Evidence map›Paper›PMID 38984666›Full record

ArticleAutism research : official journal of the International Society for Autism Research2025

A common genetic variant in the Neurexin family member CNTNAP2 is related to language but not communication skills in youth with Autism Spectrum Disorder.

Vardan Arutiunian, Megha Santhosh, Emily Neuhaus, Catherine A W Sullivan, Raphael A Bernier, Susan Y Bookheimer, Mirella Dapretto, Daniel H Geschwind, Allison Jack, James C McPartland and 5 more

Abstract read
In one paragraph

Article in Autism research : official journal of the International Society for Autism Research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

15 authors.

Vardan ArutiunianCenter for Child Health, Behavior and Development, Seattle Children's Research Institute, Seattle, Washington, USA.ORCID 0000-0001-9417-0913
Megha SanthoshCenter for Child Health, Behavior and Development, Seattle Children's Research Institute, Seattle, Washington, USA.
Emily NeuhausCenter for Child Health, Behavior and Development, Seattle Children's Research Institute, Seattle, Washington, USA.ORCID 0000-0003-1762-0348
Catherine A W SullivanDepartment of Pediatrics, Yale School of Medicine, New Haven, Connecticut, USA.ORCID 0000-0003-2515-6901
Raphael A BernierDepartment of Psychiatry and Behavioral Science, University of Washington, Seattle, Washington, USA.ORCID 0000-0003-1854-2804
Susan Y BookheimerDepartment of Psychiatry and Biobehavioral Sciences, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA.
Mirella DaprettoDepartment of Psychiatry and Biobehavioral Sciences, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA.ORCID 0000-0003-2914-6858
Daniel H GeschwindDepartment of Psychiatry and Biobehavioral Sciences, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA.
Allison JackDepartment of Psychology, George Mason University, Fairfax, Virginia, USA.
James C McPartlandYale Child Study Center, Yale School of Medicine, New Haven, Connecticut, USA.
John D Van HornDepartment of Psychology, University of Virginia, Charlottesville, Virginia, USA.
Kevin A PelphreyDepartment of Neurology, School of Medicine, University of Virginia, Virginia, USA.
Abha R GuptaDepartment of Pediatrics, Yale School of Medicine, New Haven, Connecticut, USA.
Sara Jane WebbCenter for Child Health, Behavior and Development, Seattle Children's Research Institute, Seattle, Washington, USA.ORCID 0000-0003-4101-6255
ACE GENDAAR Network

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Multimodal Developmental Neurogenetics of Females with ASDR01MH100028 · NIMH · YALE UNIVERSITY · PI Allison Elizabeth Jack, LAUREN KENWORTHY · 2012 to 2026
$37.8M
Mechanisms of Brain Dysmorphology in MN1 C-Terminal Truncation Syndrome, a Novel Intellectual Developmental Disability Disorder P50HD103524 · NICHD · UNIVERSITY OF WASHINGTON · PI Sandra E Juul · 2020 to 2026
$9.9M
Subnetwork-based Quantitative Imaging Biomarkers for Therapy Assessment in AutismR01NS035193 · NINDS · YALE UNIVERSITY · PI JAMES S DUNCAN, LAWRENCE H. STAIB · 1996 to 2026
$9.2M
NCATS NIH HHS UL1 TR001863NICHD NIH HHS P50 HD103524NIMH NIH HHS R01 MH100028NINDS NIH HHS R01 NS035193
6 · The paper itself

Abstract

One of the candidate genes related to language variability in individuals with Autism Spectrum Disorder (ASD) is the contactin-associated protein-like 2 gene (CNTNAP2), a member of the Neurexin family. However, due to the different assessment tools used, it is unknown whether the polymorphisms of the CNTNAP2 gene are linked to structural language skills or more general communication abilities. A total of 302 youth aged 7 to 18 years participated in the present study: 131 verbal youth with ASD (62 female), 130 typically developing (TD) youth (64 female), and 41 unaffected siblings (US) of youth with ASD (25 female). Blood samples were collected to obtain genomic DNA and processed by the Rutgers University Cell and Data Repository or using standard protocols (Gentra Puregene Blood DNA extraction kit; Qiagen). Language and verbal communication skills were screened with the Clinical Evaluation of Language Fundamental-4 (CELF-4) and Vineland-II Communication domain, subsequently. The results showed that the polymorphism of CNTNAP2 (SNP rs2710102) was related to structural language abilities, such that participants carrying the A-allele had lower language skills in comparison to the G-allele homozygotes. No relationship was found between the polymorphism of CNTNAP2 and more general communication abilities. Although the study revealed genetic mechanisms that are associated with CELF-4 measures but not Vineland-II in youth with ASD, follow-up studies are needed that will include measures of language and communication that are less correlated to each other as well as will include a group of minimally and/or non-verbal individuals with ASD.

Indexed as

Autism Spectrum DisorderCommunicationMembrane ProteinsNerve Tissue ProteinsAdolescentChildFemaleGenotypeHumansMalePolymorphism, Single NucleotideCNTNAP2 protein, humanMembrane ProteinsNerve Tissue ProteinsAutism Spectrum DisordercommunicationlanguageSNP rs2710102the polymorphism of CNTNAP2

Identifiers

PMID38984666
PMCPMC11717989

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.