Niki Armstrong, MS, CGC is the Vice President of Genetic Services and Education at the Foundation for Angelman Syndrome Therapeutics. Niki is a board-certified genetic counselor, providing counseling to families, developing educational tools on genetics and clinical trials, and directing data strategy related to Angelman syndrome. Niki previously worked in the advancement of newborn screening for Duchenne and as a clinical genetic counselor in an academic children’s hospital. She is a graduate of the University of Minnesota genetic counseling program.