Evidence map›Paper›PMID 41657078›Full record

ArticleAutism research : official journal of the International Society for Autism Research2026

Behavioral Phenotype Associations With Resting State EEG Signal Complexity and Power Spectral Density in Fragile X Syndrome.

Mélodie Proteau-Lemieux, Inga S Knoth, Saeideh Davoudi, Rae Buckser, Charles-Olivier Martin, Anne-Marie Bélanger, Valérie K Fontaine, Hazel Maridith Barlahan Biag, Leonard Abbeduto, Sébastien Jacquemont and 5 more

Abstract read
In one paragraph

Article in Autism research : official journal of the International Society for Autism Research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Mélodie Proteau-LemieuxDepartment of Psychology, University of Montreal, Montreal, Quebec, Canada.ORCID 0009-0007-7789-1170
Inga S KnothAzrieli Research Center of the Sainte-Justine University Hospital, Montreal, Quebec, Canada.
Saeideh DavoudiAzrieli Research Center of the Sainte-Justine University Hospital, Montreal, Quebec, Canada.
Rae BuckserAzrieli Research Center of the Sainte-Justine University Hospital, Montreal, Quebec, Canada.
Charles-Olivier MartinAzrieli Research Center of the Sainte-Justine University Hospital, Montreal, Quebec, Canada.
Anne-Marie BélangerAzrieli Research Center of the Sainte-Justine University Hospital, Montreal, Quebec, Canada.
Valérie K FontaineAzrieli Research Center of the Sainte-Justine University Hospital, Montreal, Quebec, Canada.
Hazel Maridith Barlahan BiagMIND Institute, University of California Davis School of Medicine, Sacramento, California, USA.
Leonard AbbedutoMIND Institute, University of California Davis School of Medicine, Sacramento, California, USA.ORCID 0000-0002-2311-7194
Sébastien JacquemontAzrieli Research Center of the Sainte-Justine University Hospital, Montreal, Quebec, Canada.
David HesslMIND Institute, University of California Davis School of Medicine, Sacramento, California, USA.
Randi J HagermanMIND Institute, University of California Davis School of Medicine, Sacramento, California, USA.
Andrea SchneiderMIND Institute, University of California Davis School of Medicine, Sacramento, California, USA.
François V BolducDepartment of Pediatrics, University of Montreal, Montreal, Quebec, Canada.
Sarah LippéDepartment of Psychology, University of Montreal, Montreal, Quebec, Canada.

Funding

Azrieli FoundationCIHRNatural Sciences and Engineering Research Council of CanadaUC David Mind Institute 103526
6 · The paper itself

Abstract

Fragile X Syndrome (FXS), an X-linked genetic condition, is associated with a wide range of phenotypic manifestations, namely intellectual disability (ID), autism spectrum disorder (ASD), attention deficit hyperactivity disorder (ADHD), and atypical behaviors. Individuals with FXS present robust electrophysiological (EEG) alterations, notably on signal complexity and power spectral density (PSD) resting state measures. To which extent they are associated to specific behavioral phenotypes in the FXS population remains to be comprehensively addressed. This study aimed to investigate the relations between resting state EEG markers and the most frequently observed symptoms in FXS. EEG and behavioral data from 41 individuals with FXS aged between 7 and 34 years old were collected, and correlational approaches were used to analyze the associations between EEG markers and symptomatology. We observed positive associations between complexity in higher scales and non-verbal intelligence quotient (NVIQ). Reduced alpha power, a robust biomarker in FXS, was associated with more social avoidance, a hallmark in FXS. Decreased high gamma power was linked to hyperactive symptoms. Our results suggest powerful relations between known biomarkers and core symptoms in FXS, highlighting that EEG biomarkers correspond to symptom severity which further supports their potential as objective, translational treatment outcome measures.

Indexed as

ElectroencephalographyFragile X SyndromeAdolescentAdultChildFemaleHumansMalePhenotypeRestYoung AdultbehaviorcognitionEEGfragile X syndromePSDresting statesignal complexity

Identifiers

PMID41657078
PMCPMC12996851

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.