Non-coding variants in Usher Syndrome

K08 EY033789 

Rapid neonatal genetic diagnosis of retinoblastoma utilizing targeted long-read sequencing technology

Young Investigator Grant Award 

Targeted long-read sequencing to identify phased pathogenic variants in inherited retinal diseases

Career Development Award

 Deciphering the Missing Heritability in Inherited Retinal Diseases with Targeted Long-Read Genome Sequencing

Vision Innovation Award