Area of research
Neurology · Genetics
Research interest
Research interests include Amyotrophic Lateral Sclerosis Research, Neurogenetic and Muscular Disorders Research, Parkinson's Disease Mechanisms and Treatments, and Genetic Neurodegenerative Diseases.
TDP-43 loss induces cryptic polyadenylation in ALS/FTD
Efficacy and Safety of Zilucoplan in Amyotrophic Lateral Sclerosis
Author Correction: TDP-43 loss and ALS-risk SNPs drive mis-splicing and depletion of UNC13A
COURAGE-ALS: a randomized, double-blind phase 3 study designed to improve participant experience and increase the probability of success
TDP-43 loss and ALS-risk SNPs drive mis-splicing and depletion of UNC13A
Cell environment shapes TDP-43 function with implications in neuronal and muscle disease
An integrated multi-omic analysis of iPSC-derived motor neurons from C9ORF72 ALS patients
Ethical Considerations in Dementia Diagnosis and Care
Structural and functional characterization of fosfomycin resistance conferred by <scp>FosB</scp> from <scp><i>Enterococcus faecium</i></scp>
<scp>COVID‐19–associated Guillain‐Barré</scp> syndrome: The early pandemic experience
Primary lateral sclerosis: consensus diagnostic criteria
Effect of Ezogabine on Cortical and Spinal Motor Neuron Excitability in Amyotrophic Lateral Sclerosis
Clinical features of <scp>LRP4</scp>/agrin‐antibody–positive myasthenia gravis: A multicenter study
Amyotrophic lateral sclerosis care and research in the United States during the <scp>COVID</scp>‐19 pandemic: Challenges and opportunities
A Phase 2, Double-Blind, Randomized, Dose-Ranging Trial Of <i>Reldesemtiv</i> In Patients With ALS
Preface: promoting research in PLS: current knowledge and future challenges
Postmortem Cortex Samples Identify Distinct Molecular Subtypes of ALS: Retrotransposon Activation, Oxidative Stress, and Activated Glia
Primary lateral sclerosis (PLS) functional rating scale: PLS‐specific clinimetric scale
Unexpected similarities between C9ORF72 and sporadic forms of ALS/FTD suggest a common disease mechanism
Amyotrophic lateral sclerosis
Hydration measured by doubly labeled water in ALS and its effects on survival
Pain in amyotrophic lateral sclerosis: Patient and physician perspectives and practices
Relationship of creatine kinase to body composition, disease state, and longevity in ALS
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