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Neuron|January 19, 2022
Genome-wide identification of the genetic basis of amyotrophic lateral sclerosisSai Zhang, Johnathan Cooper-Knock, Annika K Weimer, et al.BMC Medicine|March 25, 2026
Digenic inheritance of mutations in SPG7 and AFG3L2 causes motor neuron and cerebellar disordersMehrdad A Estiar, Eric Yu, Parizad Varghaei, et al.NAR Genomics and Bioinformatics|February 8, 2021
Cross-reactive probes on Illumina DNA methylation arrays: a large study on ALS shows that a cautionary approach is warranted in interpreting epigenome-wide association studiesPaul J Hop, Ramona A J Zwamborn, Eilis J Hannon, 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.The Journal of Infectious Diseases|February 25, 2012
Multicohort genomewide association study reveals a new signal of protection against HIV-1 acquisitionSophie Limou, Olivier Delaneau, Daniëlle van Manen, 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.Acta Neuropathologica|January 9, 2016
Serotonin 2B receptor slows disease progression and prevents degeneration of spinal cord mononuclear phagocytes in amyotrophic lateral sclerosisHajer El Oussini, Hanna Bayer, Jelena Scekic-Zahirovic, et al.Neurology|October 6, 2017
Meta-analysis of pharmacogenetic interactions in amyotrophic lateral sclerosis clinical trialsRuben P A van Eijk, Ashley R Jones, William Sproviero, et al.Brain Communications|October 28, 2021
SCFD1 expression quantitative trait loci in amyotrophic lateral sclerosis are differentially expressedAlfredo Iacoangeli, Isabella Fogh, Sashika Selvackadunco, et al.Acta Neuropathologica Communications|September 17, 2024
Molecular pathology, developmental changes and synaptic dysfunction in (pre-) symptomatic human C9ORF72-ALS/FTD cerebral organoidsAstrid T van der Geest, Channa E Jakobs, Tijana Ljubikj, et al.Pageof 28