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Article

A new single-nucleotide mutation (rs362719) of the reelin (RELN) gene associated with schizophrenia in female Chinese Han.

Genetics and molecular research : GMR - 1 Jan 2011

Kuang W J, Sun R F, Zhu Y S, Li S B

Abstract excerpt

Reelin is an extracellular signaling protein that plays an important role in the development of the central nervous system. Post-mortem studies have shown lower reelin protein levels in the brains of patients with schizophrenia and bipolar disorder compared with controls. Genetic studies have also shown that mutations in the reelin gene (RELN) increase the risk for schizophrenia and bipolar disorder. We evaluated...

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Identifiers

PMID: 21863557
DOI: 10.4238/vol10-3gmr1343

Genes

RELN

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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A new single-nucleotide mutation (rs362719) of the reelin (RELN) gene associated with schizophrenia in female Chinese Han.PMID 21863557Read ↗

Association study of RELN polymorphisms with schizophrenia in Han Chinese population.Semantic proximity Read ↗

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The genetic variation of RELN expression in schizophrenia and bipolar disorder.Semantic proximity Read ↗

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Further evidence for the association between LRP8 and schizophrenia.Semantic proximity Read ↗

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

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Analysis of common genetic variants identifies RELN as a risk gene for schizophrenia in Chinese population.Semantic proximity Read ↗

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