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 screen for nuclear mitochondrial gene associations with Parkinson's disease.

Journal of neural transmission (Vienna, Austria : 1996) - 1 Feb 2004

Mellick G D, Silburn P A, Prince J A, Brookes A J

Abstract excerpt

Genetic factors play an important role in the aetiology of Parkinson's disease (PD). We have screened nuclear genes encoding subunits of mitochondrial complex I for associations between single nucleotide polymorphisms (SNPs) and PD. Abnormal functioning of complex I is well documented in human PD...

Read the complete abstract on PubMed

Topics

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

Share to Cell Nucleus
Share to Chi-Square Distribution
Share to Confidence Intervals

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Electron Transport Complex I

Share to Hybridization, Genetic

Share to Logistic Models

Share to Odds Ratio

Share to Parkinson Disease

Source

Identifiers

PMID: 14767722
DOI: 10.1007/s00702-003-0085-8

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-14767722-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A novel screen for nuclear mitochondrial gene associations with Parkinson's disease.PMID 14767722Read ↗

Parkinson's Disease, Parkinsonisms, and Mitochondria: the Role of Nuclear and Mitochondrial DNA.Semantic proximity Read ↗

Interactions between nuclear and mitochondrial SNPs and Parkinson's disease risk.Semantic proximity Read ↗

Interactions between nuclear and mitochondrial SNPs and Parkinson’s disease riskSemantic proximity Read ↗

Population genetic approaches to neurological disease: Parkinson's disease as an example.Semantic proximity Read ↗

Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease.Semantic proximity Read ↗

NR4A2 genetic variation in sporadic Parkinson's disease: a genewide approach.Semantic proximity Read ↗

Parkinson disease: analysis of mitochondrial DNA in monozygotic twins.Semantic proximity Read ↗

Novel mutations of mitochondrial complex I in pathologically proven Parkinson disease.Semantic proximity Read ↗

Mitochondrial DNA analysis in Parkinson's diseaseSemantic proximity Read ↗

Genotype in the 24-kDa subunit gene (NDUFV2) of mitochondrial complex I and susceptibility to Parkinson disease.Semantic proximity Read ↗

Mitochondrial DNA variants modulate genetic susceptibility to Parkinson's disease in Han Chinese.Semantic proximity Read ↗

Mitochondrial transcription factor A (TFAM) gene variation in Parkinson's disease.Semantic proximity Read ↗

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