Publicaciones en colaboración con investigadoras/es de University of Sydney (8)

2021

  1. Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1

    Autophagy, Vol. 17, Núm. 1, pp. 1-382

2018

  1. Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study

    The Lancet Neurology, Vol. 17, Núm. 6, pp. 548-558

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

2015

  1. A rare P2X7 variant Arg307Gln with absent pore formation function protects against neuroinflammation in multiple sclerosis

    Human Molecular Genetics, Vol. 24, Núm. 19, pp. 5644-5654

2014

  1. Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

    Nature Genetics, Vol. 46, Núm. 9, pp. 989-993

2013

  1. The International Society for bipolar Disorders (ISBD) task force report on antidepressant use in bipolar disorders

    American Journal of Psychiatry, Vol. 170, Núm. 11, pp. 1249-1262

2010

  1. Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions

    Nature Genetics, Vol. 42, Núm. 3, pp. 234-239

2007

  1. Functional outcome in bipolar disorder: The role of clinical and cognitive factors

    Bipolar Disorders, Vol. 9, Núm. 1-2, pp. 103-113