No evidence of association between common European mitochondrial DNA variants in Alzheimer, Parkinson, and migraine in the Spanish population.

doi:10.1002/ajmg.b.32276

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

Community

Back to search

Article

No evidence of association between common European mitochondrial DNA variants in Alzheimer, Parkinson, and migraine in the Spanish population.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics - 1 Jan 2015

Fachal Laura, Mosquera-Miguel Ana, Pastor Pau, Ortega-Cubero Sara, Lorenzo Elena, Oterino-Durán Agustín, Toriello María, Quintáns Beatriz, Camiña-Tato Montse, Sesar Angel, Vega Ana, Sobrido María-Jesús, Salas Antonio

Abstract excerpt

Certain mitochondrial DNA (mtDNA) variants and haplogroups have been found to be associated with neurological disorders. Several studies have suggested that mtDNA variation could have an etiologic role in these disorders by affecting the ATP production on high-energy demanding organs, such as the brain. We have analyzed 15 mtDNA SNPs (mtSNPs) in five cohorts of cases presenting Alzheimer disease (AD), Parkinson...

Read the complete abstract on PubMed

Topics

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

Share to Alzheimer Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA, Mitochondrial

Share to Genetic Association Studies

Share to Migraine Disorders

Share to Mitochondria

Share to Parkinson Disease

Share to Polymorphism, Single Nucleotide

Share to Spain

Source

Open in PubMed

Identifiers

PMID: 25349034
DOI: 10.1002/ajmg.b.32276

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

No evidence of association between common European mitochondrial DNA variants in Alzheimer, Parkinson, and migraine in the Spanish population.PMID 25349034Read ↗

Mitochondrial genome-wide association study of migraine - the HUNT Study.Semantic proximity Read ↗

Association between mitochondrial DNA variations and Alzheimer's disease in the ADNI cohort.Semantic proximity Read ↗

No consistent evidence for association between mtDNA variants and Alzheimer disease.Semantic proximity Read ↗

mtDNA mutations and common neurodegenerative disorders.Semantic proximity Read ↗

Is there a primary role of the mitochondrial genome in Alzheimer's disease?Semantic proximity Read ↗

Analysis of European mitochondrial haplogroups with Alzheimer disease risk.Semantic proximity Read ↗

Is Mitochondria DNA Variation a Biomarker for AD?Semantic proximity Read ↗

Association study of two genetic variants in mitochondrial transcription factor A (TFAM) in Alzheimer's and Parkinson's disease.Semantic proximity Read ↗

Role of mitochondrial DNA in longevity, aging and age-related diseases in humans: a reappraisal.Semantic proximity Read ↗

Possible association of mitochondrial transcription factor A (TFAM) genotype with sporadic Alzheimer disease.Semantic proximity Read ↗

[Research progress on mitochondrial genetic mechanisms underlying the onset of migraine].Semantic proximity Read ↗

The impact of mitochondrial and nuclear DNA variants on late-onset Alzheimer's disease risk.Semantic proximity Read ↗

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