Publicacions en col·laboració amb investigadors/es de Instituto de Biomedicina de Sevilla (4)

2024

  1. Genome sequence analyses identify novel risk loci for multiple system atrophy

    Neuron, Vol. 112, Núm. 13, pp. 2142-2156.e5

2023

  1. Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) (npj Parkinson's Disease, (2023), 9, 1, (100), 10.1038/s41531-023-00526-9)

    npj Parkinson's Disease

  2. Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)

    npj Parkinson's Disease, Vol. 9, Núm. 1

2021

  1. A versatile workflow to integrate RNA-seq genomic and transcriptomic data into mechanistic models of signaling pathways

    PLoS Computational Biology, Vol. 17, Núm. 2