Shen-Yang Lim
Universiti Malaya
H-index: 39
Asia-Malaysia
Top articles of Shen-Yang Lim
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
Longitudinal Changes in the Retinal Nerve Fiber Layer Thickness in Amyotrophic Lateral Sclerosis and Parkinson’s Disease | Journal of Clinical Neurology | Sharifah Azira Taufik Norlina Ramli Ai Huey Tan Shen-Yang Lim Mohd Taufiq Abdul Ghani | 2024/5/1 |
Loss-of-function SMPD1 gene variant in Progressive Supranuclear Palsy-Richardson Syndrome patients of Chinese ancestry | Journal of Movement Disorders | Shen-Yang Lim Ai Huey Tan Jia Nee Foo Yi Jayne Tan Elaine GY Chew | 2024/1/31 |
Orthostatic Hypotension in Parkinson's disease: Sit-to-Stand vs. Supine-to-Stand Protocol and Clinical Correlates | Parkinsonism & Related Disorders | Kai Bin Lim Shen-Yang Lim Jia Wei Hor Heamah Krishnan Firdaus Mortadza | 2024/4/22 |
Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome | The American Journal of Human Genetics | Vincenzo Salpietro Reza Maroofian Maha S Zaki Jamie Wangen Andrea Ciolfi | 2024/1/4 |
Parkinson’s disease is predominantly a genetic disease | Shen-Yang Lim Christine Klein | 2024/3/25 | |
Neurostimulation for Advanced Parkinson Disease and Quality of Life at 5 Years: A Nonrandomized Controlled Trial | JAMA network open | Stefanie T Jost Salima Aloui Julian Evans Keyoumars Ashkan Anna Sauerbier | 2024/1/2 |
Understanding monogenic Parkinson's disease at a global scale | medRxiv | Johanna Junker Lara M Lange Eva-Juliane Vollstedt Karisha Roopnarain Maria Leila M Doquenia | 2024 |
GBA1 rs3115534 Is Associated with REM Sleep Behavior Disorder in Parkinson's Disease in Nigerians | Movement Disorders | Oluwadamilola Omolara Ojo Sara Bandres‐Ciga Mary B Makarious Peter Wild Crea Dena G Hernandez | 2024/2/23 |
Genetic testing for Parkinson's disease and movement disorders in less privileged areas: Barriers and opportunities | Movement disorders clinical practice | Ai Huey Tan Mario Cornejo-Olivas Njideka Okubadejo Pramod Kumar Pal Gerard Saranza | 2024/1 |
A statement of the MDS on biological definition, staging, and classification of Parkinson's disease | Movement Disorders | Francisco Cardoso Christopher G Goetz Tiago A Mestre Cristina Sampaio Charles H Adler | 2024/2 |
Embracing monogenic Parkinson's disease: the MJFF Global Genetic PD cohort | Movement Disorders | Eva‐Juliane Vollstedt Susen Schaake Katja Lohmann Shalini Padmanabhan Alexis Brice | 2023/2 |
Different pieces of the same puzzle: a multifaceted perspective on the complex biological basis of Parkinson’s disease | Amica C Müller-Nedebock Marieke CJ Dekker Matthew J Farrer Nobutaka Hattori Shen-Yang Lim | 2023/7/13 | |
Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study | The Lancet Neurology | Mie Rizig Sara Bandres-Ciga Mary B Makarious Oluwadamilola Omolara Ojo Peter Wild Crea | 2023/11/1 |
Gastrointestinal Dysfunction in Parkinson’s Disease: Neuro-Gastroenterology Perspectives on a Multifaceted Problem | Ai Huey Tan Kee Huat Chuah Yuan Ye Beh Jie Ping Schee Sanjiv Mahadeva | 2023/5 | |
REAL-WORLD EXPERIENCE OF DEEP BRAIN STIMULATION SURGERY IN A DEVELOPING SOUTHEAST ASIAN COUNTRY | medRxiv | Alfand Marl F Dy Closas Ai Huey Tan Yi Wen Tay Jia Wei Hor Tzi Shin Toh | 2023 |
Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) | npj Parkinson's Disease | Lara M Lange Micol Avenali Melina Ellis Anastasia Illarionova Ignacio J Keller Sarmiento | 2023/6/27 |
Deep brain stimulation in Dopa-Responsive Parkinsonism-Look out for red flags: Expert commentary | Shen-Yang Lim Ai Huey Tan Yi Wen Tay | 2023/5 | |
Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson’s Disease … | Plos one | Eva-Juliane Vollstedt Harutyun Madoev Anna Aasly Azlina Ahmad-Annuar Bashayer Al-Mubarak | 2023/10/3 |
Exome sequencing in Asian populations identifies rare deficient SMPD1 alleles that increase risk of Parkinson's disease | medRxiv | Elaine GY Chew Zhehao Liu Zheng Li Sun Ju Chung Michelle M Lian | 2023 |
Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) | npj Parkinson's Disease | Lara M Lange Micol Avenali Melina Ellis Anastasia Illarionova Ignacio J Keller Sarmiento | 2023/9/13 |
Co-Authors
