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

Sexual dimorphic effect in the genetic association of monoamine oxidase A (MAOA) markers with autism spectrum disorder.

Progress in neuro-psychopharmacology & biological psychiatry - 3 Apr 2014

Verma Deepak, Chakraborti Barnali, Karmakar Arijit, Bandyopadhyay Tirthankar, Singh Asem Surindro, Sinha Swagata, Chatterjee Anindita, Ghosh Saurabh, Mohanakumar Kochupurackal P, Mukhopadhyay Kanchan, Rajamma Usha

Abstract excerpt

Autism spectrum disorders are heritable and behaviorally-defined neurodevelopmental disorders having skewed sex ratio. Serotonin as modulator of behavior and implication of serotonergic dysfunction in ASD etiology corroborates that serotonergic system genes are potential candidates for autism susceptibility. In the current study X-chromosomal gene, MAOA responsible for degradation of serotonin is investigated for...

Read the complete abstract on PubMed

Topics

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

Share to Child Development Disorders, Pervasive
Share to Child, Preschool

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Association Studies

Share to Genetic Markers

Share to Haplotypes

Share to Linkage Disequilibrium

Share to Monoamine Oxidase

Share to Sex Characteristics

Source

Identifiers

PMID: 24291416
DOI: 10.1016/j.pnpbp.2013.11.010

Genes

MAOA
SRY

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

Sexual dimorphic effect in the genetic association of monoamine oxidase A (MAOA) markers with autism spectrum disorder.PMID 24291416Read ↗

Genetic variants of MAOB affect serotonin level and specific behavioral attributes to increase autism spectrum disorder (ASD) susceptibility in males.Semantic proximity Read ↗

Genetic association and gene-gene interaction analyses suggest likely involvement of ITGB3 and TPH2 with autism spectrum disorder (ASD) in the Indian population.Semantic proximity Read ↗

The involvement of serotonin polymorphisms in autistic spectrum symptomatology.Semantic proximity Read ↗

Association and gene-gene interaction of SLC6A4 and ITGB3 in autism.Semantic proximity Read ↗

Differential association between MAOA, ADHD and neuropsychological functioning in boys and girls.Semantic proximity Read ↗

Genetic variants of neurotransmitter-related genes and miRNAs in Egyptian autistic patients.Semantic proximity Read ↗

Analysis of serotonin receptor 2A gene (HTR2A): association study with autism spectrum disorder in the Indian population and investigation of the gene expression in peripheral blood leukocytes.Semantic proximity Read ↗

Association between autism spectrum disorder and polymorphisms in genes encoding serotine and dopamine receptors.Semantic proximity Read ↗

Expression analysis of selected genes involved in tryptophan metabolic pathways in Egyptian children with Autism Spectrum Disorder and learning disabilitiesSemantic proximity Read ↗

Population-based association study and contrasting linkage disequilibrium pattern reveal genetic association of SLC6A4 with autism in the Indian population from West Bengal.Semantic proximity Read ↗

Towards understanding sex differences in autism spectrum disorders.Semantic proximity Read ↗

MAOA, DBH, and SLC6A4 variants in CHARGE: a case-control study of autism spectrum disorders.Semantic proximity Read ↗

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