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A Mackey

Showing results (661-670 of 763) with videos related to

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Plos Genetics|May 21, 2010
Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thicknessYi Lu, David P Dimasi, Pirro G Hysi, et al.
Neuropsychologia|October 1, 2008
Genetic influences on handedness: data from 25,732 Australian and Dutch twin familiesSarah E Medland, David L Duffy, Margaret J Wright, et al.
JAMA Ophthalmology|September 30, 2018
Myocilin Gene Gln368Ter Variant Penetrance and Association With Glaucoma in Population-Based and Registry-Based StudiesXikun Han, Emmanuelle Souzeau, Jue-Sheng Ong, et al.
JAMA Ophthalmology|April 8, 2021
Evaluation of Shared Genetic Susceptibility to High and Low Myopia and HyperopiaJ Willem L Tideman, Olavi Pärssinen, Annechien E G Haarman, et al.
Analytical and Bioanalytical Chemistry|February 1, 2007
Development and certification of the new SRM 695 trace elements in multi-nutrient fertilizerE A Mackey, M P Cronise, C N Fales, et al.
Clinical & Experimental Ophthalmology|December 17, 2011
Australian and New Zealand Registry of Advanced Glaucoma: methodology and recruitmentEmmanuelle Souzeau, Ivan Goldberg, Paul R Healey, et al.
JAMA Ophthalmology|January 18, 2019
Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital GlaucomaOwen M Siggs, Emmanuelle Souzeau, Francesca Pasutto, et al.
American Journal of Human Genetics|October 28, 2005
Mutations in TCF8 cause posterior polymorphous corneal dystrophy and ectopic expression of COL4A3 by corneal endothelial cellsCharles M Krafchak, Hemant Pawar, Sayoko E Moroi, et al.
Nature Communications|August 23, 2025
Large-scale GWAS of strabismus identifies risk loci and provides support for a link with maternal smokingWeixiong He, Peter J van der Most, Jue-Sheng Ong, et al.
Human Mutation|May 12, 2017
Haplotype reference consortium panel: Practical implications of imputations with large reference panelsAdriana I Iglesias, Sven J van der Lee, Pieter W M Bonnemaijer, et al.
Pageof 77

Showing results (661-670 of 763) with videos related to

Sort By:
Pageof 77
Plos Genetics|May 21, 2010
Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thicknessYi Lu, David P Dimasi, Pirro G Hysi, et al.
Neuropsychologia|October 1, 2008
Genetic influences on handedness: data from 25,732 Australian and Dutch twin familiesSarah E Medland, David L Duffy, Margaret J Wright, et al.
JAMA Ophthalmology|September 30, 2018
Myocilin Gene Gln368Ter Variant Penetrance and Association With Glaucoma in Population-Based and Registry-Based StudiesXikun Han, Emmanuelle Souzeau, Jue-Sheng Ong, et al.
JAMA Ophthalmology|April 8, 2021
Evaluation of Shared Genetic Susceptibility to High and Low Myopia and HyperopiaJ Willem L Tideman, Olavi Pärssinen, Annechien E G Haarman, et al.
Analytical and Bioanalytical Chemistry|February 1, 2007
Development and certification of the new SRM 695 trace elements in multi-nutrient fertilizerE A Mackey, M P Cronise, C N Fales, et al.
Clinical & Experimental Ophthalmology|December 17, 2011
Australian and New Zealand Registry of Advanced Glaucoma: methodology and recruitmentEmmanuelle Souzeau, Ivan Goldberg, Paul R Healey, et al.
JAMA Ophthalmology|January 18, 2019
Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital GlaucomaOwen M Siggs, Emmanuelle Souzeau, Francesca Pasutto, et al.
American Journal of Human Genetics|October 28, 2005
Mutations in TCF8 cause posterior polymorphous corneal dystrophy and ectopic expression of COL4A3 by corneal endothelial cellsCharles M Krafchak, Hemant Pawar, Sayoko E Moroi, et al.
Nature Communications|August 23, 2025
Large-scale GWAS of strabismus identifies risk loci and provides support for a link with maternal smokingWeixiong He, Peter J van der Most, Jue-Sheng Ong, et al.
Human Mutation|May 12, 2017
Haplotype reference consortium panel: Practical implications of imputations with large reference panelsAdriana I Iglesias, Sven J van der Lee, Pieter W M Bonnemaijer, et al.
Pageof 77