Daniela Felicio
Porto, Portugal
Last Updated: 09/26/2026
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Found 8 publications
Retrotransposition Events Shape the Evolution of the Ataxin-3 Gene Family in Primates.
Journal: Genome biology and evolution
Published: February 20, 2026
Missense variant in TTBK2 kinase domain causes loss of function and impaired protein phosphorylation.
Journal: Scientific reports
Published: July 04, 2025
Evolutionary model of repeat insertions in Ataxin-3 traces the origin of the polyglutamine stretch to an ancestral ubiquitin binding module.
Journal: Protein science : a publication of the Protein Society
Published: August 05, 2024
Functional implications of paralog genes in polyglutamine spinocerebellar ataxias.
Journal: Human genetics
Published: July 10, 2023
Non-coding variants in VAMP2 and SNAP25 affect gene expression: potential implications in migraine susceptibility.
Journal: The journal of headache and pain
Published: May 15, 2023
Spinocerebellar ataxia type 11 (SCA11): TTBK2 variants, functions and associated disease mechanisms.
Spinocerebellar ataxia type 11 (SCA11): TTBK2 variants, functions and associated disease mechanisms.
Journal: Cerebellum (London, England)
Published: March 02, 2023
Integrating functional scoring and regulatory data to predict the effect of non-coding SNPs in a complex neurological disease.
Journal: Briefings in functional genomics
Published: January 26, 2023
Showing 1-8 of 8
Last Updated: 09/26/2026