Evidence map›Paper›PMID 42127906›Full record

ArticleCell reports. Medicine2026

Traumatic life experiences during critical periods lead to diverse developmental trajectories.

Giovanni Morelli, Greta Visintin, Elisa Gelli, Angelo Serani, Martina Bartolucci, Sara Uccella, Maria D'Apruzzo, Deborah Preiti, Mariam Marie Chellali, Alessandra Cucinelli and 7 more

Abstract read
In one paragraph

Article in Cell reports. Medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

17 authors.

Giovanni MorelliBrain Development and Disease Laboratory, Istituto Italiano di Tecnologia, Genoa, Italy.
Greta VisintinBrain Development and Disease Laboratory, Istituto Italiano di Tecnologia, Genoa, Italy; University of Genoa, Genoa, Italy.
Elisa GelliGenetics and Epigenetics of Behavior Laboratory, Istituto Italiano di Tecnologia, Genoa, Italy.
Angelo SeraniGenetics and Epigenetics of Behavior Laboratory, Istituto Italiano di Tecnologia, Genoa, Italy.
Martina BartolucciCore Facilities - Clinical Proteomics and Metabolomics, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Sara UccellaDepartment of Neurosciences, Rehabilitation, Ophthalmology, Genetics, and Maternal and Child Health (DINOGMI), University of Genoa, Genoa, Italy; Child Neuropsychiatry Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Maria D'ApruzzoChild Neuropsychiatry Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Deborah PreitiChild Neuropsychiatry Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy; Patologia Neonatale, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Mariam Marie ChellaliBrain Development and Disease Laboratory, Istituto Italiano di Tecnologia, Genoa, Italy; University of Genoa, Genoa, Italy.
Alessandra CucinelliBrain Development and Disease Laboratory, Istituto Italiano di Tecnologia, Genoa, Italy; University of Genoa, Genoa, Italy.
Mohit RastogiBrain Development and Disease Laboratory, Istituto Italiano di Tecnologia, Genoa, Italy; University of Genoa, Genoa, Italy.
Matteo FalappaGenetics and Epigenetics of Behavior Laboratory, Istituto Italiano di Tecnologia, Genoa, Italy.
Andrea ScalabriniDepartment of Human and Social Sciences, University of Bergamo, Bergamo, Italy.
Gustavo TureckiDouglas Institute, Department of Psychiatry, McGill University, Montreal, QC, Canada.
Andrea PetrettoCore Facilities - Clinical Proteomics and Metabolomics, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Valter TucciGenetics and Epigenetics of Behavior Laboratory, Istituto Italiano di Tecnologia, Genoa, Italy.
Laura CanceddaBrain Development and Disease Laboratory, Istituto Italiano di Tecnologia, Genoa, Italy. Electronic address: laura.cancedda@iit.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Traumatic events can disrupt neurodevelopment, increasing the risk for neuropsychiatric disorders. However, the relationships between specific types of traumas and the emergence of particular neuropsychiatric traits remain elusive. Here, we examine the long-term consequences of different life-threatening events experienced during four distinct developmental periods in mice. Our findings at the behavioral and molecular/cellular levels in adulthood suggest a crucial role for timing (rather than type) of stress during development in shaping long-term outcomes. Our parallel analysis of individuals exposed to trauma at diverse life stages reveals similar results. Finally, our proteomic data suggest the brain-derived neurotrophic factor (BDNF)-pathway as a promising therapeutic target for ameliorating psychopathology related to trauma experienced specifically in early adulthood in mice and potentially in individuals. Our results point to the existence of critical periods for trauma exposure that uniquely influence adult behavioral outcomes and induce time-specific molecular/cellular patterns in the brain, which may have therapeutic implications.

Indexed as

Critical Period, PsychologicalStress, PsychologicalAnimalsBrainBrain-Derived Neurotrophic FactorFemaleHumansMaleMiceNeurodevelopmentProteomicsBrain-Derived Neurotrophic Factorcritical periodsdevelopmental trajectoriesearly-life stresstrauma

Identifiers

PMID42127906
PMCPMC13293931

What OpenQuestion holds

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Registered trials

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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.