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

A large-scale screen for coding variants in SERT/SLC6A4 in autism spectrum disorders.

Autism research : official journal of the International Society for Autism Research - 1 Aug 2008

Sakurai Takeshi, Reichert Jennifer, Hoffman Ellen J, Cai Guiqing, Jones Hywel B, Faham Malek, Buxbaum Joseph D

Abstract excerpt

In the current study we explored the hypothesis that rare variants in SLC6A4 contribute to autism susceptibility and to rigid-compulsive behaviors in autism. We made use of a large number of unrelated cases with autism spectrum disorders (approximately 350) and controls (approximately 420) and screened for rare exonic variants in SLC6A4 by a high-throughput method followed by sequencing. We observed no difference...

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to Autistic Disorder

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Variation

Share to Pedigree

Share to Serotonin Plasma Membrane Transport Proteins

Share to Young Adult

Source

Open in PubMed Open full text

Identifiers

PMID: 19360675
DOI: 10.1002/aur.30
PMCID: PMC2678895

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

A large-scale screen for coding variants in SERT/SLC6A4 in autism spectrum disorders.PMID 19360675Read ↗

Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors.Semantic proximity Read ↗

Lack of evidence for association of the serotonin transporter gene SLC6A4 with autism.Semantic proximity Read ↗

Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid-compulsive subset of autism.Semantic proximity Read ↗

SERT Ileu425Val in autism, Asperger syndrome and obsessive-compulsive disorder.Semantic proximity Read ↗

Association analysis of the NrCAM gene in autism and in subsets of families with severe obsessive-compulsive or self-stimulatory behaviors.Semantic proximity Read ↗

Single Nucleotide Polymorphisms in SLC19A1 and SLC25A9 Are Associated with Childhood Autism Spectrum Disorder in the Chinese Han Population.Semantic proximity Read ↗

Lack of association between autism and SLC25A12.Semantic proximity Read ↗

Association study of the SLC25A12 gene and autism in Han Chinese in Taiwan.Semantic proximity Read ↗

A large case-control study of common functional SLC6A4 and BDNF variants in obsessive-compulsive disorder.Semantic proximity Read ↗

A case of drug-resistant epilepsy and autism with de novo SLC6A8 gene variant.Semantic 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 ↗

Enhanced activity of human serotonin transporter variants associated with autism.Semantic proximity Read ↗

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