Back to search

Article

Rare risk variants associate with epigenetic dysregulation in migraine

2021-12-21

Abstract excerpt

<h4>ABSTRACT</h4> Migraine has a heritability of up to 65%. Genome-wide association studies (GWAS) on migraine have identified 123 risk loci, explaining only 10.6% of migraine heritability. Thus, there is a considerable genetic component not identified with GWAS. Further, the causality of the identified risk loci remains inconclusive. Rare variants contribute to the risk of migraine but GWAS are often underpowered...

Topics

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

Identifiers and source

Literature Corpus work
fed6fa26-d722-5883-bbd9-e62a0b372fc7
DOI
10.1101/2021.12.20.21268001
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Rare risk variants associate with epigenetic dysregulation in migraineDOI 10.1101/2021.12.20.21268001
Select a neighboring publication to make it the new centre.