Célia Kun-Rodrigues
3PUBLICATIONS
10CO-AUTHORS
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Publications (3)
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|Sep 17, 2022
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.Miguel Tábuas-Pereira, Rita Guerreiro, Célia Kun-Rodrigues
|Dec 03, 2020
Whole-exome sequencing of Finnish patients with vascular cognitive impairment.Saana Mönkäre, Liina Kuuluvainen, Celia Kun-Rodrigues
|Apr 29, 2020
Novel MAG Variant Causes Cerebellar Ataxia with Oculomotor Apraxia: Molecular Basis and Expanded Clinical Phenotype.Mariana Santos, Joana Damásio, Célia Kun-Rodrigues
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Frequent Collaborators
2 joint publications
Rita Guerreiro
1 joint publications
Mariana Santos
1 joint publications
Jorge Sequeiros
1 joint publications
Saana Mönkäre
1 joint publications
Johanna Schleutker
1 joint publications
Liisa Myllykangas
1 joint publications
Miguel Tábuas-Pereira
1 joint publications
Maria Rosário Almeida
1 joint publications
José Brás
1 joint publications
Isabel Santana
