ArticleCommunications biology2025
Diffusion trajectory of atypical morphological development in autism spectrum disorder.
Article in Communications biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- Alteration of individual morphological brain networks in preschool children with autism spectrum disorder.Brain imaging and behavior · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
14 authors.
Funding
Abstract
Brain development from childhood through adolescence is crucial for understanding autism spectrum disorder (ASD). Yet how functional networks regulate developmental changes in brain morphology remains unclear. Here, we analyzed gray matter volume (GMV) and functional connectivity (FC) in 301 individuals with ASD and 375 typically developing controls (TDCs), aged 8-18 years, from the Autism Brain Imaging Data Exchange (ABIDE). Using a sliding-window approach, participants were stratified by age, and GMV distribution deviations (DEV) were quantified with Kullback-Leibler divergence and expected value analysis. Network diffusion modeling (NDM) was applied to predict developmental alterations and evaluate how functional networks constrain atypical neurodevelopment. Results revealed a developmental shift in GMV divergence: during early adolescence, ASD participants showed positive GMV deviations relative to TDCs, which shifted to negative in late adolescence. The largest DEV were observed in the superior temporal sulcus, cingulate gyrus, insula, and superior parietal lobule. Furthermore, NDM demonstrated cross-stage predictability, as DEV values of atypical brain regions at preceding age stages significantly predicting subsequent ones, constrained by network architecture. These findings highlight a dynamic developmental shift from GMV overgrowth to delayed maturation during adolescence in ASD and revealing the role of intrinsic functional networks in constraining atypical anatomical development.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.