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

A cis-eQTL in AHI1 confers risk to schizophrenia in European populations.

Neuroscience letters - 6 Oct 2016

Ren Zhimin, Qiu Anli, Zhang Aiqi, Huang Lijun, Rao Shuquan

Abstract excerpt

Schizophrenia is a devastating mental disorder, with heritability as high as 80%. Although genome-wide association studies have identified multiple promising risk variants of schizophrenia, they could only explain a small portion of the disease heritability, and other variants with low to moderate effect remain to be identified. Abelson helper integration site 1 (AHI1) is highly expressed in mammals throughout...

Read the complete abstract on PubMed

Topics

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

Share to Adaptor Proteins, Signal Transducing
Share to Adaptor Proteins, Vesicular Transport

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Alleles

Share to Case-Control Studies

Share to Gene Frequency

Share to Quantitative Trait Loci

Share to Schizophrenia

Share to White People

Source

Identifiers

PMID: 27585752
DOI: 10.1016/j.neulet.2016.08.050

Genes

AHI1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A cis-eQTL in AHI1 confers risk to schizophrenia in European populations.PMID 27585752Read ↗

Fine mapping of AHI1 as a schizophrenia susceptibility gene: from association to evolutionary evidence.Semantic proximity Read ↗

A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia.Semantic proximity Read ↗

Impact of the AHI1 gene on the vulnerability to schizophrenia: a case-control association study.Semantic proximity Read ↗

Lymphoblast and brain expression of AHI1 and the novel primate-specific gene, C6orf217, in schizophrenia and bipolar disorder.Semantic proximity Read ↗

AHI1, a pivotal neurodevelopmental gene, and C6orf217 are associated with susceptibility to schizophrenia.Semantic proximity Read ↗

The influence of AHI1 variants on the diagnosis and treatment outcome in schizophrenia.Semantic proximity Read ↗

Genome-wide association study followed by trans-ancestry meta-analysis identify 17 new risk loci for schizophrenia.Semantic proximity Read ↗

Association of common variants in the Joubert syndrome gene (AHI1) with autism.Semantic proximity Read ↗

Abelson Helper Integration Site-1 Gene Variants on Major Depressive Disorder and Bipolar DisorderSemantic proximity Read ↗

Revisiting Schizophrenia from an Evolutionary Perspective: An Association Study of Recent Evolutionary Markers and Schizophrenia.Semantic proximity Read ↗

Genetic variations in evolutionary accelerated regions disrupt cognition in schizophrenia.Semantic proximity Read ↗

Integrative analyses indicate an association between ITIH3 polymorphisms with autism spectrum disorder.Semantic proximity Read ↗

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