NARETTO, VALERIA GIORGIA
 Distribuzione geografica
Continente #
NA - Nord America 311
EU - Europa 190
AS - Asia 53
SA - Sud America 3
OC - Oceania 2
AF - Africa 1
Totale 560
Nazione #
US - Stati Uniti d'America 305
IT - Italia 60
CN - Cina 33
SE - Svezia 32
DE - Germania 21
IE - Irlanda 21
AT - Austria 10
VN - Vietnam 10
DK - Danimarca 9
FR - Francia 8
UA - Ucraina 7
CA - Canada 5
GB - Regno Unito 5
FI - Finlandia 4
PL - Polonia 4
JP - Giappone 3
BR - Brasile 2
CZ - Repubblica Ceca 2
IN - India 2
KR - Corea 2
NL - Olanda 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
SG - Singapore 1
TH - Thailandia 1
Totale 560
Città #
Chandler 54
Ann Arbor 42
Dublin 19
Fairfield 19
Torino 19
Ashburn 15
Houston 12
Beijing 11
Vienna 10
Nyköping 9
Woodbridge 8
Wilmington 7
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
Medford 3
Redwood City 3
Asti 2
Buffalo 2
Guangzhou 2
Hangzhou 2
Jinan 2
Legnano 2
Leiden 2
Ljubljana 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
Boardman 1
Bonn 1
Brussels 1
Cairo 1
Chatsworth 1
Edemissen 1
Esslingen am Neckar 1
Falls Church 1
Genova 1
Guiyang 1
Helsinki 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
Singapore 1
Stockholm 1
São Paulo 1
Tallinn 1
Uppsala 1
Victoria 1
Totale 371
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 238
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 100
Congenital Sensorineural Hearing Loss and Inborn Pigmentary Disorders: First Report of Multilocus Syndrome in Piebaldism 95
Evidence that FGFRL1 contributes to congenital diaphragmatic hernia development in humans 90
Family-based whole exome sequencing allows a 25% diagnostic yield in patients with autism spectrum disorder 63
Totale 586
Categoria #
all - tutte 1.914
article - articoli 0
book - libri 0
conference - conferenze 338
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 2.252


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20193 0 0 0 0 0 0 0 0 0 0 3 0
2019/202067 6 0 1 14 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
2023/202438 6 11 3 2 1 8 0 1 0 5 1 0
Totale 586