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Acta Neuropathologica|April 5, 2019
ADAR2 mislocalization and widespread RNA editing aberrations in C9orf72-mediated ALS/FTDStephen Moore, Eric Alsop, Ileana Lorenzini, et al.Neurobiology of Disease|August 24, 2013
Genetic ablation of phospholipase C delta 1 increases survival in SOD1(G93A) miceKim A Staats, Lawrence Van Helleputte, Ashley R Jones, et al.Orphanet Journal of Rare Diseases|May 23, 2013
Olmsted syndrome: exploration of the immunological phenotypeDina Danso-Abeam, Jianguo Zhang, James Dooley, et al.Human Molecular Genetics|February 8, 2018
Elongator subunit 3 (ELP3) modifies ALS through tRNA modificationAndre Bento-Abreu, Gunilla Jager, Bart Swinnen, et al.Nature Medicine|August 28, 2012
EPHA4 is a disease modifier of amyotrophic lateral sclerosis in animal models and in humansAnnelies Van Hoecke, Lies Schoonaert, Robin Lemmens, et al.Journal of Experimental Neurology|September 22, 2025
Protein Assembly Modulation: A New Approach to Amyotrophic Lateral Sclerosis (ALS) TherapeuticsShao Feng Yu, Kumar Paulvannan, Dennis Solas, et al.Nature Medicine|February 6, 2018
Haploinsufficiency leads to neurodegeneration in C9ORF72 ALS/FTD human induced motor neuronsYingxiao Shi, Shaoyu Lin, Kim A Staats, et al.Nature Genetics|July 26, 2016
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosisWouter van Rheenen, Aleksey Shatunov, Annelot M Dekker, et al.Pageof 8