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

International journal of environmental research and public health - 30 Oct 2020

Hernández-García Ignacio, Chamorro Antonio-Javier, Ternavasio-de la Vega Hugo Guillermo, Carbonell Cristina, Marcos Miguel, Mirón-Canelo José-Antonio

Abstract excerpt

Autistic spectrum disorder (ASD) is a complex neurodevelopmental disability with a genetic basis, and several studies have suggested a potential role of the reelin gene (RELN) in ASD susceptibility. Accordingly, genetic association studies have explored this potential association, but the results have been controversial thus far. For this reason, we assessed the association of four genetic variants of RELN (the...

Read the complete abstract on PubMed

Topics

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

Share to Autism Spectrum Disorder
Share to Cell Adhesion Molecules, Neuronal

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Extracellular Matrix Proteins

Share to Genetic Association Studies

Share to Nerve Tissue Proteins

Share to Reelin Protein

Share to Serine Endopeptidases

Source

Open in PubMed Open full text

Identifiers

PMID: 33143244
DOI: 10.3390/ijerph17218010
PMCID: PMC7663127

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 · 12 closest

Association of Allelic Variants of the Reelin Gene with Autistic Spectrum Disorder: A Systematic Review and Meta-Analysis of Candidate Gene Association Studies.PMID 33143244Read ↗

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

Two single-nucleotide polymorphisms of the RELN gene and symptom-based and developmental deficits among children and adolescents with autistic spectrum disorders in the Tianjin, China.Semantic proximity Read ↗

No significant association between RELN polymorphism and autism in case-control and family-based association study in Chinese Han population.Semantic proximity Read ↗

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

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

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

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

The association analysis of RELN and GRM8 genes with autistic spectrum disorder in Chinese Han population.Semantic proximity Read ↗

Meta-analyses of RELN variants in neuropsychiatric disorders.Semantic proximity Read ↗

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

Association and gene-gene interactions study of reelin signaling pathway related genes with autism in the Han Chinese population.Semantic proximity Read ↗

Polymorphisms of candidate genes in Slovak autistic patients.Semantic proximity Read ↗

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