Research Output per year
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
Network
Recent external collaboration on country level. Dive into details by clicking on the dots.
Research Output 1988 2019
Congenital glycosylation disorder: a novel presentation of coexisting anterior and posterior segment pathology and its implications in pediatric cataract management
Etzel, J. D., Neely, K. & Ely, A., Jan 1 2019, In : Journal of AAPOS.Research output: Contribution to journal › Article
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 1 2019, In : Ophthalmology. 126, 2, p. 261-273 13 p.Research output: Contribution to journal › Article
Eye Diseases
Macular Degeneration
Natural History
Confidence Intervals
Visual Acuity
7
Citations
(Scopus)
Progression of Geographic Atrophy in Age-related Macular Degeneration: AREDS2 Report Number 16
AREDS2 Research Group, Dec 1 2018, In : Ophthalmology. 125, 12, p. 1913-1928 16 p.Research output: Contribution to journal › Article
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., Brodie, S. E. & Levin, A. V., Jul 3 2015, In : Ophthalmic Genetics. 36, 3, p. 257-264 8 p.Research output: Contribution to journal › Article
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 journal › Article
Retinoschisis
Initiator Codon
Point Mutation
Mutation
Genes