Biblio

Found 4 results
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2018
J. C. Bis, Jian, X., Kunkle, B. W., Chen, Y., Hamilton-Nelson, K. L., Bush, W. S., Salerno, W. J., Lancour, D., Ma, Y., Renton, A. E., Marcora, E., Farrell, J. J., Zhao, Y., Qu, L., Ahmad, S., Amin, N., Amouyel, P., Beecham, G. W., Below, J. E., Campion, D., Charbonnier, C., Chung, J., Crane, P. K., Cruchaga, C., L Cupples, A., Dartigues, J. - F., Debette, S., Deleuze, J. - F., Fulton, L., Gabriel, S. B., Genin, E., Gibbs, R. A., Goate, A., Grenier-Boley, B., Gupta, N., Haines, J. L., Havulinna, A. S., Helisalmi, S., Hiltunen, M., Howrigan, D. P., M Ikram, A., Kaprio, J., Konrad, J., Kuzma, A., Lander, E. S., Lathrop, M., Lehtimäki, T., Lin, H., Mattila, K., Mayeux, R., Muzny, D. M., Nasser, W., Neale, B., Nho, K., Nicolas, G., Patel, D., Pericak-Vance, M. A., Perola, M., Psaty, B. M., Quenez, O., Rajabli, F., Redon, R., Reitz, C., Remes, A. M., Salomaa, V., Sarnowski, C., Schmidt, H., Schmidt, M., Schmidt, R., Soininen, H., Thornton, T. A., Tosto, G., Tzourio, C., van der Lee, S. J., van Duijn, C. M., Vardarajan, B., Wang, W., Wijsman, E., Wilson, R. K., Witten, D., Worley, K. C., Zhang, X., Bellenguez, C., Lambert, J. - C., Kurki, M. I., Palotie, A., Daly, M., Boerwinkle, E., Lunetta, K. L., DeStefano, A. L., Dupuis, J., Martin, E. R., Schellenberg, G. D., Seshadri, S., Naj, A. C., Fornage, M., and Farrer, L. A., Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation., Mol Psychiatry, 2018.
B. N. Vardarajan, Barral, S., Jaworski, J., Beecham, G. W., Blue, E., Tosto, G., Reyes-Dumeyer, D., Medrano, M., Lantigua, R., Naj, A., Thornton, T., DeStefano, A., Martin, E., San Wang, L. -, Brown, L., Bush, W., van Duijn, C., Goate, A., Farrer, L., Haines, J. L., Boerwinkle, E., Schellenberg, G., Wijsman, E., Pericak-Vance, M. A., Mayeux, R., and San Wang, L. -, Whole genome sequencing of Caribbean Hispanic families with late-onset Alzheimer's disease., Ann Clin Transl Neurol, vol. 5, no. 4, pp. 406-417, 2018.
N. S. Raghavan, Brickman, A. M., Andrews, H., Manly, J. J., Schupf, N., Lantigua, R., Wolock, C. J., Kamalakaran, S., Petrovski, S., Tosto, G., Vardarajan, B. N., Goldstein, D. B., and Mayeux, R., Whole-exome sequencing in 20,197 persons for rare variants in Alzheimer's disease., Ann Clin Transl Neurol, vol. 5, no. 7, pp. 832-842, 2018.