Keren Carss

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

Possibilities and limitations of antisense oligonucleotide therapies for the treatment of monogenic disorders

Whole genome sequencing reveals novel mutations causing autosomal dominant inherited macular degeneration

A clinical and molecular characterisation of CRB1-associated maculopathy