Clarisse Delvallée

Natural History and Phenotypic Spectrum of <scp>GAA‐<i>FGF14</i></scp> Sporadic Late‐Onset Cerebellar Ataxia (<scp>SCA27B</scp>)

Thomas Wirth, Guillemette Clément, Clarisse Delvallée et al. · Movement Disorders · 2023 · 55 citations · Full text

Medicine, Neurology, Neuroscience +16

Identification and Characterization of Known Biallelic Mutations in the IFT27 (BBS19) Gene in a Novel Family With Bardet-Biedl Syndrome

Élise Schaefer, Clarisse Delvallée, Laura Mary et al. · Frontiers in Genetics · 2019 · 37 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

A <scp> <i>BBS1</i> SVA </scp> F retrotransposon insertion is a frequent cause of <scp>Bardet‐Biedl</scp> syndrome

Clarisse Delvallée, Samuel Nicaise, Manuela Antin et al. · Clinical Genetics · 2020 · 26 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Does Spinocerebellar ataxia 27B mimic cerebellar multiple system atrophy?

Thomas Wirth, Céline Bonnet, Clarisse Delvallée et al. · Journal of Neurology · 2024 · 16 citations

Life Sciences, Neurology, Neuroscience +14

Novel<i>IQCE</i>variations confirm its role in postaxial polydactyly and cause ciliary defect phenotype in zebrafish

Alejandro Estrada‐Cuzcano, Christelle Etard, Clarisse Delvallée et al. · Human Mutation · 2019 · 11 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13