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Laurent Villard

French Institute of Health and Medical Research
Aix-Marseille University

264

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5489

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Gyrokinetic simulations of electromagnetic turbulence with global particle-in-cell codes

2021
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Gyrokinetic investigation of the nonlinear interaction of Alfvénic modes and turbulence

2021
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Rett syndrome: think outside the (skull) box.

2021
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Expansion of the Genotypic and Phenotypic Spectrum of WASF1-Related Neurodevelopmental Disorder.

2021 Brain Sciences
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Patients with KCNH1-related intellectual disability without distinctive features of Zimmermann-Laband/Temple-Baraitser syndrome

2021 Journal of Medical Genetics
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Severe offtarget effects following intravenous delivery of AAV9-MECP2 in a female mouse model of Rett syndrome.

2021 Neurobiology of Disease
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Further delineation of BCAP31-linked intellectual disability: description of 17 new families with LoF and missense variants.

2021 European Journal of Human Genetics
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Time-limited alterations in cortical activity of a Knock-in mice model of KCNQ2-related Developmental and Epileptic Encephalopathy

2021 bioRxiv
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SYNGAP1-DEE: A visual sensitive epilepsy.

2021 Clinical Neurophysiology
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A large consanguineous family with a homozygous Metabotropic Glutamate Receptor 7 (mGlu7) variant and developmental epileptic encephalopathy: Effect on protein structure and ligand affinity.

2021 Orphanet Journal of Rare Diseases
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