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Article

Allelic association of juvenile absence epilepsy with a GluR5 kainate receptor gene (GRIK1) polymorphism.

American journal of medical genetics - 25 Jul 1997

Sander T, Hildmann T, Kretz R, Fürst R, Sailer U, Bauer G, Schmitz B, Beck-Mannagetta G, Wienker T F, Janz D

Abstract excerpt

Juvenile absence epilepsy (JAE) is a common subtype of idiopathic generalized epilepsy (IGE). Hereditary factors play a major role in its etiology. The important function of glutamate receptors (GluRs) in excitatory neurotransmission, synaptic plasticity, and neurodevelopment suggests their invol...

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Source

Identifiers

PMID: 9259378

Genes

GRIK1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-9259378-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

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Allelic association of juvenile absence epilepsy with a GluR5 kainate receptor gene (GRIK1) polymorphism.PMID 9259378Read ↗

Sequencing of the GRIK1 gene in patients with juvenile absence epilepsy does not reveal mutations affecting receptor structure.Semantic proximity Read ↗

Association study of GRIK1 gene polymorphisms in schizophrenia: case-control and family-based studies.Semantic proximity Read ↗

Kainate receptor subunit 1 (GRIK1) risk variants and GRIK1 deficiency were detected in the Indian ADHD probands.Semantic proximity Read ↗

Clustered mutations in the GRIK2 kainate receptor subunit gene underlie diverse neurodevelopmental disorders.Semantic proximity Read ↗

1p34.3 deletion involving GRIK3: Further clinical implication of GRIK family glutamate receptors in the pathogenesis of developmental delay.Semantic proximity Read ↗

Association study of polymorphisms in the GluR5 kainate receptor gene (GRIK1) with schizophrenia.Semantic proximity Read ↗

Wide-ranging behavioral dysfunction in two mouse models of pathological human variants in the <i>GRIK2</i> kainate receptor geneSemantic proximity Read ↗

Role of GRM4 in idiopathic generalized epilepsies analysed by genetic association and sequence analysis.Semantic proximity Read ↗

The phenotypic spectrum related to the human epilepsy susceptibility gene "EJM1".Semantic proximity Read ↗

Glutamate AMPA receptor subunit 1 gene (GRIA1) and DSM-IV-TR schizophrenia: a pilot case-control association study in an Italian sample.Semantic proximity Read ↗

Clinical and therapeutic significance of genetic variation in the GRIN gene family encoding NMDARs.Semantic proximity Read ↗

Candidate gene analysis of the human metabotropic glutamate receptor type 4 (GRM4) in patients with juvenile myoclonic epilepsy.Semantic proximity Read ↗

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