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Lower-than-expected linkage disequilibrium between tightly linked markers in humans suggests a role for gene conversion.

Ardlie K, Liu-Cordero SN, Eberle MA, et al. Lower-than-expected linkage disequilibrium between tightly linked markers in humans suggests a role for gene conversion. Am J Hum Genet. 2001;69(3):582-9. doi:10.1086/323251

Genetic association studies of complex traits: design and analysis issues.

Newton-Cheh C, Hirschhorn JN. Genetic association studies of complex traits: design and analysis issues. Mutat Res. 2005;573(1-2):54-69. doi:10.1016/j.mrfmmm.2005.01.006

Quantifying missing heritability at known GWAS loci.

Gusev A, Bhatia G, Zaitlen N, et al. Quantifying missing heritability at known GWAS loci. PLoS Genet. 2013;9(12):e1003993. doi:10.1371/journal.pgen.1003993

The power of gene-based rare variant methods to detect disease-associated variation and test hypotheses about complex disease.

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

The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping.

Hästbacka J, de la Chapelle A, Mahtani MM, et al. The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping. Cell. 1994;78(6):1073-87.