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

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

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

Liu Jun, Yang Aiping, Zhang Qunwei, Yang Guohui, Yang Wenjun, Lei Heyue, Quan Jianjun, Qu Fei, Wang Min, Zhang Zengyu, Yu Ke

Abstract excerpt

The solute carrier family 25 (aspartate/glutamate carrier), member 12 gene (SLC25A12) has been strongly posed as a candidate gene for autism spectrum disorder (ASD) given its important role in mitochondrial function and adenosine triphosphate (ATP) synthesis. Evidence is mounting for the association between SLC25A12 variants (rs2056202 and rs2292813) and ASD risk, but the results are inconsistent. To clarify the...

Read the complete abstract on PubMed

Topics

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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

Share to Autism Spectrum Disorder
Share to Genetic Association Studies
Share to Genetic Heterogeneity
Share to Haplotypes
Share to Mitochondrial Membrane Transport Proteins
Share to Polymorphism, Single Nucleotide
Share to Publication Bias
Share to Risk Factors

Source

Identifiers

PMID: 25921325
DOI: 10.1002/ajmg.b.32304

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

Association between genetic variants in SLC25A12 and risk of autism spectrum disorders: An integrated meta-analysis.PMID 25921325Read ↗

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

Association study of the SLC25A12 gene and autism in Han Chinese in Taiwan.Semantic proximity Read ↗

Mitochondrial aspartate/glutamate carrier SLC25A12 gene is associated with autism.Semantic proximity Read ↗

A Study of Genetic Variants in Genes of Glutamate Signaling and Risk of Childhood Autism Spectrum DisorderSemantic proximity Read ↗

A Study of Genetic Variants in Genes of Glutamate Signaling and Risk of Childhood Autism Spectrum DisorderSemantic proximity Read ↗

Genetics of autism spectrum disorder: an umbrella review of systematic reviews and meta-analyses.Semantic proximity Read ↗

Linkage and association of the mitochondrial aspartate/glutamate carrier SLC25A12 gene with autism.Semantic proximity Read ↗

Confirmation of association between autism and the mitochondrial aspartate/glutamate carrier SLC25A12 gene on chromosome 2q31.Semantic proximity Read ↗

Family-based association study identifies SNAP25 as a susceptibility gene for autism in the Han Chinese population.Semantic proximity Read ↗

Comprehensive systematic review and meta-analysis of the association between common genetic variants and autism spectrum disorder.Semantic proximity Read ↗

Synaptosome-Associated Protein 25 (SNAP25) Gene Association Analysis Revealed Risk Variants for ASD, in Iranian Population.Semantic proximity Read ↗

Single Nucleotide Polymorphisms in SLC19A1 and SLC25A9 Are Associated with Childhood Autism Spectrum Disorder in the Chinese Han Population.Semantic proximity Read ↗

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