SACCUZZO, LUCIA RITA
 Distribuzione geografica
Continente #
EU - Europa 180
AS - Asia 179
NA - Nord America 165
SA - Sud America 27
AF - Africa 21
Totale 572
Nazione #
US - Stati Uniti d'America 162
IT - Italia 135
SG - Singapore 90
CN - Cina 56
BR - Brasile 22
CI - Costa d'Avorio 15
KR - Corea 13
FI - Finlandia 8
IE - Irlanda 8
VN - Vietnam 8
GB - Regno Unito 6
AR - Argentina 4
FR - Francia 4
IN - India 4
NL - Olanda 4
RU - Federazione Russa 4
BJ - Benin 3
ES - Italia 3
PL - Polonia 3
SE - Svezia 3
JP - Giappone 2
MX - Messico 2
NG - Nigeria 2
TR - Turchia 2
AZ - Azerbaigian 1
BD - Bangladesh 1
CA - Canada 1
DE - Germania 1
GR - Grecia 1
NP - Nepal 1
PY - Paraguay 1
SN - Senegal 1
UZ - Uzbekistan 1
Totale 572
Città #
Singapore 51
Catania 34
Dallas 32
Hefei 31
Santa Clara 30
Ashburn 20
Abidjan 15
Los Angeles 13
Palermo 13
Seoul 13
Milan 10
Chicago 8
Dublin 8
Boardman 6
Civitanova Marche 6
Augusta 5
Beijing 5
New York 5
Helsinki 4
Lappeenranta 4
Naples 4
Pontedera 4
Amsterdam 3
Cotonou 3
Genoa 3
Ho Chi Minh City 3
Kochi 3
Ragusa 3
Rome 3
Stockholm 3
São Paulo 3
Abuja 2
Ankara 2
Buffalo 2
Canning 2
Houston 2
London 2
Nantes 2
Orvieto 2
Phoenix 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
Atlanta 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
Da Nang 1
Dakar 1
Denver 1
Des Moines 1
Florence 1
Fort Worth 1
Foshan 1
Franca 1
Gurupi 1
Haiphong 1
Hortolândia 1
Hải Dương 1
Ibarreta 1
Itapema 1
Japeri 1
Kathmandu 1
Lawrence 1
Manaus 1
Manchester 1
Messina 1
Monte Alegre 1
Montreal 1
Newham 1
Nuremberg 1
Panambi 1
Pelotas 1
Philadelphia 1
Poplar 1
Praia Grande 1
Querétaro 1
Regalbuto 1
Reggello 1
Totale 431
Nome #
Trait - driven analysis of the 2p15p16.1 microdeletion syndrome suggests a complex pattern of interactions between candidate genes 115
Copy Number Variations in Children with Tourette Syndrome: Systematic Investigation in a Clinical Setting 107
PARK2 microdeletion in a multiplex family with autism spectrum disorder 107
Assigning single clinical features to their disease-locus in large deletions: the example of chromosome 1q23-25 deletion syndrome 107
PPP5C pathogenic variant identified: a potential key to gaining insight into developmental and epileptic encephalopathy? 80
Unveiling Secondary Mutations in Blended Phenotypes: Dual ERCC4 and OTOA Pathogenic Variants Through WES Analysis 64
Totale 580
Categoria #
all - tutte 1.629
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 1.629


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
2025/2026243 30 48 51 57 57 0 0 0 0 0 0 0
Totale 580