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

Suzanne Yzer

Showing results (61-70 of 72) with videos related to

Pageof 8
Sort By:
Investigative Ophthalmology & Visual Science|December 7, 2007
Identification of novel mutations in patients with Leber congenital amaurosis and juvenile RP by genome-wide homozygosity mapping with SNP microarraysAnneke I den Hollander, Irma Lopez, Suzanne Yzer, et al.
Human Molecular Genetics|November 5, 2005
Retinal degeneration associated with RDH12 mutations results from decreased 11-cis retinal synthesis due to disruption of the visual cycleDebra A Thompson, Andreas R Janecke, Jessica Lange, et al.
Progress in Retinal and Eye Research|July 19, 2019
Central serous chorioretinopathy: Towards an evidence-based treatment guidelineThomas J van Rijssen, Elon H C van Dijk, Suzanne Yzer, et al.
Investigative Ophthalmology & Visual Science|March 1, 2006
Microarray-based mutation detection and phenotypic characterization of patients with Leber congenital amaurosisSuzanne Yzer, Bart P Leroy, Elfride De Baere, et al.
JAMA Ophthalmology|April 20, 2023
Overlap of Genetic Loci for Central Serous Chorioretinopathy With Age-Related Macular DegenerationJoel T Rämö, Erik Abner, Elon H C van Dijk, et al.
Medrxiv : the Preprint Server for Health Sciences|June 4, 2026
GWAS Meta-analysis Identifies Novel Associated Loci and Points to Causal Tissues in Central Serous ChorioretinopathyLiyin Chen, Soo Hyun Kim, Buu Truong, et al.
Medrxiv : the Preprint Server for Health Sciences|May 20, 2024
Rare genetic variation in VE-PTP is associated with central serous chorioretinopathy, venous dysfunction and glaucomaJoel T Rämö, Bryan Gorman, Lu-Chen Weng, et al.
Scientific Reports|March 18, 2025
Genome-wide association and multi-omics analyses provide insights into the disease mechanisms of central serous chorioretinopathyYuki Mori, Elon H C van Dijk, Masahiro Miyake, et al.
Progress in Retinal and Eye Research|February 1, 2024
Central serous chorioretinopathy: An evidence-based treatment guidelineHelena M A Feenstra, Elon H C van Dijk, Chui Ming Gemmy Cheung, et al.
Nature Communications|May 3, 2025
Rare genetic variation in PTPRB is associated with central serous chorioretinopathy, varicose veins and glaucomaJoel T Rämö, Bryan R Gorman, Lu-Chen Weng, et al.
Pageof 8

Showing results (61-70 of 72) with videos related to

Sort By:
Pageof 8
Investigative Ophthalmology & Visual Science|December 7, 2007
Identification of novel mutations in patients with Leber congenital amaurosis and juvenile RP by genome-wide homozygosity mapping with SNP microarraysAnneke I den Hollander, Irma Lopez, Suzanne Yzer, et al.
Human Molecular Genetics|November 5, 2005
Retinal degeneration associated with RDH12 mutations results from decreased 11-cis retinal synthesis due to disruption of the visual cycleDebra A Thompson, Andreas R Janecke, Jessica Lange, et al.
Progress in Retinal and Eye Research|July 19, 2019
Central serous chorioretinopathy: Towards an evidence-based treatment guidelineThomas J van Rijssen, Elon H C van Dijk, Suzanne Yzer, et al.
Investigative Ophthalmology & Visual Science|March 1, 2006
Microarray-based mutation detection and phenotypic characterization of patients with Leber congenital amaurosisSuzanne Yzer, Bart P Leroy, Elfride De Baere, et al.
JAMA Ophthalmology|April 20, 2023
Overlap of Genetic Loci for Central Serous Chorioretinopathy With Age-Related Macular DegenerationJoel T Rämö, Erik Abner, Elon H C van Dijk, et al.
Medrxiv : the Preprint Server for Health Sciences|June 4, 2026
GWAS Meta-analysis Identifies Novel Associated Loci and Points to Causal Tissues in Central Serous ChorioretinopathyLiyin Chen, Soo Hyun Kim, Buu Truong, et al.
Medrxiv : the Preprint Server for Health Sciences|May 20, 2024
Rare genetic variation in VE-PTP is associated with central serous chorioretinopathy, venous dysfunction and glaucomaJoel T Rämö, Bryan Gorman, Lu-Chen Weng, et al.
Scientific Reports|March 18, 2025
Genome-wide association and multi-omics analyses provide insights into the disease mechanisms of central serous chorioretinopathyYuki Mori, Elon H C van Dijk, Masahiro Miyake, et al.
Progress in Retinal and Eye Research|February 1, 2024
Central serous chorioretinopathy: An evidence-based treatment guidelineHelena M A Feenstra, Elon H C van Dijk, Chui Ming Gemmy Cheung, et al.
Nature Communications|May 3, 2025
Rare genetic variation in PTPRB is associated with central serous chorioretinopathy, varicose veins and glaucomaJoel T Rämö, Bryan R Gorman, Lu-Chen Weng, et al.
Pageof 8