Excessive burden of lysosomal storage disorder gene variants in Parkinson’s diseaseLaurie Robak, Karin D. van Dijk, Mike A. Nalls et al.|Brain|2017Cited by 452
Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent MitophagySuzanne Lesage, Michel Borg, Valérie Drouet et al.|The American Journal of Human Genetics|2016Cited by 449
<scp>NeuroBooster</scp> Array: A Genome‐Wide Genotyping Platform to Study Neurological Disorders Across Diverse PopulationsSara Bandrés‐Ciga, Dan Vitale, Faraz Faghri et al.|Movement Disorders|2024Cited by 38
NeuroBooster Array: A Genome-Wide Genotyping Platform to Study Neurological Disorders Across Diverse PopulationsSara Bandrés‐Ciga, Dan Vitale, Faraz Faghri et al.|medRxiv|2023Cited by 23