1.
Manolio TA, Fowler DM, Starita LM, et al. Bedside Back to Bench: Building Bridges between Basic and Clinical Genomic Research. Cell. 2017;169(1):6-12. doi:10.1016/j.cell.2017.03.005.
1.
Martin AR, Gignoux CR, Walters RK, et al. Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations. Am J Hum Genet. 2017;100(4):635-649. doi:10.1016/j.ajhg.2017.03.004.
1.
Dong Z, Wang H, Chen H, et al. Identification of balanced chromosomal rearrangements previously unknown among participants in the 1000 Genomes Project: implications for interpretation of structural variation in genomes and the future of clinical cytogenetics. Genet Med. 2018;20(7):697-707. doi:10.1038/gim.2017.170.
1.
Collins FS, Doudna JA, Lander ES, Rotimi CN. Human Molecular Genetics and Genomics - Important Advances and Exciting Possibilities. N Engl J Med. 2021;384(1):1-4. doi:10.1056/NEJMp2030694.
1.
Lander ES. Scientific commentary: the scientific foundations and medical and social prospects of the Human Genome Project. J Law Med Ethics. 1998;26(3):184-8, 178.
1.
Margulies EH, Cooper GM, Asimenos G, et al. Analyses of deep mammalian sequence alignments and constraint predictions for 1% of the human genome. Genome Res. 2007;17(6):760-74. doi:10.1101/gr.6034307.
1.
de Bakker PIW, Burtt NP, Graham RR, et al. Transferability of tag SNPs in genetic association studies in multiple populations. Nat Genet. 2006;38(11):1298-303. doi:10.1038/ng1899.
1.
Hu X, Yuan J, Shi Y, et al. pIRS: Profile-based Illumina pair-end reads simulator. Bioinformatics. 2012;28(11):1533-5. doi:10.1093/bioinformatics/bts187.
1.
Ruchi R, Genovese G, Lee J, et al. Copy Number Variation at the APOL1 Locus. PLoS One. 2015;10(5):e0125410. doi:10.1371/journal.pone.0125410.
1.
Konkel MK, Walker JA, Hotard AB, et al. Sequence Analysis and Characterization of Active Human Alu Subfamilies Based on the 1000 Genomes Pilot Project. Genome Biol Evol. 2015;7(9):2608-22. doi:10.1093/gbe/evv167.