Krier JB, Kalia SS, Green RC. Genomic sequencing in clinical practice: applications, challenges, and opportunities. Dialogues Clin Neurosci. 2016;18(3):299-312.
Publications
Ubellacker JM, McAllister SS. The unresolved role of systemic factors in bone metastasis. J Bone Oncol. 2016;5(3):96-99. doi:10.1016/j.jbo.2016.03.009
Chen B, Zheng B, DeRan M, et al. ZDHHC7-mediated S-palmitoylation of Scribble regulates cell polarity. Nat Chem Biol. 2016;12(9):686-93. doi:10.1038/nchembio.2119
Herring A, Messana A, Bara AM, Hazelbaker DZ, Eggan K, Barrett LE. Generation of a TLE1 homozygous knockout human embryonic stem cell line using CRISPR-Cas9. Stem Cell Res. 2016;17(2):430-432. doi:10.1016/j.scr.2016.09.009
Bara AM, Messana A, Herring A, Hazelbaker DZ, Eggan K, Barrett LE. Generation of a TLE3 heterozygous knockout human embryonic stem cell line using CRISPR-Cas9. Stem Cell Res. 2016;17(2):441-443. doi:10.1016/j.scr.2016.09.008
Muñoz JF, Farrer RA, Desjardins CA, et al. Genome Diversity, Recombination, and Virulence across the Major Lineages of Paracoccidioides. mSphere. 2016;1(5). doi:10.1128/mSphere.00213-16
Li G, Cunin P, Wu D, et al. The Rheumatoid Arthritis Risk Variant CCR6DNP Regulates CCR6 via PARP-1. PLoS Genet. 2016;12(9):e1006292. doi:10.1371/journal.pgen.1006292
Walesky C, Goessling W. Nature and nurture: Environmental toxins and biliary atresia. Hepatology. 2016;64(3):717-9. doi:10.1002/hep.28701
High FA, Bhayani P, Wilson JM, Bult CJ, Donahoe PK, Longoni M. De novo frameshift mutation in COUP-TFII (NR2F2) in human congenital diaphragmatic hernia. Am J Med Genet A. 2016;170(9):2457-61. doi:10.1002/ajmg.a.37830
Flannick J, Florez JC. Type 2 diabetes: genetic data sharing to advance complex disease research. Nat Rev Genet. 2016;17(9):535-49. doi:10.1038/nrg.2016.56