Elisa Mani

Gene Editing for CEP290 -Associated Retinal Degeneration

Infant microbes and metabolites point to childhood neurodevelopmental disorders

Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability

Mutation of the gene encoding cellular retinaldehyde–binding protein in autosomal recessive retinitis pigmentosa