Selected Publications
Vizcarra JA, Yarlagadda S, Xie K, Ellis CA, Spindler M, Hammer LH.: Artificial Intelligence in the Diagnosis and Quantitative Phenotyping of Hyperkinetic Movement Disorders: A Systematic Review J Clin Med 13 : 7009,2024.
Ellis CA, Oliver KL, Harris RV, Ottman R, Scheffer IE, Mefford HC, Epstein MP, Berkovic SF, Bahlo M.: Inflation of polygenic risk scores caused by sample overlap and relatedness: Examples of a major risk of bias Am J Hum Genet 111 : 1805-1809,2024.
Chen S, Abou-Khalil BW, Afawi Z, Ali QZ, Amadori E, Anderson A, Anderson J, Andrade DM, Annesi G, Arslan M, Auce P, Bahlo M, Baker MD, Balagura G, Balestrini S, Banks E, Barba C, Barboza K, Bartolomei F, Bass N, Baum LW, Baumgartner TH, Baykan B, Bebek N, Becker F, Bennett CA, Beydoun A, Bianchini C, Bisulli F, Blackwood D, Blatt I, Borggräfe I, Bosselmann C, Braatz V, Brand H, Brockmann K, Buono RJ, Busch RM, Caglayan SH, Canafoglia L, Canavati C, Castellotti B, Cavalleri GL, Cerrato F, Chassoux F, Cherian C, Cherny SS, Cheung CL, Chou IJ, Chung SK, Churchhouse C, Ciullo V, Clark PO, Cole AJ, Cosico M, Cossette P, Cotsapas C, Cusick C, Daly MJ, Davis LK, Jonghe P, Delanty N, Dennig D, Depondt C, Derambure P, Devinsky O, Di Vito L, Dickerson F, Dlugos DJ, Doccini V, Doherty CP, El-Naggar H, Ellis CA, Epstein L, Evans M, Faucon A, Feng YA, Ferguson L, Ferraro TN, Da Silva IF, Ferri L, Feucht M, Fields MC, Fitzgerald M, Fonferko-Shadrach B, Fortunato F, Franceschetti S, French JA, Freri E, Fu JM, Gabriel S, Gagliardi M, Gambardella A, Gauthier L, Giangregorio T, Gili T, Glauser TA, Goldberg E, Goldman A, Goldstein DB, et al.: Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes medRxiv : 2024.
Raper AC, Weathers BL, Drivas TG, Ellis CA, Kripke CM, Oyer RA, Owens AT, Verma A, Wileyto PE, Wollack CC, Zhou W, Ritchie MD, Schnoll RA, Nathanson KL.: Protocol for a type 3 hybrid implementation cluster randomized clinical trial to evaluate the effect of patient and clinician nudges to advance the use of genomic medicine across a diverse health system Implement Sci 19 : 61,2024.
Hamedani AG, Ellis CA, Ehrlich JR, Willis AW.: Interaction between visual impairment and genetic risk of dementia and psychosis in older adults Age Ageing 53 : afae163,2024.
Xie K, Ojemann WKS, Gallagher RS, Shinohara RT, Lucas A, Hill CE, Hamilton RH, Johnson KB, Roth D, Litt B, Ellis CA.: Disparities in seizure outcomes revealed by large language models J Am Med Inform Assoc 31 : 1348-1355,2024.
Baldwin A, Copeland J, Azage M, Dratch L, Johnson K, Paul RA, Amado DA, Baer M, Deik A, Elman LB, Guo M, Hamedani AG, Irwin DJ, Lasker A, Orthmann-Murphy J, Quinn CC, Tropea TF, Scherer SS, Shinohara RT, Hamilton RH, Ellis CA.: Disparities in Genetic Testing for Neurologic Disorders Neurology 102 : e209161,2024.
Oliver KL, Scheffer IE, Ellis CA, Grinton BE; Epi4K Consortium; Berkovic SF, Bahlo M.: Investigating the effect of polygenic background on epilepsy phenotype in 'monogenic' families EBioMedicine : 2024.
Galer PD, Parthasarathy S, Xian J, McKee JL, Ruggiero SM, Ganesan S, Kaufman MC, Cohen SR, Haag S, Chen C, Ojemann WKS, Kim D, Wilmarth O, Vaidiswaran P, Sederman C, Ellis CA, Gonzalez AK, Boßelmann CM, Lal D, Sederman R, Lewis-Smith D, Litt B, Helbig I.: Clinical signatures of genetic epilepsies precede diagnosis in electronic medical records of 32,000 individuals Genet Med : 2024.
Roggenbuck J, Morales A, Ellis CA, Dratch L, Stetler M, Tan CA, Bucknor B, Hatchell KE, Aradhya S, Esplin ED, Ting YL, Scherer SS.: Diagnostic and clinical utility of comprehensive multigene panel testing for patients with neuropathy J Peripher Nerv Syst : 2024.
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Academic Contact Information
University of Pennsylvania
Department of Neurology
3 West Gates Building
Philadelphia,
PA
19104
Phone: 215-349-5166
Patient appointments: 800-789-7366