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.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2000 | 3 | 4 | 7 |
| 2001 | 6 | 5 | 11 |
| 2002 | 6 | 7 | 13 |
| 2003 | 10 | 9 | 19 |
| 2004 | 10 | 15 | 25 |
| 2005 | 30 | 23 | 53 |
| 2006 | 29 | 32 | 61 |
| 2007 | 41 | 43 | 84 |
| 2008 | 62 | 64 | 126 |
| 2009 | 66 | 80 | 146 |
| 2010 | 86 | 101 | 187 |
| 2011 | 86 | 112 | 198 |
| 2012 | 92 | 138 | 230 |
| 2013 | 86 | 123 | 209 |
| 2014 | 58 | 89 | 147 |
| 2015 | 48 | 92 | 140 |
| 2016 | 39 | 100 | 139 |
| 2017 | 49 | 78 | 127 |
| 2018 | 38 | 85 | 123 |
| 2019 | 31 | 82 | 113 |
| 2020 | 23 | 48 | 71 |
| 2021 | 17 | 57 | 74 |
| 2022 | 5 | 39 | 44 |
| 2023 | 4 | 25 | 29 |
| 2024 | 15 | 33 | 48 |
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Below are the most recent publications written about "Polymorphism, Single Nucleotide" by people in Profiles.
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Genetic variants in canonical Wnt signaling pathway associated with pediatric immune thrombocytopenia. Blood Adv. 2024 Nov 12; 8(21):5529-5538.
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Body composition in recurrent prostate cancer and the role of steroidogenic genotype. Endocr Relat Cancer. 2024 Dec 01; 31(12).
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Identification of allele-specific KIV-2 repeats and impact on Lp(a) measurements for cardiovascular disease risk. BMC Med Genomics. 2024 Oct 24; 17(1):255.
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Rare variant contribution to the heritability of coronary artery disease. Nat Commun. 2024 Oct 09; 15(1):8741.
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Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height. Nat Commun. 2024 Oct 03; 15(1):8549.
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A genome-wide Association study of the Count of Codeine prescriptions. Sci Rep. 2024 10 01; 14(1):22780.
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Reconstructing oral cavity tumor evolution through brush biopsy. Sci Rep. 2024 09 30; 14(1):22591.
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Exploring the complexity of systemic sclerosis etiology by trio whole genome sequencing. Hum Mol Genet. 2024 Sep 19; 33(19):1643-1647.
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Semi-supervised machine learning method for predicting homogeneous ancestry groups to assess Hardy-Weinberg equilibrium in diverse whole-genome sequencing studies. Am J Hum Genet. 2024 Oct 03; 111(10):2129-2138.
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Disease prediction with multi-omics and biomarkers empowers case-control genetic discoveries in the UK Biobank. Nat Genet. 2024 Sep; 56(9):1821-1831.