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Jamie E Craig

Showing results (71-80 of 352) with videos related to

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Investigative Ophthalmology & Visual Science|February 21, 2013
Association of eNOS polymorphisms with primary angle-closure glaucomaMona S Awadalla, Suman S Thapa, Alex W Hewitt, et al.
Ophthalmology|June 13, 2025
REPLYAntonia Kolovos, Ayub Qassim, Mark M Hassall, et al.
Molecular Vision|August 31, 2012
A cross-ethnicity investigation of genes previously implicated in primary angle closure glaucomaMona S Awadalla, Kathryn P Burdon, Suman S Thapa, et al.
Clinical & Experimental Ophthalmology|January 5, 2008
Objective monitoring of papilloedema using confocal scanning laser ophthalmoscopyJern Yee Chen, Deepa A Taranath, Angela J Chappell, et al.
Translational Vision Science & Technology|June 10, 2021
Risk Stratification and Clinical Utility of Polygenic Risk Scores in OphthalmologyAyub Qassim, Emmanuelle Souzeau, Georgie Hollitt, et al.
Clinical & Experimental Ophthalmology|October 23, 2004
Analysis of optineurin (OPTN) gene mutations in subjects with and without glaucoma: the Blue Mountains Eye StudyPaul N Baird, Andrea J Richardson, Jamie E Craig, et al.
Clinical & Experimental Ophthalmology|January 23, 2010
Sensitivity of confocal laser tomography versus optical coherence tomography in detecting advanced glaucomaAlex W Hewitt, Angela J Chappell, Tania Straga, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 11, 2014
Predictive genetic testing experience for myocilin primary open-angle glaucoma using the Australian and New Zealand Registry of Advanced GlaucomaEmmanuelle Souzeau, Jodi Glading, Miriam Keane, et al.
Gene|April 29, 2014
Identification of a novel MYOC mutation, p.(Trp373), in a family with open angle glaucomaApril Crawford, Emmanuelle Souzeau, Ashish Agar, et al.
Ophthalmic Genetics|April 13, 2005
Chromosomal abnormalities and glaucoma: a case of congenital glaucoma with trisomy 8q22-qter/ monosomy 9p23-pterAmy C Cohn, Lisa S Kearns, Ravi Savarirayan, et al.
Pageof 36

Showing results (71-80 of 352) with videos related to

Sort By:
Pageof 36
Investigative Ophthalmology & Visual Science|February 21, 2013
Association of eNOS polymorphisms with primary angle-closure glaucomaMona S Awadalla, Suman S Thapa, Alex W Hewitt, et al.
Ophthalmology|June 13, 2025
REPLYAntonia Kolovos, Ayub Qassim, Mark M Hassall, et al.
Molecular Vision|August 31, 2012
A cross-ethnicity investigation of genes previously implicated in primary angle closure glaucomaMona S Awadalla, Kathryn P Burdon, Suman S Thapa, et al.
Clinical & Experimental Ophthalmology|January 5, 2008
Objective monitoring of papilloedema using confocal scanning laser ophthalmoscopyJern Yee Chen, Deepa A Taranath, Angela J Chappell, et al.
Translational Vision Science & Technology|June 10, 2021
Risk Stratification and Clinical Utility of Polygenic Risk Scores in OphthalmologyAyub Qassim, Emmanuelle Souzeau, Georgie Hollitt, et al.
Clinical & Experimental Ophthalmology|October 23, 2004
Analysis of optineurin (OPTN) gene mutations in subjects with and without glaucoma: the Blue Mountains Eye StudyPaul N Baird, Andrea J Richardson, Jamie E Craig, et al.
Clinical & Experimental Ophthalmology|January 23, 2010
Sensitivity of confocal laser tomography versus optical coherence tomography in detecting advanced glaucomaAlex W Hewitt, Angela J Chappell, Tania Straga, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 11, 2014
Predictive genetic testing experience for myocilin primary open-angle glaucoma using the Australian and New Zealand Registry of Advanced GlaucomaEmmanuelle Souzeau, Jodi Glading, Miriam Keane, et al.
Gene|April 29, 2014
Identification of a novel MYOC mutation, p.(Trp373), in a family with open angle glaucomaApril Crawford, Emmanuelle Souzeau, Ashish Agar, et al.
Ophthalmic Genetics|April 13, 2005
Chromosomal abnormalities and glaucoma: a case of congenital glaucoma with trisomy 8q22-qter/ monosomy 9p23-pterAmy C Cohn, Lisa S Kearns, Ravi Savarirayan, et al.
Pageof 36