Evidence map›Paper›PMID 28524075›Full record

ArticleInternational journal of molecular sciences2017

Examining the Overlap between Autism Spectrum Disorder and 22q11.2 Deletion Syndrome.

Opal Ousley, A Nichole Evans, Samuel Fernandez-Carriba, Erica L Smearman, Kimberly Rockers, Michael J Morrier, David W Evans, Karlene Coleman, Joseph Cubells

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Decoding the genetic landscape of autism: A comprehensive review.World journal of clinical pediatrics · 2024
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Peripheral Expression ofPsychiatry and clinical psychopharmacology · 2023
    Article
  11. Review
  12. Decoding microRNAs in autism spectrum disorder.Molecular therapy. Nucleic acids · 2022
    Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. A cross-comparison of cognitive ability across 8 genomic disorders.Current opinion in genetics & development · 2021
    Review
  19. Article
  20. Review
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

9 authors.

Opal OusleyEmory Autism Center, Department of Psychiatry and Behavioral Sciences, Emory University School of Medicine, 1551 Shoup Court, Atlanta, GA 30322, USA. oousley@emory.edu.
A Nichole EvansMarcus Autism Center, Children's Healthcare of Atlanta, 1920 Briarcliff Road, Atlanta, GA 30329, USA. andrea.evans@choa.org.
Samuel Fernandez-CarribaMarcus Autism Center, Children's Healthcare of Atlanta, 1920 Briarcliff Road, Atlanta, GA 30329, USA. samuel.fernandez-carriba@emory.edu.
Erica L SmearmanDepartment of Psychology, Emory University, Psychology and Interdisciplinary Studies (PAIS) Building, 36 Eagle Row, Atlanta, GA 30322, USA. esmearm@emory.edu.
Kimberly RockersEmory Autism Center, Department of Psychiatry and Behavioral Sciences, Emory University School of Medicine, 1551 Shoup Court, Atlanta, GA 30322, USA. kimberly.rockers@gmail.com.
Michael J MorrierEmory Autism Center, Department of Psychiatry and Behavioral Sciences, Emory University School of Medicine, 1551 Shoup Court, Atlanta, GA 30322, USA. mmorrier@emory.edu.
David W EvansDepartment of Psychology, Bucknell University, 1 Dent Drive, Lewisburg, PA 17837, USA. dwevans@bucknell.edu.
Karlene ColemanMarcus Autism Center, Children's Healthcare of Atlanta, 1920 Briarcliff Road, Atlanta, GA 30329, USA. karlene.coleman@choa.org.
Joseph CubellsEmory Autism Center, Department of Psychiatry and Behavioral Sciences, Emory University School of Medicine, 1551 Shoup Court, Atlanta, GA 30322, USA. jcubell@emory.edu.

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM008169 · NIGMS · EMORY UNIVERSITY · PI GROSS, ROBERT E · 1987 to 2021
$20.3M
NIGMS NIH HHS T32 GM008169
6 · The paper itself

Abstract

22q11.2 deletion syndrome (22q11.2DS) is a genomic disorder reported to associate with autism spectrum disorders (ASDs) in 15-50% of cases; however, others suggest that individuals with 22q11.2DS present psychiatric or behavioral features associated with ASDs, but do not meet full criteria for ASD diagnoses. Such wide variability in findings may arise in part due to methodological differences across studies. Our study sought to determine whether individuals with 22q11.2DS meet strict ASD diagnostic criteria using research-based guidelines from the Collaborative Programs of Excellence in Autism (CPEA), which required a gathering of information from three sources: the Autism Diagnostic Interview-Revised (ADI-R), the Autism Diagnostic Observational Schedule (ADOS), and a clinician's best-estimate diagnosis. Our study examined a cohort of children, adolescents, and young adults (

Indexed as

AdolescentAdultAutism Spectrum DisorderAutistic DisorderChildDiGeorge SyndromeDNA Copy Number VariationsFemaleHumansMaleYoung Adult22q11.2 deletionautismautism spectrumCNVcopy number variationdiagnosisRDoCResearch Domain Criteria

Identifiers

PMID28524075
PMCPMC5454981

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.