Article

Pathogenic Epilepsy Gene Variant Prevalence and Penetrance Among U.S. Military Veterans in the Million Veteran Program Cohort

2026-08-21

Abstract excerpt

<h4>Background: </h4> and Objectives: Genetic causes of epilepsy are well-established in children, but the genetics of adult-onset epilepsy is not well understood. There are few studies of epilepsy genetics in older adults, U.S. military Veterans, and people with acquired causes of epilepsy like traumatic brain injury (TBI) and stroke. To test if rare gene variants that cause pediatric epilepsy are associated with...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: c7d57d25-9628-50ca-a7b7-4bf31c29c093
DOI: 10.64898/2026.08.18.26360604

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Pathogenic Epilepsy Gene Variant Prevalence and Penetrance Among U.S. Military Veterans in the Million Veteran Program CohortDOI 10.64898/2026.08.18.26360604Read

Epilepsies of presumed genetic etiology show enrichment of rare variants that occur in the general population.Semantic proximity Read

Primer Part 1-The building blocks of epilepsy genetics.Semantic proximity Read

Genetic Testing in Adult Patients With Epilepsy: Genetic Risk Index for Seizure Etiology for Identifying Optimal Candidates.Semantic proximity Read

Genetic testing and counseling for the unexplained epilepsies: An evidence‐based practice guideline of the National Society of Genetic CounselorsSemantic proximity Read

The complex etiology of Epilepsy in the Middle East: Genetic analysis and HLA associationsSemantic proximity Read

Long-term Penetrance of Disease Variants in Genes Prioritized for Genomic Newborn Screening: Evidence from Adult BiobanksSemantic proximity Read

Genetic Etiology of Epilepsy: A Retrospective Study From a Single-Center Cohort.Semantic proximity Read

Epilepsy panels in clinical practice: Yield, variants of uncertain significance, and treatment implications.Semantic proximity Read

Unraveling the role of non-coding rare variants in epilepsySemantic proximity Read

Whole-exome sequencing of a Saudi epilepsy cohort reveals association signals in known and potentially novel loci.Semantic proximity Read

Whole‐Exome Sequencing of a Saudi Epilepsy Cohort Reveals Association Signals in Known and Potentially Novel LociSemantic proximity Read

Early-Life Epilepsies and the Emerging Role of Genetic Testing.Semantic proximity Read