Publicaciones en colaboración con investigadores/as de Centro de Investigación Médica Aplicada (10)

2020

  1. Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis

    Scientific Reports, Vol. 10, Núm. 1

2019

  1. Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia

    Scientific Reports, Vol. 9, Núm. 1

  2. Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia

    Nature Medicine, Vol. 25, Núm. 1, pp. 152-164

2018

  1. Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies

    PLoS Medicine, Vol. 15, Núm. 1

  2. Target-enriched sequencing of chromosome 17q21.31 in sporadic tauopathies reveals no candidate variants

    Neurobiology of Aging, Vol. 66, pp. 177.e7-177.e10

2014

  1. Frontotemporal dementia and its subtypes: A genome-wide association study

    The Lancet Neurology, Vol. 13, Núm. 7, pp. 686-699

2013

  1. Fused in sarcoma (FUS) gene mutations are not a frequent cause of essential tremor in europeans

    Neurobiology of Aging, Vol. 34, Núm. 10, pp. 2441.e9-2441.e11

2011

  1. Genetic variation in APOE cluster region and Alzheimer's disease risk

    Neurobiology of Aging, Vol. 32, Núm. 11, pp. 2107.e7-2107.e17

  2. Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy

    Nature Genetics

2009

  1. Ubiquitin associated protein 1 is a risk factor for frontotemporal lobar degeneration

    Neurobiology of Aging, Vol. 30, Núm. 4, pp. 656-665