Channel:  Simons Foundation Autism Research Initiative (SFARI)

280 Articles

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Homeostatic Plasticity Commonly Fails at the Intersection of Autism-Gene Mutations and a Novel Class of Common Phenotypic Modifier
Genc, O., An, J. Y., Fetter, R. D., Kulik, Y., Zunino, G., Sanders, S. J., Davis, G. W.
10.1101/2020.01.31.927665 — Posted: 2020-01-31
FMRP Control of Ribosome Translocation Promotes Chromatin Modifications and Alternative Splicing of Neuronal Genes Linked to Autism
Shah, S., Molinaro, G., Liu, B., Wang, R., Huber, K., Richter, J.
10.1101/801076 — Posted: 2020-01-27
The stability flexibility tradeoff and the dark side of detail
Nassar, M. R., Troiani, V.
10.1101/2020.01.03.894014 — Posted: 2020-01-03
Regulation of Prefrontal Patterning, Connectivity and Synaptogenesis by Retinoic Acid
Shibata, M., Pattabiraman, K., Lorente-Galdos, B., Andreijevic, D., Xing, X., Sousa, A. M. M., Santpere, G., Sestan, N.
10.1101/2019.12.31.891036 — Posted: 2019-12-31
Increased variability but intact integration during visual navigation in Autism Spectrum Disorder
Noel, J.-P., Lakshminarasimhan, K. J., Park, H., Angelaki, D.
10.1101/2019.12.28.890004 — Posted: 2019-12-28
Massively parallel disruption of enhancers active during human corticogenesis
Geller, E., Gockley, J., Emera, D., Uebbing, S., Cotney, J., Noonan, J. P.
10.1101/852673 — Posted: 2019-12-02
Reduced sleep pressure in young children with autism
Arazi, A., Meiri, G., Danan, D., Michaelovski, A., Flusser, H., Menashe, I., Tarasiuk, A., Dinstein, I.
10.1101/706135 — Posted: 2019-11-19
G-Graph: An interactive genomic graph viewer
Andrews, P. A., Alexander, J., Kendall, J., Wigler, M.
10.1101/803015 — Posted: 2019-11-18
Transcriptome-wide transmission disequilibrium analysis identifies novel risk genes for autism spectrum disorder
Huang, K., Wu, Y., Shin, J., Zheng, Y., Fotuhi Siahpirani, A., Lin, Y., Ni, Z., Chen, J., You, J., Keles, S., Wang, D., Roy, S., Lu, Q.
10.1101/835678 — Posted: 2019-11-15
MEF2C hypofunction in neuronal and neuroimmune populations cooperate to produce MEF2C haploinsufficiency syndrome-like behaviors in mice
Harrington, A. J., Bridges, C. M., Blankenship, K., Assali, A., Berto, S., Siemsen, B. M., Moore, H. W., Cho, J. Y., Tsvetkov, E., Thielking, A., Konopka, G., Everman, D. B., Scofield, M., Skinner, S. A., Cowan, C. W.
10.1101/824151 — Posted: 2019-10-30

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