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Investigative Ophthalmology & Visual Science
|
June 29, 2021
Characterization of the Spectrum of Ophthalmic Changes in Patients With Alagille Syndrome
Mariana Matioli da Palma, Austin D Igelman, Cristy Ku, et al.
Nature Communications
|
May 3, 2025
Rare genetic variation in PTPRB is associated with central serous chorioretinopathy, varicose veins and glaucoma
Joel T Rämö, Bryan R Gorman, Lu-Chen Weng, et al.
Brain : a Journal of Neurology
|
July 19, 2022
Variant-specific changes in RAC3 function disrupt corticogenesis in neurodevelopmental phenotypes
Marcello Scala, Masashi Nishikawa, Hidenori Ito, et al.
Annals of Internal Medicine
|
July 21, 2004
Benefits and harms of doxycycline treatment for Gulf War veterans' illnesses: a randomized, double-blind, placebo-controlled trial
Sam T Donta, Charles C Engel, Joseph F Collins, et al.
American Journal of Epidemiology
|
April 19, 2011
Variations in apolipoprotein E frequency with age in a pooled analysis of a large group of older people
Gareth J McKay, Giuliana Silvestri, Usha Chakravarthy, et al.
NPJ Genomic Medicine
|
April 17, 2025
Variants in CFAP410 cause a range of retinal and skeletal phenotypes
Ryan E Schmidt, Amy E Pohodich, David Birch, et al.
Human Mutation
|
September 2, 2011
Evidence of association of APOE with age-related macular degeneration: a pooled analysis of 15 studies
Gareth J McKay, Chris C Patterson, Usha Chakravarthy, et al.
International Journal of Epidemiology
|
January 19, 2012
Complement factor H genetic variant and age-related macular degeneration: effect size, modifiers and relationship to disease subtype
Reecha Sofat, Juan P Casas, Andrew R Webster, et al.
Nature Genetics
|
September 17, 2013
Identification of a rare coding variant in complement 3 associated with age-related macular degeneration
Xiaowei Zhan, David E Larson, Chaolong Wang, et al.
Biomolecules
|
March 28, 2024
Towards Uncovering the Role of Incomplete Penetrance in Maculopathies through Sequencing of 105 Disease-Associated Genes
Rebekkah J Hitti-Malin, Daan M Panneman, Zelia Corradi, et al.
Page
of 18
Search research articles
Search
Showing results (161-170 of 175) with videos related to
Sort By:
Page
of 18
Investigative Ophthalmology & Visual Science
|
June 29, 2021
Characterization of the Spectrum of Ophthalmic Changes in Patients With Alagille Syndrome
Mariana Matioli da Palma, Austin D Igelman, Cristy Ku, et al.
Nature Communications
|
May 3, 2025
Rare genetic variation in PTPRB is associated with central serous chorioretinopathy, varicose veins and glaucoma
Joel T Rämö, Bryan R Gorman, Lu-Chen Weng, et al.
Brain : a Journal of Neurology
|
July 19, 2022
Variant-specific changes in RAC3 function disrupt corticogenesis in neurodevelopmental phenotypes
Marcello Scala, Masashi Nishikawa, Hidenori Ito, et al.
Annals of Internal Medicine
|
July 21, 2004
Benefits and harms of doxycycline treatment for Gulf War veterans' illnesses: a randomized, double-blind, placebo-controlled trial
Sam T Donta, Charles C Engel, Joseph F Collins, et al.
American Journal of Epidemiology
|
April 19, 2011
Variations in apolipoprotein E frequency with age in a pooled analysis of a large group of older people
Gareth J McKay, Giuliana Silvestri, Usha Chakravarthy, et al.
NPJ Genomic Medicine
|
April 17, 2025
Variants in CFAP410 cause a range of retinal and skeletal phenotypes
Ryan E Schmidt, Amy E Pohodich, David Birch, et al.
Human Mutation
|
September 2, 2011
Evidence of association of APOE with age-related macular degeneration: a pooled analysis of 15 studies
Gareth J McKay, Chris C Patterson, Usha Chakravarthy, et al.
International Journal of Epidemiology
|
January 19, 2012
Complement factor H genetic variant and age-related macular degeneration: effect size, modifiers and relationship to disease subtype
Reecha Sofat, Juan P Casas, Andrew R Webster, et al.
Nature Genetics
|
September 17, 2013
Identification of a rare coding variant in complement 3 associated with age-related macular degeneration
Xiaowei Zhan, David E Larson, Chaolong Wang, et al.
Biomolecules
|
March 28, 2024
Towards Uncovering the Role of Incomplete Penetrance in Maculopathies through Sequencing of 105 Disease-Associated Genes
Rebekkah J Hitti-Malin, Daan M Panneman, Zelia Corradi, et al.
Page
of 18