Jérémie Courraud

Novel mutations in NLGN3 causing autism spectrum disorder and cognitive impairment

Angélique Quartier, Jérémie Courraud, Thuong Ha et al. · Human Mutation · 2019 · 65 citations

Genetics, Molecular Biology, Nlgn3 Gene +17

Sex-specific impact of prenatal androgens on social brain default mode subsystems

Michael Lombardo, Bonnie Auyeung, Tiziano Pramparo et al. · Molecular Psychiatry · 2018 · 57 citations · Full text

Biallelic PDE2A variants: a new cause of syndromic paroxysmal dyskinesia

Diane Doummar, Christel Dentel, Romane Lyautey et al. · European Journal of Human Genetics · 2020 · 40 citations · Full text

Biallelic Pde2a Variants, Neurology, Medicine +1

De Novo Frameshift Variants in the Neuronal Splicing Factor NOVA2 Result in a Common C-Terminal Extension and Cause a Severe Form of Neurodevelopmental Disorder

Francesca Mattioli, Gaëlle Hayot, Nathalie Drouot et al. · The American Journal of Human Genetics · 2020 · 39 citations · Full text

Neurodevelopmental Disorders, Developmental Biology, Genetics +8

Integrative approach to interpret DYRK1A variants, leading to a frequent neurodevelopmental disorder

Jérémie Courraud, Eric Chater‐Diehl, Benjamin Durand et al. · Genetics in Medicine · 2021 · 31 citations · Full text

Neurodevelopmental Disorders, Developmental Biology, Molecular Neuroscience +11