Jenina Capasso

Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies, rod-cone dystrophies, Leber congenital amaurosis, and cone dysfunction syndromes

Structural basis for odorant recognition of the insect odorant receptor OR-Orco heterocomplex

Patients and animal models of CNGβ1-deficient retinitis pigmentosa support gene augmentation approach

Retinal Dystrophy with Intraretinal Cystoid Spaces Associated with Mutations in the Crumbs Homologue (CRB1) Gene