J
John H. Fingert
Researcher at University of Iowa
Publications - 171
Citations - 14975
John H. Fingert is an academic researcher from University of Iowa. The author has contributed to research in topics: Glaucoma & Myocilin. The author has an hindex of 47, co-authored 165 publications receiving 13442 citations. Previous affiliations of John H. Fingert include University of Arkansas for Medical Sciences & University of Iowa Hospitals and Clinics.
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Journal ArticleDOI
Aqueous Misdirection After Trabeculectomy in a Down Syndrome Patient With Angle-closure Glaucoma.
TL;DR: The first case of aqueous misdirection in a patient with Down syndrome after trabeculectomy is reported, and awareness of this risk may aid surgical planning and postoperative management.
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Long-Term Follow-Up of Normal Tension Glaucoma Patients With TBK1 Gene Mutations in One Large Pedigree.
TL;DR: The first report of the clinical features and long-term clinical course in a family of NTG patients withTBK1 gene duplications is provided, suggesting that it may be advantageous to set extremely low IOP targets for some patients with TBK1-associated glaucoma.
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Assessment of a three-generation pedigree with Fuchs endothelial corneal dystrophy with anticipation for expansion of the triplet repeat in the TCF4 gene.
Mark A. Greiner,Daniel C. Terveen,Jesse M. Vislisel,Ben R. Roos,Ben R. Roos,John H. Fingert,John H. Fingert +6 more
TL;DR: Assessment of a three-generation pedigree with Fuchs endothelial corneal dystrophy with anticipation for expansion of the triplet repeat in the TCF4 gene.
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Progressive optic nerve changes in cavitary optic disc anomaly: integration of copy number alteration and cis-expression quantitative trait loci to assess disease etiology
Eileen S. Hwang,Denise J. Morgan,Katie L. Pennington,Leah A. Owen,John H. Fingert,Paul S. Bernstein,Margaret M. DeAngelis +6 more
TL;DR: Clinical and genetic data indicate that in CODA, the excavated optic nerve appearance may develop after birth and into adulthood, and eQTL analysis demonstrated that this CNA region regulates expression of up to 4 genes in cis.
Journal ArticleDOI
A novel mutation (LEU396ARG) in OPA1 is associated with a severe phenotype in a large dominant optic atrophy pedigree
Michael J. Schnieders,Wesley A. Goar,M Griess,Ben R. Roos,Ben R. Roos,Todd E. Scheetz,Todd E. Scheetz,Edwin M. Stone,Edwin M. Stone,John H. Fingert,John H. Fingert +10 more
TL;DR: A novel mutation (LEU396ARG) in OPA1 is associated with a severe phenotype in a large dominant optic atrophy pedigree.