DIVIZIA, MARIA TERESA
 Distribuzione geografica
Continente #
EU - Europa 603
AS - Asia 130
NA - Nord America 107
Continente sconosciuto - Info sul continente non disponibili 19
SA - Sud America 10
Totale 869
Nazione #
IT - Italia 579
US - Stati Uniti d'America 102
SG - Singapore 46
CN - Cina 34
VN - Vietnam 23
BD - Bangladesh 12
FR - Francia 11
BR - Brasile 10
HK - Hong Kong 6
GB - Regno Unito 4
CA - Canada 3
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 850
Città #
Genoa 307
Genova 117
Rapallo 73
Vado Ligure 64
San Jose 28
Singapore 24
Ashburn 9
Hong Kong 6
New York 6
Lauterbourg 5
Marseille 5
Ho Chi Minh City 4
Turin 4
Beijing 3
Haiphong 3
Hải Dương 3
Los Angeles 3
Albany 2
Biên Hòa 2
Bordighera 2
Buffalo 2
Chicago 2
Council Bluffs 2
Dallas 2
Hanoi 2
London 2
Orem 2
Pasadena 2
Pinole 2
Tokyo 2
Atlanta 1
Baltimore 1
Bangkok 1
Belo Horizonte 1
Berlin 1
Bettendorf 1
Birmingham 1
Boca Raton 1
Boston 1
Bắc Ninh 1
Cambiano 1
Carpi 1
Chengdu 1
City of London 1
Copenhagen 1
Davenport 1
Erbil 1
Franca 1
Houston 1
Irbid 1
Kajang 1
Lahore 1
Las Vegas 1
Lisbon 1
Lithia 1
Malang 1
Manchester 1
Mandeville 1
Miami 1
Montreal 1
Mosul 1
Natal 1
Newark 1
Newport News 1
Ninh Bình 1
North Charleston 1
North York 1
Oswego 1
Padua 1
Paris 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
São Pedro 1
Tampa 1
Thái Bình 1
Thái Nguyên 1
Thủ Đức 1
Tân Tiến 1
Venice 1
Walton 1
Warsaw 1
Washington 1
Waterbury 1
Watertown 1
Xiamen 1
Zurich 1
Totale 760
Nome #
A spectrum of LMX1B mutations in Nail-Patella syndrome: New point mutations, deletion, and evidence of mosaicism in unaffected parents 175
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 156
Neurodevelopmental Disorders in Patients With Complex Phenotypes and Potential Complex Genetic Basis Involving Non-Coding Genes, and Double CNVs 145
P63 modulates the expression of the WDFY2 gene which is implicated in cancer regulation and limb development 124
Whole exome sequencing (WES) and functional analyses suggest synergistic effects of deleterious variants in two candidate genes for Poland Syndrome 113
Scoliosis with cognitive impairment in a girl with 8q11.21q11.23 microdeletion and SNTG1 disruption 78
Neuroradiologic, Clinical, and Genetic Characterization of Cerebellar Heterotopia: A Pediatric Multicentric Study. 44
Data-driven insights into post-autopsy consultations: causes of perinatal mortality and parental outcomes 34
Totale 869
Categoria #
all - tutte 3.467
article - articoli 3.026
book - libri 0
conference - conferenze 441
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 6.934


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/202244 0 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
2025/2026368 45 16 26 24 52 18 55 15 33 31 13 40
2026/202727 24 3 0 0 0 0 0 0 0 0 0 0
Totale 869