Abigail T. Fahim

Abigail T. Fahim

Ophthalmology

1000 Wall St
Elevator B Floor 2
Ann Arbor, MI 48105

Last Updated: 09/26/2026

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Found 49 publications

Correction: Raeker et al. Reduced Retinal Pigment Epithelial Autophagy Due to Loss of Rab12 Prenylation in a Human iPSC-RPE Model of Choroideremia. Cells 2024, 13, 1068.

Correction: Raeker et al. Reduced Retinal Pigment Epithelial Autophagy Due to Loss of Rab12 Prenylation in a Human iPSC-RPE Model of Choroideremia. Cells 2024, 13, 1068.

Journal: Cells

Published: June 22, 2026

High-Density Lipoprotein Nanoparticles Delivering Liver X Receptor Agonist for the Treatment of Age-Related Macular Degeneration.

High-Density Lipoprotein Nanoparticles Delivering Liver X Receptor Agonist for the Treatment of Age-Related Macular Degeneration.

Journal: Molecular pharmaceutics

Published: May 22, 2026

Addressing Challenges in Developing Treatments for Inherited Retinal Diseases: Recommendations From the Third Monaciano Symposium.

Addressing Challenges in Developing Treatments for Inherited Retinal Diseases: Recommendations From the Third Monaciano Symposium.

Journal: Translational vision science & technology

Published: August 27, 2025

Supporting Effective Peer Review at Investigative Ophthalmology & Visual Science.

Supporting Effective Peer Review at Investigative Ophthalmology & Visual Science.

Journal: Investigative ophthalmology & visual science

Published: April 29, 2025

IGFBP5 as a Novel Basolateral Secretion Marker in the Retinal Pigment Epithelium.

IGFBP5 as a Novel Basolateral Secretion Marker in the Retinal Pigment Epithelium.

Journal: Advances in experimental medicine and biology

Published: February 10, 2025

Female Simplex Carriers of X-Linked Retinal Dystrophies: A Case Series.

Female Simplex Carriers of X-Linked Retinal Dystrophies: A Case Series.

Journal: Case reports in ophthalmology

Published: February 09, 2025

Characterizing the Genetic Basis for Inherited Retinal Disease: Lessons Learned From the Foundation Fighting Blindness Clinical Consortium's Gene Poll.

Characterizing the Genetic Basis for Inherited Retinal Disease: Lessons Learned From the Foundation Fighting Blindness Clinical Consortium's Gene Poll.

Journal: Investigative ophthalmology & visual science

Published: February 05, 2025

Racial Disparities in Genetic Detection Rates for Inherited Retinal Diseases.

Racial Disparities in Genetic Detection Rates for Inherited Retinal Diseases.

Journal: JAMA ophthalmology

Published: November 07, 2024

Multimodal Imaging-Guided Stem Cell Ocular Treatment.

Multimodal Imaging-Guided Stem Cell Ocular Treatment.

Journal: ACS nano

Published: May 27, 2024

Visual Acuity, Full-field Stimulus Thresholds, and Electroretinography for 4 Years in The Rate of Progression of USH2A-related Retinal Degeneration (RUSH2A) Study.

Visual Acuity, Full-field Stimulus Thresholds, and Electroretinography for 4 Years in The Rate of Progression of USH2A-related Retinal Degeneration (RUSH2A) Study.

Journal: Ophthalmology science

Published: May 13, 2024

Reduced Retinal Pigment Epithelial Autophagy Due to Loss of Rab12 Prenylation in a Human iPSC-RPE Model of Choroideremia.

Reduced Retinal Pigment Epithelial Autophagy Due to Loss of Rab12 Prenylation in a Human iPSC-RPE Model of Choroideremia.

Journal: Cells

Published: April 23, 2024

Autoantibodies Against Bestrophin in Non-Paraneoplastic Acute Exudative Polymorphous Vitelliform Maculopathy.

Autoantibodies Against Bestrophin in Non-Paraneoplastic Acute Exudative Polymorphous Vitelliform Maculopathy.

Journal: Ophthalmic surgery, lasers & imaging retina

Published: January 08, 2024

Showing 1-12 of 49

Last Updated: 09/26/2026