LOMARTIRE, SILVIA
 Distribuzione geografica
Continente #
NA - Nord America 252
EU - Europa 179
AS - Asia 144
AF - Africa 23
SA - Sud America 9
Totale 607
Nazione #
US - Stati Uniti d'America 248
CN - Cina 49
IT - Italia 46
SG - Singapore 39
GB - Regno Unito 37
SE - Svezia 27
VN - Vietnam 26
DE - Germania 21
HK - Hong Kong 13
IN - India 10
CI - Costa d'Avorio 9
NL - Olanda 9
RU - Federazione Russa 9
BR - Brasile 7
FR - Francia 7
TG - Togo 7
IE - Irlanda 5
ZA - Sudafrica 4
AT - Austria 3
BG - Bulgaria 3
EE - Estonia 3
FI - Finlandia 3
JO - Giordania 3
MX - Messico 3
UA - Ucraina 3
AR - Argentina 2
ID - Indonesia 2
SC - Seychelles 2
CA - Canada 1
CH - Svizzera 1
EG - Egitto 1
JP - Giappone 1
PH - Filippine 1
PL - Polonia 1
SI - Slovenia 1
Totale 607
Città #
Ashburn 40
Southend 29
Bologna 24
Fairfield 24
Singapore 23
Chandler 22
Seattle 19
Dong Ket 18
Hong Kong 13
Houston 12
Cambridge 10
Santa Clara 10
Abidjan 9
Wilmington 8
Woodbridge 8
Beijing 7
Lomé 7
New York 7
Princeton 6
Dublin 5
Boardman 4
Guangzhou 4
Nanjing 4
Amman 3
Berlin 3
Haikou 3
Hebei 3
Helsinki 3
Padova 3
Saint Petersburg 3
Sofia 3
Tappahannock 3
Turin 3
Westminster 3
Ann Arbor 2
Buffalo 2
Bühl 2
Council Bluffs 2
Dallas 2
Florence 2
Graz 2
Ho Chi Minh City 2
Jakarta 2
Jinan 2
Los Angeles 2
Mexico City 2
Phoenix 2
Shanghai 2
Shenyang 2
Tianjin 2
Wuxi 2
Zhengzhou 2
Baoding 1
Bauru 1
Belém de São Francisco 1
Bengaluru 1
Bern 1
Bexley 1
Brasília 1
Bremen 1
Caruaru 1
Chicago 1
Dearborn 1
Detroit 1
Düsseldorf 1
El Gouna 1
Falkenstein 1
Falls Church 1
Frankfurt Am Main 1
Frankfurt am Main 1
Gualtieri 1
Ha Long 1
Hanoi 1
Huizhou 1
Hyderabad 1
Hưng Yên 1
Itapitanga 1
Johannesburg 1
Kuban 1
Linfen 1
Linlithgow 1
Ljubljana 1
London 1
Lviv 1
Manila 1
Nanchang 1
Napoli 1
Ningbo 1
Norwalk 1
Phú Thọ 1
Pinhais 1
Poplar 1
Quận Chín 1
Ramos Mejía 1
Redondo Beach 1
Saltillo 1
Suzhou 1
Taiyuan 1
Tokyo 1
Toronto 1
Totale 430
Nome #
A CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum disorder. 216
Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients. 185
Analysis of CHRNA7 rare variants in autism spectrum disorder susceptibility 96
null 81
Corrigendum: Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients(EMBO Mol Med, (2014), 6, (795–809), 10.1002/emmm.201303235) 42
Totale 620
Categoria #
all - tutte 1.559
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 1.559


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202140 0 0 0 0 0 1 3 1 9 3 1 22
2021/202276 3 4 3 4 7 7 2 3 3 6 24 10
2022/202388 8 15 6 10 3 9 4 3 17 2 6 5
2023/202438 2 2 4 2 5 12 6 1 1 3 0 0
2024/202592 4 4 7 8 15 3 6 8 1 11 10 15
2025/2026102 14 22 16 22 24 4 0 0 0 0 0 0
Totale 620