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Rinki Ratnapriya

Showing results (41-50 of 56) with videos related to

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Research Square|July 3, 2023
QTL mapping of human retina DNA methylation identifies 87 gene-epigenome interactions in age-related macular degenerationJayshree Advani, Ximena Corso-Diaz, Madeline Kwicklis, et al.
Human Molecular Genetics|January 19, 2018
Genome-wide analysis of disease progression in age-related macular degenerationQi Yan, Ying Ding, Yi Liu, et al.
Human Mutation|June 17, 2015
Nonsyndromic Early-Onset Cone-Rod Dystrophy and Limb-Girdle Muscular Dystrophy in a Consanguineous Israeli Family are Caused by Two Independent yet Linked Mutations in ALMS1 and DYSFCsilla H Lazar, Adva Kimchi, Prasanthi Namburi, et al.
JAMA Ophthalmology|May 24, 2019
Assessment of Novel Genome-Wide Significant Gene Loci and Lesion Growth in Geographic Atrophy Secondary to Age-Related Macular DegenerationFelix Grassmann, Sebastian Harsch, Caroline Brandl, et al.
Developmental Cell|December 14, 2017
Molecular Anatomy of the Developing Human RetinaAkina Hoshino, Rinki Ratnapriya, Matthew J Brooks, et al.
Nature Genetics|May 10, 2019
Author Correction: Retinal transcriptome and eQTL analyses identify genes associated with age-related macular degenerationRinki Ratnapriya, Olukayode A Sosina, Margaret R Starostik, et al.
Human Molecular Genetics|February 25, 2016
A secreted WNT-ligand-binding domain of FZD5 generated by a frameshift mutation causes autosomal dominant colobomaChunqiao Liu, Sonya A Widen, Kathleen A Williamson, et al.
Nature Genetics|February 12, 2019
Retinal transcriptome and eQTL analyses identify genes associated with age-related macular degenerationRinki Ratnapriya, Olukayode A Sosina, Margaret R Starostik, et al.
Nature Communications|March 4, 2024
QTL mapping of human retina DNA methylation identifies 87 gene-epigenome interactions in age-related macular degenerationJayshree Advani, Puja A Mehta, Andrew R Hamel, et al.
Human Molecular Genetics|April 4, 2017
REEP6 mediates trafficking of a subset of Clathrin-coated vesicles and is critical for rod photoreceptor function and survivalShobi Veleri, Jacob Nellissery, Bibhudatta Mishra, et al.
Pageof 6

Showing results (41-50 of 56) with videos related to

Sort By:
Pageof 6
Research Square|July 3, 2023
QTL mapping of human retina DNA methylation identifies 87 gene-epigenome interactions in age-related macular degenerationJayshree Advani, Ximena Corso-Diaz, Madeline Kwicklis, et al.
Human Molecular Genetics|January 19, 2018
Genome-wide analysis of disease progression in age-related macular degenerationQi Yan, Ying Ding, Yi Liu, et al.
Human Mutation|June 17, 2015
Nonsyndromic Early-Onset Cone-Rod Dystrophy and Limb-Girdle Muscular Dystrophy in a Consanguineous Israeli Family are Caused by Two Independent yet Linked Mutations in ALMS1 and DYSFCsilla H Lazar, Adva Kimchi, Prasanthi Namburi, et al.
JAMA Ophthalmology|May 24, 2019
Assessment of Novel Genome-Wide Significant Gene Loci and Lesion Growth in Geographic Atrophy Secondary to Age-Related Macular DegenerationFelix Grassmann, Sebastian Harsch, Caroline Brandl, et al.
Developmental Cell|December 14, 2017
Molecular Anatomy of the Developing Human RetinaAkina Hoshino, Rinki Ratnapriya, Matthew J Brooks, et al.
Nature Genetics|May 10, 2019
Author Correction: Retinal transcriptome and eQTL analyses identify genes associated with age-related macular degenerationRinki Ratnapriya, Olukayode A Sosina, Margaret R Starostik, et al.
Human Molecular Genetics|February 25, 2016
A secreted WNT-ligand-binding domain of FZD5 generated by a frameshift mutation causes autosomal dominant colobomaChunqiao Liu, Sonya A Widen, Kathleen A Williamson, et al.
Nature Genetics|February 12, 2019
Retinal transcriptome and eQTL analyses identify genes associated with age-related macular degenerationRinki Ratnapriya, Olukayode A Sosina, Margaret R Starostik, et al.
Nature Communications|March 4, 2024
QTL mapping of human retina DNA methylation identifies 87 gene-epigenome interactions in age-related macular degenerationJayshree Advani, Puja A Mehta, Andrew R Hamel, et al.
Human Molecular Genetics|April 4, 2017
REEP6 mediates trafficking of a subset of Clathrin-coated vesicles and is critical for rod photoreceptor function and survivalShobi Veleri, Jacob Nellissery, Bibhudatta Mishra, et al.
Pageof 6