James E. Elder

Parkville, VIC, Australia

Last Updated: 09/26/2026

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Found 42 publications

The Burden of Treatment for Sporadic Unilateral Retinoblastoma in Australia.

The Burden of Treatment for Sporadic Unilateral Retinoblastoma in Australia.

Journal: Clinical & experimental ophthalmology

Published: July 02, 2025

NEOVASCULAR GLAUCOMA AS A PREDICTOR OF RETINOBLASTOMA HIGH-RISK HISTOPATHOLOGY IN AN INTERNATIONAL MULTICENTER STUDY.

NEOVASCULAR GLAUCOMA AS A PREDICTOR OF RETINOBLASTOMA HIGH-RISK HISTOPATHOLOGY IN AN INTERNATIONAL MULTICENTER STUDY.

Journal: Retina (Philadelphia, Pa.)

Published: December 02, 2024

HIGH-RISK HISTOPATHOLOGICAL FEATURES OF RETINOBLASTOMA FOLLOWING PRIMARY ENUCLEATION: A Global Study Of 1,426 Patients From 5 Continents.

HIGH-RISK HISTOPATHOLOGICAL FEATURES OF RETINOBLASTOMA FOLLOWING PRIMARY ENUCLEATION: A Global Study Of 1,426 Patients From 5 Continents.

Journal: Retina (Philadelphia, Pa.)

Published: August 16, 2024

Treatment Outcomes and Definition Inconsistencies in High-Risk Unilateral Retinoblastoma.

Treatment Outcomes and Definition Inconsistencies in High-Risk Unilateral Retinoblastoma.

Journal: American journal of ophthalmology

Published: June 24, 2024

Multicenter Validation of Deep Learning Algorithm ROP.AI for the Automated Diagnosis of Plus Disease in ROP.

Multicenter Validation of Deep Learning Algorithm ROP.AI for the Automated Diagnosis of Plus Disease in ROP.

Journal: Translational vision science & technology

Published: August 14, 2023

Development of a joint set of database parameters for the EU-ROP and Fight Childhood Blindness! ROP Registries.

Development of a joint set of database parameters for the EU-ROP and Fight Childhood Blindness! ROP Registries.

Journal: The British journal of ophthalmology

Published: May 12, 2023

Pathogenic genetic variants identified in Australian families with paediatric cataract.

Pathogenic genetic variants identified in Australian families with paediatric cataract.

Journal: BMJ open ophthalmology

Published: May 11, 2022

Infantile hemangioma affecting the iris.

Infantile hemangioma affecting the iris.

Journal: Pediatric dermatology

Published: October 11, 2021

Inflammatory choroiditis and papillitis from Crohn's disease in a child.

Inflammatory choroiditis and papillitis from Crohn's disease in a child.

Journal: Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus

Published: July 16, 2021

Spontaneous resolution of schitic cavities in XLRS.

Spontaneous resolution of schitic cavities in XLRS.

Journal: Ophthalmic genetics

Published: July 05, 2021

Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresis.

Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresis.

Journal: Nature genetics

Published: March 17, 2021

Recessive variants in COL25A1 gene as novel cause of arthrogryposis multiplex congenita with ocular congenital cranial dysinnervation disorder.

Recessive variants in COL25A1 gene as novel cause of arthrogryposis multiplex congenita with ocular congenital cranial dysinnervation disorder.

Journal: Human mutation

Published: March 16, 2021

Showing 1-12 of 42

Last Updated: 09/26/2026