Dr. Maya Chopra, MBBS, FRACP is a Clinical Geneticist with an interest the delineation of rare neurodevelopmental syndromes and clinical trial readiness programs for such disorders. She obtained her medical qualifications from the University of New South Wales in in 2000, and her speciality qualifications the Royal Australasian College of Physicians and the Human Genetics Society of Australasia in 2010. Dr Chopra has experience in practicing Clinical Genetics in a range of healthcare systems and cultural settings, having held positions at Royal Prince Alfred Hospital (Sydney, Australia), Shanghai First Maternity and Infant Hospital (Shanghai, China) and The Imagine Institute for Genetic Disease (Paris, France). Currently she is appointed at Boston Children's Hospital, serving as Director of Translational Genomic Medicine at the RSZ - Translational Neuroscience Center, as well as Medical Co-Director, Neurogenetics and Neurodevelopment Section, and Attending Physician, Division of Genetics & Genomics. She is Assistant Professor of Neurology at Harvard Medical School. Dr. Chopra serves as one of the Chairs of the ClinGen Intellectual Disability /Autism Gene Curation Expert Panel. She is the Principal Investigator of an internationally-recruiting longitudinal natural history study of ANKRD17-Neurodevelopmental Syndrome (Chopra-Amiel-Gordon syndrome).