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

Rando Allikmets

Showing results (121-130 of 180) with videos related to

Pageof 18
Sort By:
Investigative Ophthalmology & Visual Science|November 10, 2015
Quantitative Fundus Autofluorescence and Optical Coherence Tomography in ABCA4 CarriersTobias Duncker, Gregory E Stein, Winston Lee, et al.
American Journal of Human Genetics|March 13, 2018
Identification and Rescue of Splice Defects Caused by Two Neighboring Deep-Intronic ABCA4 Mutations Underlying Stargardt DiseaseSilvia Albert, Alejandro Garanto, Riccardo Sangermano, et al.
Ophthalmology|March 26, 2013
Inclusion of genotype with fundus phenotype improves accuracy of predicting choroidal neovascularization and geographic atrophyLorah T Perlee, Aruna T Bansal, Karen Gehrs, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 9, 2020
Mapping the <i>cis</i>-regulatory architecture of the human retina reveals noncoding genetic variation in diseaseTimothy J Cherry, Marty G Yang, David A Harmin, et al.
Ophthalmology|October 15, 2014
Clinical and molecular characteristics of childhood-onset Stargardt diseaseKaoru Fujinami, Jana Zernant, Ravinder K Chana, et al.
Retina (Philadelphia, Pa.)|December 30, 2014
New best1 mutations in autosomal recessive bestrophinopathyAdrian T Fung, Suzanne Yzer, Naomi Goldberg, et al.
Investigative Ophthalmology & Visual Science|January 27, 2005
Early-onset macular degeneration with drusen in a cynomolgus monkey (Macaca fascicularis) pedigree: exclusion of 13 candidate genes and lociShinsuke Umeda, Radha Ayyagari, Rando Allikmets, et al.
Investigative Ophthalmology & Visual Science|August 27, 2005
Genotyping microarray (disease chip) for Leber congenital amaurosis: detection of modifier allelesJana Zernant, Maigi Külm, Sharola Dharmaraj, et al.
Communications Biology|March 3, 2021
Identification of genetic factors influencing metabolic dysregulation and retinal support for MacTel, a retinal disorderRoberto Bonelli, Victoria E Jackson, Aravind Prasad, et al.
Nature Genetics|March 3, 2017
Genome-wide analyses identify common variants associated with macular telangiectasia type 2Thomas S Scerri, Anna Quaglieri, Carolyn Cai, et al.
Pageof 18

Showing results (121-130 of 180) with videos related to

Sort By:
Pageof 18
Investigative Ophthalmology & Visual Science|November 10, 2015
Quantitative Fundus Autofluorescence and Optical Coherence Tomography in ABCA4 CarriersTobias Duncker, Gregory E Stein, Winston Lee, et al.
American Journal of Human Genetics|March 13, 2018
Identification and Rescue of Splice Defects Caused by Two Neighboring Deep-Intronic ABCA4 Mutations Underlying Stargardt DiseaseSilvia Albert, Alejandro Garanto, Riccardo Sangermano, et al.
Ophthalmology|March 26, 2013
Inclusion of genotype with fundus phenotype improves accuracy of predicting choroidal neovascularization and geographic atrophyLorah T Perlee, Aruna T Bansal, Karen Gehrs, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 9, 2020
Mapping the <i>cis</i>-regulatory architecture of the human retina reveals noncoding genetic variation in diseaseTimothy J Cherry, Marty G Yang, David A Harmin, et al.
Ophthalmology|October 15, 2014
Clinical and molecular characteristics of childhood-onset Stargardt diseaseKaoru Fujinami, Jana Zernant, Ravinder K Chana, et al.
Retina (Philadelphia, Pa.)|December 30, 2014
New best1 mutations in autosomal recessive bestrophinopathyAdrian T Fung, Suzanne Yzer, Naomi Goldberg, et al.
Investigative Ophthalmology & Visual Science|January 27, 2005
Early-onset macular degeneration with drusen in a cynomolgus monkey (Macaca fascicularis) pedigree: exclusion of 13 candidate genes and lociShinsuke Umeda, Radha Ayyagari, Rando Allikmets, et al.
Investigative Ophthalmology & Visual Science|August 27, 2005
Genotyping microarray (disease chip) for Leber congenital amaurosis: detection of modifier allelesJana Zernant, Maigi Külm, Sharola Dharmaraj, et al.
Communications Biology|March 3, 2021
Identification of genetic factors influencing metabolic dysregulation and retinal support for MacTel, a retinal disorderRoberto Bonelli, Victoria E Jackson, Aravind Prasad, et al.
Nature Genetics|March 3, 2017
Genome-wide analyses identify common variants associated with macular telangiectasia type 2Thomas S Scerri, Anna Quaglieri, Carolyn Cai, et al.
Pageof 18