Search research articles
Contact Us
Filters
Showing results (341-350 of 499) with videos related to
Page
of 50
Sort By:
Nature Communications
|
October 22, 2024
Uncovering genetic loci and biological pathways associated with age-related cataracts through GWAS meta-analysis
Santiago Diaz-Torres, Samantha Sze-Yee Lee, Luis M García-Marín, et al.
European Journal of Human Genetics : EJHG
|
May 29, 2002
Mutations in a protein target of the Pim-1 kinase associated with the RP9 form of autosomal dominant retinitis pigmentosa
T Jeffrey Keen, Matthew M Hims, Arthur B McKie, et al.
Clinical & Experimental Ophthalmology
|
September 2, 2022
Low-concentration atropine eyedrops for myopia control in a multi-racial cohort of Australian children: A randomised clinical trial
Samantha Sze-Yee Lee, Gareth Lingham, Magdalena Blaszkowska, et al.
Molecular Vision
|
April 10, 2007
Investigation of founder effects for the Thr377Met Myocilin mutation in glaucoma families from differing ethnic backgrounds
Alex W Hewitt, John R Samples, R Rand Allingham, et al.
Investigative Ophthalmology & Visual Science
|
February 21, 2013
Association mapping of the high-grade myopia MYP3 locus reveals novel candidates UHRF1BP1L, PTPRR, and PPFIA2
Felicia Hawthorne, Sheng Feng, Ravikanth Metlapally, et al.
Scientific Reports
|
June 1, 2016
Assessment of polygenic effects links primary open-angle glaucoma and age-related macular degeneration
Gabriel Cuellar-Partida, Jamie E Craig, Kathryn P Burdon, et al.
G3 (Bethesda, Md.)
|
August 26, 2017
High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern Australia
Shari Javadiyan, Jamie E Craig, Emmanuelle Souzeau, et al.
Investigative Ophthalmology & Visual Science
|
June 15, 2022
Axial Length Distributions in Patients With Genetically Confirmed Inherited Retinal Diseases
Katie M Williams, Michalis Georgiou, Angelos Kalitzeos, et al.
American Journal of Human Genetics
|
October 20, 2021
Establishing risk of vision loss in Leber hereditary optic neuropathy
M Isabel G Lopez Sanchez, Lisa S Kearns, Sandra E Staffieri, et al.
Human Genetics
|
August 29, 2009
Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genes
David P Dimasi, Jern Y Chen, Alex W Hewitt, et al.
Page
of 50
Search research articles
Search
Showing results (341-350 of 499) with videos related to
Sort By:
Page
of 50
Nature Communications
|
October 22, 2024
Uncovering genetic loci and biological pathways associated with age-related cataracts through GWAS meta-analysis
Santiago Diaz-Torres, Samantha Sze-Yee Lee, Luis M García-Marín, et al.
European Journal of Human Genetics : EJHG
|
May 29, 2002
Mutations in a protein target of the Pim-1 kinase associated with the RP9 form of autosomal dominant retinitis pigmentosa
T Jeffrey Keen, Matthew M Hims, Arthur B McKie, et al.
Clinical & Experimental Ophthalmology
|
September 2, 2022
Low-concentration atropine eyedrops for myopia control in a multi-racial cohort of Australian children: A randomised clinical trial
Samantha Sze-Yee Lee, Gareth Lingham, Magdalena Blaszkowska, et al.
Molecular Vision
|
April 10, 2007
Investigation of founder effects for the Thr377Met Myocilin mutation in glaucoma families from differing ethnic backgrounds
Alex W Hewitt, John R Samples, R Rand Allingham, et al.
Investigative Ophthalmology & Visual Science
|
February 21, 2013
Association mapping of the high-grade myopia MYP3 locus reveals novel candidates UHRF1BP1L, PTPRR, and PPFIA2
Felicia Hawthorne, Sheng Feng, Ravikanth Metlapally, et al.
Scientific Reports
|
June 1, 2016
Assessment of polygenic effects links primary open-angle glaucoma and age-related macular degeneration
Gabriel Cuellar-Partida, Jamie E Craig, Kathryn P Burdon, et al.
G3 (Bethesda, Md.)
|
August 26, 2017
High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern Australia
Shari Javadiyan, Jamie E Craig, Emmanuelle Souzeau, et al.
Investigative Ophthalmology & Visual Science
|
June 15, 2022
Axial Length Distributions in Patients With Genetically Confirmed Inherited Retinal Diseases
Katie M Williams, Michalis Georgiou, Angelos Kalitzeos, et al.
American Journal of Human Genetics
|
October 20, 2021
Establishing risk of vision loss in Leber hereditary optic neuropathy
M Isabel G Lopez Sanchez, Lisa S Kearns, Sandra E Staffieri, et al.
Human Genetics
|
August 29, 2009
Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genes
David P Dimasi, Jern Y Chen, Alex W Hewitt, et al.
Page
of 50