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Edwin oh
Edwin oh
Dirección de correo verificada de duke.edu
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Gene expression elucidates functional impact of polygenic risk for schizophrenia
M Fromer, P Roussos, SK Sieberts, JS Johnson, DH Kavanagh, ...
Nature neuroscience 19 (11), 1442-1453, 2016
10322016
Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC)
BM Neale, J Fagerness, R Reynolds, L Sobrin, M Parker, S Raychaudhuri, ...
Proceedings of the National Academy of Sciences 107 (16), 7395-7400, 2010
4942010
KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant
C Golzio, J Willer, ME Talkowski, EC Oh, Y Taniguchi, S Jacquemont, ...
Nature 485 (7398), 363-367, 2012
4542012
Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights
A Gusev, N Mancuso, H Won, M Kousi, HK Finucane, Y Reshef, L Song, ...
Nature genetics 50 (4), 538-548, 2018
4182018
Planar cell polarity acts through septins to control collective cell movement and ciliogenesis
SK Kim, A Shindo, TJ Park, EC Oh, S Ghosh, RS Gray, RA Lewis, ...
Science 329 (5997), 1337-1340, 2010
3852010
Targeting of GFP to newborn rods by Nrl promoter and temporal expression profiling of flow-sorted photoreceptors
M Akimoto, H Cheng, D Zhu, JA Brzezinski, R Khanna, E Filippova, ...
Proceedings of the National Academy of Sciences 103 (10), 3890-3895, 2006
3752006
Photoreceptor-specific nuclear receptor NR2E3 functions as a transcriptional activator in rod photoreceptors
H Cheng, H Khanna, ECT Oh, D Hicks, KP Mitton, A Swaroop
Human molecular genetics 13 (15), 1563-1575, 2004
2812004
Nde1-mediated inhibition of ciliogenesis affects cell cycle re-entry
S Kim, NA Zaghloul, E Bubenshchikova, EC Oh, S Rankin, N Katsanis, ...
Nature cell biology 13 (4), 351-360, 2011
2532011
DISC1-dependent switch from progenitor proliferation to migration in the developing cortex
K Ishizuka, A Kamiya, EC Oh, H Kanki, S Seshadri, JF Robinson, ...
Nature 473 (7345), 92-96, 2011
2362011
Cilia in vertebrate development and disease
EC Oh, N Katsanis
Development 139 (3), 443-448, 2012
1922012
Expression profiling of the developing and mature Nrl −/− mouse retina: identification of retinal disease candidates and transcriptional regulatory …
S Yoshida, AJ Mears, JS Friedman, T Carter, S He, E Oh, Y Jing, R Farjo, ...
Human molecular genetics 13 (14), 1487-1503, 2004
1892004
Transformation of cone precursors to functional rod photoreceptors by bZIP transcription factor NRL
ECT Oh, N Khan, E Novelli, H Khanna, E Strettoi, A Swaroop
Proceedings of the National Academy of Sciences 104 (5), 1679-1684, 2007
1852007
Loss of δ-catenin function in severe autism
TN Turner, K Sharma, EC Oh, YP Liu, RL Collins, MX Sosa, DR Auer, ...
Nature 520 (7545), 51-56, 2015
1652015
Mutations in LOXHD1, a recessive-deafness locus, cause dominant late-onset Fuchs corneal dystrophy
SA Riazuddin, DS Parker, EJ McGlumphy, EC Oh, BW Iliff, T Schmedt, ...
The American Journal of Human Genetics 90 (3), 533-539, 2012
1632012
Retinoid-related orphan nuclear receptor RORβ is an early-acting factor in rod photoreceptor development
L Jia, ECT Oh, L Ng, M Srinivas, M Brooks, A Swaroop, D Forrest
Proceedings of the National Academy of Sciences 106 (41), 17534-17539, 2009
1472009
Functional analyses of variants reveal a significant role for dominant negative and common alleles in oligogenic Bardet–Biedl syndrome
NA Zaghloul, Y Liu, JM Gerdes, C Gascue, EC Oh, CC Leitch, Y Bromberg, ...
Proceedings of the National Academy of Sciences 107 (23), 10602-10607, 2010
1422010
Rod differentiation factor NRL activates the expression of nuclear receptor NR2E3 to suppress the development of cone photoreceptors
ECT Oh, H Cheng, H Hao, L Jia, NW Khan, A Swaroop
Brain research 1236, 16-29, 2008
1412008
Whole genome sequencing in patients with retinitis pigmentosa reveals pathogenic DNA structural changes and NEK2 as a new disease gene
KM Nishiguchi, RG Tearle, YP Liu, EC Oh, N Miyake, P Benaglio, ...
Proceedings of the National Academy of Sciences 110 (40), 16139-16144, 2013
1362013
Bardet-Biedl syndrome-associated small GTPase ARL6 (BBS3) functions at or near the ciliary gate and modulates Wnt signaling
CJ Wiens, Y Tong, MA Esmail, E Oh, JM Gerdes, J Wang, W Tempel, ...
Journal of Biological Chemistry 285 (21), 16218-16230, 2010
1272010
Recurrent de novo mutations in PACS1 cause defective cranial-neural-crest migration and define a recognizable intellectual-disability syndrome
JHM Schuurs-Hoeijmakers, EC Oh, LELM Vissers, MEM Swinkels, ...
The American Journal of Human Genetics 91 (6), 1122-1127, 2012
1262012
El sistema no puede realizar la operación en estos momentos. Inténtalo de nuevo más tarde.
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