Genome-Wide Association Study
"Genome-Wide Association Study" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
An analysis comparing the allele frequencies of all available (or a whole GENOME representative set of) polymorphic markers in unrelated patients with a specific symptom or disease condition, and those of healthy controls to identify markers associated with a specific disease or condition.
Descriptor ID |
D055106
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MeSH Number(s) |
E05.318.416.249 E05.318.780.392 E05.393.385.500 E05.393.522.500 E05.393.760.640.500 N06.850.520.445.392 N06.850.520.470.500
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Concept/Terms |
Genome-Wide Association Study- Genome-Wide Association Study
- Association Studies, Genome-Wide
- Association Study, Genome-Wide
- Genome-Wide Association Studies
- Studies, Genome-Wide Association
- Study, Genome-Wide Association
- Genome Wide Association Scan
- Genome Wide Association Studies
- GWA Study
- GWA Studies
- Studies, GWA
- Study, GWA
- Whole Genome Association Analysis
- Whole Genome Association Study
- Genome Wide Association Analysis
- Genome Wide Association Study
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Below are MeSH descriptors whose meaning is more general than "Genome-Wide Association Study".
Below are MeSH descriptors whose meaning is more specific than "Genome-Wide Association Study".
This graph shows the total number of publications written about "Genome-Wide Association Study" by people in this website by year, and whether "Genome-Wide Association Study" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2008 | 0 | 2 | 2 |
2009 | 3 | 6 | 9 |
2010 | 5 | 7 | 12 |
2011 | 9 | 7 | 16 |
2012 | 4 | 8 | 12 |
2013 | 2 | 12 | 14 |
2014 | 3 | 8 | 11 |
2015 | 4 | 8 | 12 |
2016 | 4 | 10 | 14 |
2017 | 3 | 8 | 11 |
2018 | 1 | 7 | 8 |
2019 | 3 | 7 | 10 |
2020 | 2 | 6 | 8 |
2021 | 2 | 10 | 12 |
2022 | 4 | 4 | 8 |
2023 | 1 | 3 | 4 |
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Below are the most recent publications written about "Genome-Wide Association Study" by people in Profiles.
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Pervasive Sharing of Causal Genetic Risk Factors Contributes to Clinical and Molecular Overlap between Sj?gren's Disease and Systemic Lupus Erythematosus. Int J Mol Sci. 2023 Sep 22; 24(19).
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Polygenic architecture of rare coding variation across 394,783 exomes. Nature. 2023 02; 614(7948):492-499.
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Genome-Wide Association Study in Acute Tubulointerstitial Nephritis. J Am Soc Nephrol. 2023 05 01; 34(5):895-908.
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Ancestral origins are associated with SARS-CoV-2 susceptibility and protection in a Florida patient population. PLoS One. 2023; 18(1):e0276700.
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Massively parallel reporter assays and variant scoring identified functional variants and target genes for melanoma loci and highlighted cell-type specificity. Am J Hum Genet. 2022 12 01; 109(12):2210-2229.
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A saturated map of common genetic variants associated with human height. Nature. 2022 10; 610(7933):704-712.
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Rare germline deleterious variants increase susceptibility for lung cancer. Hum Mol Genet. 2022 Oct 10; 31(20):3558-3565.
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Defining novel causal SNPs and linked phenotypes at melanoma-associated loci. Hum Mol Genet. 2022 08 25; 31(17):2845-2856.
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Rare genetic variants explain missing heritability in smoking. Nat Hum Behav. 2022 11; 6(11):1577-1586.
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Genome-wide association study identifies Sjögren's risk loci with functional implications in immune and glandular cells. Nat Commun. 2022 07 27; 13(1):4287.