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Genome-wide association study identifies risk loci for cluster headache
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
SNCA and mTOR Pathway Single Nucleotide Polymorphisms Interact to Modulate the Age at Onset of Parkinson's Disease
PDXK mutations cause polyneuropathy responsive to pyridoxal 5 '-phosphate supplementation
Moving beyond neurons: the role of cell type-specific gene regulation in Parkinson's disease heritability
Loss of VPS1 3C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
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
