Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

RE: Six novel rare non-synonymous mutations for migraine without aura identified by exome sequencing.

Journal of neurogenetics - 1 Dec 2017

Albury Cassie L, Gerring Zachary F, Griffiths Lyn R, Nyholt Dale R, Rodriguez-Acevedo Astrid J

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Epilepsy
Share to Exome
Share to Genetic Predisposition to Disease
Share to Migraine without Aura

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation, Missense

Source

Identifiers

PMID: 29105529
DOI: 10.1080/01677063.2017.1382490

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

RE: Six novel rare non-synonymous mutations for migraine without aura identified by exome sequencing.PMID 29105529Read ↗

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

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

Whole-exome sequencing reveals migraine associated novel functional variantsSemantic proximity Read ↗

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

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

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

Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles.Semantic proximity Read ↗

Genome-wide association analysis identifies susceptibility loci for migraine without aura.Semantic proximity Read ↗

Migraine genetics: from genome-wide association studies to translational insights.Semantic proximity Read ↗

Genome-wide association study reveals three susceptibility loci for common migraine in the general population.Semantic proximity Read ↗

Update on the genetics of migraine.Semantic proximity Read ↗

PharmGKB summary: very important pharmacogene information for RYR1.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.