DIVIZIA, MARIA TERESA
 Distribuzione geografica
Continente #
EU - Europa 602
AS - Asia 128
NA - Nord America 82
SA - Sud America 9
Totale 821
Nazione #
IT - Italia 578
US - Stati Uniti d'America 78
SG - Singapore 46
CN - Cina 34
VN - Vietnam 22
BD - Bangladesh 11
FR - Francia 11
BR - Brasile 9
HK - Hong Kong 6
GB - Regno Unito 4
CA - Canada 2
IQ - Iraq 2
JP - Giappone 2
RU - Federazione Russa 2
CH - Svizzera 1
DE - Germania 1
DK - Danimarca 1
ID - Indonesia 1
JM - Giamaica 1
JO - Giordania 1
LT - Lituania 1
MX - Messico 1
MY - Malesia 1
PK - Pakistan 1
PL - Polonia 1
PT - Portogallo 1
SK - Slovacchia (Repubblica Slovacca) 1
TH - Thailandia 1
Totale 821
Città #
Genoa 307
Genova 117
Rapallo 73
Vado Ligure 64
San Jose 27
Singapore 24
Ashburn 9
Hong Kong 6
Lauterbourg 5
Marseille 5
New York 4
Turin 4
Beijing 3
Haiphong 3
Ho Chi Minh City 3
Hải Dương 3
Los Angeles 3
Biên Hòa 2
Bordighera 2
Council Bluffs 2
Hanoi 2
London 2
Orem 2
Tokyo 2
Atlanta 1
Baltimore 1
Bangkok 1
Belo Horizonte 1
Berlin 1
Birmingham 1
Boca Raton 1
Boston 1
Buffalo 1
Bắc Ninh 1
Cambiano 1
Carpi 1
Chengdu 1
Chicago 1
City of London 1
Copenhagen 1
Dallas 1
Davenport 1
Erbil 1
Franca 1
Irbid 1
Kajang 1
Lahore 1
Lisbon 1
Malang 1
Manchester 1
Mandeville 1
Miami 1
Montreal 1
Mosul 1
Natal 1
Newport News 1
Ninh Bình 1
Padua 1
Paris 1
Pasadena 1
Paulista 1
Peruíbe 1
Potomac 1
Providence 1
Querétaro 1
Quận Chín 1
Recife 1
Richmond 1
Salinas 1
Sete Lagoas 1
Shanghai 1
Smolensk 1
St Petersburg 1
Suzhou 1
São José 1
São Paulo 1
Tampa 1
Thái Bình 1
Thái Nguyên 1
Thủ Đức 1
Tân Tiến 1
Venice 1
Walton 1
Warsaw 1
Waterbury 1
Watertown 1
Xiamen 1
Zurich 1
Totale 738
Nome #
A spectrum of LMX1B mutations in Nail-Patella syndrome: New point mutations, deletion, and evidence of mosaicism in unaffected parents 169
Case Report: Whole Exome Sequencing Revealed Disease-Causing Variants in Two Genes in a Patient With Autism Spectrum Disorder, Intellectual Disability, Hyperactivity, Sleep and Gastrointestinal Disturbances 151
Neurodevelopmental Disorders in Patients With Complex Phenotypes and Potential Complex Genetic Basis Involving Non-Coding Genes, and Double CNVs 143
P63 modulates the expression of the WDFY2 gene which is implicated in cancer regulation and limb development 121
Whole exome sequencing (WES) and functional analyses suggest synergistic effects of deleterious variants in two candidate genes for Poland Syndrome 110
Scoliosis with cognitive impairment in a girl with 8q11.21q11.23 microdeletion and SNTG1 disruption 77
Neuroradiologic, Clinical, and Genetic Characterization of Cerebellar Heterotopia: A Pediatric Multicentric Study. 38
Data-driven insights into post-autopsy consultations: causes of perinatal mortality and parental outcomes 31
Totale 840
Categoria #
all - tutte 3.263
article - articoli 2.846
book - libri 0
conference - conferenze 417
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 6.526


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/202245 1 0 4 5 0 1 2 14 4 4 1 9
2022/202396 9 6 3 5 11 11 5 9 17 1 15 4
2023/202473 2 5 0 8 6 18 8 4 3 4 3 12
2024/2025176 8 10 4 10 23 16 18 29 6 8 26 18
2025/2026366 45 16 26 24 52 18 55 15 33 31 13 38
Totale 840