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BMC 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 MorrisBMC Proceedings|March 1, 2012
Estimating heritability using family and unrelated individuals dataPriya B Shetty, Huaizhen Qin, Junghyun Namkung, et al.BMC Proceedings|March 1, 2012
Association tests for rare and common variants based on genotypic and phenotypic measures of similarity between individualsAnbupalam Thalamuthu, Jingyuan Zhao, Garrett Teoh Hor Keong, et al.BMC Proceedings|March 1, 2012
Enrichment analysis of genetic association in genes and pathways by aggregating signals from both rare and common variantsWei Yang, C Charles GuBMC Proceedings|March 1, 2012
Detection of rare functional variants using group ISISYue S Niu, Ning Hao, Lingling AnBMC Proceedings|March 1, 2012
Pathway analysis following association studyJulius S Ngwa, Alisa K Manning, Jonna L Grimsby, et al.BMC Proceedings|March 1, 2012
Successful identification of rare variants using oligogenic segregation analysis as a prioritizing tool for whole-exome sequencing studiesFrance Gagnon, Nicole M Roslin, Mathieu LemirePageof 101