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Neuropsychologia|October 1, 2008
Genetic influences on handedness: data from 25,732 Australian and Dutch twin familiesSarah E Medland, David L Duffy, Margaret J Wright, et al.
JAMA Ophthalmology|September 30, 2018
Myocilin Gene Gln368Ter Variant Penetrance and Association With Glaucoma in Population-Based and Registry-Based StudiesXikun Han, Emmanuelle Souzeau, Jue-Sheng Ong, et al.
JAMA Ophthalmology|April 8, 2021
Evaluation of Shared Genetic Susceptibility to High and Low Myopia and HyperopiaJ Willem L Tideman, Olavi Pärssinen, Annechien E G Haarman, et al.
Clinical & Experimental Ophthalmology|December 17, 2011
Australian and New Zealand Registry of Advanced Glaucoma: methodology and recruitmentEmmanuelle Souzeau, Ivan Goldberg, Paul R Healey, et al.
JAMA Ophthalmology|January 18, 2019
Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital GlaucomaOwen M Siggs, Emmanuelle Souzeau, Francesca Pasutto, et al.
American Journal of Human Genetics|October 28, 2005
Mutations in TCF8 cause posterior polymorphous corneal dystrophy and ectopic expression of COL4A3 by corneal endothelial cellsCharles M Krafchak, Hemant Pawar, Sayoko E Moroi, et al.
Nature Communications|August 23, 2025
Large-scale GWAS of strabismus identifies risk loci and provides support for a link with maternal smokingWeixiong He, Peter J van der Most, Jue-Sheng Ong, et al.
Human Mutation|May 12, 2017
Haplotype reference consortium panel: Practical implications of imputations with large reference panelsAdriana I Iglesias, Sven J van der Lee, Pieter W M Bonnemaijer, et al.
European Journal of Human Genetics : EJHG|May 18, 2017
Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variantsEmmanuelle Souzeau, Owen M Siggs, Tiger Zhou, et al.
Ophthalmology|April 23, 2021
Childhood and Early Onset Glaucoma Classification and Genetic Profile in a Large Australasian Disease RegistryLachlan S W Knight, Jonathan B Ruddle, Deepa A Taranath, et al.
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