|Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma|
PG Hysi, CY Cheng, H Springelkamp, S Macgregor, JNC Bailey, ...
Nature genetics 46 (10), 1126, 2014
|Mitochondrial oxidative phosphorylation compensation may preserve vision in patients with OPA1-linked autosomal dominant optic atrophy|
NJ Van Bergen, JG Crowston, LS Kearns, SE Staffieri, AW Hewitt, ...
PLoS One 6 (6), 2011
|Effectiveness of a binocular video game vs placebo video game for improving visual functions in older children, teenagers, and adults with amblyopia: a randomized clinical trial|
TY Gao, CX Guo, RJ Babu, JM Black, WR Bobier, A Chakraborty, S Dai, ...
JAMA ophthalmology 136 (2), 172-181, 2018
|Rock, paper and scissors? Traumatic paediatric cataract in Victoria 1992–2006|
SE Staffieri, JB Ruddle, DA Mackey
Clinical & experimental ophthalmology 38 (3), 237-241, 2010
|Retinoblastoma in Victoria, 1976− 2000: changing management trends and outcomes|
JC Dondey, S Staffieri, J McKenzie, G Davie, J Elder
Clinical & experimental ophthalmology 32 (4), 354-359, 2004
|Mutations in the EPHA2 gene are a major contributor to inherited cataracts in South-Eastern Australia|
A Dave, K Laurie, SE Staffieri, D Taranath, DA Mackey, P Mitchell, ...
PLoS One 8 (8), 2013
|Incidence and predictors of glaucoma following surgery for congenital cataract in the first year of life in V ictoria, A ustralia|
JB Ruddle, SE Staffieri, JG Crowston, JC Sherwin, DA Mackey
Clinical & experimental ophthalmology 41 (7), 653-661, 2013
|Heritability of strabismus: genetic influence is specific to eso-deviation and independent of refractive error|
PG Sanfilippo, CJ Hammond, SE Staffieri, LS Kearns, SHM Liew, ...
Twin Research and Human Genetics 15 (5), 624-630, 2012
|Binocular treatment of amblyopia using videogames (BRAVO): study protocol for a randomised controlled trial|
CX Guo, RJ Babu, JM Black, WR Bobier, CSY Lam, S Dai, TY Gao, ...
Trials 17 (1), 504, 2016
|Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants|
E Souzeau, OM Siggs, T Zhou, A Galanopoulos, T Hodson, D Taranath, ...
European Journal of Human Genetics 25 (7), 839-847, 2017
|Optical treatment of amblyopia in older children and adults is essential prior to enrolment in a clinical trial|
TY Gao, N Anstice, RJ Babu, JM Black, WR Bobier, S Dai, CX Guo, ...
Ophthalmic and Physiological Optics 38 (2), 129-143, 2018
|Superselective intra-arterial chemotherapy for advanced retinoblastoma complicated by metastatic disease|
AA Mathew, N Sachdev, SE Staffieri, JD McKenzie, JE Elder
Journal of American Association for Pediatric Ophthalmology and Strabismus …, 2015
|Best's macular dystrophy in Australia: phenotypic profile and identification of novel BEST1 mutations|
AC Cohn, C Turnbull, JB Ruddle, RH Guymer, LS Kearns, S Staffieri, ...
Eye 25 (2), 208-217, 2011
|Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases|
AI Iglesias, A Mishra, V Vitart, Y Bykhovskaya, R Höhn, H Springelkamp, ...
Nature communications 9 (1), 1-11, 2018
|High-throughput genetic screening of 51 pediatric cataract genes identifies causative mutations in inherited pediatric cataract in south eastern Australia|
S Javadiyan, JE Craig, E Souzeau, S Sharma, KM Lower, DA Mackey, ...
G3: Genes, Genomes, Genetics 7 (10), 3257-3268, 2017
|Managing fetuses at high risk of retinoblastoma: lesion detection on screening MRI|
SE Staffieri, G McGillivray, JE Elder, A Bristowe, S Cole, JD McKenzie, ...
Prenatal diagnosis 35 (2), 174-178, 2015
|Telemedicine model to prevent blindness from familial glaucoma|
SE Staffieri, JB Ruddle, LS Kearns, JM Barbour, TL Edwards, P Paul, ...
Clinical & experimental ophthalmology 39 (8), 760-765, 2011
|Familial retinal detachment associated with COL2A1 exon 2 and FZD4 mutations|
TL Edwards, BO Burt, GCM Black, R Perveen, LS Kearns, SE Staffieri, ...
Clinical & experimental ophthalmology 40 (5), 476-483, 2012
|CYP1B1 copy number variation is not a major contributor to primary congenital glaucoma|
E Souzeau, M Hayes, JB Ruddle, JE Elder, SE Staffieri, LS Kearns, ...
Molecular vision 21, 160, 2015
|Prevalence of FOXC1 variants in individuals with a suspected diagnosis of primary congenital glaucoma|
OM Siggs, E Souzeau, F Pasutto, A Dubowsky, JEH Smith, D Taranath, ...
JAMA ophthalmology 137 (4), 348-355, 2019