
Stephanie M. Morris, MD
Medical Director, Center for Autism and Related Disorders, Kennedy Krieger Institute
EmailMorrsSt@kennedykrieger.org
Washington University School of Medicine
660 S. Euclid Ave., CB 8111
St. Louis, MO 63110
Education
- BS, Molecular and Cellular Biology,: University of Arizona, Tucson, AZ, (2007)
- MD,: University of Arizona, Phoenix, AZ, (2011)
- Residency in Pediatrics,: St. Louis Children's Hospital, St. Louis, MO, (2013)
- Residency in Child Neurology,: St. Louis Children's Hospital, St. Louis, MO, (2016)
Recognition
Magna Cum Laude graduate, University of Arizona, Tucson, AZ, 2007
Outstanding Student in a Third Year Clerkship – Pediatrics & Neurology, University of Arizona College of Medicine, Phoenix, AZ, 2010 – 2011
Neurological Sciences Academic Development Award, Washington University School of Medicine, 2015
Clinical Interests
Pediatric Neurology, Neurofibromatosis, Autism Spectrum Disorder
Publications
In Press: Anastasaki C, Morris SM, Gao F, Gutmann DH. Children with 5’-end NF1 gene mutations are more likely to harbor glioma. Neurology.
In Press: Vogel AC, Gutmann DH, Morris SM. Neurodevelopmental disorders in children with neurofibromatosis Type 1. Dev Med Child Neurol.
INVITED PUBLICATIONS:
Morris SM, Kim YM, Waubant E, Van Haren K, Mar S. Poliomyelitis-Like Syndome. In: Waubant E, Lotze T, eds. Demyelinating Diseases and their Mimics: Case Studies. Springer Science and Business Media New York 2016.
POSTERS:
Morris SM, Munoz R, Von Hoff D (2012). Identification of Novel Therapeutic Compounds for the Treatment of Pancreatic Cancer Using High-Throughput Screening. Poster presented at: Translational Genomics Research Institute Summer Intern Poster Symposium; Phoenix, AZ.
Morris SM, Prengler R, White A, Bayliss S, Mar S. (2015). Neurologic Findings and Serial Neuroimaging in Patients with Linear Scleroderma en Coup de Sabre (ECDS) and Parry Romberg Syndrome (PRS). Poster presented at: Child Neurology Society Meeting; National Harbor, MD.