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 |
|---|
| 2003 | 1 | 0 | 1 |
| 2004 | 0 | 1 | 1 |
| 2005 | 2 | 2 | 4 |
| 2006 | 4 | 2 | 6 |
| 2007 | 11 | 5 | 16 |
| 2008 | 12 | 9 | 21 |
| 2009 | 10 | 8 | 18 |
| 2010 | 10 | 8 | 18 |
| 2011 | 8 | 10 | 18 |
| 2012 | 5 | 8 | 13 |
| 2013 | 10 | 13 | 23 |
| 2014 | 12 | 7 | 19 |
| 2015 | 11 | 14 | 25 |
| 2016 | 4 | 13 | 17 |
| 2017 | 6 | 10 | 16 |
| 2018 | 2 | 8 | 10 |
| 2019 | 1 | 9 | 10 |
| 2020 | 3 | 17 | 20 |
| 2021 | 2 | 5 | 7 |
| 2022 | 0 | 7 | 7 |
| 2023 | 0 | 5 | 5 |
| 2024 | 1 | 5 | 6 |
| 2025 | 1 | 6 | 7 |
| 2026 | 0 | 4 | 4 |
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Below are the most recent publications written about "Polymorphism, Single Nucleotide" by people in Profiles.
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Genetic survey of biomarkers at early and mid-pregnancy identifies pregnancy-specialized immune regulation. PLoS Genet. 2026 Jun; 22(6):e1012204.
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Multi-ancestry genome-wide association analyses of refractive error augment genetic discovery and polygenic prediction. Nat Genet. 2026 May; 58(5):1030-1039.
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Genetic risk factors modulate the association between physical activity and colorectal cancer. BMC Med. 2026 02 05; 24(1).
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Repeated Independent Formation of Triploid Lineages Contributes to Clonal Diversity in Heteronotia binoei Parthenogens. Mol Ecol. 2026 Jan; 35(2):e70240.
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A multi-ancestry meta genome-wide association study of migraine among veterans:?associations with traumatic brain injury, depression, and post-traumatic stress disorder. Mol Psychiatry. 2026 May; 31(5):2660-2674.
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Multiple polygenic score approach in colorectal cancer risk prediction. Sci Rep. 2025 Oct 30; 15(1):38006.
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Large-scale GWAS of strabismus identifies risk loci and provides support for a link with maternal smoking. Nat Commun. 2025 Aug 23; 16(1):7890.
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Whole Exome Sequencing Study Uncovers Novel Candidate Genes and Protein-Coding Variants for Cataract. Invest Ophthalmol Vis Sci. 2025 Aug 01; 66(11):32.
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Large-scale multi-omics analyses in Hispanic/Latino populations identify genes for cardiometabolic traits. Nat Commun. 2025 Apr 11; 16(1):3438.
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SARS-CoV-2 Omicron subvariant genomic variation associations with immune evasion in Northern California: A retrospective cohort study. PLoS One. 2025; 20(2):e0319218.