Publications by authors named "Maria Guarnaccia"

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Unraveling the missing heritability of amyotrophic lateral sclerosis: Should we focus more on copy number variations?
Maria Guarnaccia, Valentina La Cognata, Giulia Gentile, Giovanna Morello, Sebastiano Cavallaro

Neural Regen Res· May 2026

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Multi-Omics Integration for Advancing Glioma Precision Medicine.
Maria Guarnaccia, Valentina La Cognata, Giulia Gentile, Giovanna Morello, Sebastiano Cavallaro

Ann Clin Transl Neurol· November 2025

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Predicting amyotrophic lateral sclerosis in the pre-symptomatic phase: Insights from SOD1G93A mouse gene expression profiles.
Valentina La Cognata, Maria Guarnaccia, Giovanna Morello, Giulia Gentile, Sebastiano Cavallaro

Exp Neurol· October 2025

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Artificial Intelligence-Driven Multi-Omics Approaches in Glioblastoma.
Giovanna Morello, Valentina La Cognata, Maria Guarnaccia, Giulia Gentile, Sebastiano Cavallaro

Int J Mol Sci· September 2025

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Oncological and Functional Outcomes After Type III Cordectomy for Early Glottic Cancer (Tis, T1a): A Retrospective Study Based on Our 10-Year Experience.
Eleonora Lovati, Elisabetta Genovese, Livio Presutti, Marco Trebbi, Luca Pingani, Maria Consolazione Guarnaccia

J Clin Med· November 2024

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Prognostic Factors in Idiopathic Sudden Sensorineural Hearing Loss: The Experience of Two Audiology Tertiary Referral Centres.
Valeria Caragli, Leonardo Franz, Alessandro Incognito, Salvatore Bitonti, Maria Guarnaccia

Medicina (Kaunas)· July 2024

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Increased copy-number variant load of associated risk genes in sporadic cases of amyotrophic lateral sclerosis.
Maria Guarnaccia, Giovanna Morello, Valentina La Cognata, Vincenzo La Bella, Francesca Luisa Conforti

Cell Mol Life Sci· July 2024

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The multifaceted role of the CXC chemokines and receptors signaling axes in ALS pathophysiology.
Valentina La Cognata, Giovanna Morello, Maria Guarnaccia, Sebastiano Cavallaro

Prog Neurobiol· April 2024

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Transcriptomic Analysis in the Hippocampus and Retina of Tg2576 AD Mice Reveals Defective Mitochondrial Oxidative Phosphorylation and Recovery by Tau 12A12mAb Treatment.
Giovanna Morello, Maria Guarnaccia, Valentina La Cognata, Valentina Latina, Pietro Calissano

Cells· September 2023

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The ε-Isozyme of Protein Kinase C (PKCε) Is Impaired in ALS Motor Cortex and Its Pulse Activation by Bryostatin-1 Produces Long Term Survival in Degenerating SOD1-G93A Motor Neuron-like Cells.
Valentina La Cognata, Agata Grazia D'Amico, Grazia Maugeri, Giovanna Morello, Maria Guarnaccia

Int J Mol Sci· August 2023

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CXCR2 Is Deregulated in ALS Spinal Cord and Its Activation Triggers Apoptosis in Motor Neuron-Like Cells Overexpressing hSOD1-G93A.
Valentina La Cognata, Agata Grazia D'Amico, Grazia Maugeri, Giovanna Morello, Maria Guarnaccia

Cells· July 2023

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A Diagnostic Gene-Expression Signature in Fibroblasts of Amyotrophic Lateral Sclerosis.
Giovanna Morello, Valentina La Cognata, Maria Guarnaccia, Vincenzo La Bella, Francesca Luisa Conforti

Cells· July 2023

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Detection of Single-Nucleotide and Copy Number Defects Underlying Hyperphenylalaninemia by Next-Generation Sequencing.
Elisabetta Anna Tendi, Giovanna Morello, Maria Guarnaccia, Valentina La Cognata, Salvatore Petralia

Biomedicines· July 2023

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Cracking the Code of Neuronal Cell Fate.
Giovanna Morello, Valentina La Cognata, Maria Guarnaccia, Velia D'Agata, Sebastiano Cavallaro

Cells· March 2023

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A Targeted Next-Generation Sequencing Panel to Genotype Gliomas.
Maria Guarnaccia, Laura Guarnaccia, Valentina La Cognata, Stefania Elena Navone, Rolando Campanella

Life (Basel)· June 2022

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Dysregulated miRNAs as Biomarkers and Therapeutical Targets in Neurodegenerative Diseases.
Giulia Gentile, Giovanna Morello, Valentina La Cognata, Maria Guarnaccia, Francesca Luisa Conforti

J Pers Med· May 2022

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The Utility of Genomic Testing for Hyperphenylalaninemia.
Elisabetta Anna Tendi, Maria Guarnaccia, Giovanna Morello, Sebastiano Cavallaro

J Clin Med· February 2022

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Transcriptional Profiles of Cell Fate Transitions Reveal Early Drivers of Neuronal Apoptosis and Survival.
Giovanna Morello, Ambra Villari, Antonio Gianmaria Spampinato, Valentina La Cognata, Maria Guarnaccia

Cells· November 2021

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Design and Validation of a Custom NGS Panel Targeting a Set of Lysosomal Storage Diseases Candidate for NBS Applications.
Valentina La Cognata, Maria Guarnaccia, Giovanna Morello, Martino Ruggieri, Agata Polizzi

Int J Mol Sci· September 2021

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miRNA and mRNA Profiling Links Connexin Deficiency to Deafness via Early Oxidative Damage in the Mouse .
Giulia Gentile, Fabiola Paciello, Veronica Zorzi, Antonio Gianmaria Spampinato, Maria Guarnaccia

Front Cell Dev Biol· January 2021

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Genomic Portrait of a Sporadic Amyotrophic Lateral Sclerosis Case in a Large Spinocerebellar Ataxia Type 1 Family.
Giovanna Morello, Giulia Gentile, Rossella Spataro, Antonio Gianmaria Spampinato, Maria Guarnaccia

J Pers Med· December 2020

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Development of a Pharmacogenetic Lab-on-Chip Assay Based on the In-Check Technology to Screen for Genetic Variations Associated to Adverse Drug Reactions to Common Chemotherapeutic Agents.
Rosario Iemmolo, Valentina La Cognata, Giovanna Morello, Maria Guarnaccia, Mariamena Arbitrio

Biosensors (Basel)· December 2020

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Deletion of Voltage-Dependent Anion Channel 1 knocks mitochondria down triggering metabolic rewiring in yeast.
Andrea Magrì, Maria Carmela Di Rosa, Ivan Orlandi, Francesca Guarino, Simona Reina, Maria Guarnaccia

Cell Mol Life Sci· August 2020

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Highlights on Genomics Applications for Lysosomal Storage Diseases.
Valentina La Cognata, Maria Guarnaccia, Agata Polizzi, Martino Ruggieri, Sebastiano Cavallaro

Cells· August 2020

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A Systems Biology Approach for Personalized Medicine in Refractory Epilepsy.
Giuseppina Daniela Naimo, Maria Guarnaccia, Teresa Sprovieri, Carmine Ungaro, Francesca Luisa Conforti

Int J Mol Sci· July 2019

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