Usher syndrome: An effective sequencing approach to establish a genetic and clinical diagnosis 366
Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals 365
A catalog of genetic loci associated with kidney function from analyses of a million individuals. 353
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
Cx26 partial loss causes accelerated presbycusis by redox imbalance and dysregulation of Nfr2 pathway 349
Pharmacogenetics driving personalized medicine: Analysis of genetic polymorphisms related to breast cancer medications in Italian isolated populations 340
Mutations in L-type amino acid transporter-2 support SLC7A8 as a novel gene involved in age-related hearing loss 331
Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss 327
Whole-genome sequencing reveals new insights into age-related hearing loss: cumulative effects, pleiotropy and the role of selection 309
Next Generation Sequencing and Animal Models Reveal SLC9A3R1 as a New Gene Involved in Human Age-Related Hearing Loss 299
Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment 282
Common Variants in UMOD Associate with Urinary Uromodulin Levels: A Meta-Analysis. 278
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels 276
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk 272
Evidence of Inbreeding Depression on Human Height 259
TBL1Y: a new gene involved in syndromic hearing loss 258
Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability 256
A novel P2RX2 mutation in an Italian family affected by autosomal dominant nonsyndromic hearing loss 251
Genetic landscape of populations along the Silk Road: admixture and migration patterns 248
Associations of autozygosity with a broad range of human phenotypes 246
Linkage Study and Exome Sequencing Identify a BDP1 Mutation Associated with Hereditary Hearing Loss 244
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney 244
Consanguinity and Hereditary Hearing Loss in Qatar 241
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair 240
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals 240
Genome-wide analysis identifies 12 loci influencing human reproductive behavior. 230
Estrogen-related receptor gamma and hearing function: evidence of a role in humans and mice 229
Age-related hearing loss and level of education: an epidemiological study on a large cohort of isolated popu-lations 226
GJB2 and GJB6 genes and the A1555G mitochondrial mutation are only minor causes of nonsyndromic hearing loss in the Qatari population 225
MYH9 related disease: four novel mutations of the tail domain of myosin-9 correlating with a mild clinical phenotype 223
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits 223
Next generation sequencing study in a cohort of Italian patients with syndromic hearing loss 217
Effects of Calcium, Magnesium, and Potassium Concentrations on Ventricular Repolarization in Unselected Individuals. 216
Genetic and Phenotypic Characterization of Nexilin (NEXN)-Related Cardiomyopathy: Results From a Multicentric Study 212
New age-related hearing loss candidate genes in humans: an ongoing challenge 207
Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci 206
Hereditary hearing loss: a 96 gene targeted sequencing protocol reveals novel alleles in a series of Italian and Qatari patients 203
Salt-inducible kinase 3, SIK3, is a new gene associated with hearing. 203
Frequency of hearing loss in a series of rural communities of five developing countries located along the Silk Road 202
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) 200
Increased rate of deleterious variants in long runs of homozygosity of an inbred population from Qatar 197
A novel founder MYO15A frameshift duplication is the major cause of genetic hearing loss in Oman 196
Genome-wide association study identifies 74 loci associated with educational attainment 195
Targeted sequencing identifies novel variants involved in autosomal recessive hereditary hearing loss in Qatari families 195
Directional dominance on stature and cognition in diverse human populations 194
Expression and Replication Studies to Identify New Candidate Genes Involved in Normal Hearing Function 188
Lifestyle and normal hearing function in Italy and Central Asia: The potential role of coffee 186
Lights and shadows in the genetics of syndromic and non-syndromic hearing loss in the Italian population 184
Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations. 181
Genetic variants linked to education predict longevity. 181
Challenging Occam's Razor: Dual Molecular Diagnoses Explain Entangled Clinical Pictures 175
Rare and low-frequency coding variants alter human adult height 172
Hearing function and thresholds: a genome-wide association study in European isolated populations identifies new loci and pathways. 169
A bird’s-eye view of Italian genomic variation through whole-genome sequencing 169
Genome-wide meta-analysis of common variant differences between men and women 168
Seventy-five genetic loci influencing the human red blood cell. 167
A saturated map of common genetic variants associated with human height 166
The power of genetic diversity in genome-wide association studies of lipids 165
Genetics, odor perception and food liking: The intriguing role of cinnamon 161
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals 158
Maps of open chromatin highlight cell type-restricted patterns of regulatory sequence variation at hematological trait loci. 158
TTC5 syndrome: Clinical and molecular spectrum of a severe and recognizable condition 156
Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity 155
Proangiogenic properties of complement protein C1q can contribute to endometriosis 154
Natural human knockouts and Mendelian disorders: deep phenotyping in Italian isolates 153
Pendred syndrome, or not pendred syndrome? That is the question 151
Prognostic Prediction of Genotype vs Phenotype in Genetic Cardiomyopathies 149
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences 148
Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color 144
Genetics of hearing loss (from congenital forms to presbycusis) 143
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways 142
There Is More Than Meets the Eye: Identification of Dual Molecular Diagnosis in Patients Affected by Hearing Loss 142
Long QT syndrome and left ventricular non-compaction in a family with KCNH2 mutation: A case report 141
Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function 141
Odontostomatological Traits in North-Eastern Italy's Isolated Populations: An Epidemiological Cross-Sectional Study 139
Genetic dissection of temperament personality traits in Italian isolates 139
Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour 138
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids 137
Mutations in PLS1, encoding fimbrin, cause autosomal dominant nonsyndromic hearing loss 137
Ancestry-related distribution of Runs of homozygosity and functional variants in Qatari population 136
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits 135
Cardiovascular Risk Factors and MRI Markers of Cerebral Small Vessel Disease 135
A possible association between low MBL/lectin pathway functionality and microbiota dysbiosis in endometriosis patients 134
The Enigmatic Genetic Landscape of Hereditary Hearing Loss: A Multistep Diagnostic Strategy in the Italian Population 131
Haploinsufficiency as a Foreground Pathomechanism of Poirer-Bienvenu Syndrome and Novel Insights Underlying the Phenotypic Continuum of CSNK2B-Associated Disorders 131
Puzzling Out the Genetic Architecture of Endometriosis: Whole-Exome Sequencing and Novel Candidate Gene Identification in a Deeply Clinically Characterised Cohort 130
Whole-exome sequencing: Clinical characterization of pediatric and adult Italian patients affected by different forms of hereditary cardiovascular diseases 130
Genome‐Wide Interaction Analyses of Serum Calcium on Ventricular Repolarization Time in 125 393 Participants 130
The role of knockout olfactory receptor genes in odor discrimination 129
The Bittersweet Symphony of COVID-19: Associations between TAS1Rs and TAS2R38 Genetic Variations and COVID-19 Symptoms 125
Hearing loss and brain abnormalities due to pathogenic mutations in ADGRV1 gene: a case report 124
A new case of TAR syndrome confirms the importance of noncoding variants in the etiopathogenesis of the disease 124
Hearing Function: Identification of New Candidate Genes Further Explaining the Complexity of This Sensory Ability 124
Totale 21.856
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Categoria #
all - tutte 75.628
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 75.628
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021362 0 0 0 0 0 0 0 0 0 198 51 113
2021/20221.147 74 39 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
2025/202610.051 1.032 710 906 1.016 924 925 1.567 392 1.210 1.369 0 0
Totale 26.961