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 | 38 | 43 | 81 | | 2012 | 25 | 66 | 91 | | 2013 | 38 | 62 | 100 | | 2014 | 39 | 62 | 101 | | 2015 | 26 | 62 | 88 | | 2016 | 29 | 63 | 92 | | 2017 | 23 | 79 | 102 | | 2018 | 23 | 50 | 73 | | 2019 | 17 | 55 | 72 | | 2020 | 18 | 40 | 58 | | 2021 | 17 | 52 | 69 | | 2022 | 9 | 41 | 50 | | 2023 | 5 | 24 | 29 | | 2024 | 17 | 35 | 52 | | 2025 | 4 | 56 | 60 | | 2026 | 3 | 27 | 30 |
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Below are the most recent publications written about "Polymorphism, Single Nucleotide" by people in Profiles.
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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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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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Orchard P, Blackwell TW, Kachuri L, Castaldi PJ, Cho MH, Christenson SA, Durda P, Gabriel S, Hersh CP, Huntsman S, Hwang S, Joehanes R, Johnson M, Li X, Lin H, Liu CT, Liu Y, Mak ACY, Manichaikul AW, Paik DT, Saferali A, Smith JD, Taylor KD, Tracy RP, Wang J, Wang M, Weinstock JS, Weiss J, Wheeler HE, Zhou Y, Zöllner S, Wu JC, Mestroni L, Graw S, Taylor MRG, Ortega VE, Johnson WC, Gan W, Abecasis G, Nickerson DA, Gupta N, Ardlie K, Woodruff PG, Bowler RP, Meyers DA, Reiner A, Kooperberg C, Ziv E, Vasan RS, Larson MG, Cupples LA, Silverman EK, Rich SS, Heard-Costa N, Tang H, Rotter JI, Smith AV, Levy D, Aguet F, Scott LJ, Raffield LM, Parker SCJ, Abe N, Almasy L, Ament S, Anugu P, Auer P, Avramopoulos D, Balasubramanian A, Barr RG, Barwick L, Beaty T, Becker D, Becker L, Beitelshees A, Benos T, Bezerra M, Bis J, Brody J, Broeckel U, Broome J, Bunting K, Buth E, Carey V, Carty C, Casaburi R, Chaffin M, Chang C, Chang YC, Chavan S, Chen BJ, Chen WM, Choi SH, Chuang LM, Chung RH, Conomos M, Cornell E, Crandall C, Crapo J, Curtis J, Damcott C, David S, de Las Fuentes L, de Vries P, Deka R, DeMeo D, Devine S, Dinh H, Doddapaneni H, Duan Q, Duggirala R, Eaton C, Ekunwe L, El Boueiz A, Emery L, Farber C, Farek J, Franceschini N, Frazar C, Fu M, Fullerton SM, Fulton L, Gao S, Gao Y, Gass M, Geiger H, Ghosh A, Gignoux C, Glahn D, Gogarten S, Gong DW, Goring H, Grine D, Gu CC, Guan Y, Hall M, Han Y, Harris D, Heavner B, Herrington D, Hobbs B, Hong E, Hoth K, Hsiung CA, Hu J, Hung YJ, Huston H, Hwu CM, Jackson R, Jain D, Johnsen J, Johnston R, Jones K, Kessler M, Khan A, Khan Z, Kim W, Kimoff J, Kinney G, Kramer H, Lange C, Lange E, Laurie C, Laurie C, LeBoff M, Lee S, Lee WJ, Levine D, Lewis J, Li Y, Lin X, Liu S, Liu Y, Make B, Manning A, Manson J, Martin L, Marton M, Mathai S, May S, McArdle P, McDonald ML, McFarland S, McGoldrick D, McHugh C, Mei H, Meigs J, Menon V, Min N, Moll M, Momin Z, Montasser M, Mychaleckyj JC, Naik R, Naseri T, Natarajan P, Nelson SC, Neltner B, Nessner C, Nkechinyere O, O'Connell J, O'Connor T, Ochs-Balcom H, Okwuonu G, Pankow J, Parker C, Peloso G, Peralta JM, Perez M, Perry J, Peters U, Phillips LS, Pollin T, Becker JP, Boorgula MP, Psaty B, Qiao D, Rafaels N, Rajendran M, Rasmussen-Torvik L, Ratan A, Reed R, Regan E, Reupena MS, Robillard R, Roselli C, Ruczinski I, Runnels A, Russell P, Ryan K, Sabino EC, Salimi S, Salvi S, Salzberg S, Sandow K, Santibanez J, Schwander K, Sciurba F, Sériès F, Shetty A, Shetty A, Silver B, Skomro R, Smith T, Smoller S, Snively B, Stilp AM, Storm G, Streeten E, Su JL, Sung YJ, Sylvia J, Szpiro A, Taub M, Taylor S, Thornton TA, Threlkeld M, Tinker L, Tirschwell D, Tiwari H, Tong C, Tsai M, Vaidya D, Walker T, Wallace R, Walts A, Wang FF, Wang H, Watson K, Watt J, Weng LC, Wessel J, Williams K, Wilson C, Wilson J, Winterkorn L, Wong Q, Wu B, Xu H, Yanek L, Yang I, Zekavat SM, Zhao SX, Zhao W, Zhu X. Cross-cohort analysis of expression and splicing quantitative trait loci in TOPMed. Science. 2026 Jul 16; 393(6808):eadx2989.
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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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Shadid A, Rich HE, Hok KD, Doursout MF, Restrepo MI, Banda NK, Gunamalai L, Shivshankar P. Comprehensive Prediction Analysis of Novel Noncoding Regulatory Variants Identified in the MicroRNA Binding Regions in Complement System Genes. Int J Mol Sci. 2026 Jun 30; 27(13).
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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 Jun; 17(3):e70293.
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Ockerman F, Chen BD, Sun Q, Kharitonova EV, Chen C, Zhou LY, Loos RJF, Kooperberg C, Peters U, Haessler J, Reiner AP, Jung SY, Manson JE, Nassir R, North KE, Buyske S, Haiman CA, Conti DV, Wilkens LR, Lange EM, Cox NJ, Cao H, Raffield LM, Li Y, Tao R. An efficient LASSO framework for admixture-aware polygenic scores. HGG Adv. 2026 Jul 09; 7(3):100628.
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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.
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Sapin E, Kelly KM, Keller MC. A novel method for across-chromosome phasing without relative data. Bioinformatics. 2026 May 03; 42(5).
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