Dr. Kendra J. Bjoraker is a pediatric neuropsychologist with specialized expertise in rare genetic and metabolic diseases. She has held faculty positions at the University of Minnesota and Children’s Hospital Colorado, with advanced training in genetics, metabolism, and neuroimaging. Dr. Bjoraker is known for her work in lysosomal storage disorders, peroxisomal disorders, and inherited metabolic diseases. Her multidisciplinary research focuses on neuropsychological outcomes, disease progression, and the psychosocial factors that impact quality of life in individuals with rare and metabolic conditions. She also leads her own consultancy business, providing expert guidance in clinical care, research, and program development, and is a frequent presenter at national and international conferences.