Cristy A. Ku

Detailed Clinical Phenotype and Molecular Genetic Findings in <i>CLN3</i>-Associated Isolated Retinal Degeneration

Cristy A. Ku, Sarah Hull, Gavin Arno et al. · JAMA Ophthalmology · 2017 · 76 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Molecular and Clinical Findings in Patients With Knobloch Syndrome

Sarah Hull, Gavin Arno, Cristy A. Ku et al. · JAMA Ophthalmology · 2016 · 66 citations · Full text

Medicine, Molecular Genetics, Ophthalmology +17

Three‐Year Safety Results of SAR422459 (EIAV‐ABCA4) Gene Therapy in Patients With ABCA4‐Associated Stargardt Disease: An Open‐Label Dose‐Escalation Phase I/IIa Clinical Trial, Cohorts 1‐5

Maria A. Parker, Laura Erker, Isabelle Audo et al. · American Journal of Ophthalmology · 2022 · 56 citations · Full text

Medicine, Ophthalmology, Optometry +15

Specific Alleles of <i>CLN7</i> / <i>MFSD8</i> , a Protein That Localizes to Photoreceptor Synaptic Terminals, Cause a Spectrum of Nonsyndromic Retinal Dystrophy

Kamron N. Khan, Mohammed E. El‐Asrag, Cristy A. Ku et al. · Investigative Ophthalmology & Visual Science · 2017 · 52 citations · Full text

Medicine, Genetics, Ophthalmology +17

Gene therapy using self-complementary Y733F capsid mutant AAV2/8 restores vision in a model of early onset Leber congenital amaurosis

Cristy A. Ku, Vince A. Chiodo, Sanford L. Boye et al. · Human Molecular Genetics · 2011 · 45 citations · Full text

Medicine, Genetics, Ophthalmology +15