ArTS Archivio della ricerca di Trieste

GIROTTO, GIORGIA
 Distribuzione geografica
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Continente #
NA - Nord America 5.988
EU - Europa 4.789
AS - Asia 1.444
AF - Africa 47
SA - Sud America 39
OC - Oceania 10
Continente sconosciuto - Info sul continente non disponibili 6
Totale 12.323
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Nazione #
US - Stati Uniti d'America 5.973
PL - Polonia 1.929
IT - Italia 1.206
SE - Svezia 509
CN - Cina 465
HK - Hong Kong 389
SG - Singapore 356
UA - Ucraina 213
DE - Germania 157
FI - Finlandia 152
BG - Bulgaria 137
IE - Irlanda 109
TR - Turchia 101
GB - Regno Unito 75
CH - Svizzera 66
BE - Belgio 55
VN - Vietnam 54
RU - Federazione Russa 50
SN - Senegal 44
FR - Francia 32
BR - Brasile 26
CZ - Repubblica Ceca 25
NL - Olanda 25
KR - Corea 24
JP - Giappone 17
IN - India 15
CA - Canada 13
AT - Austria 12
AU - Australia 9
ES - Italia 9
CL - Cile 7
EU - Europa 5
IR - Iran 5
GR - Grecia 4
IL - Israele 4
LU - Lussemburgo 4
PT - Portogallo 4
CO - Colombia 3
DK - Danimarca 3
AE - Emirati Arabi Uniti 2
CY - Cipro 2
HR - Croazia 2
IM - Isola di Man 2
IS - Islanda 2
JO - Giordania 2
KG - Kirghizistan 2
MX - Messico 2
RO - Romania 2
A2 - ???statistics.table.value.countryCode.A2??? 1
BD - Bangladesh 1
BN - Brunei Darussalam 1
CM - Camerun 1
DZ - Algeria 1
EC - Ecuador 1
EE - Estonia 1
EG - Egitto 1
HU - Ungheria 1
LA - Repubblica Popolare Democratica del Laos 1
LK - Sri Lanka 1
LV - Lettonia 1
MY - Malesia 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
PE - Perù 1
PY - Paraguay 1
SI - Slovenia 1
TW - Taiwan 1
Totale 12.323
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Città #
Warsaw 1.928
Chandler 661
Fairfield 610
Houston 589
Woodbridge 566
Ashburn 482
Ann Arbor 456
Hong Kong 373
Wilmington 335
Trieste 319
Seattle 316
Singapore 297
Jacksonville 245
Cambridge 240
Princeton 176
Sofia 137
Beijing 126
Dublin 109
Izmir 95
Boardman 80
Milan 76
Helsinki 68
Bern 61
Dearborn 61
Dong Ket 50
Santa Clara 47
Brussels 45
Dakar 44
Bremen 42
San Diego 42
Turin 40
Saint Petersburg 28
Nanjing 27
Rome 26
Brno 22
Los Angeles 22
Munich 22
Des Moines 21
Hefei 21
Shanghai 20
Barletta 19
Redwood City 19
Seoul 19
Falls Church 18
Guangzhou 18
Boydton 17
Dallas 17
Florence 16
Lappeenranta 16
Chicago 15
Jinan 15
Pignone 14
Shenyang 13
Bologna 12
Kunming 12
London 12
Redmond 12
Norwalk 11
Phoenix 11
Fremont 10
Nanchang 10
Scuola 10
Udine 10
Vienna 10
Washington 10
Dongguan 9
Pordenone 9
Pune 9
São Paulo 9
Paris 8
Quinto di Treviso 8
Waanrode 8
Berlin 7
Grottaglie 7
Tianjin 7
Venezia 7
Frankfurt am Main 6
Fuzhou 6
Gorizia 6
Leawood 6
Mestre 6
Padova 6
Philadelphia 6
Triggiano 6
Venice 6
Wuhan 6
Amsterdam 5
Campinas 5
Columbus 5
Düsseldorf 5
Erechim 5
Ferrara 5
Grafing 5
Islington 5
New York 5
Tappahannock 5
Turi 5
Auburn Hills 4
Bochum 4
Buffalo 4
Totale 9.486
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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 426
PSIP1/LEDGF: A new gene likely involved in sensorineural progressive hearing loss 362
1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function 334
Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss 328
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 322
The p.Cys169Tyr variant of connexin 26 is not a polymorphism 308
Pharmacogenetics driving personalized medicine: Analysis of genetic polymorphisms related to breast cancer medications in Italian isolated populations 301
Mutations in L-type amino acid transporter-2 support SLC7A8 as a novel gene involved in age-related hearing loss 285
Cx26 partial loss causes accelerated presbycusis by redox imbalance and dysregulation of Nfr2 pathway 277
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 260
Whole-genome sequencing reveals new insights into age-related hearing loss: cumulative effects, pleiotropy and the role of selection 256
Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss 242
A catalog of genetic loci associated with kidney function from analyses of a million individuals. 233
Next Generation Sequencing and Animal Models Reveal SLC9A3R1 as a New Gene Involved in Human Age-Related Hearing Loss 219
Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment 190
Usher syndrome: An effective sequencing approach to establish a genetic and clinical diagnosis 187
Evidence of Inbreeding Depression on Human Height 179
TBL1Y: a new gene involved in syndromic hearing loss 179
A novel P2RX2 mutation in an Italian family affected by autosomal dominant nonsyndromic hearing loss 164
Frequency of hearing loss in a series of rural communities of five developing countries located along the Silk Road 161
Targeted sequencing identifies novel variants involved in autosomal recessive hereditary hearing loss in Qatari families 161
Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability 159
Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus 158
Common Variants in UMOD Associate with Urinary Uromodulin Levels: A Meta-Analysis. 156
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair 156
Linkage Study and Exome Sequencing Identify a BDP1 Mutation Associated with Hereditary Hearing Loss 155
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney 155
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk 152
MYH9 related disease: four novel mutations of the tail domain of myosin-9 correlating with a mild clinical phenotype 151
Genetic landscape of populations along the Silk Road: admixture and migration patterns 151
Estrogen-related receptor gamma and hearing function: evidence of a role in humans and mice 149
Consanguinity and Hereditary Hearing Loss in Qatar 148
Salt-inducible kinase 3, SIK3, is a new gene associated with hearing. 147
GJB2 and GJB6 genes and the A1555G mitochondrial mutation are only minor causes of nonsyndromic hearing loss in the Qatari population 147
Lifestyle and normal hearing function in Italy and Central Asia: The potential role of coffee 141
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits 137
Age-related hearing loss and level of education: an epidemiological study on a large cohort of isolated popu-lations 134
A novel founder MYO15A frameshift duplication is the major cause of genetic hearing loss in Oman 129
Hereditary hearing loss: a 96 gene targeted sequencing protocol reveals novel alleles in a series of Italian and Qatari patients 128
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals 126
Next generation sequencing study in a cohort of Italian patients with syndromic hearing loss 126
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels 124
Hearing function and thresholds: a genome-wide association study in European isolated populations identifies new loci and pathways. 123
Increased rate of deleterious variants in long runs of homozygosity of an inbred population from Qatar 123
Genome-wide analysis identifies 12 loci influencing human reproductive behavior. 123
Seventy-five genetic loci influencing the human red blood cell. 123
Expression and Replication Studies to Identify New Candidate Genes Involved in Normal Hearing Function 118
Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations. 114
Effects of Calcium, Magnesium, and Potassium Concentrations on Ventricular Repolarization in Unselected Individuals. 113
Associations of autozygosity with a broad range of human phenotypes 108
Mutations in PLS1, encoding fimbrin, cause autosomal dominant nonsyndromic hearing loss 102
Rare and low-frequency coding variants alter human adult height 98
Genetic variants linked to education predict longevity. 97
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) 97
Directional dominance on stature and cognition in diverse human populations 96
Genome-wide association study identifies 74 loci associated with educational attainment 91
Lights and shadows in the genetics of syndromic and non-syndromic hearing loss in the Italian population 90
Genome-wide meta-analysis of common variant differences between men and women 89
Maps of open chromatin highlight cell type-restricted patterns of regulatory sequence variation at hematological trait loci. 86
New age-related hearing loss candidate genes in humans: an ongoing challenge 82
Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci 78
Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color 78
Hearing loss and brain abnormalities due to pathogenic mutations in ADGRV1 gene: a case report 76
Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour 76
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution 67
Genetics of hearing loss (from congenital forms to presbycusis) 66
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences 64
Genetics, odor perception and food liking: The intriguing role of cinnamon 63
A bird’s-eye view of Italian genomic variation through whole-genome sequencing 62
MYH9 related disease: a novel missense Ala95Asp mutation of the MYH9 gene. 61
Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function 58
Natural human knockouts and Mendelian disorders: deep phenotyping in Italian isolates 57
Sordità da cause genetiche 55
There Is More Than Meets the Eye: Identification of Dual Molecular Diagnosis in Patients Affected by Hearing Loss 52
Functional analysis of candidate genes from genome-wide association studies of hearing 51
The power of genetic diversity in genome-wide association studies of lipids 50
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals 49
A new case of TAR syndrome confirms the importance of noncoding variants in the etiopathogenesis of the disease 49
Benefit of cochlear implantation in a patient with Myhre syndrome 49
Genetic dissection of temperament personality traits in Italian isolates 48
Pendred syndrome, or not pendred syndrome? That is the question 47
Publisher Correction: Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability (Nature Genetics, (2018), 50, 5, (652-656), 10.1038/s41588-018-0100-5) 45
Variants in USP48 encoding ubiquitin hydrolase are associated with autosomal dominant non-syndromic hereditary hearing loss 44
TBC1D24 and non-syndromic autosomal dominant hearing loss: the identification of an additional Italo-American family carrying the p.(S178L) mutation 44
Primary Ciliary Dyskinesia: The Impact of Taste Receptor (TAS2R38) Gene Polymorphisms on Disease Outcome and Severity 43
Meta-GWAS Reveals Novel Genetic Variants Associated with Urinary Excretion of Uromodulin 42
Hearing Function: Identification of New Candidate Genes Further Explaining the Complexity of This Sensory Ability 42
A saturated map of common genetic variants associated with human height 41
The role of knockout olfactory receptor genes in odor discrimination 41
Sensory Capacities and Eating Behavior: Intriguing Results from a Large Cohort of Italian Individuals 40
Non-syndromic autosomal dominant hearing loss: The first italian family carrying a mutation in the NCOA3 gene 40
SLC12A2: a new gene associated with autosomal dominant Non-Syndromic hearing loss in humans 39
Odontostomatological Traits in North-Eastern Italy's Isolated Populations: An Epidemiological Cross-Sectional Study 38
Long QT syndrome and left ventricular non-compaction in a family with KCNH2 mutation: A case report 38
Prognostic Prediction of Genotype vs Phenotype in Genetic Cardiomyopathies 38
Non-syndromic sensorineural prelingual and postlingual hearing loss due to col11a1 gene mutation 38
TTC5 syndrome: Clinical and molecular spectrum of a severe and recognizable condition 37
Molecular testing for the study of non-syndromic hearing loss 37
Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals 37
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways 35
Totale 12.291
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Categoria #
all - tutte 38.713
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 38.713
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20202.131 0 0 114 356 175 336 254 205 237 140 174 140
2020/20211.920 162 120 188 179 231 197 162 119 200 198 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
2023/20241.821 130 117 98 159 121 169 357 301 24 62 138 145
2024/2025704 168 227 309 0 0 0 0 0 0 0 0 0
Totale 12.929