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 of Reelin gene polymorphisms with autism.

Genomics - 1 Jan 2006

Serajee Fatema J, Zhong Hailang, Mahbubul Huq A H M

Abstract excerpt

Genome scans indicate a linkage of autism to the chromosome 7q21-q36 region. Recent studies suggest that the Reelin gene may be one of the loci contributing to the positive linkage between chromosome 7q and autism. However, these studies were relatively small scale, using a few markers in the gene. We investigated 34 single nucleotide polymorphisms (SNPs) in the Reelin gene with an average spacing between the...

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 Cell Adhesion Molecules, Neuronal
Share to Chromosomes, Human, Pair 7

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Extracellular Matrix Proteins

Share to Introns

Share to Nerve Tissue Proteins

Share to Reelin Protein

Share to Serine Endopeptidases

Source

Identifiers

PMID: 16311013
DOI: 10.1016/j.ygeno.2005.09.008

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 of Reelin gene polymorphisms with autism.PMID 16311013Read ↗

Genetic analysis of reelin gene (RELN) SNPs: no association with autism spectrum disorder in the Indian population.Semantic proximity Read ↗

Analysis of reelin as a candidate gene for autism.Semantic proximity Read ↗

Association of Allelic Variants of the Reelin Gene with Autistic Spectrum Disorder: A Systematic Review and Meta-Analysis of Candidate Gene Association Studies.Semantic proximity Read ↗

Reelin gene variants and risk of autism spectrum disorders: an integrated meta-analysis.Semantic proximity Read ↗

Analysis of the RELN gene as a genetic risk factor for autism.Semantic proximity Read ↗

Reelin gene alleles and susceptibility to autism spectrum disorders.Semantic proximity Read ↗

Reelin gene polymorphisms in the Indian population: a possible paternal 5'UTR-CGG-repeat-allele effect on autism.Semantic proximity Read ↗

Absence of association between a polymorphic GGC repeat in the 5' untranslated region of the reelin gene and autism.Semantic proximity Read ↗

RELN gene polymorphisms and susceptibility to autism in Chinese Han population.Semantic proximity Read ↗

Alleles of a reelin CGG repeat do not convey liability to autism in a sample from the CPEA network.Semantic proximity Read ↗

Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder.Semantic proximity Read ↗

Association analysis of two single-nucleotide polymorphisms of the RELN gene with autism in the South African population.Semantic proximity Read ↗

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