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Amanda Thomas-Wilson

Amanda Thomas-Wilson

New York Genome Center
Amanda Thomas-Wilson received her Masters of Science from the University of North Carolina at Greensboro and her PhD from the Department of Molecular and Human Genetics at Baylor College of Medicine (Houston, Texas). She completed fellowships in Clinical Biochemical Genetics at the University of Utah (Salt Lake City, Utah), followed by Laboratory Genetics and Genomics at Columbia University (New York, New York). Amanda was Board Certified by the American Board of Medical Genetics and Genomics in Clinical Biochemical Genetics (2017) and Laboratory Genetics and Genomics (2019) and has been a Fellow of the American College of Medical Genetics and Genomics since 2017. Amanda is currently a Director of Molecular Diagnostics at New York Genome Center where she is primarily involved in Clinical Genome Sequencing for undiagnosed disease. Amanda is also an active participant in the Clinicial Genome Resource (ClinGen) where she serves as chair of the Urea Cycle Disorders Expert Panel, serves as an expert and biocurator for the Cerebral Creatine Deficiency Syndromes Expert Panel, and a biocurator for the Prenatal Gene Curation Expert Panel.
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