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BMC Proceedings|March 1, 2012
Pathway-based joint effects analysis of rare genetic variants using Genetic Analysis Workshop 17 exon sequence dataPingzhao Hu, Wei Xu, Lu Cheng, et al.BMC Proceedings|March 1, 2012
Use of principal components to aggregate rare variants in case-control and family-based association studies in the presence of multiple covariatesRémi Kazma, Thomas J Hoffmann, John S WitteBMC Proceedings|March 1, 2012
Evaluation of a LASSO regression approach on the unrelated samples of Genetic Analysis Workshop 17Wei Guo, Robert C Elston, Xiaofeng ZhuBMC Proceedings|March 1, 2012
Large-scale risk prediction applied to Genetic Analysis Workshop 17 mini-exome sequence dataGengxin Li, John Ferguson, Wei Zheng, et al.BMC Proceedings|March 1, 2012
Power of association tests in the presence of multiple causal variantsYanming Di, Gu Mi, Luna Sun, et al.BMC Proceedings|March 1, 2012
Evaluating aggregate effects of rare and common variants in the 1000 Genomes Project exon sequencing data using latent variable structural equation modelingNl Nock, Lx ZhangBMC Proceedings|March 1, 2012
Evaluating methods for combining rare variant data in pathway-based tests of genetic associationAshley Petersen, Alexandra Sitarik, Alexander Luedtke, et al.BMC Proceedings|March 1, 2012
A pathway-based association analysis model using common and rare variantsLu Cheng, Pingzhao Hu, Jenna Sykes, et al.BMC Proceedings|March 1, 2012
Association screening for genes with multiple potentially rare variants: an inverse-probability weighted clustering approachYing Liu, Chien Hsun Huang, Inchi Hu, et al.BMC Proceedings|March 1, 2012
Assessing the impact of missing genotype data in rare variant association analysisReedik Mägi, Ashish Kumar, Andrew P MorrisPageof 102