Celia Kun-Rodrigues (Célia Kun-Rodrigues)

Publication Activity (10 Years)

Years Active: 2020-2022
Publications (10 Years): 3

Top Topics

Cognitive Impairment

Gene Expression

Top Venues

Journal of clinical medicine

European journal of human genetics : EJHG

This page only lists publications with an associated author ORCID identifier.

Publications

Miguel Tábuas-Pereira, Rita Guerreiro, Celia Kun-Rodrigues, Maria Rosário Almeida, Jose T Bras, Isabel Santana
Whole-exome sequencing reveals PSEN1 and ATP7B combined variants as a possible cause of early-onset Lewy body dementia: a case study of genotype-phenotype correlation. Neurogenetics 23 (4) (2022)
Saana Mönkäre, Liina Kuuluvainen, Celia Kun-Rodrigues, Susana Carmona, Johanna Schleutker, Jose Bras, Minna Pöyhönen, Rita Guerreiro, Liisa Myllykangas
Whole-exome sequencing of Finnish patients with vascular cognitive impairment. European journal of human genetics : EJHG 29 (4) (2020)
Mariana Santos, Joana Damásio, Celia Kun-Rodrigues, Clara Barbot, Leonor Correia Guedes, José Brás, Isabel Alonso, Rita Guerreiro
Novel MAG Variant Causes Cerebellar Ataxia with Oculomotor Apraxia: Molecular Basis and Expanded Clinical Phenotype. Journal of clinical medicine 9 (4) (2020)