Lea Bennett to Humans
This is a "connection" page, showing publications Lea Bennett has written about Humans.
Connection Strength
0.339
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Expanding the Mutation Spectrum for Inherited Retinal Diseases. Genes (Basel). 2024 Dec 28; 16(1).
Score: 0.055
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Delineating the Clinical Phenotype of Patients With the c.629C>G, p.Pro210Arg Mutation in Peripherin-2. Invest Ophthalmol Vis Sci. 2022 07 08; 63(8):19.
Score: 0.047
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Functional Evaluation of Splicing for Variants of Uncertain Significance in Patients with Inherited Retinal Diseases. Genes (Basel). 2021 06 29; 12(7).
Score: 0.043
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Variable expressivity in patients with autosomal recessive retinitis pigmentosa associated with the gene CNGB1. Ophthalmic Genet. 2021 02; 42(1):15-22.
Score: 0.041
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Disease Progression in Patients with Autosomal Dominant Retinitis Pigmentosa due to a Mutation in Inosine Monophosphate Dehydrogenase 1 (IMPDH1). Transl Vis Sci Technol. 2020 04; 9(5):14.
Score: 0.040
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Regional Variations and Intra-/Intersession Repeatability for Scotopic Sensitivity in Normal Controls and Patients With Inherited Retinal Degenerations. Invest Ophthalmol Vis Sci. 2019 03 01; 60(4):1122-1131.
Score: 0.037
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Structure/Psychophysical Relationships in X-Linked Retinoschisis. Invest Ophthalmol Vis Sci. 2016 Feb; 57(2):332-7.
Score: 0.030
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Current Progress in Deciphering Importance of VLC-PUFA in the Retina. Adv Exp Med Biol. 2016; 854:145-51.
Score: 0.030
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Prospective Evaluation of Patients With X-Linked Retinoschisis During 18 Months. Invest Ophthalmol Vis Sci. 2018 12 03; 59(15):5941-5956.
Score: 0.009
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Long-term Follow-up of Patients With Retinitis Pigmentosa Receiving Intraocular Ciliary Neurotrophic Factor Implants. Am J Ophthalmol. 2016 Oct; 170:10-14.
Score: 0.008