Pediatric Neurology
Jillian Lee Mckee, MD
Independent provider
Accepting new patients
Sees newborns through age 18
CHOP Specialty Care, Lancaster

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

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.
Dr. Mckee is an independent physician who is not employed by Penn Medicine Lancaster General Health.

Qualifications and experience

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