Tallaksen, Chantal Me E.

Top Publications

Top Publications Authored or Co-Authored by "Tallaksen, Chantal Me E."

• Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration

  Brain, Volume 131, No. 3, Year 2008, Citations 213
• Mutation analysis of the paraplegin gene (SPG7) in patients with hereditary spastic paraplegia

  Neurology, Volume 66, No. 5, Year 2006, Citations 102
• Efficacy of exome-targeted capture sequencing to detect mutations in known cerebellar ataxia genes

  JAMA Neurology, Volume 75, No. 5, Year 2018, Citations 97
• Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment

  Genetics in Medicine, Volume 22, No. 11, Year 2020, Citations 89