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Jonathan B Ruddle

Showing results (41-50 of 79) with videos related to

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Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|October 7, 2009
Twins eye study in Tasmania (TEST): rationale and methodology to recruit and examine twinsDavid A Mackey, Jane R Mackinnon, Shayne A Brown, et al.
Disease Models & Mechanisms|December 1, 2022
Lysosomal alterations and decreased electrophysiological activity in CLN3 disease patient-derived cortical neuronsSueanne Chear, Sharn Perry, Richard Wilson, et al.
American Journal of Ophthalmology|October 26, 2010
Associations of birth weight with ocular biometry, refraction, and glaucomatous endophenotypes: the Australian Twins Eye StudyCong Sun, Anne-Louise Ponsonby, Shayne A Brown, et al.
Hypertension (Dallas, Tex. : 1979)|January 14, 2009
Effect of birth parameters on retinal vascular caliber: the Twins Eye Study in TasmaniaCong Sun, Anne-Louise Ponsonby, Tien Y Wong, et al.
Hypertension (Dallas, Tex. : 1979)|August 19, 2009
Quantitative genetic analysis of the retinal vascular caliber: the Australian Twins Eye StudyCong Sun, Gu Zhu, Tien Y Wong, et al.
Ophthalmology|March 5, 2013
Higher prevalence of myocilin mutations in advanced glaucoma in comparison with less advanced disease in an Australasian disease registryEmmanuelle Souzeau, Kathryn P Burdon, Andrew Dubowsky, et al.
Ophthalmology|October 30, 2007
Genetic dissection of myopia: evidence for linkage of ocular axial length to chromosome 5qGu Zhu, Alex W Hewitt, Jonathan B Ruddle, et al.
Molecular Vision|October 26, 2022
The phenotypic spectrum of <i>ADAMTSL4-</i>associated ectopia lentis: Additional cases, complications, and review of literatureLachlan S W Knight, Sean Mullany, Deepa A Taranath, et al.
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.
BMJ Open Ophthalmology|September 26, 2022
Pathogenic genetic variants identified in Australian families with paediatric cataractJohanna L Jones, Bennet J McComish, Sandra E Staffieri, et al.
Pageof 8

Showing results (41-50 of 79) with videos related to

Sort By:
Pageof 8
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|October 7, 2009
Twins eye study in Tasmania (TEST): rationale and methodology to recruit and examine twinsDavid A Mackey, Jane R Mackinnon, Shayne A Brown, et al.
Disease Models & Mechanisms|December 1, 2022
Lysosomal alterations and decreased electrophysiological activity in CLN3 disease patient-derived cortical neuronsSueanne Chear, Sharn Perry, Richard Wilson, et al.
American Journal of Ophthalmology|October 26, 2010
Associations of birth weight with ocular biometry, refraction, and glaucomatous endophenotypes: the Australian Twins Eye StudyCong Sun, Anne-Louise Ponsonby, Shayne A Brown, et al.
Hypertension (Dallas, Tex. : 1979)|January 14, 2009
Effect of birth parameters on retinal vascular caliber: the Twins Eye Study in TasmaniaCong Sun, Anne-Louise Ponsonby, Tien Y Wong, et al.
Hypertension (Dallas, Tex. : 1979)|August 19, 2009
Quantitative genetic analysis of the retinal vascular caliber: the Australian Twins Eye StudyCong Sun, Gu Zhu, Tien Y Wong, et al.
Ophthalmology|March 5, 2013
Higher prevalence of myocilin mutations in advanced glaucoma in comparison with less advanced disease in an Australasian disease registryEmmanuelle Souzeau, Kathryn P Burdon, Andrew Dubowsky, et al.
Ophthalmology|October 30, 2007
Genetic dissection of myopia: evidence for linkage of ocular axial length to chromosome 5qGu Zhu, Alex W Hewitt, Jonathan B Ruddle, et al.
Molecular Vision|October 26, 2022
The phenotypic spectrum of <i>ADAMTSL4-</i>associated ectopia lentis: Additional cases, complications, and review of literatureLachlan S W Knight, Sean Mullany, Deepa A Taranath, et al.
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.
BMJ Open Ophthalmology|September 26, 2022
Pathogenic genetic variants identified in Australian families with paediatric cataractJohanna L Jones, Bennet J McComish, Sandra E Staffieri, et al.
Pageof 8