Kaitryn E. Ronning

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

Lactylation-driven FTO targets CDK2 to aggravate microvascular anomalies in diabetic retinopathy

Molecular profiling of resident and infiltrating mononuclear phagocytes during rapid adult retinal degeneration using single-cell RNA sequencing

Loss of cone function without degeneration in a novel Gnat2 knock-out mouse