Emma C. Davies, MD
Research Area(s): Cornea, Infectious Disease Profiles: Harvard Catalyst Profile Mass. Eye and Ear Profile (Research) Mass. Eye and Ear Profile (Clinical)
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1349 results found
Adipose-derived circulating miRNAs regulate gene expression in other tissues
Thomou, Thomas, Marcelo Mori, Jonathan Dreyfuss, Masahiro Konishi, Masaji Sakaguchi, Christian Wolfrum, Tata Nageswara Rao, et al. 2017. “Adipose-Derived Circulating MiRNAs Regulate Gene Expression in Other Tissues”. Nature 542 (7642): 450-55.
Loss of astrocyte cholesterol synthesis disrupts neuronal function and alters whole-body metabolism
Ferris, Heather, Rachel Perry, Gabriela Moreira, Gerald Shulman, Jay Horton, and C. Ronald Kahn. 2017. “Loss of Astrocyte Cholesterol Synthesis Disrupts Neuronal Function and Alters Whole-Body Metabolism”. Proc Natl Acad Sci U S A 114 (5): 1189-94.
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BIDMC Article about our High Sch Summer Research Program
BIDMC article released Oct 26, 2017
Summer Internship
*****NOTE: THIS PROGRAM IS CLOSED***** This official BIDMC High School Summer Research Program allows the students to experience scientific research and gain generic skills. All students receive a stipend during this Program. You can read about this program here. Take a look at our past students'...
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia
Verhoeven, Virginie, Pirro Hysi, Robert Wojciechowski, Qiao Fan, Jeremy Guggenheim, René Höhn, Stuart Macgregor, et al. 2013. “Genome-Wide Meta-Analyses of Multiancestry Cohorts Identify Multiple New Susceptibility Loci for Refractive Error and Myopia”. Nat Genet 45 (3): 314-8.
Mutations in LOXHD1, a recessive-deafness locus, cause dominant late-onset Fuchs corneal dystrophy
Riazuddin, Amer, David Parker, Elyse McGlumphy, Edwin Oh, Benjamin Iliff, Thore Schmedt, Ula Jurkunas, Robert Schleif, Nicholas Katsanis, and John Gottsch. 2012. “Mutations in LOXHD1, a Recessive-Deafness Locus, Cause Dominant Late-Onset Fuchs Corneal Dystrophy”. Am J Hum Genet 90 (3): 533-9.
A multicenter study to map genes for Fuchs endothelial corneal dystrophy: baseline characteristics and heritability
Louttit, Megan, Laura Kopplin, Robert Igo, Jeremy Fondran, Angela Tagliaferri, David Bardenstein, Anthony Aldave, et al. 2012. “A Multicenter Study to Map Genes for Fuchs Endothelial Corneal Dystrophy: Baseline Characteristics and Heritability”. Cornea 31 (1): 26-35.
Molecular bases of corneal endothelial dystrophies
Schmedt, Thore, Mariana Mazzini Silva, Alireza Ziaei, and Ula Jurkunas. 2012. “Molecular Bases of Corneal Endothelial Dystrophies”. Exp Eye Res 95 (1): 24-34.