K08 EY033789
Non-coding variants in Usher Syndrome
Rapid neonatal genetic diagnosis of retinoblastoma utilizing targeted long-read sequencing technology
Young Investigator Grant AwardÂ
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
Clinical & Research Synergy Pilot Award
Patient-derived retinal organoid models for mechanistic and therapeutic discovery
Pediatric Retina Researc Award
Vision Innovation Award