NARETTO, VALERIA GIORGIA
 Distribuzione geografica
Continente #
NA - Nord America 347
EU - Europa 198
AS - Asia 82
SA - Sud America 3
OC - Oceania 2
AF - Africa 1
Totale 633
Nazione #
US - Stati Uniti d'America 339
IT - Italia 61
CN - Cina 33
SE - Svezia 32
SG - Singapore 27
DE - Germania 25
IE - Irlanda 21
AT - Austria 11
VN - Vietnam 10
DK - Danimarca 9
FR - Francia 8
CA - Canada 7
UA - Ucraina 7
FI - Finlandia 5
GB - Regno Unito 5
PL - Polonia 4
ID - Indonesia 3
JP - Giappone 3
NL - Olanda 3
BR - Brasile 2
CZ - Repubblica Ceca 2
IN - India 2
KR - Corea 2
SI - Slovenia 2
AR - Argentina 1
AU - Australia 1
BE - Belgio 1
EE - Estonia 1
EG - Egitto 1
IL - Israele 1
MX - Messico 1
NZ - Nuova Zelanda 1
RO - Romania 1
TH - Thailandia 1
Totale 633
Città #
Chandler 54
Ann Arbor 42
Singapore 23
Dublin 19
Fairfield 19
Torino 19
Ashburn 16
Santa Clara 14
Houston 12
Beijing 11
Vienna 11
Nyköping 9
Woodbridge 8
Wilmington 7
Boardman 6
Columbus 5
Dearborn 5
Milan 5
New Milton 5
Princeton 5
Seattle 5
Fremont 4
Jacksonville 4
Nanjing 4
New York 4
Rome 4
Villeurbanne 4
Ziebice 4
Boston 3
Cambridge 3
Dallas 3
Dong Ket 3
Hebei 3
Jakarta 3
Medford 3
Munich 3
Redwood City 3
Asti 2
Buffalo 2
Guangzhou 2
Hangzhou 2
Helsinki 2
Jinan 2
Legnano 2
Leiden 2
Ljubljana 2
London 2
Los Angeles 2
Lyndhurst 2
Lübeck 2
Norwalk 2
Ottawa 2
Rochester 2
San Diego 2
Tokyo 2
Toronto 2
Wuhan 2
Aachen 1
Auckland 1
Bangkok 1
Blaine 1
Bonn 1
Brussels 1
Cairo 1
Chatsworth 1
Edemissen 1
Esslingen am Neckar 1
Falls Church 1
Genova 1
Guiyang 1
Kunming 1
Malagueno 1
Mexico 1
Nanning 1
North York 1
Novara 1
Pantigliate 1
Perth 1
Provo 1
Pulsano 1
Sacramento 1
Salt Lake City 1
Seoul 1
Shanghai 1
Shenzhen 1
Siena 1
Stockholm 1
São Paulo 1
Tallinn 1
Uppsala 1
Victoria 1
Totale 429
Nome #
Copy number variants analysis in a cohort of isolated and syndromic developmental delay/intellectual disability reveals novel genomic disorders, position effects and candidate disease genes 254
Evidence that FGFRL1 contributes to congenital diaphragmatic hernia development in humans 111
Bilaterally cleft lip and bilateral thumb polydactyly with triphalangeal component in a patient with two de novo deletions of HSA 4q32 and 4q34 involving PDGFC, GRIA2, and FBXO8 genes 110
Congenital Sensorineural Hearing Loss and Inborn Pigmentary Disorders: First Report of Multilocus Syndrome in Piebaldism 108
Family-based whole exome sequencing allows a 25% diagnostic yield in patients with autism spectrum disorder 76
Totale 659
Categoria #
all - tutte 2.369
article - articoli 0
book - libri 0
conference - conferenze 422
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 2.791


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202046 0 0 0 0 6 12 2 5 7 3 5 6
2020/202175 4 6 2 4 6 4 5 1 5 3 5 30
2021/2022166 16 11 15 19 10 9 7 8 12 11 28 20
2022/2023138 11 14 15 11 13 32 4 11 16 1 5 5
2023/202448 6 11 3 2 1 8 0 1 0 5 3 8
2024/202563 3 3 5 12 40 0 0 0 0 0 0 0
Totale 659