This profile is built from public research funding records (CIHR, NSERC and SSHRC) and PubMed. We have not imported them from a Université de Montréal directory, so their courses and email address may be missing. Find their university profile.
Research
Latest papers
Brain morphology in Anorexia Nervosa and its subtypes: A multi-cohort study of individual participant data.
PLoS medicine · 2026
Cortical differences across psychiatric disorders and associated common and rare genetic variants.
medRxiv : the preprint server for health sciences · 2025
Functional connectivity subtypes associate robustly with ASD diagnosis.
eLife · 2022
Latest funding
- $772,650
Multifeature brain investigation of genetic liability for neurodevelopmental and psychiatric disorders
CIHR · 2025 · Principal investigator
7 publications.
Brain morphology in Anorexia Nervosa and its subtypes: A multi-cohort study of individual participant data.
Bernardoni F, Arold D, Schoppik L, Bahnsen K, Ge R, Moreau C, Bang L, D'Agata F, Abbate-Daga G, Tamnes CK, Campbell I, O'Daly O, Schmidt U, Frank G, Horndasch S, Hess A, Dörfler A, Friederich HC, Simon J, Favaro A, Lavagnino L, Wierenga CE, Bischoff-Grethe A, Miles AE, Kaplan A, Voineskos A, Smeets PAM, van Elburg AA, Danner U, Thomopoulos SI, Berner L, Jahanshad N, Frangou S, King JA, Thompson P, Ehrlich S
Cortical differences across psychiatric disorders and associated common and rare genetic variants.
Kumar K, Liao Z, Kopal J, Moreau C, Ching CRK, Modenato C, Snyder W, Kazem S, Martin CO, Bélanger AM, Fontaine VK, Jizi K, Boen R, Huguet G, Saci Z, Kushan L, Silva AI, 16p11.2 European Consortium, Simons Searchlight Consortium, van den Bree MBM, Linden DEJ, Owen MJ, Hall J, Lippé S, Dumas G, Draganski B, Almasy L, Thomopoulos SI, Jahanshad N, Sønderby IE, Andreassen OA, Glahn DC, Raznahan A, Bearden CE, Paus T, Thompson PM, Jacquemont S
Functional connectivity subtypes associate robustly with ASD diagnosis.
Urchs SGW, Tam A, Orban P, Moreau C, Benhajali Y, Nguyen HD, Evans AC, Bellec P
1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans.
Sønderby IE, van der Meer D, Moreau C, Kaufmann T, Walters GB, Ellegaard M, Abdellaoui A, Ames D, Amunts K, Andersson M, Armstrong NJ, Bernard M, Blackburn NB, Blangero J, Boomsma DI, Brodaty H, Brouwer RM, Bülow R, Bøen R, Cahn W, Calhoun VD, Caspers S, Ching CRK, Cichon S, Ciufolini S, Crespo-Facorro B, Curran JE, Dale AM, Dalvie S, Dazzan P, de Geus EJC, de Zubicaray GI, de Zwarte SMC, Desrivieres S, Doherty JL, Donohoe G, Draganski B, Ehrlich S, Eising E, Espeseth T, Fejgin K, Fisher SE, Fladby T, Frei O, Frouin V, Fukunaga M, Gareau T, Ge T, Glahn DC, Grabe HJ, Groenewold NA, Gústafsson Ó, Haavik J, Haberg AK, Hall J, Hashimoto R, Hehir-Kwa JY, Hibar DP, Hillegers MHJ, Hoffmann P, Holleran L, Holmes AJ, Homuth G, Hottenga JJ, Hulshoff Pol HE, Ikeda M, Jahanshad N, Jockwitz C, Johansson S, Jönsson EG, Jørgensen NR, Kikuchi M, Knowles EEM, Kumar K, Le Hellard S, Leu C, Linden DEJ, Liu J, Lundervold A, Lundervold AJ, Maillard AM, Martin NG, Martin-Brevet S, Mather KA, Mathias SR, McMahon KL, McRae AF, Medland SE, Meyer-Lindenberg A, Moberget T, Modenato C, Sánchez JM, Morris DW, Mühleisen TW, Murray RM, Nielsen J, Nordvik JE, Nyberg L, Loohuis LMO, Ophoff RA, Owen MJ, Paus T, Pausova Z, Peralta JM, Pike GB, Prieto C, Quinlan EB, Reinbold CS, Marques TR, Rucker JJH, Sachdev PS, Sando SB, Schofield PR, Schork AJ, Schumann G, Shin J, Shumskaya E, Silva AI, Sisodiya SM, Steen VM, Stein DJ, Strike LT, Suzuki IK, Tamnes CK, Teumer A, Thalamuthu A, Tordesillas-Gutiérrez D, Uhlmann A, Ulfarsson MO, van 't Ent D, van den Bree MBM, Vanderhaeghen P, Vassos E, Wen W, Wittfeld K, Wright MJ, Agartz I, Djurovic S, Westlye LT, Stefansson H, Stefansson K, Jacquemont S, Thompson PM, Andreassen OA, ENIGMA-CNV working group
Autonomic regulation of the heart and arrhythmogenesis in trained breath-hold divers.
Costalat G, Godin B, Balmain BN, Moreau C, Brotherton E, Billaut F, Lemaitre F
Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition.
Writing Committee for the ENIGMA-CNV Working Group, van der Meer D, Sønderby IE, Kaufmann T, Walters GB, Abdellaoui A, Ames D, Amunts K, Andersson M, Armstrong NJ, Bernard M, Blackburn NB, Blangero J, Boomsma DI, Brodaty H, Brouwer RM, Bülow R, Cahn W, Calhoun VD, Caspers S, Cavalleri GL, Ching CRK, Cichon S, Ciufolini S, Corvin A, Crespo-Facorro B, Curran JE, Dalvie S, Dazzan P, de Geus EJC, de Zubicaray GI, de Zwarte SMC, Delanty N, den Braber A, Desrivieres S, Di Forti M, Doherty JL, Donohoe G, Ehrlich S, Eising E, Espeseth T, Fisher SE, Fladby T, Frei O, Frouin V, Fukunaga M, Gareau T, Glahn DC, Grabe HJ, Groenewold NA, Gústafsson Ó, Haavik J, Haberg AK, Hashimoto R, Hehir-Kwa JY, Hibar DP, Hillegers MHJ, Hoffmann P, Holleran L, Hottenga JJ, Hulshoff Pol HE, Ikeda M, Jacquemont S, Jahanshad N, Jockwitz C, Johansson S, Jönsson EG, Kikuchi M, Knowles EEM, Kwok JB, Le Hellard S, Linden DEJ, Liu J, Lundervold A, Lundervold AJ, Martin NG, Mather KA, Mathias SR, McMahon KL, McRae AF, Medland SE, Moberget T, Moreau C, Morris DW, Mühleisen TW, Murray RM, Nordvik JE, Nyberg L, Olde Loohuis LM, Ophoff RA, Owen MJ, Paus T, Pausova Z, Peralta JM, Pike B, Prieto C, Quinlan EB, Reinbold CS, Reis Marques T, Rucker JJH, Sachdev PS, Sando SB, Schofield PR, Schork AJ, Schumann G, Shin J, Shumskaya E, Silva AI, Sisodiya SM, Steen VM, Stein DJ, Strike LT, Tamnes CK, Teumer A, Thalamuthu A, Tordesillas-Gutiérrez D, Uhlmann A, Úlfarsson MÖ, van 't Ent D, van den Bree MBM, Vassos E, Wen W, Wittfeld K, Wright MJ, Zayats T, Dale AM, Djurovic S, Agartz I, Westlye LT, Stefánsson H, Stefánsson K, Thompson PM, Andreassen OA
Estimating the effect size of the 15Q11.2 BP1-BP2 deletion and its contribution to neurodevelopmental symptoms: recommendations for practice.
Jønch AE, Douard E, Moreau C, Van Dijck A, Passeggeri M, Kooy F, Puechberty J, Campbell C, Sanlaville D, Lefroy H, Richetin S, Pain A, Geneviève D, Kini U, Le Caignec C, Lespinasse J, Skytte AB, Isidor B, Zweier C, Caberg JH, Delrue MA, Møller RS, Bojesen A, Hjalgrim H, Brasch-Andersen C, Lemyre E, Ousager LB, Jacquemont S, 15q11.2 Working Group
Multifeature brain investigation of genetic liability for neurodevelopmental and psychiatric disorders
Principal investigators: Jacquemont, Sebastien; Dumas, Guillaume; Lippé, Sarah; Moreau, Clara A; Paus, Tomas
Keywords: Brain Endophenotypes; Brain Imaging; Electroencephalography; Genomic Variants; Neurodevelopmental Disorders; Psychiatric Disorders
From CIHR, NSERC and SSHRC funding decisions: CIHR since 2008, NSERC since 1991 and SSHRC since 1998, including their latest published competition results.
Frequent collaborators
- Pediatrics
- Psychiatry
- Department of Psychiatry
- Neurology and Neurosurgery
- Informatique et recherche opérationnelle
- Other
Co-authors at Université de Montréal, colored by department. Thicker lines mean more shared papers; select anyone to open their profile and their own map.
Zdenka Pausova
Faculty
2 shared papers, latest 2021
Tomas Paus
Faculty
2 shared papers, latest 2021
Allan Kaplan
Department of Psychiatry
1 shared papers, latest 2026
Aristotle Voineskos
Psychiatry
1 shared papers, latest 2026
Pierre Bellec
Neurology and Neurosurgery
1 shared papers, latest 2022
Pierre Bellec
Informatique et recherche opérationnelle
1 shared papers, latest 2022
Pierre Orban
Faculty
1 shared papers, latest 2022
Tomas Paus
Pediatrics
1 shared papers, latest 2025
Sophia Frangou
Psychiatry
1 shared papers, latest 2026
Guillaume Dumas
Pediatrics
1 shared papers, latest 2025
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