Paterson AH, Damon S, Hewitt JD, et al. Mendelian factors underlying quantitative traits in tomato: comparison across species, generations, and environments. Genetics. 1991;127(1):181-97.
Kuntzen T, Berical A, Ndjomou J, et al. A set of reference sequences for the hepatitis C genotypes 4d, 4f, and 4k covering the full open reading frame. J Med Virol. 2008;80(8):1370-8. doi:10.1002/jmv.21240
Inoue K, Dewar K, Katsanis N, et al. The 1.4-Mb CMT1A duplication/HNPP deletion genomic region reveals unique genome architectural features and provides insights into the recent evolution of new genes. Genome Res. 2001;11(6):1018-33. doi:10.1101/gr.180401
Petit E, Giraud T, de Vienne DM, et al. Linkage to the mating-type locus across the genus Microbotryum: insights into nonrecombining chromosomes. Evolution. 2012;66(11):3519-33. doi:10.1111/j.1558-5646.2012.01703.x
Haldi M, Perrot V, Saumier M, et al. Large human YACs constructed in a rad52 strain show a reduced rate of chimerism. Genomics. 1994;24(3):478-84. doi:10.1006/geno.1994.1656
Drier Y, Lawrence MS, Carter SL, et al. Somatic rearrangements across cancer reveal classes of samples with distinct patterns of DNA breakage and rearrangement-induced hypermutability. Genome Res. 2013;23(2):228-35. doi:10.1101/gr.141382.112
Lehesjoki AE, Koskiniemi M, Norio R, et al. Localization of the EPM1 gene for progressive myoclonus epilepsy on chromosome 21: linkage disequilibrium allows high resolution mapping. Hum Mol Genet. 1993;2(8):1229-34.
Koren A, Polak P, Nemesh J, et al. Differential relationship of DNA replication timing to different forms of human mutation and variation. Am J Hum Genet. 2012;91(6):1033-40. doi:10.1016/j.ajhg.2012.10.018
Wade CM, Kulbokas EJ, Kirby AW, et al. The mosaic structure of variation in the laboratory mouse genome. Nature. 2002;420(6915):574-8. doi:10.1038/nature01252
Genovese G, Friedman DJ, Pollak MR. APOL1 variants and kidney disease in people of recent African ancestry. Nat Rev Nephrol. 2013;9(4):240-4. doi:10.1038/nrneph.2013.34