Kimberly Neely, MD, PhD

    • 280 Citations
    • 10 h-Index
    1988 …2019
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    Fingerprint Dive into the research topics where Kimberly Neely is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

    • 4 Similar Profiles
    Macular Degeneration Medicine & Life Sciences
    Vitreous Hemorrhage Medicine & Life Sciences
    Retinoschisis Medicine & Life Sciences
    Cryotherapy Medicine & Life Sciences
    Eye Diseases Medicine & Life Sciences
    Optic Disk Medicine & Life Sciences
    Cats Medicine & Life Sciences
    Geographic Atrophy Medicine & Life Sciences

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    Research Output 1988 2019

    • 280 Citations
    • 10 h-Index
    • 14 Article
    • 3 Letter
    • 1 Comment/debate
    Congenital Disorders of Glycosylation
    Cataract
    Pediatrics
    Pathology
    Optic Atrophy
    1 Citation (Scopus)

    Natural History of Drusenoid Pigment Epithelial Detachment Associated with Age-Related Macular Degeneration: Age-Related Eye Disease Study 2 Report No. 17

    Age-Related Eye Disease Study 2 Research Group, Feb 2019, In : Ophthalmology. 126, 2, p. 261-273 13 p.

    Research output: Contribution to journalArticle

    Eye Diseases
    Macular Degeneration
    Natural History
    Confidence Intervals
    Visual Acuity
    8 Citations (Scopus)

    Progression of Geographic Atrophy in Age-related Macular Degeneration: AREDS2 Report Number 16

    AREDS2 Research Group, Dec 2018, In : Ophthalmology. 125, 12, p. 1913-1928 16 p.

    Research output: Contribution to journalArticle

    Geographic Atrophy
    Eye Diseases
    Macular Degeneration
    12 Citations (Scopus)

    Retinal Dystrophy with Intraretinal Cystoid Spaces Associated with Mutations in the Crumbs Homologue (CRB1) Gene

    Cordovez, J. A., Traboulsi, E. I., Capasso, J. E., Sadagopan, K. A., Ganesh, A., Rychwalski, P. J., Neely, K. A., Brodie, S. E. & Levin, A. V., Jul 3 2015, In : Ophthalmic Genetics. 36, 3, p. 257-264 8 p.

    Research output: Contribution to journalArticle

    Retinal Dystrophies
    Carbonic Anhydrase Inhibitors
    Mutation
    Genes
    Visual Acuity
    8 Citations (Scopus)

    X-linked retinoschisis: Novel mutation in the initiation codon of the xlrs1 gene in a large family

    Kim, D. Y., Neely, K., Sassani, J., Vrabec, T. R., Tantri, A., Frost, A. & Donoso, L. A., Oct 1 2006, In : Retina. 26, 8, p. 940-946 7 p.

    Research output: Contribution to journalArticle

    Retinoschisis
    Initiator Codon
    Point Mutation
    Mutation
    Genes