CNR Institutional Research Information System

VERRILLO, LUCIA
 Distribuzione geografica
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Continente #
NA - Nord America 103
AS - Asia 65
EU - Europa 25
Totale 193
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Nazione #
US - Stati Uniti d'America 103
SG - Singapore 63
IT - Italia 25
CN - Cina 2
Totale 193
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Città #
Santa Clara 54
Singapore 47
Boardman 18
Queens 6
Naples 5
New York 5
Rome 3
Fiorano Modenese 2
Florence 2
Milan 2
Nashville 2
Saline 2
Udine 2
Arlington 1
Ashburn 1
Casandrino 1
Des Moines 1
Guangzhou 1
Totale 155
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Nome #
Conserved functions of mouse ARX and Caenorhabditis elegans alr-1 in controlling pathways damaged in neurodevelopmental disorders (NDDs) 24
Characterization of highly conserved molecular pathways involved in neurodevelopmental disorders (NDDs) 13
The Chromatin-Oxygen Sensor Gene KDM5C Associates with Novel Hypoxia-Related Signatures in Glioblastoma Multiforme. 12
Dissecting the Aristaless-related Homeobox Epilepsy path to find druggable target molecules 7
Evidences for an evolutionary conserved druggable pathway damaged in models for ARX polyalanine expansions linked to Refractory Epilepsy and Intellectual Disability. 7
Sulfavant A: a novel modulator of microglia activity 7
Le connessioni sinaptiche- La Notte Europea dei Ricercatori 2021 - Meet me tonight. FACCIA A FACCIA CON LA RICERCA. 6
Identification of a novel class of small molecules for the treatment of TREM2-related neurodegenerative dysfunctions 6
Deregulation of microtubule organization and RNA metabolism in Arx models for lissencephaly and developmental epileptic encephalopathy 6
Clinical and molecular characterization of FOXP1 variants in subjects with neurodevelopmental disorders. 6
A novel promising therapeutic paradigm in a preclinical mouse model for developmental and epileptic encephalopathy 5
Siamo tutti connessi - XXXIV edizione di "FUTURO REMOTO: PIANETA - tra cambiamenti epocali e sfide globali. 5
Deregulation of microtubule organization and RNA metabolism in Arx models for DEE 5
Exploring transcriptional single-cell signatures in a mouse model of epilepsy caused by a polyalanine expansion mutation in Aristaless-related homeobox gene. 5
Microtubule organization and splicing switches are altered in Arx animal models for neurodevelopmental disorders 5
Analysis of transcriptome landscapes in the epileptogenic cortex of the Arx(GCG)7/Y mouse 5
Expanding the genetics and phenotypic spectrum of Lysine-specific demethylase 5C (KDM5C): a report of 13 novel variants. 5
Particular musical aptitude in a female patient with speech disorders: analysis of a de novo FOXP1 truncating mutation and possible role in song-learning. 5
DNA Hypermethylation and Unstable Repeat Diseases: A Paradigm of Transcriptional Silencing to Decipher the Basis of Pathogenic Mechanisms 5
Exploitation of the Bio-MEMORY collection CNR-IBBR-CeLITABASE for the characterization of highly conserved molecular pathways involved in neurodevelopmental disorders (NDD). 5
Connessioni Neuronali & Sviluppo - La Notte Europea dei Ricercatori 2020- FACCIA A FACCIA CON LA RICERCA. 5
Cell type-specific changes identified by single-cell transcriptomics in Arx mouse model of developmental and epileptic encephalopathy 4
Defective corticogenesis in Arx mouse model of developmental and epileptic encephalopathy caused by polyalanine elongations 4
A reliable strategy for single-cell RNA sequencing analysis using cryoconserved primary cortical cells. 4
Suberoylanilide Hydroxamic Acid (SAHA) Is a Driver Molecule of Neuroplasticity: Implication for Neurological Diseases 4
Analysis of the X-chromosome cancer driver gene Lysine-specific demethylase 5C (KDM5C) in Glioblastoma Multiforme (GBM) reveals novel molecular signatures 4
Quantitative proteomic analysis of mouse brain in models of neurodevelopmental disorders caused by mutations in Aristaless-related homeobox gene 4
Expanding the genetics and phenotypic spectrum of Lysine-specific demethylase 5C (KDM5C): a report of 13 novel variants 4
A novel promising therapeutic paradigm for the treatment of drug-resistant seizures in a genetic mouse model of developmental and epileptic encephalopathy 4
Analysis of cortical gene expression variability in a mouse model of X-linked Infantile spsms syndrome 3
Phytocannabinoid treatment in a mouse model of West syndrome with spontaneous seizures 3
Further Delineation of Duplications of ARX Locus Detected in Male Patients with Varying Degrees of Intellectual Disability. 3
Analysis of the X-chromosome cancer driver gene Lysine-specific demethylase 5C (KDM5C) in Glioblastoma Multiforme (GBM 3
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Verrillo L, Mangano E, Drongitis D, Merelli I, Pischedda F, Piccoli G, Consolandi C, Bordoni R and Miano MG. 1
Totale 196
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Categoria #
all - tutte 868
article - articoli 270
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 1.138
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202447 0 0 0 0 0 0 0 0 15 2 5 25
2024/2025149 6 1 70 26 46 0 0 0 0 0 0 0
Totale 196