Dr. William Dobyns

Dr. William Dobyns is a globally renowned authority in pediatric neurology, neurogenetics, and brain malformations, whose groundbreaking work has shaped the modern understanding of neurodevelopmental disorders. Dr. Dobyns is best known for his pioneering research on lissencephaly, polymicrogyria, megalencephaly, and other disorders of cortical development, as well as for defining new genetic syndromes that affect brain structure and function.

Based in the United States, Dr. Dobyns has held academic and clinical positions at some of the world’s leading institutions, where he has combined meticulous research with compassionate clinical care. His contributions to the fields of fetal and pediatric neuroimaging, clinical genetics, and developmental neuroscience have led to earlier diagnoses, improved classification systems, and better outcomes for children with complex neurological conditions.

As a Board Member of the Fetal Brain Society, Dr. Dobyns brings unparalleled expertise in correlating prenatal imaging findings with genetic and postnatal phenotypes, helping clinicians and researchers around the world interpret complex fetal brain anomalies with greater accuracy and depth. His work has been instrumental in linking genotype to phenotype in brain development—an essential aspect of personalized fetal medicine.

A prolific scholar, dedicated mentor, and international thought leader, Dr. Dobyns continues to inspire innovation and collaboration at the intersection of imaging, genetics, and pediatric neuroscience. His involvement in the Fetal Brain Society strengthens its mission to deliver globally impactful, evidence-based care for the developing brain.