Amanda Thomas-Wilson is the Director of Molecular Diagnostics at the New York Genome Center, specializing in clinical genomics and the diagnosis of rare genetic disorders. She holds a PhD in Human and Molecular Genetics from Baylor College of Medicine and is a board-certified Biochemical and Laboratory Geneticist.
[Predicted] Outside of her core research, Amanda appears passionate about bridging the gap between genomic research and patient care. Her work suggests a dedication to translating complex genetic findings into actionable insights that can directly benefit families affected by rare diseases.
She serves on an FDA-recognized expert panel that collaborates with patient advocacy groups to classify genetic variants for rare diseases.
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