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Beau James Fenner

11PUBLICATIONS

103CO-AUTHORS

Sensory systemsGene and molecular therapyOptical technologyDeep learningAboriginal and Torres Strait Islander artefacts

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Publications (11)

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|Jan 09, 2026

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

Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova

|Oct 07, 2025

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

Tien-En Tan, Christopher Z Y Sun, Stanley S J Poh

|Aug 26, 2025

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

Saadia Z Farooqui, Mathieu Quinodoz, Tien-En Tan

|Jul 01, 2025

Enhancing diagnostic accuracy in rare and common fundus diseases with a knowledge-rich vision-language model.

Meng Wang, Tian Lin, Aidi Lin

|Jun 03, 2025

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

Mathieu Quinodoz, Yixin Lai, Rachael Wei Chao Tang

|Mar 21, 2025

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

Jane Andrea Lieviant, Choi Mun Chan, Yasmin Bylstra

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Frequent Collaborators

2 joint publications

Yih Chung Tham

2 joint publications

Ai Fujita Sajiki

2 joint publications

Carlo Rivolta

1 joint publications

Tyler Rim

1 joint publications

Kelvin Teo

1 joint publications

Tien Yin Wong

1 joint publications

Chui Ming Gemmy Cheung

1 joint publications

Christopher Sun

1 joint publications

Taro Kominami

1 joint publications

Junya Ota

Frequent Collaborators

2 joint publications

Yih Chung Tham

2 joint publications

Ai Fujita Sajiki

2 joint publications

Carlo Rivolta

1 joint publications

Tyler Rim

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