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Brain Communications|March 25, 2024
Healthcare utilization and clinical characteristics of genetic epilepsy in electronic health recordsChristian M Boßelmann, Alina Ivaniuk, Mark St John, et al.
Scientific Reports|September 17, 2020
Neurological disorder-associated genetic variants in individuals with psychogenic nonepileptic seizuresCostin Leu, Jocelyn F Bautista, Monica Sudarsanam, et al.
Epilepsy & Behavior Reports|March 4, 2022
Incidence and prevalence of major epilepsy-associated brain lesionsJavier A López-Rivera, Victoria Smuk, Costin Leu, et al.
Nature Communications|July 20, 2023
Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individualsLudovica Montanucci, David Lewis-Smith, Ryan L Collins, et al.
Bioinformatics (Oxford, England)|May 16, 2019
Variant Score Ranker-a web application for intuitive missense variant prioritizationJuanjiangmeng Du, Monica Sudarsanam, Eduardo Pérez-Palma, et al.
Human Heredity|April 2, 2010
Feasible and successful: genome-wide interaction analysis involving all 1.9 x 10(11) pair-wise interaction testsMichael Steffens, Tim Becker, Thomas Sander, et al.
Epilepsy Research|November 23, 2015
Variants in KCNJ11 and BAD do not predict response to ketogenic dietary therapies for epilepsyNatasha E Schoeler, Costin Leu, Jon White, et al.
European Journal of Human Genetics : EJHG|July 31, 2019
Assessment of genetic variant burden in epilepsy-associated brain lesionsLisa-Marie Niestroj, Patrick May, Mykyta Artomov, et al.
Epilepsia|March 26, 2026
Underutilization of syndrome-specific ICD-10 codes for genetic epilepsies: Implications for precision medicineÉmile Moura Coelho da Silva, Tobias Brünger, Gary Taylor, et al.
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