Craig J E

Dimasi D P, Burdon K P, Craig J E

This review highlights CCT's high heritability and ethnic differences, despite unknown specific genes. Understanding CCT genetics is crucial for open-angle glaucoma risk assessment and future treatments.

Kakaday T, Hewitt A W, Voelcker N H, Li J S J, Craig J E

This review explores telemetric continuous IOP assessment technologies, finding miniaturized sensors and wireless communication offer superior, more accurate glaucoma monitoring than traditional clinic-based methods.

Hewitt A W, Sanfilippo P, Ring M A, Craig J E, Mackey D A

This study found open-angle glaucoma patients had a significantly higher risk of death from ischemic heart disease. Clinically, this highlights the need for increased awareness of the cardiovascular link in OAG.

Mimiwati Z, Mackey D A, Craig J E, Mackinnon J R, Rait J L, Liebelt J E et al.

This study found Australian Nail-patella syndrome (NPS) patients have an increased glaucoma risk. Regular glaucoma screening is recommended for NPS patients, though exact risk remains unclear.

Craig J E, Hewitt A W, Dimasi D P, Howell N, Toomes C, Cohn A C et al.

This study found the OPTN Met98Lys variant isn't a strong risk factor for glaucoma, ADOA, or LHON, but a weak association with normal-tension glaucoma was observed.

Craig J E, Baird P N, Healey D L, McNaught A I, McCartney P J, Rait J L et al.

Studying Gln368STOP mutation families, researchers found this mutation causes earlier-onset, more severe glaucoma with higher IOP, often requiring surgery. This highlights its significant role in disease expression.

Baird P N, Dickinson J, Craig J E, Mackey D A

This study found the Taa1 restriction enzyme reliably detects the Q368STOP myocilin gene mutation, offering a simple, rapid diagnostic tool for this glaucoma-linked allele.

Fingert J H, Clark A F, Craig J E, Alward W L, Snibson G R, McLaughlin M et al.

This study found no significant link between MYOC gene variations and steroid-induced ocular hypertension in humans or monkeys, suggesting MYOC mutations aren't a primary cause of this condition.

Craig J E, Mackey D A

This review highlights rapid advances in glaucoma genetics, identifying multiple genes linked to different glaucoma types, which is crucial for understanding disease mechanisms and future clinical management.