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David A Mackey

Showing results (421-430 of 499) with videos related to

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JAMA Ophthalmology|December 20, 2019
Association of Genetic Variation With KeratoconusBennet J McComish, Srujana Sahebjada, Yelena Bykhovskaya, et al.
American Journal of Human Genetics|January 31, 2012
X-linked megalocornea caused by mutations in CHRDL1 identifies an essential role for ventroptin in anterior segment developmentTom R Webb, Mar Matarin, Jessica C Gardner, et al.
Genome Medicine|September 27, 2017
Key challenges in bringing CRISPR-mediated somatic cell therapy into the clinicDianne Nicol, Lisa Eckstein, Michael Morrison, et al.
Human Molecular Genetics|April 17, 2010
Genome-wide association identifies ATOH7 as a major gene determining human optic disc sizeStuart Macgregor, Alex W Hewitt, Pirro G Hysi, et al.
The Journal of Clinical Investigation|November 7, 2017
Angiopoietin-1 is required for Schlemm's canal development in mice and humansBenjamin R Thomson, Tomokazu Souma, Stuart W Tompson, et al.
Cell Genomics|February 13, 2023
Retinal ganglion cell-specific genetic regulation in primary open-angle glaucomaMaciej Daniszewski, Anne Senabouth, Helena H Liang, et al.
Nature Genetics|September 14, 2010
A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25Pirro G Hysi, Terri L Young, David A Mackey, et al.
Investigative Ophthalmology & Visual Science|May 26, 2007
Heritable features of the optic disc: a novel twin method for determining genetic significanceAlex W Hewitt, Johan P Poulsen, Wallace L M Alward, et al.
American Journal of Human Genetics|December 3, 2013
Recessive mutations in SLC38A8 cause foveal hypoplasia and optic nerve misrouting without albinismJames A Poulter, Musallam Al-Araimi, Ivan Conte, et al.
Nature Genetics|April 2, 2020
Meta-analysis of 542,934 subjects of European ancestry identifies new genes and mechanisms predisposing to refractive error and myopiaPirro G Hysi, Hélène Choquet, Anthony P Khawaja, et al.
Pageof 50

Showing results (421-430 of 499) with videos related to

Sort By:
Pageof 50
JAMA Ophthalmology|December 20, 2019
Association of Genetic Variation With KeratoconusBennet J McComish, Srujana Sahebjada, Yelena Bykhovskaya, et al.
American Journal of Human Genetics|January 31, 2012
X-linked megalocornea caused by mutations in CHRDL1 identifies an essential role for ventroptin in anterior segment developmentTom R Webb, Mar Matarin, Jessica C Gardner, et al.
Genome Medicine|September 27, 2017
Key challenges in bringing CRISPR-mediated somatic cell therapy into the clinicDianne Nicol, Lisa Eckstein, Michael Morrison, et al.
Human Molecular Genetics|April 17, 2010
Genome-wide association identifies ATOH7 as a major gene determining human optic disc sizeStuart Macgregor, Alex W Hewitt, Pirro G Hysi, et al.
The Journal of Clinical Investigation|November 7, 2017
Angiopoietin-1 is required for Schlemm's canal development in mice and humansBenjamin R Thomson, Tomokazu Souma, Stuart W Tompson, et al.
Cell Genomics|February 13, 2023
Retinal ganglion cell-specific genetic regulation in primary open-angle glaucomaMaciej Daniszewski, Anne Senabouth, Helena H Liang, et al.
Nature Genetics|September 14, 2010
A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25Pirro G Hysi, Terri L Young, David A Mackey, et al.
Investigative Ophthalmology & Visual Science|May 26, 2007
Heritable features of the optic disc: a novel twin method for determining genetic significanceAlex W Hewitt, Johan P Poulsen, Wallace L M Alward, et al.
American Journal of Human Genetics|December 3, 2013
Recessive mutations in SLC38A8 cause foveal hypoplasia and optic nerve misrouting without albinismJames A Poulter, Musallam Al-Araimi, Ivan Conte, et al.
Nature Genetics|April 2, 2020
Meta-analysis of 542,934 subjects of European ancestry identifies new genes and mechanisms predisposing to refractive error and myopiaPirro G Hysi, Hélène Choquet, Anthony P Khawaja, et al.
Pageof 50