Channel:  Simons Foundation Autism Research Initiative (SFARI)

280 Articles

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An open resource of structural variation for medical and population genetics
Collins, R. L., Brand, H., Karczewski, K. J., Zhao, X., Alföldi, J., Francioli, L. C., Khera, A. V., Lowther, C., Gauthier, L. D., Wang, H., Watts, N. A., Solomonson, M., O'Donnell-Luria, A., Baumann, A., Munshi, R., Walker, M., Whelan, C., Huang, Y., Brookings, T., Sharpe, T., Stone, M. R., Valkanas, E., Fu, J., Tiao, G., Laricchia, K. M., Ruano-Rubio, V., Stevens, C., Gupta, N., Margolin, L., Genome Aggregation Database Consortium, , Taylor, K. D., Lin, H. J., Rich, S. S., Post, W., Chen, Y.-D. I., Rotter, J. I., Nusbaum, C., Philippakis, A., Lander, E., Gabriel, S., Neale, B. M., Kathire
10.1101/578674 — Posted: 2019-10-21
A sex difference in the composition of the rodent postsynaptic density
Mastro, T. L., Preza, A., Basu, S., Chattarji, S., Till, S. M., Kind, P. C., Kennedy, M. B.
10.1101/802538 — Posted: 2019-10-12
Multi-model functionalization of disease-associated PTEN missense mutations identifies multiple molecular mechanisms underlying protein dysfunction
Post, K. L., Belmadani, M., Ganguly, P., Meili, F., Dingwall, R., McDiarmid, T. A., Meyers, W. M., Herrington, C., Young, B. P., Callaghan, D. B., Rogic, S., Edwards, M., Niciforovic, A., Cau, A., Rankin, C., OConnor, T. P., Bamji, S. X., Loewen, C. J., Allan, D. W., Pavlidis, P., Haas, K.
10.1101/800011 — Posted: 2019-10-10
Acute and repeated intranasal oxytocin differentially modulate brain-wide functional connectivity
Pagani, M., De Felice, A., Montani, C., Galbusera, A., Papaleo, F., Gozzi, A.
10.1101/798025 — Posted: 2019-10-09
FMRP binding to a ranked subset of long genes is revealed by coupled CLIP and TRAP in specific neuronal cell types
Van Driesche, S. J., Sawicka, K., Zhang, C., Hung, S. K. Y., Park, C. Y., Fak, J. J., Yang, C., Darnell, R. B., Darnell, J. C.
10.1101/762500 — Posted: 2019-09-09
Psychotic symptoms in 16p11.2 copy number variant carriers
Jutla, A., Turner, J. B., Green Snyder, L., Chung, W. K., Veenstra-VanderWeele, J.
10.1101/621250 — Posted: 2019-09-06
Shared risk alleles with discordant polygenic effects: Disentangling the genetic overlap between ASD and ADHD
Verhoef, E., Grove, J., Shapland, C. Y., Demontis, D., Burgess, S., Rai, D., Borglum, A. D., St Pourcain, B.
10.1101/580365 — Posted: 2019-09-04
Ketamine disinhibits dendrites and enhances calcium signals in prefrontal dendritic spines
Ali, F., Gerhard, D. M., Sweasy, K., Pothula, S., Pittenger, C., Duman, R. S., Kwan, A. C.
10.1101/659292 — Posted: 2019-08-23
Robust Hi-C chromatin loop maps in human neurogenesis and brain tissues at high-resolution
LU, L., Liu, X., Huang, W.-K., Giusti-Rodriguez, P., Cui, J., Zhang, S., Xu, W., Wen, Z., Ma, S., Rosen, J. D., Xu, Z., Bartels, C., Riki Kawaguchi, R., Hu, M., Scacheri, P., Rong, Z., Li, Y., Sullivan, P. F., Song, H., Ming, G.-l., Li, Y., Jin, F.
10.1101/744540 — Posted: 2019-08-22
Human cerebral organoids capture the spatiotemporal complexity and disease dynamics of UBE3A
Sen, D., Voulgaropoulos, A., Drobna, Z., Keung, A. J.
10.1101/742213 — Posted: 2019-08-22

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