ArTS Archivio della ricerca di Trieste

VOZZI, DIEGO
 Distribuzione geografica
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Continente #
NA - Nord America 4.099
EU - Europa 2.721
AS - Asia 1.835
SA - Sud America 325
AF - Africa 59
OC - Oceania 13
Continente sconosciuto - Info sul continente non disponibili 3
Totale 9.055
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Nazione #
US - Stati Uniti d'America 4.039
PL - Polonia 1.072
SG - Singapore 681
CN - Cina 434
IT - Italia 407
SE - Svezia 288
BR - Brasile 255
HK - Hong Kong 233
VN - Vietnam 186
DE - Germania 155
UA - Ucraina 133
FR - Francia 111
GB - Regno Unito 86
FI - Finlandia 83
RU - Federazione Russa 81
TR - Turchia 72
NL - Olanda 71
IE - Irlanda 56
KR - Corea 49
IN - India 48
BG - Bulgaria 43
BE - Belgio 36
MX - Messico 27
CA - Canada 25
BD - Bangladesh 23
AT - Austria 22
AR - Argentina 21
ES - Italia 21
MA - Marocco 16
JP - Giappone 15
SN - Senegal 15
CZ - Repubblica Ceca 12
ID - Indonesia 12
VE - Venezuela 12
AU - Australia 11
SA - Arabia Saudita 11
ZA - Sudafrica 11
CH - Svizzera 10
DK - Danimarca 9
UZ - Uzbekistan 9
CL - Cile 8
IQ - Iraq 8
CO - Colombia 7
PH - Filippine 7
AE - Emirati Arabi Uniti 6
EC - Ecuador 6
PE - Perù 6
PK - Pakistan 6
PY - Paraguay 6
DZ - Algeria 5
IR - Iran 5
PT - Portogallo 5
AL - Albania 3
AZ - Azerbaigian 3
DO - Repubblica Dominicana 3
GR - Grecia 3
LT - Lituania 3
TH - Thailandia 3
AM - Armenia 2
BO - Bolivia 2
EG - Egitto 2
EU - Europa 2
IL - Israele 2
JO - Giordania 2
KE - Kenya 2
KG - Kirghizistan 2
KZ - Kazakistan 2
LK - Sri Lanka 2
NO - Norvegia 2
PA - Panama 2
PS - Palestinian Territory 2
RO - Romania 2
SK - Slovacchia (Repubblica Slovacca) 2
TT - Trinidad e Tobago 2
TW - Taiwan 2
UG - Uganda 2
UY - Uruguay 2
BH - Bahrain 1
BN - Brunei Darussalam 1
BW - Botswana 1
CG - Congo 1
EE - Estonia 1
ET - Etiopia 1
GE - Georgia 1
HN - Honduras 1
HU - Ungheria 1
KH - Cambogia 1
LA - Repubblica Popolare Democratica del Laos 1
LU - Lussemburgo 1
MD - Moldavia 1
MG - Madagascar 1
MT - Malta 1
MY - Malesia 1
NA - Namibia 1
NC - Nuova Caledonia 1
NP - Nepal 1
NZ - Nuova Zelanda 1
OM - Oman 1
TN - Tunisia 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 9.055
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Città #
Warsaw 1.041
Ashburn 455
Singapore 415
Fairfield 330
Chandler 289
Houston 279
Woodbridge 269
Ann Arbor 256
Hong Kong 219
Wilmington 172
San Jose 161
Seattle 159
Jacksonville 135
Trieste 124
Cambridge 111
Beijing 81
Boardman 73
Princeton 72
Chicago 71
Los Angeles 65
Dearborn 60
Dublin 55
Hanoi 47
Izmir 45
Seoul 44
Sofia 43
Ho Chi Minh City 42
Lauterbourg 40
Munich 40
Columbus 38
New York 38
Hefei 36
Helsinki 36
Brussels 32
Moscow 32
Santa Clara 32
Dallas 29
Frankfurt am Main 29
Council Bluffs 28
Zgierz 28
Düsseldorf 27
Buffalo 22
The Dalles 22
Milan 21
Amsterdam 20
Orem 20
São Paulo 19
Bremen 18
London 18
Des Moines 17
Salt Lake City 17
Shanghai 17
Stockholm 17
San Diego 16
Dakar 15
Dong Ket 14
Redwood City 13
Tokyo 13
Ankara 12
Casablanca 12
Guangzhou 12
Nanjing 12
Washington 11
Kunming 10
Redondo Beach 10
Tampa 10
Brooklyn 9
Falls Church 9
Manchester 9
Montreal 9
Nuremberg 9
Portsmouth 9
St Louis 9
Tashkent 9
Vienna 9
Atlanta 8
Da Nang 8
Florence 8
Haiphong 8
Istanbul 8
Johannesburg 8
Nanchang 8
Scuola 8
Sterling 8
Boston 7
Brno 7
Fremont 7
Jinan 7
Paris 7
Pignone 7
Tianjin 7
Bologna 6
Chennai 6
Fuzhou 6
Hebei 6
Melbourne 6
Mexico City 6
North Bergen 6
Shenyang 6
Turku 6
Totale 6.222
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Nome #
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 442
Rare coding variants and X-linked loci associated with age at menarche 437
Type i interferon-mediated autoinflammation due to DNase II deficiency 389
Two‑gene mutation in a single patient: Biochemical and functional analysis for a correct interpretation of exome results. 379
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
Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss 326
Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype 276
Novel NOD2 Mutation in Early-Onset Inflammatory Bowel Phenotype 273
TBL1Y: a new gene involved in syndromic hearing loss 257
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
Target sequencing approach intended to discover new mutations in non-syndromic intellectual disability 243
Linkage Study and Exome Sequencing Identify a BDP1 Mutation Associated with Hereditary Hearing Loss 242
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
Mevalonate kinase deficiency and IBD: shared genetic background 238
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals 236
Alagille syndrome: A new missense mutation detected by whole-exome sequencing in a case previously found to be negative by DHPLC and MLPA 213
Putative modifier genes in mevalonate kinase deficiency 210
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. 205
Hereditary hearing loss: a 96 gene targeted sequencing protocol reveals novel alleles in a series of Italian and Qatari patients 203
Molecular Diagnosis of Usher Syndrome: Application of Two Different Next Generation Sequencing-Based Procedures 201
The Challenge of Next Generation Sequencing in a Boy with Severe Mononucleosis and EBV-related Lymphoma 198
Increased rate of deleterious variants in long runs of homozygosity of an inbred population from Qatar 195
Targeted sequencing identifies novel variants involved in autosomal recessive hereditary hearing loss in Qatari families 193
Directional dominance on stature and cognition in diverse human populations 192
Molecular epidemiology of Usher syndrome in Italy 190
Next generation sequencing in nonsyndromic intellectual disability: From a negative molecular karyotype to a possible causative mutation detection 187
Genetic variants linked to education predict longevity. 179
Rare and low-frequency coding variants alter human adult height 172
Microarray and large-scale in silico-based identification of genes functionally related to Haptoglobin and/or Hemopexin. 148
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences 148
Excess of runs of homozygosity is associated with severe cognitive impairment in intellectual disability. 139
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders 128
null 124
Integrative multi-omic analysis reveals conserved cell-projection deficits in human Down syndrome brains 106
Organo-silane coated substrates for DNA purification 94
Totale 9.322
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Categoria #
all - tutte 24.267
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 24.267
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021173 0 0 0 0 0 0 0 0 0 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
2024/20251.393 37 33 79 124 120 99 73 97 171 196 285 79
2025/20262.406 326 184 140 164 267 239 422 100 292 272 0 0
Totale 9.322