Publicaciones en colaboración con investigadoras/es de University of Sydney (5)

2017

  1. Response to interferon-beta treatment in multiple sclerosis patients: A genome-wide association study

    Pharmacogenomics Journal, Vol. 17, Núm. 4, pp. 312-318

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

2013

  1. MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis

    Brain, Vol. 136, Núm. 6, pp. 1778-1782

2008

  1. Refining genetic associations in multiple sclerosis

    The Lancet Neurology

2007

  1. Corrigendum to "Linkage disequilibrium screening for multiple sclerosis implicates JAG1 and POU2AF1 as susceptibility genes in Europeans" [J. Neuroimmunol. 179 (2006) 108-116] (DOI:10.1016/j.jneuroim.2006.06.003)

    Journal of Neuroimmunology