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

SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample.

European journal of human genetics : EJHG - 1 Jan 2006

Blasi Francesca, Bacchelli Elena, Carone Simona, Toma Claudio, Monaco Anthony P, Bailey Anthony J, Maestrini Elena

Abstract excerpt

Autism is a severe neurodevelopmental disorder with a complex genetic predisposition. Linkage findings from several genome scans suggest the presence of an autism susceptibility locus on chromosome 2q24-q33, making this region the focus of candidate gene and association studies. Recently, significant association with autism has been reported for single-nucleotide polymorphisms (SNPs) in the SLC25A12 and CMYA3...

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 DNA-Binding Proteins

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to International Cooperation

Share to LIM Domain Proteins

Share to Membrane Transport Proteins

Share to Mitochondrial Membrane Transport Proteins

Share to Mitochondrial Proteins

Share to Nuclear Proteins

Source

Identifiers

PMID: 16205742
DOI: 10.1038/sj.ejhg.5201444

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 11 closest

SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample.PMID 16205742Read ↗

Lack of association between autism and SLC25A12.Semantic proximity Read ↗

Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families. The International Molecular Genetic Study of Autism Consortium.Semantic proximity Read ↗

No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder.Semantic proximity Read ↗

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

Lack of association between markers in the ITGA3, ITGAV, ITGA6 and ITGB3 and autism in an Irish sample.Semantic proximity Read ↗

Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families.Semantic proximity Read ↗

NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population.Semantic proximity Read ↗

Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism.Semantic proximity Read ↗

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

Lack of association between HoxA1 and HoxB1 gene variants and autism in 110 multiplex families.Semantic proximity Read ↗

Protein kinase C-beta 1 gene variants are not associated with autism in the Irish population.Semantic proximity Read ↗

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