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Klaver

Showing results (901-910 of 1,112) with videos related to

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Plos One|September 19, 2014
Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 lociClaire L Simpson, Robert Wojciechowski, Konrad Oexle, et al.
Journal of Clinical Immunology|January 10, 2014
First report of the Hyper-IgM syndrome Registry of the Latin American Society for Immunodeficiencies: novel mutations, unique infections, and outcomesOtavio Cabral-Marques, Stefanie Klaver, Lena F Schimke, et al.
International Journal of Epidemiology|January 19, 2012
Complement factor H genetic variant and age-related macular degeneration: effect size, modifiers and relationship to disease subtypeReecha Sofat, Juan P Casas, Andrew R Webster, et al.
Plos Genetics|May 10, 2012
Common genetic determinants of intraocular pressure and primary open-angle glaucomaLeonieke M E van Koolwijk, Wishal D Ramdas, M Kamran Ikram, et al.
Communications Biology|December 14, 2020
Common variants in SOX-2 and congenital cataract genes contribute to age-related nuclear cataractEkaterina Yonova-Doing, Wanting Zhao, Robert P Igo, et al.
HGG Advances|February 14, 2023
Whole genome sequencing for <i>USH2A</i>-associated disease reveals several pathogenic deep-intronic variants that are amenable to splice correctionJanine Reurink, Nicole Weisschuh, Alejandro Garanto, et al.
Nature Genetics|September 17, 2013
Identification of a rare coding variant in complement 3 associated with age-related macular degenerationXiaowei Zhan, David E Larson, Chaolong Wang, et al.
Human Molecular Genetics|March 12, 2013
Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive errorDwight Stambolian, Robert Wojciechowski, Konrad Oexle, et al.
Nature Communications|May 16, 2018
Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseasesAdriana I Iglesias, Aniket Mishra, Veronique Vitart, et al.
Communications Biology|March 21, 2020
Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive errorQiao Fan, Alfred Pozarickij, Nicholas Y Q Tan, et al.
Pageof 112

Showing results (901-910 of 1,112) with videos related to

Sort By:
Pageof 112
Plos One|September 19, 2014
Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 lociClaire L Simpson, Robert Wojciechowski, Konrad Oexle, et al.
Journal of Clinical Immunology|January 10, 2014
First report of the Hyper-IgM syndrome Registry of the Latin American Society for Immunodeficiencies: novel mutations, unique infections, and outcomesOtavio Cabral-Marques, Stefanie Klaver, Lena F Schimke, et al.
International Journal of Epidemiology|January 19, 2012
Complement factor H genetic variant and age-related macular degeneration: effect size, modifiers and relationship to disease subtypeReecha Sofat, Juan P Casas, Andrew R Webster, et al.
Plos Genetics|May 10, 2012
Common genetic determinants of intraocular pressure and primary open-angle glaucomaLeonieke M E van Koolwijk, Wishal D Ramdas, M Kamran Ikram, et al.
Communications Biology|December 14, 2020
Common variants in SOX-2 and congenital cataract genes contribute to age-related nuclear cataractEkaterina Yonova-Doing, Wanting Zhao, Robert P Igo, et al.
HGG Advances|February 14, 2023
Whole genome sequencing for <i>USH2A</i>-associated disease reveals several pathogenic deep-intronic variants that are amenable to splice correctionJanine Reurink, Nicole Weisschuh, Alejandro Garanto, et al.
Nature Genetics|September 17, 2013
Identification of a rare coding variant in complement 3 associated with age-related macular degenerationXiaowei Zhan, David E Larson, Chaolong Wang, et al.
Human Molecular Genetics|March 12, 2013
Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive errorDwight Stambolian, Robert Wojciechowski, Konrad Oexle, et al.
Nature Communications|May 16, 2018
Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseasesAdriana I Iglesias, Aniket Mishra, Veronique Vitart, et al.
Communications Biology|March 21, 2020
Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive errorQiao Fan, Alfred Pozarickij, Nicholas Y Q Tan, et al.
Pageof 112