Beau J. Fenner

Ophthalmology

200 Hawkins Dr
Iowa City, IA 52242

Last Updated: 09/26/2026

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Found 68 publications

Defining a Novel RPGR Phenotype of Sector Retinitis Pigmentosa With Cone Dystrophy.

Defining a Novel RPGR Phenotype of Sector Retinitis Pigmentosa With Cone Dystrophy.

Journal: Investigative ophthalmology & visual science

Published: August 10, 2026

COQ8 chaperones coenzyme Q lipid intermediates through ATP-driven structural gating.

COQ8 chaperones coenzyme Q lipid intermediates through ATP-driven structural gating.

Journal: Science advances

Published: July 29, 2026

The Trajectory of Gene Discovery in Retinitis Pigmentosa.

The Trajectory of Gene Discovery in Retinitis Pigmentosa.

Journal: Genes

Published: July 06, 2026

Aflibercept With Versus Without Reduced-Fluence Photodynamic Therapy for Polypoidal Choroidal Vasculopathy: Optical Coherence Tomography Angiographic Changes From a Randomized Clinical Trial.

Aflibercept With Versus Without Reduced-Fluence Photodynamic Therapy for Polypoidal Choroidal Vasculopathy: Optical Coherence Tomography Angiographic Changes From a Randomized Clinical Trial.

Journal: American journal of ophthalmology

Published: March 17, 2026

Drusenoid macular dystrophies in Singaporean Chinese: first report of Doyne honeycomb retinal dystrophy and late-onset retinal degeneration from Southeast Asia.

Drusenoid macular dystrophies in Singaporean Chinese: first report of Doyne honeycomb retinal dystrophy and late-onset retinal degeneration from Southeast Asia.

Journal: Ophthalmic genetics

Published: March 16, 2026

Advances in Polypoidal Choroidal Vasculopathy (PCV) Management: Emerging Evidence for Faricimab and Aflibercept 8 mg.

Advances in Polypoidal Choroidal Vasculopathy (PCV) Management: Emerging Evidence for Faricimab and Aflibercept 8 mg.

Journal: Ophthalmology and therapy

Published: March 13, 2026

Phenotypic Divergence in C19ORF44-Associated Retinal Degeneration despite an Identical Genotype: A Case Report.

Phenotypic Divergence in C19ORF44-Associated Retinal Degeneration despite an Identical Genotype: A Case Report.

Journal: Case reports in ophthalmology

Published: February 20, 2026

A novel missense TUBB4B variant outside of the canonical hotspot is associated with cone-rod dystrophy and sensorineural hearing loss.

A novel missense TUBB4B variant outside of the canonical hotspot is associated with cone-rod dystrophy and sensorineural hearing loss.

Journal: Ophthalmic genetics

Published: October 07, 2025

One down but many more to go: the state of gene therapy for inherited retinal disease.

One down but many more to go: the state of gene therapy for inherited retinal disease.

Journal: Regenerative medicine

Published: October 07, 2025

Cuticular drusen in Asian neovascular age-related macular degeneration: Clinical features and polypoidal choroidal vasculopathy association.

Cuticular drusen in Asian neovascular age-related macular degeneration: Clinical features and polypoidal choroidal vasculopathy association.

Journal: Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie

Published: September 19, 2025

A survey of genotypes associated with Leber congenital amaurosis and early-onset severe retinal degeneration identified in a Singaporean patient cohort.

A survey of genotypes associated with Leber congenital amaurosis and early-onset severe retinal degeneration identified in a Singaporean patient cohort.

Journal: Ophthalmic genetics

Published: August 26, 2025

Management of incontinentia pigmenti retinopathy.

Management of incontinentia pigmenti retinopathy.

Journal: Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie

Published: July 07, 2025

Showing 1-12 of 68

Last Updated: 09/26/2026