Obaldia N, Baro NK, Calzada JE, et al. Clonal outbreak of Plasmodium falciparum infection in eastern Panama. J Infect Dis. 2015;211(7):1087-96. doi:10.1093/infdis/jiu575
Xu Q, Wu X, Li M, et al. Association studies of genomic variants with treatment response to risperidone, clozapine, quetiapine and chlorpromazine in the Chinese Han population. Pharmacogenomics J. 2016;16(4):357-65. doi:10.1038/tpj.2015.61
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
Musunuru K, Kathiresan S. HapMap and mapping genes for cardiovascular disease. Circ Cardiovasc Genet. 2008;1(1):66-71. doi:10.1161/CIRCGENETICS.108.813675
Zody MC, Garber M, Sharpe T, et al. Analysis of the DNA sequence and duplication history of human chromosome 15. Nature. 2006;440(7084):671-5. doi:10.1038/nature04601
Boettger LM, Handsaker RE, Zody MC, McCarroll SA. Structural haplotypes and recent evolution of the human 17q21.31 region. Nat Genet. 2012;44(8):881-5. doi:10.1038/ng.2334
Van der Auwera GA, Carneiro MO, Hartl C, et al. From FastQ data to high confidence variant calls: the Genome Analysis Toolkit best practices pipeline. Curr Protoc Bioinformatics. 2013;43:11.10.1-33. doi:10.1002/0471250953.bi1110s43
Lee JM, Kim KH, Shin A, et al. Sequence-Level Analysis of the Major European Huntington Disease Haplotype. Am J Hum Genet. 2015;97(3):435-44. doi:10.1016/j.ajhg.2015.07.017
Walsh EC, Mather KA, Schaffner SF, et al. An integrated haplotype map of the human major histocompatibility complex. Am J Hum Genet. 2003;73(3):580-90. doi:10.1086/378101
Raychaudhuri S, Remmers EF, Lee AT, et al. Common variants at CD40 and other loci confer risk of rheumatoid arthritis. Nat Genet. 2008;40(10):1216-23. doi:10.1038/ng.233