Channel:  Simons Foundation Autism Research Initiative (SFARI)

280 Articles

De novo damaging coding mutations are strongly associated with obsessive-compulsive disorder and overlap with autism
Cappi, C., Oliphant, M. E., Peter, Z., Zai, G., Sullivan, C. A., Gupta, A. R., Hoffman, E. J., Virdee, M., Willsey, A. J., Shavitt, R. G., Miguel, E. C., Kennedy, J. L., Richter, M. A., Fernandez, T. V.
10.1101/127712 — Posted: 2017-09-21
Developmental diversification of cortical inhibitory interneurons.
Mayer, C., Hafemeister, C., Bandler, R. C., Machold, R., Allaway, K., Jaglin, X., Brito, R. B., Butler, A., Fishell, G., Satija, R.
10.1101/105312 — Posted: 2017-09-13
Genetic analysis of very obese children with autism spectrum disorder
Cortes, H. D., Wevrick, R.
10.1101/185900 — Posted: 2017-09-12
Increased axonal bouton stability during learning in the mouse model of MECP2 duplication syndrome
Ash, R. T., Fahey, P. G., Park, J., Zoghbi, H. Y., Smirnakis, S. M.
10.1101/186239 — Posted: 2017-09-08
TiSAn: Estimating Tissue Specific Effects of Coding and Non-coding Variants
Vervier, K., Michaelson, J. J.
10.1101/141408 — Posted: 2017-08-30
Whole Genome Sequencing in Psychiatric Disorders: the WGSPD Consortium
Sanders, S. J., Neale, B. M., Huang, H., Werling, D. M., An, J.-Y., Dong, S., - Whole Genome Sequencing for Psychiatric Disorders, , Abecasis, G., Arguello, P. A., Blangero, J., Boehnke, M., Daly, M., Eggan, K., Geschwind, D. H., Glahn, D., Goldstein, D. B., Gur, R. E., Handsaker, R. E., McCarroll, S. A., Ophoff, R. A., Palotie, A., Pato, C., Sabatti, C., State, M. W., Willsey, A. J., Hyman, S. E., Addington, A., Lehner, T., Freimer, N. B.
10.1101/160499 — Posted: 2017-07-07
An insula-central amygdala circuit for behavioral inhibition
Schiff, H. C., Bouhuis, A. L., Yu, K., Penzo, M. A., Li, H., He, M., Li, B.
10.1101/156216 — Posted: 2017-06-26
Distinct contributions of three GABAergic interneuron populations to a mouse model of Rett Syndrome.
Mossner, J., Batista-Brito, R., Pant, R., Cardin, J.
10.1101/155382 — Posted: 2017-06-25
Normal CA1 place fields but discoordinated network discharge in a Fmr1-null mouse model of fragile X syndrome
Sparks, F. T., Talbot, Z. N., Dvorak, D., Curran, B. M., Alarcon, J. M., Fenton, A. A.
10.1101/152462 — Posted: 2017-06-20
Mutational sequencing for accurate count and long-range assembly
Kumar, V., Rosenbaum, J., Wang, Z., Forcier, T., Ronemus, M., Wigler, M., Levy, D.
10.1101/149740 — Posted: 2017-06-13

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