Genetic variants of SNCA and LRRK2 genes are associated with sporadic PD susceptibility: A replication study in a Taiwanese cohort

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The Structure of Haplotype Blocks in the Human Genome

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Genetics, Genetic Epidemiology, Human Polymorphism +18

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Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology

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Mendelian Disorder, Genetic Disorder, Parkinson Disease +5

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Genome-wide Association Study, Genetics, Genetic Epidemiology +6