ArTS Archivio della ricerca di Trieste

ATHANASAKIS, EMMANOUIL
 Distribuzione geografica
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Continente #
NA - Nord America 4.416
EU - Europa 2.689
AS - Asia 1.974
SA - Sud America 242
AF - Africa 73
OC - Oceania 6
Continente sconosciuto - Info sul continente non disponibili 2
Totale 9.402
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Nazione #
US - Stati Uniti d'America 4.363
IT - Italia 771
SG - Singapore 736
PL - Polonia 628
CN - Cina 401
SE - Svezia 270
VN - Vietnam 207
BR - Brasile 199
FR - Francia 198
HK - Hong Kong 190
DE - Germania 173
UA - Ucraina 138
BD - Bangladesh 99
GB - Regno Unito 88
RU - Federazione Russa 82
FI - Finlandia 79
KR - Corea 72
NL - Olanda 58
IN - India 56
BG - Bulgaria 52
TR - Turchia 50
IE - Irlanda 42
BE - Belgio 26
CA - Canada 24
SA - Arabia Saudita 24
ID - Indonesia 23
TH - Thailandia 21
ES - Italia 19
MA - Marocco 18
JP - Giappone 17
MX - Messico 16
IQ - Iraq 14
EG - Egitto 13
AT - Austria 12
ZA - Sudafrica 12
MY - Malesia 11
PH - Filippine 11
CO - Colombia 10
SN - Senegal 10
AR - Argentina 9
RO - Romania 8
VE - Venezuela 8
AL - Albania 7
NO - Norvegia 6
UZ - Uzbekistan 6
AE - Emirati Arabi Uniti 5
AU - Australia 5
CH - Svizzera 5
CZ - Repubblica Ceca 5
DZ - Algeria 5
EC - Ecuador 5
PE - Perù 5
PK - Pakistan 5
IR - Iran 4
JO - Giordania 4
KE - Kenya 4
PT - Portogallo 4
CL - Cile 3
DK - Danimarca 3
GR - Grecia 3
LT - Lituania 3
TN - Tunisia 3
AZ - Azerbaigian 2
BB - Barbados 2
EU - Europa 2
GA - Gabon 2
HN - Honduras 2
JM - Giamaica 2
KG - Kirghizistan 2
KZ - Kazakistan 2
LB - Libano 2
NG - Nigeria 2
NP - Nepal 2
PA - Panama 2
PR - Porto Rico 2
PY - Paraguay 2
TW - Taiwan 2
AO - Angola 1
BA - Bosnia-Erzegovina 1
BW - Botswana 1
BY - Bielorussia 1
CI - Costa d'Avorio 1
CR - Costa Rica 1
CY - Cipro 1
DO - Repubblica Dominicana 1
EE - Estonia 1
ET - Etiopia 1
HU - Ungheria 1
IL - Israele 1
IS - Islanda 1
KH - Cambogia 1
LV - Lettonia 1
MK - Macedonia 1
NZ - Nuova Zelanda 1
OM - Oman 1
PS - Palestinian Territory 1
RS - Serbia 1
SK - Slovacchia (Repubblica Slovacca) 1
SV - El Salvador 1
SY - Repubblica araba siriana 1
Totale 9.401
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Città #
Warsaw 586
Ashburn 529
Woodbridge 425
Singapore 413
Fairfield 380
Ann Arbor 339
Chandler 308
Houston 239
San Jose 223
Hong Kong 179
Seattle 162
Wilmington 162
Jacksonville 137
Cambridge 115
Beijing 101
Dallas 101
Trieste 85
Dearborn 80
Princeton 76
Seoul 71
Ho Chi Minh City 65
Boardman 63
Chicago 52
Rome 51
Sofia 51
Los Angeles 48
Milan 46
Columbus 45
Frankfurt am Main 45
Hanoi 44
Dublin 42
Hefei 38
New York 38
Izmir 37
Lauterbourg 37
Zgierz 33
Munich 32
Santa Clara 31
The Dalles 31
London 25
Council Bluffs 23
Moscow 23
Helsinki 21
São Paulo 21
Guangzhou 20
Brussels 19
Bangkok 18
Bremen 18
San Diego 18
Buffalo 17
Casablanca 15
Riyadh 15
Turku 15
Düsseldorf 14
Shanghai 14
Jakarta 13
Orem 13
Redwood City 13
Dong Ket 12
Des Moines 11
Falls Church 11
Naples 11
Tokyo 11
Chennai 10
Dakar 10
Nanjing 10
Redondo Beach 10
Manila 9
Phoenix 9
Rio de Janeiro 9
Denver 8
Florence 8
Hebei 8
Johannesburg 8
Palermo 8
Paris 8
Cagliari 7
Da Nang 7
Edinburgh 7
Tirana 7
Belo Horizonte 6
Bologna 6
Cairo 6
Dhaka 6
Fremont 6
Hangzhou 6
Hải Dương 6
Jinan 6
Kuala Selangor 6
Madrid 6
Manchester 6
Miano 6
Montreal 6
Perugia 6
Stockholm 6
Tashkent 6
Toronto 6
Turin 6
Waanrode 6
Washington 6
Totale 6.194
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Nome #
Genetic profiling of autoinflammatory disorders in patients with periodic fever: a prospective study 522
Valutazione del background genetico di una coorte di individui dislessici mediante l'utilizzo di tecnologie ad alta processività 505
Developmental dyslexia and its complex genetic puzzle 430
A semi-nested real-time PCR method to detect low chimerism percentage in small quantity of hematopoietic stem cell transplant DNA samples. 418
Impact of methylmercury and other heavy metals exposure on neurocognitive function in children of 7 years old: study protocol of the follow-up 299
Association of a variant in the CHRNA5-A3-B4 gene cluster region to heavy smoking in the Italian population. 290
A Novel CRYBB2 Missense Mutation Causing Congenital Autosomal Dominant Cataract in an Italian Family. 284
MYO5B Gene Mutations: A Not Negligible Cause of Intrahepatic Cholestasis of Infancy with Normal Gamma-glutamyl Transferase Phenotype 283
A polymorphism in the 5' UTR of the DEFB1 gene is associated with the lung phenotype in F508del homozygous Italian cystic fibrosis patients 277
Puzzling results from BAP1 germline mutations analysis in a group of asbestos-exposed patients in a high-risk area of northeast Italy 276
Genetics of Food Preferences: A First View from Silk Road Populations 264
Analysis of DEFB1 regulatory SNPs in cystic fibrosis patients from North-Eastern Italy. 263
Abnormal expression of leiomyoma cytoskeletal proteins involved in cell migration 259
A 3'UTR SNP in NLRP3 gene is associated with susceptibility to HIV-1 infection 250
Congenital hyperinsulinism: clinical and molecular analysis of a large Italian cohort. 245
F402L variant in NLRP12 in subjects with undiagnosed periodic fevers and in healthy controls 233
Autosomal recessive stickler syndrome due to a loss of function mutation in theCOL9A3gene 229
Polymorphisms in innate immunity genes and patients response to dendritic cell-based HIV immuno-treatment. 223
Co-inheritance of two ABCC8 mutations causing an unresponsive congenital hyperinsulinism: Clinical and functional characterization of two novel ABCC8 mutations 223
Molecular epidemiology of Usher syndrome in Italy 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
Phospholipase C-β3 is a key modulator of IL-8 expression in cystic fibrosis bronchial epithelial cells. 209
A novel mutation in the vWFA2 domain of the COCH gene in an Italian DFNA9 family 209
High-throughput Genotyping Robot-assisted Method for Mutation Detection in Patients With Hypertrophic Cardiomyopathy. 207
TNF-α SNP rs1800629 and risk of relapse in childhood acute lymphoblastic leukemia: relation to immunophenotype 205
Molecular Diagnosis of Usher Syndrome: Application of Two Different Next Generation Sequencing-Based Procedures 204
Next generation sequencing in nonsyndromic intellectual disability: From a negative molecular karyotype to a possible causative mutation detection 194
Genetic and immunologic findings in children with recurrent aphthous stomatitis with systemic inflammation 186
Copy number variation, gene expression and histological localization of human beta-defensin 2 in patients with adeno-tonsillar hypertrophy 182
Vertebral defects in patients with Peters plus syndrome and mutations in B3GALTL 180
Proteins involved in oxidative stress in leiomyoma tissues treated with ulipristal acetate 178
Two Novel COH1 Mutations in an Italian Patient with Cohen Syndrome. 176
The Genetic Diagnosis of Ultrarare DEEs: An Ongoing Challenge 158
Complex rearrangement of the exon 6 genomic region among Opitz G/BBB Syndrome MID1 alterations 152
Systematic analysis of factors that improve homologous direct repair (HDR) efficiency in CRISPR/Cas9 technique 152
Identification of a new mutation (L46P) in the human NOG gene in an Italian patient with Symphalangism syndrome 148
GNE-related thrombocytopenia: evidence for a mutational hotspot in the ADP/substrate domain of the GNE bifunctional enzyme 146
Could the MED13 mutations manifest as a Kabuki-like syndrome? 139
Sensitive Detection of Gynecological Cancer Recurrence Using Circulating Tumor DNA and Digital PCR: A Comparative Study with Serum Biochemical Markers 120
Genomic instability in congenital lung malformations in children 119
null 96
Totale 9.565
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Categoria #
all - tutte 25.650
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 25.650
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202169 0 0 0 0 0 0 0 0 0 0 0 69
2021/2022610 18 48 27 39 51 38 28 30 76 63 50 142
2022/2023878 82 126 82 118 92 135 6 87 83 9 39 19
2023/2024463 31 30 19 20 48 49 80 83 11 14 40 38
2024/20251.188 24 34 64 99 119 103 68 94 201 148 126 108
2025/20262.809 338 92 195 236 235 289 440 76 273 363 125 147
Totale 9.565