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A Mackey

Showing results (641-650 of 763) with videos related to

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Ophthalmology|September 29, 2022
Vitamin D Supplementation and the Incidence of Cataract Surgery in Older Australian AdultsSabbir T Rahman, Mary Waterhouse, Briony Duarte Romero, et al.
Ebiomedicine|April 13, 2023
A new polygenic score for refractive error improves detection of children at risk of high myopia but not the prediction of those at risk of myopic macular degenerationRosie Clark, Samantha Sze-Yee Lee, Ran Du, et al.
Investigative Ophthalmology & Visual Science|March 11, 2017
Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle GlaucomaTiger Zhou, Emmanuelle Souzeau, Owen M Siggs, et al.
American Journal of Human Genetics|March 17, 2004
Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11qCarmel Toomes, Helen M Bottomley, Richard M Jackson, et al.
JAMA Ophthalmology|May 8, 2015
Occurrence of CYP1B1 Mutations in Juvenile Open-Angle Glaucoma With Advanced Visual Field LossEmmanuelle Souzeau, Melanie Hayes, Tiger Zhou, et al.
Ebiomedicine|May 18, 2023
Disentangling the genetic overlap and causal relationships between primary open-angle glaucoma, brain morphology and four major neurodegenerative disordersSantiago Diaz-Torres, Weixiong He, Jackson Thorp, et al.
Plos One|March 7, 2017
Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucomaTiger Zhou, Emmanuelle Souzeau, Shiwani Sharma, et al.
Human Molecular Genetics|April 10, 1999
Analysis of myocilin mutations in 1703 glaucoma patients from five different populationsJ H Fingert, E Héon, J M Liebmann, et al.
American Journal of Human Genetics|December 24, 2022
Is the disease risk and penetrance in Leber hereditary optic neuropathy actually low?David A Mackey, Jue-Sheng Ong, Stuart MacGregor, et al.
European Journal of Human Genetics : EJHG|November 18, 2010
LTBP2 and CYP1B1 mutations and associated ocular phenotypes in the Roma/Gypsy founder populationDimitar N Azmanov, Stanislava Dimitrova, Laura Florez, et al.
Pageof 77

Showing results (641-650 of 763) with videos related to

Sort By:
Pageof 77
Ophthalmology|September 29, 2022
Vitamin D Supplementation and the Incidence of Cataract Surgery in Older Australian AdultsSabbir T Rahman, Mary Waterhouse, Briony Duarte Romero, et al.
Ebiomedicine|April 13, 2023
A new polygenic score for refractive error improves detection of children at risk of high myopia but not the prediction of those at risk of myopic macular degenerationRosie Clark, Samantha Sze-Yee Lee, Ran Du, et al.
Investigative Ophthalmology & Visual Science|March 11, 2017
Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle GlaucomaTiger Zhou, Emmanuelle Souzeau, Owen M Siggs, et al.
American Journal of Human Genetics|March 17, 2004
Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11qCarmel Toomes, Helen M Bottomley, Richard M Jackson, et al.
JAMA Ophthalmology|May 8, 2015
Occurrence of CYP1B1 Mutations in Juvenile Open-Angle Glaucoma With Advanced Visual Field LossEmmanuelle Souzeau, Melanie Hayes, Tiger Zhou, et al.
Ebiomedicine|May 18, 2023
Disentangling the genetic overlap and causal relationships between primary open-angle glaucoma, brain morphology and four major neurodegenerative disordersSantiago Diaz-Torres, Weixiong He, Jackson Thorp, et al.
Plos One|March 7, 2017
Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucomaTiger Zhou, Emmanuelle Souzeau, Shiwani Sharma, et al.
Human Molecular Genetics|April 10, 1999
Analysis of myocilin mutations in 1703 glaucoma patients from five different populationsJ H Fingert, E Héon, J M Liebmann, et al.
American Journal of Human Genetics|December 24, 2022
Is the disease risk and penetrance in Leber hereditary optic neuropathy actually low?David A Mackey, Jue-Sheng Ong, Stuart MacGregor, et al.
European Journal of Human Genetics : EJHG|November 18, 2010
LTBP2 and CYP1B1 mutations and associated ocular phenotypes in the Roma/Gypsy founder populationDimitar N Azmanov, Stanislava Dimitrova, Laura Florez, et al.
Pageof 77