Channel:  Simons Foundation Autism Research Initiative (SFARI)

280 Articles

Common risk variants identified in autism spectrum disorder
Grove, J., Ripke, S., Als, T. D., Mattheisen, M., Walters, R., Won, H., Pallesen, J., Agerbo, E., Andreassen, O. A., Anney, R., Belliveau, R., Bettella, F., Buxbaum, J. D., Bybjerg-Grauholm, J., Baekved-Hansen, M., Cerrato, F., Chambert, K., Christensen, J. H., Churchhouse, C., Dellenvall, K., Demontis, D., De Rubeis, S., Devlin, B., Djurovic, S., Dumont, A., Goldstein, J., Hansen, C. S., Hauberg, M. E., Hollegaard, M. V., Hope, S., Howrigan, D. P., Huang, H., Hultman, C., Klei, L., Maller, J., Martin, J., Martin, A. R., Moran, J., Nyegaard, M., Naerland, T., Palmer, D. S., Palotie, A., Peders
10.1101/224774 — Posted: 2017-11-27
Elevated polygenic burden for autism is associated with differential DNA methylation at birth.
Hannon, E., Schendel, D., Ladd-Acosta, C., Grove, J., iPSYCH-Broad ASD Group, , Hansen, C. S., Andrews, S. V., Hougaard, D., Bresnahan, M., Mors, O., Hollegaard, M. V., Baekvad-Hansen, M., Hornig, M., Mortensen, P. B., Borglum, A., Werge, T., Pedersen, M. G., Nordentoft, M., Buxbaum, J., Fallin, D., Bybjerg-Grauholm, J., Reichenberg, A., Mill, J.
10.1101/225193 — Posted: 2017-11-26
Two-Photon Imaging of Striatum Demonstrates Distinct Functions for Striosomes and Matrix in Reinforcement Learning
Bloem, B., Huda, R., Sur, M., Graybiel, A. M.
10.1101/199497 — Posted: 2017-11-24
Impaired perceptual learning in Fragile X syndrome is mediated by parvalbumin neuron dysfunction in V1 and is reversible.
Goel, A., Cantu, D., Guilfoyle, J., Chaudhari, G. R., Newadkar, A., Todisco, B., Alba, D. d., Kourdougli, N., Schmitt, L. M., Pedapati, E., Erickson, C. A., Portera-Cailliau, C.
10.1101/217414 — Posted: 2017-11-13
Abnormal Speech Motor Control in Individuals with 16p11.2 Deletions
Demopoulos, C., Kothare, H., Mizuiri, D., Henderson-Sabes, J., Fregeau, B., Tjernagel, J., Houde, J., Sherr, E., Nagarajan, S. S.
10.1101/165316 — Posted: 2017-11-01
Prediction and interpretation of deleterious coding variants in terms of protein structural stability
Ancien, F., Pucci, F., Godfroid, M., Rooman, M.
10.1101/210120 — Posted: 2017-10-27
Robust identification of deletions in exome and genome sequence data based on clustering of Mendelian errors
Manheimer, K. B., Patel, N., Richter, F., Gorham, J., Tai, A. C., Homsy, J., Boskovski, M. T., Parfenov, M., Goldmuntz, E., Chung, W. K., Brueckner, M., Tristani-Firouzi, M., Srivastava, D., Seidman, J. G., Seidman, C. E., Gelb, B. D., Sharp, A. J.
10.1101/209478 — Posted: 2017-10-26
Single-cell transcriptomic catalog of mouse cortical development
Loo, L., Simon, J. M., McCoy, E. S., Niehaus, J. K., Zylka, M. J.
10.1101/208744 — Posted: 2017-10-25
Quantification of autism recurrence risk by direct assessment of paternal sperm mosaicism
Breuss, M., Kleiber, M., George, R. D., Antaki, D., James, K. N., Ball, L. L., Hong, O., Garcia, C. A. B., Musaev, D., Nguyen, A., McEvoy-Venneri, J., Knox, R., Sticca, E., Devinsky, O., Gymrek, M., Sebat, J., Gleeson, J. G.
10.1101/208165 — Posted: 2017-10-24
Paternal-age-related de novo mutations and risk for five disorders
Taylor, J., Debost, J.-C. P. G., Morton, S. U., Wigdor, E. M., Heyne, H. O., Lal, D., Howrigan, D. P., Bloemendal, A., Larsen, J. T., Kosmicki, J. A., Weiner, D. J., Pediatric Cardiac Genomics Consortium, , Homsy, J., Seidman, J. G., Seidman, C. E., Agerbo, E., McGrath, J. J., Mortensen, P. B., Petersen, L., Daly, M. J., Robinson, E. B.
10.1101/192740 — Posted: 2017-09-22

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