Robert Hufnagel to Eye Diseases, Hereditary
This is a "connection" page, showing publications Robert Hufnagel has written about Eye Diseases, Hereditary.
Connection Strength
3.969
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Genotype-Phenotype Spectrum of eyeGENE Patients With Familial Exudative Vitreoretinopathy: Novel Variants in Norrin/?-Catenin Signaling Pathway Genes. Invest Ophthalmol Vis Sci. 2025 Feb 03; 66(2):9.
Score: 0.978
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Phenotypic and Genetic Spectrum of Autosomal Recessive Bestrophinopathy and Best Vitelliform Macular Dystrophy. Invest Ophthalmol Vis Sci. 2021 05 03; 62(6):22.
Score: 0.754
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Novel TMEM98, MFRP, PRSS56 variants in a large United States high hyperopia and nanophthalmos cohort. Sci Rep. 2020 11 17; 10(1):19986.
Score: 0.730
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Genetic testing for inherited eye conditions in over 6,000 individuals through the eyeGENE network. Am J Med Genet C Semin Med Genet. 2020 09; 184(3):828-837.
Score: 0.720
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Seeing in Color: Inclusion and Characterization of Hereditary Eye Disease in African Americans. Transl Vis Sci Technol. 2024 Sep 03; 13(9):4.
Score: 0.237
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Characterization of the Spectrum of Ophthalmic Changes in Patients With Alagille Syndrome. Invest Ophthalmol Vis Sci. 2021 06 01; 62(7):27.
Score: 0.189
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Ocular genetics in the genomics age. Am J Med Genet C Semin Med Genet. 2020 09; 184(3):860-868.
Score: 0.180
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Ophthalmic genetics in South America. Am J Med Genet C Semin Med Genet. 2020 09; 184(3):753-761.
Score: 0.180