Works matching AU Huguet, Guillaume

Results: 33
    1
    2

    Copy-number variants and polygenic risk for intelligence confer risk for autism spectrum disorder irrespective of their effects on cognitive ability.

    Published in:
    Frontiers in Psychiatry, 2024, p. 1, doi. 10.3389/fpsyt.2024.1369767
    By:
    • Schmilovich, Zoe;
    • Bourque, Vincent-Raphaël;
    • Douard, Elise;
    • Huguet, Guillaume;
    • Poulain, Cécile;
    • Ross, Jay P.;
    • Alipour, Paria;
    • Castonguay, Charles-Étienne;
    • Younis, Nadine;
    • Jean-Louis, Martineau;
    • Saci, Zohra;
    • Pausova, Zdenka;
    • Paus, Tomas;
    • Schuman, Gunter;
    • Porteous, David;
    • Davies, Gail;
    • Redmond, Paul;
    • Harris, Sarah E.;
    • Deary, Ian J.;
    • Whalley, Heather
    Publication type:
    Article
    3

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

    Published in:
    Nature Communications, 2025, v. 16, n. 1, p. 1, doi. 10.1038/s41467-025-56855-1
    By:
    • Liao, Zhijie;
    • Kumar, Kuldeep;
    • Kopal, Jakub;
    • Huguet, Guillaume;
    • Saci, Zohra;
    • Jean-Louis, Martineau;
    • Pausova, Zdenka;
    • Jurisica, Igor;
    • Bearden, Carrie E.;
    • 16p11.2 European Consortium;
    • Jacquemont, Sebastien;
    • Paus, Tomas
    Publication type:
    Article
    4

    Effects of Alzheimer's disease genetic risk on brain morphometric development in three multiple‐ancestry pediatric datasets.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.080302
    By:
    • Vogel, Jacob W;
    • Schultz, Laura M;
    • Larsen, Bart;
    • Seidlitz, Jakob;
    • Al‐Sharif, Noor B;
    • Barzilay, Ran;
    • Cieslak, Matthew;
    • Covitz, Sydney;
    • Gur, Raquel E;
    • Gur, Ruben C;
    • Huguet, Guillaume;
    • La Joie, Renaud;
    • McMillan, Corey T;
    • Nilsson, Nathalie I.V.;
    • Poline, Jean‐Baptiste;
    • Ruparel, Kosha;
    • Shinohara, Russell T.;
    • Wisse, Laura EM;
    • Wolf, Daniel;
    • Wolk, David A.
    Publication type:
    Article
    5
    6

    Investigating the contributions of circadian pathway and insomnia risk genes to autism and sleep disturbances.

    Published in:
    Translational Psychiatry, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41398-022-02188-2
    By:
    • Tesfaye, Rackeb;
    • Huguet, Guillaume;
    • Schmilovich, Zoe;
    • Renne, Thomas;
    • Loum, Mor Absa;
    • Douard, Elise;
    • Saci, Zohra;
    • Jean-Louis, Martineau;
    • Martineau, Jean Luc;
    • Whelan, Rob;
    • Desrivieres, Sylvane;
    • Heinz, Andreas;
    • Schumann, Gunter;
    • Hayward, Caroline;
    • Elsabbagh, Mayada;
    • Jacquemont, Sebastien
    Publication type:
    Article
    7

    Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments.

    Published in:
    PLoS Genetics, 2014, v. 10, n. 9, p. 1, doi. 10.1371/journal.pgen.1004580
    By:
    • Leblond, Claire S.;
    • Nava, Caroline;
    • Polge, Anne;
    • Gauthier, Julie;
    • Huguet, Guillaume;
    • Lumbroso, Serge;
    • Giuliano, Fabienne;
    • Stordeur, Coline;
    • Depienne, Christel;
    • Mouzat, Kevin;
    • Pinto, Dalila;
    • Howe, Jennifer;
    • Lemière, Nathalie;
    • Durand, Christelle M.;
    • Guibert, Jessica;
    • Ey, Elodie;
    • Toro, Roberto;
    • Peyre, Hugo;
    • Mathieu, Alexandre;
    • Amsellem, Frédérique
    Publication type:
    Article
    8

    Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders.

    Published in:
    PLoS Genetics, 2012, v. 8, n. 2, p. 1, doi. 10.1371/journal.pgen.1002521
    By:
    • Leblond, Claire S.;
    • Heinrich, Jutta;
    • Delorme, Richard;
    • Proepper, Christian;
    • Betancur, Catalina;
    • Huguet, Guillaume;
    • Konyukh, Marina;
    • Chaste, Pauline;
    • Ey, Elodie;
    • Rastam, Maria;
    • Anckarsäter, Henrik;
    • Nygren, Gudrun;
    • Gillberg, I. Carina;
    • Melke, Jonas;
    • Toro, Roberto;
    • Regnault, Beatrice;
    • Fauchereau, Fabien;
    • Mercati, Oriane;
    • Lemière, Nathalie;
    • Skuse, David
    Publication type:
    Article
    9

    Copy Number Variant Risk Scores Associated With Cognition, Psychopathology, and Brain Structure in Youths in the Philadelphia Neurodevelopmental Cohort.

    Published in:
    2022
    By:
    • Alexander-Bloch, Aaron;
    • Huguet, Guillaume;
    • Schultz, Laura M.;
    • Huffnagle, Nicholas;
    • Jacquemont, Sebastien;
    • Seidlitz, Jakob;
    • Saci, Zohra;
    • Moore, Tyler M.;
    • Bethlehem, Richard A. I.;
    • Mollon, Josephine;
    • Knowles, Emma K.;
    • Raznahan, Armin;
    • Merikangas, Alison;
    • Chaiyachati, Barbara H.;
    • Raman, Harshini;
    • Schmitt, J. Eric;
    • Barzilay, Ran;
    • Calkins, Monica E.;
    • Shinohara, Russel T.;
    • Satterthwaite, Theodore D.
    Publication type:
    journal article
    10
    11

    Measuring and Estimating the Effect Sizes of Copy Number Variants on General Intelligence in Community-Based Samples.

    Published in:
    2018
    By:
    • Huguet, Guillaume;
    • Schramm, Catherine;
    • Douard, Elise;
    • Jiang, Lai;
    • Labbe, Aurélie;
    • Tihy, Frédérique;
    • Mathonnet, Géraldine;
    • Nizard, Sonia;
    • Lemyre, Emmanuelle;
    • Mathieu, Alexandre;
    • Poline, Jean-Baptiste;
    • Loth, Eva;
    • Toro, Roberto;
    • Schumann, Gunter;
    • Conrod, Patricia;
    • Pausova, Zdenka;
    • Greenwood, Celia;
    • Paus, Tomas;
    • Bourgeron, Thomas;
    • Jacquemont, Sébastien
    Publication type:
    journal article
    12

    Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia.

    Published in:
    Translational Psychiatry, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41398-019-0402-0
    By:
    • Gialluisi, Alessandro;
    • Andlauer, Till F. M.;
    • Mirza-Schreiber, Nazanin;
    • Moll, Kristina;
    • Becker, Jessica;
    • Hoffmann, Per;
    • Ludwig, Kerstin U.;
    • Czamara, Darina;
    • St Pourcain, Beate;
    • Brandler, William;
    • Honbolygó, Ferenc;
    • Tóth, Dénes;
    • Csépe, Valéria;
    • Huguet, Guillaume;
    • Morris, Andrew P.;
    • Hulslander, Jacqueline;
    • Willcutt, Erik G.;
    • DeFries, John C.;
    • Olson, Richard K.;
    • Smith, Shelley D.
    Publication type:
    Article
    13

    Single-cell analysis reveals inflammatory interactions driving macular degeneration.

    Published in:
    Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-37025-7
    By:
    • Kuchroo, Manik;
    • DiStasio, Marcello;
    • Song, Eric;
    • Calapkulu, Eda;
    • Zhang, Le;
    • Ige, Maryam;
    • Sheth, Amar H.;
    • Majdoubi, Abdelilah;
    • Menon, Madhvi;
    • Tong, Alexander;
    • Godavarthi, Abhinav;
    • Xing, Yu;
    • Gigante, Scott;
    • Steach, Holly;
    • Huang, Jessie;
    • Huguet, Guillaume;
    • Narain, Janhavi;
    • You, Kisung;
    • Mourgkos, George;
    • Dhodapkar, Rahul M.
    Publication type:
    Article
    14

    Both rare and common genetic variants contribute to autism in the Faroe Islands.

    Published in:
    NPJ Genomic Medicine, 2019, v. 4, n. 1, p. N.PAG, doi. 10.1038/s41525-018-0075-2
    By:
    • Leblond, Claire S;
    • Cliquet, Freddy;
    • Carton, Coralie;
    • Huguet, Guillaume;
    • Mathieu, Alexandre;
    • Kergrohen, Thomas;
    • Buratti, Julien;
    • Lemière, Nathalie;
    • Cuisset, Laurence;
    • Bienvenu, Thierry;
    • Boland, Anne;
    • Deleuze, Jean-François;
    • Stora, Tormodur;
    • Biskupstoe, Rannva;
    • Halling, Jónrit;
    • Andorsdóttir, Guðrið;
    • Billstedt, Eva;
    • Gillberg, Christopher;
    • Bourgeron, Thomas
    Publication type:
    Article
    15

    Both rare and common genetic variants contribute to autism in the Faroe Islands.

    Published in:
    NPJ Genomic Medicine, 2019, v. 4, n. 1, p. N.PAG, doi. 10.1038/s41525-018-0075-2
    By:
    • Leblond, Claire S;
    • Cliquet, Freddy;
    • Carton, Coralie;
    • Huguet, Guillaume;
    • Mathieu, Alexandre;
    • Kergrohen, Thomas;
    • Buratti, Julien;
    • Lemière, Nathalie;
    • Cuisset, Laurence;
    • Bienvenu, Thierry;
    • Boland, Anne;
    • Deleuze, Jean-François;
    • Stora, Tormodur;
    • Biskupstoe, Rannva;
    • Halling, Jónrit;
    • Andorsdóttir, Guðrið;
    • Billstedt, Eva;
    • Gillberg, Christopher;
    • Bourgeron, Thomas
    Publication type:
    Article
    16

    Author Correction: Using rare genetic mutations to revisit structural brain asymmetry.

    Published in:
    Nature Communications, 2024, v. 15, p. 1, doi. 10.1038/s41467-024-47545-5
    By:
    • Kopal, Jakub;
    • Kumar, Kuldeep;
    • Shafighi, Kimia;
    • Saltoun, Karin;
    • Modenato, Claudia;
    • Moreau, Clara A.;
    • Huguet, Guillaume;
    • Jean-Louis, Martineau;
    • Martin, Charles-Olivier;
    • Saci, Zohra;
    • Younis, Nadine;
    • Douard, Elise;
    • Jizi, Khadije;
    • Beauchamp-Chatel, Alexis;
    • Kushan, Leila;
    • Silva, Ana I.;
    • van den Bree, Marianne B. M.;
    • Linden, David E. J.;
    • Owen, Michael J.;
    • Hall, Jeremy
    Publication type:
    Article
    17

    Author Correction: Using rare genetic mutations to revisit structural brain asymmetry.

    Published in:
    2024
    By:
    • Kopal, Jakub;
    • Kumar, Kuldeep;
    • Shafighi, Kimia;
    • Saltoun, Karin;
    • Modenato, Claudia;
    • Moreau, Clara A.;
    • Huguet, Guillaume;
    • Jean-Louis, Martineau;
    • Martin, Charles-Olivier;
    • Saci, Zohra;
    • Younis, Nadine;
    • Douard, Elise;
    • Jizi, Khadije;
    • Beauchamp-Chatel, Alexis;
    • Kushan, Leila;
    • Silva, Ana I.;
    • van den Bree, Marianne B. M.;
    • Linden, David E. J.;
    • Owen, Michael J.;
    • Hall, Jeremy
    Publication type:
    Correction Notice
    18

    Using rare genetic mutations to revisit structural brain asymmetry.

    Published in:
    Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-46784-w
    By:
    • Kopal, Jakub;
    • Kumar, Kuldeep;
    • Shafighi, Kimia;
    • Saltoun, Karin;
    • Modenato, Claudia;
    • Moreau, Clara A.;
    • Huguet, Guillaume;
    • Jean-Louis, Martineau;
    • Martin, Charles-Olivier;
    • Saci, Zohra;
    • Younis, Nadine;
    • Douard, Elise;
    • Jizi, Khadije;
    • Beauchamp-Chatel, Alexis;
    • Kushan, Leila;
    • Silva, Ana I.;
    • van den Bree, Marianne B. M.;
    • Linden, David E. J.;
    • Owen, Michael J.;
    • Hall, Jeremy
    Publication type:
    Article
    19

    Genomic and Developmental Models to Predict Cognitive and Adaptive Outcomes in Autistic Children.

    Published in:
    JAMA Pediatrics, 2025, v. 179, n. 6, p. 655, doi. 10.1001/jamapediatrics.2025.0205
    By:
    • Bourque, Vincent-Raphaël;
    • Schmilovich, Zoe;
    • Huguet, Guillaume;
    • England, Jade;
    • Okewole, Adeniran;
    • Poulain, Cécile;
    • Renne, Thomas;
    • Jean-Louis, Martineau;
    • Saci, Zohra;
    • Zhang, Xinhe;
    • Rolland, Thomas;
    • Labbé, Aurélie;
    • Vorstman, Jacob;
    • Rouleau, Guy A.;
    • Baron-Cohen, Simon;
    • Mottron, Laurent;
    • Bethlehem, Richard A. I.;
    • Warrier, Varun;
    • Jacquemont, Sébastien
    Publication type:
    Article
    20

    Effects of eight neuropsychiatric copy number variants on human brain structure.

    Published in:
    Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01490-9
    By:
    • Modenato, Claudia;
    • Kumar, Kuldeep;
    • Moreau, Clara;
    • Martin-Brevet, Sandra;
    • Huguet, Guillaume;
    • Schramm, Catherine;
    • Jean-Louis, Martineau;
    • Martin, Charles-Olivier;
    • Younis, Nadine;
    • Tamer, Petra;
    • Douard, Elise;
    • Thébault-Dagher, Fanny;
    • Côté, Valérie;
    • Charlebois, Audrey-Rose;
    • Deguire, Florence;
    • Maillard, Anne M.;
    • Rodriguez-Herreros, Borja;
    • Pain, Aurèlie;
    • Richetin, Sonia;
    • 16p11.2 European Consortium
    Publication type:
    Article
    21

    Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders.

    Published in:
    Human Genetics, 2014, v. 133, n. 6, p. 781, doi. 10.1007/s00439-013-1416-y
    By:
    • Waltes, Regina;
    • Duketis, Eftichia;
    • Knapp, Michael;
    • Anney, Richard;
    • Huguet, Guillaume;
    • Schlitt, Sabine;
    • Jarczok, Tomasz;
    • Sachse, Michael;
    • Kämpfer, Laura;
    • Kleinböck, Tina;
    • Poustka, Fritz;
    • Bölte, Sven;
    • Schmötzer, Gabriele;
    • Voran, Anette;
    • Huy, Ellen;
    • Meyer, Jobst;
    • Bourgeron, Thomas;
    • Klauck, Sabine;
    • Freitag, Christine;
    • Chiocchetti, Andreas
    Publication type:
    Article
    22

    11q24.2-25 Micro-Rearrangements in Autism Spectrum Disorders: Relation to Brain Structures.

    Published in:
    American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 12, p. 3019, doi. 10.1002/ajmg.a.37345
    By:
    • Maruani, Anna;
    • Huguet, Guillaume;
    • Beggiato, Anita;
    • ElMaleh, Monique;
    • Toro, Roberto;
    • Leblond, Claire S.;
    • Mathieu, Alexandre;
    • Amsellem, Frederique;
    • Lemière, Nathalie;
    • Verloes, Alain;
    • Leboyer, Marion;
    • Gillberg, Christopher;
    • Bourgeron, Thomas;
    • Delorme, Richard
    Publication type:
    Article
    23

    Brain functional connectivity mirrors genetic pleiotropy in psychiatric conditions.

    Published in:
    Brain: A Journal of Neurology, 2023, v. 146, n. 4, p. 1686, doi. 10.1093/brain/awac315
    By:
    • Moreau, Clara A;
    • Kumar, Kuldeep;
    • Harvey, Annabelle;
    • Huguet, Guillaume;
    • Urchs, Sebastian G W;
    • Schultz, Laura M;
    • Sharmarke, Hanad;
    • Jizi, Khadije;
    • Martin, Charles-Olivier;
    • Younis, Nadine;
    • Tamer, Petra;
    • Martineau, Jean-Louis;
    • Orban, Pierre;
    • Silva, Ana Isabel;
    • Hall, Jeremy;
    • Bree, Marianne B M van den;
    • Owen, Michael J;
    • Linden, David E J;
    • Lippé, Sarah;
    • Bearden, Carrie E
    Publication type:
    Article
    24

    Mutations associated with neuropsychiatric conditions delineate functional brain connectivity dimensions contributing to autism and schizophrenia.

    Published in:
    Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-18997-2
    By:
    • Moreau, Clara A.;
    • Urchs, Sebastian G. W.;
    • Kuldeep, Kumar;
    • Orban, Pierre;
    • Schramm, Catherine;
    • Dumas, Guillaume;
    • Labbe, Aurélie;
    • Huguet, Guillaume;
    • Douard, Elise;
    • Quirion, Pierre-Olivier;
    • Lin, Amy;
    • Kushan, Leila;
    • Grot, Stephanie;
    • Luck, David;
    • Mendrek, Adrianna;
    • Potvin, Stephane;
    • Stip, Emmanuel;
    • Bourgeron, Thomas;
    • Evans, Alan C.;
    • Bearden, Carrie E.
    Publication type:
    Article
    25
    26

    Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders.

    Published in:
    Journal of Pineal Research, 2011, v. 51, n. 4, p. 394, doi. 10.1111/j.1600-079X.2011.00902.x
    By:
    • Chaste, Pauline;
    • Clement, Nathalie;
    • Botros, Hany Goubran;
    • Guillaume, Jean-Luc;
    • Konyukh, Marina;
    • Pagan, Cécile;
    • Scheid, Isabelle;
    • Nygren, Gudrun;
    • Anckarsäter, Henrik;
    • Rastam, Maria;
    • Ståhlberg, Ola;
    • Gillberg, I. Carina;
    • Melke, Jonas;
    • Delorme, Richard;
    • Leblond, Claire;
    • Toro, Roberto;
    • Huguet, Guillaume;
    • Fauchereau, Fabien;
    • Durand, Christelle;
    • Boudarene, Lydia
    Publication type:
    Article
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    Effects of Alzheimer's disease genetic risk on brain morphometric development in three multiple‐ancestry pediatric datasets.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, n. 10, p. 1, doi. 10.1002/alz.081996
    By:
    • Vogel, Jacob W;
    • Schultz, Laura M;
    • Larsen, Bart;
    • Seidlitz, Jakob;
    • Al‐Sharif, Noor B;
    • Barzilay, Ran;
    • Cieslak, Matthew;
    • Covitz, Sydney;
    • Gur, Raquel E;
    • Gur, Ruben C;
    • Huguet, Guillaume;
    • La Joie, Renaud;
    • McMillan, Corey T;
    • Nilsson, Nathalie I.V.;
    • Poline, Jean‐Baptiste;
    • Ruparel, Kosha;
    • Shinohara, Russell T.;
    • Wisse, Laura EM;
    • Wolf, Daniel;
    • Wolk, David A.
    Publication type:
    Article
    31
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    Heterozygous FA2H mutations in autism spectrum disorders.

    Published in:
    BMC Medical Genetics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2350-14-124
    By:
    • Scheid, Isabelle;
    • Maruani, Anna;
    • Huguet, Guillaume;
    • Leblond, Claire S.;
    • Nygren, Gudrun;
    • Anckarsäter, Henrik;
    • Beggiato, Anita;
    • Rastam, Maria;
    • Fréderique Amsellem;
    • Carina Gillberg, I.;
    • Elmaleh, Monique;
    • Leboyer, Marion;
    • Gillberg, Christopher;
    • Betancur, Catalina;
    • Coleman, Mary;
    • Hama, Hiroko;
    • Cook, Edwin H.;
    • Bourgeron, Thomas;
    • Delorme, Richard
    Publication type:
    Article