DIVIZIA, MARIA TERESA
 Distribuzione geografica
Continente #
EU - Europa 654
AS - Asia 136
NA - Nord America 56
SA - Sud America 10
Totale 856
Nazione #
IT - Italia 628
SG - Singapore 54
US - Stati Uniti d'America 53
CN - Cina 38
VN - Vietnam 26
FR - Francia 11
BR - Brasile 9
HK - Hong Kong 6
GB - Regno Unito 5
CA - Canada 2
IQ - Iraq 2
JO - Giordania 2
JP - Giappone 2
RU - Federazione Russa 2
AR - Argentina 1
BE - Belgio 1
CH - Svizzera 1
DE - Germania 1
DK - Danimarca 1
ID - Indonesia 1
IL - Israele 1
LT - Lituania 1
MX - Messico 1
MY - Malesia 1
PK - Pakistan 1
PL - Polonia 1
PT - Portogallo 1
SA - Arabia Saudita 1
SK - Slovacchia (Repubblica Slovacca) 1
TH - Thailandia 1
Totale 856
Città #
Genoa 350
Genova 117
Vado Ligure 77
Rapallo 73
Singapore 30
San Jose 21
Ashburn 6
Hong Kong 6
Hanoi 5
Lauterbourg 5
Marseille 5
Ho Chi Minh City 4
New York 4
Beijing 3
Haiphong 3
Hải Dương 3
Los Angeles 3
Biên Hòa 2
Bordighera 2
Council Bluffs 2
London 2
Orem 2
Tokyo 2
Turin 2
Bangkok 1
Belo Horizonte 1
Bend 1
Berlin 1
Boston 1
Brussels 1
Buffalo 1
Bắc Ninh 1
Cambiano 1
Cardiff 1
Carpi 1
Chengdu 1
City of London 1
Copenhagen 1
Erbil 1
Fall River 1
Franca 1
Hangzhou 1
Irbid 1
Jeddah 1
Kajang 1
Lahore 1
Lisbon 1
Malang 1
Manchester 1
Montreal 1
Mosul 1
Natal 1
Ninh Bình 1
Paris 1
Paulista 1
Peruíbe 1
Querétaro 1
Quận Chín 1
Recife 1
San Miguel de Tucumán 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
Warsaw 1
Waterbury 1
Watertown 1
Xiamen 1
Zurich 1
Totale 782
Nome #
A spectrum of LMX1B mutations in Nail-Patella syndrome: New point mutations, deletion, and evidence of mosaicism in unaffected parents 165
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 147
Neurodevelopmental Disorders in Patients With Complex Phenotypes and Potential Complex Genetic Basis Involving Non-Coding Genes, and Double CNVs 123
P63 modulates the expression of the WDFY2 gene which is implicated in cancer regulation and limb development 115
Whole exome sequencing (WES) and functional analyses suggest synergistic effects of deleterious variants in two candidate genes for Poland Syndrome 106
Novel SYNGAP1 Variant in an Adult Individual Affected by Intellectual Disability and Epilepsy: A Cold Case Solved through Whole-Exome Sequencing 87
Scoliosis with cognitive impairment in a girl with 8q11.21q11.23 microdeletion and SNTG1 disruption 74
Neuroradiologic, Clinical, and Genetic Characterization of Cerebellar Heterotopia: A Pediatric Multicentric Study. 33
Data-driven insights into post-autopsy consultations: causes of perinatal mortality and parental outcomes 26
Totale 876
Categoria #
all - tutte 3.327
article - articoli 2.928
book - libri 0
conference - conferenze 399
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 6.654


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20212 0 0 0 0 0 0 0 0 0 0 2 0
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
2023/202483 2 5 0 8 6 18 12 6 3 5 3 15
2024/2025210 9 13 4 15 26 18 18 35 6 9 35 22
2025/2026358 52 19 30 27 58 20 61 17 38 36 0 0
Totale 876