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Plos Genetics|May 21, 2010
Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thicknessYi Lu, David P Dimasi, Pirro G Hysi, et al.Nature Communications|June 9, 2023
A village in a dish model system for population-scale hiPSC studiesDrew R Neavin, Angela M Steinmann, Nona Farbehi, et al.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.Nature|December 13, 2023
The landscape of genomic structural variation in Indigenous AustraliansAndre L M Reis, Melissa Rapadas, Jillian M Hammond, 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.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.Nature Communications|November 17, 2024
Genome-wide meta-analysis identifies 22 loci for normal tension glaucoma with significant overlap with high tension glaucomaSantiago Diaz-Torres, Weixiong He, Regina Yu, et al.The EMBO Journal|August 23, 2019
A single-cell transcriptome atlas of the adult human retinaSamuel W Lukowski, Camden Y Lo, Alexei A Sharov, et al.Pageof 59