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

Family- and population-based association studies of monoamine oxidase A and autism spectrum disorders in Korean.

Neuroscience research - 1 Mar 2009

Yoo Hee Jeong, Lee Seong Kyu, Park Mira, Cho In Hee, Hyun Seung Hee, Lee Je Chul, Yang So Young, Kim Soon Ae

Abstract excerpt

Monoamine oxidase A gene (MAOA) has been thought to be a candidate gene implicated in autism spectrum disorder (ASD). This study evaluates the relationship between ASDs and MAOA markers (i.e., uVNTR and four single nucleotide polymorphisms (SNPs)) in 151 Korean family trios with children diagnosed with ASDs, and 193 unrelated Korean controls. The result of case-control global haplotype analysis also showed a...

Read the complete abstract on PubMed

Topics

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

Share to Autistic Disorder
Share to Chi-Square Distribution

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Family Health

Share to Linkage Disequilibrium

Share to Minisatellite Repeats

Share to Monoamine Oxidase

Share to Sex Factors

Source

Identifiers

PMID: 19100789
DOI: 10.1016/j.neures.2008.11.007

Genes

MAOA

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

Family- and population-based association studies of monoamine oxidase A and autism spectrum disorders in Korean.PMID 19100789Read ↗

Association between monoamine oxidase gene polymorphisms and attention deficit hyperactivity disorder in Korean children.Semantic proximity Read ↗

Family-based association study between NOS-I and -IIA polymorphisms and autism spectrum disorders in Korean trios.Semantic proximity Read ↗

Family-based association study of 5-HTTLPR and the 5-HT2A receptor gene polymorphisms with autism spectrum disorder in Korean trios.Semantic proximity Read ↗

Family-based association study of microsatellites in the 5' flanking region of AVPR1A with autism spectrum disorder in the Korean population.Semantic proximity Read ↗

Association study of the vesicular monoamine transporter 1 (VMAT1) gene with autism in an Iranian population.Semantic proximity Read ↗

MAOA Variants and Genetic Susceptibility to Major Psychiatric Disorders.Semantic proximity Read ↗

Association of the catechol-o-methyltransferase gene polymorphisms with Korean autism spectrum disorders.Semantic proximity Read ↗

Genome-Wide Association Study for Autism Spectrum Disorder in Taiwanese Han Population.Semantic proximity Read ↗

Association study between single nucleotide polymorphisms in promoter region of AVPR1A and Korean autism spectrum disorders.Semantic proximity Read ↗

Association between PTGS2 polymorphism and autism spectrum disorders in Korean trios.Semantic proximity Read ↗

No association of the norepinephrine transporter gene (SLC6A2) and cognitive and behavioural phenotypes of patients with autism spectrum disorder.Semantic proximity Read ↗

CNTNAP2 gene polymorphisms in autism spectrum disorder and language impairment among Bangladeshi children: a case-control study combined with a meta-analysis.Semantic proximity Read ↗

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