NARETTO, VALERIA GIORGIA
 Distribuzione geografica
Continente #
NA - Nord America 104
EU - Europa 88
AS - Asia 78
SA - Sud America 7
AF - Africa 1
Totale 278
Nazione #
US - Stati Uniti d'America 96
CN - Cina 51
IT - Italia 32
PL - Polonia 12
FR - Francia 9
VN - Vietnam 9
CA - Canada 8
DE - Germania 7
BR - Brasile 5
CZ - Repubblica Ceca 5
ES - Italia 5
ID - Indonesia 5
GB - Regno Unito 4
IL - Israele 4
RU - Federazione Russa 4
TW - Taiwan 3
IR - Iran 2
NL - Olanda 2
RO - Romania 2
AE - Emirati Arabi Uniti 1
AR - Argentina 1
BE - Belgio 1
CH - Svizzera 1
CL - Cile 1
FI - Finlandia 1
HK - Hong Kong 1
HU - Ungheria 1
IE - Irlanda 1
JO - Giordania 1
SE - Svezia 1
TR - Turchia 1
ZA - Sudafrica 1
Totale 278
Città #
Shenyang 13
Fairfield 11
Ashburn 10
Guangzhou 10
Santa Cruz 8
Woodbridge 8
Summerville 6
Buffalo 5
Warsaw 5
Bologna 4
Cambridge 4
Changsha 4
Dong Ket 4
Salvador 4
Ann Arbor 3
Harbin 3
Ottawa 3
Torino 3
Wilmington 3
Xian 3
Boardman 2
Brasov 2
Chicago 2
Hanoi 2
Hebei 2
Houston 2
Lübeck 2
New York 2
Nijmegen 2
Nordhorn 2
Rome 2
Seattle 2
Amman 1
Bari 1
Beijing 1
Boston 1
Brescia 1
Brno 1
Brussels 1
Budapest 1
Buenos Aires 1
Bydgoszcz 1
Central 1
Dong Nai 1
Edmonton 1
Encino 1
Ferrara 1
Forlì 1
Frisco 1
Haikou 1
Heidelberg 1
Herndon 1
Istanbul 1
Jakarta 1
Kansas City 1
Kiryat Ono 1
Lake Forest 1
Langley 1
Lanzhou 1
Lodz 1
Los Angeles 1
Manchester 1
Milan 1
Milpitas 1
Monmouth Junction 1
Mountain View 1
Muizenberg 1
Nanjing 1
Nanning 1
Ningbo 1
North York 1
Níjar 1
Oulu 1
Padova 1
Palo Alto 1
Québec 1
Reutov 1
Rosh Ha‘Ayin 1
San Biagio di Callalta 1
San Jose 1
Sennori 1
Taipei 1
Troina 1
University Park 1
Uppsala 1
Vancouver 1
Verona 1
Vigo 1
Vitória da Conquista 1
Wahlen 1
Wenzhou 1
Xining 1
Ziebice 1
Zurich 1
Totale 200
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, file e27ce42b-f0f5-2581-e053-d805fe0acbaa 180
Congenital Sensorineural Hearing Loss and Inborn Pigmentary Disorders: First Report of Multilocus Syndrome in Piebaldism, file e27ce42e-4c48-2581-e053-d805fe0acbaa 82
Evidence that FGFRL1 contributes to congenital diaphragmatic hernia development in humans, file e27ce431-c67b-2581-e053-d805fe0acbaa 17
Evidence that FGFRL1 contributes to congenital diaphragmatic hernia development in humans, file e27ce431-bf36-2581-e053-d805fe0acbaa 4
Evidence that FGFRL1 contributes to congenital diaphragmatic hernia development in humans, file e27ce431-e18f-2581-e053-d805fe0acbaa 1
Totale 284
Categoria #
all - tutte 459
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 459


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202037 1 2 3 5 1 2 1 4 10 2 4 2
2020/2021112 6 6 3 5 13 13 7 4 30 10 3 12
2021/202265 4 5 3 2 3 8 3 11 4 5 6 11
2022/202359 2 3 9 9 7 4 9 9 3 1 2 1
2023/20248 0 0 1 0 1 0 2 2 2 0 0 0
Totale 284