Evidence map›Paper›PMID 41023420›Full record

ReviewMolecular psychiatry2025

Asymmetric developmental bifurcations in polarized environments: a new class of human variants, which may include autism.

Laurent Mottron, Alix Lavigne-Champagne, Boris Bernhardt, Guillaume Dumas, Sébastien Jacquemont, David Gagnon

Abstract readReview
In one paragraph

Review in Molecular psychiatry, 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

6 authors.

Laurent MottronDépartement de Psychiatrie et d'Addictologie, Université de Montréal, Montréal, QC, Canada. Laurent.mottron@gmail.com.ORCID 0000-0001-5668-5422
Alix Lavigne-ChampagneDépartement de Psychiatrie et d'Addictologie, Université de Montréal, Montréal, QC, Canada.ORCID 0009-0003-7893-3900
Boris BernhardtMultimodal Imaging and Connectome Analysis Laboratory, McConnell Brain Imaging Centre, McGill University, Montreal, QC, Canada.ORCID 0000-0001-9256-6041
Guillaume DumasDépartement de Psychiatrie et d'Addictologie, Université de Montréal, Montréal, QC, Canada.
Sébastien JacquemontDepartment of Pediatrics, University of Montreal, Montréal, QC, Canada.ORCID 0000-0001-6838-8767
David GagnonDépartement de Psychiatrie et d'Addictologie, Université de Montréal, Montréal, QC, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inspired by discrete stable alternative states that often coexist with the dominant phenotypes of a species, we propose that asymmetric developmental bifurcations (ADB) may provide a biological framework for grouping autism together with some human alternative organizations rather than with disorders or diseases. These include minority embryological or obstetrical variants, such as twinning and breech presentation, as well as minority information processing variants, such as left-handedness and importantly prototypical autism. Four common contextual, developmental, adaptive, and mechanistic features unify these alternative conditions as ADBs: 1) ADBs occur in a dynamic system formed by an individual and his environment with two polarized stable solutions. 2) The bifurcation occurs in a critical period of development and is significantly shorter than the stable states that precede and follow it. 3) While the frequent branch of the ADB optimizes evolutionary success, its rare branch has an adaptive cost, which is still compatible with survival. 4) Both rare and frequent branches of the ADB are human possibilities, favoured without major/deleterious changes by familial and/or sexual predispositions. Framing autism as a categorical, alternative phenotypic prototype in a polarized choice between social bias and its absence, elucidates autism's recurrent divergence within the species, its developmental and information processing characteristics, and its adaptive challenges.

Indexed as

Autistic DisorderBiological EvolutionHumansPhenotype

Identifiers

PMID41023420
PMCPMC12602325

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.