Dr. John Fingert, MD

• Ophthalmology

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• Yorkshire Co Hospital

  2006

• Molecular Ophthalmology Fellowship, University Of Iowa, Carver College Of Medicine, Department Of Ophthalmology And Visual Sciences

  Fellowship Hospital, 2006

• Youngstown General Hospital

  Residency Hospital, 2004

• St Lukes Aurora Med

  Internship Hospital, 2001

• University Of Iowa Carver College Of Medicine

  Medical School, 2000

• Youngstown Hospital Assn|luth Medical Center

  Undergraduate School, 1992

• Dartmouth College

  Undergraduate School, 1991

• LystMutation in Mice Recapitulates Iris Defects of Human Exfoliation Syndrome, 2008-11-21

• Statistical tests for detecting rare variants using variance-stabilizing transformations, 2012-06-25

• Progressive optic disc cupping over 20 years in a patient withTBK1-associated glaucoma, 2019-11-16

• Novel Intragenic PAX6 Deletion in a Pedigree with Aniridia, Morbid Obesity, and Diabetes, 2019-08-14

• Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy, 2017-03-30

• Genetic correlations between diabetes and glaucoma: an analysis of continuous and dichotomous phenotypes, 2019-05-20

• A common variant mapping toCACNA1Ais associated with susceptibility to Exfoliation syndrome, 2015-02-23

• Evaluation of variants in the selectin genes in age-related macular degeneration, 2011-04-26

• Genomic organization ofTBK1copy number variations in glaucoma patients, 2017-09-20

• Chromosome 7q31 POAG locus: ocular expression of caveolins and lack of association with POAG in a US cohort, 2011-02-08

• CRISPR-CAS9 GENOME ENGINEERING: TREATING INHERITED RETINAL DEGENERATION, 2018-03-22

• Genetic association study of exfoliation syndrome identifies a protective rare variant atLOXL1and five new susceptibility loci, 2017-05-29

• Heterozygous triplication of upstream regulatory sequences leads to dysregulation of matrix metalloproteinase 19 (MMP19) in patients with cavitary optic disc anomaly (CODA), 2015-09-16

• Update on Animal Models of Exfoliation Syndrome, 2018-06-01

• Animal models of exfoliation syndrome, now and future, 2015-03-25

• Identification of Proteins that Interact with TANK Binding Kinase 1 and Testing for Mutations Associated with Glaucoma, 2013-01-03

• The Heritability of Pigment Dispersion Syndrome and Pigmentary Glaucoma, 2019-02-21

• Cell-Matrix Interactions in the Eye: From Cornea to Choroid, 2021-03-20

• Mutations that are a common cause of Leber congenital amaurosis in northern America are rare in Southern India, 2009-09-04

• Automated Axon Counting in Rodent Optic Nerve Sections with AxonJ, 2016-05-26

• CLINICAL AND GENETIC CHARACTERIZATION OF A LARGE PRIMARY OPEN ANGLE GLAUCOMA PEDIGREE, 2016-06-29

• Duplication of TBK1 Stimulates Autophagy in iPSC-derived Retinal Cells from a Patient with Normal Tension Glaucoma, 2014-01-25

• Automated Segmentation of Choroidal Layers from 3-Dimensional Macular Optical Coherence Tomography Scans, 2021-06-19

• A Genome-Wide Association Study for Primary Open Angle Glaucoma and Macular Degeneration Reveals Novel Loci, 2013-03-11

• Nanophthalmos patient with a THR518MET mutation inMYRF, a case report, 2020-10-01

• Genome-wide analysis of copy number variants in age-related macular degeneration, 2010-10-28

• Calpain-5 Mutations Cause Autoimmune Uveitis, Retinal Neovascularization, and Photoreceptor Degeneration, 2012-10-04

• TBK1gene duplication and normal-tension glaucoma, 2015-02-13

• Confirmation ofTBK1duplication in normal tension glaucoma, 2012-01-02

• Clinical and genetic characterization of a Danish family with North Carolina macular dystrophy, 2010-12-09

• Long-Term Follow-Up of Normal Tension Glaucoma Patients WithTBK1Gene Mutations in One Large Pedigree, 2020-01-24

• TBK1and Flanking Genes in Human Retina, 2013-02-20

• SQSTM1 Mutations and Glaucoma, 2016-06-08

• North Carolina Macular Dystrophy is caused by dysregulation of the retinal transcription factor PRDM13, 2015-10-24

• Assessment of SNPs associated with the human glucocorticoid receptor in primary open-angle glaucoma and steroid responders, 2010-04-03

• Circumferential iris trans-illumination defects in exfoliation syndrome, 2012-04-30

• Histochemical Analysis of Glaucoma Caused by a Myocilin Mutation in a Human Donor Eye, 2018-08-17

• Genome-wide association analysis identifiesTXNRD2, ATXN2andFOXC1as susceptibility loci for primary open angle glaucoma, 2016-01-11

• Mendelian Genes in Primary Open Angle Glaucoma, 2019-06-22

• Progressive optic nerve changes in cavitary optic disc anomaly: integration of copy number alteration and cis-expression quantitative trait loci to assess disease etiology, 2019-04-27

• Glaucoma Risk Alleles in the Ocular Hypertension Treatment Study (OHTS), 2016-10-01

• Evaluation of sFLT1 Protein Levels in Human Eyes with theFLT1rs9943922 Polymorphism, 2017-09-26

• Exome-based investigation of the genetic basis of human pigmentary glaucoma, 2021-06-26