BOERI, SILVIA
 Distribuzione geografica
Continente #
EU - Europa 698
AS - Asia 148
NA - Nord America 66
SA - Sud America 7
AF - Africa 1
Totale 920
Nazione #
IT - Italia 674
SG - Singapore 63
US - Stati Uniti d'America 63
CN - Cina 35
VN - Vietnam 32
BR - Brasile 5
FR - Francia 5
JP - Giappone 4
GB - Regno Unito 3
BD - Bangladesh 2
DE - Germania 2
HK - Hong Kong 2
ID - Indonesia 2
MX - Messico 2
NL - Olanda 2
AR - Argentina 1
AT - Austria 1
BE - Belgio 1
CA - Canada 1
DK - Danimarca 1
EC - Ecuador 1
ES - Italia 1
FI - Finlandia 1
HR - Croazia 1
IE - Irlanda 1
IL - Israele 1
IN - India 1
IQ - Iraq 1
JO - Giordania 1
LB - Libano 1
MY - Malesia 1
PL - Polonia 1
PT - Portogallo 1
RS - Serbia 1
RU - Federazione Russa 1
SA - Arabia Saudita 1
TR - Turchia 1
UA - Ucraina 1
ZA - Sudafrica 1
Totale 920
Città #
Genoa 465
Vado Ligure 90
Rapallo 63
Singapore 33
San Jose 22
Genova 20
Ho Chi Minh City 14
Hanoi 7
Ashburn 4
Beijing 4
Milan 4
New York 4
Orem 4
Tokyo 4
Turin 4
Bordighera 3
Buffalo 3
Lauterbourg 3
Los Angeles 3
Frankfurt am Main 2
Haiphong 2
Hong Kong 2
London 2
Mexico City 2
Ninh Bình 2
Santa Clara 2
Thái Bình 2
Achinsk 1
Ambato 1
Beirut 1
Belgrade 1
Bend 1
Boston 1
Brasília 1
Brussels 1
Cambiano 1
Can Tho 1
Canal Winchester 1
Cardiff 1
Cecina 1
Chennai 1
Conceição do Jacuípe 1
Copenhagen 1
Council Bluffs 1
Da Nang 1
Dublin 1
Erbil 1
Florence 1
Franca 1
Helsinki 1
Houston 1
Jeddah 1
Johannesburg 1
Kajang 1
Kyiv 1
Lagoa Santa 1
Lisbon 1
Madrid 1
Malang 1
Naples 1
Paoli 1
Paris 1
Piscataway 1
Qujing 1
Quận Ba 1
Registro 1
Rome 1
San Francisco 1
San Miguel de Tucumán 1
Seattle 1
Toronto 1
Warsaw 1
Watertown 1
Totale 816
Nome #
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
Phenotypic spectrum overview of patients with neurodevelopmental disorders sharing one recurrent copy number variant (CNV) and carrying different additional CNVs 121
Complex cases with Autism Spectrum Disorder (ASD), developmental delay, hyperactivity and sleep disturbance explained by oligogenic mechanisms 90
Novel SYNGAP1 Variant in an Adult Individual Affected by Intellectual Disability and Epilepsy: A Cold Case Solved through Whole-Exome Sequencing 85
Relevance of double-hit mechanisms in patients with Neurodevelopmental Disorders (NDDs): a re-evaluation of 526 patients with non-benign copy number variants (CNVs). 84
Phenotypic Spectrum revealed by two hits model mechanism in Neurodevelopmental Disorder patients with Syndromic and Recurrent CNVs. 82
MYT1L variant inherited by a mosaic father in a case of severe developmental and epileptic encephalopathy 65
Decreased free D-aspartate levels in the blood serum of patients with schizophrenia 52
Supratentorial Demyelinating Lesions Following Severe Acute Respiratory Syndrome Coronavirus-2 Infection: A Pediatric Case Report 40
Subclinical rhythmic EEG discharge of adults (SREDA) in pediatric population: A case series with systematic review of the literature 37
Polygenic variants in DNA repair genes are associated with neurodevelopmental disorders, regression and increased burdens of somatic variants and short tandem repeat expansions 8
null 3
null 3
Totale 940
Categoria #
all - tutte 3.350
article - articoli 1.935
book - libri 0
conference - conferenze 1.415
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 6.700


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/202229 0 0 0 3 0 0 0 9 0 2 0 15
2022/202391 12 10 2 4 7 8 5 3 18 0 19 3
2023/2024108 1 5 2 11 7 30 13 7 6 9 6 11
2024/2025286 8 14 3 18 35 24 20 51 9 19 47 38
2025/2026426 57 20 35 42 60 42 61 21 45 43 0 0
Totale 940