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

Influence of MTHFR genotype on contingent negative variation and MRI abnormalities in migraine.

Headache - 1 Feb 2007

de Tommaso Marina, Difruscolo Olimpia, Sardaro Michele, Losito Luciana, Serpino Claudia, Pietrapertosa Anna, Santeramo Maria Teresa, Dicuonzo Franca, Carella Aristide, Lamberti Paolo, Livrea Paolo

Abstract excerpt

BACKGROUND: The MTHFR C677T genotype has been associated with increased risk of migraine, particularly of migraine with aura (MA) in selected clinical samples and with elevated homocysteine. The hyper-homocysteinemia may favor the vascular and neuronal mechanism underlying migraine, and the risk of stroke. OBJECTIVE: The first aim of the present study was to examine the Contingent Negative Variation (CNV)...

Read the complete abstract on PubMed

Topics

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

Share to Case-Control Studies
Share to Homocysteine

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Homozygote

Share to Magnetic Resonance Imaging

Share to Methylenetetrahydrofolate Reductase (NADPH2)

Share to Migraine Disorders

Share to Risk Factors

Share to Stroke

Source

Identifiers

PMID: 17300365
DOI: 10.1111/j.1526-4610.2006.00690.x

Genes

MTHFR

Variants

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

Influence of MTHFR genotype on contingent negative variation and MRI abnormalities in migraine.PMID 17300365Read ↗

Effects of MTHFR gene polymorphism on the clinical and electrophysiological characteristics of migraine.Semantic proximity Read ↗

The methylenetetrahydrofolate reductase gene variant C677T influences susceptibility to migraine with aura.Semantic proximity Read ↗

Search for correlations between genotypes and electrophysiological patterns in migraine: the MTHFR C677T polymorphism and visual evoked potentials.Semantic proximity Read ↗

Migraine and MTHFR C677T genotype in a population-based sample.Semantic proximity Read ↗

Frequency of the C677T variant of the methylenetetrahydrofolate reductase (MTHFR) gene in patients with migraine with or without aura - a preliminary report.Semantic proximity Read ↗

A Comprehensive Investigation into the Association Between Mthfr C677t, A1298c, and Ace I/D Variants and Risk of Migraine: an Updated Meta-Analysis of Genetic Association Studies with Trial Sequential Analysis and Meta-Regression.Semantic proximity Read ↗

Analysis of the MTHFR C677T variant with migraine phenotypesSemantic proximity Read ↗

Association of MTHFR gene polymorphisms with migraine in North Indian population.Semantic proximity Read ↗

Association of the C677T and A1298C polymorphisms in the 5,10 methylenetetrahydrofolate reductase gene in patients with migraine risk.Semantic proximity Read ↗

The homozygous C677T mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for migraine.Semantic proximity Read ↗

Interrelationships among the MTHFR 677C>T polymorphism, migraine, and cardiovascular disease.Semantic proximity Read ↗

MTHFR T677 Homozygosis Influences the Presence of Aura in MigraineursSemantic proximity Read ↗

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