Team: Translational research in neurogenetic diseases (NRGEN) PhD student |
Evolutionary model of repeat insertions in Ataxin-3 traces the origin of the polyglutamine stretch to an ancestral ubiquitin binding module Daniela Felício, Sandra Martins, Guilherme Pimenta Alves, António Amorim, Sandra Macedo‐Ribeiro, Matthew Merski Protein Science. 2024-11-26 10.1002/pro.5236
Functional implications of paralog genes in polyglutamine spinocerebellar ataxias Daniela Felício, Tanguy Rubat du Mérac, António Amorim, Sandra Martins Hum. Genet.. 2023-10-16 10.1007/s00439-023-02607-4
Non-coding variants in VAMP2 and SNAP25 affect gene expression: potential implications in migraine susceptibility Daniela Felício, Andreia Dias, Sandra Martins, Estefânia Carvalho, Alexandra M. Lopes, Nádia Pinto, Carolina Lemos, Mariana Santos, Miguel Alves-Ferreira J Headache Pain. 2023-06-29 10.1186/s10194-023-01615-z
Integrating functional scoring and regulatory data to predict the effect of non-coding SNPs in a complex neurological disease Daniela Felício, Miguel Alves-Ferreira, Mariana Santos, Marlene Quintas, Alexandra M Lopes, Carolina Lemos, Nádia Pinto, Sandra Martins Briefings in Functional Genomics. 2023-05-30 10.1093/bfgp/elad020
Functional characterization of a novel PRRT2 variant found in a Portuguese patient with hemiplegic migraine Andreia Dias, Mariana Santos, Estefânia Carvalho, Daniela Felício, Paulo Silva, Ivânia Alves, Teresa Pinho, Alda Sousa, Miguel Alves‐Ferreira, Carolina Lemos Clinical Genetics. 2023-05-26 10.1111/cge.14379
Spinocerebellar ataxia type 11 (SCA11): TTBK2 variants, functions and associated disease mechanisms Daniela Felício, Mariana Santos Cerebellum. 2023-03-09 10.1007/s12311-023-01540-6