Channel:  Simons Foundation Autism Research Initiative (SFARI)

280 Articles

CRISPR activation rescues abnormalities in SCN2A haploinsufficiency-associated autism spectrum disorder
Tamura, S., Nelson, A. D., Spratt, P. W., Kyoung, H., Zhou, X., Li, Z., Zhao, J., Holden, S. S., Sahagun, A., Keeshen, C. M., Lu, C., Hamada, E. C., Ben-Shalom, R., Pan, J. Q., Paz, J. T., Sanders, S. J., Matharu, N., Ahituv, N., Bender, K. J.
10.1101/2022.03.30.486483 — Posted: 2022-04-01
Glial dysregulation in human brain in Fragile X-related disorders
Dias, C. M., Talukdar, M., Akula, S., Walsh, K. G., Walsh, C. A.
10.1101/2022.03.29.486195 — Posted: 2022-03-29
Mobile elements in human population-specific genome and phenotype divergence
Kojima, S., Koyama, S., Ka, M., Saito, Y., Parrish, E. H., Endo, M., Takata, S., Mizukoshi, M., Hikino, K., Takeda, A., Gelinas, A. F., Heaton, S. M., Koide, R., Kamada, A. J., Noguchi, M., Hamada, M., Biobank Japan Project Consortium, , Kamatani, Y., Murakawa, Y., Ishigaki, K., Nakamura, Y., Ito, K., Terao, C., Momozawa, Y., Parrish, N. F.
10.1101/2022.03.25.485726 — Posted: 2022-03-27
Dissociable Cellular and Genetic Mechanisms of Cortical Thinning at Different Life Stages
Modabbernia, A., Vidal-Pineiro, D., Agartz, I., Andreassen, O. A., Ayesa-Arriola, R., Bertolino, A., Boomsma, D. I., Bourque, J., Breier, A., Brouwer, R. M., Buitelaar, J. K., Canales-Rodriguez, E. J., Caseras, X., Conrod, P. J., Crespo-Facorro, B., Crivello, F., Crone, E. A., de Zubicaray, G. I., Dickie, E. W., Dima, D., Frenzel, S., Fisher, S. E., Franke, B., Glahn, D. C., Grabe, H.-J., Grotegerd, D., Gruber, O., Guerrero-Pedraza, A., Gur, R. E., Gur, R. C., Hartman, C. A., Hoekstra, P. J., Hulshoff Pol, H. E., Jahanshad, N., Jernigan, T. L., Jiang, J., Kalnin, A. J., Kochan, N. A., Mazoyer
10.1101/2022.03.21.484899 — Posted: 2022-03-22
Multi-omic analysis along the gut-brain axis points to a functional architecture of autism
Morton, J. T., Jin, D.-m., Mills, R., Shao, Y., Rahman, G., McDonald, D., Harold-Berding, K., Needham, B. D., Zurita, M. F., David, M., Averina, O., Kovtun, A., Noto, A., Mussap, M., Wang, M., Frank, D., Li, E., Zhou, W., Fanos, V., Danilenko, V., Wall, D. P., Cardenas, P. A., Baldeon, M., xavier, r. j., Mazmanian, S., Knight, R., Gilbert, J., Donovan, S., Lawley, T., Carpenter, B., Bonneau, R., Taroncher-Oldenburg, G.
10.1101/2022.02.25.482050 — Posted: 2022-03-09
Measuring the response to visually presented faces in the human lateral prefrontal cortex
Nikel, L., Sliwinska, M., Kucuk, E., Ungerleider, L., Pitcher, D.
10.1101/2022.03.06.483119 — Posted: 2022-03-07
Patterns of connectome variability in autism across five functional activation tasks. Findings from the LEAP project
Looden, T., Floris, D. L., Llera Arenas, A., Chauvin, R. J., Charman, T., Banaschewski, T., Murphy, D., Marquand, A. F., Buitelaar, J. K., Beckmann, C. F., the AIMS-2-TRIALS group
10.1101/2022.02.22.481408 — Posted: 2022-02-28
Autism is associated with inter-individual variations of gray and white matter morphology
Mei, T., Forde, N. J., Floris, D. L., Dell'Acqua, F., Stones, R., Ilioska, I., Durston, S., Moessnang, C., Banaschewski, T., Holt, R. J., Baron-Cohen, S., Rausch, A., Loth, E., Oakley, B., Charman, T., Ecker, C., Murphy, D. G. M., the EU-AIMS LEAP group, , Beckmann, C. F., Llera, A., Buitelaar, J. K.
10.1101/2022.02.16.480649 — Posted: 2022-02-17
Quantitative fate mapping: Reconstructing progenitor field dynamics via retrospective lineage barcoding
Fang, W., Bell, C. M., Sapirstein, A., Asami, S., Leeper, K., Zack, D. J., Ji, H., Kalhor, R.
10.1101/2022.02.13.480215 — Posted: 2022-02-14
Variability in sampling of cortex-wide neural dynamics explains individual differences in functional connectivity and behavioral phenotype
MacDowell, C. J., Briones, B. A., Lenzi, M. J., Gustison, M. L., Buschman, T. J.
10.1101/2022.01.24.477572 — Posted: 2022-01-25

RSS  Channel RSS