Evidence map›Paper›PMID 20155310›Full record

ArticleJournal of autism and developmental disorders2010

Glutamate transporter gene (SLC1A1) single nucleotide polymorphism (rs301430) and repetitive behaviors and anxiety in children with autism spectrum disorder.

Kenneth D Gadow, Jasmin Roohi, Carla J DeVincent, Sarah Kirsch, Eli Hatchwell

Abstract read
In one paragraph

Article in Journal of autism and developmental disorders, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Pathology and Astrocytes in Autism.Neuropsychiatric disease and treatment · 2023
    Review
  6. Article
  7. Review
  8. Light-Adapted Electroretinogram Differences in Autism Spectrum Disorder.Journal of autism and developmental disorders · 2020
    Article
  9. Gene-environment interaction: New insights into perceived parenting and social anxiety among adolescents.European psychiatry : the journal of the Association of European Psychiatrists · 2020
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Comprehensive family-based association study of the glutamate transporter gene SLC1A1 in obsessive-compulsive disorder.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2011
    Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Kenneth D GadowDepartment of Psychiatry, Stony Brook University, New York, NY, USA. kenneth.gadow@stonybrook.edu
Jasmin Roohi
Carla J DeVincent
Sarah Kirsch
Eli Hatchwell

Funding

World Trade Center Worker and Volunteer Medical Screening ProgramM01RR010710 · NCRR · STATE UNIVERSITY NEW YORK STONY BROOK · PI CHEN, WEN Y · 1998 to 2009
$17.6M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM008444 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI FROHMAN, MICHAEL A. · 1992 to 2024
$12.6M
NCRR NIH HHS M01 RR010710NCRR NIH HHS M01RR10710NIGMS NIH HHS T32 GM008444
6 · The paper itself

Abstract

Investigated association of single nucleotide polymorphism (SNP) rs301430 in glutamate transporter gene (SLC1A1) with severity of repetitive behaviors (obsessive-compulsive behaviors, tics) and anxiety in children with autism spectrum disorder (ASD). Mothers and/or teachers completed a validated DSM-IV-referenced rating scale for 67 children with autism spectrum disorder. Although analyses were not significant for repetitive behaviors, youths homozygous for the high expressing C allele had more severe anxiety than carriers of the T allele. Allelic variation in SLC1A1 may be a biomarker for or modifier of anxiety symptom severity in children with ASD, but study findings are best conceptualized as tentative pending replication with larger independent samples.

Indexed as

AdolescentAllelesAnxietyChildChild Development Disorders, PervasiveChild, PreschoolExcitatory Amino Acid Transporter 3FemaleGenotypeHumansMaleObsessive-Compulsive DisorderPolymorphism, Single NucleotideStereotypic Movement DisorderExcitatory Amino Acid Transporter 3SLC1A1 protein, human

Identifiers

PMID20155310
PMCPMC4348063

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.