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Genetic Epidemiology|March 19, 2008
Estimation of the multiple testing burden for genomewide association studies of nearly all common variantsItsik Pe'er, Roman Yelensky, David Altshuler, et al.Genetic Epidemiology|March 12, 2008
Using disease symptoms to improve detection of linkage under genetic heterogeneityAlexandre Bureau, Aurélie Labbe, Jordie Croteau, et al.Genetic Epidemiology|February 12, 2008
Comparison of approaches for machine-learning optimization of neural networks for detecting gene-gene interactions in genetic epidemiologyAlison A Motsinger-Reif, Scott M Dudek, Lance W Hahn, et al.Genetic Epidemiology|October 25, 2018
Variance components genetic association test for zero-inflated count outcomesMatthew O Goodman, Lori Chibnik, Tianxi CaiGenetic Epidemiology|April 11, 2017
Inclusion of biological knowledge in a Bayesian shrinkage model for joint estimation of SNP effectsMiguel Pereira, John R Thompson, Christian X Weichenberger, et al.Genetic Epidemiology|March 29, 2019
Subset testing and analysis of multiple phenotypesAndriy Derkach, Ruth M PfeifferGenetic Epidemiology|March 29, 2019
Bayesian meta-analysis across genome-wide association studies of diverse phenotypesHolly Trochet, Matti Pirinen, Gavin Band, et al.Genetic Epidemiology|February 16, 2017
Genetic risk models: Influence of model size on risk estimates and precisionYing Shan, Gerard Tromp, Helena Kuivaniemi, et al.Genetic Epidemiology|March 21, 2017
Semiparametric methods for estimation of a nonlinear exposure-outcome relationship using instrumental variables with application to Mendelian randomizationJames R Staley, Stephen BurgessGenetic Epidemiology|January 24, 2017
Bayesian latent variable models for hierarchical clustered count outcomes with repeated measures in microbiome studiesLizhen Xu, Andrew D Paterson, Wei XuPageof 285