The New Field Of Epigenomics: Implications for Cancer and Other Common Disease Research

Por Bjornsson, H.T., Cui, H., Gius, D., Fallin, M.D., Feinberg, A.P.
Publicado no Cold Spring Harb Symp Quant Biol (2004)

Haplotype Diversity in 11 Candidate Genes Across Four Populations

Por Beaty, T. H., Fallin, M. D., Hetmanski, J. B., McIntosh, I., Chong, S. S., Ingersoll, R., Sheng, X., Chakraborty, R., Scott, A. F.
Publicado em 2005

TRANSCOBALAMIN-II VARIANTS, DECREASED VITAMIN B12 AVAILABILITY AND INCREASED RISK OF FRAILTY

Por MATTEINI, A.M., WALSTON, J.D., BANDEEN-ROCHE, K., ARKING, D.E., ALLEN, R.H., FRIED, L.P., CHAKRAVARTI, A., STABLER, S.P., FALLIN, M.D.
Publicado em 2010

The association of genetic variants in interleukin-1 genes with cognition: Findings from the cardiovascular health study

Por Benke, K.S., Carlson, M.C., Doan, B.Q., Walston, J.D., Xue, Q.L., Reiner, A.P., Fried, L.P., Arking, D.E., Chakravarti, A., Fallin, M.D.
Publicado em 2011

High throughput SNP and expression analyses of candidate genes for non‐syndromic oral clefts

Por Park, J W, Cai, J, McIntosh, I, Jabs, E W, Fallin, M D, Ingersoll, R, Hetmanski, J B, Vekemans, M, Attie‐Bitach, T, Lovett, M, Scott, A F, Beaty, T H
Publicado em 2006

Independent and epistatic effects of variants in VPS10-d receptors on Alzheimer disease risk and processing of the amyloid precursor protein (APP)

Por Reitz, C, Tosto, G, Vardarajan, B, Rogaeva, E, Ghani, M, Rogers, R S, Conrad, C, Haines, J L, Pericak-Vance, M A, Fallin, M D, Foroud, T, Farrer, L A, Schellenberg, G D, George-Hyslop, P S, Mayeux, R
Publicado em 2013