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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| 2005 | 1 | 0 | 1 | | 2008 | 1 | 2 | 3 | | 2009 | 14 | 13 | 27 | | 2010 | 16 | 30 | 46 | | 2011 | 13 | 27 | 40 | | 2012 | 16 | 32 | 48 | | 2013 | 18 | 29 | 47 | | 2014 | 32 | 44 | 76 | | 2015 | 14 | 34 | 48 | | 2016 | 22 | 34 | 56 | | 2017 | 23 | 41 | 64 | | 2018 | 14 | 44 | 58 | | 2019 | 18 | 65 | 83 | | 2020 | 15 | 29 | 44 | | 2021 | 30 | 39 | 69 | | 2022 | 42 | 39 | 81 | | 2023 | 20 | 42 | 62 | | 2024 | 27 | 30 | 57 | | 2025 | 14 | 50 | 64 | | 2026 | 7 | 16 | 23 |
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Below are the most recent publications written about "Genome-Wide Association Study" by people in Profiles.
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Peljto AL, Furusawa H, Puthenvedu D, Lee JS, Steele MP, Brancato J, Cardwell J, Blumhagen RZ, de Andrade J, Bendstrup E, Blackwell TS, Bonella F, Borie R, Braybrooke R, Brown KK, Carbone RG, Christie JD, Costabel U, Crestani B, Davidsen JR, Dieude P, Donnelly SC, Egan J, Eickelberg O, Fernández Pérez ER, Fiddler CA, Foster EE, Gibson KF, Gudmundsson G, Guthridge JM, Henry MT, Hirani N, Jenkins RG, Kass DJ, Keane MP, Kokturk N, Kropski JA, Lederer D, Leone PM, Linderholm AL, Maher TM, Mathai SK, McCarthy C, McElroy AN, Mogulkoc N, Molina-Molina M, Molyneaux PL, Montesi SB, Nathan SD, Noth I, Olaniyi JA, Oldham JM, O'Reilly KMA, Palmisciano AJ, Pardo A, Parfrey H, Planas-Cerezales L, Poletti V, Porteous MK, Puppo F, Richeldi L, Rojas M, Salinas M, Schluger N, Selman M, Shea BS, Sterclova M, Solomon JJ, Tomassetti S, Vasakova MK, Zhang Y, Corte TJ, Dickinson JL, Glaspole I, Moodley YP, Prele CMA, Ryerson CJ, Wolters PJ, Jinno M, Miyata Y, Akagawa S, Narumoto O, Kita T, Shibayama T, Li T, Owan I, Wakamatsu K, Arai T, Hirose M, Kim DS, Ohta K, Ohta S, Park JS, Park MS, Yang IV, Fingerlin TE, Miyazaki Y, Okamoto T, Inoue Y, Song JW, Schwartz DA. Idiopathic pulmonary fibrosis risk loci in East Asian populations mirror those of European populations. Am J Respir Crit Care Med. 2026 07 01; 212(7):1522-1532.
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Chiles JW, Rocco A, Srinivasasainagendra V, Rossiter HB, Casaburi R, Thalacker-Mercer A, Wells JM, Wan ES, Silverman EK, Cho MH, Hersh CP, Psaty BM, Gharib SA, Gao Y, O'Connor GT, Lange LA, Rich SS, Manichaikul AW, Barr RG, Ortega VE, Meyers DA, Smith AV, Tiwari HK, McDonald MN. Whole Genome Sequence Analysis of Weight Loss in 16?972 Participants With COPD Reveals Novel Risk Loci in DRAIC and RFX3. J Cachexia Sarcopenia Muscle. 2026 06; 17(3):e70293.
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Purdy AL, Bakhshian Nik A, Arkatkar AA, Hasan P, Flinn MA, Choudhury P, Wood C, Takizawa A, Malloy L, Tutaj M, Drysdale TA, Bridgewater D, Link BA, Plageman TF, Kwitek AE, Dwinell MR, Saba LM, O'Meara CC, Patterson M. Genome-wide association mapping and targeted loss of function studies identify Shroom3 as a driver of hyperpolyploidy and ventricular dilation. Proc Natl Acad Sci U S A. 2026 Jun 02; 123(22):e2522068123.
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Zhang J, Moll M, Debban CL, Hobbs BD, Rijhwani H, Washko GR, Celli BR, Silverman EK, Bakke P, Oelsner EC, Barr RG, Agustí A, Faner R, Bruselle GG, Humphries SM, Lynch DA, Dupuis J, Manichaikul AW, O'Connor GT, Cho MH. Body Mass Index-related genetic factors and COPD imaging phenotypes. Ann Am Thorac Soc. 2026 05 01; 23(5):720-727.
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Moolhuijsen LME, Zhu J, Mullin BH, Pujol-Gualdo N, Actkins KV, Mack JA, Rao H, Trivedi B, Kentistou KA, Zhao Y, Westergaard D, Tyrmi JS, Thorleifsson G, Zhang Y, Wittemans L, DeVries A, Brewer K, Sisk R, Danning R, Preuss MH, Jones MR, Ruth KS, Andersen M, Azziz R, Banasik K, Boehnke M, Broer L, Brunak S, Chan YM, Chasman DI, Daly M, Ehrmann DA, Fauser BC, Fritsche LG, Hayes MG, He C, Huang H, Kowalska I, Kraft P, Legro RS, Lin N, Loos RJ, Louwers YV, Magi R, McCarthy MI, Morin-Papunen L, Morrison JV, Morton C, Nadkarni GN, Neale BM, Nielsen HS, Nyegaard M, Ostrowski SR, Pedersen OBV, Sørensen E, Mikkelsen C, Erikstrup C, Kaspersen KA, Bruun MT, Aagaard B, Ullum H, Obermayer-Pietsch B, Palotie A, Reeve MP, Salumets A, Saxena R, Spector TD, Stuckey BGA, Thorsteinsdottir U, Uitterlinden AG, Urbanek M, Zöllner S, van Heel DA, Hirschhorn JN, Stefansson K, Perry JRB, Styrkarsdottir U, Wilson SG, Piltonen T, Laisk T, Jarvelin MR, Burns K, Justice AE, Laivuori H, Ong KK, Goodarzi MO, Davis LK, Dunaif A, Lindgren CM, Laven JSE, Franks S, Visser JA, Welt CK, Karaderi T, Day FR. Genomic analyses implicate hormonal and metabolic dysregulation in polycystic ovary syndrome. Nat Genet. 2026 May; 58(5):1040-1050.
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Weisburd B, Dolzhenko E, Bennett MF, Danzi MC, Xu IRL, Tanudisastro H, Gu B, English A, Hiatt L, Mokveld T, De Sena Brandine G, Chiu R, Kurtas NE, Jam HZ, Brand H, Rajan-Babu IS, Bahlo M, Chaisson MJP, Züchner S, Gymrek M, Dashnow H, Eberle MA, Rehm HL. Defining a tandem repeat catalog and variation clusters for genome-wide analyses and population databases. Am J Hum Genet. 2026 May 07; 113(5):915-928.
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Dahl A, Sajuthi S, Rappaport N, Galanter J, Gignoux C, Burchard E, Seibold M, Zaitlen N. Context-specific genetic effects inform endotypes and treatment in asthma. J Allergy Clin Immunol. 2026 Jul; 158(1):91-103.
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Hu X, Araujo DS, Khunsriraksakul C, Wang L, Sun Q, Wen J, Zhou L, Ekunwe L, Lange LA, Lange EM, Montgomery SB, Reiner AP, Aguet F, Ardlie KG, Lappalainen T, Gignoux CR, Burchard EG, Taylor KD, Guo X, Rotter JI, Rich SS, Cornell E, Durda P, Tracy RP, Liu Y, Johnson WC, Papanicolaou GP, Perera MA, Cho MH, Liu DJ, Raffield LM, Li Y, Wheeler HE, Im HK, Manichaikul A. Multi-ancestry transcriptome prediction with functionally informed variants in TOPMed MESA improves performance of transcriptome-wide association studies. Am J Hum Genet. 2026 Apr 02; 113(4):828-841.
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Rader L, Zorina-Lichtenwalter K, Hatoum AS, Stallings MC, Wager TD, Friedman NP. Genetic overlap of chronic pain, musculoskeletal-specific pain, substance use disorders and substance use consumption: Common addiction and substance-specific effects. Addiction. 2026 Jul; 121(7):1683-1698.
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Rader L, Zorina-Lichtenwalter K, Gustavson DE, Wager TD, Friedman NP. Adolescent pain reports share genetic overlap with adult chronic pain conditions: A polygenic score analysis using the ABCD study. J Pain. 2026 Jun; 43:106260.
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