CGG Repeat-Associated Translation Mediates Neurodegeneration in Fragile X Tremor Ataxia Syndrome
2013 · Neuron · 484 citations
https://doi.org/10.1016/j.neuron.2013.03.026
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Chantal Sellier
Inserm(FR)
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Chantal Sellier is an academic researcher from Inserm. The author has contributed to research in topics: Genetic Neurodegenerative Diseases & Genetics and Neurodevelopmental Disorders & Amyotrophic Lateral Sclerosis Research. The author has an h-index of 24, co-authored 35 publications.
ORCID: 0000-0003-2933-5464Papers by this author
worksTranslation of Expanded CGG Repeats into FMRpolyG Is Pathogenic and May Contribute to Fragile X Tremor Ataxia Syndrome
2017 · Neuron · 235 citations
https://doi.org/10.1016/j.neuron.2016.12.016
Repeat-associated non-AUG (RAN) translation and other molecular mechanisms in Fragile X Tremor Ataxia Syndrome
2018 · Brain Research · 88 citations
https://doi.org/10.1016/j.brainres.2018.02.006
FMRpolyG-positive inclusions in CNS and non-CNS organs of a fragile X premutation carrier with fragile X-associated tremor/ataxia syndrome
2014 · Acta Neuropathologica Communications · 84 citations
https://doi.org/10.1186/s40478-014-0162-2
Integrative genetic analysis illuminates ALS heritability and identifies risk genes
2023 · Nature Communications · 40 citations
https://doi.org/10.1038/s41467-022-35724-1
Potential pathogenic mechanisms underlying Fragile X Tremor Ataxia Syndrome: RAN translation and/or RNA gain-of-function?
2017 · European Journal of Medical Genetics · 31 citations
https://doi.org/10.1016/j.ejmg.2017.11.001
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