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

No association between catechol-O-methyltransferase polymorphisms and neurotic disorders among mainland Chinese university students.

Psychiatry research - 30 Jul 2012

Kou Changgui, Meng Xiangfei, Xie Bing, Shi Jieping, Yu Qiong, Yu Yaqin, D'Arcy Carl

Abstract excerpt

This study investigates the genetic association between catechol-O-methyltransferase (COMT) gene polymorphisms and neurotic disorders. Data were derived from a case-control association study of 255 undergraduates affected by neurotic disorders and 269 matched healthy undergraduate controls. The p...

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 Case-Control Studies
Share to Catechol O-Methyltransferase

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Association Studies

Share to Neurotic Disorders

Share to Polymorphism, Single Nucleotide

Share to Students

Share to Universities

Source

Identifiers

PMID: 22401966
DOI: 10.1016/j.psychres.2011.10.020

Genes

COMT

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-22401966-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

No association between catechol-O-methyltransferase polymorphisms and neurotic disorders among mainland Chinese university students.PMID 22401966Read ↗

The catechol-O-methyl transferase (COMT) gene and its potential association with schizophrenia: findings from a large German case-control and family-based sample.Semantic proximity Read ↗

No association of catechol-O-methyltransferase polymorphisms with schizophrenia in the Han Chinese population.Semantic proximity Read ↗

Identification of a BglI polymorphism of catechol-O-methyltransferase (COMT) gene, and association study with schizophrenia.Semantic proximity Read ↗

Association study of catechol-O-methyltransferase gene polymorphisms with schizophrenia and psychopathological symptoms in Han Chinese.Semantic proximity Read ↗

Low activity allele of catechol-o-methyltransferase gene and Japanese unipolar depression.Semantic proximity Read ↗

No associations exist between five functional polymorphisms in the catechol-O-methyltransferase gene and schizophrenia in a Japanese population.Semantic proximity Read ↗

Catechol-O-methyltransferase genetic variant associated with the risk of Alzheimer's disease in a Brazilian population.Semantic proximity Read ↗

In Silico Prediction of the Effects of Nonsynonymous Single Nucleotide Polymorphisms in the Human Catechol-O-Methyltransferase (COMT) Gene.Semantic proximity Read ↗

Human catechol-O-methyltransferase pharmacogenetics: description of a functional polymorphism and its potential application to neuropsychiatric disorders.Semantic proximity Read ↗

Association of catechol-O-methyltransferase gene polymorphisms with schizophrenia and negative symptoms in a Chinese population.Semantic proximity Read ↗

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

Association study between high and low activity polymorphism of catechol-O-methyltransferase gene and alcoholismSemantic proximity Read ↗

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