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Article

Uncovering common genetic risk factors in migraine and epilepsy through whole exome sequencing.

Epileptic disorders : international epilepsy journal with videotape - 1 Apr 2026

Sahu Prachi, Kashyap Sohit, Kumar Anil, Munshi Anjana

Abstract excerpt

BACKGROUND: Migraine and epilepsy are distinct neurological disorders that co-occur as comorbid conditions as well. Despite their clinical differences, these disorders exhibit some overlapping symptoms and share underlying pathophysiological mechanisms driven by a common genetic contribution. AIM: The current study aimed to explore the genetic predisposition associated with epilepsy, migraine, and their...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 41386636
DOI: 10.1002/epd2.70147

Genes

SCN1A
ADGRV1
ATP1A2
COL4A1
DEPDC5
EFHC1
GABRA5
KCNMA1
KIF1A
SCN1B
SCN2A
SCN9A
SETD1B
SLC2A1
SLC6A1
STXBP1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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