SACCUZZO, LUCIA RITA
 Distribuzione geografica
Continente #
EU - Europa 162
AS - Asia 138
NA - Nord America 123
SA - Sud America 22
AF - Africa 18
Totale 463
Nazione #
IT - Italia 129
US - Stati Uniti d'America 122
SG - Singapore 68
CN - Cina 47
BR - Brasile 19
CI - Costa d'Avorio 15
KR - Corea 13
FI - Finlandia 8
IE - Irlanda 8
FR - Francia 4
GB - Regno Unito 4
IN - India 4
NL - Olanda 3
VN - Vietnam 3
AR - Argentina 2
JP - Giappone 2
NG - Nigeria 2
PL - Polonia 2
AZ - Azerbaigian 1
DE - Germania 1
GR - Grecia 1
MX - Messico 1
PY - Paraguay 1
RU - Federazione Russa 1
SE - Svezia 1
SN - Senegal 1
Totale 463
Città #
Singapore 40
Catania 33
Dallas 31
Santa Clara 30
Hefei 29
Abidjan 15
Palermo 13
Seoul 13
Ashburn 10
Milan 10
Dublin 8
Los Angeles 8
Chicago 7
Boardman 6
Civitanova Marche 6
Augusta 5
Beijing 4
Helsinki 4
Lappeenranta 4
Pontedera 4
Genoa 3
Kochi 3
Ragusa 3
Rome 3
São Paulo 3
Abuja 2
Amsterdam 2
Ho Chi Minh City 2
London 2
Nantes 2
Orvieto 2
Piacenza 2
Priolo Gargallo 2
Rieti 2
Valenciennes 2
Żory 2
Aci Bonaccorsi 1
Aci Castello 1
Aci Catena 1
Alessandria 1
Andover 1
Arujá 1
Asunción 1
Baku 1
Belo Horizonte 1
Belpasso 1
Bento Gonçalves 1
Biên Hòa 1
Boston 1
Brasília 1
Bresso 1
Brooklyn 1
Burzaco 1
Camberwell 1
Cambridge 1
Chengdu 1
Chennai 1
Cincinnati 1
Dakar 1
Des Moines 1
Florence 1
Fort Worth 1
Franca 1
Gurupi 1
Hortolândia 1
Houston 1
Ibarreta 1
Itapema 1
Japeri 1
Lawrence 1
Messina 1
Monte Alegre 1
Naples 1
Newham 1
Nuremberg 1
Panambi 1
Philadelphia 1
Phoenix 1
Reggello 1
Ribeirão Bonito 1
Rio Branco 1
Riverside 1
Seattle 1
Stockholm 1
São Gonçalo 1
São Vicente 1
Várzea Paulista 1
Washington 1
Wuhan 1
Totale 370
Nome #
PARK2 microdeletion in a multiplex family with autism spectrum disorder 96
Assigning single clinical features to their disease-locus in large deletions: the example of chromosome 1q23-25 deletion syndrome 96
Trait - driven analysis of the 2p15p16.1 microdeletion syndrome suggests a complex pattern of interactions between candidate genes 95
Copy Number Variations in Children with Tourette Syndrome: Systematic Investigation in a Clinical Setting 89
PPP5C pathogenic variant identified: a potential key to gaining insight into developmental and epileptic encephalopathy? 56
Unveiling Secondary Mutations in Blended Phenotypes: Dual ERCC4 and OTOA Pathogenic Variants Through WES Analysis 39
Totale 471
Categoria #
all - tutte 1.440
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 1.440


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202111 0 0 0 0 0 0 1 7 3 0 0 0
2021/202222 0 1 0 0 1 0 1 0 0 1 0 18
2022/202354 3 0 0 0 0 2 0 9 13 6 10 11
2023/202475 5 3 10 10 5 14 6 3 4 4 5 6
2024/2025175 7 16 9 10 35 17 8 5 14 12 23 19
2025/2026134 30 48 51 5 0 0 0 0 0 0 0 0
Totale 471