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Biblio

Found 34 results
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B
G. W. Beecham, Hamilton, K., Naj, A. C., Martin, E. R., Huentelman, M., Myers, A. J., Corneveaux, J. J., Hardy, J., Vonsattel, J. - P., Younkin, S. G., Bennett, D. A., De Jager, P. L., Larson, E. B., Crane, P. K., M Kamboh, I., Kofler, J. K., Mash, D. C., Duque, L., Gilbert, J. R., Gwirtsman, H., Buxbaum, J. D., Kramer, P., Dickson, D. W., Farrer, L. A., Frosch, M. P., Ghetti, B., Haines, J. L., Hyman, B. T., Kukull, W. A., Mayeux, R. P., Pericak-Vance, M. A., Schneider, J. A., Trojanowski, J. Q., Reiman, E. M., Schellenberg, G. D., and Montine, T. J., Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias., PLoS Genet, vol. 10, no. 9, p. e1004606, 2014.
D. A. Bennett, Schneider, J. A., Arvanitakis, Z., and Wilson, R. S., Overview and findings from the religious orders study., Curr Alzheimer Res, vol. 9, no. 6, pp. 628-45, 2012.
D. A. Bennett, Schneider, J. A., Buchman, A. S., Barnes, L. L., Boyle, P. A., and Wilson, R. S., Overview and findings from the rush Memory and Aging Project., Curr Alzheimer Res, vol. 9, no. 6, pp. 646-63, 2012.
E. E. Blue, Bis, J. C., Dorschner, M. O., Tsuang, D. W., Barral, S. M., Beecham, G., Below, J. E., Bush, W. S., Butkiewicz, M., Cruchaga, C., DeStefano, A., Farrer, L. A., Goate, A., Haines, J., Jaworski, J., Jun, G., Kunkle, B., Kuzma, A., Lee, J. J., Lunetta, K. L., Ma, Y., Martin, E., Naj, A., Nato, A. Q., Navas, P., Nguyen, H., Reitz, C., Reyes, D., Salerno, W., Schellenberg, G. D., Seshadri, S., Sohi, H., Thornton, T. A., Valadares, O., van Duijn, C., Vardarajan, B. N., San Wang, L. -, Boerwinkle, E., Dupuis, J., Pericak-Vance, M. A., Mayeux, R., and Wijsman, E. M., Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project., Dement Geriatr Cogn Disord, vol. 45, no. 1-2, pp. 1-17, 2018.
A. L. Boyles, Scott, W. K., Martin, E. R., Schmidt, S., Li, Y. - J., Ashley-Koch, A., Bass, M. P., Schmidt, M., Pericak-Vance, M. A., Speer, M. C., and Hauser, E. R., Linkage disequilibrium inflates type I error rates in multipoint linkage analysis when parental genotypes are missing., Hum Hered, vol. 59, no. 4, pp. 220-7, 2005.
L
J. H. Lee, Mayeux, R., Mayo, D., Mo, J., Santana, V., Williamson, J., Flaquer, A., Ciappa, A., Rondon, H., Estevez, P., Lantigua, R., Kawarai, T., Toulina, A., Medrano, M., Torres, M., Stern, Y., Tycko, B., Rogaeva, E., St George-Hyslop, P., and Knowles, J. A., Fine mapping of 10q and 18q for familial Alzheimer's disease in Caribbean Hispanics., Mol Psychiatry, vol. 9, no. 11, pp. 1042-51, 2004.
J. H. Lee, Cheng, R., Graff-Radford, N., Foroud, T., and Mayeux, R., Analyses of the National Institute on Aging Late-Onset Alzheimer's Disease Family Study: implication of additional loci., Arch Neurol, vol. 65, no. 11, pp. 1518-26, 2008.
Z. Li, Del-Aguila, J. L., Dube, U., Budde, J., Martinez, R., Black, K., Xiao, Q., Cairns, N. J., Dougherty, J. D., Lee, J. - M., Morris, J. C., Bateman, R. J., Karch, C. M., Cruchaga, C., and Harari, O., Genetic variants associated with Alzheimer's disease confer different cerebral cortex cell-type population structure., Genome Med, vol. 10, no. 1, p. 43, 2018.
Z. Li, Del-Aguila, J. L., Dube, U., Budde, J., Martinez, R., Black, K., Xiao, Q., Cairns, N. J., Dougherty, J. D., Lee, J. - M., Morris, J. C., Bateman, R. J., Karch, C. M., Cruchaga, C., and Harari, O., Genetic variants associated with Alzheimer's disease confer different cerebral cortex cell-type population structure., Genome Med, vol. 10, no. 1, p. 43, 2018.
Y. Li, Chen, J. A., Sears, R. L., Gao, F., Klein, E. D., Karydas, A., Geschwind, M. D., Rosen, H. J., Boxer, A. L., Guo, W., Pellegrini, M., Horvath, S., Miller, B. L., Geschwind, D. H., and Coppola, G., An epigenetic signature in peripheral blood associated with the haplotype on 17q21.31, a risk factor for neurodegenerative tauopathy., PLoS Genet, vol. 10, no. 3, p. e1004211, 2014.