ArTS Archivio della ricerca di Trieste

VOZZI, DIEGO
 Distribuzione geografica
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Continente #
NA - Nord America 4.576
EU - Europa 2.834
AS - Asia 2.002
SA - Sud America 335
Continente sconosciuto - Info sul continente non disponibili 270
AF - Africa 59
OC - Oceania 17
Totale 10.093
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Nazione #
US - Stati Uniti d'America 4.480
PL - Polonia 1.072
SG - Singapore 685
IT - Italia 507
CN - Cina 449
SE - Svezia 289
BR - Brasile 260
HK - Hong Kong 237
VN - Vietnam 186
DE - Germania 155
BD - Bangladesh 147
UA - Ucraina 133
FR - Francia 116
GB - Regno Unito 89
FI - Finlandia 83
RU - Federazione Russa 81
TR - Turchia 72
NL - Olanda 71
IE - Irlanda 56
IN - India 49
KR - Corea 49
CA - Canada 45
BG - Bulgaria 43
BE - Belgio 36
MX - Messico 29
AR - Argentina 23
AT - Austria 23
JP - Giappone 23
ES - Italia 22
MA - Marocco 16
AU - Australia 15
SN - Senegal 15
CZ - Repubblica Ceca 14
ID - Indonesia 14
VE - Venezuela 12
PK - Pakistan 11
SA - Arabia Saudita 11
ZA - Sudafrica 11
CH - Svizzera 10
CL - Cile 9
CO - Colombia 9
DK - Danimarca 9
UZ - Uzbekistan 9
IQ - Iraq 8
PH - Filippine 8
AE - Emirati Arabi Uniti 6
EC - Ecuador 6
PE - Perù 6
PY - Paraguay 6
CR - Costa Rica 5
DZ - Algeria 5
IR - Iran 5
PT - Portogallo 5
TW - Taiwan 4
AL - Albania 3
AZ - Azerbaigian 3
BB - Barbados 3
DO - Repubblica Dominicana 3
GR - Grecia 3
IL - Israele 3
LT - Lituania 3
TH - Thailandia 3
AM - Armenia 2
BO - Bolivia 2
EG - Egitto 2
EU - Europa 2
GT - Guatemala 2
JM - Giamaica 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
GP - Guadalupe 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
Totale 9.820
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Città #
Warsaw 1.041
Ashburn 536
Singapore 417
Fairfield 330
Chandler 289
Houston 282
Woodbridge 269
Ann Arbor 256
Hong Kong 221
San Jose 187
Wilmington 173
Seattle 162
Jacksonville 135
Trieste 124
Cambridge 112
Council Bluffs 94
Beijing 83
Los Angeles 81
Chicago 80
Boardman 75
Princeton 73
Dearborn 60
Dublin 56
New York 50
Hanoi 47
Columbus 46
Izmir 45
Seoul 44
Sofia 43
Ho Chi Minh City 42
Milan 42
Santa Clara 42
Lauterbourg 40
Munich 40
Hefei 36
Helsinki 36
Dallas 34
Brussels 32
Moscow 32
Buffalo 31
Frankfurt am Main 29
Zgierz 28
Düsseldorf 27
The Dalles 22
Amsterdam 20
Orem 20
Salt Lake City 20
London 19
São Paulo 19
Bremen 18
Des Moines 17
Shanghai 17
Stockholm 17
San Diego 16
Dakar 15
Dong Ket 14
Redwood City 13
Tokyo 13
Ankara 12
Brooklyn 12
Casablanca 12
Guangzhou 12
Montreal 12
Nanjing 12
Phoenix 12
Rome 11
Washington 11
Atlanta 10
Denver 10
Kunming 10
Naples 10
Redondo Beach 10
Tampa 10
Vienna 10
Boston 9
Falls Church 9
Manchester 9
Nuremberg 9
Portsmouth 9
San Francisco 9
St Louis 9
Sterling 9
Tashkent 9
Da Nang 8
Florence 8
Haiphong 8
Istanbul 8
Johannesburg 8
Mexico City 8
Nanchang 8
Scuola 8
Toronto 8
Bologna 7
Brno 7
Cagliari 7
Fremont 7
Jinan 7
Lahore 7
Paris 7
Pignone 7
Totale 6.547
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Nome #
Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss 459
Rare coding variants and X-linked loci associated with age at menarche 457
PSIP1/LEDGF: A new gene likely involved in sensorineural progressive hearing loss 455
Type i interferon-mediated autoinflammation due to DNase II deficiency 419
Usher syndrome: An effective sequencing approach to establish a genetic and clinical diagnosis 416
Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals 399
Two‑gene mutation in a single patient: Biochemical and functional analysis for a correct interpretation of exome results. 391
Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss 335
Novel NOD2 Mutation in Early-Onset Inflammatory Bowel Phenotype 315
TBL1Y: a new gene involved in syndromic hearing loss 309
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals 296
Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype 291
A novel P2RX2 mutation in an Italian family affected by autosomal dominant nonsyndromic hearing loss 262
Genetic landscape of populations along the Silk Road: admixture and migration patterns 259
Target sequencing approach intended to discover new mutations in non-syndromic intellectual disability 256
Mevalonate kinase deficiency and IBD: shared genetic background 254
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair 254
Linkage Study and Exome Sequencing Identify a BDP1 Mutation Associated with Hereditary Hearing Loss 251
Consanguinity and Hereditary Hearing Loss in Qatar 250
Targeted sequencing identifies novel variants involved in autosomal recessive hereditary hearing loss in Qatari families 229
Hereditary hearing loss: a 96 gene targeted sequencing protocol reveals novel alleles in a series of Italian and Qatari patients 225
Alagille syndrome: A new missense mutation detected by whole-exome sequencing in a case previously found to be negative by DHPLC and MLPA 224
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. 223
Directional dominance on stature and cognition in diverse human populations 222
Molecular epidemiology of Usher syndrome in Italy 222
Putative modifier genes in mevalonate kinase deficiency 222
Molecular Diagnosis of Usher Syndrome: Application of Two Different Next Generation Sequencing-Based Procedures 213
The Challenge of Next Generation Sequencing in a Boy with Severe Mononucleosis and EBV-related Lymphoma 210
Increased rate of deleterious variants in long runs of homozygosity of an inbred population from Qatar 209
Next generation sequencing in nonsyndromic intellectual disability: From a negative molecular karyotype to a possible causative mutation detection 201
Genetic variants linked to education predict longevity. 192
Excess of runs of homozygosity is associated with severe cognitive impairment in intellectual disability. 186
Rare and low-frequency coding variants alter human adult height 178
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences 158
Microarray and large-scale in silico-based identification of genes functionally related to Haptoglobin and/or Hemopexin. 157
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders 141
Integrative multi-omic analysis reveals conserved cell-projection deficits in human Down syndrome brains 126
null 124
Organo-silane coated substrates for DNA purification 103
Totale 10.093
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Categoria #
all - tutte 27.275
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 27.275
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022497 0 0 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
2026/2027329 90 136 103 0 0 0 0 0 0 0 0 0
Totale 10.093