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

Failure to confirm an association between the PLXNA2 gene and schizophrenia in a Japanese population.

Progress in neuro-psychopharmacology & biological psychiatry - 9 May 2007

Fujii Takashi, Iijima Yoshimi, Kondo Hitomi, Shizuno Tomoko, Hori Hiroaki, Nakabayashi Tetsuo, Arima Kunimasa, Saitoh Osamu, Kunugi Hiroshi

Abstract excerpt

Plexins are receptors for multiple classes of semaphorins, either alone or in combination with neuropilins. Plexins participate in many cellular events that include axonal repulsion, axonal attraction, cell migration, axon pruning, and synaptic plasticity. PLXNA2 maps to chromosome 1q32. Several linkage studies reported schizophrenia susceptibility loci in the 1q22-42 region. A recent study reported that intronic...

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to Chi-Square Distribution

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Gene Frequency

Share to Nerve Tissue Proteins

Share to Polymorphism, Single Nucleotide

Share to Receptors, Cell Surface

Share to Schizophrenia

Source

Identifiers

PMID: 17346868
DOI: 10.1016/j.pnpbp.2007.01.027

Genes

PLXNA2

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

Failure to confirm an association between the PLXNA2 gene and schizophrenia in a Japanese population.PMID 17346868Read ↗

Genetic examination of the PLXNA2 gene in Japanese and Chinese people with schizophrenia.Semantic proximity Read ↗

Identification of the semaphorin receptor PLXNA2 as a candidate for susceptibility to schizophrenia.Semantic proximity Read ↗

Failure to confirm genetic association of the FXYD6 gene with schizophrenia: the Japanese population and meta-analysis.Semantic proximity Read ↗

Possible association of the semaphorin 3D gene (SEMA3D) with schizophrenia.Semantic proximity Read ↗

No association between the PTGS2/PLA2G4A locus and schizophrenia in a Chinese population.Semantic proximity Read ↗

Lack of a genetic association between the TNXB locus and schizophrenia in a Chinese population.Semantic proximity Read ↗

No genetic association between the SLC1A2 gene and Japanese patients with schizophrenia.Semantic proximity Read ↗

No association between tagging SNPs of SNARE complex genes (STX1A, VAMP2 and SNAP25) and schizophrenia in a Japanese population.Semantic proximity Read ↗

No evidence for an association between variants at the gamma-amino-n-butyric acid type A receptor beta2 locus and schizophrenia.Semantic proximity Read ↗

Association analysis of a functional variant in ATXN2 with schizophrenia.Semantic proximity Read ↗

Association of NKAPL, TSPAN18, and MPC2 gene variants with schizophrenia based on new data and a meta-analysis in Han Chinese.Semantic proximity Read ↗

Genetic association analysis of tagging SNPs in alpha4 and beta2 subunits of neuronal nicotinic acetylcholine receptor genes (CHRNA4 and CHRNB2) with schizophrenia in the Japanese population.Semantic proximity Read ↗

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