Alzheimer Disease
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JAMA, vol. 287, no. 3, pp. 329-36, 2002.
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“Genetic overlap between Alzheimer's disease and Parkinson's disease at the MAPT locus.”,
Mol Psychiatry, vol. 20, no. 12, pp. 1588-95, 2015.
P. M. Erlich, Lunetta, K. L., L Cupples, A., Huyck, M., Green, R. C., Baldwin, C. T., and Farrer, L. A.,
“Polymorphisms in the PON gene cluster are associated with Alzheimer disease.”,
Hum Mol Genet, vol. 15, no. 1, pp. 77-85, 2006.
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.
M. Ghani, Reitz, C., Cheng, R., Vardarajan, B. Narayan, Jun, G., Sato, C., Naj, A., Rajbhandary, R., San Wang, L. -, Valladares, O., Lin, C. - F., Larson, E. B., Graff-Radford, N. R., Evans, D., De Jager, P. L., Crane, P. K., Buxbaum, J. D., Murrell, J. R., Raj, T., Ertekin-Taner, N., Logue, M., Baldwin, C. T., Green, R. C., Barnes, L. L., Cantwell, L. B., M Fallin, D., Go, R. C. P., Griffith, P. A., Obisesan, T. O., Manly, J. J., Lunetta, K. L., M Kamboh, I., Lopez, O. L., Bennett, D. A., Hendrie, H., Hall, K. S., Goate, A. M., Byrd, G. S., Kukull, W. A., Foroud, T. M., Haines, J. L., Farrer, L. A., Pericak-Vance, M. A., Lee, J. H., Schellenberg, G. D., St George-Hyslop, P., Mayeux, R., and Rogaeva, E.,
“Association of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals.”,
JAMA Neurol, vol. 72, no. 11, pp. 1313-23, 2015.
M. Saleh, Vaillancourt, J. P., Graham, R. K., Huyck, M., Srinivasula, S. M., Alnemri, E. S., Steinberg, M. H., Nolan, V., Baldwin, C. T., Hotchkiss, R. S., Buchman, T. G., Zehnbauer, B. A., Hayden, M. R., Farrer, L. A., Roy, S., and Nicholson, D. W.,
“Differential modulation of endotoxin responsiveness by human caspase-12 polymorphisms.”,
Nature, vol. 429, no. 6987, pp. 75-9, 2004.
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.
M. Malik, Chiles, J., Xi, H. S., Medway, C., Simpson, J., Potluri, S., Howard, D., Liang, Y., Paumi, C. M., Mukherjee, S., Crane, P., Younkin, S., Fardo, D. W., and Estus, S.,
“Genetics of CD33 in Alzheimer's disease and acute myeloid leukemia.”,
Hum Mol Genet, vol. 24, no. 12, pp. 3557-70, 2015.
C. A. Reynolds, Hong, M. - G., Eriksson, U. K., Blennow, K., Wiklund, F., Johansson, B., Malmberg, B., Berg, S., Alexeyenko, A., Grönberg, H., Gatz, M., Pedersen, N. L., and Prince, J. A.,
“Analysis of lipid pathway genes indicates association of sequence variation near SREBF1/TOM1L2/ATPAF2 with dementia risk.”,
Hum Mol Genet, vol. 19, no. 10, pp. 2068-78, 2010.
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.
M. Victoria Fernández, Black, K., Carrell, D., Saef, B., Budde, J., Deming, Y., Howells, B., Del-Aguila, J. L., Ma, S., Bi, C., Norton, J., Chasse, R., Morris, J., Goate, A., and Cruchaga, C.,
“SORL1 variants across Alzheimer's disease European American cohorts.”,
Eur J Hum Genet, vol. 24, no. 12, pp. 1828-1830, 2016.
P. L. De Jager, Shulman, J. M., Chibnik, L. B., Keenan, B. T., Raj, T., Wilson, R. S., Yu, L., Leurgans, S. E., Tran, D., Aubin, C., Anderson, C. D., Biffi, A., Corneveaux, J. J., Huentelman, M. J., Rosand, J., Daly, M. J., Myers, A. J., Reiman, E. M., Bennett, D. A., and Evans, D. A.,
“A genome-wide scan for common variants affecting the rate of age-related cognitive decline.”,
Neurobiol Aging, vol. 33, no. 5, pp. 1017.e1-15, 2012.
R. S. Desikan, Schork, A. J., Wang, Y., Thompson, W. K., Dehghan, A., Ridker, P. M., Chasman, D. I., McEvoy, L. K., Holland, D., Chen, C. - H., Karow, D. S., Brewer, J. B., Hess, C. P., Williams, J., Sims, R., O'Donovan, M. C., Choi, S. Hoan, Bis, J. C., M Ikram, A., Gudnason, V., DeStefano, A. L., van der Lee, S. J., Psaty, B. M., van Duijn, C. M., Launer, L., Seshadri, S., Pericak-Vance, M. A., Mayeux, R., Haines, J. L., Farrer, L. A., Hardy, J., Ulstein, I. Dina, Aarsland, D., Fladby, T., White, L. R., Sando, S. B., Rongve, A., Witoelar, A., Djurovic, S., Hyman, B. T., Snaedal, J., Steinberg, S., Stefansson, H., Stefansson, K., Schellenberg, G. D., Andreassen, O. A., and Dale, A. M.,
“Polygenic Overlap Between C-Reactive Protein, Plasma Lipids, and Alzheimer Disease.”,
Circulation, vol. 131, no. 23, pp. 2061-2069, 2015.
G. R. Jun, Chung, J., Mez, J., Barber, R., Beecham, G. W., Bennett, D. A., Buxbaum, J. D., Byrd, G. S., Carrasquillo, M. M., Crane, P. K., Cruchaga, C., De Jager, P., Ertekin-Taner, N., Evans, D., M Fallin, D., Foroud, T. M., Friedland, R. P., Goate, A. M., Graff-Radford, N. R., Hendrie, H., Hall, K. S., Hamilton-Nelson, K. L., Inzelberg, R., M Kamboh, I., Kauwe, J. S. K., Kukull, W. A., Kunkle, B. W., Kuwano, R., Larson, E. B., Logue, M. W., Manly, J. J., Martin, E. R., Montine, T. J., Mukherjee, S., Naj, A., Reiman, E. M., Reitz, C., Sherva, R., St George-Hyslop, P. H., Thornton, T., Younkin, S. G., Vardarajan, B. N., San Wang, L. -, Wendlund, J. R., Winslow, A. R., Haines, J., Mayeux, R., Pericak-Vance, M. A., Schellenberg, G., Lunetta, K. L., and Farrer, L. A.,
“Transethnic genome-wide scan identifies novel Alzheimer's disease loci.”,
Alzheimers Dement, vol. 13, no. 7, pp. 727-738, 2017.
S. Swaminathan, Huentelman, M. J., Corneveaux, J. J., Myers, A. J., Faber, K. M., Foroud, T., Mayeux, R., Shen, L., Kim, S., Turk, M., Hardy, J., Reiman, E. M., and Saykin, A. J.,
“Analysis of copy number variation in Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals.”,
PLoS One, vol. 7, no. 12, p. e50640, 2012.
S. Mukherjee, Walter, S., Kauwe, J. S. K., Saykin, A. J., Bennett, D. A., Larson, E. B., Crane, P. K., and M Glymour, M.,
“Genetically predicted body mass index and Alzheimer's disease-related phenotypes in three large samples: Mendelian randomization analyses.”,
Alzheimers Dement, vol. 11, no. 12, pp. 1439-1451, 2015.
Y. Deming, Li, Z., Kapoor, M., Harari, O., Del-Aguila, J. L., Black, K., Carrell, D., Cai, Y., Fernández, M. Victoria, Budde, J., Ma, S., Saef, B., Howells, B., Huang, K. - L., Bertelsen, S., Fagan, A. M., Holtzman, D. M., Morris, J. C., Kim, S., Saykin, A. J., De Jager, P. L., Albert, M., Moghekar, A., O'Brien, R., Riemenschneider, M., Petersen, R. C., Blennow, K., Zetterberg, H., Minthon, L., Van Deerlin, V. M., Lee, V. Man- Yee, Shaw, L. M., Trojanowski, J. Q., Schellenberg, G., Haines, J. L., Mayeux, R., Pericak-Vance, M. A., Farrer, L. A., Peskind, E. R., Li, G., Di Narzo, A. F., Kauwe, J. S. K., Goate, A. M., and Cruchaga, C.,
“Genome-wide association study identifies four novel loci associated with Alzheimer's endophenotypes and disease modifiers.”,
Acta Neuropathol, vol. 133, no. 5, pp. 839-856, 2017.
J. J. Corneveaux, Myers, A. J., Allen, A. N., Pruzin, J. J., Ramirez, M., Engel, A., Nalls, M. A., Chen, K., Lee, W., Chewning, K., Villa, S. E., Meechoovet, H. B., Gerber, J. D., Frost, D., Benson, H. L., O'Reilly, S., Chibnik, L. B., Shulman, J. M., Singleton, A. B., Craig, D. W., Van Keuren-Jensen, K. R., Dunckley, T., Bennett, D. A., De Jager, P. L., Heward, C., Hardy, J., Reiman, E. M., and Huentelman, M. J.,
“Association of CR1, CLU and PICALM with Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals.”,
Hum Mol Genet, vol. 19, no. 16, pp. 3295-301, 2010.
C. M. Karch, Cruchaga, C., and Goate, A. M.,
“Alzheimer's disease genetics: from the bench to the clinic.”,
Neuron, vol. 83, no. 1, pp. 11-26, 2014.
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