Aarti Sevilimedu

This study identifies biallelic CCN2 variants as the cause of autosomal recessive kyphomelic dysplasia through clinical, genetic, and zebrafish model analyses.

This study investigates ovarian development defects in zebrafish fmr1 knockout models, identifying three mechanisms involving neuroendocrine signaling, germ cell gene expression, and mitochondrial impairment.

The paper presents a cost-effective method for introducing multiple mutations into DNA, demonstrated using the Omicron Spike DNA construct.

The paper applies AI/ML to identify potential drugs for Fragile X Syndrome by comparing disease gene profiles with drug-induced perturbation profiles.