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Molecular Genetics & Genomic Medicine|September 6, 2019
LRRK2 N551K and R1398H variants are protective in Malays and Chinese in Malaysia: A case-control association study for Parkinson's diseaseAroma Agape Gopalai, Jia Lun Lim, Hui-Hua Li, et al.Parkinsonism & Related Disorders|October 9, 2025
No anti-IgLON5 antibody in carefully diagnosed PSP patients with "atypical" or variant clinical featuresAnis Nadhirah Khairul Anuar, Ai Huey Tan, Jeremy Christopher Fernandiz, et al.Movement Disorders : Official Journal of the Movement Disorder Society|April 20, 2026
Ex Vivo LRRK2 Activation in Asian G2385R and R1628P Variant Carriers and Idiopathic Parkinson's DiseaseTzi Shin Toh, Lei Cheng Lit, Shen-Yang Lim, et al.Journal of Neural Transmission (Vienna, Austria : 1996)|November 15, 2021
Glucocerebrosidase (GBA) gene variants in a multi-ethnic Asian cohort with Parkinson's disease: mutational spectrum and clinical featuresJia Lun Lim, Katja Lohmann, Ai Huey Tan, et al.Parkinsonism & Related Disorders|January 22, 2023
New insights from a multi-ethnic Asian progressive supranuclear palsy cohortShen-Yang Lim, Alfand Marl F Dy Closas, Ai Huey Tan, et al.Journal of Movement Disorders|January 31, 2024
Loss-of-Function Variant in the SMPD1 Gene in Progressive Supranuclear Palsy-Richardson Syndrome Patients of Chinese AncestryShen-Yang Lim, Ai Huey Tan, Jia Nee Foo, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 9, 2021
Association study of MCCC1/LAMP3 and DGKQ variants with Parkinson's disease in patients of Malay ancestryJia Lun Lim, Ebonne Yulin Ng, Shen-Yang Lim, et al.Journal of Parkinson'S Disease|February 20, 2025
New insights from a Malaysian real-world deep brain stimulation cohortAlfand Marl F Dy Closas, Ai Huey Tan, Yi Wen Tay, et al.Parkinsonism & Related Disorders|May 20, 2023
Genetic study of early-onset Parkinson's disease in the Malaysian populationYi Wen Tay, Ai Huey Tan, Jia Lun Lim, et al.NPJ Parkinson'S Disease|February 23, 2025
Clinical and functional evidence for the pathogenicity of the LRRK2 p.Arg1067Gln variantShen-Yang Lim, Tzi Shin Toh, Jia Wei Hor, et al.Pageof 3