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

Common variants in SLC1A2 and schizophrenia: Association and cognitive function in patients with schizophrenia and healthy individuals.

Schizophrenia research - 1 Dec 2015

Zhang Bao, Guan Fanglin, Chen Gang, Lin Huali, Zhang Tianxiao, Feng Jiali, Li Lu, Fu Dongke

Abstract excerpt

SLC1A2 is reported to be responsible for the majority of glutamate uptake, which has a crucial role in neural development and synaptic plasticity, and a disturbance in glutamatergic transmission has been suggested to be involved in the pathophysiology of schizophrenia (SCZ) and cognition. To evaluate the relationship of common variants within SLC1A2 with SCZ and cognition in Han Chinese, 28 tag SNPs were...

Read the complete abstract on PubMed

Topics

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

Share to Cognition
Share to Datasets as Topic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Excitatory Amino Acid Transporter 2

Share to Genotyping Techniques

Share to Linkage Disequilibrium

Share to Neuropsychological Tests

Share to Schizophrenia

Share to Schizophrenic Psychology

Source

Identifiers

PMID: 26459047
DOI: 10.1016/j.schres.2015.10.012

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

Common variants in SLC1A2 and schizophrenia: Association and cognitive function in patients with schizophrenia and healthy individuals.PMID 26459047Read ↗

Association of common variants in H2AFZ gene with schizophrenia and cognitive function in patients with schizophrenia.Semantic proximity Read ↗

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

Common variants in MAGI2 gene are associated with increased risk for cognitive impairment in schizophrenic patients.Semantic proximity Read ↗

Differential effects of common variants in SCN2A on general cognitive ability, brain physiology, and messenger RNA expression in schizophrenia cases and control individuals.Semantic proximity Read ↗

Cognitive Characterization of Schizophrenia Risk Variants Involved in Synaptic Transmission: Evidence of CACNA1C's Role in Working Memory.Semantic proximity Read ↗

Evaluation of association of common variants in HTR1A and HTR5A with schizophrenia and executive function.Semantic proximity Read ↗

Glutamate Networks Implicate Cognitive Impairments in Schizophrenia: Genome-Wide Association Studies of 52 Cognitive Phenotypes.Semantic proximity Read ↗

Association analysis of CHRNA3 polymorphisms with schizophrenia in a Chinese Han population: A case-control study.Semantic proximity Read ↗

Polymorphism of rs12294045 in EAAT2 gene is potentially associated with schizophrenia in Chinese Han population.Semantic proximity Read ↗

Evaluation of genetic susceptibility of common variants in CACNA1D with schizophrenia in Han Chinese.Semantic proximity Read ↗

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

The CSMD1 genome-wide associated schizophrenia risk variant rs10503253 affects general cognitive ability and executive function in healthy males.Semantic proximity Read ↗

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