Genetic analysis of the RAB39B gene in Chinese Han patients with Parkinson's disease

Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease

Wataru Satake, Yuko Nakabayashi, Ikuko Mizuta et al. · Nature Genetics · 2009 · 1.3K citations

Life Sciences, Genetics, Molecular Genetics +11

Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase

Alfredo Ramı́rez, André Heimbach, Jan Gründemann et al. · Nature Genetics · 2006 · 1.2K citations

Life Sciences, Genetics, Molecular Genetics +16

A Mutation in VPS35, Encoding a Subunit of the Retromer Complex, Causes Late-Onset Parkinson Disease

Alexander Zimprich, Anna Benet‐Pagès, Walter Struhal et al. · The American Journal of Human Genetics · 2011 · 902 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Mapping of a Gene for Parkinson's Disease to Chromosome 4q21-q23

Mihael H. Polymeropoulos, Joseph Higgins, Lawrence I. Golbe et al. · Science · 1996 · 782 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Bayesian Haplotype Inference for Multiple Linked Single-Nucleotide Polymorphisms

Tianhua Niu, Zhaohui Qin, Xiping Xu et al. · The American Journal of Human Genetics · 2002 · 645 citations · Full text

Public Health, Biostatistics, Genetics +12