Lenz TL, Deutsch AJ, Han B, et al. Widespread non-additive and interaction effects within HLA loci modulate the risk of autoimmune diseases. Nat Genet. 2015;47(9):1085-90. doi:10.1038/ng.3379
Publications
Chan K, Roberts SA, Klimczak LJ, et al. An APOBEC3A hypermutation signature is distinguishable from the signature of background mutagenesis by APOBEC3B in human cancers. Nat Genet. 2015;47(9):1067-72. doi:10.1038/ng.3378
Paull D, Sevilla A, Zhou H, et al. Automated, high-throughput derivation, characterization and differentiation of induced pluripotent stem cells. Nat Methods. 2015;12(9):885-92. doi:10.1038/nmeth.3507
Karjalainen MK, Ojaniemi M, Haapalainen AM, et al. CXCR3 Polymorphism and Expression Associate with Spontaneous Preterm Birth. J Immunol. 2015;195(5):2187-98. doi:10.4049/jimmunol.1501174
Stachler MD, Taylor-Weiner A, Peng S, et al. Paired exome analysis of Barrett’s esophagus and adenocarcinoma. Nat Genet. 2015;47(9):1047-55. doi:10.1038/ng.3343
Lal D, Pernhorst K, Klein KM, et al. Extending the phenotypic spectrum of RBFOX1 deletions: Sporadic focal epilepsy. Epilepsia. 2015;56(9):e129-33. doi:10.1111/epi.13076
Baxt LA, Xavier RJ. Role of Autophagy in the Maintenance of Intestinal Homeostasis. Gastroenterology. 2015;149(3):553-62. doi:10.1053/j.gastro.2015.06.046
Ozkumur AY, Goods BA, Love C. Development of a High-Throughput Functional Screen Using Nanowell-Assisted Cell Patterning. Small. 2015;11(36):4643-50. doi:10.1002/smll.201500674
Guda S, Brendel C, Renella R, et al. miRNA-embedded shRNAs for Lineage-specific BCL11A Knockdown and Hemoglobin F Induction. Mol Ther. 2015;23(9):1465-74. doi:10.1038/mt.2015.113
Chen CY, Han J, Hunter DJ, Kraft P, Price AL. Explicit Modeling of Ancestry Improves Polygenic Risk Scores and BLUP Prediction. Genet Epidemiol. 2015;39(6):427-38. doi:10.1002/gepi.21906