Area of research
Molecular Biology · Ophthalmology
Research interest
Research interests include Mitochondrial Function and Pathology, Retinal Development and Disorders, Glaucoma and retinal disorders, and Retinal Diseases and Treatments.
Molecular Basis of Mitochondrial Complex I Disruption by m.14484T>C-Induced Leber Hereditary Optic Neuropathy
Retinal ganglion cell vulnerability to pathogenic tau in Alzheimer’s disease
Recessive variants in mitochondrial Complex I nuclear subunits are an underrated cause of optic atrophy
Alzheimer's disease pathophysiology in the Retina
Mitochondrial retinopathies and optic neuropathies: The impact of retinal imaging on modern understanding of pathogenesis, diagnosis, and management
Five-Year Outcomes of Lenadogene Nolparvovec Gene Therapy in Leber Hereditary Optic Neuropathy
How crosstalk between mitochondria, lysosomes, and other organelles can prevent or promote dry age-related macular degeneration
Coenzyme Q10 trapping in mitochondrial complex I underlies Leber’s hereditary optic neuropathy
Randomized trial of bilateral gene therapy injection for m.11778G&gt;A <i>MT-ND4</i> Leber optic neuropathy
Pathological mitophagy disrupts mitochondrial homeostasis in Leber’s hereditary optic neuropathy
Indirect Comparison of Lenadogene Nolparvovec Gene Therapy Versus Natural History in Patients with Leber Hereditary Optic Neuropathy Carrying the m.11778G>A MT-ND4 Mutation
Safety of Lenadogene Nolparvovec Gene Therapy Over 5 Years in 189 Patients With Leber Hereditary Optic Neuropathy
Efficacy and Safety of Intravitreal Gene Therapy for Leber Hereditary Optic Neuropathy Treated within 6 Months of Disease Onset
Glaucoma as Neurodegeneration in the Brain
Natural history of patients with Leber hereditary optic neuropathy—results from the REALITY study
Intravitreal Gene Therapy vs. Natural History in Patients With Leber Hereditary Optic Neuropathy Carrying the m.11778G>A ND4 Mutation: Systematic Review and Indirect Comparison
Retinal ganglion cell dysfunction in preclinical Alzheimer’s disease: an electrophysiologic biomarker signature
Bilateral visual improvement with unilateral gene therapy injection for Leber hereditary optic neuropathy
Inhibition of autophagy curtails visual loss in a model of autosomal dominant optic atrophy
Long-Term Follow-Up After Unilateral Intravitreal Gene Therapy for Leber Hereditary Optic Neuropathy: The RESTORE Study
Chromatic Pupillometry Findings in Alzheimer’s Disease
The Retina in Alzheimer's Disease: Histomorphometric Analysis of an Ophthalmologic Biomarker
Peripapillary vessel density changes in Leber's hereditary optic neuropathy: a new biomarker
Topographic Macular Microvascular Changes and Correlation With Visual Loss in Chronic Leber Hereditary Optic Neuropathy
Optic neuropathies: the tip of the neurodegeneration iceberg
Retinal Ganglion Cells and Circadian Rhythms in Alzheimer’s Disease, Parkinson’s Disease, and Beyond
Accuracy of Diagnostic Imaging Modalities for Classifying Pediatric Eyes as Papilledema Versus Pseudopapilledema
Natural History of Conversion of Leber's Hereditary Optic Neuropathy
Optical coherence tomography angiography in acute arteritic and non-arteritic anterior ischemic optic neuropathy
Melanopsin retinal ganglion cell loss in <scp>A</scp>lzheimer disease