We’re moving! Datasets in the NIAGADS database are being transitioned to the DSS database, more info coming soon.

Biblio

Found 155 results
Author Keyword Title Type [ Year(Asc)]
Filters: First Letter Of Keyword is H  [Clear All Filters]
2014
A. Sonnega, Faul, J. D., Ofstedal, M. Beth, Langa, K. M., Phillips, J. W. R., and Weir, D. R., Cohort Profile: the Health and Retirement Study (HRS)., Int J Epidemiol, vol. 43, no. 2, pp. 576-85, 2014.
A. Sonnega, Faul, J. D., Ofstedal, M. Beth, Langa, K. M., Phillips, J. W. R., and Weir, D. R., Cohort Profile: the Health and Retirement Study (HRS)., Int J Epidemiol, vol. 43, no. 2, pp. 576-85, 2014.
A. C. Naj, Jun, G., Reitz, C., Kunkle, B. W., Perry, W., Park, Y. Son, Beecham, G. W., Rajbhandary, R. A., Hamilton-Nelson, K. L., San Wang, L. -, Kauwe, J. S. K., Huentelman, M. J., Myers, A. J., Bird, T. D., Boeve, B. F., Baldwin, C. T., Jarvik, G. P., Crane, P. K., Rogaeva, E., M Barmada, M., F Demirci, Y., Cruchaga, C., Kramer, P. L., Ertekin-Taner, N., Hardy, J., Graff-Radford, N. R., Green, R. C., Larson, E. B., St George-Hyslop, P. H., Buxbaum, J. D., Evans, D. A., Schneider, J. A., Lunetta, K. L., M Kamboh, I., Saykin, A. J., Reiman, E. M., De Jager, P. L., Bennett, D. A., Morris, J. C., Montine, T. J., Goate, A. M., Blacker, D., Tsuang, D. W., Hakonarson, H., Kukull, W. A., Foroud, T. M., Martin, E. R., Haines, J. L., Mayeux, R. P., Farrer, L. A., Schellenberg, G. D., Pericak-Vance, M. A., Albert, M. S., Albin, R. L., Apostolova, L. G., Arnold, S. E., Barber, R., Barnes, L. L., Beach, T. G., Becker, J. T., Beekly, D., Bigio, E. H., Bowen, J. D., Boxer, A., Burke, J. R., Cairns, N. J., Cantwell, L. B., Cao, C., Carlson, C. S., Carney, R. M., Carrasquillo, M. M., Carroll, S. L., Chui, H. C., Clark, D. G., Corneveaux, J., Cribbs, D. H., Crocco, E. A., DeCarli, C., DeKosky, S. T., Dick, M., Dickson, D. W., Duara, R., Faber, K. M., Fallon, K. B., Farlow, M. R., Ferris, S., Frosch, M. P., Galasko, D. R., Ganguli, M., Gearing, M., Geschwind, D. H., Ghetti, B., Gilbert, J. R., Glass, J. D., Growdon, J. H., Hamilton, R. L., Harrell, L. E., Head, E., Honig, L. S., Hulette, C. M., Hyman, B. T., Jicha, G. A., Jin, L. - W., Karydas, A., Kaye, J. A., Kim, R., Koo, E. H., Kowall, N. W., Kramer, J. H., LaFerla, F. M., Lah, J. J., Leverenz, J. B., Levey, A. I., Li, G., Lieberman, A. P., Lin, C. - F., Lopez, O. L., Lyketsos, C. G., Mack, W. J., Martiniuk, F., Mash, D. C., Masliah, E., McCormick, W. C., McCurry, S. M., McDavid, A. N., McKee, A. C., Mesulam, M., Miller, B. L., Miller, C. A., Miller, J. W., Murrell, J. R., Olichney, J. M., Pankratz, V. S., Parisi, J. E., Paulson, H. L., Peskind, E., Petersen, R. C., Pierce, A., Poon, W. W., Potter, H., Quinn, J. F., Raj, A., Raskind, M., Reisberg, B., Ringman, J. M., Roberson, E. D., Rosen, H. J., Rosenberg, R. N., Sano, M., Schneider, L. S., Seeley, W. W., Smith, A. G., Sonnen, J. A., Spina, S., Stern, R. A., Tanzi, R. E., Thornton-Wells, T. A., Trojanowski, J. Q., Troncoso, J. C., Valladares, O., Van Deerlin, V. M., Van Eldik, L. J., Vardarajan, B. N., Vinters, H. V., Vonsattel, J. Paul, Weintraub, S., Welsh-Bohmer, K. A., Williamson, J., Wishnek, S., Woltjer, R. L., Wright, C. B., Younkin, S. G., Yu, C. - E., and Yu, L., Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study., JAMA Neurol, vol. 71, no. 11, pp. 1394-404, 2014.
Y. Li, Chen, J. A., Sears, R. L., Gao, F., Klein, E. D., Karydas, A., Geschwind, M. D., Rosen, H. J., Boxer, A. L., Guo, W., Pellegrini, M., Horvath, S., Miller, B. L., Geschwind, D. H., and Coppola, G., An epigenetic signature in peripheral blood associated with the haplotype on 17q21.31, a risk factor for neurodegenerative tauopathy., PLoS Genet, vol. 10, no. 3, p. e1004211, 2014.
Y. Li, Chen, J. A., Sears, R. L., Gao, F., Klein, E. D., Karydas, A., Geschwind, M. D., Rosen, H. J., Boxer, A. L., Guo, W., Pellegrini, M., Horvath, S., Miller, B. L., Geschwind, D. H., and Coppola, G., An epigenetic signature in peripheral blood associated with the haplotype on 17q21.31, a risk factor for neurodegenerative tauopathy., PLoS Genet, vol. 10, no. 3, p. e1004211, 2014.
A. Patel, Rees, S. D., M Kelly, A., Bain, S. C., Barnett, A. H., Prasher, A., Arshad, H., and Prasher, V. P., Genetic variants conferring susceptibility to Alzheimer's disease in the general population; do they also predispose to dementia in Down's syndrome., BMC Res Notes, vol. 7, p. 42, 2014.
S. Barral, Reitz, C., Small, S. A., and Mayeux, R., Genetic variants in a 'cAMP element binding protein' (CREB)-dependent histone acetylation pathway influence memory performance in cognitively healthy elderly individuals., Neurobiol Aging, vol. 35, no. 12, pp. 2881.e7-2881.e10, 2014.
S. Barral, Reitz, C., Small, S. A., and Mayeux, R., Genetic variants in a 'cAMP element binding protein' (CREB)-dependent histone acetylation pathway influence memory performance in cognitively healthy elderly individuals., Neurobiol Aging, vol. 35, no. 12, pp. 2881.e7-2881.e10, 2014.
G. W. Beecham, Hamilton, K., Naj, A. C., Martin, E. R., Huentelman, M., Myers, A. J., Corneveaux, J. J., Hardy, J., Vonsattel, J. - P., Younkin, S. G., Bennett, D. A., De Jager, P. L., Larson, E. B., Crane, P. K., M Kamboh, I., Kofler, J. K., Mash, D. C., Duque, L., Gilbert, J. R., Gwirtsman, H., Buxbaum, J. D., Kramer, P., Dickson, D. W., Farrer, L. A., Frosch, M. P., Ghetti, B., Haines, J. L., Hyman, B. T., Kukull, W. A., Mayeux, R. P., Pericak-Vance, M. A., Schneider, J. A., Trojanowski, J. Q., Reiman, E. M., Schellenberg, G. D., and Montine, T. J., Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias., PLoS Genet, vol. 10, no. 9, p. e1004606, 2014.
G. W. Beecham, Hamilton, K., Naj, A. C., Martin, E. R., Huentelman, M., Myers, A. J., Corneveaux, J. J., Hardy, J., Vonsattel, J. - P., Younkin, S. G., Bennett, D. A., De Jager, P. L., Larson, E. B., Crane, P. K., M Kamboh, I., Kofler, J. K., Mash, D. C., Duque, L., Gilbert, J. R., Gwirtsman, H., Buxbaum, J. D., Kramer, P., Dickson, D. W., Farrer, L. A., Frosch, M. P., Ghetti, B., Haines, J. L., Hyman, B. T., Kukull, W. A., Mayeux, R. P., Pericak-Vance, M. A., Schneider, J. A., Trojanowski, J. Q., Reiman, E. M., Schellenberg, G. D., and Montine, T. J., Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias., PLoS Genet, vol. 10, no. 9, p. e1004606, 2014.
J. S. K. Kauwe, Bailey, M. H., Ridge, P. G., Perry, R., Wadsworth, M. E., Hoyt, K. L., Staley, L. A., Karch, C. M., Harari, O., Cruchaga, C., Ainscough, B. J., Bales, K., Pickering, E. H., Bertelsen, S., Fagan, A. M., Holtzman, D. M., Morris, J. C., and Goate, A. M., Genome-wide association study of CSF levels of 59 alzheimer's disease candidate proteins: significant associations with proteins involved in amyloid processing and inflammation., PLoS Genet, vol. 10, no. 10, p. e1004758, 2014.
G. Han, Sun, J., Wang, J., Bai, Z., Song, F., and Lei, H., Genomics in neurological disorders., Genomics Proteomics Bioinformatics, vol. 12, no. 4, pp. 156-63, 2014.
R. Guerreiro, Brás, J., Hardy, J., and Singleton, A., Next generation sequencing techniques in neurological diseases: redefining clinical and molecular associations., Hum Mol Genet, vol. 23, no. R1, pp. R47-53, 2014.
R. Guerreiro, Brás, J., Hardy, J., and Singleton, A., Next generation sequencing techniques in neurological diseases: redefining clinical and molecular associations., Hum Mol Genet, vol. 23, no. R1, pp. R47-53, 2014.
C. Cruchaga, Karch, C. M., Jin, S. Chih, Benitez, B. A., Cai, Y., Guerreiro, R., Harari, O., Norton, J., Budde, J., Bertelsen, S., Jeng, A. T., Cooper, B., Skorupa, T., Carrell, D., Levitch, D., Hsu, S., Choi, J., Ryten, M., Sassi, C., Brás, J., Gibbs, R. J., Hernandez, D. G., Lupton, M. K., Powell, J., Forabosco, P., Ridge, P. G., Corcoran, C. D., Tschanz, J. A. T., Norton, M. C., Munger, R. G., Schmutz, C., Leary, M., F Demirci, Y., Bamne, M. N., Wang, X., Lopez, O. L., Ganguli, M., Medway, C., Turton, J., Lord, J., Braae, A., Barber, I., Brown, K., Pastor, P., Lorenzo-Betancor, O., Brkanac, Z., Scott, E., Topol, E., Morgan, K., Rogaeva, E., Singleton, A., Hardy, J., M Kamboh, I., St George-Hyslop, P., Cairns, N., Morris, J. C., Kauwe, J. S. K., and Goate, A. M., Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer's disease., Nature, vol. 505, no. 7484, pp. 550-554, 2014.
P. Ryvkin, Leung, Y. Yee, Ungar, L. H., Gregory, B. D., and San Wang, L. -, Using machine learning and high-throughput RNA sequencing to classify the precursors of small non-coding RNAs., Methods, vol. 67, no. 1, pp. 28-35, 2014.
P. Ryvkin, Leung, Y. Yee, Ungar, L. H., Gregory, B. D., and San Wang, L. -, Using machine learning and high-throughput RNA sequencing to classify the precursors of small non-coding RNAs., Methods, vol. 67, no. 1, pp. 28-35, 2014.
2013
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.
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. - F. Lin, Naj, A. C., and San Wang, L. -, Analyzing copy number variation using SNP array data: protocols for calling CNV and association tests., Curr Protoc Hum Genet, vol. 79, p. Unit 1.27., 2013.
C. - F. Lin, Naj, A. C., and San Wang, L. -, Analyzing copy number variation using SNP array data: protocols for calling CNV and association tests., Curr Protoc Hum Genet, vol. 79, p. Unit 1.27., 2013.
Y. Yee Leung, Ryvkin, P., Ungar, L. H., Gregory, B. D., and San Wang, L. -, CoRAL: predicting non-coding RNAs from small RNA-sequencing data., Nucleic Acids Res, vol. 41, no. 14, p. e137, 2013.
S. Barral, Cosentino, S., Costa, R., Andersen, S. L., Christensen, K., Eckfeldt, J. H., Newman, A. B., Perls, T. T., Province, M. A., Hadley, E. C., Rossi, W. K., and Mayeux, R., Exceptional memory performance in the Long Life Family Study., Neurobiol Aging, vol. 34, no. 11, pp. 2445-8, 2013.
C. Cruchaga, Kauwe, J. S. K., Harari, O., Jin, S. Chih, Cai, Y., Karch, C. M., Benitez, B. A., Jeng, A. T., Skorupa, T., Carrell, D., Bertelsen, S., Bailey, M., McKean, D., Shulman, J. M., De Jager, P. L., Chibnik, L., Bennett, D. A., Arnold, S. E., Harold, D., Sims, R., Gerrish, A., Williams, J., Van Deerlin, V. M., Lee, V. M. - Y., Shaw, L. M., Trojanowski, J. Q., Haines, J. L., Mayeux, R., Pericak-Vance, M. A., Farrer, L. A., Schellenberg, G. D., Peskind, E. R., Galasko, D., Fagan, A. M., Holtzman, D. M., Morris, J. C., and Goate, A. M., GWAS of cerebrospinal fluid tau levels identifies risk variants for Alzheimer's disease., Neuron, vol. 78, no. 2, pp. 256-68, 2013.
P. Ryvkin, Leung, Y. Yee, Silverman, I. M., Childress, M., Valladares, O., Dragomir, I., Gregory, B. D., and San Wang, L. -, HAMR: high-throughput annotation of modified ribonucleotides., RNA, vol. 19, no. 12, pp. 1684-92, 2013.