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Kathryn P Burdon

Showing results (1-10 of 185) with videos related to

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Clinical & Experimental Ophthalmology|December 17, 2011
Genome-wide association studies in the hunt for genes causing primary open-angle glaucoma: a reviewKathryn P Burdon
Clinical & Experimental Ophthalmology|July 7, 2021
The utility of genomic testing in the ophthalmology clinic: A reviewKathryn P Burdon
Clinical & Experimental Optometry|February 8, 2013
Insights into keratoconus from a genetic perspectiveKathryn P Burdon, Andrea L Vincent
Annual Review of Vision Science|April 23, 2020
Genetic and Environmental Risk Factors for KeratoconusSionne E M Lucas, Kathryn P Burdon
Methods in Molecular Biology (Clifton, N.J.)|June 16, 2023
A Guide to Genome-Wide Association Study Design for Diabetic RetinopathyRajya L Gurung, Kathryn P Burdon, Bennet J McComish
Diabetes|July 10, 2009
A systematic meta-analysis of genetic association studies for diabetic retinopathySotoodeh Abhary, Alex W Hewitt, Kathryn P Burdon, et al.
Clinical & Experimental Ophthalmology|October 12, 2013
Chromosome 9p21 primary open-angle glaucoma susceptibility locus: a reviewSoo Khai Ng, Robert J Casson, Kathryn P Burdon, et al.
Frontiers in Immunology|April 4, 2019
The Association Between Vitamin D and Multiple Sclerosis Risk: 1,25(OH)<sub>2</sub>D<sub>3</sub> Induces Super-Enhancers Bound by VDRMing Lu, Bennet J McComish, Kathryn P Burdon, et al.
Gene|April 10, 2013
A Turkish family with Nance-Horan Syndrome due to a novel mutationEsra Tug, Nihal F Dilek, Shahrbanou Javadiyan, et al.
Ophthalmic Genetics|April 21, 2016
Ferritin light chain gene mutation in a large Australian family with hereditary hyperferritinemia-cataract syndromeSeyhan Yazar, Maria Franchina, Jamie E Craig, et al.
Pageof 19

Showing results (1-10 of 185) with videos related to

Sort By:
Pageof 19
Clinical & Experimental Ophthalmology|December 17, 2011
Genome-wide association studies in the hunt for genes causing primary open-angle glaucoma: a reviewKathryn P Burdon
Clinical & Experimental Ophthalmology|July 7, 2021
The utility of genomic testing in the ophthalmology clinic: A reviewKathryn P Burdon
Clinical & Experimental Optometry|February 8, 2013
Insights into keratoconus from a genetic perspectiveKathryn P Burdon, Andrea L Vincent
Annual Review of Vision Science|April 23, 2020
Genetic and Environmental Risk Factors for KeratoconusSionne E M Lucas, Kathryn P Burdon
Methods in Molecular Biology (Clifton, N.J.)|June 16, 2023
A Guide to Genome-Wide Association Study Design for Diabetic RetinopathyRajya L Gurung, Kathryn P Burdon, Bennet J McComish
Diabetes|July 10, 2009
A systematic meta-analysis of genetic association studies for diabetic retinopathySotoodeh Abhary, Alex W Hewitt, Kathryn P Burdon, et al.
Clinical & Experimental Ophthalmology|October 12, 2013
Chromosome 9p21 primary open-angle glaucoma susceptibility locus: a reviewSoo Khai Ng, Robert J Casson, Kathryn P Burdon, et al.
Frontiers in Immunology|April 4, 2019
The Association Between Vitamin D and Multiple Sclerosis Risk: 1,25(OH)<sub>2</sub>D<sub>3</sub> Induces Super-Enhancers Bound by VDRMing Lu, Bennet J McComish, Kathryn P Burdon, et al.
Gene|April 10, 2013
A Turkish family with Nance-Horan Syndrome due to a novel mutationEsra Tug, Nihal F Dilek, Shahrbanou Javadiyan, et al.
Ophthalmic Genetics|April 21, 2016
Ferritin light chain gene mutation in a large Australian family with hereditary hyperferritinemia-cataract syndromeSeyhan Yazar, Maria Franchina, Jamie E Craig, et al.
Pageof 19