Replogle JM, De Jager PL. Reply: To PMID 25545807. Ann Neurol. 2015;78(4):659-60. doi:10.1002/ana.24456
Housley WJ, Fernandez SD, Vera K, et al. Genetic variants associated with autoimmunity drive NFκB signaling and responses to inflammatory stimuli. Sci Transl Med. 2015;7(291):291ra93. doi:10.1126/scitranslmed.aaa9223
Hohman TJ, Cooke-Bailey JN, Reitz C, et al. Global and local ancestry in African-Americans: Implications for Alzheimer’s disease risk. Alzheimers Dement. 2016;12(3):233-43. doi:10.1016/j.jalz.2015.02.012
Usher CL, Handsaker RE, Esko T, et al. Structural forms of the human amylase locus and their relationships to SNPs, haplotypes and obesity. Nat Genet. 2015;47(8):921-5. doi:10.1038/ng.3340
Kim K, Jiang X, Cui J, et al. Interactions between amino acid-defined major histocompatibility complex class II variants and smoking in seropositive rheumatoid arthritis. Arthritis Rheumatol. 2015;67(10):2611-23. doi:10.1002/art.39228
Tandon A, Chen CJ, Penman A, et al. African Ancestry Analysis and Admixture Genetic Mapping for Proliferative Diabetic Retinopathy in African Americans. Invest Ophthalmol Vis Sci. 2015;56(6):3999-4005. doi:10.1167/iovs.15-16674
Fu Q, Hajdinjak M, Moldovan OT, et al. An early modern human from Romania with a recent Neanderthal ancestor. Nature. 2015;524(7564):216-9. doi:10.1038/nature14558
Taft DH, Ambalavanan N, Schibler KR, et al. Center Variation in Intestinal Microbiota Prior to Late-Onset Sepsis in Preterm Infants. PLoS One. 2015;10(6):e0130604. doi:10.1371/journal.pone.0130604
Radmanesh F, Falcone GJ, Anderson CD, et al. Rare Coding Variation and Risk of Intracerebral Hemorrhage. Stroke. 2015;46(8):2299-301. doi:10.1161/STROKEAHA.115.009838
Joshi PK, Esko T, Mattsson H, et al. Directional dominance on stature and cognition in diverse human populations. Nature. 2015;523(7561):459-62. doi:10.1038/nature14618