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Ebonne Ng

Observed names: E Ng, E.Y. Ng, Ebonne Y Ng, Ebonne Y. L. Ng, Ebonne Y. Ng, Ebonne Y.L. Ng, Ebonne YL Ng
OpenAlex ID: A5113830081
Identification of Risk Loci for Parkinson Disease in Asians and Comparison of Risk Between Asians and Europeans
2020 · Jia Nee Foo, Elaine Guo Yan Chew, et al. · JAMA Neurology · 249
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Association of NOTCH2NLC Repeat Expansions With Parkinson Disease
2020 · Dongrui Ma, Yi Jayne Tan, et al. · JAMA Neurology · 97
Serum uric acid level and its association with motor subtypes and non-motor symptoms in early Parkinson's disease: PALS study
2018 · Xinxin Huang, Samuel Yong-Ern Ng, et al. · Parkinsonism & Related Disorders · 67
Multiancestry analysis of the HLA locus in Alzheimer’s and Parkinson’s diseases uncovers a shared adaptive immune response mediated by HLA-DRB1*04 subtypes
2023 · Yann Le Guen, Guo Luo, et al. · Proceedings of the National Academy of Sciences · 60
Plasma alpha‐synuclein detected by single molecule array is increased in PD
2019 · Adeline S. L. Ng, Yi Jayne Tan, et al. · Annals of Clinical and Translational Neurology · 53
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NOTCH2NLC GGC Repeat Expansions Are Associated with Sporadic Essential Tremor: Variable Disease Expressivity on Long‐Term Follow‐up
2020 · Adeline S. L. Ng, Weng Khong Lim, et al. · Annals of Neurology · 46
Greater motor progression in patients with Parkinson disease who carry LRRK2 risk variants
2015 · Linda P. Oosterveld, John C. Allen, et al. · Neurology · 36
Higher serum triglyceride levels are associated with Parkinson's disease mild cognitive impairment
2018 · Xinxin Huang, Samuel Yong‐Ern Ng, et al. · Movement Disorders · 28
SNCA Rep1 promoter variability influences cognition in Parkinson's disease
2019 · Adeline S.L. Ng, Yi Jayne Tan, et al. · Movement Disorders · 20
Exome sequencing in Asian populations identifies low-frequency and rare coding variation influencing Parkinson’s disease risk
2024 · Elaine GY Chew, Zhehao Liu, et al. · Nature Aging · 19
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Targeted exome sequencing reveals homozygous TREM2 R47C mutation presenting with behavioral variant frontotemporal dementia without bone involvement
2018 · Adeline S.L. Ng, Yi Jayne Tan, et al. · Neurobiology of Aging · 19
Identifying clinical features and blood biomarkers associated with mild cognitive impairment in Parkinson disease using machine learning
2023 · Xiao Deng, Yilin Ning, et al. · European Journal of Neurology · 18
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Parkinson’s disease GWAS-linked Park16 carriers show greater motor progression
2019 · Xiao Deng, Bin Xiao, et al. · Journal of Medical Genetics · 11
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Four-Year Longitudinal Study of Motor and Non-motor Symptoms in LRRK2-Related Parkinson's Disease
2020 · Xiao Deng, Bin Xiao, et al. · Frontiers in Neurology · 10
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Case-control analysis of LRRK2 protective variants in Essential Tremor
2018 · Adeline S. L. Ng, Ebonne Y. L. Ng, et al. · Scientific Reports · 7
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Case-control analysis of leucine-rich repeat kinase 2 protective variants in Alzheimer's disease
2017 · Adeline S.L. Ng, Ebonne Y.L. Ng, et al. · Neurobiology of Aging · 7
Exome sequencing in Asian populations identifies rare deficient SMPD1 alleles that increase risk of Parkinson’s disease
2023 · Elaine GY Chew, Zhehao Liu, et al. · medRxiv · 4
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Serum peroxiredoxin 3 is reduced in genetic carriers of Parkinson’s disease
2022 · Adeline SL Ng, Jayne Tan, et al. · Journal of Neurology Neurosurgery & Psychiatry · 4
Longitudinal Study of SNCA Rep1 Polymorphism on Executive Function in Early Parkinson’s Disease
2022 · Yi Jayne Tan, Seyed Ehsan Saffari, et al. · Journal of Parkinson s Disease · 3
iTRAQ‐based proteomic analysis reveals myeloperoxidase (MPO) as a diagnostic and prognostic biomarker of cognitive decline in Parkinson’s disease
2023 · Yi Jayne Tan, Ebonne YL Ng, et al. · Alzheimer s & Dementia · 2
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Carriers of Parkinson’s disease-linked SNCA Rep1 variant have greater non-motor decline: a 4 year follow up study
2025 · Aarthi Santhanakrishnan, Yi Jayne Tan, et al. · Aging
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Interaction between caffeine intake and polymorphisms of MCCC1 modifies Parkinson’s Disease risk
2024 · Y. Yang, E.K. Tan, et al. · Parkinsonism & Related Disorders
Interaction between caffeine intake and polymorphisms of PARK16 modifies Parkinson’s Disease risk
2024 · E.K. Tan, Y. Yang, et al. · Parkinsonism & Related Disorders
Screening for TMEM230 mutations in young onset Parkinson’s disease
2018 · D. Ma, S.H. Ng, et al. · Parkinsonism & Related Disorders
Glucocerebrosidase gene mutation in Parkinson’s disease
2018 · M. Macas, E.Y. Ng, et al. · Parkinsonism & Related Disorders
Works count: 28
Citation count: 759
H-index: 12
I10-index: 14
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