Search Results - Jacques L Michaud

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  1. 1

    Unraveling the role of non-coding rare variants in epilepsy by Alexandre Girard, Claudia Moreau, Jacques L. Michaud, Berge Minassian, Patrick Cossette, Simon L. Girard

    Published in PLoS ONE (2023-01-01)
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  2. 2

    Unraveling the role of non-coding rare variants in epilepsy. by Alexandre Girard, Claudia Moreau, Jacques L Michaud, Berge Minassian, Patrick Cossette, Simon L Girard

    Published in PLoS ONE (2023-01-01)
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  3. 3

    Syngap1 regulates the synaptic drive and membrane excitability of Parvalbumin-positive interneurons in mouse auditory cortex by Ruggiero Francavilla, Bidisha Chattopadhyaya, Jorelle Linda Damo Kamda, Vidya Jadhav, Said Kourrich, Jacques L Michaud, Graziella Di Cristo

    Published in eLife (2025-08-01)
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  4. 4

    Auditory repetition suppression alterations in relation to cognitive functioning in fragile X syndrome: a combined EEG and machine learning approach by Inga Sophia Knoth, Tarek Lajnef, Simon Rigoulot, Karine Lacourse, Phetsamone Vannasing, Jacques L. Michaud, Sébastien Jacquemont, Philippe Major, Karim Jerbi, Sarah Lippé

    Published in Journal of Neurodevelopmental Disorders (2018-01-01)
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  5. 5

    Assessment of burden and segregation profiles of CNVs in patients with epilepsy by Claudia Moreau, Frédérique Tremblay, Stefan Wolking, Alexandre Girard, Catherine Laprise, Fadi F. Hamdan, Jacques L. Michaud, Berge A. Minassian, Patrick Cossette, Simon L. Girard

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  6. 6

    Mice doubly-deficient in lysosomal hexosaminidase A and neuraminidase 4 show epileptic crises and rapid neuronal loss. by Volkan Seyrantepe, Pablo Lema, Aurore Caqueret, Larbi Dridi, Samar Bel Hadj, Stephane Carpentier, Francine Boucher, Thierry Levade, Lionel Carmant, Roy A Gravel, Edith Hamel, Pascal Vachon, Graziella Di Cristo, Jacques L Michaud, Carlos R Morales, Alexey V Pshezhetsky

    Published in PLoS Genetics (2010-09-01)
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  7. 7

    Global characterization of copy number variants in epilepsy patients from whole genome sequencing. by Jean Monlong, Simon L Girard, Caroline Meloche, Maxime Cadieux-Dion, Danielle M Andrade, Ron G Lafreniere, Micheline Gravel, Dan Spiegelman, Alexandre Dionne-Laporte, Cyrus Boelman, Fadi F Hamdan, Jacques L Michaud, Guy Rouleau, Berge A Minassian, Guillaume Bourque, Patrick Cossette

    Published in PLoS Genetics (2018-04-01)
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  8. 8

    Whole-exome sequencing reveals a rapid change in the frequency of rare functional variants in a founding population of humans. by Ferran Casals, Alan Hodgkinson, Julie Hussin, Youssef Idaghdour, Vanessa Bruat, Thibault de Maillard, Jean-Christophe Grenier, Elias Gbeha, Fadi F Hamdan, Simon Girard, Jean-François Spinella, Mathieu Larivière, Virginie Saillour, Jasmine Healy, Isabel Fernández, Daniel Sinnett, Jacques L Michaud, Guy A Rouleau, Elie Haddad, Françoise Le Deist, Philip Awadalla

    Published in PLoS Genetics (2013-01-01)
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