CURRO', AURORA
 Distribuzione geografica
Continente #
EU - Europa 491
NA - Nord America 404
AS - Asia 47
OC - Oceania 3
Totale 945
Nazione #
US - Stati Uniti d'America 402
IT - Italia 187
GB - Regno Unito 124
IE - Irlanda 70
SE - Svezia 36
DE - Germania 24
CN - Cina 22
FR - Francia 18
VN - Vietnam 14
ES - Italia 7
FI - Finlandia 6
UA - Ucraina 6
TR - Turchia 5
BE - Belgio 3
CZ - Repubblica Ceca 3
NL - Olanda 3
SG - Singapore 3
AU - Australia 2
BA - Bosnia-Erzegovina 2
CA - Canada 2
RU - Federazione Russa 2
IN - India 1
IR - Iran 1
NZ - Nuova Zelanda 1
TW - Taiwan 1
Totale 945
Città #
Southend 116
Fairfield 69
Dublin 67
Woodbridge 50
Chandler 42
Ashburn 39
Siena 27
Houston 25
Seattle 21
Ann Arbor 20
Wilmington 18
Cambridge 17
Dong Ket 14
Padova 12
Princeton 11
Beijing 10
Dearborn 9
New York 9
Jacksonville 8
Aachen 7
Florence 6
Helsinki 6
Málaga 6
Bolzano 5
Brescia 5
Shanghai 5
Munich 4
Phoenix 4
San Floriano del Collio 4
Venice 4
Brno 3
Cossato 3
Dallas 3
Farra di Soligo 3
Izmir 3
London 3
Milan 3
Modica 3
Nanjing 3
Rome 3
San Diego 3
San Mateo 3
Turin 3
Washington 3
Ardea 2
Bihać 2
Boardman 2
Bologna 2
Bracciano 2
Brussels 2
Castleknock 2
Conversano 2
Fremont 2
Los Angeles 2
Moscow 2
Olgiate Olona 2
Quartu Sant'Elena 2
Rimini 2
Rotterdam 2
Vicenza 2
Alghero 1
Andover 1
Bangalore 1
Berlin 1
Canberra 1
Fano 1
Frankfurt am Main 1
Glasgow 1
Grottaglie 1
Hounslow 1
Louvain-la-Neuve 1
Macchiagodena 1
Melbourne 1
Menfi 1
Messina 1
New Bedfont 1
Ningbo 1
Norwalk 1
Ottawa 1
Palermo 1
Pisa 1
Prescot 1
Rhoon 1
Sacramento 1
San Francisco 1
Santa Maria Capua Vetere 1
Santa Marinella 1
Segrate 1
Singapore 1
Sioux Falls 1
Teggiano 1
Xian 1
Zhengzhou 1
Totale 747
Nome #
MEIS2 gene is responsible for intellectual disability, cardiac defects and a distinct facial phenotype 277
Evidence of predisposing epimutation in retinoblastoma 240
Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants 167
IQSEC2 disorder: A new disease entity or a Rett spectrum continuum? 130
CDKL5 mutations may mimic Pitt-Hopkins syndrome phenotype 77
Cell-free DNA next-generation sequencing liquid biopsy as a new revolutionary approach for arteriovenous malformation 73
Totale 964
Categoria #
all - tutte 3.155
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 3.155


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020209 9 16 8 33 19 23 19 22 22 12 9 17
2020/2021219 7 9 9 12 18 8 12 18 28 51 19 28
2021/2022159 15 13 11 20 5 9 12 11 9 11 17 26
2022/2023139 7 16 20 17 12 20 8 10 11 7 9 2
2023/2024182 5 4 23 13 9 39 36 2 7 22 6 16
2024/20258 8 0 0 0 0 0 0 0 0 0 0 0
Totale 964