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A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

artículo científico publicado en 2011

C9orf72, AAO and ancestry help discriminating behavioural from language variants in FTLD cohorts

scientific article published on 17 September 2020

Erratum to: Mitochondrial DNA point mutations and relative copy number in 1363 disease and control human brains

artículo científico publicado en 2017

Frontotemporal dementia and its subtypes: a genome-wide association study

artículo científico publicado en 2014

Genetic compendium of 1511 human brains available through the UK Medical Research Council Brain Banks Network Resource

artículo científico publicado en 2016

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

artículo científico publicado en 2018

Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD

scientific article published on 09 February 2019

Mitochondrial DNA point mutations and relative copy number in 1363 disease and control human brains

artículo científico publicado en 2017

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

artículo científico publicado en 2018

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