Jean-Loup Méreaux

7PUBLICATIONS
27CO-AUTHORS
Aerospace structuresEpigenetics (incl. genome methylation and epigenomics)NeurogeneticsGene expression (incl. microarray and other genome-wide approaches)Neurology and neuromuscular diseases
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Publications (7)

|Sep 22, 2026
ATXN8OS Intermediate Expansion Acts as a Genetic Modifier in Spinocerebellar Ataxia Type 48 (SCA48/STUB1).

|Jun 26, 2026
Biallelic ATG9B Variants Define a Novel Autophagy-Related Neurodevelopmental Disorder with Cerebellar Ataxia.

|Dec 19, 2025
Sequence Variants in Small CAG Repeat Expansions of the HTT Gene and Disease Onset and Progression in Huntington Disease.

Anna Heinzmann, Emilien Petit, Jessica Dawson

|Jan 04, 2023
Fast and reliable detection of repeat expansions in spinocerebellar ataxia using exomes.

Jean-Loup Méreaux, Claire-Sophie Davoine, Marie Coutelier

|Jan 04, 2022
Clinical and genetic spectra of 1550 index patients with hereditary spastic paraplegia.

Jean-Loup Méreaux, Guillaume Banneau, Mélanie Papin

|Jun 22, 2019
Trigeminal Neuralgia and Charcot-Marie-Tooth Disease: An Intriguing Association. Lessons From a Large Family Case Report and Review of Literature.

Jean-Loup Méreaux, Romain Lefaucheur, Benjamin Hebant

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Frequent Collaborators

2 joint publications

Emilien Petit

2 joint publications

Giulia Coarelli

2 joint publications

Léna Guillot-Noel

2 joint publications

Alexandra Durr