Pendergraft WF, Nachman PH. Recent pathogenetic advances in ANCA-associated vasculitis. Presse Med. 2015;44(6 Pt 2):e223-9. doi:10.1016/j.lpm.2015.04.007
McLaren PJ, Coulonges C, Bartha I, et al. Polymorphisms of large effect explain the majority of the host genetic contribution to variation of HIV-1 virus load. Proc Natl Acad Sci U S A. 2015;112(47):14658-63. doi:10.1073/pnas.1514867112
Cleynen I, Boucher G, Jostins L, et al. Inherited determinants of Crohn’s disease and ulcerative colitis phenotypes: a genetic association study. Lancet. 2016;387(10014):156-67. doi:10.1016/S0140-6736(15)00465-1
Delaneau O, Marchini J, 1000 Genomes Project Consortium, 1000 Genomes Project Consortium. Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel. Nat Commun. 2014;5:3934. doi:10.1038/ncomms4934
Mikkelsen TS, Ku M, Jaffe DB, et al. Genome-wide maps of chromatin state in pluripotent and lineage-committed cells. Nature. 2007;448(7153):553-60. doi:10.1038/nature06008
Carter SL, Cibulskis K, Helman E, et al. Absolute quantification of somatic DNA alterations in human cancer. Nat Biotechnol. 2012;30(5):413-21. doi:10.1038/nbt.2203
Isobe N, Gourraud PA, Harbo HF, et al. Genetic risk variants in African Americans with multiple sclerosis. Neurology. 2013;81(3):219-27. doi:10.1212/WNL.0b013e31829bfe2f
Kukurba KR, Zhang R, Li X, et al. Allelic expression of deleterious protein-coding variants across human tissues. PLoS Genet. 2014;10(5):e1004304. doi:10.1371/journal.pgen.1004304
Perry JRB, Day F, Elks CE, et al. Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche. Nature. 2014;514(7520):92-7. doi:10.1038/nature13545
Thormaehlen AS, Schuberth C, Won HH, et al. Systematic cell-based phenotyping of missense alleles empowers rare variant association studies: a case for LDLR and myocardial infarction. PLoS Genet. 2015;11(2):e1004855. doi:10.1371/journal.pgen.1004855