Biblio

Found 6 results

Author Keyword Title [ Type

] Year

Filters: Keyword is Genetic Association Studies [Clear All Filters]

Journal Article

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.

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.

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.

M. Malik, Chiles, J., Xi, H. S., Medway, C., Simpson, J., Potluri, S., Howard, D., Liang, Y., Paumi, C. M., Mukherjee, S., Crane, P., Younkin, S., Fardo, D. W., and Estus, S., “Genetics of CD33 in Alzheimer's disease and acute myeloid leukemia.”, Hum Mol Genet, vol. 24, no. 12, pp. 3557-70, 2015.

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.

Y. Le Guen, Belloy, M. E., Napolioni, V., Eger, S. J., Kennedy, G., Tao, R., He, Z., and Greicius, M. D., “A novel age-informed approach for genetic association analysis in Alzheimer's disease.”, Alzheimers Res Ther, vol. 13, no. 1, p. 72, 2021.