Evidence map›Paper›PMID 40713507›Full record

ArticleJournal of neurodevelopmental disorders2025

Distinct early development trajectories in Nf1

Helena Ferreira, Sofia Santos, João Martins, Miguel Castelo-Branco, Joana Gonçalves

Abstract read
In one paragraph

Article in Journal of neurodevelopmental disorders, 2025. 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.

Helena FerreiraUniversity of Coimbra, Coimbra Institute for Biomedical Imaging and Translational Research (CIBIT), Health Sciences Campus, Azinhaga de Santa Comba, Celas, Coimbra, 3000-548, Portugal.
Sofia SantosUniversity of Coimbra, Coimbra Institute for Biomedical Imaging and Translational Research (CIBIT), Health Sciences Campus, Azinhaga de Santa Comba, Celas, Coimbra, 3000-548, Portugal.
João MartinsUniversity of Coimbra, Coimbra Institute for Biomedical Imaging and Translational Research (CIBIT), Health Sciences Campus, Azinhaga de Santa Comba, Celas, Coimbra, 3000-548, Portugal.
Miguel Castelo-BrancoUniversity of Coimbra, Coimbra Institute for Biomedical Imaging and Translational Research (CIBIT), Health Sciences Campus, Azinhaga de Santa Comba, Celas, Coimbra, 3000-548, Portugal.
Joana GonçalvesUniversity of Coimbra, Coimbra Institute for Biomedical Imaging and Translational Research (CIBIT), Health Sciences Campus, Azinhaga de Santa Comba, Celas, Coimbra, 3000-548, Portugal. jgoncalves@icnas.uc.pt.

Funding

Fundação Luso-Americana para o Desenvolvimento FLAD Life Sciences Ed 2 2016Fundação para a Ciência e a Tecnologia 2022.01066.PTDCFundação para a Ciência e a Tecnologia FCT/UIDP&B/04950/2020
6 · The paper itself

Abstract

backgroundAutism spectrum disorder (ASD) is a neurodevelopmental condition characterized by deficits in social communication and interaction, and repetitive behaviors. Males are three times more likely to be diagnosed with ASD than females, and sex-dependent alterations in behavior and communication have been reported both in clinical and animal research. Animal models are useful for understanding ASD-related manifestations and their associated neurobiological mechanisms. However, even though ASD is diagnosed during childhood, relatively few animal studies have focused on neonatal development.

methodsHere, we performed a detailed analysis of neonatal developmental milestones and maternal separation-induced ultrasonic vocalizations (USVs) in two genetic animal models of ASD, neurofibromatosis type 1 (Nf1

resultsNf1

conclusionsThis study provides a nuanced understanding of how these two ASD models differ in their developmental trajectories. It underscores the importance of studying sex differences and early-life developmental markers, as these could offer crucial insights into ASD's progression and neurobiology. The distinct profiles of these models may help guide more targeted therapeutic strategies in the future.

Indexed as

Autism Spectrum DisorderNeurofibromatosis 1Neurofibromin 1Tuberous Sclerosis Complex 2 ProteinVocalization, AnimalAnimalsAnimals, NewbornDisease Models, AnimalFemaleMaleMaternal DeprivationMiceMice, Inbred C57BLSex CharacteristicsTuberous SclerosisNeurofibromin 1Tsc2 protein, mouseTuberous Sclerosis Complex 2 ProteinASDDevelopmental milestonesNeurofibromatosis type 1Tuberous sclerosis complex 2Ultrasonic vocalizations

Identifiers

PMID40713507
PMCPMC12296589

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.