The possible interplay of synaptic and clock genes in autism spectrum disorders von Bourgeron, T

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SHANK3 mutations identified in autism lead to modification of dendritic spine morphology via an actin-dependent mechanism von Durand, C M, Perroy, J, Loll, F, Perrais, D, Fagni, L, Bourgeron, T, Montcouquiol, M, Sans, N

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Cntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmission von Karayannis, T., Au, E., Patel, J. C., Kruglikov, I., Markx, S., Delorme, R., Héron, D., Salomon, D., Glessner, J., Restituito, S., Gordon, A., Rodriguez-Murillo, L., Roy, N. C., Gogos, J. A., Rudy, B., Rice, M. E., Karayiorgou, M., Hakonarson, H., Keren, B., Huguet, G., Bourgeron, T., Hoeffer, C., Tsien, R. W., Peles, E., Fishell, G.

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Genome-wide meta-analysis of cognitive empathy: heritability, and correlates with sex, neuropsychiatric conditions and cognition von Warrier, V, Grasby, K L, Uzefovsky, F, Toro, R, Smith, P, Chakrabarti, B, Khadake, J, Mawbey-Adamson, E, Litterman, N, Hottenga, J-J, Lubke, G, Boomsma, D I, Martin, N G, Hatemi, P K, Medland, S E, Hinds, D A, Bourgeron, T, Baron-Cohen, S

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The serotonin-N-acetylserotonin–melatonin pathway as a biomarker for autism spectrum disorders von Pagan, C, Delorme, R, Callebert, J, Goubran-Botros, H, Amsellem, F, Drouot, X, Boudebesse, C, Le Dudal, K, Ngo-Nguyen, N, Laouamri, H, Gillberg, C, Leboyer, M, Bourgeron, T, Launay, J-M

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Adaptation of a quantitative trait to a changing environment: New analytical insights on the asexual and infinitesimal sexual models von Garnier, J., Cotto, O., Bouin, E., Bourgeron, T., Lepoutre, T., Ronce, O., Calvez, V.

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Genomic architecture of human neuroanatomical diversity von Toro, R, Poline, J-B, Huguet, G, Loth, E, Frouin, V, Banaschewski, T, Barker, G J, Bokde, A, Büchel, C, Carvalho, F M, Conrod, P, Fauth-Bühler, M, Flor, H, Gallinat, J, Garavan, H, Gowland, P, Heinz, A, Ittermann, B, Lawrence, C, Lemaître, H, Mann, K, Nees, F, Paus, T, Pausova, Z, Rietschel, M, Robbins, T, Smolka, M N, Ströhle, A, Schumann, G, Bourgeron, T

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Absence of deficits in social behaviors and ultrasonic vocalizations in later generations of mice lacking neuroligin4 von Ey, E., Yang, M., Katz, A. M., Woldeyohannes, L., Silverman, J. L., Leblond, C. S., Faure, P., Torquet, N., Le Sourd, A.‐M., Bourgeron, T., Crawley, J. N.

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Differentiation from human pluripotent stem cells of cortical neurons of the superficial layers amenable to psychiatric disease modeling and high-throughput drug screening von Boissart, C, Poulet, A, Georges, P, Darville, H, Julita, E, Delorme, R, Bourgeron, T, Peschanski, M, Benchoua, A

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CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders von Mercati, O, Huguet, G, Danckaert, A, André-Leroux, G, Maruani, A, Bellinzoni, M, Rolland, T, Gouder, L, Mathieu, A, Buratti, J, Amsellem, F, Benabou, M, Van-Gils, J, Beggiato, A, Konyukh, M, Bourgeois, J-P, Gazzellone, M J, Yuen, R K C, Walker, S, Delépine, M, Boland, A, Régnault, B, Francois, M, Van Den Abbeele, T, Mosca-Boidron, A L, Faivre, L, Shimoda, Y, Watanabe, K, Bonneau, D, Rastam, M, Leboyer, M, Scherer, S W, Gillberg, C, Delorme, R, Cloëz-Tayarani, I, Bourgeron, T

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Abnormal melatonin synthesis in autism spectrum disorders von Melke, J, Goubran Botros, H, Chaste, P, Betancur, C, Nygren, G, Anckarsäter, H, Rastam, M, Ståhlberg, O, Gillberg, I C, Delorme, R, Chabane, N, Mouren-Simeoni, M-C, Fauchereau, F, Durand, C M, Chevalier, F, Drouot, X, Collet, C, Launay, J-M, Leboyer, M, Gillberg, C, Bourgeron, T

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Disentangling the Myriad Genomics of Complex Disorders, Specifically Focusing on Autism, Epilepsy, and Schizophrenia von Poot, M., van der Smagt, J.J., Brilstra, E.H., Bourgeron, T.

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Analysis of the chromosome X exome in patients with autism spectrum disorders identified novel candidate genes, including TMLHE von Nava, C, Lamari, F, Héron, D, Mignot, C, Rastetter, A, Keren, B, Cohen, D, Faudet, A, Bouteiller, D, Gilleron, M, Jacquette, A, Whalen, S, Afenjar, A, Périsse, D, Laurent, C, Dupuits, C, Gautier, C, Gérard, M, Huguet, G, Caillet, S, Leheup, B, Leboyer, M, Gillberg, C, Delorme, R, Bourgeron, T, Brice, A, Depienne, C

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Linkage and association of the glutamate receptor 6 gene with autism von Jamain, S, Betancur, C, Quach, H, Philippe, A, Fellous, M, Giros, B, Gillberg, C, Leboyer, M, Bourgeron, T

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S.01.02 - Genetics of autism spectrum disorder: impact on neuroanatomy and synaptic plasticity von Bourgeron, T.

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Genetics of autism spectrum disorder: impact on neuroanatomy and synaptic plasticity von Bourgeron, T.

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Linkage and association of the glutamate receptor 6 gene with autism von JAMAIN, S, BETANCUR, C, QUACH, H, PHILIPPE, A, FELLOUS, M, GIROS, B, GILLBERG, C, LEBOYER, M, BOURGERON, T

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Biochemical and molecular investigations in respiratory chain deficiencies von Rustin, P., Chretien, D., Bourgeron, T., Gérard, B., Rötig, A., Saudubray, J.M., Munnich, A.

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S.12.02 A human pluripotent stem cell-derived neuronal model for characterisation of pathways regulating the autism and schizophrenia-related gene SHANK-3 von Darville, H, Poulet, A, Pernelle, J, Delorme, R, Coge, F, Millan, M.J, Bourgeron, T, Peschanski, M, Benchoua, A

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The Genetic Landscapes of Autism Spectrum Disorders von Huguet, Guillaume, Ey, Elodie, Bourgeron, Thomas

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