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

An association study between polymorphism of L1CAM gene and schizophrenia in a Japanese sample.

American journal of medical genetics - 8 Jan 2001

Kurumaji A, Nomoto H, Okano T, Toru M

Abstract excerpt

L1CAM, a neural cell adhesion molecule, plays an important role in the development of the central nervous system. The human L1CAM gene is located in Xq28. Mutations in the gene are responsible for a wide spectrum of neurological abnormalities and mental retardation. Schizophrenia may result from early neurodevelopmental abnormalities. We screened 30 male and 30 female schizophrenic patients for their genomic...

Read the complete abstract on PubMed

Topics

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

Share to Gene Order
Share to Genetic Testing
Share to Japan

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Leukocyte L1 Antigen Complex

Share to Membrane Glycoproteins

Share to Neural Cell Adhesion Molecules

Share to Polymorphism, Restriction Fragment Length

Share to Schizophrenia

Source

Identifiers

PMID: 11425011

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

An association study between polymorphism of L1CAM gene and schizophrenia in a Japanese sample.PMID 11425011Read ↗

An association between a missense polymorphism in the close homologue of L1 (CHL1, CALL) gene and schizophrenia.Semantic proximity Read ↗

L1CAM mutations in three fetuses diagnosed by medical exome sequencing.Semantic proximity Read ↗

Analysis of L1CAM gene mutation and imaging appearance in three Chinese families with L1 syndrome: Three case reports.Semantic proximity Read ↗

Case-control association study of the close homologue of L1 (CHL1) gene and schizophrenia in the Chinese population.Semantic proximity Read ↗

Evidence for Association of Cell Adhesion Molecules Pathway and NLGN1 Polymorphisms with Schizophrenia in Chinese Han Population.Semantic proximity Read ↗

Intronic mutations in the L1CAM gene may cause X-linked hydrocephalus by aberrant splicing.Semantic proximity Read ↗

A new mutation of the L1CAM gene in an X-linked hydrocephalus family.Semantic proximity Read ↗

L1CAM mutation in a Japanese family with X-linked hydrocephalus: a study for genetic counseling.Semantic proximity Read ↗

A missense mutation in the ITGA8 gene, a cell adhesion molecule gene, is associated with schizophrenia in Japanese female patients.Semantic proximity Read ↗

Comprehensive bioinformatics analysis of <i>L1CAM</i> gene revealed Novel Pathological mutations associated with L1 syndromeSemantic proximity Read ↗

Promoter variant rs2301228 on the neural cell adhesion molecule 1 gene confers risk of schizophrenia in Han Chinese.Semantic proximity Read ↗

Prenatal molecular diagnosis of a severe type of L1 syndrome (X-linked hydrocephalus).Semantic proximity Read ↗

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