Teslovich TM, Musunuru K, Smith AV, et al. Biological, clinical and population relevance of 95 loci for blood lipids. Nature. 2010;466(7307):707-13. doi:10.1038/nature09270
Fraser HB, Xie X. Common polymorphic transcript variation in human disease. Genome Res. 2009;19(4):567-75. doi:10.1101/gr.083477.108
Ackerman KG, Huang H, Grasemann H, et al. Interacting genetic loci cause airway hyperresponsiveness. Physiol Genomics. 2005;21(1):105-11. doi:10.1152/physiolgenomics.00267.2004
Sankaran VG, Orkin SH. Genome-wide association studies of hematologic phenotypes: a window into human hematopoiesis. Curr Opin Genet Dev. 2013;23(3):339-44. doi:10.1016/j.gde.2013.02.006
Almendro V, Cheng YK, Randles A, et al. Inference of tumor evolution during chemotherapy by computational modeling and in situ analysis of genetic and phenotypic cellular diversity. Cell Rep. 2014;6(3):514-27. doi:10.1016/j.celrep.2013.12.041
Satija R, Shalek AK. Heterogeneity in immune responses: from populations to single cells. Trends Immunol. 2014;35(5):219-29. doi:10.1016/j.it.2014.03.004
Duda M, Kosmicki JA, Wall DP. Testing the accuracy of an observation-based classifier for rapid detection of autism risk. Transl Psychiatry. 2014;4:e424. doi:10.1038/tp.2014.65
Golan D, Lander ES, Rosset S. Measuring missing heritability: inferring the contribution of common variants. Proc Natl Acad Sci U S A. 2014;111(49):E5272-81. doi:10.1073/pnas.1419064111
Walford GA, Colomo N, Todd JN, et al. The study to understand the genetics of the acute response to metformin and glipizide in humans (SUGAR-MGH): design of a pharmacogenetic resource for type 2 diabetes. PLoS One. 2015;10(3):e0121553. doi:10.1371/journal.pone.0121553
Chen CY, Han J, Hunter DJ, Kraft P, Price AL. Explicit Modeling of Ancestry Improves Polygenic Risk Scores and BLUP Prediction. Genet Epidemiol. 2015;39(6):427-38. doi:10.1002/gepi.21906