The caudal infrasylvian surface in dyslexia : Novel magnetic resonance imaging-based findings von GREEN, R. L, HUTSLER, J. J, LOFTUS, W. C, TRAMO, M. J, THOMAS, C. E, SILBERFARB, A. W, NORDGREN, R. E, NORDGREN, R. A, GAZZANIGA, M. S

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Evidence for long-lived components in developing mouse tissues labeled with leucine von Nordgren, R.A., Hirsch, G.P., Menzies, R.A., Hendley, D.D., Kutsky, R., Strehler, B.L.

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Evidence for long-lived lipid components in developing mouse tissues von Gee, M, Nordgren, R A, Menzies, R A, Hirsch, G P, Kutsky, R, Strehler, B L

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Evidence for long-lived lipid components in developing mouse tissues von Gee, M., Nordgren, R.A., Menzies, R.A., Hirsch, G.P., Kutsky, R., Strehler, B.L.

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Assessment of the efficacy of a single dose of a recombinant vaccine against West Nile virus in response to natural challenge with West Nile virus-infected mosquitoes in horses von Siger, L, Bowen, R.A, Karaca, K, Murray, M.J, Gordy, P.W, Loosmore, S.M, Audonnet, J.C.F, Nordgren, R.M, Minke, J.M

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Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders von Wang, T., Hoekzema, K., Vecchio, D., Wu, H.D., Sulovari, A., Coe, B.P., Gillentine, M.A., Wilfert, A.B., Perez-Jurado, L.A., Kvarnung, M., Sleyp, Y., Earl, R.K., Rosenfeld, J.A., Geisheker, M.R., Han, L., , B. du, Barnett, C., Thompson, E., Shaw, M., Carroll, R., Friend, K., Catford, R., Palmer, E.E., Zou, X.B., Ou, J.J., Li, H.H., Guo, H., Gerdts, J., Avola, E., Calabrese, G., Elia, M., Greco, D., Lindstrand, A., Nordgren, A., Anderlid, B.M., Vandeweyer, G., Dijck, A. van, Aa, N. van der, McKenna, B., Hancarova, M., Bendova, S., Havlovicova, M., Malerba, G., Bernardina, B. dalla, Muglia, P., Haeringen, A. van, Hoffer, M.J.V., Franke, B., Cappuccio, G., Delatycki, M., Lockhart, P.J., Manning, M.A., Liu, P.F., Scheffer, I.E., Brunetti-Pierri, N., Rommelse, N., Amaral, D.G., Santen, G.W.E., Trabetti, E., Sedlacek, Z., Michaelson, J.J., Pierce, K., Courchesne, E., Kooy, R.F., Nordenskjold, M., Romano, C., Peeters, H., Bernier, R.A., Gecz, J., Xia, K., Eichler, E.E.

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Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains von Geisheker, M.R., Heymann, G., Wang, T.Y., Coe, B.P., Turner, T.N., Stessman, H.A.F., Hoekzema, K., Kvarnung, M., Shaw, M., Friend, K., Liebelt, J., Barnett, C., Thompson, E.M., Haan, E., Guo, H., Anderlid, B.M., Nordgren, A., Lindstrand, A., Vandeweyer, G., Alberti, A., Avola, E., Vinci, M., Giusto, S., Pramparo, T., Pierce, K., Nalabolu, S., Michaelson, J.J., Sedlacek, Z., Santen, G.W.E., Peeters, H., Hakonarson, H., Courchesne, E., Romano, C., Kooy, R.F., Bernier, R.A., Nordenskjold, M., Gecz, J., Xia, K., Zweifel, L.S., Eichler, E.E.

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Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases von Stessman, H.A.F., Xiong, B., Coe, B.P., Wang, T.Y., Hoekzema, K., Fenckova, M., Kvarnung, M., Gerdts, J., Trinh, S., Cosemans, N., Vives, L., Lin, J., Turner, T.N., Santen, G., Ruivenkamp, C., Kriek, M., Haeringen, A. van, Aten, E., Friend, K., Liebelt, J., Barnett, C., Haan, E., Shaw, M., Gecz, J., Anderlid, B.M., Nordgren, A., Lindstrand, A., Schwartz, C., Kooy, R.F., Vandeweyer, G., Helsmoortel, C., Romano, C., Alberti, A., Vinci, M., Avola, E., Giusto, S., Courchesne, E., Pramparo, T., Pierce, K., Nalabolu, S., Amaral, D.G., Scheffer, I.E., Delatycki, M.B., Lockhart, P.J., Hormozdiari, F., Harich, B., Castells-Nobau, A., Xia, K., Peeters, H., Nordenskjold, M., Schenck, A., Bernier, R.A., Eichler, E.E.

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