LERONE, MARGHERITA
 Distribuzione geografica
Continente #
EU - Europa 1.039
AS - Asia 172
NA - Nord America 79
SA - Sud America 22
AF - Africa 1
Totale 1.313
Nazione #
IT - Italia 1.022
US - Stati Uniti d'America 78
SG - Singapore 77
CN - Cina 44
VN - Vietnam 30
BR - Brasile 16
HK - Hong Kong 6
FR - Francia 5
AR - Argentina 4
GB - Regno Unito 3
IQ - Iraq 3
RU - Federazione Russa 3
ID - Indonesia 2
IL - Israele 2
BD - Bangladesh 1
BE - Belgio 1
BW - Botswana 1
CA - Canada 1
DE - Germania 1
DK - Danimarca 1
EC - Ecuador 1
FI - Finlandia 1
IN - India 1
JO - Giordania 1
JP - Giappone 1
MY - Malesia 1
PK - Pakistan 1
PL - Polonia 1
PS - Palestinian Territory 1
PT - Portogallo 1
SA - Arabia Saudita 1
UY - Uruguay 1
Totale 1.313
Città #
Genoa 465
Genova 336
Vado Ligure 117
Rapallo 86
Singapore 43
Ashburn 29
San Jose 21
Ho Chi Minh City 9
Hanoi 8
Beijing 7
Hong Kong 6
Bordighera 5
Lauterbourg 5
New York 4
Haiphong 3
Palermo 3
Turin 3
Biên Hòa 2
Buffalo 2
London 2
Los Angeles 2
Orem 2
São Paulo 2
Ahmedabad 1
Atlanta 1
Banfield 1
Belo Horizonte 1
Bend 1
Blumenau 1
Boituva 1
Boston 1
Brussels 1
Bắc Ninh 1
Cambiano 1
Cardiff 1
Caxias do Sul 1
Chicago 1
Copenhagen 1
Council Bluffs 1
Erbil 1
Fall River 1
Florence 1
Franca 1
Frankfurt am Main 1
Gaborone 1
Goiás 1
Guayaquil 1
Hebron 1
Helsinki 1
Iguaba Grande 1
Jeddah 1
Kajang 1
Kazan' 1
Lahore 1
Lisbon 1
Malang 1
Montevideo 1
Montreal 1
Mosul 1
Ninh Bình 1
Peruíbe 1
Quilmes 1
Recife 1
Riachão 1
San Justo 1
San Miguel de Tucumán 1
Saratov 1
Smolensk 1
Sumaré 1
Tel Aviv 1
Teresina 1
Thái Bình 1
Tijucas 1
Tokyo 1
Três Marias 1
Verona 1
Vinh 1
Warsaw 1
Watertown 1
Xiamen 1
Totale 1.219
Nome #
Intragenic duplication of KCNQ5 gene results in aberrant splicing leading to a premature termination codon in a patient with intellectual disability 202
Diagnostic Criteria of Pediatric Intestinal Myopathies 169
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 114
null 96
Novel SYNGAP1 Variant in an Adult Individual Affected by Intellectual Disability and Epilepsy: A Cold Case Solved through Whole-Exome Sequencing 86
Exclusion of the Sonic Hedgehog gene as responsible for Currarino syndrome and anorectal malformations with sacral hypodevelopment 58
Diagnostic and therapeutic approach to multiple endocrine neoplasia type 2B in pediatric patients 57
Consensus based recommendations for diagnosis and medical management of Poland syndrome (sequence) 51
Response to Klinger and Merlob re: Case description with review of the literature. Am J Med Genet Part A 149A:1597-1602, 2009 41
Dextrocardia in patients with Poland syndrome: Phenotypic characterization provides insight into the pathogenesis 41
Totale 1.350
Categoria #
all - tutte 4.750
article - articoli 4.750
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 9.500


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202124 0 0 0 0 0 0 0 0 0 9 2 13
2021/202281 4 1 4 9 3 9 4 19 5 11 2 10
2022/2023115 11 10 2 6 14 10 5 9 21 1 21 5
2023/2024104 4 6 1 8 5 13 12 13 6 7 4 25
2024/2025312 14 19 6 18 39 30 21 62 7 12 47 37
2025/2026457 76 21 41 31 82 32 65 24 39 46 0 0
Totale 1.350