Publicaciones en colaboración con investigadores/as de University of Trento (8)

2023

  1. A second update on mapping the human genetic architecture of COVID-19

    Nature

2021

  1. Correction: Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment (Genetics in Medicine, (2020), 22, 11, (1851-1862), 10.1038/s41436-020-0899-x)

    Genetics in Medicine

  2. Delivery of oligonucleotide-based therapeutics: challenges and opportunities

    EMBO Molecular Medicine, Vol. 13, Núm. 4

2020

  1. Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment

    Genetics in Medicine, Vol. 22, Núm. 11, pp. 1851-1862

2018

  1. Joint data analysis in nutritional epidemiology: Identification of observational studies and minimal requirements

    Journal of Nutrition, Vol. 148, Núm. 2, pp. 285-297

2017

  1. Delivery is key: lessons learnt from developing splice-switching antisense therapies

    EMBO Molecular Medicine, Vol. 9, Núm. 5, pp. 545-557

2016

  1. Erratum to: Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (Autophagy, 12, 1, 1-222, 10.1080/15548627.2015.1100356

    Autophagy

  2. Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

    Autophagy, Vol. 12, Núm. 1, pp. 1-222