Li H. BGT: efficient and flexible genotype query across many samples. Bioinformatics. 2016;32(4):590-2. doi:10.1093/bioinformatics/btv613
Llamas B, Fehren-Schmitz L, Valverde G, et al. Ancient mitochondrial DNA provides high-resolution time scale of the peopling of the Americas. Sci Adv. 2016;2(4):e1501385. doi:10.1126/sciadv.1501385
Boettger LM, Salem RM, Handsaker RE, et al. Recurring exon deletions in the HP (haptoglobin) gene contribute to lower blood cholesterol levels. Nat Genet. 2016;48(4):359-66. doi:10.1038/ng.3510
Keum JW, Shin A, Gillis T, et al. The HTT CAG-Expansion Mutation Determines Age at Death but Not Disease Duration in Huntington Disease. Am J Hum Genet. 2016;98(2):287-98. doi:10.1016/j.ajhg.2015.12.018
Sekar A, Bialas AR, de Rivera H, et al. Schizophrenia risk from complex variation of complement component 4. Nature. 2016;530(7589):177-83. doi:10.1038/nature16549
Palamara PF, Francioli LC, Wilton PR, et al. Leveraging Distant Relatedness to Quantify Human Mutation and Gene-Conversion Rates. Am J Hum Genet. 2015;97(6):775-89. doi:10.1016/j.ajhg.2015.10.006
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 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
Li Y, Beckman KB, Caberto C, et al. Association of Genes, Pathways, and Haplogroups of the Mitochondrial Genome with the Risk of Colorectal Cancer: The Multiethnic Cohort. PLoS One. 2015;10(9):e0136796. doi:10.1371/journal.pone.0136796
Ward LD, Kellis M. HaploReg v4: systematic mining of putative causal variants, cell types, regulators and target genes for human complex traits and disease. Nucleic Acids Res. 2016;44(D1):D877-81. doi:10.1093/nar/gkv1340