Area of research
Neurology · Cellular and Molecular Neuroscience
Research interest
Research focused on Progressive supranuclear palsy and Genome-wide association study, with related work in Movement disorders, Palsy, Missense mutation. Notable publications include 'Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteria', 'Alpha‐synuclein p.H50Q, a novel pathogenic mutation for Parkinson's disease', and 'Which ante mortem clinical features predict progressive supranuclear palsy pathology?'.
RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analyses
Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy
Correction: Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy
Whole-Genome Sequencing Analysis Reveals New Susceptibility Loci and Structural Variants Associated with Progressive Supranuclear Palsy
Long‐Duration Progressive Supranuclear Palsy: Clinical Course and Pathological Underpinnings
Common Variants Near <scp>ZIC1</scp> and <scp>ZIC4</scp> in Autopsy‐Confirmed Multiple System Atrophy
Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study
Clinical Conditions “Suggestive of Progressive Supranuclear Palsy”—Diagnostic Performance
How to apply the movement disorder society criteria for diagnosis of progressive supranuclear palsy
Validation of the Movement Disorder Society Criteria for the Diagnosis of 4‐Repeat Tauopathies
Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteria
Which ante mortem clinical features predict progressive supranuclear palsy pathology?
Genome-wide association study in essential tremor identifies three new loci
Alpha‐synuclein p.H50Q, a novel pathogenic mutation for Parkinson's disease