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

Mark M Hassall

Showing results (11-20 of 30) with videos related to

Pageof 3
Sort By:
International Journal of Molecular Sciences|August 27, 2020
Analysis of Early Cone Dysfunction in an In Vivo Model of Rod-Cone DystrophyMark M Hassall, Michelle E McClements, Alun R Barnard, et al.
Clinical & Experimental Ophthalmology|September 8, 2024
Healthcare professionals' knowledge and attitudes towards polygenic risk testing for glaucomaGeorgina L Hollitt, Miriam C Keane, Thi T Nguyen, et al.
Investigative Ophthalmology & Visual Science|December 29, 2018
A Novel Achromatopsia Mouse Model Resulting From a Naturally Occurring Missense Change in Cngb3Mark M Hassall, Alun R Barnard, Harry O Orlans, et al.
The British Journal of Ophthalmology|March 30, 2021
Normal-tension glaucoma is associated with cognitive impairmentSean Mullany, Lewis Xiao, Ayub Qassim, et al.
Scientific Reports|July 7, 2023
Phenotypic consequences of a nanophthalmos-associated TMEM98 variant in human and mouseMark M Hassall, Shari Javadiyan, Sonja Klebe, et al.
Clinical & Experimental Ophthalmology|October 19, 2017
Visual outcomes following vitrectomy for diabetic retinopathy amongst Indigenous and non-Indigenous Australians in South Australia and the Northern TerritoryGeorgia Kaidonis, Mark M Hassall, Russell Phillips, et al.
Human Mutation|May 11, 2021
A novel GSN variant outside the G2 calcium-binding domain associated with Amyloidosis of the Finnish typeSean Mullany, Emmanuelle Souzeau, Sonja Klebe, et al.
Human Molecular Genetics|December 7, 2019
Genome-wide association analysis of 95 549 individuals identifies novel loci and genes influencing optic disc morphologyXikun Han, Ayub Qassim, Jiyuan An, et al.
Molecular Genetics & Genomic Medicine|August 19, 2022
Diagnostic yield of candidate genes in an Australian corneal dystrophy cohortEmmanuelle Souzeau, Owen M Siggs, Sean Mullany, et al.
Ophthalmology|November 27, 2020
Corneal Stiffness Parameters Are Predictive of Structural and Functional Progression in Glaucoma Suspect EyesAyub Qassim, Sean Mullany, Farshad Abedi, et al.
Pageof 3

Showing results (11-20 of 30) with videos related to

Sort By:
Pageof 3
International Journal of Molecular Sciences|August 27, 2020
Analysis of Early Cone Dysfunction in an In Vivo Model of Rod-Cone DystrophyMark M Hassall, Michelle E McClements, Alun R Barnard, et al.
Clinical & Experimental Ophthalmology|September 8, 2024
Healthcare professionals' knowledge and attitudes towards polygenic risk testing for glaucomaGeorgina L Hollitt, Miriam C Keane, Thi T Nguyen, et al.
Investigative Ophthalmology & Visual Science|December 29, 2018
A Novel Achromatopsia Mouse Model Resulting From a Naturally Occurring Missense Change in Cngb3Mark M Hassall, Alun R Barnard, Harry O Orlans, et al.
The British Journal of Ophthalmology|March 30, 2021
Normal-tension glaucoma is associated with cognitive impairmentSean Mullany, Lewis Xiao, Ayub Qassim, et al.
Scientific Reports|July 7, 2023
Phenotypic consequences of a nanophthalmos-associated TMEM98 variant in human and mouseMark M Hassall, Shari Javadiyan, Sonja Klebe, et al.
Clinical & Experimental Ophthalmology|October 19, 2017
Visual outcomes following vitrectomy for diabetic retinopathy amongst Indigenous and non-Indigenous Australians in South Australia and the Northern TerritoryGeorgia Kaidonis, Mark M Hassall, Russell Phillips, et al.
Human Mutation|May 11, 2021
A novel GSN variant outside the G2 calcium-binding domain associated with Amyloidosis of the Finnish typeSean Mullany, Emmanuelle Souzeau, Sonja Klebe, et al.
Human Molecular Genetics|December 7, 2019
Genome-wide association analysis of 95 549 individuals identifies novel loci and genes influencing optic disc morphologyXikun Han, Ayub Qassim, Jiyuan An, et al.
Molecular Genetics & Genomic Medicine|August 19, 2022
Diagnostic yield of candidate genes in an Australian corneal dystrophy cohortEmmanuelle Souzeau, Owen M Siggs, Sean Mullany, et al.
Ophthalmology|November 27, 2020
Corneal Stiffness Parameters Are Predictive of Structural and Functional Progression in Glaucoma Suspect EyesAyub Qassim, Sean Mullany, Farshad Abedi, et al.
Pageof 3