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Parkinsonism & Related Disorders|December 21, 2010
Lrrk2 S1647T and BDNF V66M interact with environmental factors to increase risk of Parkinson's diseaseChin-Hsien Lin, Ruey-Meei Wu, Chun-Hwei Tai, et al.
Neurobiology of Aging|July 8, 2015
Mutational analysis of SYNJ1 gene (PARK20) in Parkinson's disease in a Taiwanese populationKai-Hsiang Chen, Ruey-Meei Wu, Hang-I Lin, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 17, 2013
Reaffirmation of GAK, but not HLA-DRA, as a Parkinson's disease susceptibility gene in a Taiwanese populationChin-Hsien Lin, Meng-Ling Chen, Yi-Cheng Tai, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 5, 2010
Feeling-of-knowing in episodic memory in patients with Parkinson's disease with various motor symptomsRwei-Ling Yu, Ruey-Meei Wu, Chun-Hwei Tai, et al.
Parkinsonism & Related Disorders|February 15, 2018
Catechol-O-methyltransferase (COMT) genetic variants are associated with cognitive decline in patients with Parkinson's diseaseChin-Hsien Lin, Jun-Yu Fan, Han-I Lin, et al.
Parkinsonism & Related Disorders|October 9, 2014
Risk of Parkinson's disease following severe constipation: a nationwide population-based cohort studyChin-Hsien Lin, Jou-Wei Lin, Ying-Chun Liu, et al.
Cerebral Cortex (New York, N.Y. : 1991)|August 24, 2021
Neural Basis of Somatosensory Spatial and Temporal Discrimination in Humans: The Role of Sensory DetectionCheng-Wei Huang, Chin-Hsien Lin, Yi-Hsuan Lin, et al.
Clinical Neuropharmacology|November 17, 2010
Effectiveness of quetiapine for poststroke pathological laughing: case report and review of the literatureYu-Ren Chen, Ya-Ping Huang, Shan-Ju Lin, et al.
Human Genetics|June 25, 2011
Novel variant Pro143Ala in HTRA2 contributes to Parkinson's disease by inducing hyperphosphorylation of HTRA2 protein in mitochondriaChin-Hsien Lin, Meng-Ling Chen, Grace Shiahuy Chen, et al.
Frontiers in Neurology|May 8, 2014
Lack of c9orf72 repeat expansion in taiwanese patients with mixed neurodegenerative disordersChin-Hsien Lin, Ta-Fu Chen, Ming-Jang Chiu, et al.
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