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David A Mackey

Showing results (301-310 of 499) with videos related to

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Ophthalmology Science|October 17, 2022
Atrophy Expansion Rates in Stargardt Disease Using Ultra-Widefield Fundus AutofluorescenceRachael C Heath Jeffery, Jennifer A Thompson, Johnny Lo, et al.
Acta Ophthalmologica|January 10, 2021
Time spent outdoors through childhood and adolescence - assessed by 25-hydroxyvitamin D concentration - and risk of myopia at 20 yearsGareth Lingham, David A Mackey, Kun Zhu, et al.
Investigative Ophthalmology & Visual Science|November 20, 2023
Changes in Refractive Error During Young Adulthood: The Effects of Longitudinal Screen Time, Ocular Sun Exposure, and Genetic PredispositionSamantha Sze-Yee Lee, Gareth Lingham, Carol A Wang, et al.
Frontiers in Genetics|June 23, 2023
A multiethnic genome-wide analysis of 19,420 individuals identifies novel loci associated with axial length and shared genetic influences with refractive error and myopiaChen Jiang, Ronald B Melles, Jie Yin, et al.
Molecular Vision|March 10, 2015
CYP1B1 copy number variation is not a major contributor to primary congenital glaucomaEmmanuelle Souzeau, Melanie Hayes, Jonathan B Ruddle, et al.
Ophthalmic Epidemiology|October 31, 2013
Birth order and myopiaJeremy A Guggenheim, George McMahon, Kate Northstone, et al.
Aging|April 30, 2016
Study of mitochondrial respiratory defects on reprogramming to human induced pluripotent stem cellsSandy S C Hung, Nicole J Van Bergen, Stacey Jackson, et al.
Human Mutation|September 27, 2002
Broad phenotypic variability in a single pedigree with a novel 1410delC mutation in the PST domain of the PAX6 geneMichèle M Sale, Jamie E Craig, Jacinta C Charlesworth, et al.
Investigative Ophthalmology & Visual Science|May 4, 2010
Genetic association of insulin-like growth factor-1 polymorphisms with high-grade myopia in an international family cohortRavikanth Metlapally, Chang-Seok Ki, Yi-Ju Li, et al.
Human Mutation|March 24, 2009
Mutations of the EPHA2 receptor tyrosine kinase gene cause autosomal dominant congenital cataractTianxiao Zhang, Rui Hua, Wei Xiao, et al.
Pageof 50

Showing results (301-310 of 499) with videos related to

Sort By:
Pageof 50
Ophthalmology Science|October 17, 2022
Atrophy Expansion Rates in Stargardt Disease Using Ultra-Widefield Fundus AutofluorescenceRachael C Heath Jeffery, Jennifer A Thompson, Johnny Lo, et al.
Acta Ophthalmologica|January 10, 2021
Time spent outdoors through childhood and adolescence - assessed by 25-hydroxyvitamin D concentration - and risk of myopia at 20 yearsGareth Lingham, David A Mackey, Kun Zhu, et al.
Investigative Ophthalmology & Visual Science|November 20, 2023
Changes in Refractive Error During Young Adulthood: The Effects of Longitudinal Screen Time, Ocular Sun Exposure, and Genetic PredispositionSamantha Sze-Yee Lee, Gareth Lingham, Carol A Wang, et al.
Frontiers in Genetics|June 23, 2023
A multiethnic genome-wide analysis of 19,420 individuals identifies novel loci associated with axial length and shared genetic influences with refractive error and myopiaChen Jiang, Ronald B Melles, Jie Yin, et al.
Molecular Vision|March 10, 2015
CYP1B1 copy number variation is not a major contributor to primary congenital glaucomaEmmanuelle Souzeau, Melanie Hayes, Jonathan B Ruddle, et al.
Ophthalmic Epidemiology|October 31, 2013
Birth order and myopiaJeremy A Guggenheim, George McMahon, Kate Northstone, et al.
Aging|April 30, 2016
Study of mitochondrial respiratory defects on reprogramming to human induced pluripotent stem cellsSandy S C Hung, Nicole J Van Bergen, Stacey Jackson, et al.
Human Mutation|September 27, 2002
Broad phenotypic variability in a single pedigree with a novel 1410delC mutation in the PST domain of the PAX6 geneMichèle M Sale, Jamie E Craig, Jacinta C Charlesworth, et al.
Investigative Ophthalmology & Visual Science|May 4, 2010
Genetic association of insulin-like growth factor-1 polymorphisms with high-grade myopia in an international family cohortRavikanth Metlapally, Chang-Seok Ki, Yi-Ju Li, et al.
Human Mutation|March 24, 2009
Mutations of the EPHA2 receptor tyrosine kinase gene cause autosomal dominant congenital cataractTianxiao Zhang, Rui Hua, Wei Xiao, et al.
Pageof 50