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Jonathan B Ruddle

Showing results (61-70 of 79) with videos related to

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JAMA Ophthalmology|May 7, 2026
Association of FOXC1 Duplications With Juvenile Open-Angle GlaucomaGiorgina E Maxwell, Joshua M Schmidt, Antonia Kolovos, et al.
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.
Clinical Genetics|February 14, 2020
The genetic and clinical landscape of nanophthalmos and posterior microphthalmos in an Australian cohortOwen M Siggs, Mona S Awadalla, Emmanuelle Souzeau, 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.
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.
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.
European Journal of Human Genetics : EJHG|October 13, 2017
Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variantsEmmanuelle Souzeau, Owen M Siggs, Tiger Zhou, et al.
Plos One|August 6, 2014
Association of CHRDL1 mutations and variants with X-linked megalocornea, Neuhäuser syndrome and central corneal thicknessAlice E Davidson, Sek-Shir Cheong, Pirro G Hysi, et al.
Pageof 8

Showing results (61-70 of 79) with videos related to

Sort By:
Pageof 8
JAMA Ophthalmology|May 7, 2026
Association of FOXC1 Duplications With Juvenile Open-Angle GlaucomaGiorgina E Maxwell, Joshua M Schmidt, Antonia Kolovos, et al.
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.
Clinical Genetics|February 14, 2020
The genetic and clinical landscape of nanophthalmos and posterior microphthalmos in an Australian cohortOwen M Siggs, Mona S Awadalla, Emmanuelle Souzeau, 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.
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.
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.
European Journal of Human Genetics : EJHG|October 13, 2017
Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variantsEmmanuelle Souzeau, Owen M Siggs, Tiger Zhou, et al.
Plos One|August 6, 2014
Association of CHRDL1 mutations and variants with X-linked megalocornea, Neuhäuser syndrome and central corneal thicknessAlice E Davidson, Sek-Shir Cheong, Pirro G Hysi, et al.
Pageof 8