GIROTTO, GIORGIA
 Distribuzione geografica
Continente #
NA - Nord America 5.782
EU - Europa 4.591
AS - Asia 967
AF - Africa 53
SA - Sud America 20
OC - Oceania 7
Continente sconosciuto - Info sul continente non disponibili 6
Totale 11.426
Nazione #
US - Stati Uniti d'America 5.771
PL - Polonia 1.927
IT - Italia 1.083
SE - Svezia 505
CN - Cina 387
HK - Hong Kong 380
UA - Ucraina 212
FI - Finlandia 139
BG - Bulgaria 137
DE - Germania 131
BE - Belgio 115
IE - Irlanda 108
TR - Turchia 100
CH - Svizzera 64
GB - Regno Unito 60
VN - Vietnam 52
SN - Senegal 44
RU - Federazione Russa 34
NL - Olanda 21
FR - Francia 18
BR - Brasile 15
IN - India 13
CA - Canada 10
JP - Giappone 8
CI - Costa d'Avorio 7
SG - Singapore 7
AT - Austria 6
AU - Australia 6
CZ - Repubblica Ceca 5
ES - Italia 5
EU - Europa 5
IR - Iran 5
KR - Corea 5
GR - Grecia 4
CL - Cile 3
IL - Israele 3
PT - Portogallo 3
AE - Emirati Arabi Uniti 2
HR - Croazia 2
IM - Isola di Man 2
IS - Islanda 2
JO - Giordania 2
LU - Lussemburgo 2
RO - Romania 2
SI - Slovenia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
BN - Brunei Darussalam 1
CM - Camerun 1
DZ - Algeria 1
EE - Estonia 1
LK - Sri Lanka 1
MX - Messico 1
MY - Malesia 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
PE - Perù 1
PY - Paraguay 1
Totale 11.426
Città #
Warsaw 1.926
Chandler 661
Fairfield 610
Houston 589
Woodbridge 566
Ashburn 480
Ann Arbor 456
Hong Kong 371
Wilmington 333
Seattle 315
Trieste 291
Jacksonville 245
Cambridge 240
Princeton 176
Sofia 137
Beijing 119
Dublin 108
Brussels 106
Izmir 94
Boydton 73
Boardman 71
Helsinki 62
Bern 61
Dearborn 61
Milan 60
Dong Ket 50
Dakar 44
Bremen 42
San Diego 42
Turin 40
Saint Petersburg 28
Nanjing 22
Des Moines 21
Hefei 21
Barletta 19
Redwood City 19
Rome 19
Falls Church 18
Florence 16
Jinan 15
Guangzhou 14
Pignone 14
Kunming 12
London 12
Munich 12
Redmond 12
Chicago 11
Norwalk 11
Phoenix 11
Shanghai 11
Fremont 10
Hanover 10
Nanchang 10
Scuola 10
Udine 10
Washington 10
Dongguan 9
Lappeenranta 9
Pordenone 9
Pune 9
Bologna 8
Paris 8
Quinto di Treviso 8
Shenyang 8
São Paulo 8
Waanrode 8
Abidjan 7
Berlin 7
Venezia 7
Fuzhou 6
Gorizia 6
Leawood 6
Mestre 6
Triggiano 6
Venice 6
Wuhan 6
Amsterdam 5
Brno 5
Columbus 5
Ferrara 5
Grafing 5
Tappahannock 5
Turi 5
Vienna 5
Auburn Hills 4
Central 4
Dallas 4
Edinburgh 4
Hagen 4
Imola 4
Ivrea 4
Lainate 4
Naaldwijk 4
Padova 4
Philadelphia 4
Southend 4
Tavagnacco 4
Tokyo 4
Xian 4
Zhengzhou 4
Totale 9.058
Nome #
Il Registro Regionale delle Morti Cardiache Improvvise in età giovanile del Friuli Venezia Giulia. Protocolli operativi e risultati di un progetto multidisciplinare 380
PSIP1/LEDGF: A new gene likely involved in sensorineural progressive hearing loss 349
1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function 337
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 321
Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss 320
The p.Cys169Tyr variant of connexin 26 is not a polymorphism 307
Pharmacogenetics driving personalized medicine: Analysis of genetic polymorphisms related to breast cancer medications in Italian isolated populations 300
Mutations in L-type amino acid transporter-2 support SLC7A8 as a novel gene involved in age-related hearing loss 273
Cx26 partial loss causes accelerated presbycusis by redox imbalance and dysregulation of Nfr2 pathway 270
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 259
Whole-genome sequencing reveals new insights into age-related hearing loss: cumulative effects, pleiotropy and the role of selection 255
Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss 241
A catalog of genetic loci associated with kidney function from analyses of a million individuals. 232
Next Generation Sequencing and Animal Models Reveal SLC9A3R1 as a New Gene Involved in Human Age-Related Hearing Loss 213
Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment 188
Evidence of Inbreeding Depression on Human Height 172
TBL1Y: a new gene involved in syndromic hearing loss 169
Targeted sequencing identifies novel variants involved in autosomal recessive hereditary hearing loss in Qatari families 161
Frequency of hearing loss in a series of rural communities of five developing countries located along the Silk Road 160
A novel P2RX2 mutation in an Italian family affected by autosomal dominant nonsyndromic hearing loss 159
Usher syndrome: An effective sequencing approach to establish a genetic and clinical diagnosis 159
Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability 157
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair 153
Linkage Study and Exome Sequencing Identify a BDP1 Mutation Associated with Hereditary Hearing Loss 151
MYH9 related disease: four novel mutations of the tail domain of myosin-9 correlating with a mild clinical phenotype 150
Genetic landscape of populations along the Silk Road: admixture and migration patterns 148
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney 147
Salt-inducible kinase 3, SIK3, is a new gene associated with hearing. 146
Consanguinity and Hereditary Hearing Loss in Qatar 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
Lifestyle and normal hearing function in Italy and Central Asia: The potential role of coffee 139
GJB2 and GJB6 genes and the A1555G mitochondrial mutation are only minor causes of nonsyndromic hearing loss in the Qatari population 139
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits 136
Age-related hearing loss and level of education: an epidemiological study on a large cohort of isolated popu-lations 131
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk 130
A novel founder MYO15A frameshift duplication is the major cause of genetic hearing loss in Oman 127
Hereditary hearing loss: a 96 gene targeted sequencing protocol reveals novel alleles in a series of Italian and Qatari patients 125
Seventy-five genetic loci influencing the human red blood cell. 122
Hearing function and thresholds: a genome-wide association study in European isolated populations identifies new loci and pathways. 120
Increased rate of deleterious variants in long runs of homozygosity of an inbred population from Qatar 119
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels 119
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals 117
Next generation sequencing study in a cohort of Italian patients with syndromic hearing loss 117
Expression and Replication Studies to Identify New Candidate Genes Involved in Normal Hearing Function 116
Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations. 112
Genome-wide analysis identifies 12 loci influencing human reproductive behavior. 110
Effects of Calcium, Magnesium, and Potassium Concentrations on Ventricular Repolarization in Unselected Individuals. 109
Mutations in PLS1, encoding fimbrin, cause autosomal dominant nonsyndromic hearing loss 101
Genetic variants linked to education predict longevity. 95
Rare and low-frequency coding variants alter human adult height 95
Directional dominance on stature and cognition in diverse human populations 93
Associations of autozygosity with a broad range of human phenotypes 93
Genome-wide association study identifies 74 loci associated with educational attainment 89
Maps of open chromatin highlight cell type-restricted patterns of regulatory sequence variation at hematological trait loci. 83
Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color 78
Genome-wide meta-analysis of common variant differences between men and women 76
Lights and shadows in the genetics of syndromic and non-syndromic hearing loss in the Italian population 71
Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci 70
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) 67
Genetics of hearing loss (from congenital forms to presbycusis) 65
A bird’s-eye view of Italian genomic variation through whole-genome sequencing 64
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution 63
Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour 63
MYH9 related disease: a novel missense Ala95Asp mutation of the MYH9 gene. 61
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences 61
Hearing loss and brain abnormalities due to pathogenic mutations in ADGRV1 gene: a case report 61
Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function 60
New age-related hearing loss candidate genes in humans: an ongoing challenge 58
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals 48
Natural human knockouts and Mendelian disorders: deep phenotyping in Italian isolates 47
Genetic dissection of temperament personality traits in Italian isolates 47
Pendred syndrome, or not pendred syndrome? That is the question 46
Benefit of cochlear implantation in a patient with Myhre syndrome 46
A new case of TAR syndrome confirms the importance of noncoding variants in the etiopathogenesis of the disease 45
Puzzling Out the Genetic Architecture of Endometriosis: Whole-Exome Sequencing and Novel Candidate Gene Identification in a Deeply Clinically Characterised Cohort 43
Whole-exome sequencing: Clinical characterization of pediatric and adult Italian patients affected by different forms of hereditary cardiovascular diseases 43
Genetics, odor perception and food liking: The intriguing role of cinnamon 43
Variants in USP48 encoding ubiquitin hydrolase are associated with autosomal dominant non-syndromic hereditary hearing loss 43
Sensory Capacities and Eating Behavior: Intriguing Results from a Large Cohort of Italian Individuals 40
Hearing Function: Identification of New Candidate Genes Further Explaining the Complexity of This Sensory Ability 40
Non-syndromic autosomal dominant hearing loss: The first italian family carrying a mutation in the NCOA3 gene 39
The role of knockout olfactory receptor genes in odor discrimination 38
A saturated map of common genetic variants associated with human height 37
Odontostomatological Traits in North-Eastern Italy's Isolated Populations: An Epidemiological Cross-Sectional Study 37
Meta-GWAS Reveals Novel Genetic Variants Associated with Urinary Excretion of Uromodulin 37
There Is More Than Meets the Eye: Identification of Dual Molecular Diagnosis in Patients Affected by Hearing Loss 37
Functional analysis of candidate genes from genome-wide association studies of hearing 36
TTC5 syndrome: Clinical and molecular spectrum of a severe and recognizable condition 35
Prognostic Prediction of Genotype vs Phenotype in Genetic Cardiomyopathies 35
Sordità da cause genetiche 35
Molecular testing for the study of non-syndromic hearing loss 35
TBC1D24 and non-syndromic autosomal dominant hearing loss: the identification of an additional Italo-American family carrying the p.(S178L) mutation 35
Impact of cultural and genetic structure on food choices along the Silk Road 34
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) 34
SLC12A2: a new gene associated with autosomal dominant Non-Syndromic hearing loss in humans 33
Chronic Rhinosinusitis: T2r38 Genotyping and Nasal Cytology in Primary Ciliary Dyskinesia 33
High Throughput Genetic Characterisation of Caucasian Patients Affected by Multi-Drug Resistant Rheumatoid or Psoriatic Arthritis 32
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways 32
Identifying missing pieces in color vision defects: a genome-wide association study in Silk Road populations 32
Totale 11.559
Categoria #
all - tutte 30.224
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 30.224


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019724 0 0 0 0 0 0 0 0 56 153 333 182
2019/20202.401 125 145 114 356 175 336 254 205 237 140 174 140
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
2022/20232.292 176 250 128 308 216 331 48 324 265 57 131 58
2023/20241.519 139 151 104 162 133 169 357 301 3 0 0 0
Totale 12.006