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Association of variants in the SPTLC1 gene with juvenile amyotrophic lateral sclerosis
Pathogenic huntingtin repeat expansion in patients with frontotemporal dementia and amyotrophic lateral sclerosis
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene
Common genetic variants influence human subcortical brain structures
NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases
Genetic comorbidities in Parkinson's disease
Genome-wide meta-analysis identifies new susceptibility loci for migraine
A Two-Stage Meta-Analysis Identifies Several New Loci for Parkinson's Disease
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies