Channel:  Simons Foundation Autism Research Initiative (SFARI)

280 Articles

The autism-associated gene Scn2a plays an essential role in synaptic stability and learning
Spratt, P., Ben-Shalom, R., Keeshen, C., Burke, K., Clarkson, R., Sanders, S., Bender, K.
10.1101/366781 — Posted: 2018-07-10
Both rare and common genetic variants contribute to autism in the Faroe Islands
Leblond, C., Cliquet, F., Carton, C., Huguet, G., Mathieu, A., Kergrohen, T., Buratti, J., Lemiere, N., Cuisset, L., Bienvenu, T., Boland, A., Deleuze, J.-F., Stora, T., Biskupstoe, R., Halling, J., Andorsdottir, G., Billstedt, E., Gillberg, C., Bourgeron, T.
10.1101/363853 — Posted: 2018-07-09
Whole genome sequencing in multiplex families reveals novel inherited and de novo genetic risk in autism
Ruzzo, E. K., Perez-Cano, L., Jung, J.-Y., Wang, L.-k., Kashef-Haghighi, D., Hartl, C., Hoekstra, J., Leventhal, O., Gandal, M. J., Paskov, K., Stockham, N., Polioudakis, D., Lowe, J. K., Geschwind, D. H., Wall, D. P.
10.1101/338855 — Posted: 2018-06-06
Rbfox1 mediates cell-type-specific splicing in cortical interneurons
Jaglin, X. H., Wamsley, B., Favuzzi, E., Quattracolo, G., Nigro, M. J., Yusef, N., Khodadadi-Jamayran, A., Rudy, B., Fishell, G.
10.1101/305904 — Posted: 2018-05-17
Dynamics of social representation in the mouse prefrontal cortex
Levy, D. R., Tamir, T., Kaufman, M., Weissbrod, A., Schneidman, E., Yizhar, O.
10.1101/321182 — Posted: 2018-05-14
Widespread Alterations in Translation Elongation in the Brain of Juvenile Fmr1 Knock-Out Mice
Das Sharma, S., Metz, J. B., Li, H., Hobson, B. D., Hornstein, N., Sulzer, D., Tang, G., Sims, P. A.
10.1101/319368 — Posted: 2018-05-10
Increased excitation-inhibition ratio stabilizes synapse and circuit excitability in four autism mouse models.
Antoine, M. W., Schnepel, P., Langberg, T., Feldman, D. E.
10.1101/317693 — Posted: 2018-05-09
Disentangling genetically confounded polygenic associations between Attention-Deficit/Hyperactivity Disorder, literacy and language
Verhoef, E., Demontis, D., Burgess, S., Shapland, C. Y., Dale, P. S., Okbay, A., Neale, B. M., Faraone, S. V., iPSYCH-Broad-PGC ADHD Consortium, , Stergiakouli, E., Davey Smith, G., Fisher, S. E., Borglum, A., St Pourcain, B.
10.1101/276527 — Posted: 2018-05-03
Rare variants in the genetic background modulate the expressivity of neurodevelopmental disorders
Pizzo, L., Jensen, M., Polyak, A., Rosenfeld, J. A., Mannik, K., Krishnan, A., McCready, E., Pichon, O., Le Caignec, C., Van Dijck, A., Pope, K., Voorhoeve, E., Yoon, J., Stankiewicz, P., Cheung, S. W., Pazuchanics, D., Huber, E., Kumar, V., Kember, R., Mari, F., Curro, A., Castiglia, L., Galesi, O., Avola, E., Mattina, T., Fichera, M., Mandara, L., Vincent, M., Nizon, M., Mercier, S., Beneteau, C., Blesson, S., Martin-Coignard, D., Mosca-Boidron, A.-L., Caberg, J. H., Bucan, M., Zeesman, S., Nowaczyk, M. J. M., Lefebvre, M., Faivre, L., Callier, P., Skinner, C., Keren, B., Perrine, C., Pronte
10.1101/257758 — Posted: 2018-04-18
MVP: predicting pathogenicity of missense variants by deep learning
Qi, H., Chen, C., Zhang, H., Long, J. J., Chung, W. K., Guan, Y., Shen, Y.
10.1101/259390 — Posted: 2018-04-02

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