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Neurobiology of Aging|May 9, 2016
TBK1 is associated with ALS and ALS-FTD in Sardinian patientsGiuseppe Borghero, Maura Pugliatti, Francesco Marrosu, et al.Scientific Reports|April 13, 2019
Exome array analysis of rare and low frequency variants in amyotrophic lateral sclerosisAnnelot M Dekker, Frank P Diekstra, Sara L Pulit, et al.Neurobiology of Aging|July 16, 2015
HFE p.H63D polymorphism does not influence ALS phenotype and survivalAdriano Chiò, Gabriele Mora, Mario Sabatelli, et al.Neurobiology of Aging|March 2, 2015
CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patientsAdriano Chiò, Gabriele Mora, Mario Sabatelli, et al.Biomedicines|March 29, 2023
The HFE p.H63D (p.His63Asp) Polymorphism Is a Modifier of ALS Outcome in Italian and French Patients with SOD1 MutationsAntonio Canosa, Andrea Calvo, Gabriele Mora, et al.Neurobiology of Aging|January 7, 2016
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansionAdriano Chiò, Gabriele Mora, Mario Sabatelli, et al.Neurobiology of Aging|December 15, 2022
Whole genome sequencing analysis reveals post-zygotic mutation variability in monozygotic twins discordant for amyotrophic lateral sclerosisGijs H P Tazelaar, Paul J Hop, Meinie Seelen, et al.Brain : a Journal of Neurology|April 22, 2026
Machine learning model based on plasma proteomics for the identification of Parkinson's diseaseBoluwatife Adewale, Ruth Chia, Ruin Moaddel, et al.Neuron|December 15, 2010
Exome sequencing reveals VCP mutations as a cause of familial ALSJanel O Johnson, Jessica Mandrioli, Michael Benatar, et al.Nature Medicine|August 19, 2025
A plasma proteomics-based candidate biomarker panel predictive of amyotrophic lateral sclerosisRuth Chia, Ruin Moaddel, Justin Y Kwan, et al.Pageof 8