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

Evidence for association between Disrupted-in-Schizophrenia 1 (DISC1) gene polymorphisms and autism in Chinese Han population: a family-based association study.

Behavioral and brain functions : BBF - 15 May 2011

Zheng Fanfan, Wang Lifang, Jia Meixiang, Yue Weihua, Ruan Yan, Lu Tianlan, Liu Jing, Li Jun, Zhang Dai

Abstract excerpt

BACKGROUND: Disrupted-in-Schizophrenia 1 (DISC1) gene is one of the most promising candidate genes for major mental disorders. In a previous study, a Finnish group demonstrated that DISC1 polymorphisms were associated with autism and Asperger syndrome. However, the results were not replicated in Korean population. To determine whether DISC1 is associated with autism in Chinese Han population, we performed a...

Read the complete abstract on PubMed

Topics

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

Share to Asian People
Share to Autistic Disorder

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Child, Preschool

Share to Family

Share to Genetic Association Studies

Share to Haplotypes

Share to Nerve Tissue Proteins

Source

Open in PubMed Open full text

Identifiers

PMID: 21569632
DOI: 10.1186/1744-9081-7-14
PMCID: PMC3113723

Genes

DISC1

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

Evidence for association between Disrupted-in-Schizophrenia 1 (DISC1) gene polymorphisms and autism in Chinese Han population: a family-based association study.PMID 21569632Read ↗

Case-control association study of Disrupted-in-Schizophrenia-1 (DISC1) gene and schizophrenia in the Chinese population.Semantic proximity Read ↗

Limited association between Disrupted in Schizophrenia 1 (DISC1) gene and bipolar disorder in the Chinese population.Semantic proximity Read ↗

Positive association of the Disrupted-in-Schizophrenia-1 gene (DISC1) with schizophrenia in the Chinese Han population.Semantic proximity Read ↗

Gene polymorphisms of DISC1 is associated with schizophrenia: Evidence from a meta-analysis.Semantic proximity Read ↗

Association between variations in the disrupted in schizophrenia 1 gene and schizophrenia: A meta-analysis.Semantic proximity Read ↗

Association between genes of Disrupted in schizophrenia 1 (DISC1) interactors and schizophrenia supports the role of the DISC1 pathway in the etiology of major mental illnesses.Semantic proximity Read ↗

Schizophrenia in translation: disrupted in schizophrenia (DISC1): integrating clinical and basic findings.Semantic proximity Read ↗

Disrupted in schizophrenia 1 (DISC1): association with schizophrenia, schizoaffective disorder, and bipolar disorder.Semantic proximity Read ↗

Disrupted‐in‐Schizophrenia‐1 (DISC1)Semantic proximity Read ↗

Disrupted-in-Schizophrenia-1 (DISC1) protein disturbs neural function in multiple disease-risk pathways.Semantic proximity Read ↗

Association analysis of the DISC1 gene with schizophrenia in the Japanese population and DISC1 immunoreactivity in the postmortem brain.Semantic proximity Read ↗

Association study of DISC1 genetic variants with the risk of schizophrenia.Semantic proximity Read ↗

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