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Nature Genetics|December 2, 2024
Genome-wide association analyses identify distinct genetic architectures for age-related macular degeneration across ancestriesBryan R Gorman, Georgios Voloudakis, Robert P Igo, et al.
Nature Communications|March 31, 2017
Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophyNatalie A Afshari, Robert P Igo, Nathan J Morris, et al.
Plos One|October 25, 2011
A 32 kb critical region excluding Y402H in CFH mediates risk for age-related macular degenerationTheru A Sivakumaran, Robert P Igo, Jeffrey M Kidd, et al.
Plos One|December 21, 2018
Correction: A 32 kb Critical Region Excluding Y402H in CFH Mediates Risk for Age-Related Macular DegenerationTheru A Sivakumaran, Robert P Igo, Jeffrey M Kidd, et al.
American Journal of Human Genetics|July 3, 2021
Targeted long-read sequencing identifies missing disease-causing variationDanny E Miller, Arvis Sulovari, Tianyun Wang, et al.
American Journal of Respiratory and Critical Care Medicine|June 30, 2022
A MUC5B Gene Polymorphism, rs35705950-T, Confers Protective Effects Against COVID-19 Hospitalization but Not Severe Disease or MortalityAnurag Verma, Jessica Minnier, Emily S Wan, et al.
American Journal of Human Genetics|December 30, 2019
Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry CohortsLaura M Raffield, Apoorva K Iyengar, Biqi Wang, 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.
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