Area of research
Neurology · Cellular and Molecular Neuroscience
Research interest
Research interests include Parkinson's Disease Mechanisms and Treatments, Neurological diseases and metabolism, Amyotrophic Lateral Sclerosis Research, and Genetic Neurodegenerative Diseases.
Association between Human Leukocyte Antigen Alleles and Neuropathological Outcomes in Lewy Body Disease
Detection of mosaic and population-level structural variants with Sniffles2
<scp>NeuroBooster</scp> Array: A Genome‐Wide Genotyping Platform to Study Neurological Disorders Across Diverse Populations
Mechanism-Free Repurposing of Drugs For&nbsp;C9orf72-related ALS/FTD Using Large-Scale Genomic Data
Mechanism-Free Repurposing of Drugs For&nbsp;C9orf72-Related ALS/FTD Using Large-Scale Genomic Data
Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation
Large-scale rare variant burden testing in Parkinson's disease
Genome‐Wide Analysis of Structural Variants in Parkinson Disease
Unexpected frequency of the pathogenic <i>AR</i> CAG repeat expansion in the general population
A reference human induced pluripotent stem cell line for large-scale collaborative studies
Identification and prediction of Parkinson’s disease subtypes and progression using machine learning in two cohorts
Dementia with Lewy bodies: Impact of co‐pathologies and implications for clinical trial design
Personality traits are consistently associated with blood mitochondrial DNA copy number estimated from genome sequences in two genetic cohort studies
Challenges in the diagnosis of Parkinson's disease
Finding genetically-supported drug targets for Parkinson’s disease using Mendelian randomization of the druggable genome
Accelerating Medicines Partnership: Parkinson's Disease. Genetic Resource
A reference induced pluripotent stem cell line for large-scale collaborative studies
Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study
Large-scale pathway specific polygenic risk and transcriptomic community network analysis identifies novel functional pathways in Parkinson disease
Human Herpesvirus 6 Detection in Alzheimer’s Disease Cases and Controls across Multiple Cohorts
Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Parkinson's disease age at onset genome‐wide association study: Defining heritability, genetic loci, and α‐synuclein mechanisms
Genetic modifiers of risk and age at onset in GBA associated Parkinson’s disease and Lewy body dementia
Mitochondria function associated genes contribute to Parkinson’s Disease risk and later age at onset
A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity
Moving beyond neurons: the role of cell type-specific gene regulation in Parkinson’s disease heritability
A critique of the second consensus criteria for multiple system atrophy
Heritability and genetic variance of dementia with Lewy bodies
Parkinson disease age of onset GWAS: defining heritability, genetic loci and a-synuclein mechanisms