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
|
| MeSH Number(s) |
G05.365.795.598
|
| Concept/Terms |
Polymorphism, Single Nucleotide- Polymorphism, Single Nucleotide
- Nucleotide Polymorphism, Single
- Nucleotide Polymorphisms, Single
- Polymorphisms, Single Nucleotide
- Single Nucleotide Polymorphisms
- SNPs
- Single Nucleotide Polymorphism
|
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 | 9 | 5 | 14 | | 2005 | 10 | 15 | 25 | | 2006 | 17 | 19 | 36 | | 2007 | 18 | 28 | 46 | | 2008 | 38 | 33 | 71 | | 2009 | 31 | 42 | 73 | | 2010 | 30 | 57 | 87 | | 2011 | 41 | 44 | 85 | | 2012 | 25 | 68 | 93 | | 2013 | 38 | 62 | 100 | | 2014 | 40 | 68 | 108 | | 2015 | 27 | 60 | 87 | | 2016 | 27 | 63 | 90 | | 2017 | 23 | 81 | 104 | | 2018 | 26 | 50 | 76 | | 2019 | 17 | 61 | 78 | | 2020 | 18 | 41 | 59 | | 2021 | 16 | 52 | 68 | | 2022 | 9 | 41 | 50 | | 2023 | 5 | 24 | 29 | | 2024 | 15 | 35 | 50 | | 2025 | 4 | 57 | 61 | | 2026 | 3 | 19 | 22 |
To return to the timeline, click here.
Below are the most recent publications written about "Polymorphism, Single Nucleotide" by people in Profiles.
-
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.
-
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.
-
Font-Porterias N, Nemat-Gorgani N, Kichula KM, Al-Hindi DR, Harrison GF, Tao S, Zhu F, Montero-Martin G, Fernández-Viña MA, Guethlein LA, Parham P, Oppenheimer SJ, Ioannidis AG, Moreno-Estrada A, Pomat W, Mentzer AJ, Henn BM, Norman PJ. Signatures of pathogen-driven selection and Austronesian gene flow of Papua New Guinea HLA alleles. Am J Hum Genet. 2026 Jun 04; 113(6):1175-1193.
-
Sapin E, Kelly KM, Keller MC. A novel method for across-chromosome phasing without relative data. Bioinformatics. 2026 May 03; 42(5).
-
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.
-
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.
-
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.
-
Evans LM, Arehart CH, Gibson RA, Bowman GI, Gignoux CR. A simple approach for multiple observations improves power to detect genetic effects and genomic prediction accuracy. HGG Adv. 2026 Apr 09; 7(2):100586.
-
Shemirani R, Belbin GM, Cullina S, Caggiano C, Gignoux CR, Zaitlen N, Kenny EE. A spectral component approach leveraging identity-by-descent graphs to address recent population structure in genomic analysis. Genome Res. 2026 03 02; 36(3):534-546.
-
Gupta A, Dahlin A, Macario A, Gally F, Weaver MR, Guarino S, Kahn L, Sanford L, Gruca MA, Cho MH, Dowell RD, Weiss ST, Sasse SK, Gerber AN. Functional Variant Discovery Identifies a Novel Genetic Link between SPRY2, Wood Smoke, and Asthma. Am J Respir Cell Mol Biol. 2026 03 01; 74(3):326-338.
|
People  People who have written about this concept. _
Similar Concepts
People who have written about this concept.
_
Top Journals
Top journals in which articles about this concept have been published.
|