Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

E Branham

Showing results (41-50 of 62) with videos related to

Pageof 7
Sort By:
Human Molecular Genetics|November 7, 2023
Whole genome sequencing of 4,787 individuals identifies gene-based rare variants in age-related macular degenerationAlan Kwong, Matthew Zawistowski, Lars G Fritsche, et al.
Molecular Vision|December 10, 2013
Mutations in the small nuclear riboprotein 200 kDa gene (SNRNP200) cause 1.6% of autosomal dominant retinitis pigmentosaSara J Bowne, Lori S Sullivan, Cheryl E Avery, et al.
Genomics|March 8, 2014
exomeSuite: Whole exome sequence variant filtering tool for rapid identification of putative disease causing SNVs/indelsB Maranhao, P Biswas, J L Duncan, et al.
Nature Genetics|March 18, 2014
Ancestry estimation and control of population stratification for sequence-based association studiesChaolong Wang, Xiaowei Zhan, Jennifer Bragg-Gresham, et al.
Annals of Human Genetics|April 3, 2019
Associations of the melanocortin 3 receptor C17A + G241A haplotype with body composition and inflammation in African-American adultsAndrew P Demidowich, Viraj J Parikh, Nicket Dedhia, et al.
Cell Reports|December 31, 2013
Hypomethylation of the IL17RC promoter in peripheral blood leukocytes is not a hallmark of age-related macular degenerationVerity F Oliver, Maria Franchina, Andrew E Jaffe, et al.
Investigative Ophthalmology & Visual Science|February 11, 2015
Advancing therapeutic strategies for inherited retinal degeneration: recommendations from the Monaciano SymposiumDebra A Thompson, Robin R Ali, Eyal Banin, et al.
Investigative Ophthalmology & Visual Science|May 27, 2017
A Novel Dominant Mutation in SAG, the Arrestin-1 Gene, Is a Common Cause of Retinitis Pigmentosa in Hispanic Families in the Southwestern United StatesLori S Sullivan, Sara J Bowne, Daniel C Koboldt, et al.
Nature Genetics|May 5, 2026
Population-level super-pangenome reveals genome evolution and empowers precision breeding in watermelonHonghe Sun, Jie Zhang, Shengjin Liao, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 18, 2010
Loss of lysophosphatidylcholine acyltransferase 1 leads to photoreceptor degeneration in rd11 miceJames S Friedman, Bo Chang, Daniel S Krauth, et al.
Pageof 7

Showing results (41-50 of 62) with videos related to

Sort By:
Pageof 7
Human Molecular Genetics|November 7, 2023
Whole genome sequencing of 4,787 individuals identifies gene-based rare variants in age-related macular degenerationAlan Kwong, Matthew Zawistowski, Lars G Fritsche, et al.
Molecular Vision|December 10, 2013
Mutations in the small nuclear riboprotein 200 kDa gene (SNRNP200) cause 1.6% of autosomal dominant retinitis pigmentosaSara J Bowne, Lori S Sullivan, Cheryl E Avery, et al.
Genomics|March 8, 2014
exomeSuite: Whole exome sequence variant filtering tool for rapid identification of putative disease causing SNVs/indelsB Maranhao, P Biswas, J L Duncan, et al.
Nature Genetics|March 18, 2014
Ancestry estimation and control of population stratification for sequence-based association studiesChaolong Wang, Xiaowei Zhan, Jennifer Bragg-Gresham, et al.
Annals of Human Genetics|April 3, 2019
Associations of the melanocortin 3 receptor C17A + G241A haplotype with body composition and inflammation in African-American adultsAndrew P Demidowich, Viraj J Parikh, Nicket Dedhia, et al.
Cell Reports|December 31, 2013
Hypomethylation of the IL17RC promoter in peripheral blood leukocytes is not a hallmark of age-related macular degenerationVerity F Oliver, Maria Franchina, Andrew E Jaffe, et al.
Investigative Ophthalmology & Visual Science|February 11, 2015
Advancing therapeutic strategies for inherited retinal degeneration: recommendations from the Monaciano SymposiumDebra A Thompson, Robin R Ali, Eyal Banin, et al.
Investigative Ophthalmology & Visual Science|May 27, 2017
A Novel Dominant Mutation in SAG, the Arrestin-1 Gene, Is a Common Cause of Retinitis Pigmentosa in Hispanic Families in the Southwestern United StatesLori S Sullivan, Sara J Bowne, Daniel C Koboldt, et al.
Nature Genetics|May 5, 2026
Population-level super-pangenome reveals genome evolution and empowers precision breeding in watermelonHonghe Sun, Jie Zhang, Shengjin Liao, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 18, 2010
Loss of lysophosphatidylcholine acyltransferase 1 leads to photoreceptor degeneration in rd11 miceJames S Friedman, Bo Chang, Daniel S Krauth, et al.
Pageof 7