Kari E Branham
Clinical Associate Professor of Ophthalmology and Visual Sciences
Clinical Associate Professor of Human Genetics and Program Assistant
Human Genetics
[email protected]

Available to mentor
Kari E Branham
Clinical Associate Professor
  • Recent Publications
    • Recent Publications See All Publications
    • Journal Article
      Whole genome sequencing of 4,787 individuals identifies gene-based rare variants in age-related macular degeneration.
      Kwong A, Zawistowski M, Fritsche LG, Zhan X, Bragg-Gresham J, Branham KE, Advani J, Othman M, Ratnapriya R, Teslovich TM, Stambolian D, Chew EY, Abecasis GR, Swaroop A. Hum Mol Genet, 2024 Feb 1; 33 (4): 374 - 385. DOI:10.1093/hmg/ddad189
      PMID: 37934784
    • Journal Article
      Clinical sequencing of the retinitis pigmentosa gene RPGR in over 1,000 cases of vision loss.
      Pantrangi M, Rath J, Kaetterhenry N, Branham K, Talsness D, Weber JL. Mol Vis, 2024 30: 49 - 57.
      PMID: 38586605
    • Journal Article
      Readability, Content, and Accountability Assessment of Online Health Information for Retinitis Pigmentosa & Retinitis Pigmentosa Treatment Options.
      Partin S, Westfall E, Sanda G, Branham K, Muir K, Bellcross C, Jain N. Ophthalmic Genet, 2023 Feb; 44 (1): 43 - 48. DOI:10.1080/13816810.2022.2135113
      PMID: 36239593
    • Journal Article
      Clinical and imaging findings of choroideremia in a pediatric patient due to a novel frameshift mutation.
      Moussa MT, Scoles D, Branham K, Fahim AT, Capone A. Am J Ophthalmol Case Rep, 2022 Dec; 28: 101718 DOI:10.1016/j.ajoc.2022.101718
      PMID: 36247208
    • Journal Article
      Automated Segmentation of Autofluorescence Lesions in Stargardt Disease.
      Zhao PY, Branham K, Schlegel D, Fahim AT, Jayasundera KT. Ophthalmol Retina, 2022 Nov; 6 (11): 1098 - 1104. DOI:10.1016/j.oret.2022.05.020
      PMID: 35644472
    • Journal Article
      Real-world outcomes of voretigene neparvovec treatment in pediatric patients with RPE65-associated Leber congenital amaurosis.
      Deng C, Zhao PY, Branham K, Schlegel D, Fahim AT, Jayasundera TK, Khan N, Besirli CG. Graefes Arch Clin Exp Ophthalmol, 2022 May; 260 (5): 1543 - 1550. DOI:10.1007/s00417-021-05508-2
      PMID: 35001204
    • Journal Article
      Automated Segmentation of Autofluorescence Lesions in Stargardt Disease.
      Zhao PY, Branham K, Schlegel D, Fahim AT, Jayasundera KT. Ophthalmology. Retina, 2022 Jan 26;
    • Journal Article
      Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia.
      Solaki M, Baumann B, Reuter P, Andreasson S, Audo I, Ayuso C, Balousha G, Benedicenti F, Birch D, Bitoun P, Blain D, Bocquet B, Branham K, Català-Mora J, De Baere E, Dollfus H, Falana M, Giorda R, Golovleva I, Gottlob I, Heckenlively JR, Jacobson SG, Jones K, Jägle H, Janecke AR, Kellner U, Liskova P, Lorenz B, Martorell-Sampol L, Messias A, Meunier I, Belga Ottoni Porto F, Papageorgiou E, Plomp AS, de Ravel TJL, Reiff CM, Renner AB, Rosenberg T, Rudolph G, Salati R, Sener EC, Sieving PA, Stanzial F, Traboulsi EI, Tsang SH, Varsanyi B, Weleber RG, Zobor D, Stingl K, Wissinger B, Kohl S. Hum Mutat, 2022 Jul; 43 (7): 832 - 858. DOI:10.1002/humu.24371
      PMID: 35332618