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Ophthalmology
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September 29, 2022
Vitamin D Supplementation and the Incidence of Cataract Surgery in Older Australian Adults
Sabbir 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 degeneration
Rosie 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 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.
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.
Human Molecular Genetics
|
April 10, 1999
Analysis of myocilin mutations in 1703 glaucoma patients from five different populations
J 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 population
Dimitar N Azmanov, Stanislava Dimitrova, Laura Florez, et al.
Page
of 77
Search research articles
Search
Showing results (641-650 of 763) with videos related to
Sort By:
Page
of 77
Ophthalmology
|
September 29, 2022
Vitamin D Supplementation and the Incidence of Cataract Surgery in Older Australian Adults
Sabbir 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 degeneration
Rosie 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 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.
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.
Human Molecular Genetics
|
April 10, 1999
Analysis of myocilin mutations in 1703 glaucoma patients from five different populations
J 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 population
Dimitar N Azmanov, Stanislava Dimitrova, Laura Florez, et al.
Page
of 77