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Connection

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
  1. 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.
    View in: PubMed
    Score: 0.978
  2. Phenotypic and Genetic Spectrum of Autosomal Recessive Bestrophinopathy and Best Vitelliform Macular Dystrophy. Invest Ophthalmol Vis Sci. 2021 05 03; 62(6):22.
    View in: PubMed
    Score: 0.754
  3. Novel TMEM98, MFRP, PRSS56 variants in a large United States high hyperopia and nanophthalmos cohort. Sci Rep. 2020 11 17; 10(1):19986.
    View in: PubMed
    Score: 0.730
  4. 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.
    View in: PubMed
    Score: 0.720
  5. Seeing in Color: Inclusion and Characterization of Hereditary Eye Disease in African Americans. Transl Vis Sci Technol. 2024 Sep 03; 13(9):4.
    View in: PubMed
    Score: 0.237
  6. Characterization of the Spectrum of Ophthalmic Changes in Patients With Alagille Syndrome. Invest Ophthalmol Vis Sci. 2021 06 01; 62(7):27.
    View in: PubMed
    Score: 0.189
  7. Ocular genetics in the genomics age. Am J Med Genet C Semin Med Genet. 2020 09; 184(3):860-868.
    View in: PubMed
    Score: 0.180
  8. Ophthalmic genetics in South America. Am J Med Genet C Semin Med Genet. 2020 09; 184(3):753-761.
    View in: PubMed
    Score: 0.180

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