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The Lancet Regional Health. Western Pacific|March 11, 2026
Genetic risk loci for Parkinson's disease and dementia in a large-scale population-based Taiwanese cohort (TPMI)Chin-Hsien Lin, Chien-Ching Chang, Hung-Hsin Chen, et al.
NPJ Parkinson'S Disease|February 2, 2026
Association of LRRK2 p.A419V with Parkinson's Disease in East Asians and analysis of age at onsetKai Shi Lim, Maria Teresa Periñan, Elaine Guo Yan Chew, et al.
Medrxiv : the Preprint Server for Health Sciences|September 15, 2025
The <i>LRRK2</i> p.A419V variant associates with risk of Parkinson's disease in the East Asian population and an evaluation on age of onsetKai Shi Lim, Maria Teresa Periñan, Elaine Guo Yan Chew, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 11, 2025
Rare but Relevant? Assessing Variants in Dystonia-Linked Genes in Parkinson's DiseaseLara M Lange, Zih-Hua Fang, Laurel Screven, et al.
Medrxiv : the Preprint Server for Health Sciences|July 17, 2025
Rare but Relevant: Assessing Variants in Dystonia-linked Genes in Parkinson's DiseaseLara M Lange, Zih-Hua Fang, Laurel Screven, et al.
Movement Disorders Clinical Practice|August 29, 2024
Exercise Habits in People with Parkinson's: A Multinational SurveyPriya Jagota, Phanupong Phutrakool, Nitish Kamble, et al.
Medrxiv : the Preprint Server for Health Sciences|July 3, 2026
<i>GCH1</i> p.Ser80Asn Confers Risk for Parkinson's Disease in East Asian PopulationsYi Wen Tay, Andrew Leslie Lee, Jie Ping Schee, et al.
Medrxiv : the Preprint Server for Health Sciences|July 3, 2026
Repeat expansions in Parkinson's disease and parkinsonism across ancestries: insights from a global genetic cohortLara M Lange, Catalina Cerquera-Cleves, Ai Huey Tan, et al.
Epilepsia|June 25, 2026
Variability in epilepsy polygenic risk prediction across Taiwanese population and clinical cohortsYi-Syuan Ke, Meng-Han Tsai, Chen-Rui Ho, et al.
Neurobiology of Aging|August 22, 2013
Protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variantsMichael G Heckman, Alexis Elbaz, Alexandra I Soto-Ortolaza, et al.
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