Area of research
Neurology · General Health Professions
Research interest
Research interests include Parkinson's Disease Mechanisms and Treatments, Neurological disorders and treatments, Health and Medical Studies, and Genetic Associations and Epidemiology.
Opioid overdoses involving xylazine in emergency department patients: a multicenter study
Genetics and Pathogenesis of Parkinson's Syndrome
Finding genetically-supported drug targets for Parkinson’s disease using Mendelian randomization of the druggable genome
Contribution of a positive psychology-based conceptual framework in reducing physician burnout and improving well-being: a systematic review
Targeted Quantification of Detergent-Insoluble RNA-Binding Proteins in Human Brain Reveals Stage and Disease Specific Co-aggregation in Alzheimer’s Disease
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
Tau-Mediated Disruption of the Spliceosome Triggers Cryptic RNA Splicing and Neurodegeneration in Alzheimer’s Disease
Progressive parkinsonism in older adults is related to the burden of mixed brain pathologies
Moving beyond neurons: the role of cell type-specific gene regulation in Parkinson’s disease heritability
cindr, the Drosophila Homolog of the CD2AP Alzheimer’s Disease Risk Gene, Is Required for Synaptic Transmission and Proteostasis
The Dementias Platform UK (DPUK) Data Portal
Tau Activates Transposable Elements in Alzheimer’s Disease
A Druggable Genome Screen Identifies Modifiers of α-Synuclein Levels via a Tiered Cross-Species Validation Approach
Parkinson disease age of onset GWAS: defining heritability, genetic loci and a-synuclein mechanisms
Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease
NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases
Discovery and functional prioritization of Parkinson’s disease candidate genes from large-scale whole exome sequencing
NMNAT2:HSP90 Complex Mediates Proteostasis in Proteinopathies
Genome-wide association study in essential tremor identifies three new loci
Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease
GWAS for executive function and processing speed suggests involvement of the CADM2 gene
Using genetics to test the causal relationship of total adiposity and periodontitis: Mendelian randomization analyses in the Gene-Lifestyle Interactions and Dental Endpoints (GLIDE) Consortium
A Mitocentric View of Parkinson's Disease
Genome-wide Studies of Verbal Declarative Memory in Nondemented Older People: The Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium
GWAS of Cerebrospinal Fluid Tau Levels Identifies Risk Variants for Alzheimer’s Disease
Genome‐wide association study of the rate of cognitive decline in Alzheimer's disease
A Genome-Wide Association Study of Depressive Symptoms