Ohcanbohtosat - Courraud, Jérémie

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  1. 1
    Sex-specific impact of prenatal androgens on social brain default mode subsystems

    Sex-specific impact of prenatal androgens on social brain default mode subsystems Dahkki Lombardo, Michael V., Auyeung, Bonnie, Pramparo, Tiziano, Quartier, Angélique, Courraud, Jérémie, Holt, Rosemary J., Waldman, Jack, Ruigrok, Amber N. V., Mooney, Natasha, Bethlehem, Richard A. I., Lai, Meng-Chuan, Kundu, Prantik, Bullmore, Edward T., Mandel, Jean-Louis, Piton, Amélie, Baron-Cohen, Simon

    Almmustuhtton 2018
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  2. 2
    Conditional switching of KIF2A mutation provides new insights into cortical malformation pathogeny

    Conditional switching of KIF2A mutation provides new insights into cortical malformation pathogeny Dahkki Gilet, Johan G, Ivanova, Ekaterina L, Trofimova, Daria, Rudolf, Gabrielle, Meziane, Hamid, Broix, Loic, Drouot, Nathalie, Courraud, Jeremie, Skory, Valerie, Voulleminot, Paul, Osipenko, Maria, Bahi-Buisson, Nadia, Yalcin, Binnaz, Birling, Marie-Christine, Hinckelmann, Maria-Victoria, Kwok, Benjamin H, Allingham, John S, Chelly, Jamel

    Almmustuhtton 2020
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  3. 3
    De Novo Frameshift Variants in the Neuronal Splicing Factor NOVA2 Result in a Common C-Terminal Extension and Cause a Severe Form of Neurodevelopmental Disorder

    De Novo Frameshift Variants in the Neuronal Splicing Factor NOVA2 Result in a Common C-Terminal Extension and Cause a Severe Form of Neurodevelopmental Disorder Dahkki Mattioli, Francesca, Hayot, Gaelle, Drouot, Nathalie, Isidor, Bertrand, Courraud, Jérémie, Hinckelmann, Maria-Victoria, Mau-Them, Frederic Tran, Sellier, Chantal, Goldman, Alica, Telegrafi, Aida, Boughton, Alicia, Gamble, Candace, Moutton, Sebastien, Quartier, Angélique, Jean, Nolwenn, Van Ness, Paul, Grotto, Sarah, Nambot, Sophie, Douglas, Ganka, Si, Yue Cindy, Chelly, Jamel, Shad, Zohra, Kaplan, Elisabeth, Dineen, Richard, Golzio, Christelle, Charlet-Berguerand, Nicolas, Mandel, Jean-Louis, Piton, Amélie

    Almmustuhtton 2020
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  4. 4
    Biallelic PDE2A variants: a new cause of syndromic paroxysmal dyskinesia

    Biallelic PDE2A variants: a new cause of syndromic paroxysmal dyskinesia Dahkki Doummar, Diane, Dentel, Christel, Lyautey, Romane, Metreau, Julia, Keren, Boris, Drouot, Nathalie, Malherbe, Ludivine, Bouilleret, Viviane, Courraud, Jérémie, Valenti-Hirsch, Maria Paola, Minotti, Lorella, Dozieres-Puyravel, Blandine, Bär, Séverine, Scholly, Julia, Schaefer, Elise, Nava, Caroline, Wirth, Thomas, Nasser, Hala, de Salins, Marie, de Saint Martin, Anne, Warde, Marie Thérèse Abi, Kahane, Philippe, Hirsch, Edouard, Anheim, Mathieu, Friant, Sylvie, Chelly, Jamel, Mignot, Cyril, Rudolf, Gabrielle

    Almmustuhtton 2020
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