Editorial: Advancements and prospects of genome-wide association studies.
作者信息
Doumatey Ayo P, Li Yafang, Fernandez-Lopez Juan Carlos
机构信息
Center for Research on Genomics and Global Health, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, United States.
University of New Mexico Comprehensive Cancer Center, Albuquerque, NM, United States.
出版信息
Front Genet. 2025 Feb 19;16:1564006. doi: 10.3389/fgene.2025.1564006. eCollection 2025.
Abstract
摘要
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Editorial: Advancements and prospects of genome-wide association studies.
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本文引用的文献
1
Imputation accuracy across global human populations.
Am J Hum Genet. 2024 May 2;111(5):979-989. doi: 10.1016/j.ajhg.2024.03.011. Epub 2024 Apr 10.
2
Genomic data in the All of Us Research Program.
Nature. 2024 Mar;627(8003):340-346. doi: 10.1038/s41586-023-06957-x. Epub 2024 Feb 19.
3
Whole Genome Sequencing Identifies Novel Common and Low-Frequency Variants Associated With Age-Related Macular Degeneration.
Invest Ophthalmol Vis Sci. 2023 Nov 1;64(14):24. doi: 10.1167/iovs.64.14.24.
4
Genes, environment, and African ancestry in cardiometabolic disorders.
Trends Endocrinol Metab. 2023 Oct;34(10):601-621. doi: 10.1016/j.tem.2023.07.007. Epub 2023 Aug 17.
5
Genome-wide association study using whole-genome sequencing identifies risk loci for Parkinson's disease in Chinese population.
NPJ Parkinsons Dis. 2023 Feb 9;9(1):22. doi: 10.1038/s41531-023-00456-6.
6
The NHGRI-EBI GWAS Catalog: knowledgebase and deposition resource.
Nucleic Acids Res. 2023 Jan 6;51(D1):D977-D985. doi: 10.1093/nar/gkac1010.
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10
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PLoS Genet. 2019 Dec 23;15(12):e1008500. doi: 10.1371/journal.pgen.1008500. eCollection 2019 Dec.
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