H., Bryois, Julien, Buttenschon, Henriette N., Bybjerg-Grauholm, Jonas, Cai, Na, Castelao, Enrique, Christensen, Jane Hvarregaard, Clarke, Toni-Kim, Coleman, Jonathan I. T., Bigdeli, Tim B., Binder, Elisabeth B., Blackwood, Douglas R. F., Bacanu, Silviu-Alin, Baekvad-Hansen, Marie, Beekman, Aartjan F. Wray, Naomi R., Ripke, Stephan, Mattheisen, Manuel, Trzaskowski, Maciej, Byrne, Enda M., Abdellaoui, Abdel, Adams, Mark J., Agerbo, Esben, Air, Tracy M., Andlauer, Till M. Prediction of Individual Risk to Disease from Genome-wide Association studies. Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs. Lee SH, DeCandia T, Ripke S, Yang J, PGC-SCZ, ISC, MGS, Sullivan PF, Goddard ME, Keller MC*, Visscher PM*, Wray NR (*joint last) (2012). American Journal of Human Genetics 88:294-305. Estimating Missing Heritability for Disease from Genome-wide Association Studies. Lee SH, Wray NR, Goddard ME, Visscher PM (2011).
Finding the missing heritability of complex diseases.
Manolio TA, Collins FS, Cox NJ, Goldstein DB, Hindorff LA, Hunter DJ, McCarthy MI, Ramos EM, Cardon LR, Chakravarti A, Cho JH, Guttmacher AE, Kong A, Kruglyak L, Mardis E, Rotimi CN, Slatkin M, Valle D, Whittemore AS, Boehnke M, Clark AG, Eichler EE, Gibson G, Haines JL, Mackay TF, McCarroll SA, Visscher PM. Common SNPs explain a large proportion of the heritability for human height. Yang J, Benyamin B, McEvoy BP, Gordon S, Henders AK, Nyholt DR, Madden PA, Heath AC, Martin NG, Montgomery GW, Goddard ME, Visscher PM (2010).
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