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| Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes JK White, AK Gerdin, NA Karp, E Ryder, M Buljan, JN Bussell, J Salisbury, ... Cell 154 (2), 452-464, 2013 | 405 | 2013 |
| Unexpected mutations after CRISPR–Cas9 editing in vivo KA Schaefer, WH Wu, DF Colgan, SH Tsang, AG Bassuk, VB Mahajan Nature methods 14 (6), 547-548, 2017 | 366 | 2017 |
| A drosophila genetic resource of mutants to study mechanisms underlying human genetic diseases S Yamamoto, M Jaiswal, WL Charng, T Gambin, E Karaca, G Mirzaa, ... Cell 159 (1), 200-214, 2014 | 286 | 2014 |
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| Long-term safety and efficacy of human-induced pluripotent stem cell (iPS) grafts in a preclinical model of retinitis pigmentosa Y Li, YT Tsai, CW Hsu, D Erol, J Yang, WH Wu, RJ Davis, D Egli, ... Molecular medicine 18 (9), 1312-1319, 2012 | 174 | 2012 |
| Precision medicine: genetic repair of retinitis pigmentosa in patient-derived stem cells AG Bassuk, A Zheng, Y Li, SH Tsang, VB Mahajan Scientific reports 6 (1), 1-6, 2016 | 160 | 2016 |
| Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia S Kohl, D Zobor, WC Chiang, N Weisschuh, J Staller, IG Menendez, ... Nature genetics 47 (7), 757-765, 2015 | 158 | 2015 |
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| Quantitative fundus autofluorescence in recessive Stargardt disease TR Burke, T Duncker, RL Woods, JP Greenberg, J Zernant, SH Tsang, ... Investigative ophthalmology & visual science 55 (5), 2841-2852, 2014 | 137 | 2014 |
| A comparison of fundus autofluorescence and retinal structure in patients with Stargardt disease NL Gomes, VC Greenstein, JN Carlson, SH Tsang, RT Smith, RE Carr, ... Investigative ophthalmology & visual science 50 (8), 3953-3959, 2009 | 133 | 2009 |
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| Structural assessment of hyperautofluorescent ring in patients with retinitis pigmentosa LH Lima, W Cella, VC Greenstein, NK Wang, M Busuioc, RT Smith, ... Retina (Philadelphia, Pa.) 29 (7), 1025, 2009 | 97 | 2009 |
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