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Communications Biology|April 6, 2024
A multi-ancestry GWAS of Fuchs corneal dystrophy highlights the contributions of laminins, collagen, and endothelial cell regulationBryan R Gorman, Michael Francis, Cari L Nealon, et al.Ophthalmic Epidemiology|November 25, 2021
Development and Evaluation of a Rules-based Algorithm for Primary Open-Angle Glaucoma in the VA Million Veteran ProgramCari L Nealon, Christopher W Halladay, Tyler G Kinzy, et al.Cornea|May 12, 2023
Association Between Fuchs Endothelial Corneal Dystrophy, Diabetes Mellitus, and MultimorbidityCari L Nealon, Christopher W Halladay, Bryan R Gorman, et al.Ophthalmology|June 19, 2022
Glaucoma Genetic Risk Scores in the Million Veteran ProgramAndrea R Waksmunski, Tyler G Kinzy, Lauren A Cruz, et al.Medrxiv : the Preprint Server for Health Sciences|May 20, 2024
Rare genetic variation in VE-PTP is associated with central serous chorioretinopathy, venous dysfunction and glaucomaJoel T Rämö, Bryan Gorman, Lu-Chen Weng, et al.Journal of the American Medical Informatics Association : JAMIA|August 19, 2024
Development of electronic health record based algorithms to identify individuals with diabetic retinopathyJoseph H Breeyear, Sabrina L Mitchell, Cari L Nealon, et al.Medrxiv : the Preprint Server for Health Sciences|November 28, 2023
Development of Portable Electronic Health Record Based Algorithms to Identify Individuals with Diabetic RetinopathyJoseph H Breeyear, Sabrina L Mitchell, Cari L Nealon, et al.Ophthalmology Science|June 8, 2026
A Primary Open-Angle Glaucoma Locus Near Transcription Factor PRRX1 Identified in the Million Veteran ProgramTyler G Kinzy, Osahon J Asowata, Lauren A Cruz, et al.Nature Communications|May 3, 2025
Rare genetic variation in PTPRB is associated with central serous chorioretinopathy, varicose veins and glaucomaJoel T Rämö, Bryan R Gorman, Lu-Chen Weng, et al.Nature Medicine|June 25, 2024
Adaptive selection at G6PD and disparities in diabetes complicationsJoseph H Breeyear, Jacklyn N Hellwege, Philip H Schroeder, et al.Pageof 4