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Journal Article

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.

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.

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.

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.

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.

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.

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.

G. C. Román, Tatemichi, T. K., Erkinjuntti, T., Cummings, J. L., Masdeu, J. C., Garcia, J. H., Amaducci, L., Orgogozo, J. M., Brun, A., and Hofman, A., “Vascular dementia: diagnostic criteria for research studies. Report of the NINDS-AIREN International Workshop.”, Neurology, vol. 43, no. 2, pp. 250-60, 1993.

A. J. Myers, Marshall, H., Holmans, P., Compton, D., Crook, R. J. P., Mander, A. P., Nowotny, P., Smemo, S., Dunstan, M., Jehu, L., Wang, J. C., Hamshere, M., Morris, J. C., Norton, J., Chakraventy, S., Tunstall, N., Lovestone, S., Petersen, R., O'Donovan, M., Jones, L., Williams, J., Owen, M. J., Hardy, J., and Goate, A., “Variation in the urokinase-plasminogen activator gene does not explain the chromosome 10 linkage signal for late onset AD.”, Am J Med Genet B Neuropsychiatr Genet, vol. 124B, no. 1, pp. 29-37, 2004.

A. J. Myers, Marshall, H., Holmans, P., Compton, D., Crook, R. J. P., Mander, A. P., Nowotny, P., Smemo, S., Dunstan, M., Jehu, L., Wang, J. C., Hamshere, M., Morris, J. C., Norton, J., Chakraventy, S., Tunstall, N., Lovestone, S., Petersen, R., O'Donovan, M., Jones, L., Williams, J., Owen, M. J., Hardy, J., and Goate, A., “Variation in the urokinase-plasminogen activator gene does not explain the chromosome 10 linkage signal for late onset AD.”, Am J Med Genet B Neuropsychiatr Genet, vol. 124B, no. 1, pp. 29-37, 2004.

A. J. Myers, Marshall, H., Holmans, P., Compton, D., Crook, R. J. P., Mander, A. P., Nowotny, P., Smemo, S., Dunstan, M., Jehu, L., Wang, J. C., Hamshere, M., Morris, J. C., Norton, J., Chakraventy, S., Tunstall, N., Lovestone, S., Petersen, R., O'Donovan, M., Jones, L., Williams, J., Owen, M. J., Hardy, J., and Goate, A., “Variation in the urokinase-plasminogen activator gene does not explain the chromosome 10 linkage signal for late onset AD.”, Am J Med Genet B Neuropsychiatr Genet, vol. 124B, no. 1, pp. 29-37, 2004.

A. J. Myers, Marshall, H., Holmans, P., Compton, D., Crook, R. J. P., Mander, A. P., Nowotny, P., Smemo, S., Dunstan, M., Jehu, L., Wang, J. C., Hamshere, M., Morris, J. C., Norton, J., Chakraventy, S., Tunstall, N., Lovestone, S., Petersen, R., O'Donovan, M., Jones, L., Williams, J., Owen, M. J., Hardy, J., and Goate, A., “Variation in the urokinase-plasminogen activator gene does not explain the chromosome 10 linkage signal for late onset AD.”, Am J Med Genet B Neuropsychiatr Genet, vol. 124B, no. 1, pp. 29-37, 2004.

C. Reitz, Jun, G., Naj, A., Rajbhandary, R., Vardarajan, B. Narayan, 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., 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., Schellenberg, G. D., and Mayeux, R., “Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4,and the risk of late-onset Alzheimer disease in African Americans.”, JAMA, vol. 309, no. 14, pp. 1483-92, 2013.

C. Reitz, Jun, G., Naj, A., Rajbhandary, R., Vardarajan, B. Narayan, 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., 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., Schellenberg, G. D., and Mayeux, R., “Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4,and the risk of late-onset Alzheimer disease in African Americans.”, JAMA, vol. 309, no. 14, pp. 1483-92, 2013.

C. Reitz, Jun, G., Naj, A., Rajbhandary, R., Vardarajan, B. Narayan, 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., 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., Schellenberg, G. D., and Mayeux, R., “Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4,and the risk of late-onset Alzheimer disease in African Americans.”, JAMA, vol. 309, no. 14, pp. 1483-92, 2013.

S. Smemo, Nowotny, P., Hinrichs, A. L., Kauwe, J. S. K., Cherny, S., Erickson, K., Myers, A. J., Kaleem, M., Marlowe, L., Gibson, A. M., Hollingworth, P., O'Donovan, M. C., Morris, C. M., Holmans, P., Lovestone, S., Morris, J. C., Thal, L., Li, Y., Grupe, A., Hardy, J., Owen, M. J., Williams, J., and Goate, A., “Ubiquilin 1 polymorphisms are not associated with late-onset Alzheimer's disease.”, Ann Neurol, vol. 59, no. 1, pp. 21-6, 2006.

S. Smemo, Nowotny, P., Hinrichs, A. L., Kauwe, J. S. K., Cherny, S., Erickson, K., Myers, A. J., Kaleem, M., Marlowe, L., Gibson, A. M., Hollingworth, P., O'Donovan, M. C., Morris, C. M., Holmans, P., Lovestone, S., Morris, J. C., Thal, L., Li, Y., Grupe, A., Hardy, J., Owen, M. J., Williams, J., and Goate, A., “Ubiquilin 1 polymorphisms are not associated with late-onset Alzheimer's disease.”, Ann Neurol, vol. 59, no. 1, pp. 21-6, 2006.

S. Smemo, Nowotny, P., Hinrichs, A. L., Kauwe, J. S. K., Cherny, S., Erickson, K., Myers, A. J., Kaleem, M., Marlowe, L., Gibson, A. M., Hollingworth, P., O'Donovan, M. C., Morris, C. M., Holmans, P., Lovestone, S., Morris, J. C., Thal, L., Li, Y., Grupe, A., Hardy, J., Owen, M. J., Williams, J., and Goate, A., “Ubiquilin 1 polymorphisms are not associated with late-onset Alzheimer's disease.”, Ann Neurol, vol. 59, no. 1, pp. 21-6, 2006.

S. Smemo, Nowotny, P., Hinrichs, A. L., Kauwe, J. S. K., Cherny, S., Erickson, K., Myers, A. J., Kaleem, M., Marlowe, L., Gibson, A. M., Hollingworth, P., O'Donovan, M. C., Morris, C. M., Holmans, P., Lovestone, S., Morris, J. C., Thal, L., Li, Y., Grupe, A., Hardy, J., Owen, M. J., Williams, J., and Goate, A., “Ubiquilin 1 polymorphisms are not associated with late-onset Alzheimer's disease.”, Ann Neurol, vol. 59, no. 1, pp. 21-6, 2006.

M. A. Slifer, Martin, E. R., Haines, J. L., and Pericak-Vance, M. A., “The ubiquilin 1 gene and Alzheimer's disease.”, N Engl J Med, vol. 352, no. 26, pp. 2752-3; author reply 2752-3, 2005.

J. Mez, Chung, J., Jun, G., Kriegel, J., Bourlas, A. P., Sherva, R., Logue, M. W., Barnes, L. L., Bennett, D. A., Buxbaum, J. D., Byrd, G. S., Crane, P. K., Ertekin-Taner, N., Evans, D., M Fallin, D., Foroud, T., Goate, A., Graff-Radford, N. R., Hall, K. S., M Kamboh, I., Kukull, W. A., Larson, E. B., Manly, J. J., Haines, J. L., Mayeux, R., Pericak-Vance, M. A., Schellenberg, G. D., Lunetta, K. L., and Farrer, L. A., “Two novel loci, COBL and SLC10A2, for Alzheimer's disease in African Americans.”, Alzheimers Dement, vol. 13, no. 2, pp. 119-129, 2017.