| Year |
Citation |
Score |
| 2023 |
Ku CA, Wei LW, Sieving PA. X-Linked Retinoschisis. Cold Spring Harbor Perspectives in Medicine. PMID 36690462 DOI: 10.1101/cshperspect.a041288 |
0.355 |
|
| 2021 |
Igelman AD, Ku C, da Palma MM, Georgiou M, Schiff ER, Lam BL, Sankila EM, Ahn J, Pyers L, Vincent A, Ferraz Sallum JM, Zein WM, Oh JK, Maldonado RS, Ryu J, et al. Expanding the clinical phenotype in patients with disease causing variants associated with atypical Usher syndrome. Ophthalmic Genetics. 1-10. PMID 34223797 DOI: 10.1080/13816810.2021.1946704 |
0.343 |
|
| 2020 |
Ku CA, Pennesi ME. The new landscape of retinal gene therapy. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. PMID 32888388 DOI: 10.1002/ajmg.c.31842 |
0.404 |
|
| 2017 |
Ku CA, Hull S, Arno G, Vincent A, Carss K, Kayton R, Weeks D, Anderson GW, Geraets R, Parker C, Pearce DA, Michaelides M, MacLaren RE, Robson AG, Holder GE, et al. Detailed Clinical Phenotype and Molecular Genetic Findings in CLN3-Associated Isolated Retinal Degeneration. Jama Ophthalmology. PMID 28542676 DOI: 10.1001/Jamaophthalmol.2017.1401 |
0.413 |
|
| 2015 |
Ku CA, Pennesi ME. Retinal Gene Therapy: Current Progress and Future Prospects. Expert Review of Ophthalmology. 10: 281-299. PMID 26609316 DOI: 10.1586/17469899.2015.1035711 |
0.444 |
|
| 2015 |
Ku CA, Chiodo VA, Boye SL, Hayes A, Goldberg AF, Hauswirth WW, Ramamurthy V. Viral-mediated vision rescue of a novel AIPL1 cone-rod dystrophy model. Human Molecular Genetics. 24: 670-84. PMID 25274777 DOI: 10.1093/Hmg/Ddu487 |
0.435 |
|
| 2011 |
Ku CA, Chiodo VA, Boye SL, Goldberg AF, Li T, Hauswirth WW, Ramamurthy V. Gene therapy using self-complementary Y733F capsid mutant AAV2/8 restores vision in a model of early onset Leber congenital amaurosis. Human Molecular Genetics. 20: 4569-81. PMID 21880665 DOI: 10.1093/Hmg/Ddr391 |
0.463 |
|
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