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1
Measures of Function and Structure to Determine Phenotypic Features, Natural History, and Treatment Outcomes in Inherited Retinal Diseases.
Annu Rev Vis Sci. 2021 Sep 15;7:747-772. doi: 10.1146/annurev-vision-032321-091738. Epub 2021 Jul 13.
3
Assessing Photoreceptor Status in Retinal Dystrophies: From High-Resolution Imaging to Functional Vision.
Am J Ophthalmol. 2021 Oct;230:12-47. doi: 10.1016/j.ajo.2021.04.013. Epub 2021 May 14.
5
Clinical Perspectives and Trends: Microperimetry as a Trial Endpoint in Retinal Disease.
Ophthalmologica. 2021;244(5):418-450. doi: 10.1159/000515148. Epub 2021 Feb 10.
6
The Michigan Vision-Related Anxiety Questionnaire: A Psychosocial Outcomes Measure for Inherited Retinal Degenerations.
Am J Ophthalmol. 2021 May;225:137-146. doi: 10.1016/j.ajo.2020.12.001. Epub 2020 Dec 9.
7
Advancing Clinical Trials for Inherited Retinal Diseases: Recommendations from the Second Monaciano Symposium.
Transl Vis Sci Technol. 2020 Jun 3;9(7):2. doi: 10.1167/tvst.9.7.2. eCollection 2020 Jun.
8
Progression of Stargardt Disease as Determined by Fundus Autofluorescence Over a 12-Month Period: ProgStar Report No. 11.
JAMA Ophthalmol. 2019 Oct 1;137(10):1134-1145. doi: 10.1001/jamaophthalmol.2019.2885.
9
Depicting brighter possibilities for treating blindness.
Sci Transl Med. 2019 May 29;11(494). doi: 10.1126/scitranslmed.aax2324.
10
A Workshop on Measuring the Progression of Atrophy Secondary to Stargardt Disease in the ProgStar Studies: Findings and Lessons Learned.
Transl Vis Sci Technol. 2019 Apr 12;8(2):16. doi: 10.1167/tvst.8.2.16. eCollection 2019 Apr.

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