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Investigative Ophthalmology & Visual Science
|
July 20, 2019
Determining Possible Shared Genetic Architecture Between Myopia and Primary Open-Angle Glaucoma
Adriana 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 Glaucoma
Soo Khai Ng, Kathryn P Burdon, Jude T Fitzgerald, et al.
Ophthalmology
|
July 31, 2020
Cardiovascular Disease Predicts Structural and Functional Progression in Early Glaucoma
Henry 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 Loss
Emmanuelle 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 disorders
Santiago 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 glaucoma
Tiger 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 Glaucoma
Tiger 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 11q
Carmel 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 glaucoma
Adrian A Lahola-Chomiak, Tim Footz, Kim Nguyen-Phuoc, et al.
Page
of 36
Search research articles
Search
Showing results (261-270 of 352) with videos related to
Sort By:
Page
of 36
Investigative Ophthalmology & Visual Science
|
July 20, 2019
Determining Possible Shared Genetic Architecture Between Myopia and Primary Open-Angle Glaucoma
Adriana 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 Glaucoma
Soo Khai Ng, Kathryn P Burdon, Jude T Fitzgerald, et al.
Ophthalmology
|
July 31, 2020
Cardiovascular Disease Predicts Structural and Functional Progression in Early Glaucoma
Henry 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 Loss
Emmanuelle 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 disorders
Santiago 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 glaucoma
Tiger 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 Glaucoma
Tiger 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 11q
Carmel 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 glaucoma
Adrian A Lahola-Chomiak, Tim Footz, Kim Nguyen-Phuoc, et al.
Page
of 36