Rare and common variants analysis of the EMB gene in patients with schizophrenia.

doi:10.1186/s12888-020-02513-3

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

Community

Back to search

Article

Rare and common variants analysis of the EMB gene in patients with schizophrenia.

BMC psychiatry - 25 Mar 2020

Zhou Juan, Ma Chuanchuan, Wang Ke, Li Xiuli, Zhang Han, Chen Jianhua, Li Zhiqiang, Shi Yongyong

Abstract excerpt

BACKGROUND: Recent genome-wide association study showed rs10940346 locus near EMB gene was significantly associated with schizophrenia and suggested that EMB gene is one of the potentially causal genes for schizophrenia, but no causal variant has been identified. Our study aims to further verify EMB gene is a susceptibility gene for schizophrenia and to identify potentially causal variants in EMB gene that lead...

Read the complete abstract on PubMed

Topics

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

Share to Asian People

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Case-Control Studies

Share to Genetic Predisposition to Disease

Share to Genome-Wide Association Study

Share to Membrane Glycoproteins

Share to Molecular Chaperones

Share to Polymorphism, Single Nucleotide

Share to Schizophrenia

Source

Open in PubMed Open full text

Identifiers

PMID: 32213169
DOI: 10.1186/s12888-020-02513-3
PMCID: PMC7093976

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Rare and common variants analysis of the EMB gene in patients with schizophrenia.PMID 32213169Read ↗

Genome-wide burden of deleterious coding variants increased in schizophrenia.Semantic proximity Read ↗

Rare variants are common in schizophrenia.Semantic proximity Read ↗

Increased exonic de novo mutation rate in individuals with schizophrenia.Semantic proximity Read ↗

Rare PDCD11 variations are not associated with risk of schizophrenia in Japan.Semantic proximity Read ↗

Genome-wide association study with the risk of schizophrenia in a Korean population.Semantic proximity Read ↗

Exome sequencing in 53 sporadic cases of schizophrenia identifies 18 putative candidate genes.Semantic proximity Read ↗

Rare truncating variations and risk of schizophrenia: Whole-exome sequencing in three families with affected siblings and a three-stage follow-up study in a Japanese population.Semantic proximity Read ↗

Genome-wide tandem repeat expansions contribute to schizophrenia riskSemantic proximity Read ↗

Association study of a new schizophrenia susceptibility locus of 10q24.32-33 in a Han Chinese population.Semantic proximity Read ↗

Genome-wide tandem repeat expansions contribute to schizophrenia risk.Semantic proximity Read ↗

Non-synonymous variants in the AMACR gene are associated with schizophrenia.Semantic proximity Read ↗

Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia.Semantic proximity Read ↗

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