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

Association study on tardive dyskinesia and polymorphisms in COMT and MAOA in Chinese population.

Psychiatric genetics - 1 Aug 2013

Li Hui, Tan Yunlong, Wang Zhiren, Yang Fude, Zuo Lingjun, Luo Xingguang

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Aged
Share to Asian People
Share to Catechol O-Methyltransferase
Share to China

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Association Studies

Share to Monoamine Oxidase

Share to Movement Disorders

Share to Polymorphism, Genetic

Source

Identifiers

PMID: 23344637
DOI: 10.1097/YPG.0b013e32835e8df6

Genes

COMT
MAOA

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Association study on tardive dyskinesia and polymorphisms in COMT and MAOA in Chinese population.PMID 23344637Read ↗

Antipsychotic-induced tardive dyskinesia and polymorphic variations in COMT, DRD2, CYP1A2 and MnSOD genes: a meta-analysis of pharmacogenetic interactions.Semantic proximity Read ↗

Catechol-O-methyltransferase and Parkinson's disease.Semantic proximity Read ↗

Tardive dyskinesia is not associated with the polymorphisms of 5-HT2A receptor gene, serotonin transporter gene and catechol-<i>o</i>-methyltransferase gene <sup>⋆</sup>Semantic proximity Read ↗

[Genetic polymorphism of COMT in mental disorders].Semantic proximity Read ↗

Association of Catechol-O-Methyltransferase and monoamine oxidase B gene polymorphisms with motor complications in parkinson's disease in a Chinese population.Semantic proximity Read ↗

Association study of tardive dyskinesia and five DRD4 polymorphisms in schizophrenia patientsSemantic proximity Read ↗

Association of TaqI A polymorphism of dopamine D2 receptor gene and tardive dyskinesia in schizophrenia.Semantic proximity Read ↗

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

Associations between Catechol-O-methyltransferase (COMT) polymorphisms and cognitive impairments, psychiatric symptoms and tardive dyskinesia in schizophrenia.Semantic proximity Read ↗

Pharmacogenetics of tardive dyskinesia: an updated review of the literature.Semantic proximity Read ↗

Negative association between catechol-O-methyltransferase (COMT) gene Val158Met polymorphism and persistent tardive dyskinesia in schizophrenia.Semantic proximity Read ↗

Association between a COMT polymorphism and clinical response to risperidone treatment: a pharmacogenetic study.Semantic proximity Read ↗

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