IRIS
CERMINARA, MARIA
 Distribuzione geografica
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Continente #
EU - Europa 1.169
AS - Asia 101
NA - Nord America 17
SA - Sud America 10
Totale 1.297
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Nazione #
IT - Italia 1.163
SG - Singapore 38
VN - Vietnam 32
CN - Cina 24
US - Stati Uniti d'America 14
BR - Brasile 6
HK - Hong Kong 5
NL - Olanda 4
AR - Argentina 3
MX - Messico 2
CA - Canada 1
HR - Croazia 1
ID - Indonesia 1
IN - India 1
RU - Federazione Russa 1
VE - Venezuela 1
Totale 1.297
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Città #
Genoa 721
Vado Ligure 153
Genova 148
Rapallo 135
Hanoi 9
Ho Chi Minh City 9
Singapore 9
Beijing 7
Staten Island 7
Bordighera 5
Hong Kong 5
Oegstgeest 4
Ashburn 3
Haiphong 2
Mexico City 2
Thái Bình 2
Achinsk 1
Buenos Aires 1
Bình Dương 1
Cao Lanh 1
Cecina 1
Chennai 1
Conceição do Jacuípe 1
Cumanacoa 1
Des Moines 1
Franca 1
Guaiçara 1
Guaratinga 1
Hải Dương 1
Jaú 1
Lomas de Zamora 1
Ninh Bình 1
Orem 1
Quảng Ngãi 1
Registro 1
San Miguel de Tucumán 1
Seattle 1
Tianjin 1
Toronto 1
Totale 1.244
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Nome #
Genetic inactivation of mGlu5 receptor improves motor coordination in the Grm1crv4 mouse model of SCAR13 ataxia 213
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 121
Studio di meccanismi oligogenici alla base di patologie complesse dello sviluppo: disturbi del neurosviluppo e sindrome di Poland. 110
Phenotypic spectrum overview of patients with neurodevelopmental disorders sharing one recurrent copy number variant (CNV) and carrying different additional CNVs 103
Neurodevelopmental Disorders in Patients With Complex Phenotypes and Potential Complex Genetic Basis Involving Non-Coding Genes, and Double CNVs 102
In-vitro and in-vivo studies depict metabotropic glutamate receptor 5 as a potential pharmacological target to modulate disease progression in ALS 100
Genetic Downregulation of the Metabotropic Glutamate Receptor Type 5 Dampens the Reactive and Neurotoxic Phenotype of Adult ALS Astrocytes 90
Whole exome sequencing (WES) and functional analyses suggest synergistic effects of deleterious variants in two candidate genes for Poland Syndrome 85
An example of parenchymal renal sparing in the context of complex malformations due to a novel mutation in the PBX1 gene 83
Complex cases with Autism Spectrum Disorder (ASD), developmental delay, hyperactivity and sleep disturbance explained by oligogenic mechanisms 76
Relevance of double-hit mechanisms in patients with Neurodevelopmental Disorders (NDDs): a re-evaluation of 526 patients with non-benign copy number variants (CNVs). 68
Novel SYNGAP1 Variant in an Adult Individual Affected by Intellectual Disability and Epilepsy: A Cold Case Solved through Whole-Exome Sequencing 67
Phenotypic Spectrum revealed by two hits model mechanism in Neurodevelopmental Disorder patients with Syndromic and Recurrent CNVs. 67
Partial deletion of mGluR5 affects microglia inflammatory phenotype, bioenergetic characteristics, and red-ox state during ALS progression in SOD1G93A mice 51
null 3
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Totale 1.342
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Categoria #
all - tutte 5.338
article - articoli 2.549
book - libri 0
conference - conferenze 2.348
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 10.235
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202114 0 0 0 0 0 2 0 5 5 1 1 0
2021/202283 0 1 1 4 0 2 8 13 1 12 13 28
2022/2023177 17 14 7 11 16 24 6 11 27 3 35 6
2023/2024187 1 19 4 20 12 44 16 16 9 16 10 20
2024/2025445 13 40 4 30 47 36 36 89 17 22 61 50
2025/2026349 89 33 53 62 105 7 0 0 0 0 0 0
Totale 1.342