A photo of Shannon M. Standridge.

Director, Rett Syndrome Clinic

Epilepsy Specialist, Division of Neurology

Assistant Professor, UC Department of Pediatrics

513-636-4222

513-636-1888

Board Certified

My Biography & Research

Clinical Interests

General neurology

Academic Affiliation

Assistant Professor, UC Department of Pediatrics

Departments

Neurology, Epilepsy, Rett Syndrome, Neurology

My Locations

My Education

Fellowship: Neurophysiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 2008; Neurology, Nationwide Children's Hospital, Columbus, OH, 2007.

Residency: Pediatrics, Nationwide Children's Hospital, Columbus, OH, 2004.

MPH: The Ohio State University College of Public Health, Columbus, OH, 2008.

DO: Kansas City University of Medicine and Biosciences, Kansas City, MO, 2002.

BS: Biology, Lyon College, Batesville, AS, 1997.

My Publications

Characterizing the phenotypic effect of Xq28 duplication size in MECP2 duplication syndrome. Peters, SU; Fu, C; Suter, B; Marsh, E; Benke, TA; Skinner, SA; Lieberman, DN; Standridge, S; Jones, M; Beisang, A; et al. Clinical Genetics: an international journal of genetics and molecular medicine. 2019; 95:575-581.

The array of clinical phenotypes of males with mutations in Methyl-CpG binding protein 2. Neul, JL; Benke, TA; Marsh, ED; Skinner, SA; Merritt, J; Lieberman, DN; Standridge, S; Feyma, T; Heydemann, P; Peters, S; et al. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 2019; 180:55-67.

A Case of An Unusual Bell's Palsy Mimic. Lutley, AL; Standridge, SM. Seminars in Pediatric Neurology. 2018; 26:77-79.

An Atypical Rett Syndrome Phenotype Due to a Novel Missense Mutation in CACNA1A. Epperson, MV; Haws, ME; Standridge, SM; Gilbert, DL. Journal of Child Neurology. 2018; 33:286-289.

Drug-resistant epilepsy in children with partial onset epilepsy treated with carbamazepine. Aungaroon, G; Holland, KD; Horn, PS; Standridge, SM; Imming, CM. International Journal of Neuroscience. 2017; 127:849-853.

The Clinical Predictors That Facilitate a Clinician's Decision to Order Genetic Testing for Rett Syndrome. Knight, VM; Horn, PS; Gilbert, DL; Standridge, SM. Pediatric Neurology. 2016; 63:66-70.

Methodological Issues in Predicting Pediatric Epilepsy Surgery Candidates Through Natural Language Processing and Machine Learning. Cohen, KB; Glass, B; Greiner, HM; Holland-Bouley, K; Standridge, S; Arya, R; Faist, R; Morita, D; Mangano, F; Connolly, B; et al. Biomedical Informatics Insights. 2016; 8:BII.S38308-BII.S38308.

The Clinical Utility of a Single-Nucleotide Polymorphism Microarray in Patients With Epilepsy at a Tertiary Medical Center. Hrabik, SA; Standridge, SM; Greiner, HM; Neilson, DE; Pilipenko, VV; Zimmerman, SL; Connor, JA; Spaeth, CG. Journal of Child Neurology. 2015; 30:1770-1777.

Diagnoses in Pediatric Patients With Magnetic Resonance Imaging (MRI) Lesions Suspicious for Demyelination. Sweeney, ML; Kukreja, M; Horn, PS; Standridge, SM. Journal of Child Neurology. 2015; 30:1651-1657.

Costs and Clinical Outcomes of Epilepsy Surgery in Children With Drug-Resistant Epilepsy. Oldham, MS; Horn, PS; Tsevat, J; Standridge, S. Pediatric Neurology. 2015; 53:216-220.