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JOHN FINGERT, MD
MD
Ophthalmology Physician
NPI: 1306847454IndividualAccepts Medicare
Specialties, Licenses & Credentials
Ophthalmology PhysicianPrimary
Ophthalmology
Code: 207W00000X
35581(IA)
CMS Specialties
PrimaryOPHTHALMOLOGY
Education
UNIVERSITY OF IOWA, RJ & L CARVER COLLEGE OF MEDICINE
Class of 2000
Research & Publications (20)
Association of a novel mutation in the retinol dehydrogenase 12 (RDH12) gene with autosomal dominant retinitis pigmentosa.
PMID 18779497·Arch Ophthalmol·2008
8-other
Mitochondrial variant G4132A is associated with familial non-arteritic anterior ischemic optic neuropathy in one large pedigree.
PMID 17454741·Ophthalmic Genet·2007
8-other
Familial cavitary optic disk anomalies: identification of a novel genetic locus.
PMID 17368552·Am J Ophthalmol·2007
8-other
The C677T variant in the methylenetetrahydrofolate reductase gene is not associated with disease in cohorts of pseudoexfoliation glaucoma and primary open-angle glaucoma patients from Iowa.
PMID 16754204·Ophthalmic Genet·2006
8-other
Evaluation of the myocilin (MYOC) glaucoma gene in monkey and human steroid-induced ocular hypertension.
PMID 11133859·Invest Ophthalmol Vis Sci·2001
4-observational
Lyst mutation in mice recapitulates iris defects of human exfoliation syndrome.
PMID 19029039·Invest Ophthalmol Vis Sci·2009
7-preclinical
Familial non-arteritic anterior ischemic optic neuropathy.
PMID 18587597·Graefes Arch Clin Exp Ophthalmol·2008
8-other
Mutation in the SLC4A11 gene associated with autosomal recessive congenital hereditary endothelial dystrophy in a large Saudi family.
PMID 18363173·Ophthalmic Genet·2008
8-other
Evidence for a novel x-linked modifier locus for leber hereditary optic neuropathy.
PMID 18363168·Ophthalmic Genet·2008
8-other
Increased expression of the WNT antagonist sFRP-1 in glaucoma elevates intraocular pressure.
PMID 18274669·J Clin Invest·2008
7-preclinical
Increased expression of serum amyloid A in glaucoma and its effect on intraocular pressure.
PMID 18223246·Invest Ophthalmol Vis Sci·2008
8-other
LOXL1 mutations are associated with exfoliation syndrome in patients from the midwestern United States.
PMID 18036875·Am J Ophthalmol·2007
8-other
Heritable features of the optic disc: a novel twin method for determining genetic significance.
PMID 17525172·Invest Ophthalmol Vis Sci·2007
4-observational
Automated segmentation of the optic disc from stereo color photographs using physiologically plausible features.
PMID 17389498·Invest Ophthalmol Vis Sci·2007
4-observational
Familial cavitary optic disk anomalies: clinical features of a large family with examples of progressive optic nerve head cupping.
PMID 17362864·Am J Ophthalmol·2007
8-other
No association between variations in the WDR36 gene and primary open-angle glaucoma.
PMID 17353431·Arch Ophthalmol·2007
8-other
Myocilin Gly252Arg mutation and glaucoma of intermediate severity in Caucasian individuals.
PMID 17210859·Arch Ophthalmol·2007
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 200 HAWKINS DR, DEPT OF OPHTHALMOLOGY AND VISUAL SCIENCES
IOWA CITY, IA 52242 - Phone
- (319) 353-7699
Quick Facts
- NPI
- 1306847454
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 26
- Publications
- 20
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