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Jonathan B Ruddle

Showing results (71-80 of 79) with videos related to

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American Journal of Human Genetics|January 31, 2012
X-linked megalocornea caused by mutations in CHRDL1 identifies an essential role for ventroptin in anterior segment developmentTom R Webb, Mar Matarin, Jessica C Gardner, et al.
Human Molecular Genetics|April 17, 2010
Genome-wide association identifies ATOH7 as a major gene determining human optic disc sizeStuart Macgregor, Alex W Hewitt, Pirro G Hysi, et al.
Plos Genetics|April 28, 2020
Mutations in SPATA13/ASEF2 cause primary angle closure glaucomaNaushin H Waseem, Sancy Low, Amna Z Shah, et al.
Nature Genetics|July 29, 2018
Genome-wide association study of intraocular pressure uncovers new pathways to glaucomaStuart MacGregor, Jue-Sheng Ong, Jiyuan An, et al.
The Journal of Clinical Investigation|June 9, 2016
Angiopoietin receptor TEK mutations underlie primary congenital glaucoma with variable expressivityTomokazu Souma, Stuart W Tompson, Benjamin R Thomson, et al.
Nature Genetics|September 1, 2014
Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucomaPuya Gharahkhani, Kathryn P Burdon, Rhys Fogarty, et al.
Investigative Ophthalmology & Visual Science|May 14, 2024
Retinal Dystrophies Associated With Peripherin-2: Genetic Spectrum and Novel Clinical Observations in 241 PatientsRachael C Heath Jeffery, Jennifer A Thompson, Johnny Lo, et al.
Cell|January 16, 2010
Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidanceMax A Tischfield, Hagit N Baris, Chen Wu, et al.
Nature Genetics|January 22, 2020
Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progressionJamie E Craig, Xikun Han, Ayub Qassim, et al.
Pageof 8

Showing results (71-80 of 79) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 79 results.
American Journal of Human Genetics|January 31, 2012
X-linked megalocornea caused by mutations in CHRDL1 identifies an essential role for ventroptin in anterior segment developmentTom R Webb, Mar Matarin, Jessica C Gardner, et al.
Human Molecular Genetics|April 17, 2010
Genome-wide association identifies ATOH7 as a major gene determining human optic disc sizeStuart Macgregor, Alex W Hewitt, Pirro G Hysi, et al.
Plos Genetics|April 28, 2020
Mutations in SPATA13/ASEF2 cause primary angle closure glaucomaNaushin H Waseem, Sancy Low, Amna Z Shah, et al.
Nature Genetics|July 29, 2018
Genome-wide association study of intraocular pressure uncovers new pathways to glaucomaStuart MacGregor, Jue-Sheng Ong, Jiyuan An, et al.
The Journal of Clinical Investigation|June 9, 2016
Angiopoietin receptor TEK mutations underlie primary congenital glaucoma with variable expressivityTomokazu Souma, Stuart W Tompson, Benjamin R Thomson, et al.
Nature Genetics|September 1, 2014
Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucomaPuya Gharahkhani, Kathryn P Burdon, Rhys Fogarty, et al.
Investigative Ophthalmology & Visual Science|May 14, 2024
Retinal Dystrophies Associated With Peripherin-2: Genetic Spectrum and Novel Clinical Observations in 241 PatientsRachael C Heath Jeffery, Jennifer A Thompson, Johnny Lo, et al.
Cell|January 16, 2010
Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidanceMax A Tischfield, Hagit N Baris, Chen Wu, et al.
Nature Genetics|January 22, 2020
Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progressionJamie E Craig, Xikun Han, Ayub Qassim, et al.
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