John N De Roach (John De Roach)

Publication Activity (10 Years)

Years Active: 2020-2022
Publications (10 Years): 4

Top Topics

Induced Pluripotent Stem Cells

Diabetic Retinopathy

Optical Coherence Tomography

Top Venues

Molecular genetics & genomic medicine

Documenta ophthalmologica. Advances in ophthalmology

This page only lists publications with an associated author ORCID identifier.

Publications

Heather G Mack, Alexis Ceecee Zhang, Myra B McGuiness, Fred K Chen, John R B Grigg, Robyn V Jamieson, Thomas L Edwards, John N De Roach, Fleur O'Hare, Keith R Martin, Lauren N Ayton
Survey of perspectives of people with inherited retinal diseases on ocular gene therapy in Australia. Gene therapy (2022)
Juanita Pappalardo, Rachael C Heath Jeffery, Jennifer A Thompson, Enid Chelva, Quang Pham, Ian J Constable, Terri L McLaren, Tina M Lamey, John N De Roach, Fred K Chen
A novel phenotype in a family with autosomal dominant retinal dystrophy due to c.1430A > G in retinoid isomerohydrolase (RPE65) and c.37C > T in bestrophin 1 (BEST1). Documenta ophthalmologica. Advances in ophthalmology 143 (1) (2021)
Xiao Zhang, Dan Zhang, Jennifer A Thompson, Shang-Chih Chen, Zhiqin Huang, Luke Jennings, Terri L McLaren, Tina M Lamey, John N De Roach, Fred K Chen, Samuel McLenachan
Gene correction of the CLN3 c.175G>A variant in patient-derived induced pluripotent stem cells prevents pathological changes in retinal organoids. Molecular genetics & genomic medicine 9 (3) (2021)
Di Huang, Jennifer A Thompson, Jason Charng, Enid Chelva, Samuel McLenachan, Shang-Chih Chen, Dan Zhang, Terri L McLaren, Tina M Lamey, Ian J Constable, John N De Roach, May Thandar Aung-Htut, Abbie Adams, Susan Fletcher, Steve D Wilton, Fred K Chen
Phenotype-genotype correlations in a pseudodominant Stargardt disease pedigree due to a novel ABCA4 deletion-insertion variant causing a splicing defect. Molecular genetics & genomic medicine 8 (7) (2020)