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

Ben R Roos

Showing results (11-20 of 22) with videos related to

Pageof 3
Sort By:
Molecular Vision|September 23, 2015
Novel TMEM98 mutations in pedigrees with autosomal dominant nanophthalmosDavid Khorram, Michael Choi, Ben R Roos, et al.
Ophthalmic Genetics|September 25, 2012
Confirmation of the association between the TCF4 risk allele and Fuchs endothelial corneal dystrophy in patients from the Midwestern United StatesJohn F Stamler, Ben R Roos, Michael D Wagoner, et al.
Ophthalmology. Glaucoma|May 24, 2023
Mutations in EFEMP1 in Patients with Juvenile Open-Angle GlaucomaAminatta Z Tejan-Kamara, Erin A Boese, Andrew E Pouw, et al.
Ophthalmic Genetics|February 21, 2013
TBK1 and flanking genes in human retinaJohn H Fingert, Benjamin W Darbro, Qining Qian, et al.
Plos One|June 9, 2016
SQSTM1 Mutations and GlaucomaTodd E Scheetz, Ben R Roos, Frances Solivan-Timpe, et al.
Human Molecular Genetics|July 17, 2012
Analysis of ASB10 variants in open angle glaucomaJohn H Fingert, Ben R Roos, Frances Solivan-Timpe, et al.
JAMA Ophthalmology|April 5, 2014
TBK1 gene duplication and normal-tension glaucomaRobert Ritch, Ben Darbro, Geeta Menon, et al.
Molecular Vision|April 18, 2012
Localization of SH3PXD2B in human eyes and detection of rare variants in patients with anterior segment diseases and glaucomaMao Mao, Frances Solivan-Timpe, Ben R Roos, et al.
Ophthalmology. Glaucoma|April 25, 2025
Prevalence of Myocilin Mutations in a Cohort of Patients with Juvenile Open-Angle Glaucoma from sub-Saharan AfricaOlusola Olawoye, Brian P Young, Angela W Nyunt, et al.
Human Molecular Genetics|March 31, 2011
Copy number variations on chromosome 12q14 in patients with normal tension glaucomaJohn H Fingert, Alan L Robin, Jennifer L Stone, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Molecular Vision|September 23, 2015
Novel TMEM98 mutations in pedigrees with autosomal dominant nanophthalmosDavid Khorram, Michael Choi, Ben R Roos, et al.
Ophthalmic Genetics|September 25, 2012
Confirmation of the association between the TCF4 risk allele and Fuchs endothelial corneal dystrophy in patients from the Midwestern United StatesJohn F Stamler, Ben R Roos, Michael D Wagoner, et al.
Ophthalmology. Glaucoma|May 24, 2023
Mutations in EFEMP1 in Patients with Juvenile Open-Angle GlaucomaAminatta Z Tejan-Kamara, Erin A Boese, Andrew E Pouw, et al.
Ophthalmic Genetics|February 21, 2013
TBK1 and flanking genes in human retinaJohn H Fingert, Benjamin W Darbro, Qining Qian, et al.
Plos One|June 9, 2016
SQSTM1 Mutations and GlaucomaTodd E Scheetz, Ben R Roos, Frances Solivan-Timpe, et al.
Human Molecular Genetics|July 17, 2012
Analysis of ASB10 variants in open angle glaucomaJohn H Fingert, Ben R Roos, Frances Solivan-Timpe, et al.
JAMA Ophthalmology|April 5, 2014
TBK1 gene duplication and normal-tension glaucomaRobert Ritch, Ben Darbro, Geeta Menon, et al.
Molecular Vision|April 18, 2012
Localization of SH3PXD2B in human eyes and detection of rare variants in patients with anterior segment diseases and glaucomaMao Mao, Frances Solivan-Timpe, Ben R Roos, et al.
Ophthalmology. Glaucoma|April 25, 2025
Prevalence of Myocilin Mutations in a Cohort of Patients with Juvenile Open-Angle Glaucoma from sub-Saharan AfricaOlusola Olawoye, Brian P Young, Angela W Nyunt, et al.
Human Molecular Genetics|March 31, 2011
Copy number variations on chromosome 12q14 in patients with normal tension glaucomaJohn H Fingert, Alan L Robin, Jennifer L Stone, et al.
Pageof 3