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Neurobiology of Aging|January 19, 2016
Large-scale screening in sporadic amyotrophic lateral sclerosis identifies genetic modifiers in C9orf72 repeat carriersAnnelot M Dekker, Meinie Seelen, Perry T C van Doormaal, et al.Neurology. Genetics|February 12, 2020
Analysis of FUS, PFN2, TDP-43, and PLS3 as potential disease severity modifiers in spinal muscular atrophyRenske I Wadman, Marc D Jansen, Chantall A D Curial, et al.Nature Communications|January 20, 2016
Genomic signals of migration and continuity in Britain before the Anglo-SaxonsRui Martiniano, Anwen Caffell, Malin Holst, et al.Nature Genetics|February 24, 2023
Brain expression quantitative trait locus and network analyses reveal downstream effects and putative drivers for brain-related diseasesNiek de Klein, Ellen A Tsai, Martijn Vochteloo, et al.Brain Communications|December 22, 2025
The role of disease-associated short tandem repeats in amyotrophic lateral sclerosisJoke J F A van Vugt, Ramona A J Zwamborn, Egor Dolzhenko, et al.Iscience|May 19, 2025
Comprehensive analysis across SMN2 excludes DNA methylation as an epigenetic biomarker for spinal muscular atrophyMaria M Zwartkruis, Joris V Kortooms, Demi Gommers, 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.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.Pageof 8