Area of research
Neurology · Genetics
Research interest
Research interests include Parkinson's Disease Mechanisms and Treatments, Genetic Associations and Epidemiology, Neurological diseases and metabolism, and Genomics and Rare Diseases.
Insights into ancestral diversity in Parkinson’s disease risk: a comparative assessment of polygenic risk scores
Mis-spliced transcripts generate de novo proteins in TDP-43–related ALS/FTD
<scp>NeuroBooster</scp> Array: A Genome‐Wide Genotyping Platform to Study Neurological Disorders Across Diverse Populations
GenoTools: an open-source Python package for efficient genotype data quality control and analysis
African ancestry neurodegeneration risk variant disrupts an intronic branchpoint in GBA1
Exome sequencing in Asian populations identifies low-frequency and rare coding variation influencing Parkinson’s disease risk
A new AI-assisted data standard accelerates interoperability in biomedical research
A cellular taxonomy of the adult human spinal cord
Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study
Multi-ancestry meta-analysis and fine-mapping in Alzheimer’s disease
Parallel CRISPR-Cas9 screens identify mechanisms of PLIN2 and lipid droplet regulation
Genome-wide association study using whole-genome sequencing identifies risk loci for Parkinson’s disease in Chinese population
The Foundational Data Initiative for Parkinson Disease: Enabling efficient translation from genetic maps to mechanism
Large-scale rare variant burden testing in Parkinson's disease
Genome‐Wide Analysis of Structural Variants in Parkinson Disease
Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)
Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2)
Artificial intelligence for dementia genetics and omics
A reference human induced pluripotent stem cell line for large-scale collaborative studies
A CRISPRi/a platform in human iPSC-derived microglia uncovers regulators of disease states
Identification and prediction of Parkinson’s disease subtypes and progression using machine learning in two cohorts
Type 2 Diabetes Partitioned Polygenic Scores Associate With Disease Outcomes in 454,193 Individuals Across 13 Cohorts
Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning
Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries
Stroke genetics informs drug discovery and risk prediction across ancestries
Genome-wide CRISPRi/a screens in human neurons link lysosomal failure to ferroptosis
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
Identification of Risk Loci for Parkinson Disease in Asians and Comparison of Risk Between Asians and Europeans