Goto A, Chen BH, Chan KHK, et al. Genetic variants in sex hormone pathways and the risk of type 2 diabetes among African American, Hispanic American, and European American postmenopausal women in the US. J Diabetes. 2018;10(6):524-533. doi:10.1111/1753-0407.12648
Stein MB, McCarthy MJ, Chen CY, et al. Genome-wide analysis of insomnia disorder. Mol Psychiatry. 2018;23(11):2238-2250. doi:10.1038/s41380-018-0033-5
Zhang JY, Wang M, Tian L, et al. modifies -induced kidney disease risk. Proc Natl Acad Sci U S A. 2018;115(13):3446-3451. doi:10.1073/pnas.1716113115
Raffield LM, Ulirsch JC, Naik RP, et al. Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease. PLoS Genet. 2018;14(3):e1007293. doi:10.1371/journal.pgen.1007293
Hayden MA, Ordulu Z, Gallagher S, et al. Clinical, pathologic, cytogenetic, and molecular profiling in self-identified black women with uterine leiomyomata. Cancer Genet. 2018;222-223:1-8. doi:10.1016/j.cancergen.2018.01.001
Naik RP, Derebail VK, Grams ME, et al. Association of sickle cell trait with chronic kidney disease and albuminuria in African Americans. JAMA. 2014;312(20):2115-25. doi:10.1001/jama.2014.15063
Bryc K, Durand EY, Macpherson M, Reich D, Mountain JL. The genetic ancestry of African Americans, Latinos, and European Americans across the United States. Am J Hum Genet. 2015;96(1):37-53. doi:10.1016/j.ajhg.2014.11.010
Musunuru K, Lettre G, Young T, et al. Candidate gene association resource (CARe): design, methods, and proof of concept. Circ Cardiovasc Genet. 2010;3(3):267-75. doi:10.1161/CIRCGENETICS.109.882696
Chan Y, Salem RM, Hsu YHH, et al. Genome-wide Analysis of Body Proportion Classifies Height-Associated Variants by Mechanism of Action and Implicates Genes Important for Skeletal Development. Am J Hum Genet. 2015;96(5):695-708. doi:10.1016/j.ajhg.2015.02.018
Altshuler D, Clark AG. Genetics. Harvesting medical information from the human family tree. Science. 2005;307(5712):1052-3. doi:10.1126/science.1109682