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Rando Allikmets

Showing results (161-170 of 180) with videos related to

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Human Molecular Genetics|August 2, 2014
Analysis of the ABCA4 genomic locus in Stargardt diseaseJana Zernant, Yajing Angela Xie, Carmen Ayuso, et al.
American Journal of Ophthalmology|August 10, 2024
Cross-Sectional Analysis of Outer Retinal Tubulation in Inherited Retinal Diseases: A Multicenter StudyPei-Kang Liu, Winston Lee, Pei-Yin Su, et al.
Experimental Eye Research|September 15, 2022
Systems genomics in age-related macular degenerationAnneke I den Hollander, Robert F Mullins, Luz D Orozco, et al.
Ophthalmology|December 22, 2009
The complement component 5 gene and age-related macular degenerationDominique C Baas, Lintje Ho, Sarah Ennis, et al.
Neuromolecular Medicine|February 15, 2015
A Candidate Gene Association Study Identifies DAPL1 as a Female-Specific Susceptibility Locus for Age-Related Macular Degeneration (AMD)Felix Grassmann, Ulrike Friedrich, Sascha Fauser, 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.
Proceedings of the National Academy of Sciences of the United States of America|April 14, 2010
Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC)Benjamin M Neale, Jesen Fagerness, Robyn Reynolds, et al.
European Journal of Human Genetics : EJHG|April 26, 2002
The ABCA4 2588G>C Stargardt mutation: single origin and increasing frequency from South-West to North-East EuropeAlessandra Maugeri, Kris Flothmann, Nadine Hemmrich, et al.
Molecular Vision|April 18, 2012
Multicenter cohort association study of SLC2A1 single nucleotide polymorphisms and age-related macular degenerationDominique C Baas, Lintje Ho, Michael W T Tanck, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 5, 2005
A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degenerationGregory S Hageman, Don H Anderson, Lincoln V Johnson, et al.
Pageof 18

Showing results (161-170 of 180) with videos related to

Sort By:
Pageof 18
Human Molecular Genetics|August 2, 2014
Analysis of the ABCA4 genomic locus in Stargardt diseaseJana Zernant, Yajing Angela Xie, Carmen Ayuso, et al.
American Journal of Ophthalmology|August 10, 2024
Cross-Sectional Analysis of Outer Retinal Tubulation in Inherited Retinal Diseases: A Multicenter StudyPei-Kang Liu, Winston Lee, Pei-Yin Su, et al.
Experimental Eye Research|September 15, 2022
Systems genomics in age-related macular degenerationAnneke I den Hollander, Robert F Mullins, Luz D Orozco, et al.
Ophthalmology|December 22, 2009
The complement component 5 gene and age-related macular degenerationDominique C Baas, Lintje Ho, Sarah Ennis, et al.
Neuromolecular Medicine|February 15, 2015
A Candidate Gene Association Study Identifies DAPL1 as a Female-Specific Susceptibility Locus for Age-Related Macular Degeneration (AMD)Felix Grassmann, Ulrike Friedrich, Sascha Fauser, 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.
Proceedings of the National Academy of Sciences of the United States of America|April 14, 2010
Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC)Benjamin M Neale, Jesen Fagerness, Robyn Reynolds, et al.
European Journal of Human Genetics : EJHG|April 26, 2002
The ABCA4 2588G>C Stargardt mutation: single origin and increasing frequency from South-West to North-East EuropeAlessandra Maugeri, Kris Flothmann, Nadine Hemmrich, et al.
Molecular Vision|April 18, 2012
Multicenter cohort association study of SLC2A1 single nucleotide polymorphisms and age-related macular degenerationDominique C Baas, Lintje Ho, Michael W T Tanck, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 5, 2005
A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degenerationGregory S Hageman, Don H Anderson, Lincoln V Johnson, et al.
Pageof 18