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Rinki Ratnapriya

Showing results (51-60 of 56) with videos related to

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Human Molecular Genetics|April 5, 2020
Family-based exome sequencing identifies rare coding variants in age-related macular degenerationRinki Ratnapriya, İlhan E Acar, Maartje J Geerlings, et al.
Scientific Reports|August 27, 2015
Whole Exome Sequencing Reveals Mutations in Known Retinal Disease Genes in 33 out of 68 Israeli Families with Inherited RetinopathiesAvigail Beryozkin, Elia Shevah, Adva Kimchi, et al.
Ophthalmology|April 17, 2017
Whole-Exome Sequencing Identifies Biallelic IDH3A Variants as a Cause of Retinitis Pigmentosa Accompanied by PseudocolobomaLaurence H M Pierrache, Adva Kimchi, Rinki Ratnapriya, et al.
Nature Genetics|September 17, 2013
Identification of a rare coding variant in complement 3 associated with age-related macular degenerationXiaowei Zhan, David E Larson, Chaolong Wang, et al.
Human Molecular Genetics|June 6, 2014
Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degenerationRinki Ratnapriya, Xiaowei Zhan, Robert N Fariss, et al.
Nature Genetics|December 23, 2015
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variantsLars G Fritsche, Wilmar Igl, Jessica N Cooke Bailey, et al.
Pageof 6

Showing results (51-60 of 56) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 56 results.
Human Molecular Genetics|April 5, 2020
Family-based exome sequencing identifies rare coding variants in age-related macular degenerationRinki Ratnapriya, İlhan E Acar, Maartje J Geerlings, et al.
Scientific Reports|August 27, 2015
Whole Exome Sequencing Reveals Mutations in Known Retinal Disease Genes in 33 out of 68 Israeli Families with Inherited RetinopathiesAvigail Beryozkin, Elia Shevah, Adva Kimchi, et al.
Ophthalmology|April 17, 2017
Whole-Exome Sequencing Identifies Biallelic IDH3A Variants as a Cause of Retinitis Pigmentosa Accompanied by PseudocolobomaLaurence H M Pierrache, Adva Kimchi, Rinki Ratnapriya, et al.
Nature Genetics|September 17, 2013
Identification of a rare coding variant in complement 3 associated with age-related macular degenerationXiaowei Zhan, David E Larson, Chaolong Wang, et al.
Human Molecular Genetics|June 6, 2014
Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degenerationRinki Ratnapriya, Xiaowei Zhan, Robert N Fariss, et al.
Nature Genetics|December 23, 2015
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variantsLars G Fritsche, Wilmar Igl, Jessica N Cooke Bailey, et al.
Pageof 6