Researcher | Research Overview
Dr. Chopra's focus is the discovery and delineation of new and emerging rare monogenic neurodevelopmental syndromes and the evaluation of treatment options for such disorders based on underlying mechanism.
Researcher | Research Background
Dr. Chopra is fully qualified as a Clinical Geneticist and Pediatrician, having obtained her specialist qualifications in Australia in 2010 through the Royal Australasian College of Physicians and the Human Genetics Society of Australasia. She has experience in the assessment and diagnosis of children with rare genetic disorders, with previous positions in Sydney (Royal Prince Alfred Hospital), Shanghai (Shanghai First Maternity and Infant Hospital) and Paris (Imagine Institute of Genetic Diseases). In her role as Director of Translational Genomic Medicine at the RSZ-Translational Neuroscience Center, she leads the evaluation of genetic disorders for suitability for gene-based therapies, clinical-trial readiness, and multidisciplinary clinics.