Lipson M, Loh PR, Sankararaman S, Patterson N, Berger B, Reich D. Calibrating the Human Mutation Rate via Ancestral Recombination Density in Diploid Genomes. PLoS Genet. 2015;11(11):e1005550. doi:10.1371/journal.pgen.1005550
Liu JM, Bittker JA, Lonshteyn M, Liu DR. Functional dissection of sRNA translational regulators by nonhomologous random recombination and in vivo selection. Chem Biol. 2005;12(7):757-67. doi:10.1016/j.chembiol.2005.05.014
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
Lander ES, Lincoln SE. The appropriate threshold for declaring linkage when allowing sex-specific recombination rates. Am J Hum Genet. 1988;43(4):396-400.
Bittker JA, Le BV, Liu DR. Nucleic acid evolution and minimization by nonhomologous random recombination. Nat Biotechnol. 2002;20(10):1024-9. doi:10.1038/nbt736
Levine RL, Wadleigh M, Cools J, et al. Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis. Cancer Cell. 2005;7(4):387-97. doi:10.1016/j.ccr.2005.03.023
Donis-Keller H, Green P, Helms C, et al. A genetic linkage map of the human genome. Cell. 1987;51(2):319-37.
Miretti MM, Walsh EC, Ke X, et al. A high-resolution linkage-disequilibrium map of the human major histocompatibility complex and first generation of tag single-nucleotide polymorphisms. Am J Hum Genet. 2005;76(4):634-46. doi:10.1086/429393
Lander ES, Botstein D. Mapping mendelian factors underlying quantitative traits using RFLP linkage maps. Genetics. 1989;121(1):185-99.
Altshuler D, Clark AG. Genetics. Harvesting medical information from the human family tree. Science. 2005;307(5712):1052-3. doi:10.1126/science.1109682