Academic Journal
Q2Seizure
About Seizure
Seizure is a scholarly journal published by W.B. Saunders Ltd. SCImago 2025 lists it in Q2, with an SJR of 0.826 and H-index of 110.
Coverage: 1992-2026. Research categories: Medicine (miscellaneous) (Q2); Neurology (Q2); Neurology (clinical) (Q2).
Source-backed journal facts
Topics in published research
Epilepsy research and treatment; Pharmacological Effects and Toxicity Studies; Psychosomatic Disorders and Their Treatments; Neuroscience and Neuropharmacology Research; EEG and Brain-Computer Interfaces; Neurological disorders and treatments.
OpenAlex classifies topics from published works. These topics are not the publisher’s official aims and scope.
Reported open-access list prices
2,970.00 USD; 2,780.00 EUR; 2,380.00 GBP; 368,370.00 JPY
APC list prices reported by OpenAlex, which obtains this information from DOAJ. Confirm current charges, taxes, waivers and eligibility with the publisher; this is not a fee quotation.
Source: OpenAlex source record. Retrieved 2026-10-03. Source record updated 2026-10-02. OpenAlex metrics are different from SCImago metrics and the Clarivate Journal Impact Factor.
Journal Metrics
Quartile, SJR and the listed SCImago H-index use the 2025 imported SCImago dataset. A quartile may vary by subject category. Values without a source or reporting year are unverified historical entries. Verify the current Journal Impact Factor with Clarivate or the publisher before using it.
Aims & Scope
The publisher’s official aims and scope have not yet been verified for this profile. Use the journal website to check subject fit and accepted article types before submitting.
Recent Research Articles
Latest publications matched automatically by ISSN.
Artificial intelligence in epilepsy diagnosis: Clinical readiness, failure modes, and standards for Implementation
Juan Manuel Escobar-Montalvo, Ana Maria Torres, Fredy Escobar-Ipuz, Jorge Mateo et al.
2026-12 · DOI: 10.1016/j.seizure.2026.09.013Electrophysiological characteristics and syndrome specificity of generalized paroxysmal fast activity in genetic generalized epilepsy
Haipo Yang, Xiaoyan Liu, Jiaoyang Lu, Chenlu Jia et al.
2026-12 · DOI: 10.1016/j.seizure.2026.09.014A qualitative study of the barriers and enablers to antiseizure medication adherence in children with epilepsy
Eric Amankona Abrefa Kyeremaa, Andy Stewart, Caroline Smith, Charlotte Lawthom et al.
2026-12 · DOI: 10.1016/j.seizure.2026.09.022A novel CUL4B missense variant in a Chinese family with cabezas syndrome and epilepsy: A case report
Jinghan Gao, Jingli Wang, Zhiguo Yin, Shiguo Liu et al.
2026-12 · DOI: 10.1016/j.seizure.2026.09.017Expanding the epilepsy spectrum in primary coenzyme Q10 deficiency with COQ4 variants - Case series and literature review
Ju-Yin Hou, I-Jun Chou, Cheng-Yen Kuo, Kuang-Lin Lin et al.
2026-12 · DOI: 10.1016/j.seizure.2026.09.020Epilepsy phenotypes and Alzheimer’s disease biomarkers in adults with down syndrome: beyond diagnostic codes
Giuseppe d’Orsi
2026-12 · DOI: 10.1016/j.seizure.2026.09.024Tear fluid CGRP changes in epilepsy – evidence from an exploratory pilot study
Cem Thunstedt, Selina Trapp, Katharina Kamm, Ruth Ruscheweyh et al.
2026-12 · DOI: 10.1016/j.seizure.2026.09.019Electroencephalographic and neuroimaging prognosticators in pediatric FIRES with claustrum lesions: A 21-case retrospective study
Xiaodi Han, Changhong Ren, Weihua Zhang, Jiuwei Li et al.
2026-11 · DOI: 10.1016/j.seizure.2026.08.019Age-stratified interictal epileptiform discharges in SCN1A-related epilepsy: Association with early sodium channel-blocking antiseizure medication exposure
Samaneh Esteghamat, Mahmoud Mohammadi, Zahra Rezaei, Sedighe Nikbakht et al.
2026-11 · DOI: 10.1016/j.seizure.2026.07.028Late-onset unprovoked seizures and subsequent risk of dementia in older adults: A target trial emulation
Anderson Matheus Pereira da Silva, Daniel Vicente de Siqueira Lima, Leonardo Januario Campos Cardoso, Gabriel Caruso Novaes Tudella et al.
2026-11 · DOI: 10.1016/j.seizure.2026.08.026Phenotype-driven response to sodium channel blockers in neonatal and infantile genetic epilepsies with tonic seizures
Evelina Carapancea, Benoit Semal, Nathalie Mercier, Rosa Pugliano et al.
2026-11 · DOI: 10.1016/j.seizure.2026.08.028Anatomical and functional alterations in patients with functional/dissociative seizures and posttraumatic stress disorders
Clélia Galmiche, Louise Tyvaert, Pierre Fauvé, Cyril Husson et al.
2026-11 · DOI: 10.1016/j.seizure.2026.08.025Epilepsy and subsequent dementia in adults with down syndrome: a propensity score–matched cohort study using federated electronic health records
Anderson Matheus Pereira da Silva, Gabriel Caruso Novaes Tudella, Alice Mi Lee, Diogo Haddad Santos et al.
2026-11 · DOI: 10.1016/j.seizure.2026.08.023Deep brain stimulation outcomes in pediatric drug-resistant epilepsy: A systematic review and meta-analysis
Asmaa Mhanna, Michael A. Ciliberto, Sreenath Thati Ganganna, Brian J Dlouhy et al.
2026-11 · DOI: 10.1016/j.seizure.2026.09.009Non-convulsive status epilepticus is not a benign entity: The etiology determines mortality and its form of presentation predicts the functional prognosis
Alfonso Canabal-Berlanga, Isabel Magaña, Claudia Alvargonzález, Marta Sánchez et al.
2026-11 · DOI: 10.1016/j.seizure.2026.08.006Photosensitive absence seizures: a rare endophenotype with clinical and prognostic implications
Rodi Sari Polat, Ozgu Kizek, Pinar Topaloğlu, Ferda Uslu et al.
2026-11 · DOI: 10.1016/j.seizure.2026.09.010A novel SEMA6B splice-site variant (c.1680-2A>G) causes incompletely penetrant epilepsy via diverse aberrant transcripts
Shuyao Zhu, Jin Wang, Zemin Luo, Ping Zhou et al.
2026-11 · DOI: 10.1016/j.seizure.2026.08.015Expanding the clinical spectrum of ARV1-related disease beyond classical developmental and epileptic encephalopathy
Raneem H. Alghamdi, Alanoud Almatrafi, Hesham Aldhalaan, Sameena Khan et al.
2026-11 · DOI: 10.1016/j.seizure.2026.08.017A clinical nomogram for predicting drug-resistant epilepsy and its long-term persistence in children: a cohort study
Ohcheol Kwon, Yun Sung Nam, Hyun-Jin Kim, Hye-Ryun Yeh et al.
2026-11 · DOI: 10.1016/j.seizure.2026.07.021Genetic backround of developmental and epileptic encephalopathies is wider than monogenic aetiologies: Clinical and prognostic implications
Mario Mastrangelo, Francesco Pisani
2026-11 · DOI: 10.1016/j.seizure.2026.08.010Reviews
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October 2, 2026 at 8:47 pm
October 2, 2026