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Lim, Shen -Yang and Closas, Alfand Marl F. Dy and Tan, Ai Huey and Lim, Jia Lun and Tan, Yi Jayne and Vijayanathan, Yuganthini and Tay, Yi Wen and Khalid, Raihanah Binti Abdul and Ng, Wai Keong and Kanesalingam, Ruban and -Martin, Pablo Martinez and Annuar, Azlina Ahmad and Lit, Lei Cheng and Foo, Jia Nee and Lim, Weng Khong and Ng, Adeline Su Lyn and Tan, Eng-King (2023) New insights from a multi-ethnic Asian progressive supranuclear palsy cohort. Parkinsonism & Related Disorders, 108. ISSN 1353-8020, DOI https://doi.org/10.1016/j.parkreldis.2023.105296.
Closas, Alfand Marl F. Dy and Lohmann, Katja and Tan, Ai Huey and Ibrahim, Norlinah Mohamed and Lim, Jia Lun and Tay, Yi Wen and Muthusamy, Kalai Arasu and Ahmad Annuar, Azlina and Klein, Christine and Lim, Shen -Yang (2023) A KMT2B frameshift variant causing focal dystonia restricted to the oromandibular region after long-term follow-up. Journal of Movement Disorders, 16 (1). 91+. ISSN 2005-940X, DOI https://doi.org/10.14802/jmd.22109.
Lim, Jia Lun and Lohmann, Katja and Tan, Ai Huey and Tay, Yi Wen and Ibrahim, Khairul Azmi and Aziz, Zariah Abdul and Mawardi, Ahmad Shahir and Puvanarajah, Santhi Datuk and Lim, Thien Thien and Looi, Irene and Ooi, Joshua Chin Ern and Chia, Yuen Kang and Muthusamy, Kalai Arasu and Bauer, Peter and Rolfs, Arndt and Klein, Christine and Ahmad-Annuar, Azlina and Lim, Shen-Yang (2022) Glucocerebrosidase (GBA) gene variants in a multi-ethnic Asian cohort with Parkinson's disease: Mutational spectrum and clinical features. Journal of Neural Transmission, 129 (1). pp. 37-48. ISSN 0300-9564, DOI https://doi.org/10.1007/s00702-021-02421-0.
Lim, Jia Lun and Ng, Ebonne Yulin and Lim, Shen-Yang and Tan, Ai Huey and Abdul-Aziz, Zariah and Ibrahim, Khairul Azmi and Gopalai, Aroma Agape and Tay, Yi Wen and Vijayanathan, Yuganthini and Toh, Tzi Shin and Lim, Soo Kun and Bee, Ping-Chong and Puvanarajah, Santhi Datuk and Viswanathan, Shanthi and Looi, Irene and Lim, Thien Thien and Eow, Gaik Bee and Cheah, Wee Kooi and Tan, Eng-King and Ahmad-Annuar, Azlina (2021) Association study of MCCC1/LAMP3 and DGKQ variants with Parkinson's disease in patients of Malay ancestry. Neurological Sciences, 42 (10). pp. 4203-4207. ISSN 1590-1874, DOI https://doi.org/10.1007/s10072-021-05056-x.
Lim, Shen-Yang and Ahmad-Annuar, Azlina and Lohmann, Katja and Tan, Ai Huey and Tay, Yi Wen and Lim, Jia Lun and Lim, Kai Bin and Lit, Lei Cheng and Bauer, Peter and Rolfs, Arndt and Klein, Christine (2021) Clinical phenotype of Parkinson's disease with a homozygous PRKN p.Cys441Arg mutation. Neurology Asia, 26 (1). pp. 161-166. ISSN 1823-6138,
Lim, Shen-Yang and Ahmad-Annuar, Azlina and Lohmann, Katja and Tan, Ai Huey and Tay, Yi Wen and Lim, Jia Lun and Ramli, Norlisah and Teh, Pei Chiek and Kuppusamy, Rishikesan and Tan, Chong Tin and Goh, Khean Jin and Viswanathan, Shanthi and Bauer, Peter and Rolfs, Arndt and Klein, Christine (2021) Parkinson's disease with homozygous PINK1 p.Leu489Pro mutations in two Indian sisters. Neurology Asia, 26 (1). pp. 167-173. ISSN 1823-6138,
Lim, Shen-Yang and Lim, Jia Lun and Ahmad-Annuar, Azlina and Lohmann, Katja and Tan, Ai Huey and Lim, Kai Bin and Tay, Yi Wen and Shing, Yee Lee and Muthusamy, Kalai Arasu and Bauer, Peter and Rolfs, Arndt and Klein, Christine (2020) Clinical phenotype of LRRK2R1441C in 2 Chinese sisters. Neurodegenerative Diseases, 20 (1). pp. 39-45. ISSN 1660-2854, DOI https://doi.org/10.1159/000508131.
Lim, Shen-Yang and Lim, Jia Lun and Ahmad-Annuar, Azlina and Lohmann, Katja and Tan, Ai Huey and Lim, Kai Bin and Tay, Yi Wen and Shing, Yee Lee and Muthusamy, Kalai Arasu and Bauer, Peter and Rolfs, Arndt and Klein, Christine (2020) Clinical phenotype ofLRRK2R1441C in 2 Chinese sisters. Neurodegenerative Diseases, 20 (1). pp. 39-45. ISSN 1660-2854, DOI https://doi.org/10.1159/000508131.
