Faculty profile

Sebastien Jacquemont

ResearcherMcGill University

This profile is built from public research funding records (CIHR, NSERC and SSHRC) and PubMed. We have not imported them from a McGill University directory, so their courses and email address may be missing. Find their university profile.

Sebastien Jacquemont

Researcher

Health Sciences

McGill University

Montreal, Quebec, Canada

Supervision signals

Has led research grants, which requires an independent research appointment. Ask their department whether they supervise graduate students.
22 publications in the last five years, latest in 2026.
Senior (last) author on 4 recent papers, a sign of leading a research group.
Principal investigator on 1 research grant (1 CIHR), most recently in 2023.

These signals come from public records, including CIHR, NSERC and SSHRC funding decisions. Ask the professor or the graduate program whether they are taking new students.

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Publications

Citations

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Collaborators

Grants

Publications by year

Counts cover the works listed on the university profile; citation counts come from Dimensions.

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Signals and details

Research

16p11.2 Copy Number Variations Autism Spectrum Disorders Brain Networks Computational Models Functional Connectivity Magnetic Resonance Imaging Myelination Neuroimaging

Latest papers

Recent Progress of Large-Scale Biomarker Consortia and Paths Forward in Autism Biomarker Development.
Biological psychiatry · 2026
Prevention of hydrocephalus with a small oligonucleotide.
Molecular therapy : the journal of the American Society of Gene Therapy · 2026
Mirror effect of genomic deletions and duplications on cognitive ability across the human cerebral cortex.
bioRxiv : the preprint server for biology · 2025 · senior author

All 35 publications

Latest funding

Atypical cerebral myelination in individuals with 16p11.2 copy number variations and its relationship with functional connectivity and behaviour
CIHR · 2023 · Principal investigator
$585,225
Studying prenatal exposure to maternal immune activation as risk factor for neurodevelopmental disorders: from the fetus to adulthood
CIHR · 2019 · Co-investigator
$803,250

All 2 grants and awards

35 publications.

Recent Progress of Large-Scale Biomarker Consortia and Paths Forward in Autism Biomarker Development.

Griffin JW, Cairney B, Carson WE, Chetcuti L, Dubois AEE, Dumas G, Jacquemont S, Jeste S, Momsen JP, Naples AJ, McPartland JC

Biological psychiatry2026

DOI: 10.1016/j.biopsych.2026.08.005 PMID: 42595244

Prevention of hydrocephalus with a small oligonucleotide.

Antonyan L, Bossini L, Zhang X, Ni A, Hagel MD, Baronchelli E, Geusa M, Peng H, Semenak A, Fleming P, Alsuwaidi S, Zhang Y, Hu B, Fontana D, Crippa V, Codazzi S, Macintosh J, Arriaga-Sierra A, Khan B, Hettige N, Jefri M, Liang Y, Klein S, du Toit A, Phan NTN, Schuppert A, Zhou Y, Piazza R, Murai K, Jacquemont S, Sessa A, Ernst C

Molecular therapy : the journal of the American Society of Gene Therapy2026

DOI: 10.1016/j.ymthe.2026.01.034 PMID: 41612697

Mirror effect of genomic deletions and duplications on cognitive ability across the human cerebral cortex.

Kumar K, Kazem S, Huguet G, Engchuan W, Kopal J, Renne T, Shanta O, Thiruvahindrapuram B, MacDonald JR, Mollon J, Schultz LM, Knowles EEM, Porteous D, Davies G, Redmond P, Harris SE, Cox SR, Schumann G, Pausova Z, Greenwood CMT, Paus T, Scherer SW, Almasy L, Sebat J, Glahn DC, Dumas G, Jacquemont S

bioRxiv : the preprint server for biology2025Senior author

DOI: 10.1101/2025.01.06.631492 PMID: 41292898

The interplay between genomic copy number variants, sleep, and cognition in the general population.

Poulain C, Tesfaye R, Douard E, Martineau JL, Saci Z, Labbe A, Glahn DC, Almasy L, Elsabbagh M, Huguet G, Jacquemont S

Translational psychiatry2025Senior author

DOI: 10.1038/s41398-025-03579-x PMID: 41053002

Analyzing the Quality of Life in Individuals with Fragile X Syndrome in Relation to Sleep and Mental Health.

Minhas A, Whitlock K, Rosenfelt C, Shatto J, Finlay B, Zwicker J, Lippe S, Jacquemont S, Hagerman R, Murias K, Bolduc FV

Journal of autism and developmental disorders2025

DOI: 10.1007/s10803-024-06317-2 PMID: 38653851

Copy number variants and the tangential expansion of the cerebral cortex.

Liao Z, Kumar K, Kopal J, Huguet G, Saci Z, Jean-Louis M, Pausova Z, Jurisica I, Bearden CE, IMAGEN Consortium, 16p11.2 European Consortium, Jacquemont S, Paus T

Nature communications2025

DOI: 10.1038/s41467-025-56855-1 PMID: 39962045

Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplications.

Gur RC, Bearden CE, Jacquemont S, Swillen A, van Amelsvoort T, van den Bree M, Vorstman J, Sebat J, Ruparel K, Gallagher RS, McClellan E, White L, Crowley TB, Giunta V, Kushan L, O'Hora K, Verbesselt J, Vandensande A, Vingerhoets C, van Haelst M, Hall J, Harwood J, Chawner SJRA, Patel N, Palad K, Hong O, Guevara J, Martin CO, Jizi K, Bélanger AM, Scherer SW, Bassett AS, McDonald-McGinn DM, Gur RE

Molecular psychiatry2025

DOI: 10.1038/s41380-024-02661-y PMID: 39048645

Longitudinal follow-up of metformin treatment in Fragile X Syndrome.

Seng P, Montanaro FAM, Biag HMB, Salcedo-Arellano MJ, Kim K, Ponzini MD, Tassone F, Schneider A, Abbeduto L, Thurman AJ, Hessl D, Bolduc FV, Jacquemont S, Lippé S, Hagerman RJ

Frontiers in psychology2024

DOI: 10.3389/fpsyg.2024.1305597 PMID: 38939222

Further delineation of the rare GDACCF (global developmental delay, absent or hypoplastic corpus callosum, dysmorphic facies syndrome): genotype and phenotype of 22 patients with ZNF148 mutations.

Szakszon K, Lourenco CM, Callewaert BL, Geneviève D, Rouxel F, Morin D, Denommé-Pichon AS, Vitobello A, Patterson WG, Louie R, Pinto E Vairo F, Klee E, Kaiwar C, Gavrilova RH, Agre KE, Jacquemont S, Khadijé J, Giltay J, van Gassen K, Merő G, Gerkes E, Van Bon BW, Rinne T, Pfundt R, Brunner HG, Caluseriu O, Grasshoff U, Kehrer M, Haack TB, Khelifa MM, Bergmann AK, Cueto-González AM, Martorell AC, Ramachandrappa S, Sawyer LB, Fasel P, Braun D, Isis A, Superti-Furga A, McNiven V, Chitayat D, Ahmed SA, Brennenstuhl H, Schwaibolf EM, Battisti G, Parmentier B, Stevens SJC

Journal of medical genetics2024

DOI: 10.1136/jmg-2022-109030 PMID: 37580113

Beyond the Global Brain Differences: Intraindividual Variability Differences in 1q21.1 Distal and 15q11.2 BP1-BP2 Deletion Carriers.

Boen R, Kaufmann T, van der Meer D, Frei O, Agartz I, Ames D, Andersson M, Armstrong NJ, Artiges E, Atkins JR, Bauer J, Benedetti F, Boomsma DI, Brodaty H, Brosch K, Buckner RL, Cairns MJ, Calhoun V, Caspers S, Cichon S, Corvin AP, Crespo-Facorro B, Dannlowski U, David FS, de Geus EJC, de Zubicaray GI, Desrivières S, Doherty JL, Donohoe G, Ehrlich S, Eising E, Espeseth T, Fisher SE, Forstner AJ, Fortaner-Uyà L, Frouin V, Fukunaga M, Ge T, Glahn DC, Goltermann J, Grabe HJ, Green MJ, Groenewold NA, Grotegerd D, Grøntvedt GR, Hahn T, Hashimoto R, Hehir-Kwa JY, Henskens FA, Holmes AJ, Håberg AK, Haavik J, Jacquemont S, Jansen A, Jockwitz C, Jönsson EG, Kikuchi M, Kircher T, Kumar K, Le Hellard S, Leu C, Linden DE, Liu J, Loughnan R, Mather KA, McMahon KL, McRae AF, Medland SE, Meinert S, Moreau CA, Morris DW, Mowry BJ, Mühleisen TW, Nenadić I, Nöthen MM, Nyberg L, Ophoff RA, Owen MJ, Pantelis C, Paolini M, Paus T, Pausova Z, Persson K, Quidé Y, Marques TR, Sachdev PS, Sando SB, Schall U, Scott RJ, Selbæk G, Shumskaya E, Silva AI, Sisodiya SM, Stein F, Stein DJ, Straube B, Streit F, Strike LT, Teumer A, Teutenberg L, Thalamuthu A, Tooney PA, Tordesillas-Gutierrez D, Trollor JN, van 't Ent D, van den Bree MBM, van Haren NEM, Vázquez-Bourgon J, Völzke H, Wen W, Wittfeld K, Ching CRK, Westlye LT, Thompson PM, Bearden CE, Selmer KK, Alnæs D, Andreassen OA, Sønderby IE, ENIGMA-CNV Working Group

Biological psychiatry2024

DOI: 10.1016/j.biopsych.2023.08.018 PMID: 37661008

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Sebastien Jacquemont

Research

Latest papers

Latest funding

Recent Progress of Large-Scale Biomarker Consortia and Paths Forward in Autism Biomarker Development.

Prevention of hydrocephalus with a small oligonucleotide.

Mirror effect of genomic deletions and duplications on cognitive ability across the human cerebral cortex.

The interplay between genomic copy number variants, sleep, and cognition in the general population.

Analyzing the Quality of Life in Individuals with Fragile X Syndrome in Relation to Sleep and Mental Health.

Copy number variants and the tangential expansion of the cerebral cortex.

Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplications.

Longitudinal follow-up of metformin treatment in Fragile X Syndrome.

Further delineation of the rare GDACCF (global developmental delay, absent or hypoplastic corpus callosum, dysmorphic facies syndrome): genotype and phenotype of 22 patients with ZNF148 mutations.

Beyond the Global Brain Differences: Intraindividual Variability Differences in 1q21.1 Distal and 15q11.2 BP1-BP2 Deletion Carriers.

Atypical cerebral myelination in individuals with 16p11.2 copy number variations and its relationship with functional connectivity and behaviour

Studying prenatal exposure to maternal immune activation as risk factor for neurodevelopmental disorders: from the fetus to adulthood

Frequent collaborators

Sebastien Jacquemont

Zdenka Pausova

Guillaume Dumas

Tomas Paus

Pierre Bellec

Carl Ernst

Laurent Mottron

Pierre Bellec

Mayada Elsabbagh

Tomas Paus

Michael Wainberg

Kara Murias

Zdenka Pausova

Boris Bernhardt

Jacob Vorstman

Pierre Orban

Jennifer Zwicker

YANG ZHOU

Fidel Vila-Rodriguez

Danilo Bzdok

Adrianna Mendrek

Danilo Bzdok

Sarah Lippé