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
Physician Scientist Award
Parent-of-Origin Determination in Retinoblastoma: A Biomarker for Risk and Therapeutic Targeting
Clinical & Research Synergy Pilot Award
Patient-derived retinal organoid models for mechanistic and therapeutic discovery
STTR Rare Cancers Translational Research Grant
Transcriptional consequences of the parent-of-origin effect in RB1-associated retinoblastoma
Pediatric Retina Research Award
Vision Innovation Award