Publications
- Wu Z, Luu CD, Hodgson LAB, et al. A Secondary and Exploratory Outcomes of the Subthreshold Nanosecond Laser Intervention Randomised Trial in Age-Related Macular Degeneration: A LEAD Study Report. Ophthalmol Retina. 2019 Jul 22. pii: S2468-6530(19)30467-1. doi: 10.1016/j.oret.2019.07.008
- Teo KYC, Squirrell DM, Nguyen V, et al A Multicountry Comparison of Real-World Management and Outcomes of Polypoidal Choroidal Vasculaopthy: Fight Retina Blindness! Cohort. Ophthal Retina Mar 2019; 3 (3): 220-229.
- Nguyen CL, Gillies MC, Nguyen V. et al Characterisation of poor visual outcomes of neovascular age-related macular degeneration treated with anti-vascular endothelial growth factor agents. Ophthalmology 2018 Dec 6. Pii: S0161-6420(18)31470-2. Doi: 10.1016/j.ophtha.2018.11.036 [Epub ahead of print]
- Guymer RH, Wu Z, Hodgson LAB, et al: Sub-threshold nanosecond laser intervention in Age-related macular degeneration: the LEAD Randomized Control Clinical Trial. Ophthalmology 2018 Sep 20. Pii: S0161-6420(18)32135-3. Doi: 10.1016/j.ophtha.2018.09.015. [Epub ahead of print] (as a study group co-author)
- Lek JJ, Brassington KH, Luu CD, et al. Subthreshold nano-second laser intervention in intermediate age-relate macula degeneration. Study Design and Baseline characteristics of the Laser in Early stages of Age-Related Macula Degeneration (LEAD) study. Ophthalmol Retina 2016;: 1-13 (as a study group co-author)
- Cohn AC, Busija L, Robman LD, et al Younger Siblings, C-reactive Protein and Risk of Age-related Macular Degeneration. Am J of Epidemiology 2013; 177 (9): 933-943.
- Cohn AC, Turnbull C, Ruddle JB et al Best macular dystrophy in Australia: phenotypic profile and identification of novel BEST1 mutations. Eye 2011; 25: 208-217.
- Kearns LS, Forrest M, Cohn AC et al Does acute loss of vision in Autosomal Dominant Optic Atrophy occur in early childhood? Ophthal Genet 2010; 31(1): 44-6.
- Cohn AC, Toomes C, Hewitt AW et al The Natural History of OPA1-related Autosomal Dominant Optic Atrophy. BJO 2008; 92: 1333-1336.
- Cohn AC, Toomes C, Potter et al. Autosomal Dominant Optic Atrophy: Penetrance and Expressivity in Patients with OPA1 Mutations. AJO April 2007; 143(4) 565-662.
- Craig, JE, Hewitt, AW, Dimassi et al. The role of the Met98Lys optineurin variant in inherited optic nerve diseases. BJO 2006; 90; 1420-1424.
- McKay JD, Patterson B, Craig Je et al. The telomere of human chromosome 1p contains at least two independent congenital cataract predisposition genes. BJO 89:831-834, 2005.
- Cohn AC, Kotschet K, Veitch A, et al. Novel Opthalmological Features in Hereditary Endotheliopathy with Retinopathy, Nephropathy, and Stroke Syndrome. Clinical and Exp Ophthal. 33:181-183, 2005.
- Cohn AC, Kearns LS, Savarirayan R, et al. Chromosomal Abnormalities and Glaucoma: A Case of Congenital Glaucoma with Trisomy. 8q22-qter/Monosomy 9p23-pter. Ophthal Genet. 26:45-53, 2005.
- Cohn AC, Wilson WM, Yan B, et al. An Analysis of Clinical Outcomes Following In-Hospital Adult Cardiac Arrest. Internal Medicine Journal. 34(7): 398-402, 2004.
