Tello-Ruiz MK, Curley C, DelMonte T, et al. Haplotype-based association analysis of 56 functional candidate genes in the IBD6 locus on chromosome 19. Eur J Hum Genet. 2006;14(6):780-90. doi:10.1038/sj.ejhg.5201612
Plenge RM, Padyukov L, Remmers EF, et al. Replication of putative candidate-gene associations with rheumatoid arthritis in >4,000 samples from North America and Sweden: association of susceptibility with PTPN22, CTLA4, and PADI4. Am J Hum Genet. 2005;77(6):1044-60. doi:10.1086/498651
Freedman ML, Penney KL, Stram DO, et al. A haplotype-based case-control study of BRCA1 and sporadic breast cancer risk. Cancer Res. 2005;65(16):7516-22. doi:10.1158/0008-5472.CAN-05-0132
Freedman ML, Penney KL, Stram DO, et al. Common variation in BRCA2 and breast cancer risk: a haplotype-based analysis in the Multiethnic Cohort. Hum Mol Genet. 2004;13(20):2431-41. doi:10.1093/hmg/ddh270
Freedman ML, Reich D, Penney KL, et al. Assessing the impact of population stratification on genetic association studies. Nat Genet. 2004;36(4):388-93. doi:10.1038/ng1333
Wang TJ, Larson MG, Vasan RS, et al. Metabolite profiles and the risk of developing diabetes. Nat Med. 2011;17(4):448-53. doi:10.1038/nm.2307
Kuntzen T, Timm J, Berical A, et al. Naturally occurring dominant resistance mutations to hepatitis C virus protease and polymerase inhibitors in treatment-naïve patients. Hepatology. 2008;48(6):1769-78. doi:10.1002/hep.22549
Nyman ES, Loukola A, Varilo T, et al. Sex-specific influence of DRD2 on ADHD-type temperament in a large population-based birth cohort. Psychiatr Genet. 2012;22(4):197-201. doi:10.1097/YPG.0b013e32834c0cc8
Turchin MC, Chiang CWK, Palmer CD, et al. Evidence of widespread selection on standing variation in Europe at height-associated SNPs. Nat Genet. 2012;44(9):1015-9. doi:10.1038/ng.2368
Bick AG, Flannick J, Ito K, et al. Burden of rare sarcomere gene variants in the Framingham and Jackson Heart Study cohorts. Am J Hum Genet. 2012;91(3):513-9. doi:10.1016/j.ajhg.2012.07.017