Evidence map›Paper›PMID 31765665›Full record

ArticlePhysiology & behavior2020

Physiological regulation and social-emotional processing in female carriers of the FMR1 premutation.

Molly Winston, Kritika Nayar, Abigail L Hogan, Jamie Barstein, Chelsea La Valle, Kevin Sharp, Elizabeth Berry-Kravis, Molly Losh

Open access · greenAbstract read
In one paragraph

Article in Physiology & behavior, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Prosodic Differences in Women with theInternational journal of molecular sciences · 2025
    Article
  2. Social Communication Delay in an Unbiased Sample of Preschoolers With theJournal of speech, language, and hearing research : JSLHR · 2024
    Article
  3. Review
  4. Review
  5. Autism under the umbrella of ESSENCE.Frontiers in psychiatry · 2023
    Article
  6. Article
  7. Article
  8. Article
  9. Evidence for Three Subgroups of FemaleFrontiers in integrative neuroscience · 2021
    Article
  10. The Phenotypic Profile Associated With theFrontiers in psychiatry · 2021
    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

8 authors at 3 institutions in 1 country.

Molly WinstonRoxelyn and Richard Pepper Department of Communication Sciences and Disorders, Northwestern University, Frances Searle Building, 2240 Campus Drive, Evanston IL 60208, United States.
Kritika NayarRoxelyn and Richard Pepper Department of Communication Sciences and Disorders, Northwestern University, Frances Searle Building, 2240 Campus Drive, Evanston IL 60208, United States.
Abigail L HoganDepartment of Psychology, University of South Carolina, 1512 Pendleton Street, Barnwell College, Suite 220, Columbia, SC 29208, United States.
Jamie BarsteinRoxelyn and Richard Pepper Department of Communication Sciences and Disorders, Northwestern University, Frances Searle Building, 2240 Campus Drive, Evanston IL 60208, United States.
Chelsea La ValleRoxelyn and Richard Pepper Department of Communication Sciences and Disorders, Northwestern University, Frances Searle Building, 2240 Campus Drive, Evanston IL 60208, United States.
Kevin SharpRush University Medical Center, Jelke Building, Room 1565, 1750W. Harrison St., Chicago IL 60612, United States.
Elizabeth Berry-KravisRush University Medical Center, Jelke Building, Room 1565, 1750W. Harrison St., Chicago IL 60612, United States.
Molly LoshRoxelyn and Richard Pepper Department of Communication Sciences and Disorders, Northwestern University, Frances Searle Building, 2240 Campus Drive, Evanston IL 60208, United States. Electronic address: m-losh@northwestern.edu.
Northwestern University · USRush University Medical Center · USUniversity of South Carolina · US

Funding

A Family-Genetic Study of Autism and Fragile X SyndromeR01MH091131 · NIMH · NORTHWESTERN UNIVERSITY · PI Molly C Losh · 2012 to 2026
$10.1M
A Family-Genetic Study of Language in AutismR01DC010191 · NIDCD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Molly C Losh · 2010 to 2026
$7.8M
NIDCD NIH HHS R01 DC010191NIMH NIH HHS R01 MH091131
6 · The paper itself

Abstract

The FMR1 gene is associated with a wide range of clinical and cognitive phenotypes, ranging from intellectual disability and autism symptoms in fragile X syndrome (caused by the FMR1 full mutation), to a more varied, and still poorly understood range of clinical and cognitive phenotypes among carriers of the gene in its premutation state. Because the FMR1 premutation is relatively common among women (as high as 1 in 150), investigations of its phenotypic impact could have broad implications for understanding gene-behavior relationships underlying complex human traits, with potential clinical implications. This study investigated physiological regulation measured by pupillary responses, along with fixation patterns while viewing facial expressions among women who carry the FMR1 premutation (PM group; n = 47), to examine whether the FMR1 gene may relate to physiological regulation, social-emotional functioning, and social language skills (where subclinical differences have been previously reported among PM carriers that resemble those documented in autism-related conditions). Relative to controls (n = 25), the PM group demonstrated atypical pupillary responses and fixation patterns, controlling for IQ. In the PM group, pupillary response and fixation patterns were related to social cognition, social language abilities, and FMR1-related variation. Results indicate a pattern of atypical attention allocation among women who carry the FMR1 PM that could reflect different emotion-processing strategies mediated by autonomic dysregulation and the FMR1 gene. These findings lend insight into the FMR1 gene's potential contributions to complex human traits such as social emotional processing and social language.

Indexed as

EmotionsFacial ExpressionSocial InteractionAdultCase-Control StudiesFemaleFixation, OcularFragile X Messenger Ribonucleoprotein 1HeterozygoteHumansLanguageMutationPhenotypeReflex, PupillaryRepetitive Sequences, Nucleic AcidFMR1 protein, humanFragile X Messenger Ribonucleoprotein 1Autism spectrum disorderEndophenotypeFMR1 premutationFragile X syndromePhysiological regulationSocial cognition

Identifiers

PMID31765665
PMCPMC6992413
OpenAlexW2991124915

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.