ACCOGLI, ANDREA
 Distribuzione geografica
Continente #
NA - Nord America 301
AS - Asia 177
EU - Europa 162
SA - Sud America 45
AF - Africa 3
Totale 688
Nazione #
US - Stati Uniti d'America 297
RU - Federazione Russa 61
IT - Italia 55
SG - Singapore 51
BR - Brasile 39
HK - Hong Kong 33
CN - Cina 25
VN - Vietnam 24
BD - Bangladesh 13
IE - Irlanda 13
SE - Svezia 11
KR - Corea 8
DE - Germania 7
GB - Regno Unito 6
JO - Giordania 6
IN - India 5
FR - Francia 4
EC - Ecuador 3
AR - Argentina 2
CH - Svizzera 2
FI - Finlandia 2
ID - Indonesia 2
IQ - Iraq 2
MX - Messico 2
PK - Pakistan 2
SA - Arabia Saudita 2
TW - Taiwan 2
ZA - Sudafrica 2
CL - Cile 1
CR - Costa Rica 1
HN - Honduras 1
JP - Giappone 1
NG - Nigeria 1
NL - Olanda 1
TR - Turchia 1
Totale 688
Città #
Santa Clara 122
Singapore 38
Hong Kong 30
Ashburn 29
San Jose 18
Dublin 13
Beijing 9
Fairfield 9
Seoul 8
Woodbridge 8
Hanoi 7
Ho Chi Minh City 7
Rome 7
Pianoro 6
Cambridge 5
Chandler 5
Los Angeles 5
Milan 5
New York 5
Seattle 5
Wilmington 5
Altamura 4
Boston 4
Lawrence 4
Moscow 4
San Diego 4
Brasília 3
Buffalo 3
Council Bluffs 3
Houston 3
Lauterbourg 3
London 3
Munich 3
Naples 3
Nuremberg 3
Perugia 3
Princeton 3
Rio de Janeiro 3
São Paulo 3
Udine 3
Ancona 2
Bern 2
Chennai 2
Colle di Val d'Elsa 2
Des Moines 2
Florence 2
Kent 2
Miaoli 2
Mumbai 2
Osasco 2
Pisa 2
Reggio Emilia 2
The Dalles 2
Abuja 1
Alexander City 1
Americana 1
Ann Arbor 1
Aragoiânia 1
As Samawah 1
Austin 1
Baghdad 1
Baoding 1
Barueri 1
Belford Roxo 1
Belo Horizonte 1
Birigui 1
Brooklyn 1
Buenos Aires 1
Buritama 1
Cauquenes 1
Cedar Rapids 1
Chicago 1
Contagem 1
Coronel Fabriciano 1
Da Nang 1
Dallas 1
Dammam 1
Dhaka 1
Elk Grove Village 1
Eunápolis 1
Faisalabad 1
Go Vap 1
Guayaquil 1
Ha Long 1
Helsinki 1
Hải Dương 1
Ibirité 1
Igarapé-Açu 1
Indianapolis 1
Itatiba 1
Jaboti 1
Jakarta 1
Jeddah 1
Johannesburg 1
Lahore 1
Lappeenranta 1
Mexico City 1
Monterrey 1
Norwalk 1
Orem 1
Totale 481
Nome #
De novo DHDDS variants cause a neurodevelopmental and neurodegenerative disorder with myoclonus 205
Exome sequencing of two Italian pedigrees with non-isolated Chiari malformation type i reveals candidate genes for cranio-facial development 192
Basal Ganglia Dysmorphism in Patients With Aicardi Syndrome 144
BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlations 142
Clinical and molecular characterization of patients with YWHAG-related epilepsy 11
Totale 694
Categoria #
all - tutte 1.790
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 1.790


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/202221 0 2 0 4 0 0 0 6 0 0 3 6
2022/202365 6 10 3 6 4 13 10 1 10 0 0 2
2023/202442 1 3 3 2 4 3 2 2 0 3 11 8
2024/2025279 10 19 9 33 88 52 20 13 8 9 8 10
2025/2026247 21 46 12 12 41 11 34 11 16 22 21 0
Totale 694