An observational study of pleiotropy and penetrance of amyotrophic lateral sclerosis associated with CAG-repeat expansion of ATXN2
European Journal of Human Genetics2025cited by 6position: firstdoi
A <i>VAPB</i> (P56S) mutation in a Dutch patient with familial motor neuron disease: a case report
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration2025cited by 0position: middledoi
<i>UNC13A</i>in amyotrophic lateral sclerosis: from genetic association to therapeutic target
Journal of Neurology Neurosurgery & Psychiatry2023cited by 56position: middledoi
Lithium carbonate in amyotrophic lateral sclerosis patients homozygous for the C-allele at SNP rs12608932 in UNC13A: protocol for a confirmatory, randomized, group-sequential, event-driven, double-blind, placebo-controlled trial