Jennifer A. Thompson

2 Verdun Street
Nedlands, WA, Australia

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 79 publications

Gain of function in BEST1: photoreceptor changes and myopia in autosomal dominant vitreoretinochoroidopathy.

Gain of function in BEST1: photoreceptor changes and myopia in autosomal dominant vitreoretinochoroidopathy.

Journal: Ophthalmic genetics
Published: April 16, 2026

ABCA4 Versus PRPH2-Associated Retinopathy: Clinical and Electrophysiological Findings.

ABCA4 Versus PRPH2-Associated Retinopathy: Clinical and Electrophysiological Findings.

Journal: Investigative ophthalmology & visual science
Published: April 14, 2026

Autosomal dominant Riggs-type congenital stationary night blindness with fundus sheen and retinal atrophy due to a novel GNAT1 p.Gln200Arg variant.

Autosomal dominant Riggs-type congenital stationary night blindness with fundus sheen and retinal atrophy due to a novel GNAT1 p.Gln200Arg variant.

Journal: Documenta ophthalmologica. Advances in ophthalmology
Published: December 30, 2025

Multimodal imaging and electrophysiological features in bradyopsia associated with homozygous variants (c.895T>C) in Regulator of G-protein Signaling 9 (RGS9).

Multimodal imaging and electrophysiological features in bradyopsia associated with homozygous variants (c.895T>C) in Regulator of G-protein Signaling 9 (RGS9).

Journal: Ophthalmic genetics
Published: September 16, 2025

Sex Distributions in the Most Frequent Autosomal Genetic Causes of Retinitis Pigmentosa.

Sex Distributions in the Most Frequent Autosomal Genetic Causes of Retinitis Pigmentosa.

Journal: Investigative ophthalmology & visual science
Published: August 29, 2025

Anatomy- versus Sensitivity-Based Loci Preselection in Detecting USH2A-Retinopathy Microperimetric Progression.

Anatomy- versus Sensitivity-Based Loci Preselection in Detecting USH2A-Retinopathy Microperimetric Progression.

Journal: Ophthalmology science
Published: July 16, 2025

ROSAH syndrome presenting with recurrent vitreous hemorrhage: a multimodal imaging study.

ROSAH syndrome presenting with recurrent vitreous hemorrhage: a multimodal imaging study.

Journal: Ophthalmic genetics
Published: March 11, 2025

Elevated Plasma Complement Factors in CRB1-Associated Inherited Retinal Dystrophies.

Elevated Plasma Complement Factors in CRB1-Associated Inherited Retinal Dystrophies.

Journal: Investigative ophthalmology & visual science
Published: February 21, 2025

Generation of two induced pluripotent stem cell lines carrying the CDH23 c.1515-12G > A variant.

Generation of two induced pluripotent stem cell lines carrying the CDH23 c.1515-12G > A variant.

Journal: Stem cell research
Published: February 11, 2025

Generation of the induced pluripotent stem cell line LEIi023-A from a rod-cone dystrophy patient carrying the dominant PRPF31 c.267del variant.

Generation of the induced pluripotent stem cell line LEIi023-A from a rod-cone dystrophy patient carrying the dominant PRPF31 c.267del variant.

Journal: Stem cell research
Published: February 07, 2025

Retinal Disease Variability in Female Carriers of RPGR Variants Associated with Retinitis Pigmentosa: Clinical and Genetic Parameters.

Retinal Disease Variability in Female Carriers of RPGR Variants Associated with Retinitis Pigmentosa: Clinical and Genetic Parameters.

Journal: Genes
Published: January 16, 2025

CTNNA1-associated retinal dystrophy: novel multimodal imaging and electrophysiology features.

CTNNA1-associated retinal dystrophy: novel multimodal imaging and electrophysiology features.

Journal: Documenta ophthalmologica. Advances in ophthalmology
Published: October 29, 2024
Showing 1-12 of 79

Last Updated: 09/26/2026