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Robert Hufnagel to Tomography, Optical Coherence

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This is a "connection" page, showing publications Robert Hufnagel has written about Tomography, Optical Coherence.
Robert Hufnagel
Connection Strength
1.576
Tomography, Optical Coherence
  1. Introduction to the special issue on Ophthalmic Genetics: Vision in 2020. Am J Med Genet C Semin Med Genet. 2020 09; 184(3):535-537.
    View in: PubMed
    Score: 0.737
  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: 0.193
  3. Biallelic Loss-of-Function Variants in UBAP1L and Nonsyndromic Retinal Dystrophies. JAMA Ophthalmol. 2024 Nov 01; 142(11):1081-1086.
    View in: PubMed
    Score: 0.062
  4. A Spontaneous Nonhuman Primate Model of Myopic Foveoschisis. Invest Ophthalmol Vis Sci. 2023 Jan 03; 64(1):18.
    View in: PubMed
    Score: 0.054
  5. Ophthalmic Manifestations of ROSAH (Retinal Dystrophy, Optic Nerve Edema, Splenomegaly, Anhidrosis, and Headache) Syndrome, an Inherited NF ?B-Mediated Autoinflammatory Disease with Retinal Dystrophy. Ophthalmology. 2023 04; 130(4):423-432.
    View in: PubMed
    Score: 0.054
  6. Baseline Microperimetry and OCT in the RUSH2A Study: Structure-Function Association and Correlation With Disease Severity. Am J Ophthalmol. 2022 12; 244:98-116.
    View in: PubMed
    Score: 0.053
  7. Long-Term Anatomic and Visual Outcomes of Planned Preterm Delivery and Treatment of Norrie Disease. Ophthalmic Surg Lasers Imaging Retina. 2022 08; 53(8):464-467.
    View in: PubMed
    Score: 0.053
  8. Photoreceptor and Retinal Pigment Epithelium Relationships in Eyes With Vitelliform Macular Dystrophy Revealed by Multimodal Adaptive Optics Imaging. Invest Ophthalmol Vis Sci. 2022 07 08; 63(8):27.
    View in: PubMed
    Score: 0.052
  9. Novel ophthalmic findings and deep phenotyping in Williams-Beuren syndrome. Br J Ophthalmol. 2023 10; 107(10):1554-1559.
    View in: PubMed
    Score: 0.052
  10. Photoreceptor degeneration in ABCA4-associated retinopathy and its genetic correlates. JCI Insight. 2022 01 25; 7(2).
    View in: PubMed
    Score: 0.051
  11. 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: 0.049
  12. Retinoschisis associated with Kearns-Sayre syndrome. Ophthalmic Genet. 2020 10; 41(5):497-500.
    View in: PubMed
    Score: 0.046
  13. Homozygous Variant in ARL3 Causes Autosomal Recessive Cone Rod Dystrophy. Invest Ophthalmol Vis Sci. 2019 11 01; 60(14):4811-4819.
    View in: PubMed
    Score: 0.044
  14. DICER1 Syndrome: Characterization of the Ocular Phenotype in a Family-Based Cohort Study. Ophthalmology. 2019 02; 126(2):296-304.
    View in: PubMed
    Score: 0.040
  15. Benign Yellow Dot Maculopathy: A New Macular Phenotype. Ophthalmology. 2017 07; 124(7):1004-1013.
    View in: PubMed
    Score: 0.036

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