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Jamie E Craig

Showing results (231-240 of 352) with videos related to

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Scientific Reports|June 1, 2016
Assessment of polygenic effects links primary open-angle glaucoma and age-related macular degenerationGabriel Cuellar-Partida, Jamie E Craig, Kathryn P Burdon, et al.
Clinical & Experimental Ophthalmology|February 8, 2020
Effect of phacoemulsification cataract surgery on intraocular pressure in early glaucoma: A prospective multi-site studyAyub Qassim, Mark J Walland, John Landers, et al.
G3 (Bethesda, Md.)|August 26, 2017
High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern AustraliaShari Javadiyan, Jamie E Craig, Emmanuelle Souzeau, et al.
Molecular Vision|October 26, 2022
The phenotypic spectrum of <i>ADAMTSL4-</i>associated ectopia lentis: Additional cases, complications, and review of literatureLachlan S W Knight, Sean Mullany, Deepa A Taranath, et al.
Human Genetics|August 29, 2009
Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genesDavid P Dimasi, Jern Y Chen, Alex W Hewitt, et al.
Investigative Ophthalmology & Visual Science|March 26, 2025
Genome-Wide Association Study to Identify Genetic Variants Associated With Diabetic MaculopathyRajya L Gurung, Charvi Nangia, Tengda Cai, et al.
BMJ Open Ophthalmology|September 26, 2022
Pathogenic genetic variants identified in Australian families with paediatric cataractJohanna L Jones, Bennet J McComish, Sandra E Staffieri, et al.
American Journal of Ophthalmology|November 5, 2003
Evaluation of optineurin sequence variations in 1,048 patients with open-angle glaucomaWallace L M Alward, Young H Kwon, Kazuhide Kawase, et al.
Investigative Ophthalmology & Visual Science|January 25, 2006
A large GLC1C Greek family with a myocilin T377M mutation: inheritance and phenotypic variabilityMichael B Petersen, George Kitsos, John R Samples, et al.
Plos One|December 6, 2018
Prevalence and type of artefact with spectral domain optical coherence tomography macular ganglion cell imaging in glaucoma surveillanceMona S Awadalla, Jude Fitzgerald, Nicholas H Andrew, et al.
Pageof 36

Showing results (231-240 of 352) with videos related to

Sort By:
Pageof 36
Scientific Reports|June 1, 2016
Assessment of polygenic effects links primary open-angle glaucoma and age-related macular degenerationGabriel Cuellar-Partida, Jamie E Craig, Kathryn P Burdon, et al.
Clinical & Experimental Ophthalmology|February 8, 2020
Effect of phacoemulsification cataract surgery on intraocular pressure in early glaucoma: A prospective multi-site studyAyub Qassim, Mark J Walland, John Landers, et al.
G3 (Bethesda, Md.)|August 26, 2017
High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern AustraliaShari Javadiyan, Jamie E Craig, Emmanuelle Souzeau, et al.
Molecular Vision|October 26, 2022
The phenotypic spectrum of <i>ADAMTSL4-</i>associated ectopia lentis: Additional cases, complications, and review of literatureLachlan S W Knight, Sean Mullany, Deepa A Taranath, et al.
Human Genetics|August 29, 2009
Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genesDavid P Dimasi, Jern Y Chen, Alex W Hewitt, et al.
Investigative Ophthalmology & Visual Science|March 26, 2025
Genome-Wide Association Study to Identify Genetic Variants Associated With Diabetic MaculopathyRajya L Gurung, Charvi Nangia, Tengda Cai, et al.
BMJ Open Ophthalmology|September 26, 2022
Pathogenic genetic variants identified in Australian families with paediatric cataractJohanna L Jones, Bennet J McComish, Sandra E Staffieri, et al.
American Journal of Ophthalmology|November 5, 2003
Evaluation of optineurin sequence variations in 1,048 patients with open-angle glaucomaWallace L M Alward, Young H Kwon, Kazuhide Kawase, et al.
Investigative Ophthalmology & Visual Science|January 25, 2006
A large GLC1C Greek family with a myocilin T377M mutation: inheritance and phenotypic variabilityMichael B Petersen, George Kitsos, John R Samples, et al.
Plos One|December 6, 2018
Prevalence and type of artefact with spectral domain optical coherence tomography macular ganglion cell imaging in glaucoma surveillanceMona S Awadalla, Jude Fitzgerald, Nicholas H Andrew, et al.
Pageof 36