Publicaciones en colaboración con investigadores/as de University Hospital of Bern (3)

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. Interpreting Deep Machine Learning Models: An Easy Guide for Oncologists

    IEEE Reviews in Biomedical Engineering, Vol. 16, pp. 192-207