ArTS Archivio della ricerca di Trieste

VOZZI, DIEGO
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 4.320
EU - Europa 2.798
AS - Asia 1.974
SA - Sud America 328
AF - Africa 59
OC - Oceania 15
Continente sconosciuto - Info sul continente non disponibili 3
Totale 9.497
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 4.245
PL - Polonia 1.072
SG - Singapore 682
IT - Italia 478
CN - Cina 441
SE - Svezia 288
BR - Brasile 256
HK - Hong Kong 234
VN - Vietnam 186
DE - Germania 155
BD - Bangladesh 143
UA - Ucraina 133
FR - Francia 116
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
CA - Canada 35
MX - Messico 29
AR - Argentina 22
AT - Austria 22
ES - Italia 22
JP - Giappone 17
MA - Marocco 16
SN - Senegal 15
AU - Australia 13
CZ - Repubblica Ceca 12
ID - Indonesia 12
VE - Venezuela 12
PK - Pakistan 11
SA - Arabia Saudita 11
ZA - Sudafrica 11
CH - Svizzera 10
DK - Danimarca 9
UZ - Uzbekistan 9
CL - Cile 8
CO - Colombia 8
IQ - Iraq 8
PH - Filippine 8
AE - Emirati Arabi Uniti 6
EC - Ecuador 6
PE - Perù 6
PY - Paraguay 6
DZ - Algeria 5
IR - Iran 5
PT - Portogallo 5
TW - Taiwan 4
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
CR - Costa Rica 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
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
JM - Giamaica 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
Totale 9.495
Salva come PNG Salva come JPEG
Città #
Warsaw 1.041
Ashburn 506
Singapore 416
Fairfield 330
Chandler 289
Houston 281
Woodbridge 269
Ann Arbor 256
Hong Kong 220
San Jose 181
Wilmington 172
Seattle 160
Jacksonville 135
Trieste 124
Cambridge 111
Beijing 82
Los Angeles 76
Chicago 74
Boardman 73
Princeton 72
Dearborn 60
Dublin 56
Hanoi 47
New York 46
Izmir 45
Seoul 44
Sofia 43
Ho Chi Minh City 42
Lauterbourg 40
Munich 40
Columbus 38
Council Bluffs 36
Hefei 36
Helsinki 36
Milan 36
Santa Clara 35
Brussels 32
Dallas 32
Moscow 32
Buffalo 31
Frankfurt am Main 29
Zgierz 28
Düsseldorf 27
The Dalles 22
Amsterdam 20
Orem 20
London 19
São Paulo 19
Bremen 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
Atlanta 10
Brooklyn 10
Kunming 10
Montreal 10
Redondo Beach 10
Tampa 10
Falls Church 9
Manchester 9
Naples 9
Nuremberg 9
Phoenix 9
Portsmouth 9
St Louis 9
Tashkent 9
Vienna 9
Boston 8
Da Nang 8
Denver 8
Florence 8
Haiphong 8
Istanbul 8
Johannesburg 8
Mexico City 8
Nanchang 8
Rome 8
Scuola 8
Sterling 8
Bologna 7
Brno 7
Fremont 7
Jinan 7
Lahore 7
Paris 7
Pignone 7
Tianjin 7
Toronto 7
Chennai 6
Totale 6.381
Salva come PNG Salva come JPEG
Nome #
Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss 454
PSIP1/LEDGF: A new gene likely involved in sensorineural progressive hearing loss 452
Rare coding variants and X-linked loci associated with age at menarche 450
Type i interferon-mediated autoinflammation due to DNase II deficiency 405
Usher syndrome: An effective sequencing approach to establish a genetic and clinical diagnosis 390
Two‑gene mutation in a single patient: Biochemical and functional analysis for a correct interpretation of exome results. 386
Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals 377
Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss 331
TBL1Y: a new gene involved in syndromic hearing loss 305
Novel NOD2 Mutation in Early-Onset Inflammatory Bowel Phenotype 298
Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype 281
A novel P2RX2 mutation in an Italian family affected by autosomal dominant nonsyndromic hearing loss 256
Genetic landscape of populations along the Silk Road: admixture and migration patterns 255
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals 254
Linkage Study and Exome Sequencing Identify a BDP1 Mutation Associated with Hereditary Hearing Loss 248
Target sequencing approach intended to discover new mutations in non-syndromic intellectual disability 246
Consanguinity and Hereditary Hearing Loss in Qatar 245
Mevalonate kinase deficiency and IBD: shared genetic background 245
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair 244
Targeted sequencing identifies novel variants involved in autosomal recessive hereditary hearing loss in Qatari families 222
Hereditary hearing loss: a 96 gene targeted sequencing protocol reveals novel alleles in a series of Italian and Qatari patients 220
Molecular epidemiology of Usher syndrome in Italy 216
Putative modifier genes in mevalonate kinase deficiency 216
Alagille syndrome: A new missense mutation detected by whole-exome sequencing in a case previously found to be negative by DHPLC and MLPA 216
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. 214
Directional dominance on stature and cognition in diverse human populations 210
The Challenge of Next Generation Sequencing in a Boy with Severe Mononucleosis and EBV-related Lymphoma 204
Molecular Diagnosis of Usher Syndrome: Application of Two Different Next Generation Sequencing-Based Procedures 204
Increased rate of deleterious variants in long runs of homozygosity of an inbred population from Qatar 201
Next generation sequencing in nonsyndromic intellectual disability: From a negative molecular karyotype to a possible causative mutation detection 194
Genetic variants linked to education predict longevity. 186
Excess of runs of homozygosity is associated with severe cognitive impairment in intellectual disability. 182
Rare and low-frequency coding variants alter human adult height 175
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences 153
Microarray and large-scale in silico-based identification of genes functionally related to Haptoglobin and/or Hemopexin. 150
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders 136
null 124
Integrative multi-omic analysis reveals conserved cell-projection deficits in human Down syndrome brains 119
Organo-silane coated substrates for DNA purification 100
Totale 9.764
Salva come PNG Salva come JPEG
Categoria #
all - tutte 25.762
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 25.762
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202163 0 0 0 0 0 0 0 0 0 0 0 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
2025/20262.848 326 184 140 164 267 239 422 100 292 324 218 172
Totale 9.764