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Negative / Null Result ReportOpen accessNeurology. Diseases of the nervous system

Association of SCN1A and SCN2A Gene Polymorphisms with Antiseizure Medication Responsiveness: A Case-Control Study from Eastern India

Kollipara Sumanth; Uma Sinharoy; Anindita Joardar; Sarnava Roy; Alak Pandit; Gautam Gangopadhyay · 2026 · Annals of Indian Academy of Neurology

WASTE classifies this as Negative / Null Result Report · AI classification, approximate

The study found no significant effect — useful as a negative control or null benchmark for your own design.

Abstract

Background and Objectives: Epilepsy, with its complex interplay of neurobiological, genetic, and pharmacological factors, continues to challenge neurologists worldwide—particularly in managing drug resistance. This study aimed to evaluate the frequency of the SCN1A and SCN2A gene polymorphisms among patients with epilepsy (PWE) from Eastern India to assess their relationship with clinical profiles, electroencephalography (EEG) findings, and response to antiseizure medication. Methods: In this case–control genetic association study, a total of 110 PWE were assessed for demographic and clinical

Abstract by Kollipara Sumanth; Uma Sinharoy; Anindita Joardar; Sarnava Roy; Alak Pandit; Gautam Gangopadhyay, Annals of Indian Academy of Neurology (2026) — licensed CC BY 4.0.

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Metadata source: DOAJ · DOI 10.4103/aian.aian_616_25