Edwin Oh, Ph.D. - Publications

2008 University of Michigan, Ann Arbor, Ann Arbor, MI 
Neuroscience Biology

29 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2015 Turner TN, Sharma K, Oh EC, Liu YP, Collins RL, Sosa MX, Auer DR, Brand H, Sanders SJ, Moreno-De-Luca D, Pihur V, Plona T, Pike K, Soppet DR, Smith MW, et al. Loss of δ-catenin function in severe autism. Nature. 520: 51-6. PMID 25807484 DOI: 10.1038/nature14186  0.4
2015 Zoubovsky S, Oh EC, Cash-Padgett T, Johnson AW, Hou Z, Mori S, Gallagher M, Katsanis N, Sawa A, Jaaro-Peled H. Neuroanatomical and behavioral deficits in mice haploinsufficient for Pericentriolar material 1 (Pcm1). Neuroscience Research. PMID 25697395 DOI: 10.1016/j.neures.2015.02.002  0.4
2015 Oh EC, Vasanth S, Katsanis N. Metabolic regulation and energy homeostasis through the primary Cilium. Cell Metabolism. 21: 21-31. PMID 25543293 DOI: 10.1016/j.cmet.2014.11.019  0.4
2015 Hall G, Gbadegesin RA, Lavin P, Wu G, Liu Y, Oh EC, Wang L, Spurney RF, Eckel J, Lindsey T, Homstad A, Malone AF, Phelan PJ, Shaw A, Howell DN, et al. A novel missense mutation of Wilms' Tumor 1 causes autosomal dominant FSGS. Journal of the American Society of Nephrology : Jasn. 26: 831-43. PMID 25145932 DOI: 10.1681/ASN.2013101053  0.4
2014 Carnes MU, Liu YP, Allingham RR, Whigham BT, Havens S, Garrett ME, Qiao C, Katsanis N, Wiggs JL, Pasquale LR, Ashley-Koch A, Oh EC, Hauser MA. Discovery and functional annotation of SIX6 variants in primary open-angle glaucoma. Plos Genetics. 10: e1004372. PMID 24875647 DOI: 10.1371/journal.pgen.1004372  0.4
2014 Liu YP, Tsai IC, Morleo M, Oh EC, Leitch CC, Massa F, Lee BH, Parker DS, Finley D, Zaghloul NA, Franco B, Katsanis N. Ciliopathy proteins regulate paracrine signaling by modulating proteasomal degradation of mediators. The Journal of Clinical Investigation. 124: 2059-70. PMID 24691443 DOI: 10.1172/JCI71898  0.4
2013 Keeley PW, Luna G, Fariss RN, Skyles KA, Madsen NR, Raven MA, Poché RA, Swindell EC, Jamrich M, Oh EC, Swaroop A, Fisher SK, Reese BE. Development and plasticity of outer retinal circuitry following genetic removal of horizontal cells. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 17847-62. PMID 24198374 DOI: 10.1523/JNEUROSCI.1373-13.2013  0.4
2013 Nishiguchi KM, Tearle RG, Liu YP, Oh EC, Miyake N, Benaglio P, Harper S, Koskiniemi-Kuendig H, Venturini G, Sharon D, Koenekoop RK, Nakamura M, Kondo M, Ueno S, Yasuma TR, et al. Whole genome sequencing in patients with retinitis pigmentosa reveals pathogenic DNA structural changes and NEK2 as a new disease gene. Proceedings of the National Academy of Sciences of the United States of America. 110: 16139-44. PMID 24043777 DOI: 10.1073/pnas.1308243110  0.4
2013 Niederriter AR, Davis EE, Golzio C, Oh EC, Tsai IC, Katsanis N. In vivo modeling of the morbid human genome using Danio rerio. Journal of Visualized Experiments : Jove. e50338. PMID 23995499 DOI: 10.3791/50338  0.4
2013 Oh EC, Katsanis N. Context-dependent regulation of Wnt signaling through the primary cilium. Journal of the American Society of Nephrology : Jasn. 24: 10-8. PMID 23123400 DOI: 10.1681/ASN.2012050526  0.4
2012 Schuurs-Hoeijmakers JH, Oh EC, Vissers LE, Swinkels ME, Gilissen C, Willemsen MA, Holvoet M, Steehouwer M, Veltman JA, de Vries BB, van Bokhoven H, de Brouwer AP, Katsanis N, Devriendt K, Brunner HG. Recurrent de novo mutations in PACS1 cause defective cranial-neural-crest migration and define a recognizable intellectual-disability syndrome. American Journal of Human Genetics. 91: 1122-7. PMID 23159249 DOI: 10.1016/j.ajhg.2012.10.013  0.4
2012 Golzio C, Willer J, Talkowski ME, Oh EC, Taniguchi Y, Jacquemont S, Reymond A, Sun M, Sawa A, Gusella JF, Kamiya A, Beckmann JS, Katsanis N. KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant. Nature. 485: 363-7. PMID 22596160 DOI: 10.1038/nature11091  0.4
2012 Riazuddin SA, Parker DS, McGlumphy EJ, Oh EC, Iliff BW, Schmedt T, Jurkunas U, Schleif R, Katsanis N, Gottsch JD. Mutations in LOXHD1, a recessive-deafness locus, cause dominant late-onset Fuchs corneal dystrophy. American Journal of Human Genetics. 90: 533-9. PMID 22341973 DOI: 10.1016/j.ajhg.2012.01.013  0.4
2012 Oh EC, Katsanis N. Cilia in vertebrate development and disease. Development (Cambridge, England). 139: 443-8. PMID 22223675 DOI: 10.1242/dev.050054  0.4
2011 Oh EC, Katsanis N. Neuroscience: Imprinting in the brain. Nature. 475: 299-300. PMID 21776070 DOI: 10.1038/475299a  0.4
2011 Ishizuka K, Kamiya A, Oh EC, Kanki H, Seshadri S, Robinson JF, Murdoch H, Dunlop AJ, Kubo K, Furukori K, Huang B, Zeledon M, Hayashi-Takagi A, Okano H, Nakajima K, et al. DISC1-dependent switch from progenitor proliferation to migration in the developing cortex. Nature. 473: 92-6. PMID 21471969 DOI: 10.1038/nature09859  0.4
2011 Kim S, Zaghloul NA, Bubenshchikova E, Oh EC, Rankin S, Katsanis N, Obara T, Tsiokas L. Nde1-mediated inhibition of ciliogenesis affects cell cycle re-entry. Nature Cell Biology. 13: 351-60. PMID 21394081 DOI: 10.1038/ncb2183  0.4
2010 Kim SK, Shindo A, Park TJ, Oh EC, Ghosh S, Gray RS, Lewis RA, Johnson CA, Attie-Bittach T, Katsanis N, Wallingford JB. Planar cell polarity acts through septins to control collective cell movement and ciliogenesis. Science (New York, N.Y.). 329: 1337-40. PMID 20671153 DOI: 10.1126/science.1191184  0.4
2010 Zaghloul NA, Liu Y, Gerdes JM, Gascue C, Oh EC, Leitch CC, Bromberg Y, Binkley J, Leibel RL, Sidow A, Badano JL, Katsanis N. Functional analyses of variants reveal a significant role for dominant negative and common alleles in oligogenic Bardet-Biedl syndrome. Proceedings of the National Academy of Sciences of the United States of America. 107: 10602-7. PMID 20498079 DOI: 10.1073/pnas.1000219107  0.4
2010 Neale BM, Fagerness J, Reynolds R, Sobrin L, Parker M, Raychaudhuri S, Tan PL, Oh EC, Merriam JE, Souied E, Bernstein PS, Li B, Frederick JM, Zhang K, Brantley MA, et al. Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC). Proceedings of the National Academy of Sciences of the United States of America. 107: 7395-400. PMID 20385826 DOI: 10.1073/pnas.0912019107  0.4
2010 Wiens CJ, Tong Y, Esmail MA, Oh E, Gerdes JM, Wang J, Tempel W, Rattner JB, Katsanis N, Park HW, Leroux MR. Bardet-Biedl syndrome-associated small GTPase ARL6 (BBS3) functions at or near the ciliary gate and modulates Wnt signaling. The Journal of Biological Chemistry. 285: 16218-30. PMID 20207729 DOI: 10.1074/jbc.M109.070953  0.4
2009 Jia L, Oh EC, Ng L, Srinivas M, Brooks M, Swaroop A, Forrest D. Retinoid-related orphan nuclear receptor RORbeta is an early-acting factor in rod photoreceptor development. Proceedings of the National Academy of Sciences of the United States of America. 106: 17534-9. PMID 19805139 DOI: 10.1073/pnas.0902425106  0.4
2009 Layman WS, McEwen DP, Beyer LA, Lalani SR, Fernbach SD, Oh E, Swaroop A, Hegg CC, Raphael Y, Martens JR, Martin DM. Defects in neural stem cell proliferation and olfaction in Chd7 deficient mice indicate a mechanism for hyposmia in human CHARGE syndrome. Human Molecular Genetics. 18: 1909-23. PMID 19279158 DOI: 10.1093/hmg/ddp112  0.4
2008 Oh ECT, Cheng H, Hao H, Jia L, Khan NW, Swaroop A. Rod differentiation factor NRL activates the expression of nuclear receptor NR2E3 to suppress the development of cone photoreceptors Brain Research. 1236: 16-29. PMID 18294621 DOI: 10.1016/j.brainres.2008.01.028  0.4
2007 Raven MA, Oh EC, Swaroop A, Reese BE. Afferent control of horizontal cell morphology revealed by genetic respecification of rods and cones. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 3540-7. PMID 17392470 DOI: 10.1523/JNEUROSCI.0372-07.2007  0.4
2007 Oh EC, Khan N, Novelli E, Khanna H, Strettoi E, Swaroop A. Transformation of cone precursors to functional rod photoreceptors by bZIP transcription factor NRL. Proceedings of the National Academy of Sciences of the United States of America. 104: 1679-84. PMID 17242361 DOI: 10.1073/pnas.0605934104  0.4
2006 Akimoto M, Cheng H, Zhu D, Brzezinski JA, Khanna R, Filippova E, Oh EC, Jing Y, Linares JL, Brooks M, Zareparsi S, Mears AJ, Hero A, Glaser T, Swaroop A. Targeting of GFP to newborn rods by Nrl promoter and temporal expression profiling of flow-sorted photoreceptors. Proceedings of the National Academy of Sciences of the United States of America. 103: 3890-5. PMID 16505381 DOI: 10.1073/pnas.0508214103  0.4
2004 Cheng H, Khanna H, Oh EC, Hicks D, Mitton KP, Swaroop A. Photoreceptor-specific nuclear receptor NR2E3 functions as a transcriptional activator in rod photoreceptors. Human Molecular Genetics. 13: 1563-75. PMID 15190009 DOI: 10.1093/hmg/ddh173  0.4
2004 Yoshida S, Mears AJ, Friedman JS, Carter T, He S, Oh E, Jing Y, Farjo R, Fleury G, Barlow C, Hero AO, Swaroop A. Expression profiling of the developing and mature Nrl-/- mouse retina: identification of retinal disease candidates and transcriptional regulatory targets of Nrl. Human Molecular Genetics. 13: 1487-503. PMID 15163632 DOI: 10.1093/hmg/ddh160  0.4
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