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

The NADH-ubiquinone oxidoreductase 1 alpha subcomplex 5 (NDUFA5) gene variants are associated with autism.

Acta psychiatrica Scandinavica - 1 Feb 2011

Marui T, Funatogawa I, Koishi S, Yamamoto K, Matsumoto H, Hashimoto O, Jinde S, Nishida H, Sugiyama T, Kasai K, Watanabe K, Kano Y, Kato N

Abstract excerpt

OBJECTIVE: Autism appears to have a strong genetic component. The product of the NADH-ubiquinone oxidoreductase 1 alpha subcomplex 5 (NDUFA5) gene is included in the mitochondrial electron transport chain. METHOD: We performed a case-control study of 235 patients with autism and 214 controls and examined three single-nucleotide polymorphisms (SNPs) within this gene in a Japanese population. We then conducted a...

Read the complete abstract on PubMed

Topics

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

Share to Autistic Disorder
Share to Case-Control Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Child, Preschool

Share to Genetic Association Studies

Share to Genetic Linkage

Share to Haplotypes

Share to NADH Dehydrogenase

Share to Young Adult

Source

Identifiers

PMID: 20825370
DOI: 10.1111/j.1600-0447.2010.01600.x

Genes

NDUFA5

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

The NADH-ubiquinone oxidoreductase 1 alpha subcomplex 5 (NDUFA5) gene variants are associated with autism.PMID 20825370Read ↗

Next Generation Sequencing Mitochondrial DNA Analysis in Autism Spectrum Disorder.Semantic proximity Read ↗

Phenotypic Heterogeneity in Patients with Mutations in the Mitochondrial Complex I Assembly Gene NDUFAF5.Semantic proximity Read ↗

Brain region-specific altered expression and association of mitochondria-related genes in autismSemantic proximity Read ↗

Dysfunction in Mitochondrial Electron Transport Chain Complex I, Pyruvate Dehydrogenase Activity, and Mutations in ND1 and ND4 Gene in Autism Spectrum Disorder Subjects from Tamil Nadu Population, India.Semantic proximity Read ↗

Association of MT-ND5 gene variation with mitochondrial respiratory control ratio and NADH dehydrogenase activity in Tibet chicken embryos.Semantic proximity Read ↗

Systematic association studies of mitochondrial DNA variations in schizophrenia: focus on the ND5 gene.Semantic proximity Read ↗

Association between genetic variants in SLC25A12 and risk of autism spectrum disorders: An integrated meta-analysis.Semantic proximity Read ↗

Mitochondrial Aspartate/Glutamate Carrier SLC25A12 and Autism Spectrum Disorder: a Meta-Analysis.Semantic proximity Read ↗

The causative variants of amyloidosis in the autism.Semantic proximity Read ↗

Difference in mitochondrial DNA copy number in peripheral blood cells between probands with autism spectrum disorders and their unaffected siblings.Semantic proximity Read ↗

Association of mitochondrial complex I subunit gene NDUFV2 at 18p11 with schizophrenia in the Japanese population.Semantic proximity Read ↗

Transmission disequilibrium mapping at the serotonin transporter gene (SLC6A4) region in autistic disorderSemantic proximity Read ↗

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