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Publications

Erratum to: Type IV collagen drives alveolar epithelial-endothelial association and the morphogenetic movements of septation.

Loscertales M, Nicolaou F, Jeanne M, et al. Erratum to: Type IV collagen drives alveolar epithelial-endothelial association and the morphogenetic movements of septation. BMC Biol. 2016;14(1):73. doi:10.1186/s12915-016-0297-7

Whole Exome Sequencing in Atrial Fibrillation.

Lubitz SA, Brody JA, Bihlmeyer NA, et al. Whole Exome Sequencing in Atrial Fibrillation. PLoS Genet. 2016;12(9):e1006284. doi:10.1371/journal.pgen.1006284

Accelerating Innovation in Health IT.

Rudin RS, Bates DW, MacRae C. Accelerating Innovation in Health IT. N Engl J Med. 2016;375(9):815-7. doi:10.1056/NEJMp1606884

Accelerating global innovation to address antibacterial resistance: introducing CARB-X.

Outterson K, Rex JH, Jinks T, et al. Accelerating global innovation to address antibacterial resistance: introducing CARB-X. Nat Rev Drug Discov. 2016;15(9):589-90. doi:10.1038/nrd.2016.155

Cell Painting, a high-content image-based assay for morphological profiling using multiplexed fluorescent dyes.

Bray MA, Singh S, Han H, et al. Cell Painting, a high-content image-based assay for morphological profiling using multiplexed fluorescent dyes. Nat Protoc. 2016;11(9):1757-74. doi:10.1038/nprot.2016.105

Biallelic Variants in UBA5 Link Dysfunctional UFM1 Ubiquitin-like Modifier Pathway to Severe Infantile-Onset Encephalopathy.

Muona M, Ishimura R, Laari A, et al. Biallelic Variants in UBA5 Link Dysfunctional UFM1 Ubiquitin-like Modifier Pathway to Severe Infantile-Onset Encephalopathy. Am J Hum Genet. 2016;99(3):683-94. doi:10.1016/j.ajhg.2016.06.020

Determinants of Power in Gene-Based Burden Testing for Monogenic Disorders.

Guo MH, Dauber A, Lippincott MF, Chan YM, Salem RM, Hirschhorn JN. Determinants of Power in Gene-Based Burden Testing for Monogenic Disorders. Am J Hum Genet. 2016;99(3):527-39. doi:10.1016/j.ajhg.2016.06.031

De Novo Mutations in SON Disrupt RNA Splicing of Genes Essential for Brain Development and Metabolism, Causing an Intellectual-Disability Syndrome.

Kim JH, Shinde DN, Reijnders MRF, et al. De Novo Mutations in SON Disrupt RNA Splicing of Genes Essential for Brain Development and Metabolism, Causing an Intellectual-Disability Syndrome. Am J Hum Genet. 2016;99(3):711-9. doi:10.1016/j.ajhg.2016.06.029

Correlating Drug-Target Kinetics and In vivo Pharmacodynamics: Long Residence Time Inhibitors of the FabI Enoyl-ACP Reductase.

Daryaee F, Chang A, Schiebel J, et al. Correlating Drug-Target Kinetics and In vivo Pharmacodynamics: Long Residence Time Inhibitors of the FabI Enoyl-ACP Reductase. Chem Sci. 2016;7(9):5945-5954. doi:10.1039/C6SC01000H

Massive contribution of transposable elements to mammalian regulatory sequences.

Rayan NA, Del Rosario RCH, Prabhakar S. Massive contribution of transposable elements to mammalian regulatory sequences. Semin Cell Dev Biol. 2016;57:51-6. doi:10.1016/j.semcdb.2016.05.004