Publikationen in Zusammenarbeit mit Forschern von Hospital Universitari de Bellvitge (4)

2018

  1. Heterozygous STUB1 mutation causes familial ataxia with cognitive affective syndrome (SCA48)

    Neurology, Vol. 91, Núm. 21, pp. E1988-E1998

2017

  1. Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

    Nature Genetics, Vol. 49, Núm. 9, pp. 1373-1384

2015

  1. Analysis of the CHCHD10 gene in patients with frontotemporal dementia and amyotrophic lateral sclerosis from Spain

    Brain

2014

  1. Investigation of the role of rare TREM2 variants in frontotemporal dementia subtypes

    Neurobiology of Aging, Vol. 35, Núm. 11, pp. 2657.e13-2657.e19