Gabriel SB, Schaffner SF, Nguyen H, et al. The structure of haplotype blocks in the human genome. Science. 2002;296(5576):2225-9. doi:10.1126/science.1069424
Sander JD, Ramirez CL, Linder SJ, et al. In silico abstraction of zinc finger nuclease cleavage profiles reveals an expanded landscape of off-target sites. Nucleic Acids Res. 2013;41(19):e181. doi:10.1093/nar/gkt716
Balick DJ, Do R, Cassa CA, Reich D, Sunyaev SR. Dominance of Deleterious Alleles Controls the Response to a Population Bottleneck. PLoS Genet. 2015;11(8):e1005436. doi:10.1371/journal.pgen.1005436
Reich DE, Schaffner SF, Daly MJ, et al. Human genome sequence variation and the influence of gene history, mutation and recombination. Nat Genet. 2002;32(1):135-42. doi:10.1038/ng947
Krier J, Barfield R, Green RC, Kraft P. Reclassification of genetic-based risk predictions as GWAS data accumulate. Genome Med. 2016;8(1):20. doi:10.1186/s13073-016-0272-5
Rees MG, Seashore-Ludlow B, Cheah JH, et al. Correlating chemical sensitivity and basal gene expression reveals mechanism of action. Nat Chem Biol. 2016;12(2):109-16. doi:10.1038/nchembio.1986
Lincoln SE, Lander ES. Systematic detection of errors in genetic linkage data. Genomics. 1992;14(3):604-10.
Tucker G, Loh PR, MacLeod IM, et al. Two-Variance-Component Model Improves Genetic Prediction in Family Datasets. Am J Hum Genet. 2015;97(5):677-90. doi:10.1016/j.ajhg.2015.10.002
Bulik-Sullivan B, Finucane HK, Anttila V, et al. An atlas of genetic correlations across human diseases and traits. Nat Genet. 2015;47(11):1236-41. doi:10.1038/ng.3406
Finucane HK, Bulik-Sullivan B, Gusev A, et al. Partitioning heritability by functional annotation using genome-wide association summary statistics. Nat Genet. 2015;47(11):1228-35. doi:10.1038/ng.3404