American Board of Psychiatry and Neurology (Epilepsy) | Education
Undergraduate School
Franklin & Marshall College
2011, Lancaster, PA
Medical School
University of Rochester School of Medicine and Dentistry
2015, Rochester, NY
Residency
Pediatrics
St. Louis Children's Hospital/Washington University in St. Louis
2017, St. Louis, MO
Residency
Pediatric Neurology
St. Louis Children's Hospital/Washington University in St. Louis
2020, St. Louis, MO
Fellowship
Epilepsy
St. Louis Children's Hospital/Washington University in St. Louis
2021, St. Louis, MO
Fellowship
Neurogenetics/Epilepsy Genetics
Boston Children's Hospital
2022, Boston, MA
American Board of Psychiatry and Neurology (Epilepsy) | Publications
Expanding the phenotype and genotype spectrum of TAOK1 neurodevelopmental disorder and delineating TAOK2 neurodevelopmental disorder. Genet Med. 2025 Mar; 27(3):101348. View Expanding the phenotype and genotype spectrum of TAOK1 neurodevelopmental disorder and delineating TAOK2 neurodevelopmental disorder. Abstract
CIC-Related Neurodevelopmental Disorder: A Review of the Literature and an Expansion of Genotype and Phenotype. Genes (Basel). 2024 Oct 31; 15(11). View CIC-Related Neurodevelopmental Disorder: A Review of the Literature and an Expansion of Genotype and Phenotype. Abstract
The spectrum of movement disorders in young children with ARX-related epilepsy-dyskinesia syndrome. Ann Clin Transl Neurol. 2024 Jun; 11(6):1643-1647. View The spectrum of movement disorders in young children with ARX-related epilepsy-dyskinesia syndrome. Abstract
Consensus reporting guidelines to address gaps in descriptions of ultra-rare genetic conditions. NPJ Genom Med. 2024 Apr 06; 9(1):27. View Consensus reporting guidelines to address gaps in descriptions of ultra-rare genetic conditions. Abstract
Comprehensive phenotypes of patients with SYNGAP1-related disorder reveals high rates of epilepsy and autism. Epilepsia. 2024 May; 65(5):1428-1438. View Comprehensive phenotypes of patients with SYNGAP1-related disorder reveals high rates of epilepsy and autism. Abstract
Evaluation of the feasibility, diagnostic yield, and clinical utility of rapid genome sequencing in infantile epilepsy (Gene-STEPS): an international, multicentre, pilot cohort study. Lancet Neurol. 2023 09; 22(9):812-825. View Evaluation of the feasibility, diagnostic yield, and clinical utility of rapid genome sequencing in infantile epilepsy (Gene-STEPS): an international, multicentre, pilot cohort study. Abstract
Utility of Exome Sequencing for Diagnosis in Unexplained Pediatric-Onset Epilepsy. JAMA Netw Open. 2023 07 03; 6(7):e2324380. View Utility of Exome Sequencing for Diagnosis in Unexplained Pediatric-Onset Epilepsy. Abstract
Variants in DOCK3 cause developmental delay and hypotonia. Eur J Hum Genet. 2019 08; 27(8):1225-1234. View Variants in DOCK3 cause developmental delay and hypotonia. Abstract