Frequency of LRRK2 mutations in early-and late-onset Parkinson disease.
Different MAPT haplotypes are associated with Parkinson's disease and progressive supranuclear palsy.
Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.
Case-control study of the parkin gene in early-onset Parkinson disease.
Phenotypic associations of tau and ApoE in Parkinson's disease.
Genotype-phenotype correlations between GBA mutations and Parkinson disease risk and onset.
BDNF Val66Met polymorphism is associated with cognitive impairment in Italian patients with Parkinson's disease.
Association of DRD3 and GRIN2B with impulse control and related behaviors in Parkinson's disease.
Association of variations in monoamine oxidases A and B with Parkinson's disease subgroups.
Parkin and PINK1 mutations in early-onset Parkinson's disease: comprehensive screening in publicly available cases and control.