Area of research
Neurology · Physiology
Research interest
Research interests include Amyotrophic Lateral Sclerosis Research, Parkinson's Disease Mechanisms and Treatments, Alzheimer's disease research and treatments, and Neurological diseases and metabolism.
TDP-43 loss induces cryptic polyadenylation in ALS/FTD
Copy Number Variation and Haplotype Analysis of <scp>17q21.31</scp> Reveals Increased Risk Associated with Progressive Supranuclear Palsy and Gene Expression Changes in Neuronal Cells
MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study
Author Correction: TDP-43 loss and ALS-risk SNPs drive mis-splicing and depletion of UNC13A
Association of Structural Forms of 17q21.31 with the Risk of Progressive Supranuclear Palsy and <i>MAPT</i> Sub-haplotypes
TDP-43 loss and ALS-risk SNPs drive mis-splicing and depletion of UNC13A
Prioritization of Drug Targets for Neurodegenerative Diseases by Integrating Genetic and Proteomic Data From Brain and Blood
Common Variants Near <scp>ZIC1</scp> and <scp>ZIC4</scp> in Autopsy‐Confirmed Multiple System Atrophy
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture
Genomewide Association Studies of <scp> <i>LRRK2</i> </scp> Modifiers of Parkinson's Disease
Differences in the Presentation and Progression of Parkinson's Disease by Sex
Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodies
Machine learning suggests polygenic risk for cognitive dysfunction in amyotrophic lateral sclerosis
Postmortem Cortex Samples Identify Distinct Molecular Subtypes of ALS: Retrotransposon Activation, Oxidative Stress, and Activated Glia
Genomewide association study of Parkinson's disease clinical biomarkers in 12 longitudinal patients' cohorts
<i>TMEM106B</i> Effect on cognition in Parkinson disease and frontotemporal dementia
Primary Tau Pathology, Not Copathology, Correlates With Clinical Symptoms in PSP and CBD
C9orf72 intermediate repeats are associated with corticobasal degeneration, increased C9orf72 expression and disruption of autophagy
Heritability and genetic variance of dementia with Lewy bodies
Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia
Analysis of shared heritability in common disorders of the brain
Neurodegenerative disease concomitant proteinopathies are prevalent, age-related and APOE4-associated
Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia
Sex-specific genetic predictors of Alzheimer’s disease biomarkers
Selective Genetic Overlap Between Amyotrophic Lateral Sclerosis and Diseases of the Frontotemporal Dementia Spectrum
P1‐139: THE CONTRIBUTION OF SEX‐SPECIFIC ASSOCIATIONS IN GENETIC STUDIES OF ALZHEIMER'S DISEASE PATHOLOGY
Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study
Genome-wide association study identifies four novel loci associated with Alzheimer’s endophenotypes and disease modifiers
Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS
Large-scale exploratory genetic analysis of cognitive impairment in Parkinson's disease