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Lea Diann Bennett

TitleProf,Asst
InstitutionUniversity of Oklahoma Health Sciences Center
DepartmentOphthalmology
AddressDMEI 400
608 Stanton L Young Blvd
Oklahoma City OK 73104
Phone405/271-8316
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    Collapse Research 
    Collapse research activities and funding
    R00EY027460     (BENNETT, LEA D)Sep 30, 2018 - May 31, 2021
    NIH
    Genotype phenotype associations in inherited retinal degeneration
    Role: Principal Investigator
    K99EY027460     (BENNETT, LEA D)Mar 1, 2017 - Feb 28, 2019
    NIH
    Rod photoreceptor function in retinitis pigmentosa
    Role: Principal Investigator

    Collapse Bibliographic 
    Collapse selected publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Lynn J, Raney A, Britton N, Ramoin J, Yang RW, Radojevic B, McClard CK, Kingsley R, Coussa RG, Bennett LD. Genetic Diagnosis for 64 Patients with Inherited Retinal Disease. Genes (Basel). 2022 Dec 26; 14(1). PMID: 36672815.
      Citations: 1     Fields:    Translation:Humans
    2. Conley SM, McClard CK, Mwoyosvi ML, Alkadhem N, Radojevic B, Klein M, Birch D, Ellis A, Icks SW, Guddanti T, Bennett LD. Delineating the Clinical Phenotype of Patients With the c.629C>G, p.Pro210Arg Mutation in Peripherin-2. Invest Ophthalmol Vis Sci. 2022 07 08; 63(8):19. PMID: 35861669.
      Citations: 1     Fields:    Translation:Humans
    3. Radojevic B, Conley SM, Bennett LD. Adherent but Not Suspension-Cultured Embryoid Bodies Develop into Laminated Retinal Organoids. J Dev Biol. 2021 Sep 10; 9(3). PMID: 34564087.
      Citations: 2     
    4. Mauro-Herrera M, Chiang J, Radojevic B, Bennett LD. Functional Evaluation of Splicing for Variants of Uncertain Significance in Patients with Inherited Retinal Diseases. Genes (Basel). 2021 06 29; 12(7). PMID: 34209753.
      Citations: 1     Fields:    Translation:HumansAnimalsCells
    5. Radojevic B, Jones K, Klein M, Mauro-Herrera M, Kingsley R, Birch DG, Bennett LD. Variable expressivity in patients with autosomal recessive retinitis pigmentosa associated with the gene CNGB1. Ophthalmic Genet. 2021 02; 42(1):15-22. PMID: 33465333.
      Citations: 6     Fields:    Translation:Humans
    6. Bennett LD, Klein M, John FT, Radojevic B, Jones K, Birch DG. Disease Progression in Patients with Autosomal Dominant Retinitis Pigmentosa due to a Mutation in Inosine Monophosphate Dehydrogenase 1 (IMPDH1). Transl Vis Sci Technol. 2020 04; 9(5):14. PMID: 32821486.
      Citations: 5     Fields:    Translation:Humans
    7. Bennett LD, Metz G, Klein M, Locke KG, Khwaja A, Birch DG. Regional Variations and Intra-/Intersession Repeatability for Scotopic Sensitivity in Normal Controls and Patients With Inherited Retinal Degenerations. Invest Ophthalmol Vis Sci. 2019 03 01; 60(4):1122-1131. PMID: 30901388.
      Citations: 11     Fields:    Translation:Humans
    8. Pennesi ME, Birch DG, Jayasundera KT, Parker M, Tan O, Gurses-Ozden R, Reichley C, Beasley KN, Yang P, Weleber RG, Bennett LD, Heckenlively JR, Kothapalli K, Chulay JD. Prospective Evaluation of Patients With X-Linked Retinoschisis During 18 Months. Invest Ophthalmol Vis Sci. 2018 12 03; 59(15):5941-5956. PMID: 30551202.
      Citations: 18     Fields:    Translation:Humans
    9. Bennett LD, Klein M, Locke KG, Kiser K, Birch DG. Dark-Adapted Chromatic Perimetry for Measuring Rod Visual Fields in Patients with Retinitis Pigmentosa. Transl Vis Sci Technol. 2017 Jul; 6(4):15. PMID: 28798898.
      Citations: 22     Fields:    
    10. Carr BC, Emigh CE, Bennett LD, Pansick AD, Birch DG, Nguyen C. TOWARDS A TREATMENT FOR DIABETIC RETINOPATHY: Intravitreal Toxicity and Preclinical Safety Evaluation of Inducible Nitric Oxide Synthase Inhibitors. Retina. 2017 Jan; 37(1):22-31. PMID: 27380429.
      Citations: 4     Fields:    Translation:Animals
    11. Birch DG, Bennett LD, Duncan JL, Weleber RG, Pennesi ME. Long-term Follow-up of Patients With Retinitis Pigmentosa Receiving Intraocular Ciliary Neurotrophic Factor Implants. Am J Ophthalmol. 2016 Oct; 170:10-14. PMID: 27457255.
      Citations: 51     Fields:    Translation:HumansCTClinical Trials
    12. Bennett LD, Wang YZ, Klein M, Pennesi ME, Jayasundera T, Birch DG. Structure/Psychophysical Relationships in X-Linked Retinoschisis. Invest Ophthalmol Vis Sci. 2016 Feb; 57(2):332-7. PMID: 26830370.
      Citations: 14     Fields:    Translation:HumansCells
    13. Bennett LD, Anderson RE. Current Progress in Deciphering Importance of VLC-PUFA in the Retina. Adv Exp Med Biol. 2016; 854:145-51. PMID: 26427405.
      Citations: 6     Fields:    Translation:HumansAnimals
    14. Bennett LD, Hopiavuori BR, Brush RS, Chan M, Van Hook MJ, Thoreson WB, Anderson RE. Examination of VLC-PUFA-deficient photoreceptor terminals. Invest Ophthalmol Vis Sci. 2014 Apr 24; 55(7):4063-72. PMID: 24764063.
      Citations: 17     Fields:    Translation:AnimalsCells
    15. Bennett LD, Brush RS, Chan M, Lydic TA, Reese K, Reid GE, Busik JV, Elliott MH, Anderson RE. Effect of reduced retinal VLC-PUFA on rod and cone photoreceptors. Invest Ophthalmol Vis Sci. 2014 Apr 10; 55(5):3150-7. PMID: 24722693.
      Citations: 26     Fields:    Translation:AnimalsCells
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