Publicacións en colaboración con investigadores/as de Hospital Universitari Germans Trias i Pujol (6)

2024

  1. CSF proteomics identifies early changes in autosomal dominant Alzheimer's disease

    Cell, Vol. 187, Núm. 22, pp. 6309-6326.e15

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

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

  3. Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia

    American Journal of Human Genetics, Vol. 111, Núm. 7, pp. 1316-1329

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

  3. Proteome wide association studies of LRRK2 variants identify novel causal and druggable proteins for Parkinson’s disease

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