ArTS Archivio della ricerca di Trieste

VOZZI, DIEGO
 Distribuzione geografica
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Continente #
NA - Nord America 2.895
EU - Europa 2.160
AS - Asia 640
AF - Africa 13
SA - Sud America 12
OC - Oceania 4
Continente sconosciuto - Info sul continente non disponibili 2
Totale 5.726
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Nazione #
US - Stati Uniti d'America 2.887
PL - Polonia 1.027
IT - Italia 342
SE - Svezia 274
CN - Cina 258
SG - Singapore 158
HK - Hong Kong 132
UA - Ucraina 127
DE - Germania 65
FI - Finlandia 63
TR - Turchia 54
RU - Federazione Russa 47
IE - Irlanda 45
BG - Bulgaria 41
BE - Belgio 35
GB - Regno Unito 28
NL - Olanda 19
VN - Vietnam 15
SN - Senegal 13
FR - Francia 10
CZ - Repubblica Ceca 9
CA - Canada 7
CH - Svizzera 7
KR - Corea 7
BR - Brasile 5
DK - Danimarca 5
AU - Australia 3
CL - Cile 3
ES - Italia 3
GR - Grecia 3
IN - India 3
IR - Iran 3
PT - Portogallo 3
AE - Emirati Arabi Uniti 2
AT - Austria 2
CO - Colombia 2
EU - Europa 2
SA - Arabia Saudita 2
AL - Albania 1
AR - Argentina 1
BN - Brunei Darussalam 1
IL - Israele 1
KG - Kirghizistan 1
KZ - Kazakistan 1
LA - Repubblica Popolare Democratica del Laos 1
LK - Sri Lanka 1
LU - Lussemburgo 1
MD - Moldavia 1
MX - Messico 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
PE - Perù 1
RO - Romania 1
Totale 5.726
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Città #
Warsaw 1.026
Fairfield 329
Chandler 289
Houston 272
Woodbridge 269
Ann Arbor 256
Ashburn 195
Wilmington 169
Seattle 157
Singapore 137
Jacksonville 135
Hong Kong 128
Cambridge 111
Trieste 104
Princeton 72
Boardman 66
Dearborn 59
Dublin 45
Izmir 45
Sofia 41
Columbus 36
Beijing 33
Brussels 31
Moscow 30
Helsinki 22
Santa Clara 22
Bremen 18
Shanghai 17
Hefei 16
Des Moines 15
Munich 15
San Diego 15
Dong Ket 14
Dakar 13
Redwood City 13
Los Angeles 12
Milan 11
Kunming 10
Washington 10
Amsterdam 9
Falls Church 9
Nanjing 9
Nanchang 8
Scuola 8
Brno 7
Fremont 7
Jinan 7
Pignone 7
Chicago 6
Düsseldorf 6
Florence 6
Guangzhou 6
Hebei 6
London 6
New York 6
Seoul 6
Shenyang 6
Xian 6
Cagliari 5
Changsha 5
Dallas 5
Fuzhou 5
Grottaglie 5
Ankara 4
Dormagen 4
Grafing 4
North Bergen 4
Paris 4
Phoenix 4
Redmond 4
Rome 4
São Paulo 4
Taizhou 4
Barletta 3
Bologna 3
Detroit 3
Dongguan 3
Edinburgh 3
Genova 3
Manchester 3
Mestre 3
Montreal 3
Naples 3
San Francisco 3
Stockholm 3
Waanrode 3
Zurich 3
Assemini 2
Bogotá 2
Brescia 2
Castrovillari 2
Chengdu 2
Dubai 2
Frankfurt am Main 2
Hangzhou 2
Hanover 2
Horni Terlicko 2
Hyde Park 2
Istanbul 2
Jeddah 2
Totale 4.522
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Nome #
PSIP1/LEDGF: A new gene likely involved in sensorineural progressive hearing loss 370
Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss 338
Two‑gene mutation in a single patient: Biochemical and functional analysis for a correct interpretation of exome results. 308
Type i interferon-mediated autoinflammation due to DNase II deficiency 300
Rare coding variants and X-linked loci associated with age at menarche 290
Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss 249
Usher syndrome: An effective sequencing approach to establish a genetic and clinical diagnosis 214
TBL1Y: a new gene involved in syndromic hearing loss 184
A novel P2RX2 mutation in an Italian family affected by autosomal dominant nonsyndromic hearing loss 170
Targeted sequencing identifies novel variants involved in autosomal recessive hereditary hearing loss in Qatari families 168
Mevalonate kinase deficiency and IBD: shared genetic background 164
Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype 163
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair 163
Linkage Study and Exome Sequencing Identify a BDP1 Mutation Associated with Hereditary Hearing Loss 162
Target sequencing approach intended to discover new mutations in non-syndromic intellectual disability 162
Genetic landscape of populations along the Silk Road: admixture and migration patterns 161
Novel NOD2 Mutation in Early-Onset Inflammatory Bowel Phenotype 157
Consanguinity and Hereditary Hearing Loss in Qatar 154
Putative modifier genes in mevalonate kinase deficiency 151
Next generation sequencing in nonsyndromic intellectual disability: From a negative molecular karyotype to a possible causative mutation detection 146
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals 137
Hereditary hearing loss: a 96 gene targeted sequencing protocol reveals novel alleles in a series of Italian and Qatari patients 136
Increased rate of deleterious variants in long runs of homozygosity of an inbred population from Qatar 132
Analisi mediante metodiche di sequenziamente di nuova generazione di soggetti affetti da sordità genetica, finalizzata all’individuazione di alterazioni genomiche patogenetiche, non descritte in precedenza. 127
Alagille syndrome: A new missense mutation detected by whole-exome sequencing in a case previously found to be negative by DHPLC and MLPA 126
null 124
Molecular Diagnosis of Usher Syndrome: Application of Two Different Next Generation Sequencing-Based Procedures 121
Molecular epidemiology of Usher syndrome in Italy 111
Genetic variants linked to education predict longevity. 107
Rare and low-frequency coding variants alter human adult height 107
Directional dominance on stature and cognition in diverse human populations 104
The Challenge of Next Generation Sequencing in a Boy with Severe Mononucleosis and EBV-related Lymphoma 99
Microarray and large-scale in silico-based identification of genes functionally related to Haptoglobin and/or Hemopexin. 70
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences 70
Organo-silane coated substrates for DNA purification 67
Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals 63
Excess of runs of homozygosity is associated with severe cognitive impairment in intellectual disability. 57
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders 57
Totale 5.989
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Categoria #
all - tutte 16.402
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 16.402
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020755 0 0 0 0 0 171 154 119 111 62 91 47
2020/2021792 75 51 59 77 88 62 59 62 86 84 26 63
2021/2022545 18 30 26 36 31 39 31 17 59 44 45 169
2022/2023838 93 115 55 144 75 142 3 65 92 13 37 4
2023/2024514 15 31 33 39 32 67 103 84 7 19 47 37
2024/2025466 37 33 79 124 120 73 0 0 0 0 0 0
Totale 5.989