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Nature Neuroscience|April 2, 2014
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosisJanel O Johnson, Erik P Pioro, Ashley Boehringer, et al.
Neurobiology of Aging|May 20, 2014
Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival studyPerry T C van Doormaal, Nicola Ticozzi, Cinzia Gellera, et al.
Neurobiology of Aging|March 16, 2012
C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS populationMario Sabatelli, Francesca Luisa Conforti, Marcella Zollino, et al.
Brain : a Journal of Neurology|September 26, 2025
MYC-driven gliosis impairs neuron-glia communication in amyotrophic lateral sclerosisPaolo Vincenzo Fioretti, Anna Barbieri, Alice Migazzi, et al.
European Journal of Neurology|September 23, 2022
Effect of RNS60 in amyotrophic lateral sclerosis: a phase II multicentre, randomized, double-blind, placebo-controlled trialEttore Beghi, Elisabetta Pupillo, Elisa Bianchi, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|May 5, 2015
The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's diseaseChristina M Lill, Aina Rengmark, Lasse Pihlstrøm, et al.
The Lancet. Neurology|March 31, 2018
Prognosis for patients with amyotrophic lateral sclerosis: development and validation of a personalised prediction modelHenk-Jan Westeneng, Thomas P A Debray, Anne E Visser, et al.
Cell Genomics|June 30, 2023
Genome-wide structural variant analysis identifies risk loci for non-Alzheimer's dementiasKarri Kaivola, Ruth Chia, Jinhui Ding, et al.
The Lancet. Neurology|March 13, 2012
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional studyElisa Majounie, Alan E Renton, Kin Mok, et al.
Human Molecular Genetics|February 6, 2009
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosisAdriano Chiò, Jennifer C Schymick, Gabriella Restagno, et al.
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