Terri L. Mclaren

2 Verdun Street
Nedlands, WA, Australia

Last Updated: 09/26/2026

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Found 76 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

De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa.

De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa.

Journal: Nature genetics
Published: June 02, 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

De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa.

De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa.

Journal: medRxiv : the preprint server for health sciences
Published: January 20, 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
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Last Updated: 09/26/2026