Article

Whole-exome sequencing reveals migraine associated novel functional variants

2021-09-16

Abstract excerpt

<title>Abstract</title> <p>Background Migraine, as the 7th most disabling neurological multi-symptomatic disease condition and 26.9% prevalence in Saudi females lacks studies on SNPs for their relation with migraine aura. Methods This study was conducted on 40 Arab ancestry young female subjects, among whom 50% cases with migraine and remaining controls were used to identify the migraine associated novels genes...

Topics

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

Identifiers and source

Literature Corpus work: 931839fb-08d1-54cf-8673-75619a61da11
DOI: 10.21203/rs.3.rs-885676/v1

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Whole-exome sequencing reveals migraine associated novel functional variantsDOI 10.21203/rs.3.rs-885676/v1Read

Genome-wide meta-analysis identifies new susceptibility loci for migraine.Semantic proximity Read

A review of migraine genetics: gathering genomic and transcriptomic factors.Semantic proximity Read

Response from Original Authors - RE: Six novel rare nonsynonymous mutations for migraine without aura identified by exome sequencing.Semantic proximity Read

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

Novel Potential Risk Loci for Migraine in the Portuguese Population.Semantic proximity Read

Six novel rare non-synonymous mutations for migraine without aura identified by exome sequencing.Semantic proximity Read

Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura.Semantic proximity Read

New and sex-specific migraine susceptibility loci identified from a multiethnic genome-wide meta-analysis.Semantic proximity Read

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

Advances in genetics of migraineSemantic proximity Read

Functional characterization of a novel PRRT2 variant found in a Portuguese patient with hemiplegic migraine.Semantic proximity Read

A phenome-wide association study reveals novel phenotypic determinants of migraine risk in the UK Biobank.Semantic proximity Read