Gayle B. Collin

This paper creates a mouse model with the ARMS2A69S variant to study AMD, finding it causes mitochondrial dysfunction and AMD-like phenotypes.

This study identifies Arhgef12 and Prkci as genetic modifiers that influence the severity of retinal dysplasia in the Crb1rd8 mouse model, revealing differential disease progression and cellular mislocalization.

The paper quantifies age-related changes in axial and retinal biometry in hyperopic mouse models and identifies strain-specific differences in ocular growth.