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

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

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics - 5 Jan 2007

Dutta Shruti, Guhathakurta Subhrangshu, Sinha Swagata, Chatterjee Anindita, Ahmed Shabina, Ghosh Saurabh, Gangopadhyay Prasanta K, Singh Manoranjan, Usha Rajamma

Abstract excerpt

Autism is a neurodevelopmental disorder with high heritability factor and the reelin gene, which codes for an extracellular matrix protein involved with neuronal migration and lamination is being investigated as a positional and functional candidate gene for autism. It is located on chromosome 7q22 within the autism susceptible locus (AUTS1); identified in earlier genome scans and several investigations have been...

Read the complete abstract on PubMed

Topics

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

Share to 5' Untranslated Regions
Share to Autistic Disorder

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cell Adhesion Molecules, Neuronal

Share to Extracellular Matrix Proteins

Share to Fathers

Share to Mothers

Share to Reelin Protein

Share to Trinucleotide Repeats

Source

Identifiers

PMID: 16941662
DOI: 10.1002/ajmg.b.30419

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

Reelin gene polymorphisms in the Indian population: a possible paternal 5'UTR-CGG-repeat-allele effect on autism.PMID 16941662Read ↗

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

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

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

Association of Reelin gene polymorphisms with 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 ↗

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

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

Population-based and family-based association study of 5'UTR polymorphism of the reelin gene and schizophrenia.Semantic proximity Read ↗

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

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

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