Author

Pierre Szepetowski

InsermORCID 0000-0003-2060-8390Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Neuroscience· 2 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:rat· 2 Assay:electronic health records· 1 Organism:human· 1 Approach:statistical model· 1

Frequent Co-Authors

Emmanuelle Buhler· 2 shared Nail BurnasheviD· 2 shared Š. BaueriD· 2 shared Sarah Tarhini· 2 shared Alena Jahodová· 1 shared Alfonso RepresaiD· 1 shared Allan BayatiD· 1 shared Allyn McConkie‐RoselliD· 1 shared

Activity by Year

2022-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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2 shared papersNeuroscience

Emmanuelle Buhler

Mutual co-authors in cluster

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3 papers

Recent·Most cited

NeurosciencebioRxivPreprintFeb 11, 2025

Virus-against-virus dominant-negative interference strategy targeting a viral CC chemokine prevents cytomegalovirus-related neurodevelopmental pathogenesis

Š. Bauer, Sarah Tarhini, Emmanuelle Buhler…·Pierre Szepetowski

This study shows that a dominant-negative mutant of the viral chemokine RCK3 prevents CMV-induced neurodevelopmental disorders in a rat model.

DOI 10.1101/2025.02.11.637423

ratexperimental assay

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NeurosciencebioRxivPreprintDec 1, 2023

Pathogenic MTOR somatic variant causing focal cortical dysplasia drives hyperexcitability via overactivation of neuronal GluN2C NMDA receptors

Louison Pineau, Emmanuelle Buhler, Sarah Tarhini…·Nail Burnashev

This study shows that a somatic MTOR variant in FCD type II causes hyperexcitability through overactivation of GluN2C NMDA receptors in rat neurons.

1 citation

ratelectronic health records

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Genetic & Genomic MedicinemedRxivPreprintApr 26, 2022

Missense variants in the voltage sensing and pore domain of KCNH5 cause neurodevelopmental phenotypes including epilepsy

Hannah C. Happ, Lynette Grant Sadleir, Matthew Zemel…·Gemma L. Carvill

The paper reports a cohort of 17 patients with pathogenic KCNH5 variants causing neurodevelopmental disorders and epilepsy, identifying genotype-phenotype correlations.

DOI 10.1101/2022.04.26.22274147

humanstatistical model

𝕏 PostBluesky