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K. Mok · SciRah

Researcher profile · Semantic Scholar

K. Mok

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K. Mok — researcher profile on SciRah

h-index: 41
Works: 128
Citations: 13K

Most-cited papers

Analysis of shared heritability in common disorders of the brain
V. Anttila, B. Bulik-Sullivan, H. Finucane, R. Walters +496 more
2018Science1,869 citations Open access
Semantic Scholar
Identification of Risk Loci for Parkinson Disease in Asians and Comparison of Risk Between Asians and Europeans: A Genome-Wide Association Study.
J. Foo, E. Chew, Sun J. Chung, R. Peng +41 more
2020JAMA Neurology226 citations Open access
Semantic Scholar
Parkinson’s disease in GTP cyclohydrolase 1 mutation carriers
N. Mencacci, I. Isaias, M. Reich, C. Ganos +41 more
2014Brain : a journal of neurology198 citations Open access
Semantic Scholar
The importance of understanding individual differences in Down syndrome
A. Karmiloff-Smith, Tamara Al-Janabi, Hana D'Souza, J. Groet +8 more
2016F1000Research197 citations Open access
Semantic Scholar
Finding genetically-supported drug targets for Parkinson’s disease using Mendelian randomization of the druggable genome
C. Storm, D. Kia, Mona Almramhi, S. Bandres-Ciga +171 more
2021Nature Communications192 citations Open access
Semantic Scholar
Association of Dementia With Mortality Among Adults With Down Syndrome Older Than 35 Years
R. Hithersay, Carla M. Startin, Sarah Hamburg, K. Mok +5 more
2018JAMA Neurology164 citations Open access
Semantic Scholar
Large‐scale plasma proteomic profiling identifies a high‐performance biomarker panel for Alzheimer's disease screening and staging
Yuanbing Jiang, Xiao-Pu Zhou, Fanny C. F. Ip, P. Chan +14 more
2021Alzheimer's & Dementia154 citations Open access
Semantic Scholar
NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases
C. Blauwendraat, F. Faghri, L. Pihlstrøm, Joshua T. Geiger +37 more
2017Neurobiology of Aging142 citations Open access
Semantic Scholar
A genome-wide association study in multiple system atrophy
A. Sailer, Sonja W. Scholz, M. Nalls, C. Schulte +41 more
2016Neurology140 citations Open access
Semantic Scholar
Astrogliopathy predominates the earliest stage of corticobasal degeneration pathology.
H. Ling, G. Kovács, J. Vonsattel, Karen Davey +6 more
2016Brain : a journal of neurology125 citations Open access
Semantic Scholar
Patient-specific Alzheimer-like pathology in trisomy 21 cerebral organoids reveals BACE2 as a gene dose-sensitive AD suppressor in human brain
I. Alić, P. Goh, Aoife Murray, E. Portelius +39 more
2020bioRxiv119 citations Open access
Semantic Scholar
Non-coding variability at the APOE locus contributes to the Alzheimer’s risk
Xiao-Pu Zhou, Yu Chen, K. Mok, T. Kwok +314 more
2019Nature Communications112 citations Open access
Semantic Scholar
Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study
E. Jabbari, Shunsuke Koga, Rebecca R. Valentino, R. Reynolds +52 more
2020Lancet Neurology98 citations Open access
Semantic Scholar
Moving beyond neurons: the role of cell type-specific gene regulation in Parkinson’s disease heritability
R. Reynolds, J. Botía, M. Nalls, A. Noyce +163 more
2019npj Parkinson's Disease93 citations Open access
Semantic Scholar
Identification of genetic risk factors in the Chinese population implicates a role of immune system in Alzheimer’s disease pathogenesis
Xiao-Pu Zhou, Yu Chen, K. Mok, Qian-Hua Zhao +7 more
2018Proceedings of the National Academy of Sciences of the United States of America88 citations Open access
Semantic Scholar
Cognitive markers of preclinical and prodromal Alzheimer's disease in Down syndrome
Carla M. Startin, Sarah Hamburg, R. Hithersay, Tamara Al-Janabi +18 more
2018Alzheimer's & Dementia86 citations Open access
Semantic Scholar
Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data
K. Mok, U. Sheerin, J. Simón-Sánchez, A. Salaka +34 more
2016Lancet Neurology86 citations Open access
Semantic Scholar
Underrepresented Populations in Parkinson's Genetics Research: Current Landscape and Future Directions
A. Schumacher-Schuh, Andrei Bieger, O. Okunoye, K. Mok +17 more
2022Movement Disorders81 citations Open access
Semantic Scholar
Aging related cognitive changes associated with Alzheimer's disease in Down syndrome
Nicholas C. Firth, Carla M. Startin, R. Hithersay, Sarah Hamburg +5 more
2018bioRxiv81 citations Open access
Semantic Scholar
Identification of sixteen novel candidate genes for late onset Parkinson’s disease
A. Gialluisi, M. G. Reccia, N. Modugno, T. Nutile +173 more
2021Molecular Neurodegeneration80 citations Open access
Semantic Scholar
Plasma biomarkers for amyloid, tau, and cytokines in Down syndrome and sporadic Alzheimer’s disease
Carla M. Startin, N. Ashton, Sarah Hamburg, R. Hithersay +16 more
2019Alzheimer's Research & Therapy79 citations Open access
Semantic Scholar
Additional rare variant analysis in Parkinson’s disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance
S. Lubbe, V. Escott-Price, J. R. Gibbs, M. Nalls +21 more
2016Human Molecular Genetics64 citations Open access
Semantic Scholar
Screening a UK amyotrophic lateral sclerosis cohort provides evidence of multiple origins of the C9orf72 expansion
P. Fratta, J. Polke, J. Newcombe, S. Mizielinska +26 more
2015Neurobiology of Aging64 citations Open access
Semantic Scholar
Neurofilament light as a blood biomarker for neurodegeneration in Down syndrome
A. Strydom, A. Heslegrave, Carla M. Startin, K. Mok +9 more
2018bioRxiv61 citations Open access
Semantic Scholar
Deep learning-based polygenic risk analysis for Alzheimer’s disease prediction
Xiao-Pu Zhou, Yu Chen, Fanny C. F. Ip, Yuanbing Jiang +322 more
2023Communications Medicine60 citations Open access
Semantic Scholar
Dystonia genes functionally converge in specific neurons and share neurobiology with psychiatric disorders
N. Mencacci, R. Reynolds, Sonia Garcia Ruiz, J. Vandrovcova +45 more
2020Brain : a journal of neurology57 citations Open access
Semantic Scholar
C9orf72 Intermediate Repeats are Associated with Corticobasal Degeneration, Increased C9orf72 Expression and Disruption of Autophagy
Christopher P. Cali, M. Patiño, Yee Tai, Wan Y. Ho +22 more
2019Acta Neuropathologica55 citations Open access
Semantic Scholar
Variation at the TRIM11 locus modifies progressive supranuclear palsy phenotype
E. Jabbari, J. Woodside, M. Tan, M. Shoai +19 more
2018bioRxiv48 citations Open access
Semantic Scholar
An IL1RL1 genetic variant lowers soluble ST2 levels and the risk effects of APOE-ε4 in female patients with Alzheimer’s disease
Yuanbing Jiang, Xiao-Pu Zhou, Hiu-Yi Wong, L. Ouyang +25 more
2022Nature Aging42 citations Open access
Semantic Scholar
Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2
E. Boot, N. Butcher, S. Udow, C. Marras +30 more
2018Neurology39 citations Open access
Semantic Scholar
A blood‐based multi‐pathway biomarker assay for early detection and staging of Alzheimer's disease across ethnic groups
Yuanbing Jiang, Hyebin Uhm, Fanny C. F. Ip, Li Ouyang +17 more
2024Alzheimer's & Dementia34 citations Open access
Semantic Scholar
A multi-level developmental approach to exploring individual differences in Down syndrome: genes, brain, behaviour, and environment
Michael S. C. Thomas, Olatz Ojinaga-Alfageme, Hana D'Souza, P. Patkee +4 more
2020Research in Developmental Disabilities31 citations Open access
Semantic Scholar
Genetic and polygenic risk score analysis for Alzheimer's disease in the Chinese population
Xiao-Pu Zhou, Yu Chen, Fanny C. F. Ip, Nicole Chit Hang Lai +17 more
2020Alzheimer's & Dementia30 citations Open access
Semantic Scholar
Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genes
Kurt Farrell, J. Humphrey, Timothy S. Chang, Yi Zhao +55 more
2024Nature Communications29 citations Open access
Semantic Scholar
Lack of evidence for a role of genetic variation in TMEM230 in the risk for Parkinson’s disease in the Caucasian population
Anamika Giri, K. Mok, I. Jansen, Manu Sharma +20 more
2016Neurobiology of Aging29 citations Open access
Semantic Scholar
Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genes
Kurt Farrell, J. Humphrey, Timothy S. Chang, Yi Zhao +42 more
2023bioRxiv27 citations Open access
Semantic Scholar
Multi‐Omics‐Based Autophagy‐Related Untypical Subtypes in Patients with Cerebral Amyloid Pathology
Jong-Chan Park, Natalia Barahona-Torres, S. Jang, K. Mok +16 more
2022Advancement of science27 citations Open access
Semantic Scholar
Fulminant corticobasal degeneration: a distinct variant with predominant neuronal tau aggregates
H. Ling, E. Gelpí, Karen Davey, Z. Jaunmuktane +27 more
2020Acta Neuropathologica22 citations Open access
Semantic Scholar
Using blood transcriptome analysis for Alzheimer's disease diagnosis and patient stratification
Huan Zhong, Xiao-Pu Zhou, Hyebin Uhm, Yuanbing Jiang +14 more
2024Alzheimer's & Dementia18 citations Open access
Semantic Scholar
HLA-DRB*1501 associations with magnetic resonance imaging measures of grey matter pathology in multiple sclerosis.
Ö. Yaldizli, V. Sethi, M. Pardini, C. Tur +10 more
2016Multiple Sclerosis and Related Disorders16 citations Open access
Semantic Scholar
LRP10 in α-synucleinopathies.
D. Kia, M. Sabir, Sarah Ahmed, J. Trinh +141 more
2018Lancet Neurology15 citations Open access
Semantic Scholar
Erratum to “Polymorphisms in BACE2 may affect the age of onset Alzheimer's dementia in Down syndrome” [Neurobiol. Aging 35 (2014) 1513.e1–1513.e5]
K. Mok, E. Jones, M. Hanney, D. Harold +4 more
2014Neurobiology of Aging15 citations Open access
Semantic Scholar
Differential Associations of Apolipoprotein E ε4 Genotype With Attentional Abilities Across the Life Span of Individuals With Down Syndrome
Hana D'Souza, L. Mason, K. Mok, Carla M. Startin +6 more
2020JAMA Network Open14 citations Open access
Semantic Scholar
Parkinson's disease without nigral degeneration: a pathological correlate of scans without evidence of dopaminergic deficit (SWEDD)?
H. Ling, Seamus Kearney, H. L. K. Yip, L. Silveira-Moriyama +7 more
2015Journal of Neurology Neurosurgery & Psychiatry14 citations Open access
Semantic Scholar
Head-to-head comparison of brain-derived pTau217 and total pTau217 for brain amyloid and tau pathology classification
Yuanbing Jiang, Wen-Yue Zheng, Zengjie Xia, Wan-Wa Wong +17 more
2026Proceedings of the National Academy of Sciences of the United States of America10 citations Open access
Semantic Scholar
Creating the Pick’s disease International Consortium: Genetic association study of the MAPT H2 haplotype with risk of Pick’s disease
Rebecca R. Valentino, William J. Scotton, S. Roemer, T. Lashley +154 more
2024Lancet Neurology10 citations Open access
Semantic Scholar
Transethnic analysis identifies SORL1 variants and haplotypes protective against Alzheimer's disease
Xiao-Pu Zhou, Han-Qin Cao, Yuanbing Jiang, Yue-Wen Chen +16 more
2024Alzheimer's & Dementia9 citations Open access
Semantic Scholar
Insights into ancestral diversity in Parkinson’s disease risk: a comparative assessment of polygenic risk scores
P. Saffie-Awad, S. Grant, M. Makarious, Inas Elsayed +293 more
2025npj Parkinson's Disease8 citations Open access
Semantic Scholar
Demographics and Medication Use of Patients with Late-Onset Alzheimer’s Disease in Hong Kong
Hiu-Yi Wong, H. Zhong, Ming-Qian Zhong, Xiao-Pu Zhou +7 more
2022Journal of Alzheimer's Disease8 citations Open access
Semantic Scholar
The East Asian Parkinson Disease Genomics Consortium.
K. Mok, Ji-Feng Guo, Bei-Sha Tang, H. Shang +48 more
2021Lancet Neurology8 citations Open access
Semantic Scholar

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