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Robyn V Jamieson

Showing results (21-30 of 78) with videos related to

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Ophthalmic Genetics|June 10, 2025
Longitudinal study in autosomal recessive <i>PROM1</i> inherited retinal diseaseWilliam B Yates, John R Grigg, Benjamin M Nash, et al.
Human Mutation|May 11, 2021
Identification of missense MAB21L1 variants in microphthalmia and aniridiaSarah E Seese, Linda M Reis, Brett Deml, et al.
Ophthalmic Genetics|October 16, 2025
<i>NRL</i>-associated autosomal recessive retinopathy: novel variants expanding the phenotype, natural history and a comprehensive literature searchMarium Raza, Elisa E Cornish, Chris Ovens, et al.
Ophthalmic Genetics|September 27, 2007
PAX6 mutations may be associated with high myopiaAlex W Hewitt, Lisa S Kearns, Robyn V Jamieson, et al.
European Journal of Human Genetics : EJHG|November 30, 2017
NMNAT1 variants cause cone and cone-rod dystrophyBenjamin M Nash, Richard Symes, Himanshu Goel, et al.
Investigative Ophthalmology & Visual Science|June 25, 2010
Twist2: role in corneal stromal keratocyte proliferation and corneal thicknessLinda Weaving, Marija Mihelec, Rebecca Storen, et al.
Eye (London, England)|April 22, 2020
Outcome measures in juvenile X-linked retinoschisis: A systematic reviewJohn R Grigg, Claire Y Hooper, Clare L Fraser, et al.
Ophthalmology Science|October 17, 2022
Patient-Reported Health-Related Quality of Life in Individuals with Inherited Retinal DiseasesDeborah Schofield, Joshua Kraindler, Owen Tan, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|September 29, 2023
A natural history study of autosomal dominant GUCY2D-associated cone-rod dystrophyAmanda J Scopelliti, Robyn V Jamieson, Elizabeth H Barnes, et al.
Eye (London, England)|January 17, 2025
Hardy-Rand-Rittler colour vision testing in cone and cone-rod dystrophies: correlation with structural and functional outcome measuresBrindhan Tharmarajah, Elisa E Cornish, Jonathan Nguyen, et al.
Pageof 8

Showing results (21-30 of 78) with videos related to

Sort By:
Pageof 8
Ophthalmic Genetics|June 10, 2025
Longitudinal study in autosomal recessive <i>PROM1</i> inherited retinal diseaseWilliam B Yates, John R Grigg, Benjamin M Nash, et al.
Human Mutation|May 11, 2021
Identification of missense MAB21L1 variants in microphthalmia and aniridiaSarah E Seese, Linda M Reis, Brett Deml, et al.
Ophthalmic Genetics|October 16, 2025
<i>NRL</i>-associated autosomal recessive retinopathy: novel variants expanding the phenotype, natural history and a comprehensive literature searchMarium Raza, Elisa E Cornish, Chris Ovens, et al.
Ophthalmic Genetics|September 27, 2007
PAX6 mutations may be associated with high myopiaAlex W Hewitt, Lisa S Kearns, Robyn V Jamieson, et al.
European Journal of Human Genetics : EJHG|November 30, 2017
NMNAT1 variants cause cone and cone-rod dystrophyBenjamin M Nash, Richard Symes, Himanshu Goel, et al.
Investigative Ophthalmology & Visual Science|June 25, 2010
Twist2: role in corneal stromal keratocyte proliferation and corneal thicknessLinda Weaving, Marija Mihelec, Rebecca Storen, et al.
Eye (London, England)|April 22, 2020
Outcome measures in juvenile X-linked retinoschisis: A systematic reviewJohn R Grigg, Claire Y Hooper, Clare L Fraser, et al.
Ophthalmology Science|October 17, 2022
Patient-Reported Health-Related Quality of Life in Individuals with Inherited Retinal DiseasesDeborah Schofield, Joshua Kraindler, Owen Tan, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|September 29, 2023
A natural history study of autosomal dominant GUCY2D-associated cone-rod dystrophyAmanda J Scopelliti, Robyn V Jamieson, Elizabeth H Barnes, et al.
Eye (London, England)|January 17, 2025
Hardy-Rand-Rittler colour vision testing in cone and cone-rod dystrophies: correlation with structural and functional outcome measuresBrindhan Tharmarajah, Elisa E Cornish, Jonathan Nguyen, et al.
Pageof 8