Li Y, Zhao T, Liu B, et al. Inhibition of histone deacetylase 6 improves long-term survival in a lethal septic model. J Trauma Acute Care Surg. 2015;78(2):378-85. doi:10.1097/TA.0000000000000510
Publications
Lubitz SA, Ellinor PT. Somatic mutations and atrial fibrillation: the end or just the beginning? Circ Cardiovasc Genet. 2015;8(1):2-3. doi:10.1161/CIRCGENETICS.115.000963
Jabbari J, Olesen MS, Yuan L, et al. Common and rare variants in SCN10A modulate the risk of atrial fibrillation. Circ Cardiovasc Genet. 2015;8(1):64-73. doi:10.1161/HCG.0000000000000022
Gupta RM, Pilbrow AP, Weeke PE. Top advances in functional genomics and translational biology for 2014. Circ Cardiovasc Genet. 2015;8(1):207-10. doi:10.1161/CIRCGENETICS.115.001021
Cox DBT, Platt RJ, Zhang F. Therapeutic genome editing: prospects and challenges. Nat Med. 2015;21(2):121-31. doi:10.1038/nm.3793
Davies G, Armstrong N, Bis JC, et al. Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53949). Mol Psychiatry. 2015;20(2):183-92. doi:10.1038/mp.2014.188
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
Tonomura N, Elvers I, Thomas R, et al. Genome-wide association study identifies shared risk loci common to two malignancies in golden retrievers. PLoS Genet. 2015;11(2):e1004922. doi:10.1371/journal.pgen.1004922
Zetsche B, Volz SE, Zhang F. A split-Cas9 architecture for inducible genome editing and transcription modulation. Nat Biotechnol. 2015;33(2):139-42. doi:10.1038/nbt.3149
Dey-Guha I, Alves CP, Yeh AC, Sole X, Darp R, Ramaswamy S. A mechanism for asymmetric cell division resulting in proliferative asynchronicity. Mol Cancer Res. 2015;13(2):223-30. doi:10.1158/1541-7786.MCR-14-0474