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Biblio

Found 157 results
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Journal Article
J. H. Lee, Barral, S., Cheng, R., Chacon, I., Santana, V., Williamson, J., Lantigua, R., Medrano, M., Jimenez-Velazquez, I. Z., Stern, Y., Tycko, B., Rogaeva, E., Wakutani, Y., Kawarai, T., St George-Hyslop, P., and Mayeux, R., Age-at-onset linkage analysis in Caribbean Hispanics with familial late-onset Alzheimer's disease., Neurogenetics, vol. 9, no. 1, pp. 51-60, 2008.
V. Busby, Goossens, S., Nowotny, P., Hamilton, G., Smemo, S., Harold, D., Turic, D., Jehu, L., Myers, A., Womick, M., Woo, D., Compton, D., Doil, L. M., Tacey, K. M., Lau, K. F., Al-Saraj, S., Killick, R., Pickering-Brown, S., Moore, P., Hollingworth, P., Archer, N., Foy, C., Walter, S., Lendon, C., Iwatsubo, T., Morris, J. C., Norton, J., Mann, D., Janssens, B., Hardy, J., O'Donovan, M., Jones, L., Williams, J., Holmans, P., Owen, M. J., Grupe, A., Powell, J., van Hengel, J., Goate, A., Van Roy, F., and Lovestone, S., Alpha-T-catenin is expressed in human brain and interacts with the Wnt signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer's disease., Neuromolecular Med, vol. 5, no. 2, pp. 133-46, 2004.
V. Busby, Goossens, S., Nowotny, P., Hamilton, G., Smemo, S., Harold, D., Turic, D., Jehu, L., Myers, A., Womick, M., Woo, D., Compton, D., Doil, L. M., Tacey, K. M., Lau, K. F., Al-Saraj, S., Killick, R., Pickering-Brown, S., Moore, P., Hollingworth, P., Archer, N., Foy, C., Walter, S., Lendon, C., Iwatsubo, T., Morris, J. C., Norton, J., Mann, D., Janssens, B., Hardy, J., O'Donovan, M., Jones, L., Williams, J., Holmans, P., Owen, M. J., Grupe, A., Powell, J., van Hengel, J., Goate, A., Van Roy, F., and Lovestone, S., Alpha-T-catenin is expressed in human brain and interacts with the Wnt signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer's disease., Neuromolecular Med, vol. 5, no. 2, pp. 133-46, 2004.
V. Busby, Goossens, S., Nowotny, P., Hamilton, G., Smemo, S., Harold, D., Turic, D., Jehu, L., Myers, A., Womick, M., Woo, D., Compton, D., Doil, L. M., Tacey, K. M., Lau, K. F., Al-Saraj, S., Killick, R., Pickering-Brown, S., Moore, P., Hollingworth, P., Archer, N., Foy, C., Walter, S., Lendon, C., Iwatsubo, T., Morris, J. C., Norton, J., Mann, D., Janssens, B., Hardy, J., O'Donovan, M., Jones, L., Williams, J., Holmans, P., Owen, M. J., Grupe, A., Powell, J., van Hengel, J., Goate, A., Van Roy, F., and Lovestone, S., Alpha-T-catenin is expressed in human brain and interacts with the Wnt signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer's disease., Neuromolecular Med, vol. 5, no. 2, pp. 133-46, 2004.
V. Busby, Goossens, S., Nowotny, P., Hamilton, G., Smemo, S., Harold, D., Turic, D., Jehu, L., Myers, A., Womick, M., Woo, D., Compton, D., Doil, L. M., Tacey, K. M., Lau, K. F., Al-Saraj, S., Killick, R., Pickering-Brown, S., Moore, P., Hollingworth, P., Archer, N., Foy, C., Walter, S., Lendon, C., Iwatsubo, T., Morris, J. C., Norton, J., Mann, D., Janssens, B., Hardy, J., O'Donovan, M., Jones, L., Williams, J., Holmans, P., Owen, M. J., Grupe, A., Powell, J., van Hengel, J., Goate, A., Van Roy, F., and Lovestone, S., Alpha-T-catenin is expressed in human brain and interacts with the Wnt signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer's disease., Neuromolecular Med, vol. 5, no. 2, pp. 133-46, 2004.
V. Busby, Goossens, S., Nowotny, P., Hamilton, G., Smemo, S., Harold, D., Turic, D., Jehu, L., Myers, A., Womick, M., Woo, D., Compton, D., Doil, L. M., Tacey, K. M., Lau, K. F., Al-Saraj, S., Killick, R., Pickering-Brown, S., Moore, P., Hollingworth, P., Archer, N., Foy, C., Walter, S., Lendon, C., Iwatsubo, T., Morris, J. C., Norton, J., Mann, D., Janssens, B., Hardy, J., O'Donovan, M., Jones, L., Williams, J., Holmans, P., Owen, M. J., Grupe, A., Powell, J., van Hengel, J., Goate, A., Van Roy, F., and Lovestone, S., Alpha-T-catenin is expressed in human brain and interacts with the Wnt signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer's disease., Neuromolecular Med, vol. 5, no. 2, pp. 133-46, 2004.
P. L. Kramer, Xu, H., Woltjer, R. L., Westaway, S. K., Clark, D., Erten-Lyons, D., Kaye, J. A., Welsh-Bohmer, K. A., Troncoso, J. C., Markesbery, W. R., Petersen, R. C., R Turner, S., Kukull, W. A., Bennett, D. A., Galasko, D., Morris, J. C., and Ott, J., Alzheimer disease pathology in cognitively healthy elderly: a genome-wide study., Neurobiol Aging, vol. 32, no. 12, pp. 2113-22, 2011.
P. L. Kramer, Xu, H., Woltjer, R. L., Westaway, S. K., Clark, D., Erten-Lyons, D., Kaye, J. A., Welsh-Bohmer, K. A., Troncoso, J. C., Markesbery, W. R., Petersen, R. C., R Turner, S., Kukull, W. A., Bennett, D. A., Galasko, D., Morris, J. C., and Ott, J., Alzheimer disease pathology in cognitively healthy elderly: a genome-wide study., Neurobiol Aging, vol. 32, no. 12, pp. 2113-22, 2011.
P. L. Kramer, Xu, H., Woltjer, R. L., Westaway, S. K., Clark, D., Erten-Lyons, D., Kaye, J. A., Welsh-Bohmer, K. A., Troncoso, J. C., Markesbery, W. R., Petersen, R. C., R Turner, S., Kukull, W. A., Bennett, D. A., Galasko, D., Morris, J. C., and Ott, J., Alzheimer disease pathology in cognitively healthy elderly: a genome-wide study., Neurobiol Aging, vol. 32, no. 12, pp. 2113-22, 2011.
P. G. Ridge, Mukherjee, S., Crane, P. K., and Kauwe, J. S. K., Alzheimer's disease: analyzing the missing heritability., PLoS One, vol. 8, no. 11, p. e79771, 2013.
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.
M. Thambisetty, An, Y., and Tanaka, T., Alzheimer's disease risk genes and the age-at-onset phenotype., Neurobiol Aging, vol. 34, no. 11, pp. 2696.e1-5, 2013.
C. M. Karch, Ezerskiy, L. A., Bertelsen, S., and Goate, A. M., Alzheimer's Disease Risk Polymorphisms Regulate Gene Expression in the ZCWPW1 and the CELF1 Loci., PLoS One, vol. 11, no. 2, p. e0148717, 2016.
C. M. Karch, Ezerskiy, L. A., Bertelsen, S., and Goate, A. M., Alzheimer's Disease Risk Polymorphisms Regulate Gene Expression in the ZCWPW1 and the CELF1 Loci., PLoS One, vol. 11, no. 2, p. e0148717, 2016.
P. K. Crane, Foroud, T., Montine, T. J., and Larson, E. B., Alzheimer's Disease Sequencing Project discovery and replication criteria for cases and controls: Data from a community-based prospective cohort study with autopsy follow-up., Alzheimers Dement, vol. 13, no. 12, pp. 1410-1413, 2017.
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.
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.
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.
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.
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.
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.
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. 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.
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.
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.