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.
To see the data from this visualization as text, click here.
Year | Major Topic | Minor Topic | Total |
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2008 | 1 | 1 | 2 | 2009 | 7 | 3 | 10 | 2010 | 7 | 8 | 15 | 2011 | 6 | 8 | 14 | 2012 | 6 | 14 | 20 | 2013 | 6 | 10 | 16 | 2014 | 1 | 17 | 18 | 2015 | 10 | 6 | 16 | 2016 | 4 | 7 | 11 | 2017 | 2 | 5 | 7 | 2018 | 0 | 10 | 10 | 2019 | 1 | 4 | 5 | 2020 | 1 | 3 | 4 | 2021 | 0 | 2 | 2 | 2022 | 1 | 2 | 3 | 2023 | 0 | 4 | 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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Mullin BH, Zhu K, Brown SJ, Mullin S, Dudbridge F, Pavlos NJ, Richards JB, Grundberg E, Bell JT, Zeggini E, Walsh JP, Xu J, Wilson SG. Leveraging osteoclast genetic regulatory data to identify genes with a role in osteoarthritis. Genetics. 2023 10 04; 225(2).
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Cramer EY, Bartlett J, Chan ER, Gaedigk A, Ratsimbasoa AC, Mehlotra RK, Williams SM, Zimmerman PA. Pharmacogenomic variation in the Malagasy population: implications for the antimalarial drug primaquine metabolism. Pharmacogenomics. 2023 07; 24(11):583-597.
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Hassan N, Gregson CL, Tang H, van der Kamp M, Leo P, McInerney-Leo AM, Zheng J, Brandi ML, Tang JCY, Fraser W, Stone MD, Grundberg E, Brown MA, Duncan EL, Tobias JH. Rare and Common Variants in GALNT3 May Affect Bone Mass Independently of Phosphate Metabolism. J Bone Miner Res. 2023 05; 38(5):678-691.
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Durand A, Winkler CA, Vince N, Douillard V, Geffard E, Binns-Roemer E, Ng DK, Gourraud PA, Reidy K, Warady B, Furth S, Kopp JB, Kaskel FJ, Limou S. Identification of Novel Genetic Risk Factors for Focal Segmental Glomerulosclerosis in Children: Results From the Chronic Kidney Disease in Children (CKiD) Cohort. Am J Kidney Dis. 2023 06; 81(6):635-646.e1.
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Fasching PA, Liu D, Scully S, Ingle JN, Lyra PC, Rack B, Hein A, Ekici AB, Reis A, Schneeweiss A, Tesch H, Fehm TN, Heinrich G, Beckmann MW, Ruebner M, Huebner H, Lambrechts D, Madden E, Shen J, Romm J, Doheny K, Jenkins GD, Carlson EE, Li L, Fridley BL, Cunningham JM, Janni W, Monteiro ANA, Schaid DJ, H?berle L, Weinshilboum RM, Wang L. Identification of Two Genetic Loci Associated with Leukopenia after Chemotherapy in Patients with Breast Cancer. Clin Cancer Res. 2022 08 02; 28(15):3342-3355.
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Smail C, Ferraro NM, Hui Q, Durrant MG, Aguirre M, Tanigawa Y, Keever-Keigher MR, Rao AS, Justesen JM, Li X, Gloudemans MJ, Assimes TL, Kooperberg C, Reiner AP, Huang J, O'Donnell CJ, Sun YV, Rivas MA, Montgomery SB. Integration of rare expression outlier-associated variants improves polygenic risk prediction. Am J Hum Genet. 2022 06 02; 109(6):1055-1064.
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Kundu K, Tardaguila M, Mann AL, Watt S, Ponstingl H, Vasquez L, Von Schiller D, Morrell NW, Stegle O, Pastinen T, Sawcer SJ, Anderson CA, Walter K, Soranzo N. Genetic associations at regulatory phenotypes improve fine-mapping of causal variants for 12 immune-mediated diseases. Nat Genet. 2022 03; 54(3):251-262.
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Samanic CM, Teer JK, Thompson ZJ, Creed JH, Mokhtari S, Fridley BL, Nabors LB, Williams SL, Egan KM. Mitochondrial DNA sequence variation and risk of meningioma. J Neurooncol. 2021 Dec; 155(3):319-324.
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Zeng Y, Zhao K, Oros Klein K, Shao X, Fritzler MJ, Hudson M, Colmegna I, Pastinen T, Bernatsky S, Greenwood CMT. Thousands of CpGs Show DNA Methylation Differences in ACPA-Positive Individuals. Genes (Basel). 2021 08 29; 12(9).
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Kho PF, Amant F, Annibali D, Ashton K, Attia J, Auer PL, Beckmann MW, Black A, Brinton L, Buchanan DD, Chanock SJ, Chen C, Chen MM, Cheng THT, Cook LS, Crous-Bous M, Czene K, De Vivo I, Dennis J, D?rk T, Dowdy SC, Dunning AM, D?rst M, Easton DF, Ekici AB, Fasching PA, Fridley BL, Friedenreich CM, Garc?a-Closas M, Gaudet MM, Giles GG, Goode EL, Gorman M, Haiman CA, Hall P, Hankinson SE, Hein A, Hillemanns P, Hodgson S, Hoivik EA, Holliday EG, Hunter DJ, Jones A, Kraft P, Krakstad C, Lambrechts D, Le Marchand L, Liang X, Lindblom A, Lissowska J, Long J, Lu L, Magliocco AM, Martin L, McEvoy M, Milne RL, Mints M, Nassir R, Otton G, Palles C, Pooler L, Proietto T, Rebbeck TR, Renner SP, Risch HA, R?bner M, Runnebaum I, Sacerdote C, Sarto GE, Schumacher F, Scott RJ, Setiawan VW, Shah M, Sheng X, Shu XO, Southey MC, Tham E, Tomlinson I, Trovik J, Turman C, Tyrer JP, Van Den Berg D, Wang Z, Wentzensen N, Xia L, Xiang YB, Yang HP, Yu H, Zheng W, Webb PM, Thompson DJ, Spurdle AB, Glubb DM, O'Mara TA. Mendelian randomization analyses suggest a role for cholesterol in the development of endometrial cancer. Int J Cancer. 2021 01 15; 148(2):307-319.
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