Evidence map›Paper›PMID 42410708›Full record

ArticleDevelopmental science2026

Distinct Temporal Stages of Infant Brain Processing Associate With Early Versus Later Autism Diagnosis.

Tessel Bazelmans, Tony Charman, Mark H Johnson, Emily J H Jones, BASIS Team

Abstract read
In one paragraph

Article in Developmental science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

5 authors.

Tessel BazelmansDepartment of Psychology, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.
Tony CharmanDepartment of Psychology, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.ORCID https://orcid.org/0000-0003-1993-6549
Mark H JohnsonCentre for Brain and Cognitive Development, Birkbeck, University of London, London, UK.
Emily J H JonesCentre for Brain and Cognitive Development, Birkbeck, University of London, London, UK.
BASIS Team

Funding

Autism SpeaksEuropean Union Horizon Europe 101057385Guy's and St Thomas' Charity STR130505Innovative Medicines Initiative 777394Maudsley Charity 980Medical Research Council G0701484Medical Research Council MR/K021389/1Medical Research Council MR/R011427/1Medical Research Council MR/T003057/1Swiss State Secretariat for Education, Research and Innovation 22.00277UK government's Horizon Europe 10039383UK Medical Research Council MR/X010716/1UK Research and Innovation
6 · The paper itself

Abstract

The expression of autism traits sufficient to meet criteria for a diagnosis can occur early (by 3 years) or later (from mid-childhood onwards). It remains unknown whether variation in age of onset is due to clinical recognition or reflects distinct biological pathways. One way of addressing this question is by investigating biological differences very early in development associated with a later age of diagnosis. We use a prospective family history design to look at event-related potentials to faces, one of the most robust biomarkers in autism. A sample of 102 infants (aged 6-10 months, 54% female) with an older autistic sibling had an EEG recorded whilst viewing faces (faces vs. noise; gaze toward vs. away). Autism diagnostic assessments were conducted at 3 years and again in mid-childhood (aged 6-12 years), resulting in early diagnosed (at age 3; N = 22), later diagnosed (at mid-childhood; N = 21), and no autism in early or mid-childhood (N = 59) groups. We found that while early-stage visual processing (P100) does not associate with autism outcome, speed of structural face-versus-noise processing (N290) is slower in early-onset autism only, and semantic processing (P400) is altered in both early- and later-onset autism. Thus, temporal stages of face processing in infancy differentially associate with age of autism onset such that an earlier age of diagnosis is associated with earlier stage deviation within the event-related waveform. Early and later onset autism may represent different subtypes, challenging the view of one etiological pathway and that variation in diagnostic age is solely due to clinical ascertainment. SUMMARY: Temporal stages of face processing in infancy differentially associate with age of autism onset. N290 is slower in early-onset autism, indicating an earlier stage neural deviation. The later occurring P400 is altered in both early- and later-onset autism. Early and later-onset autism may represent distinct biological subtypes.

Indexed as

Autistic DisorderBrainChildChild, PreschoolElectroencephalographyEvoked PotentialsFemaleHumansInfantMaleautismdiagnosisface processinginfantlongitudinalmid‐childhood

Identifiers

PMID42410708
PMCPMC13338452

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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.