Biblio

Found 230 results

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2018

M. A. A. DeMichele-Sweet, Weamer, E. A., Klei, L., Vrana, D. T., Hollingshead, D. J., Seltman, H. J., Sims, R., Foroud, T., Hernandez, I., Moreno-Grau, S., Tárraga, L., Boada, M., Ruiz, A., Williams, J., Mayeux, R., Lopez, O. L., Sibille, E. L., Kamboh, M. I., Devlin, B., and Sweet, R. A., “Genetic risk for schizophrenia and psychosis in Alzheimer disease.”, Mol Psychiatry, vol. 23, no. 4, pp. 963-972, 2018.

M. A. A. DeMichele-Sweet, Weamer, E. A., Klei, L., Vrana, D. T., Hollingshead, D. J., Seltman, H. J., Sims, R., Foroud, T., Hernandez, I., Moreno-Grau, S., Tárraga, L., Boada, M., Ruiz, A., Williams, J., Mayeux, R., Lopez, O. L., Sibille, E. L., Kamboh, M. I., Devlin, B., and Sweet, R. A., “Genetic risk for schizophrenia and psychosis in Alzheimer disease.”, Mol Psychiatry, vol. 23, no. 4, pp. 963-972, 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.

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.

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.

I. Broce, Karch, C. M., Wen, N., Fan, C. C., Wang, Y., Tan, C. Hong, Kouri, N., Ross, O. A., Höglinger, G. U., Müller, U., Hardy, J., Momeni, P., Hess, C. P., Dillon, W. P., Miller, Z. A., Bonham, L. W., Rabinovici, G. D., Rosen, H. J., Schellenberg, G. D., Franke, A., Karlsen, T. H., Veldink, J. H., Ferrari, R., Yokoyama, J. S., Miller, B. L., Andreassen, O. A., Dale, A. M., Desikan, R. S., and Sugrue, L. P., “Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies.”, PLoS Med, vol. 15, no. 1, p. e1002487, 2018.

I. Broce, Karch, C. M., Wen, N., Fan, C. C., Wang, Y., Tan, C. Hong, Kouri, N., Ross, O. A., Höglinger, G. U., Müller, U., Hardy, J., Momeni, P., Hess, C. P., Dillon, W. P., Miller, Z. A., Bonham, L. W., Rabinovici, G. D., Rosen, H. J., Schellenberg, G. D., Franke, A., Karlsen, T. H., Veldink, J. H., Ferrari, R., Yokoyama, J. S., Miller, B. L., Andreassen, O. A., Dale, A. M., Desikan, R. S., and Sugrue, L. P., “Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies.”, PLoS Med, vol. 15, no. 1, p. e1002487, 2018.

I. Broce, Karch, C. M., Wen, N., Fan, C. C., Wang, Y., Tan, C. Hong, Kouri, N., Ross, O. A., Höglinger, G. U., Müller, U., Hardy, J., Momeni, P., Hess, C. P., Dillon, W. P., Miller, Z. A., Bonham, L. W., Rabinovici, G. D., Rosen, H. J., Schellenberg, G. D., Franke, A., Karlsen, T. H., Veldink, J. H., Ferrari, R., Yokoyama, J. S., Miller, B. L., Andreassen, O. A., Dale, A. M., Desikan, R. S., and Sugrue, L. P., “Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies.”, PLoS Med, vol. 15, no. 1, p. e1002487, 2018.

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.

A. C. Naj, Lin, H., Vardarajan, B. N., White, S., Lancour, D., Ma, Y., Schmidt, M., Sun, F., Butkiewicz, M., Bush, W. S., Kunkle, B. W., Malamon, J., Amin, N., Choi, S. Hoan, Hamilton-Nelson, K. L., van der Lee, S. J., Gupta, N., Koboldt, D. C., Saad, M., Wang, B., Nato, A. Q., Sohi, H. K., Kuzma, A., San Wang, L. -, L Cupples, A., van Duijn, C., Seshadri, S., Schellenberg, G. D., Boerwinkle, E., Bis, J. C., Dupuis, J., Salerno, W. J., Wijsman, E. M., Martin, E. R., and DeStefano, A. L., “Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project.”, Genomics, 2018.

A. C. Naj, Lin, H., Vardarajan, B. N., White, S., Lancour, D., Ma, Y., Schmidt, M., Sun, F., Butkiewicz, M., Bush, W. S., Kunkle, B. W., Malamon, J., Amin, N., Choi, S. Hoan, Hamilton-Nelson, K. L., van der Lee, S. J., Gupta, N., Koboldt, D. C., Saad, M., Wang, B., Nato, A. Q., Sohi, H. K., Kuzma, A., San Wang, L. -, L Cupples, A., van Duijn, C., Seshadri, S., Schellenberg, G. D., Boerwinkle, E., Bis, J. C., Dupuis, J., Salerno, W. J., Wijsman, E. M., Martin, E. R., and DeStefano, A. L., “Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project.”, Genomics, 2018.

A. C. Naj, Lin, H., Vardarajan, B. N., White, S., Lancour, D., Ma, Y., Schmidt, M., Sun, F., Butkiewicz, M., Bush, W. S., Kunkle, B. W., Malamon, J., Amin, N., Choi, S. Hoan, Hamilton-Nelson, K. L., van der Lee, S. J., Gupta, N., Koboldt, D. C., Saad, M., Wang, B., Nato, A. Q., Sohi, H. K., Kuzma, A., San Wang, L. -, L Cupples, A., van Duijn, C., Seshadri, S., Schellenberg, G. D., Boerwinkle, E., Bis, J. C., Dupuis, J., Salerno, W. J., Wijsman, E. M., Martin, E. R., and DeStefano, A. L., “Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project.”, Genomics, 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.

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.

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.

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.

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.

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.

2017

G. W. Beecham, Bis, J. C., Martin, E. R., Choi, S. - H., Destefano, A. L., van Duijn, C. M., Fornage, M., Gabriel, S. B., Koboldt, D. C., Larson, D. E., Naj, A. C., Psaty, B. M., Salerno, W., Bush, W. S., Foroud, T. M., Wijsman, E., Farrer, L. A., Goate, A., Haines, J. L., Pericak-Vance, M. A., Boerwinkle, E., Mayeux, R., Seshadri, S., and Schellenberg, G., “The Alzheimer's Disease Sequencing Project: Study design and sample selection.”, Neurol Genet, vol. 3, no. 5, p. e194, 2017.

M. Victoria Fernández, Kim, J. Hun, Budde, J. P., Black, K., Medvedeva, A., Saef, B., Deming, Y., Del-Aguila, J., Ibañez, L., Dube, U., Harari, O., Norton, J., Chasse, R., Morris, J. C., Goate, A., and Cruchaga, C., “Analysis of neurodegenerative Mendelian genes in clinically diagnosed Alzheimer Disease.”, PLoS Genet, vol. 13, no. 11, p. e1007045, 2017.

K. - L. Huang, Marcora, E., Pimenova, A. A., Di Narzo, A. F., Kapoor, M., Jin, S. Chih, Harari, O., Bertelsen, S., Fairfax, B. P., Czajkowski, J., Chouraki, V., Grenier-Boley, B., Bellenguez, C., Deming, Y., McKenzie, A., Raj, T., Renton, A. E., Budde, J., Smith, A., Fitzpatrick, A., Bis, J. C., DeStefano, A., Adams, H. H. H., M Ikram, A., van der Lee, S., Del-Aguila, J. L., Fernández, M. Victoria, Ibañez, L., Sims, R., Escott-Price, V., Mayeux, R., Haines, J. L., Farrer, L. A., Pericak-Vance, M. A., Lambert, J. Charles, van Duijn, C., Launer, L., Seshadri, S., Williams, J., Amouyel, P., Schellenberg, G. D., Zhang, B., Borecki, I., Kauwe, J. S. K., Cruchaga, C., Hao, K., and Goate, A. M., “A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease.”, Nat Neurosci, vol. 20, no. 8, pp. 1052-1061, 2017.

K. - L. Huang, Marcora, E., Pimenova, A. A., Di Narzo, A. F., Kapoor, M., Jin, S. Chih, Harari, O., Bertelsen, S., Fairfax, B. P., Czajkowski, J., Chouraki, V., Grenier-Boley, B., Bellenguez, C., Deming, Y., McKenzie, A., Raj, T., Renton, A. E., Budde, J., Smith, A., Fitzpatrick, A., Bis, J. C., DeStefano, A., Adams, H. H. H., M Ikram, A., van der Lee, S., Del-Aguila, J. L., Fernández, M. Victoria, Ibañez, L., Sims, R., Escott-Price, V., Mayeux, R., Haines, J. L., Farrer, L. A., Pericak-Vance, M. A., Lambert, J. Charles, van Duijn, C., Launer, L., Seshadri, S., Williams, J., Amouyel, P., Schellenberg, G. D., Zhang, B., Borecki, I., Kauwe, J. S. K., Cruchaga, C., Hao, K., and Goate, A. M., “A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease.”, Nat Neurosci, vol. 20, no. 8, pp. 1052-1061, 2017.

R. S. Desikan, Fan, C. Chieh, Wang, Y., Schork, A. J., Cabral, H. J., L Cupples, A., Thompson, W. K., Besser, L., Kukull, W. A., Holland, D., Chen, C. - H., Brewer, J. B., Karow, D. S., Kauppi, K., Witoelar, A., Karch, C. M., Bonham, L. W., Yokoyama, J. S., Rosen, H. J., Miller, B. L., Dillon, W. P., Wilson, D. M., Hess, C. P., Pericak-Vance, M., Haines, J. L., Farrer, L. A., Mayeux, R., Hardy, J., Goate, A. M., Hyman, B. T., Schellenberg, G. D., McEvoy, L. K., Andreassen, O. A., and Dale, A. M., “Genetic assessment of age-associated Alzheimer disease risk: Development and validation of a polygenic hazard score.”, PLoS Med, vol. 14, no. 3, p. e1002258, 2017.

R. S. Desikan, Fan, C. Chieh, Wang, Y., Schork, A. J., Cabral, H. J., L Cupples, A., Thompson, W. K., Besser, L., Kukull, W. A., Holland, D., Chen, C. - H., Brewer, J. B., Karow, D. S., Kauppi, K., Witoelar, A., Karch, C. M., Bonham, L. W., Yokoyama, J. S., Rosen, H. J., Miller, B. L., Dillon, W. P., Wilson, D. M., Hess, C. P., Pericak-Vance, M., Haines, J. L., Farrer, L. A., Mayeux, R., Hardy, J., Goate, A. M., Hyman, B. T., Schellenberg, G. D., McEvoy, L. K., Andreassen, O. A., and Dale, A. M., “Genetic assessment of age-associated Alzheimer disease risk: Development and validation of a polygenic hazard score.”, PLoS Med, vol. 14, no. 3, p. e1002258, 2017.

R. S. Desikan, Fan, C. Chieh, Wang, Y., Schork, A. J., Cabral, H. J., L Cupples, A., Thompson, W. K., Besser, L., Kukull, W. A., Holland, D., Chen, C. - H., Brewer, J. B., Karow, D. S., Kauppi, K., Witoelar, A., Karch, C. M., Bonham, L. W., Yokoyama, J. S., Rosen, H. J., Miller, B. L., Dillon, W. P., Wilson, D. M., Hess, C. P., Pericak-Vance, M., Haines, J. L., Farrer, L. A., Mayeux, R., Hardy, J., Goate, A. M., Hyman, B. T., Schellenberg, G. D., McEvoy, L. K., Andreassen, O. A., and Dale, A. M., “Genetic assessment of age-associated Alzheimer disease risk: Development and validation of a polygenic hazard score.”, PLoS Med, vol. 14, no. 3, p. e1002258, 2017.