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Jamie E Craig

Showing results (261-270 of 352) with videos related to

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Investigative Ophthalmology & Visual Science|July 20, 2019
Determining Possible Shared Genetic Architecture Between Myopia and Primary Open-Angle GlaucomaAdriana I Iglesias, Jue Sheng Ong, Anthony P Khawaja, et al.
Investigative Ophthalmology & Visual Science|July 2, 2016
Genetic Association at the 9p21 Glaucoma Locus Contributes to Sex Bias in Normal-Tension GlaucomaSoo Khai Ng, Kathryn P Burdon, Jude T Fitzgerald, et al.
Ophthalmology|July 31, 2020
Cardiovascular Disease Predicts Structural and Functional Progression in Early GlaucomaHenry Marshall, Sean Mullany, Ayub Qassim, 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.
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.
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.
Human Molecular Genetics|December 19, 2018
Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucomaAdrian A Lahola-Chomiak, Tim Footz, Kim Nguyen-Phuoc, et al.
Pageof 36

Showing results (261-270 of 352) with videos related to

Sort By:
Pageof 36
Investigative Ophthalmology & Visual Science|July 20, 2019
Determining Possible Shared Genetic Architecture Between Myopia and Primary Open-Angle GlaucomaAdriana I Iglesias, Jue Sheng Ong, Anthony P Khawaja, et al.
Investigative Ophthalmology & Visual Science|July 2, 2016
Genetic Association at the 9p21 Glaucoma Locus Contributes to Sex Bias in Normal-Tension GlaucomaSoo Khai Ng, Kathryn P Burdon, Jude T Fitzgerald, et al.
Ophthalmology|July 31, 2020
Cardiovascular Disease Predicts Structural and Functional Progression in Early GlaucomaHenry Marshall, Sean Mullany, Ayub Qassim, 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.
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.
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.
Human Molecular Genetics|December 19, 2018
Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucomaAdrian A Lahola-Chomiak, Tim Footz, Kim Nguyen-Phuoc, et al.
Pageof 36