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Alex W Hewitt

Showing results (261-270 of 425) with videos related to

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American Journal of Human Genetics|October 20, 2021
Establishing risk of vision loss in Leber hereditary optic neuropathyM 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 genesDavid P Dimasi, Jern Y Chen, Alex W Hewitt, et al.
Investigative Ophthalmology & Visual Science|March 26, 2025
Genome-Wide Association Study to Identify Genetic Variants Associated With Diabetic MaculopathyRajya L Gurung, Charvi Nangia, Tengda Cai, et al.
Stem Cell Reviews and Reports|November 22, 2015
Defined Medium Conditions for the Induction and Expansion of Human Pluripotent Stem Cell-Derived Retinal Pigment EpitheliumGrace E Lidgerwood, Shiang Y Lim, Duncan E Crombie, et al.
Psychosomatic Medicine|November 7, 2014
Associations between depression and anxiety symptoms and retinal vessel caliber in adolescents and young adultsMadeline H Meier, Nathan A Gillespie, Narelle K Hansell, et al.
JAMA Ophthalmology|November 10, 2022
Association of High Polygenic Risk With Visual Field Worsening Despite Treatment in Early Primary Open-Angle GlaucomaOwen M Siggs, Ayub Qassim, Xikun Han, et al.
Human Mutation|October 11, 2022
Specifications of the ACMG/AMP variant curation guidelines for myocilin: Recommendations from the clingen glaucoma expert panelKathryn P Burdon, Patricia Graham, Johanna Hadler, et al.
Ophthalmology|August 11, 2016
Risk Alleles Associated with Neovascularization in a Pachychoroid PhenotypeKunal K Dansingani, Lorah T Perlee, Sara Hamon, et al.
Schizophrenia Research|February 20, 2015
Retinal microvessels reflect familial vulnerability to psychotic symptoms: A comparison of twins discordant for psychotic symptoms and controlsMadeline H Meier, Nathan A Gillespie, Narelle K Hansell, et al.
Human Molecular Genetics|December 7, 2019
Genome-wide association analysis of 95 549 individuals identifies novel loci and genes influencing optic disc morphologyXikun Han, Ayub Qassim, Jiyuan An, et al.
Pageof 43

Showing results (261-270 of 425) with videos related to

Sort By:
Pageof 43
American Journal of Human Genetics|October 20, 2021
Establishing risk of vision loss in Leber hereditary optic neuropathyM 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 genesDavid P Dimasi, Jern Y Chen, Alex W Hewitt, et al.
Investigative Ophthalmology & Visual Science|March 26, 2025
Genome-Wide Association Study to Identify Genetic Variants Associated With Diabetic MaculopathyRajya L Gurung, Charvi Nangia, Tengda Cai, et al.
Stem Cell Reviews and Reports|November 22, 2015
Defined Medium Conditions for the Induction and Expansion of Human Pluripotent Stem Cell-Derived Retinal Pigment EpitheliumGrace E Lidgerwood, Shiang Y Lim, Duncan E Crombie, et al.
Psychosomatic Medicine|November 7, 2014
Associations between depression and anxiety symptoms and retinal vessel caliber in adolescents and young adultsMadeline H Meier, Nathan A Gillespie, Narelle K Hansell, et al.
JAMA Ophthalmology|November 10, 2022
Association of High Polygenic Risk With Visual Field Worsening Despite Treatment in Early Primary Open-Angle GlaucomaOwen M Siggs, Ayub Qassim, Xikun Han, et al.
Human Mutation|October 11, 2022
Specifications of the ACMG/AMP variant curation guidelines for myocilin: Recommendations from the clingen glaucoma expert panelKathryn P Burdon, Patricia Graham, Johanna Hadler, et al.
Ophthalmology|August 11, 2016
Risk Alleles Associated with Neovascularization in a Pachychoroid PhenotypeKunal K Dansingani, Lorah T Perlee, Sara Hamon, et al.
Schizophrenia Research|February 20, 2015
Retinal microvessels reflect familial vulnerability to psychotic symptoms: A comparison of twins discordant for psychotic symptoms and controlsMadeline H Meier, Nathan A Gillespie, Narelle K Hansell, et al.
Human Molecular Genetics|December 7, 2019
Genome-wide association analysis of 95 549 individuals identifies novel loci and genes influencing optic disc morphologyXikun Han, Ayub Qassim, Jiyuan An, et al.
Pageof 43