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Valerio Conti

6PUBLICATIONS

45CO-AUTHORS

Gene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)Medical infection agents (incl. prions)Infant and child healthNeurogenetics

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Publications (6)

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|Dec 11, 2025

<i>SLC35A2</i>-Related Brain Disorders: Genetics, Pathophysiology, and Therapeutic Insights.

Beatrice Risso, Antonella Riva, Greta Volpedo

|Oct 13, 2025

Mosaic expression of SLC35A2 pathogenetic variants impairs neuronal migration and dendritogenesis in the developing cortex.

Antonio Falace, Léa Corbières, Lucas Silvagnoli

|Apr 23, 2022

Prospective Evaluation of Ghrelin and Des-Acyl Ghrelin Plasma Levels in Children with Newly Diagnosed Epilepsy: Evidence for Reduced Ghrelin-to-Des-Acyl Ghrelin Ratio in Generalized Epilepsies.

Anna-Maria Costa, Tommaso Lo Barco, Elisabetta Spezia

|Feb 05, 2021

Is Focal Cortical Dysplasia/Epilepsy Caused by Somatic <i>MTOR</i> Mutations Always a Unilateral Disorder?

Renzo Guerrini, Mara Cavallin, Tommaso Pippucci

|Sep 08, 2020

International consensus recommendations on the diagnostic work-up for malformations of cortical development.

Renske Oegema, Tahsin Stefan Barakat, Martina Wilke

|Jan 27, 2019

Multiple genomic copy number variants associated with periventricular nodular heterotopia indicate extreme genetic heterogeneity.

Elena Cellini, Annalisa Vetro, Valerio Conti

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Frequent Collaborators

3 joint publications

Renzo Guerrini

2 joint publications

Elena Parrini

2 joint publications

Antonio Falace

2 joint publications

Carmen Barba

1 joint publications

Elena Cellini

1 joint publications

Annalisa Vetro

1 joint publications

Pasquale Striano

1 joint publications

Sabrina Giglio

1 joint publications

Matteo Della Monica

1 joint publications

Marco Fichera

Frequent Collaborators

3 joint publications

Renzo Guerrini

2 joint publications

Elena Parrini

2 joint publications

Antonio Falace

2 joint publications

Carmen Barba

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