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 | 67 | 107 | | 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 | 13 | 16 |
To return to the timeline, click here.
Below are the most recent publications written about "Polymorphism, Single Nucleotide" by people in Profiles.
-
Murphy JI, Barnard R, Null M, Hendricks AE. RAREsim2: flexible simulation of rare variant genetic data using real haplotypes. Bioinformatics. 2026 May 03; 42(5).
-
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.
-
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 04 02; 113(4):828-841.
-
Salmon K, Cohen CC, Lange L, Dabelea D, Perng W. Dietary Patterns, Hepatic Fat Fraction, and the Role of Genotype. Nutrients. 2026 Mar 28; 18(7).
-
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.
-
Srivastava H, Raghuvanshi S, Bhalla S, Raghuvanshi S, Singh A, Singh AK, Singh N, Nigam N, Sonkar GK, Iqbal Z, Prakash S. PIK3CA Polymorphisms in Cervical Cancer: Differential Impact of rs6443624 and rs141178472. Asian Pac J Cancer Prev. 2026 Mar 01; 27(3):1061-1068.
-
White SL, Brasher MS, Pattee J, Zhou W, Chapman S, Jee YH, Bell CC, Jamil TL, Barrio M, Arehart CH, Evans LM, Hirbo J, Cox NJ, Straub P, Namba S, Bertucci-Richter E, Guare L, Edris A, Morris S, Mulford AJ, Zhang H, Fennessy B, Tobin MD, Chen J, Williams AT, John C, van Heel DA, Mathur R, Finer S, Moksnes MR, Brumpton BM, Åsvold BO, Peculis R, Rovite V, Konrade I, Wang Y, Crooks K, Chavan S, Fisher MJ, Rafaels N, Lin M, Shortt JA, Sanders AR, Whiteman DC, MacGregor S, Medland SE, Thorsteinsdóttir U, Stefánsson K, Karaderi T, Egan KM, Bocklage T, McCrary HC, Riedlinger G, Salhia B, Shriver C, Phan MD, Farlow JL, Edge S, Kaur V, Churchman ML, Rounbehler RJ, Brock PL, Ringel MD, Pividori M, Schweppe R, Raeburn CD, Walters RG, Chen Z, Li L, Matsuda K, Okada Y, Zöllner S, Verma A, Preuss MH, Kenny E, Hendricks AE, Fishbein L, Kraft P, Daly MJ, Neale BM, Martin AR, Cole JB, Haugen BR, Gignoux CR, Pozdeyev N. Global multi-ancestry genome-wide analyses identify genes and biological pathways associated with thyroid cancer and benign thyroid diseases. Nat Genet. 2026 Feb; 58(2):307-316.
-
Aydemir O, Bailey JA, Agardh D, Lernmark Å, Noble JA, Andersson Svärd A, Blankenhorn EP, Parikh HM, Ziegler AG, Toppari J, Akolkar B, Hagopian WA, Rewers MJ, Mordes JP. Polymorphisms in intron 1 of HLA-DRA differentially associate with type 1 diabetes and celiac disease and implicate involvement of complement system genes C4A and C4B. Elife. 2026 Feb 02; 12.
|
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.
|