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Nat Commun, vol. 7, p. 13738, 2016.
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Bioinformatics, vol. 31, no. 8, pp. 1290-2, 2015.
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Nat Genet, vol. 43, no. 7, pp. 699-705, 2011.
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PLoS Med, vol. 15, no. 1, p. e1002487, 2018.
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“Independent and epistatic effects of variants in VPS10-d receptors on Alzheimer disease risk and processing of the amyloid precursor protein (APP).”,
Transl Psychiatry, vol. 3, p. e256, 2013.
B. Zhang, Gaiteri, C., Bodea, L. - G., Wang, Z., McElwee, J., Podtelezhnikov, A. A., Zhang, C., Xie, T., Tran, L., Dobrin, R., Fluder, E., Clurman, B., Melquist, S., Narayanan, M., Suver, C., Shah, H., Mahajan, M., Gillis, T., Mysore, J., MacDonald, M. E., Lamb, J. R., Bennett, D. A., Molony, C., Stone, D. J., Gudnason, V., Myers, A. J., Schadt, E. E., Neumann, H., Zhu, J., and Emilsson, V.,
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Cell, vol. 153, no. 3, pp. 707-20, 2013.
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M. T. W. Ebbert, Boehme, K. L., Wadsworth, M. E., Staley, L. A., Mukherjee, S., Crane, P. K., Ridge, P. G., and Kauwe, J. S. K.,
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H. Zhu, Gopalraj, R. K., Kelly, J. F., Bennett, D. A., and Estus, S.,
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Y. Trembath, Rosenberg, C., Ervin, J. F., Schmechel, D. E., Gaskell, P., Pericak-Vance, M., Vance, J., and Hulette, C. M.,
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“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.
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“Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease.”,
Nat Genet, vol. 45, no. 12, pp. 1452-8, 2013.
M. Wang, Beckmann, N. D., Roussos, P., Wang, E., Zhou, X., Wang, Q., Ming, C., Neff, R., Ma, W., Fullard, J. F., Hauberg, M. E., Bendl, J., Peters, M. A., Logsdon, B., Wang, P., Mahajan, M., Mangravite, L. M., Dammer, E. B., Duong, D. M., Lah, J. J., Seyfried, N. T., Levey, A. I., Buxbaum, J. D., Ehrlich, M., Gandy, S., Katsel, P., Haroutunian, V., Schadt, E., and Zhang, B.,
“The Mount Sinai cohort of large-scale genomic, transcriptomic and proteomic data in Alzheimer's disease.”,
Sci Data, vol. 5, p. 180185, 2018.
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JAMA Neurol, vol. 72, no. 4, pp. 414-22, 2015.
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