ArticleJournal of clinical neurology (Seoul, Korea)2025
Genome-Wide Association Study Identifying a Novel Gene Related to a History of Febrile Convulsions in Patients With Focal Epilepsy.
Article in Journal of clinical neurology (Seoul, Korea), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed.
- Bridging the Electroclinical Paradox to Precision Care by Elucidating Seizure Network Dynamics.Journal of clinical neurology (Seoul, Korea) · 2026Article
- Article
Corrections and comments
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Authors and funding
5 authors.
Funding
Abstract
background and purposeThe risk factors for developing epilepsy following febrile convulsion (FC) have been studied extensively, but the underlying genetic components remain largely unexplored. Our objective here was to identify the risk loci related to FC through a genome-wide association study of Korean epilepsy patients.
methodsWe examined associations between a history of FC and single-nucleotide polymorphisms (SNPs) in data obtained from 125 patients with focal epilepsy: 28 with an FC history and 97 without an FC history.
resultsAmong 288,394 SNPs, 5 candidate SNPs showed
conclusionsThis novel discovery of SNPs upstream of
Indexed as
Identifiers
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Registered trials
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