Ranjana S. Mathur

11 Third Hospital Avenue
Singapore, 168751, Singapore

Last Updated: 09/26/2026

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Found 63 publications

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

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

Fundus Autofluorescence (FAF) Alteration in Polypoidal Choroidal Vasculopathy (PCV) and Typical Neovascular Age Related Macular Degeneration (tAMD).

Fundus Autofluorescence (FAF) Alteration in Polypoidal Choroidal Vasculopathy (PCV) and Typical Neovascular Age Related Macular Degeneration (tAMD).

Journal: Retina (Philadelphia, Pa.)

Published: May 15, 2025

Clinical characteristics and progression rates of geographic atrophy in an Asian population from Singapore.

Clinical characteristics and progression rates of geographic atrophy in an Asian population from Singapore.

Journal: Eye (London, England)

Published: May 01, 2025

Inherited retinal degeneration in Malay and Indian populations of Singapore and Malaysia: a prospective multicentre study.

Inherited retinal degeneration in Malay and Indian populations of Singapore and Malaysia: a prospective multicentre study.

Journal: Ophthalmic genetics

Published: March 18, 2025

Novel founder variant in the S-antigen visual arrestin gene SAG is the most prevalent cause of autosomal dominant retinitis pigmentosa in Singaporean Chinese.

Novel founder variant in the S-antigen visual arrestin gene SAG is the most prevalent cause of autosomal dominant retinitis pigmentosa in Singaporean Chinese.

Journal: Journal of medical genetics

Published: March 11, 2025

Phenotypic Distinctions Between EYS- and USH2A-Associated Retinitis Pigmentosa in an Asian Population.

Phenotypic Distinctions Between EYS- and USH2A-Associated Retinitis Pigmentosa in an Asian Population.

Journal: Translational vision science & technology

Published: February 11, 2025

NR2E3-ASSOCIATED RETINOPATHY PRESENTING WITH BILATERAL CHOROIDAL NEOVASCULARIZATION.

NR2E3-ASSOCIATED RETINOPATHY PRESENTING WITH BILATERAL CHOROIDAL NEOVASCULARIZATION.

Journal: Retinal cases & brief reports

Published: January 09, 2025

Fundus autofluorescence features specific for EYS-associated retinitis pigmentosa.

Fundus autofluorescence features specific for EYS-associated retinitis pigmentosa.

Journal: PloS one

Published: November 21, 2024

Psychometric evaluation and computerized adaptive testing simulations of age-related macular degeneration quality of life item banks.

Psychometric evaluation and computerized adaptive testing simulations of age-related macular degeneration quality of life item banks.

Journal: Asia-Pacific journal of ophthalmology (Philadelphia, Pa.)

Published: September 18, 2024

Determinants of diagnostic yield in a multi-ethnic Asian inherited retinal disease cohort.

Determinants of diagnostic yield in a multi-ethnic Asian inherited retinal disease cohort.

Journal: European journal of human genetics : EJHG

Published: September 03, 2024

Utility of multimodal imaging in the clinical diagnosis of inherited retinal degenerations.

Utility of multimodal imaging in the clinical diagnosis of inherited retinal degenerations.

Journal: Taiwan journal of ophthalmology

Published: June 14, 2024

Showing 1-12 of 63

Last Updated: 09/26/2026