 Polymorphism, Single Nucleotide
"Polymorphism, Single Nucleotide" 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.
A single nucleotide variation in a genetic sequence that occurs at appreciable frequency in the population.
| Descriptor ID |
D020641
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| MeSH Number(s) |
G05.365.795.598
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| Concept/Terms |
Polymorphism, Single Nucleotide- Polymorphism, Single Nucleotide
- Nucleotide Polymorphism, Single
- Nucleotide Polymorphisms, Single
- Polymorphisms, Single Nucleotide
- Single Nucleotide Polymorphisms
- SNPs
- Single Nucleotide Polymorphism
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Below are MeSH descriptors whose meaning is more general than "Polymorphism, Single Nucleotide".
Below are MeSH descriptors whose meaning is more specific than "Polymorphism, Single Nucleotide".
This graph shows the total number of publications written about "Polymorphism, Single Nucleotide" by people in this website by year, and whether "Polymorphism, Single Nucleotide" 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 |
|---|
| 1999 | 1 | 0 | 1 | | 2001 | 7 | 6 | 13 | | 2002 | 2 | 4 | 6 | | 2003 | 2 | 3 | 5 | | 2004 | 10 | 5 | 15 | | 2005 | 10 | 14 | 24 | | 2006 | 17 | 19 | 36 | | 2007 | 18 | 28 | 46 | | 2008 | 38 | 34 | 72 | | 2009 | 31 | 41 | 72 | | 2010 | 28 | 57 | 85 | | 2011 | 39 | 43 | 82 | | 2012 | 26 | 67 | 93 | | 2013 | 38 | 61 | 99 | | 2014 | 38 | 61 | 99 | | 2015 | 26 | 62 | 88 | | 2016 | 29 | 67 | 96 | | 2017 | 23 | 81 | 104 | | 2018 | 23 | 57 | 80 | | 2019 | 17 | 61 | 78 | | 2020 | 18 | 40 | 58 | | 2021 | 19 | 51 | 70 | | 2022 | 9 | 38 | 47 | | 2023 | 5 | 24 | 29 | | 2024 | 17 | 36 | 53 | | 2025 | 4 | 56 | 60 | | 2026 | 3 | 35 | 38 |
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Below are the most recent publications written about "Polymorphism, Single Nucleotide" by people in Profiles.
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Mattila M, Mramba LK, Niinistö S, Erlund I, Liu X, Uusitalo U, Andrén Aronsson C, Hummel S, Frohnert BI, Parikh HM, Rich SS, Hagopian W, Toppari J, Lernmark Å, Ziegler AG, Rewers M, Krischer JP, Hakola L, Norris JM, Virtanen SM. Dietary vitamin C intake and the risk of islet autoimmunity and type 1 diabetes: The Environmental Determinants of Diabetes in the Young (TEDDY) Study. Eur J Nutr. 2026 Sep 24; 65(7).
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Gonzalez-Covarrubias V, Morales-Alfaro A, Bonilla-Jimenez O, Rodríguez-Dorantes M, Frías-Jimenez E, Soto-Perez-de-Celis E. Characterization of DPYD pharmacogenetic variation in Mexican patients with gastrointestinal malignancies. Cancer Chemother Pharmacol. 2026 Sep 17; 96(1).
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Ingold M, Gao Q, Mandel JR, McNellie JP, Keepers KG, Barb JG, Burke JM, Rieseberg LH, Hulke BS. The stability of fatty acid composition in sunflower oil is dependent on environment and affected by structural variation. Theor Appl Genet. 2026 Aug 20; 139(9).
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Peyrot WJ, Panagiotaropoulou G, Olde Loohuis LM, Adams MJ, Andreassen OA, Awasthi S, Forstner AJ, Ge T, McIntosh AM, Mitchell BL, Mullins N, O'Connell KS, Penninx BWJH, Posthuma D, Ripke S, Ruderfer DM, Uffelmann E, Vilhjalmsson BJ, Zhu Z, Smoller JW, Price AL. Distinguishing different psychiatric disorders using DDx-PRS. Nat Genet. 2026 Sep; 58(9):2371-2380.
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Sadeeq SA, Leaton LA, Kichula KM, Farias TDJ, Font-Porterias N, Pollock NR, Collora CE, Castelli EC, Gignoux CR, Norman PJ. PONG 2.0: allele imputation for the killer cell immunoglobulin-like receptors. Hum Mol Genet. 2026 Aug 10; 35(17).
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Mueller SA, Srinivasan U, Laubach ZM, Schield DR, von Rönn JAC, Safran RJ, Wolf JBW. Covariation of genetic and epigenetic divergence in barn swallows. Genome Res. 2026 Aug 03; 36(8):1561-1573.
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Wang N, DiCorpo DA, Zhang Y, Kleinbrink E, Arnett DK, Barnard J, Blangero J, Bowden DW, Carson AP, Chen YI, Chung MK, Curran JE, Darbar D, Duggirala R, Ellinor PT, Fatkin D, Fornage M, Heard-Costa N, He J, Hou L, Kardia SLR, Kooperberg C, Loos RJF, McManus DD, Mitchell BD, Minster RL, North KE, Psaty BM, Raffield LM, Redline S, Rich SS, Roden D, Rotter JI, Shoemaker MB, Smith JD, Van Wagoner DR, Aguet F, Ardlie K, Bis JC, Brody JA, Cade BE, Clish CB, de Vries PS, Floyd JS, Freedman BI, Gabriel S, Gerzsten RE, Goodarzi MO, Gu C, Guo X, Gupta N, Heckbert SR, Hsu S, Hung YJ, Kalyani RR, Kelly TN, Kinney GL, Li C, Liu S, Liu Y, Lloyd-Jones DM, Manson JE, Mathias RA, Mercader JM, Morrison AC, Naseri T, Onengut S, Palmer ND, Peyser PA, Qi Q, Raghavan S, Reiner AP, Rooney MR, Sevilla-Gonzalez M, Sarnowski C, Smith JD, Smith JA, Spartano NL, Tahir U, Taylor KD, Tobias DK, Tracy RP, Viali S, Wang H, Wood AC, Yanek LR, Zhao W, Zheng Y, Dupuis J, Liu CT, Sladek R, Wessel J, Meigs JB, Manning AK. Colocalization of eQTLs With Type 2 Diabetes and Glycemic Traits Using Whole-Genome Sequences in Diverse Populations From the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program. Diabetes. 2026 Aug 01; 75(8):1477-1491.
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Palmieri L, Dowle EJ, Nadachowska-Brzyska K, Schopf A, Dobart N, Stauffer C, Schuler H, Ragland GJ, Schebeck M. Genomic Predictors of Diapause Polymorphism in the Bark Beetle Ips typographus With Implications for Voltinism Potential and Outbreak Dynamics. Mol Ecol. 2026 Aug; 35(16):e70532.
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Bright U, Beck S, Levey DF, Deak JD, Gaziano JM, Stein MB, Gelernter J. The genetics of fibromyalgia and its relationships to psychiatric and medical traits. Nat Commun. 2026 Jul 28; 17(1).
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Irvin MR, Srinivasasainagendra V, Armstrong ND, Patki A, Broeckel U, Wang Z, Lange LA, Limdi NA, Huerta-Chagoya A, Kim J, Ng MCY, Mercader JM, Tiwari HK. Improving performance of polygenic risk scores for hypertension across two ancestry groups. PLoS One. 2026; 21(7):e0353311.
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