About me
- Instructor A of Neurology
Education and training
- Medical School: University of Chicago
- Residency: Children's Hospital of Philadelphia
- Residency: Children's Hospital of Philadelphia
- Fellowship: Children's Hospital of Philadelphia
My Locations
CHOP Specialty Care, Lancaster
Penn Medicine hospital privileges
- Hospital of the University of Pennsylvania: Has privileges to treat patients in the hospital.
- Pennsylvania Hospital: Has privileges to treat patients in the hospital.
- Lancaster General Hospital: Has privileges to treat patients in the hospital.
- Chester County Hospital: Has privileges to treat patients in the hospital.
Qualifications and experience
- Psych & Neurology/Epilepsy (AMA)
- Neurology - Child Neurology, 2021
- American Academy of Neurology, National
- American Epilepsy Society, National
- American Epilepsy Society, National
- Child Neurology Society, International
- ClinGen, International
- CURE Epilepsy, International
- SYNGAP1 Research Fund, International
Treatments and Conditions
My research
McKee JL, Magielski J, Xian J, Cohen S, Toib J, Chen C, Kim D, Rathod A, Brimble E, Fitter N, Graglia JM, Helde KA, Boland MJ, Ruggiero SM, Sederman R, Helbig I. Clinical signatures of SYNGAP1-related disorders through data integration , medRxiv (accepted to Genetics in Medicine): 2025
Magielski J, Cohen S, Kaufman M, Parthasarathy S, Xian J, Brimble E, Fitter N, Furia F, Gardella E, Moller R, Helbig I, and McKee JL. Deciphering the dynamic clinical patterns in SCN8A-related disorders using real-world data , medRxiv (accepted to Neurology): 2025
Magielski J, Ruggiero SM, Xian J, Parthasarathy S, Galer P, Ganesan S, Back A, McKee J, McSalley I, Gonzalez AK, Morgan A, Donaher J, Helbig I. The clinical and genetic spectrum of paediatric speech and language disorders in 52,143 individuals , Brain: 2025
Pierce S, Cunningham K, Coyne J, Decampo D, Demarest S, Graglia M, Goss J, Harrison A, Helde K, McKee JL, Son Rigby C, Sullivan K, Tefft S, Chao HT, Grinspan Z, Miele A, Boland M, Ruggerio S, Helbig I STXBP1 and SYNGAP1 Related Disorders: Assessing the Feasibility of Developmental Outcome Measures , AES, Los Angeles, CA: 2024
Ruggerio S, Pierce S, Cunningham K, Coyne J, Chisari T, Kaufman M, Magielski J, Decampo D, Glatts C, Kruger H, McCarthy M, McKee JL, Mercurio J, Padmanabhan V, Sullivan K, Tefft S, Thalwitzer K, Vaidiswaran P, Xian J, Chao HT, Demarest S, Grinspan Z, Miele A, Goss J, Son Rigby C, Prosser B, Boland M, Helbig I STXBP1-Related Disorder: Prospective Natural History and Reconstruction , AES, Los Angeles, CA: 2024
McKee JL, Tefft S, Toib J, Ruggerio S, Coyne J, Pierce S, Cunningham K, Harrison A, Cohen S, Sullivan K, Kaufman M, Magielski J, Decampo D, Glatts C, Kruger H, McCarthy M, Mercurio J, Padmanabhan V, Vaidiswaran P, Graglia M, Helde K, Boland M, Helbig I Delineating the Natural History of SYNGAP1-related Disorders , AES, Los Angeles, CA: 2024
Virkler A, McKee JL, Magielski J, Kaufman M, Helbig I, Kennedy BC Assessing the Impact of Corpus Callosotomy in Pediatric Epilepsy , AES, Los Angeles, CA: 2024
Wulsin A, McKee JL, Magielski J, Ruggerio S, Krueger DA, Helbig I Genotype-Phenotype Correlations in Tuberous Sclerosis-Related Epilepsy: A Study of Patients with TSC2 Variants Using Reconstructed Medical Records , AES, Los Angeles, CA: 2024
Mercurio J, Prentice A, Tefft S, Kaufman M, Magielski J, Cohen S, McKee JL, Ruggerio S, Pillai A, McGarry L, Goldberg EM, Helbig I Harmonizing Reconstructed Longitudinal Clinical and Genomic Data for SCN1A-Related Disorders , AES, Los Angeles, CA: 2024
Galer P, McKee JL, Ruggerio S, Kaufman M, Mcsalley I, Ganesan S, Ojemann W, Pattnaik A, Gonzalez A, Litt B, Helbig I, Conrad E Genetic Epilepsies Demonstrate Distinct Electrographic Signatures in STXBP1, SCN1A, and SYNGAP1 , AES, Los Angeles, CA: 2024