Selected Publications:
Matsui Rodrigo, McGuigan Iii David B, Gruzensky Michaela L, Aleman Tomas S, Schwartz Sharon B, Sumaroka Alexander, Koenekoop Robert K, Cideciyan Artur V, Jacobson Samuel G: SPATA7: Evolving phenotype from cone-rod dystrophy to retinitis pigmentosa. Ophthalmic genetics 37 (3): 333-8,2016.
Kong Xiangrong, Strauss Rupert W, Michaelides Michel, Cideciyan Artur V, Sahel José-Alain, Muñoz Beatriz, West Sheila, Scholl Hendrik P N: Visual Acuity Loss and Associated Risk Factors in the Retrospective Progression of Stargardt Disease Study (ProgStar Report No. 2). Ophthalmology : 2016.
Heon Elise, Alabduljalil Talal, Iii David B McGuigan, Cideciyan Artur V, Li Shuning, Chen Shiyi, Jacobson Samuel G: Visual Function and Central Retinal Structure in Choroideremia. Investigative ophthalmology & visual science 57 (9): OCT377-87,2016.
Sumaroka Alexander, Matsui Rodrigo, Cideciyan Artur V, McGuigan David B, Sheplock Rebecca, Schwartz Sharon B, Jacobson Samuel G: Outer Retinal Changes Including the Ellipsoid Zone Band in Usher Syndrome 1B due to MYO7A Mutations. Investigative ophthalmology & visual science 57 (9): OCT253-61,2016.
McGuigan David B, Roman Alejandro J, Cideciyan Artur V, Matsui Rodrigo, Gruzensky Michaela L, Sheplock Rebecca, Jacobson Samuel G: Automated Light- and Dark-Adapted Perimetry for Evaluating Retinitis Pigmentosa: Filling a Need to Accommodate Multicenter Clinical Trials. Investigative ophthalmology & visual science 57 (7): 3118-28,2016.
Cideciyan Artur V, Roman Alejandro J, Jacobson Samuel G, Yan Boyuan, Pascolini Michele, Charng Jason, Pajaro Simone, Nirenberg Sheila: Developing an Outcome Measure With High Luminance for Optogenetics Treatment of Severe Retinal Degenerations and for Gene Therapy of Cone Diseases. Investigative ophthalmology & visual science 57 (7): 3211-21,2016.
Vincent Ajoy, Audo Isabelle, Tavares Erika, Maynes Jason T, Tumber Anupreet, Wright Thomas, Li Shuning, Michiels Christelle, Condroyer Christel, MacDonald Heather, Verdet Robert, Sahel José-Alain, Hamel Christian P, Zeitz Christina, Héon Elise: Biallelic Mutations in GNB3 Cause a Unique Form of Autosomal-Recessive Congenital Stationary Night Blindness. American journal of human genetics 98 (5): 1011-9,2016.
Jacobson Samuel G, Matsui Rodrigo, Sumaroka Alexander, Cideciyan Artur V: Retinal Structure Measurements as Inclusion Criteria for Stem Cell-Based Therapies of Retinal Degenerations. Investigative ophthalmology & visual science 57 (5): ORSFn1-9,2016.
Jin Minghao, Li Songhua, Hu Jane, Jin Heather H, Jacobson Samuel G, Bok Dean: Functional Rescue of Retinal Degeneration-Associated Mutant RPE65 Proteins. Advances in experimental medicine and biology 854 : 525-32,2016.
Jacobson Samuel G, Cideciyan Artur V, Huang Wei Chieh, Sumaroka Alexander, Nam Hyun Ju, Sheplock Rebecca, Schwartz Sharon B: Leber Congenital Amaurosis: Genotypes and Retinal Structure Phenotypes. Advances in experimental medicine and biology 854 : 169-75,2016.
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