Pediatric Genomics & Precision Surgery
Focus: Hypospadias • Congenital Anomalies • Rare Diseases
We study the genetic basis of pediatric surgical disorders using whole-exome sequencing, transcriptomics, and epigenomic profiling. Our primary focus is hypospadias, where molecular findings are paired with detailed phenotyping to improve diagnosis, severity grading, and personalized management. We also investigate the underlying biology of pouch colon, biliary atresia, Wilms tumor, and other rare anomalies seen in surgical practice.
