Channel:  Simons Foundation Autism Research Initiative (SFARI)

bioRxiv posts many COVID19-related papers. A reminder: they have not been formally peer-reviewed and should not guide health-related behavior or be reported in the press as conclusive.

180 Articles

Systematic evaluation of genome sequencing for the assessment of fetal structural anomalies
Lowther, C., Valkanas, E., Giordano, J. L., Wang, H. Z., Currall, B. B., O'Keefe, K., Pierce-Hoffman, E., Kurtas, N. E., Whelan, C. W., Hao, S. P., Weisburd, B. W., Jalili, V., Fu, J., Wong, I., Collins, R. L., Zhao, X., Austin-Tse, C. A., Evangelista, E., Lemire, G., Aggarwal, V., Lucente, D., Gauthier, L. D., Tolonen, C., Sahakian, N., Stevens, C., An, J.-Y., Dong, S., Norton, M. E., MacKenzie, T., Devlin, B., Gilmore, K., Powell, B., Brandt, A., Vetrini, F., DiVito, M., Sanders, S. J., MacArthur, D. G., Hodge, J. C., O'Donnell-Luria, A., Rehm, H., Vora, N., Levy, B., Brand, H., Wapner, R.
10.1101/2020.08.12.248526 — Posted: 2022-09-23
A new type of mouse gaze shift is led by directed saccades
Zahler, S. H., Taylor, D. E., Wong, J. Y., Adams, J. M., Feinberg, E. H.
10.1101/2021.02.10.430669 — Posted: 2021-09-08
ASXL3 controls cortical neuron fate specification through extrinsic self-renewal pathways
McGrath, B. T., Wu, P., Salvi, S., Girgla, N., Xu, C., Zhu, J., KC, R., Tsan, Y.-C., Moccia, A., Srivastava, A., Zhou, X., Bielas, S. L.
10.1101/2021.07.20.452995 — Posted: 2021-07-21
Full-length isoform transcriptome of developing human brain provides new insights into autism
Chau, K., Zhang, P., Urresti, J., Amar, M., Pramod, A. B., Chen, J., Thomas, A., Corominas, R., Lin, G. N., Iakoucheva, L. M.
10.1101/2020.06.27.175489 — Posted: 2021-06-02
Deep multitask learning of gene risk for comorbid neurodevelopmental disorders
Beyreli, I., Karakahya, O., Cicek, A. E.
10.1101/2020.06.13.150201 — Posted: 2021-05-31
Atypical genomic cortical patterning in autism with poor early language outcome
Lombardo, M. V., Eyler, L., Pramparo, T., Gazestani, V. H., Hagler, D. J., Chen, C.-H., Dale, A. M., Seidlitz, J., Bethlehem, R. A. I., Bertelsen, N., Carter Barnes, C., Lopez, L., Campbell, K., Lewis, N. E., Pierce, K., Courchesne, E.
10.1101/2020.08.18.253443 — Posted: 2021-05-20
NRF1 Association with AUTS2-Polycomb Mediates Specific Gene Activation in the Brain
Liu, S., Aldinger, K. A., Cheng, C. V., Kiyama, T., Dave, M., McNamara, H. K., Caraffi, S. G., Ivanovski, I., Errichiello, E., Zweier, C., Zuffardi, O., Schneider, M., Papavasiliou, A. S., Perry, M. S., Cho, M. T., Weber, A., Swale, A., Badea, T. C., Mao, C.-A., Garavelli, L., Dobyns, W. B., Reinberg, D.
10.1101/2021.03.30.437620 — Posted: 2021-05-04
Chromatin remodeler Arid1a regulates subplate neuron identity and wiring of cortical connectivity
Doyle, D. Z., Lam, M. M., Qalieh, A., Qalieh, Y., Sorel, A., Funk, O. H., Kwan, K. Y.
10.1101/2020.12.14.422645 — Posted: 2021-04-14
fmr1 mutation interacts with sensory experience to alter the early development of behavior and sensory coding in zebrafish
Zhu, S., McCullough, M., Pujic, Z., Sibberas, J., Sun, B., Bucknall, B., Avitan, L., Goodhill, G.
10.1101/2021.03.16.435742 — Posted: 2021-04-14
Autism risk gene POGZ promotes chromatin accessibility and expression of clustered synaptic genes
Markenscoff, E., Binyameen, F., Whalen, S., Price, J., Lim, K., Catta-Preta, R., Pai, E. L.-L., Mu, X., Xu, D., Pollard, K. S., Nord, A., State, M. W., Rubenstein, J. L. R.
10.1101/2021.04.07.438852 — Posted: 2021-04-08

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