Portrait de Guillaume Dumas

Guillaume Dumas

Membre académique associé
Professeur agrégé, Université de Montréal, Département de psychiatrie et d’addictologie
Professeur adjoint, McGill University, Département de psychiatrie
Sujets de recherche
Apprentissage automatique médical
Apprentissage par renforcement
Apprentissage profond
Biologie computationnelle
Neurosciences computationnelles
Systèmes dynamiques
Théorie de l'apprentissage automatique

Biographie

Guillaume Dumas est professeur agrégé de psychiatrie computationnelle à la Faculté de médecine de l'Université de Montréal et chercheur principal du laboratoire de psychiatrie de précision et de physiologie sociale du Centre de recherche du CHU Sainte-Justine. Il est titulaire de la chaire IVADO IA en santé mentale et chercheur-boursier junior 1 du Fonds de recherche du Québec - Santé (FRQS) dans le domaine de l’ IA en santé et de la santé numérique. En 2023, il a été retenu dans le cadre du Programme des chercheurs mondiaux CIFAR-Azrieli pour le programme de recherche Cerveau, esprit et conscience. Il a également été nommé parmi les Futurs leaders canadiens de la recherche sur le cerveau par la Fondation Brain Canada.

Il a auparavant été chercheur permanent en neurosciences et en biologie computationnelle à l'Institut Pasteur (Paris, France), ainsi que chercheur postdoctoral au Center for Complex Systems and Brain Sciences à l’Université Florida Atlantic (FAU), aux États-Unis. Il est titulaire d'un diplôme d'ingénieur en ingénierie avancée et informatique (École centrale Paris), de deux masters (physique théorique, Université Paris-Saclay; sciences cognitives, ENS/EHESS/Paris 5) et d'un doctorat en neurosciences cognitives (Sorbonne Université).

Ses recherches visent à combiner l’intelligence artificielle, les neurosciences cognitives et la médecine numérique à travers un programme interdisciplinaire suivant deux axes principaux :

- L’intelligence artificielle en santé mentale, par la création de nouveaux algorithmes pour étudier le développement de l'architecture cognitive humaine et pour fournir une médecine personnalisée en neuropsychiatrie grâce à des données allant du génome à celles des téléphones intelligents;

- Les neurosciences sociales en intelligence artificielle, par la traduction de la recherche fondamentale sur le cerveau et le formalisme des systèmes dynamiques en des modèles hybrides neurocomputationnels et d’apprentissage automatique (NeuroML) et de nouvelles architectures présentant des capacités d'apprentissage social (NeuroIA Sociale et IHM).

Étudiants actuels

Maîtrise recherche - UdeM
Visiteur de recherche indépendant - CHU Sainte Justine / Université de Montréal
Maîtrise recherche - UdeM
Superviseur⋅e principal⋅e :
Doctorat - UdeM
Superviseur⋅e principal⋅e :

Publications

Mirror effect of genomic deletions and duplications on cognitive ability across the human cerebral cortex
Kuldeep Kumar
Sayeh Kazem
Worrawat Engchuan
Thomas Renne
Martineau Jean-Louis
Omar Shanta
Zohra Saci
Bhooma Thiruvahindrapuram
Jeffrey MacDonald
Josephine Mollon
Laura M Schultz
Emma E M Knowles
David Porteous
Gail Davies
Paul Redmond
Sarah Harris
Simon Cox
Gunter Schumann … (voir 9 de plus)
Zdenka Pausova
Celia Greenwood
Tomáš Paus
Stephen Scherer
Laura Almasy
Jonathan Sebat
David Glahn
Sébastien Jacquemont
Cognitive deficits are common across many neurodevelopmental and psychiatric conditions, including those studied in the current set of PGC-C… (voir plus)NV papers. How changes in regional gene expression across the cerebral cortex influence cognitive ability remains unknown. Population variation in gene dosage—which significantly impacts gene expression—represents a unique paradigm to address this question. We developed a cerebral-cortex gene-set burden analysis (CC-GSBA) to associate a trait with genomic deletions and duplications that disrupt genes with similar expression profiles across 180 cortical regions. We performed CC-GSBA across 180 cortical regions to test associations with cognitive ability in 260,000 individuals from general population cohorts. Most cortical gene sets were associated with a decrease in cognitive ability when deleted or duplicated, and this novel approach revealed opposing cortical patterns for the effect sizes of deletions and duplications. These cortical patterns of effect sizes followed the cortical gradient previously characterized at the molecular, cellular, and functional levels. We show that genes with preferential expression in sensorimotor regions demonstrated the largest effect on cognition when deleted. At the opposing end of the cortical gradient, genes with preferential expression in multimodal association regions affected cognition the most when duplicated. These two gene dosage cortical patterns could not be explained by particular cell types, developmental epochs, or genetic constraints, highlighting the fact that the macroscopic network organization of the cerebral cortex is key to understanding the effects of gene dosage on cognitive traits.
Determinants of pleiotropy and monotonic gene dosage responses across human traits
Sayeh Kazem
Kuldeep Kumar
Josephine Mollon
Thomas Renne
Laura M. Schultz
Emma E.M. Knowles
Worrawat Engchuan
Omar Shanta
Bhooma Thiruvahindrapuram
Jeffrey R. MacDonald
Celia M. T. Greenwood
Stephen W. Scherer
Laura Almasy
Jonathan Sebat
David C. Glahn
Sébastien Jacquemont
While pleiotropic effects of gene dosage are of particular relevance for comorbidities observed in the developmental pediatric and psychiatr… (voir plus)ic clinic, the biological processes underlying such pleiotropy remain unknown. We developed a new functional burden analysis (FunBurd) to investigate all CNVs, genome-wide, beyond well-studied recurrent CNVs. In ~500,000 UK-Biobank participants, we tested the association between 43 traits and CNVs disrupting 172 tissue or cell-type gene-sets. CNVs affected all traits. Pleiotropy was correlated with genetic constraint and was higher in the brain compared to non-brain functions, even after normalizing for genetic constraint. The levels of pleiotropy, measured by burden correlation, were similar in deletions and loss-of-function SNVs and higher compared to common variants and duplications. Gene sets under high genetic constraint showed less monotonic gene dosage responses across traits. Even in the absence of a monotonic response, we observed a negative correlation between deletion and duplication effect sizes across most traits. Overall, functional gene sets are preferentially associated with a given trait when either deleted or duplicated, but rarely both.
Towards an informational account of interpersonal coordination
Edoardo Chidichimo
Andrea Luppi
Pedro A. Mediano
Victoria Leong
Andres Canales-Johnson
Richard A.I. Bethlehem

Human sociality is grounded in the dynamic coordination of individuals as they interact with one another. Indeed, interpersonal coordinat… (voir plus)ion on various levels—neural, behavioural, physiological, affective, linguistic—are hallmarks of successful social communication and cooperation. However, describing these complex, interdependent dynamics has been limited by current methodological approaches, owing to a restrictive repertoire of tools and the absence of a unified, standardised methodological framework. Here, we identify information theory, the mathematical theory of communication, as a particularly well-suited conceptual framework to address this shortfall, given its appropriate sensitivity to complex dynamics, including potential nonlinearity and higher-order interactions, and its data-driven, model-agnostic foundations. With deep roots in computational, cognitive, and systems neuroscience, the formal introduction of information-theoretic quantities and methods into the study of interpersonal coordination is perhaps overdue. This Perspective advances the case for a unified information-theoretic framework for the field while paving the path for a new generation of empirically testable, theoretically grounded research questions.

Longitudinal intergenerational hyperscanning indexes changes in social connection
Ryssa Moffat
Emily S. Cross
Loneliness is globally acknowledged as a severe and burgeoning health risk, fuelling interest in helping people of all ages form meaningful … (voir plus)social connections. One promising approach consists of intergenerational social programs. While behavioural and qualitative evidence derived from such programs promise health and wellbeing benefits, the physiological consequences of repeated intergenerational encounters remain unknown. Insight into physiological changes will shed light on the mechanisms of social connection and can inform program design choices. We charted changes in interpersonal neural synchrony (INS) in 31 intergenerational (older/younger adult) and 30 same generation (younger adult) dyads across a six-session creative drawing program. At each session, dyads completed self-report measures, drew together and alone, and had their cortical activation recorded with fNIRS. In both groups, INS was greater while dyads drew together than alone. Across sessions, intergenerational dyads’ INS decreased and same generation dyads’ INS increased. INS in RIFG∼RTPJ and RIFG∼RIFG were predictive of loneliness levels and feelings of social closeness, respectively. The research reinforces the multi-faceted nature of INS dynamics as social connections are forged.
Sensory multi-brain stimulation enhances dyadic cooperative behavior
Ivo Leiva-Cisterna
Paulo Barraza
Eugenio Rodríguez
Hyperscanning research suggests that interbrain synchronization supports the regulation of social behavior. However, the evidence is predomi… (voir plus)nantly correlational, leaving a gap for epiphenomenal accounts, where synchrony merely represents concurrent stimulus processing rather than a mechanism relevant to interpersonal interactions. Here, we demonstrate that interbrain synchrony causally drives cooperative success, as evidenced by non-invasive stimulation enhancing coupling and subsequently improving performance in a concurrent interdependent cooperation task. We applied dual-sensory entrainment at 16 Hz and 40 Hz to dyads and compared their performance with non-entrained control dyads performing the same cooperation task. We found that dual stimulation improved interbrain synchrony at the targeted frequencies relative to controls, with 16 Hz entrainment producing the most prominent effect. Strikingly, sensory entrainment facilitated sustained behavioral coupling, allowing partners to maintain coordination over extended periods. Notably, these effects are contingent on improved response coordination, indicating the importance of interbrain coupling for facilitating coordination and demonstrating causally that partner neural attunement is necessary to produce effective joint behavior. Thus, our study supports the concept that interbrain synchrony represents a neural mechanism with functional specificity in social interactions.
Grokking Beyond the Euclidean Norm of Model Parameters
Pascal Jr Tikeng Notsawo
Grokking refers to a delayed generalization following overfitting when optimizing artificial neural networks with gradient-based methods. In… (voir plus) this work, we demonstrate that grokking can be induced by regularization, either explicit or implicit. More precisely, we show that when there exists a model with a property
Asymmetric developmental bifurcations in polarized environments: a new class of human variants, which may include autism.
Laurent Mottron
Alix Lavigne-Champagne
Boris Bernhardt
Sébastien Jacquemont
David Gagnon
Acute respiratory distress syndrome in patients with cancer: the YELENNA prospective multinational observational cohort study.
Peter Schellongowski
Michael Darmon
Philipp Eller
Laveena Munshi
Tobias Liebregts
Victoria Metaxa
Luca Montini
Tobias Lahmer
Andry Van de Louw
Martin Balik
Peter Pickkers
Pleun Hemelaar
Hemang Yadav
Andreas Barratt-Due
Thomas Karvunidis
Jordi Riera
Gennaro Martucci
Ignacio Martin-Loeches
Pedro Castro
Nina Buchtele … (voir 24 de plus)
Virginie Lemiale
Stefan Hatzl
Thomas Staudinger
Elie Azoulay
Gottfried Gürkan Christian Elisabeth Alexis Gennaro Giovanna Heinz Sengölge Zauner Lobmeyr Maillard De Pascale
Gottfried Heinz
G. Sengölge
Christian Zauner
Elisabeth Lobmeyr
Alexis Maillard
G. De Pascale
G. Panarello
Philippe R. Bauer
M. Flaksa
Brozek
Fabio S. Taccone
I. Crippa
Andreas Barrat-Due
Sandra García-Roche
Cándido Díaz-Lagares
Andrés Pacheco
A. Téllez
I. Loeches
Aperiodic and Periodic EEG Component Lifespan Trajectories: Monotonic Decrease versus Growth-then-Decline
Min Li
Ying Wang
Yaqi Chen
Adrien E. E. Dubois
Gangyong Jia
Q. M. Jonathan Wu
Maria L. Bringas-Vega
Pedro A. Valdés‐Sosa
1.1 Unraveling the lifespan trajectories of human brain development is critical for understanding brain health and … (voir plus)disease. Recent research demonstrates that electroencephalography signals are composed of periodic and aperiodic components reflecting distinct physiological substrates. This dissociation raises the possibility that they follow different developmental tendencies. Here, we delineate the lifespan trajectories of aperiodic and periodic neural oscillations using a large international cohort (N=1,563, ages 5–95, resting state, eyes closed). We reveal two fundamental developmental patterns: a Monotonic decrease in aperiodic activity and a Growth-and-Decline pattern for periodic activity. Both components have inflections around age 20 and transition to a stable senescent phase around age 40. Spatially, anterior regions mainly exhibit aperiodic activity, while periodic activity concentrate on posterior regions and these patterns remain stable throughout life. Crucially, multimodal analysis shows these trajectories map onto distinct biological substrates. The periodic component’s Growth and Decline trajectory aligns with GABAergic function and myelination. In contrast, the monotonically decreasing trajectory of aperiodic activity mirrors fundamental biomarkers of biological aging, such as DNA methylation and telomere length. Transforming age to a logarithmic scale simplifies these nonlinear trajectories into a linear decreasing and a piecewise concave linear model for aperiodic and periodic components. This form provides a robust and parsimonious framework for quantifying maturation and identifying neurological deviations. We delineate distinct lifespan trajectories of aperiodic and periodic neural activity in a large-scale international cohort (N=1,563, ages 5–95). Aperiodic activity undergoes a Monotonic Decrease with age. In contrast, periodic activity follows a Growth-then-Decline trajectory, peaking in early adulthood. Both trajectories feature a critical transition around age 20 and stabilize into a protracted senescent phase from approximately 40 onward. These neural trajectories map onto distinct biological substrates: periodic activity tracks integrative functions (myelination, GABAergic, and aperiodic decline mirrors fundamental aging processes (DNA methylation). A stable pattern observed throughout the lifespan is the spatial segregation of neural activity, where aperiodic signals are dominant in anterior regions and periodic signals are concentrated in posterior ones. Logarithmically transforming age linearized the developmental trajectories, yielding a monotonic decline for the aperiodic component and a concave piecewise for the periodic one. This process establishes robust linear norms for the personalized assessment of brain dysfunction.
Posttraumatic Growth in Intensive Care Unit Health Care Professionals After COVID-19
Elie Azoulay
Laurent Argaud
Vincent Labbé
Fabrice Bruneel
Mercé Jourdain
Christophe Guitton
Amelie Seguin
Samir Jaber
David Schnell
Isabelle Vinatier
Fanny Ardisson
Michel Ramakers
Antoine Herault
Olivier Lesieur
Alain Cariou
Antoine Vieillard-Baron
Olivier Guisset
Frédéric Pochard
Michael Darmon … (voir 1 de plus)
Nancy Kentish-Barnes
Pathfinding: a neurodynamical account of intuition
Steven Kotler
Michael Mannino
Karl Friston
Gyorgy Buzsáki
J. A. Scott Kelso
Persistent Instability in LLM's Personality Measurements: Effects of Scale, Reasoning, and Conversation History
Yorguin-Jose Mantilla-Ramos
Mahmood Hegazy
Alberto Tosato
D. Lemay