Evidence map›Paper›PMID 27355445›Full record

ArticleThe Clinical neuropsychologist2016

Broad autism spectrum and obsessive-compulsive symptoms in adults with the fragile X premutation.

A Schneider, C Johnston, F Tassone, S Sansone, R J Hagerman, E Ferrer, S M Rivera, D Hessl

Open access · greenAbstract read
In one paragraph

Article in The Clinical neuropsychologist, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 2 pooled it
3.6field-weighted citation impact, top 7% of its field
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

36 citing papers in PubMed, 2 syntheses or guidelines pooled it, 45 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Chronic pain, fatigue, and emotional distress in femaleFrontiers in molecular neuroscience · 2026
    Article
  5. Article
  6. Premutation Females with preFXTAS.International journal of molecular sciences · 2025
    Article
  7. Reduced Respiratory Sinus Arrhythmia in Infants with theInternational journal of molecular sciences · 2025
    Article
  8. Social Communication Delay in an Unbiased Sample of Preschoolers With theJournal of speech, language, and hearing research : JSLHR · 2024
    Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. The FMR1 Premutation Phenotype and Mother-Youth Synchrony in Fragile X Syndrome.American journal on intellectual and developmental disabilities · 2021
    Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Evidence for Three Subgroups of FemaleFrontiers in integrative neuroscience · 2021
    Article
  20. Fragile X Premutation: Medications, Therapy and Lifestyle Advice.Pharmacogenomics and personalized medicine · 2021
    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

8 authors at 2 institutions in 1 country.

A Schneidera MIND Institute, UC Davis Medical Center , Sacramento , CA , USA.
C Johnstona MIND Institute, UC Davis Medical Center , Sacramento , CA , USA.
F Tassonea MIND Institute, UC Davis Medical Center , Sacramento , CA , USA.
S Sansonea MIND Institute, UC Davis Medical Center , Sacramento , CA , USA.
R J Hagermana MIND Institute, UC Davis Medical Center , Sacramento , CA , USA.
E Ferrerd Department of Psychology , UC Davis , Davis , CA , USA.
S M Riveraa MIND Institute, UC Davis Medical Center , Sacramento , CA , USA.
D Hessla MIND Institute, UC Davis Medical Center , Sacramento , CA , USA.
University of California, Davis · USUniversity of California Davis Medical Center · US

Funding

Restoring FMRP Phenotypes Frpm Temporal Regional and Splice- Isoforms VarationsP30HD002274 · NICHD · UNIVERSITY OF WASHINGTON · PI GURALNICK, MICHAEL J · 1985 to 2013
$33.6M
GENOTYPE/PHENOTYPE RELATIONSHIPS IN FRAGILE X FAMILIESR01HD036071 · NICHD · UNIVERSITY OF CALIFORNIA DAVIS · PI PAUL J HAGERMAN, RANDI J. HAGERMAN · 1998 to 2026
$13.8M
Rodent Behavior CoreU54HD079125 · NICHD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CRAWLEY, JACQUELINE N · 2013 to 2019
$8.5M
Characterization and Treatment of CNS Abnormalities in Premutation Carriers (4 ofRL1AG032115 · NIA · UNIVERSITY OF CALIFORNIA AT DAVIS · PI HAGERMAN, RANDI J. · 2007 to 2011
$5.8M
Trajectories and Markers of Neurodegeneration in Fragile X Premutation CarriersR01MH078041 · NIMH · UNIVERSITY OF CALIFORNIA AT DAVIS · PI HESSL, DAVID R, RIVERA, SUSAN M · 2007 to 2017
$5.4M
POPULATION-BASED BIRTH DEFECTS SURVEILLANCE AND UTILAZATION OF SURVEILLANCE DATA U50DD000596 · DD · COLORADO STATE DEPT/PUB HLTH & ENVIRONMT · PI RUTTENBER, MARGARET · 2010 to 2015
$1.1M
NCBDD CDC HHS U50 DD000596NIA NIH HHS RL1 AG032115NICHD NIH HHS P30 HD002274NICHD NIH HHS R01 HD036071NICHD NIH HHS U54 HD079125NIMH NIH HHS R01 MH078041
6 · The paper itself

Abstract

objectiveClinical observations and a limited number of research studies provide evidence that the fragile X premutation may confer risk for autism, executive dysfunction, and psychopathology. The link to autism spectrum symptoms and social cognition deficits with the premutation remains uncertain, and thus was the focus of the present investigation.

methodOur sample included 131 individuals, 42 men/22 women with the FMR1 premutation (mean age = 31.83 ± 8.59 years) with a normal neurological exam, and 48 men/19 women healthy age-matched controls (mean age = 29.48 ± 7.29 years). Individuals completed a comprehensive neuropsychological battery with additional assessments for social cognition, broad autism spectrum, and obsessive-compulsive (OC) symptoms.

resultsPremutation carriers self-reported higher rates of autism-related symptoms (Autism Quotient; p = .001). Among males only, premutation carriers showed more atypical social interaction (p < .001) and stereotyped behavior (p = .014) during standardized clinical examination on the Autism Diagnostic Observation Schedule (ADOS) relative to controls. Female premutation carriers reported significantly higher rates of OC symptoms compared to control females (p = .012). Molecular measures defining the expanded premutation (FMR1 CGG repeat length and/or mRNA) were significantly associated with a measure of theory of mind (Reading the Mind in the Eyes Task).

conclusionsThe results of this study indicate a higher rate of broad autism spectrum symptoms in some males with the premutation and provide evidence for an obsessive-compulsive subtype in female premutation carriers.

Indexed as

AdultAutism Spectrum DisorderFemaleFragile X Messenger Ribonucleoprotein 1Fragile X SyndromeHumansMaleNeurologic ExaminationNeuropsychological TestsObsessive-Compulsive DisorderPhotic StimulationSocial BehaviorYoung AdultFragile X Messenger Ribonucleoprotein 1broad autism spectrum phenotypefragile X premutationobsessive–compulsive disorderSocial cognition

Identifiers

PMID27355445
PMCPMC5004987
OpenAlexW2474539635

What OpenQuestion holds

Textmetadata
LicenceTDM
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.