Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Jamie E Craig

Showing results (81-90 of 352) with videos related to

Pageof 36
Sort By:
American Journal of Ophthalmology|June 15, 2005
The Q368STOP myocilin mutation in a population-based cohort: the Blue Mountains Eye StudyPaul N Baird, Andrea J Richardson, Jamie E Craig, et al.
American Journal of Ophthalmology|October 18, 2005
A common disease haplotype for the Q368STOP mutation of the myocilin gene in Australian and Canadian glaucoma familiesPaul N Baird, Andrea J Richardson, David A Mackey, et al.
Investigative Ophthalmology & Visual Science|June 26, 2009
Common sequence variation in the VEGFA gene predicts risk of diabetic retinopathySotoodeh Abhary, Kathryn P Burdon, Aanchal Gupta, et al.
Clinical & Experimental Ophthalmology|March 27, 2014
Review of the prevalence of diabetic retinopathy in Indigenous AustraliansGeorgia Kaidonis, Richard A Mills, John Landers, et al.
Journal of Proteome Research|June 14, 2011
MALDI-MS-imaging of whole human lens capsuleMaurizio Ronci, Shiwani Sharma, Tim Chataway, et al.
Medrxiv : the Preprint Server for Health Sciences|February 23, 2026
Genome-wide association study of corneal dystrophy uncovers novel risk loci and enables improved polygenic prediction of Fuchs endothelial corneal dystrophyBenyapa Insawang, David A Mackey, Alex W Hewitt, et al.
Ophthalmology. Glaucoma|February 13, 2022
The Caregiver Experience in Childhood Glaucoma: An Interview StudyLachlan S W Knight, Bronwyn Ridge, Sandra E Staffieri, et al.
Biophysical Journal|September 7, 2010
Detecting protein aggregates on untreated human tissue samples by atomic force microscopy recognition imagingRhiannon Creasey, Shiwani Sharma, Jamie E Craig, et al.
Ophthalmic Genetics|October 20, 2006
Familial transmission risk of infantile glaucoma in AustraliaAlex W Hewitt, Jane R MacKinnon, Antonio Giubilato, et al.
Human Mutation|June 21, 2007
A novel deletion in the FTL gene causes hereditary hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start siteKathryn P Burdon, Shiwani Sharma, Celia S Chen, et al.
Pageof 36

Showing results (81-90 of 352) with videos related to

Sort By:
Pageof 36
American Journal of Ophthalmology|June 15, 2005
The Q368STOP myocilin mutation in a population-based cohort: the Blue Mountains Eye StudyPaul N Baird, Andrea J Richardson, Jamie E Craig, et al.
American Journal of Ophthalmology|October 18, 2005
A common disease haplotype for the Q368STOP mutation of the myocilin gene in Australian and Canadian glaucoma familiesPaul N Baird, Andrea J Richardson, David A Mackey, et al.
Investigative Ophthalmology & Visual Science|June 26, 2009
Common sequence variation in the VEGFA gene predicts risk of diabetic retinopathySotoodeh Abhary, Kathryn P Burdon, Aanchal Gupta, et al.
Clinical & Experimental Ophthalmology|March 27, 2014
Review of the prevalence of diabetic retinopathy in Indigenous AustraliansGeorgia Kaidonis, Richard A Mills, John Landers, et al.
Journal of Proteome Research|June 14, 2011
MALDI-MS-imaging of whole human lens capsuleMaurizio Ronci, Shiwani Sharma, Tim Chataway, et al.
Medrxiv : the Preprint Server for Health Sciences|February 23, 2026
Genome-wide association study of corneal dystrophy uncovers novel risk loci and enables improved polygenic prediction of Fuchs endothelial corneal dystrophyBenyapa Insawang, David A Mackey, Alex W Hewitt, et al.
Ophthalmology. Glaucoma|February 13, 2022
The Caregiver Experience in Childhood Glaucoma: An Interview StudyLachlan S W Knight, Bronwyn Ridge, Sandra E Staffieri, et al.
Biophysical Journal|September 7, 2010
Detecting protein aggregates on untreated human tissue samples by atomic force microscopy recognition imagingRhiannon Creasey, Shiwani Sharma, Jamie E Craig, et al.
Ophthalmic Genetics|October 20, 2006
Familial transmission risk of infantile glaucoma in AustraliaAlex W Hewitt, Jane R MacKinnon, Antonio Giubilato, et al.
Human Mutation|June 21, 2007
A novel deletion in the FTL gene causes hereditary hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start siteKathryn P Burdon, Shiwani Sharma, Celia S Chen, et al.
Pageof 36