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Greenwald, Scott H; Kuchenbecker, James A; Rowlan, Jessica S et al. (2017) Role of a Dual Splicing and Amino Acid Code in Myopia, Cone Dysfunction and Cone Dystrophy Associated with L/M Opsin Interchange Mutations. Transl Vis Sci Technol 6:2
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Davidoff, Candice; Neitz, Maureen; Neitz, Jay (2016) Genetic Testing as a New Standard for Clinical Diagnosis of Color Vision Deficiencies. Transl Vis Sci Technol 5:2
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Neitz, Maureen; Neitz, Jay (2014) Curing color blindness--mice and nonhuman primates. Cold Spring Harb Perspect Med 4:a017418
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Greenwald, Scott H; Kuchenbecker, James A; Roberson, Daniel K et al. (2014) S-opsin knockout mice with the endogenous M-opsin gene replaced by an L-opsin variant. Vis Neurosci 31:25-37
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