Samuel G. Jacobson, MD, PhD

faculty photo
Professor of Ophthalmology
Department: Ophthalmology

Contact information
Scheie Eye Institute
51 North 39th Street
Philadelphia, PA 19104
B.A. (Humanities)
University of Illinois, 1966.
M.D. (Medicine)
University of Illinois, 1970.
Ph.D. (Psychophysics)
University of London, 1977.
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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, Sep 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 Jul 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, Jul 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, Jul 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, Jun 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, Jun 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, May 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, Apr 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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Last updated: 07/27/2016
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