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

An adenosine A2A receptor gene haplotype is associated with migraine with aura.

Cephalalgia : an international journal of headache - 1 Feb 2007

Hohoff C, Marziniak M, Lesch K P, Deckert J, Sommer C, Mössner R

Abstract excerpt

The adenosine A2A receptor A2AR facilitates effects of calcitonin gene-related peptide and vasoactive intestinal peptide, two important neuropeptides in migraine pathophysiology, and is the molecular target of caffeine, which is used in migraine treatment. We therefore determined whether A2AR gene variation might influence migraine susceptibility. Migraine patients (n = 265) with or without aura and migraine-free...

Read the complete abstract on PubMed

Topics

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

Share to Genetic Predisposition to Disease
Share to Haplotypes

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Linkage Disequilibrium

Share to Migraine and Headache Studies

Share to Migraine with Aura

Share to Polymerase Chain Reaction

Share to Polymorphism, Genetic

Share to Receptor, Adenosine A2A

Source

Identifiers

PMID: 17257240
DOI: 10.1111/j.1468-2982.2007.01254.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

An adenosine A2A receptor gene haplotype is associated with migraine with aura.PMID 17257240Read ↗

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

A genetic risk score is differentially associated with migraine with and without aura.Semantic proximity Read ↗

Inducible nitric oxide synthase haplotype associated with migraine and aura.Semantic proximity Read ↗

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

Association of the T102C polymorphism of 5-HT2A receptor gene with aura in migraine.Semantic proximity Read ↗

Haplotype-based systematic association studies of ATP1A2 in migraine with aura.Semantic proximity Read ↗

A genotype-phenotype analysis of the 8q22.1 variant in migraine with aura.Semantic proximity Read ↗

Endothelial nitric oxide synthase haplotypes associated with aura in patients with migraine.Semantic proximity Read ↗

Association between polymorphisms in the beta2-adrenoceptor gene and migraine in women.Semantic proximity Read ↗

Clinical susceptibility to migraine with aura is modified by dopamine D2 receptor (DRD2) NcoI alleles.Semantic proximity Read ↗

Genotype-phenotype correlation in migraine without aura focusing on the rs1835740 variant on 8q22.1.Semantic proximity Read ↗

Association study of the calcitonin gene-related polypeptide-alpha (CALCA) and the receptor activity modifying 1 (RAMP1) genes with migraine.Semantic proximity Read ↗

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