McCarthy MI, Kruglyak L, Lander ES. Sib-pair collection strategies for complex diseases. Genet Epidemiol. 1998;15(4):317-40. doi:10.1002/(SICI)1098-2272(1998)15:4<317::AID-GEPI1>3.0.CO;2-#
Lander ES, Lodish H. Mitochondrial diseases: gene mapping and gene therapy. Cell. 1990;61(6):925-6.
Kruglyak L, Daly MJ, Reeve-Daly MP, Lander ES. Parametric and nonparametric linkage analysis: a unified multipoint approach. Am J Hum Genet. 1996;58(6):1347-63.
Kruglyak L, Lander ES. Complete multipoint sib-pair analysis of qualitative and quantitative traits. Am J Hum Genet. 1995;57(2):439-54.
Zheng J, Erzurumluoglu M, Elsworth BL, et al. LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis. Bioinformatics. 2017;33(2):272-279. doi:10.1093/bioinformatics/btw613
Tewhey R, Kotliar D, Park DS, et al. Direct Identification of Hundreds of Expression-Modulating Variants using a Multiplexed Reporter Assay. Cell. 2016;165(6):1519-29. doi:10.1016/j.cell.2016.04.027
Markljung E, Jiang L, Jaffe JD, et al. ZBED6, a novel transcription factor derived from a domesticated DNA transposon regulates IGF2 expression and muscle growth. PLoS Biol. 2009;7(12):e1000256. doi:10.1371/journal.pbio.1000256
Golan D, Rosset S, Lander ES. Reply to Lee: Downward bias in heritability estimation is not due to simplified linkage equilibrium SNP simulation. Proc Natl Acad Sci U S A. 2015;112(40):E5452-3. doi:10.1073/pnas.1511370112
Moutsianas L, Agarwala V, Fuchsberger C, et al. The power of gene-based rare variant methods to detect disease-associated variation and test hypotheses about complex disease. PLoS Genet. 2015;11(4):e1005165. doi:10.1371/journal.pgen.1005165
Gusev A, Lee H, Trynka G, et al. Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases. Am J Hum Genet. 2014;95(5):535-52. doi:10.1016/j.ajhg.2014.10.004