PAVINATO, LISA
 Distribuzione geografica
Continente #
NA - Nord America 188
EU - Europa 168
AS - Asia 73
SA - Sud America 4
OC - Oceania 3
AF - Africa 2
Totale 438
Nazione #
US - Stati Uniti d'America 172
IT - Italia 50
FR - Francia 29
CN - Cina 25
NL - Olanda 20
DE - Germania 19
CA - Canada 16
IN - India 14
CZ - Repubblica Ceca 12
GB - Regno Unito 10
IL - Israele 7
CH - Svizzera 6
HK - Hong Kong 6
QA - Qatar 5
VN - Vietnam 5
FI - Finlandia 4
SI - Slovenia 4
AU - Australia 3
ES - Italia 3
JP - Giappone 3
BR - Brasile 2
GR - Grecia 2
MK - Macedonia 2
RU - Federazione Russa 2
SE - Svezia 2
TR - Turchia 2
AE - Emirati Arabi Uniti 1
AR - Argentina 1
AT - Austria 1
BE - Belgio 1
CL - Cile 1
ID - Indonesia 1
IE - Irlanda 1
KR - Corea 1
LB - Libano 1
NG - Nigeria 1
TH - Thailandia 1
TW - Taiwan 1
ZA - Sudafrica 1
Totale 438
Città #
Ashburn 17
Santa Cruz 12
Turin 11
Tappahannock 8
Fairfield 7
Houston 7
Torino 6
Zoetermeer 6
Doha 5
Göttingen 5
San Diego 5
Winnipeg 5
Buffalo 4
Chicago 4
Dong Ket 4
Helsinki 4
Paris 4
Shanghai 4
Beijing 3
Bern 3
Genoa 3
Guangzhou 3
Jerusalem 3
Leerdam 3
Los Angeles 3
New York 3
Ossé 3
Pergine Valsugana 3
Saint Etienne 3
Seattle 3
Toronto 3
Vancouver 3
Angera 2
Athens 2
Bonn 2
Brisbane 2
Brugherio 2
Camparada 2
Chapel Hill 2
Chongqing 2
Cleveland 2
Delhi 2
Grass Lake 2
Hangzhou 2
Jinan 2
Kochi 2
Kozhikode 2
Leiden 2
Madison 2
Milan 2
Mountain View 2
Mumbai 2
Parsippany 2
Pisek 2
Stuttgart 2
Thornhill 2
Tilburg 2
Vienna 2
Washington 2
Wilmington 2
Aachen 1
Albuquerque 1
Alessandria 1
Alexandria 1
Amstelveen 1
Ankara 1
Ann Arbor 1
Baltimore 1
Beirut 1
Belmont 1
Boardman 1
Boulder 1
Brescia 1
Brookline 1
Buenos Aires 1
Cambridge 1
Cedar Knolls 1
Central 1
Central District 1
Changsha 1
Cincinnati 1
Columbus 1
Condat-sur-Vienne 1
Coventry 1
Davis 1
Denver 1
Dubai 1
Dublin 1
Elâzığ 1
Epsom 1
Feltham 1
Fleming Island 1
Florence 1
Friedrichsdorf 1
Gardone Val Trompia 1
Geneva 1
Grenoble 1
Haifa 1
Halifax 1
Hanoi 1
Totale 256
Nome #
Expanding the clinical phenotype of the ultra-rare Skraban-Deardorff syndrome: Two novel individuals with WDR26 loss-of-function variants and a literature review, file e27ce431-cd02-2581-e053-d805fe0acbaa 146
Drosophila functional screening of de novo variants in autism uncovers damaging variants and facilitates discovery of rare neurodevelopmental diseases, file e27ce435-2291-2581-e053-d805fe0acbaa 97
New insights into potocki-shaffer syndrome: Report of two novel cases and literature review, file e27ce430-b04b-2581-e053-d805fe0acbaa 69
Functional analysis of TLK2 variants and their proximal interactomes implicates impaired kinase activity and chromatin maintenance defects in their pathogenesis, file e27ce435-5c41-2581-e053-d805fe0acbaa 56
Kcnk18 biallelic variants associated with intellectual disability and neurodevelopmental disorders alter tresk channel activity, file e27ce432-fea9-2581-e053-d805fe0acbaa 40
Biallelic PI4KA variants cause a novel neurodevelopmental syndrome with hypomyelinating leukodystrophy, file e27ce434-b0ae-2581-e053-d805fe0acbaa 13
New insights into potocki-shaffer syndrome: Report of two novel cases and literature review, file e27ce430-b04c-2581-e053-d805fe0acbaa 6
De novo truncating NOVA2 variants affect alternative splicing and lead to heterogeneous neurodevelopmental phenotypes, file c7c94b10-51d4-4616-81be-4d111b8b3d27 5
p140Cap regulates the composition and localization of the NMDAR complex in synaptic lipid rafts, file 06991da6-e21f-4f80-8314-852fa47ee3ee 3
Missense variants in RPH3A cause defects in excitatory synaptic function and are associated with a clinically variable neurodevelopmental disorder, file 317fadea-2657-4e3d-b042-8c1365937726 3
Spinocerebellar ataxia 38: structure-function analysis shows ELOVL5 G230V is proteotoxic, conformationally altered and a mutational hotspot, file acb56ad5-8571-47de-be14-0974df86a39b 2
Expanding the clinical phenotype of the ultra-rare Skraban-Deardorff syndrome: Two novel individuals with WDR26 loss-of-function variants and a literature review, file e27ce431-c51a-2581-e053-d805fe0acbaa 2
Functional analysis of TLK2 variants and their proximal interactomes implicates impaired kinase activity and chromatin maintenance defects in their pathogenesis, file e27ce434-aeb3-2581-e053-d805fe0acbaa 2
Totale 444
Categoria #
all - tutte 1.065
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 1.065


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202130 0 0 0 0 4 2 2 2 2 3 3 12
2021/2022118 4 15 8 5 8 7 12 10 4 12 22 11
2022/2023195 12 9 23 17 6 15 50 18 8 11 13 13
2023/2024101 12 10 17 6 9 11 11 17 5 3 0 0
Totale 444