Publicaciones en colaboración con investigadores/as de National Institutes of Health (5)

2021

  1. Finding genetically-supported drug targets for Parkinson’s disease using Mendelian randomization of the druggable genome

    Nature Communications, Vol. 12, Núm. 1

  2. Investigation of Autosomal Genetic Sex Differences in Parkinson's Disease

    Annals of Neurology, Vol. 90, Núm. 1, pp. 35-42

2020

  1. Proteotoxicity and neurodegenerative diseases

    International Journal of Molecular Sciences, Vol. 21, Núm. 16, pp. 1-25

2013

  1. A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies

    JAMA Neurology, Vol. 70, Núm. 6, pp. 727-735

2009

  1. A Nonsense Mutation in COQ9 Causes Autosomal-Recessive Neonatal-Onset Primary Coenzyme Q10 Deficiency: A Potentially Treatable Form of Mitochondrial Disease

    American Journal of Human Genetics, Vol. 84, Núm. 5, pp. 558-566