11.07.2015 Views

2DkcTXceO

2DkcTXceO

2DkcTXceO

SHOW MORE
SHOW LESS

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

X. Lin 201Pearl, J. (2001). Direct and indirect effects. In Proceedings of the SeventeenthConference on Uncertainty in Artificial Intelligence. MorganKaufmannPublishers, Burlington, MA, pp. 411–420.Robinson, R. (2010). Common disease, multiple rare (and distant) variants.PLoS Biology, 8:e1000293, doi:10.1371/journal.pbio.1000293.Tennessen, J.A., Bigham, A.W., O’Connor, T.D., Fu, W., Kenny, E.E.,Gravel, S., McGee, S., Do, R., Liu, X., Jun, G., Kang, H.M., Jordan, D.,Leal, S.M., Gabriel, S., Rieder, M.J., Abecasis, G., Altshuler, D., Nickerson,D.A., Boerwinkle, E., Sunyaev, S., Bustamante, C.D., Bamshad,M.J., Akey, J.M., Broad, G.O., Seattle, G.O., and the Exome SequencingProject. (2012). Evolution and functional impact of rare coding variationfrom deep sequencing of human exomes. Science, 337:64–69.The 1000 Genomes Project Consortium (2010). A map of human genomevariation from population scale sequencing. Nature, 467:1061–1073.VanderWeele, T.J. and Vansteelandt, S. (2010). Odds ratios for mediationanalysis for a dichotomous outcome. American Journal of Epidemiology,172:1339–1348.Wray, N.R., Yang, J., Goddard, M.E., and Visscher, P.M. (2010). The geneticinterpretation of area under the ROC curve in genomic profiling. PLoSGenetics, 6:e1000864.Wu, M.C., Lee, S., Cai, T., Li, Y., Boehnke, M., and Lin, X. (2011). Rarevariantassociation testing for sequencing data with the sequence kernelassociation test. The American Journal of Human Genetics, 89:82–93.Yang, J., Benyamin, B., McEvoy, B.P., Gordon, S., Henders, A.K., Nyholt,D.R., Madden, P.A., Heath, A.C., Martin, N.G., Montgomery, G.W.,Goddard, M.E., and Visscher, P.M. (2010). Common SNPs explain alarge proportion of the heritability for human height. Nature Genetics,42:565–569.

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!