Area of research
Genetics · Sensory Systems
Research interest
Research interests include Hearing, Cochlea, Tinnitus, Genetics, Genomic variations and chromosomal abnormalities, Genomics and Rare Diseases, and COVID-19 Clinical Research Studies.
Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss
Novel GPR156 variants confirm its role in moderate sensorineural hearing loss
Spectrum of Genetic Variants Associated with Anterior Segment Dysgenesis in South Florida
Dysfunction of <i>GRAP</i> , encoding the GRB2-related adaptor protein, is linked to sensorineural hearing loss
<i>FOXF2</i>is required for cochlear development in humans and mice
Identification of candidate gene FAM183A and novel pathogenic variants in known genes: High genetic heterogeneity for autosomal recessive intellectual disability