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

A novel locus for familial migraine on Xp22.

Headache - 1 Jun 2010

Wieser Thomas, Pascual Julio, Oterino Agusto, Soso Michael, Barmada Michael, Gardner Kathy L

Abstract excerpt

INTRODUCTION: Migraine is thought to be genetically complex. There is evidence of an X-linked dominant genetic component. A locus at Xq24-q28 has already been described supporting this hypothesis. METHODS: The X chromosome in 61 migraine families was screened using markers spanning the entire chromosome. Alleles were assigned using the GeneScan Analysis software, analysis for affected relative allele sharing and...

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to Chromosomes, Human, X
Share to Family

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Linkage

Share to Genetic Loci

Share to Genetic Predisposition to Disease

Share to Lod Score

Share to Migraine Disorders

Source

Identifiers

PMID: 20412323
DOI: 10.1111/j.1526-4610.2010.01673.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A novel locus for familial migraine on Xp22.PMID 20412323Read ↗

Confirmation that Xq27 and Xq28 are susceptibility loci for migraine in independent pedigrees and a case-control cohort.Semantic proximity Read ↗

Evidence for an X-linked genetic component in familial typical migraine.Semantic proximity Read ↗

An X chromosome association scan of the Norfolk Island genetic isolate provides evidence for a novel migraine susceptibility locus at Xq12.Semantic proximity Read ↗

Familial typical migraine: significant linkage and localization of a gene to Xq24-28Semantic proximity Read ↗

A genome-wide scan provides evidence for loci influencing a severe heritable form of common migraine.Semantic proximity Read ↗

Consistently replicating locus linked to migraine on 10q22-q23.Semantic proximity Read ↗

Identification of a susceptibility locus for migraine with and without aura on 6p12.2-p21.1Semantic proximity Read ↗

Significant linkage to migraine with aura on chromosome 11q24.Semantic proximity Read ↗

A typical migraine susceptibility region localizes to chromosome 1q31.Semantic proximity Read ↗

A susceptibility locus for migraine with aura, on chromosome 4q24.Semantic proximity Read ↗

The STR cluster DXS10148-DXS8378-DXS10135 provides a powerful tool for X-chromosomal haplotyping at Xp22.Semantic proximity Read ↗

The association between candidate migraine susceptibility loci and severe migraine phenotype in a clinical sample.Semantic proximity Read ↗

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