Gymrek M, Willems T, Guilmatre A, et al. Abundant contribution of short tandem repeats to gene expression variation in humans. Nat Genet. 2016;48(1):22-9. doi:10.1038/ng.3461
Sun JX, Mullikin JC, Patterson N, Reich DE. Microsatellites are molecular clocks that support accurate inferences about history. Mol Biol Evol. 2009;26(5):1017-27. doi:10.1093/molbev/msp025
Pfeifer D, Kist R, Dewar K, et al. Campomelic dysplasia translocation breakpoints are scattered over 1 Mb proximal to SOX9: evidence for an extended control region. Am J Hum Genet. 1999;65(1):111-24. doi:10.1086/302455
Yeo TW, De Jager PL, Gregory SG, et al. A second major histocompatibility complex susceptibility locus for multiple sclerosis. Ann Neurol. 2007;61(3):228-36. doi:10.1002/ana.21063
Lee N, Daly MJ, DelMonte T, et al. A genomewide linkage-disequilibrium scan localizes the Saguenay-Lac-Saint-Jean cytochrome oxidase deficiency to 2p16. Am J Hum Genet. 2001;68(2):397-409. doi:10.1086/318197
Dutt A, Beroukhim R. Single nucleotide polymorphism array analysis of cancer. Curr Opin Oncol. 2007;19(1):43-9. doi:10.1097/CCO.0b013e328011a8c1
Cavanaugh J, IBD International Genetics Consortium. International collaboration provides convincing linkage replication in complex disease through analysis of a large pooled data set: Crohn disease and chromosome 16. Am J Hum Genet. 2001;68(5):1165-71. doi:10.1086/320119
Kamal M, Xie X, Lander ES. A large family of ancient repeat elements in the human genome is under strong selection. Proc Natl Acad Sci U S A. 2006;103(8):2740-5. doi:10.1073/pnas.0511238103
Hirschhorn JN, Lindgren CM, Daly MJ, et al. Genomewide linkage analysis of stature in multiple populations reveals several regions with evidence of linkage to adult height. Am J Hum Genet. 2001;69(1):106-16. doi:10.1086/321287
Sabeti PC, Walsh E, Schaffner SF, et al. The case for selection at CCR5-Delta32. PLoS Biol. 2005;3(11):e378. doi:10.1371/journal.pbio.0030378