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Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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R Grigg

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International Journal of Molecular Sciences|April 12, 2022

Whole Genome Sequencing, Focused Assays and Functional Studies Increasing Understanding in Cryptic Inherited Retinal DystrophiesBenjamin M Nash, Alan Ma, Gladys Ho, et al.

Data in Brief|January 6, 2022

Safety and biocompatibility of a bionic eye: Imaging, intraocular pressure, and histology dataSamuel C Eggenberger, Natalie L James, Cherry Ho, et al.

Human Molecular Genetics|August 2, 2015

Mutations in SIPA1L3 cause eye defects through disruption of cell polarity and cytoskeleton organizationRebecca Greenlees, Marija Mihelec, Saira Yousoof, et al.

Biomaterials|November 12, 2021

Implantation and long-term assessment of the stability and biocompatibility of a novel 98 channel suprachoroidal visual prosthesis in sheepSamuel C Eggenberger, Natalie L James, Cherry Ho, et al.

Human Mutation|June 8, 2021

Genome sequencing in congenital cataracts improves diagnostic yieldAlan Ma, John R Grigg, Maree Flaherty, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 6, 2020

Revealing hidden genetic diagnoses in the ocular anterior segment disordersAlan Ma, Saira Yousoof, John R Grigg, et al.

Investigative Ophthalmology & Visual Science|April 14, 2026

ABCA4 Versus PRPH2-Associated Retinopathy: Clinical and Electrophysiological FindingsRachael C Heath Jeffery, Jennifer A Thompson, Johnny Lo, et al.

Nature Genetics|July 29, 2018

Genome-wide association study of intraocular pressure uncovers new pathways to glaucomaStuart MacGregor, Jue-Sheng Ong, Jiyuan An, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 11, 2019

ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorderLloyd B Williams, Asif Javed, Amin Sabri, et al.

Investigative Ophthalmology & Visual Science|May 14, 2024

Retinal Dystrophies Associated With Peripherin-2: Genetic Spectrum and Novel Clinical Observations in 241 PatientsRachael C Heath Jeffery, Jennifer A Thompson, Johnny Lo, et al.

Pageof 15

Search research articles

Showing results (141-150 of 150) with videos related to

Sort By:

Pageof 15

You have reached the last page of results.This site can display upto 150 results.

International Journal of Molecular Sciences|April 12, 2022

Whole Genome Sequencing, Focused Assays and Functional Studies Increasing Understanding in Cryptic Inherited Retinal DystrophiesBenjamin M Nash, Alan Ma, Gladys Ho, et al.

Data in Brief|January 6, 2022

Safety and biocompatibility of a bionic eye: Imaging, intraocular pressure, and histology dataSamuel C Eggenberger, Natalie L James, Cherry Ho, et al.

Human Molecular Genetics|August 2, 2015

Mutations in SIPA1L3 cause eye defects through disruption of cell polarity and cytoskeleton organizationRebecca Greenlees, Marija Mihelec, Saira Yousoof, et al.

Biomaterials|November 12, 2021

Implantation and long-term assessment of the stability and biocompatibility of a novel 98 channel suprachoroidal visual prosthesis in sheepSamuel C Eggenberger, Natalie L James, Cherry Ho, et al.

Human Mutation|June 8, 2021

Genome sequencing in congenital cataracts improves diagnostic yieldAlan Ma, John R Grigg, Maree Flaherty, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 6, 2020

Revealing hidden genetic diagnoses in the ocular anterior segment disordersAlan Ma, Saira Yousoof, John R Grigg, et al.

Investigative Ophthalmology & Visual Science|April 14, 2026

ABCA4 Versus PRPH2-Associated Retinopathy: Clinical and Electrophysiological FindingsRachael C Heath Jeffery, Jennifer A Thompson, Johnny Lo, et al.

Nature Genetics|July 29, 2018

Genome-wide association study of intraocular pressure uncovers new pathways to glaucomaStuart MacGregor, Jue-Sheng Ong, Jiyuan An, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 11, 2019

ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorderLloyd B Williams, Asif Javed, Amin Sabri, et al.

Investigative Ophthalmology & Visual Science|May 14, 2024

Retinal Dystrophies Associated With Peripherin-2: Genetic Spectrum and Novel Clinical Observations in 241 PatientsRachael C Heath Jeffery, Jennifer A Thompson, Johnny Lo, et al.

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