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 | 4 | 4 | 8 |
| 2002 | 6 | 6 | 12 |
| 2003 | 8 | 7 | 15 |
| 2004 | 8 | 10 | 18 |
| 2005 | 23 | 19 | 42 |
| 2006 | 17 | 26 | 43 |
| 2007 | 25 | 32 | 57 |
| 2008 | 38 | 37 | 75 |
| 2009 | 44 | 48 | 92 |
| 2010 | 48 | 68 | 116 |
| 2011 | 52 | 72 | 124 |
| 2012 | 63 | 100 | 163 |
| 2013 | 57 | 70 | 127 |
| 2014 | 42 | 74 | 116 |
| 2015 | 35 | 83 | 118 |
| 2016 | 40 | 87 | 127 |
| 2017 | 44 | 64 | 108 |
| 2018 | 31 | 64 | 95 |
| 2019 | 30 | 67 | 97 |
| 2020 | 21 | 48 | 69 |
| 2021 | 14 | 55 | 69 |
| 2022 | 5 | 40 | 45 |
| 2023 | 3 | 22 | 25 |
| 2024 | 18 | 32 | 50 |
| 2025 | 7 | 50 | 57 |
| 2026 | 4 | 36 | 40 |
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Below are the most recent publications written about "Polymorphism, Single Nucleotide" by people in Profiles.
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A Genetic Risk Variant Associated With the Risk of Primary Biliary Cholangitis Is Inherited From Neanderthals. Liver Int. 2026 Oct; 46(10):e70868.
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Explaining the unexplained admixture mapping signals via rare variants: the HCHS/SOL. Hum Mol Genet. 2026 Sep 25; 35(20).
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Genome-wide association analyses highlight the neuronal contribution to multiple sclerosis susceptibility. Nat Genet. 2026 Sep; 58(9):2177-2191.
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Mapping long-read sequences to a complete reference genome reveals uncaptured variants across the ?-Globin cluster in Africans with sickle cell disease. HGG Adv. 2026 Oct 08; 7(4):100669.
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Evidence of genetic susceptibility to immune-related dermatitis in patients with melanoma treated with immune checkpoint inhibitors. Melanoma Res. 2026 Oct 01; 36(5):407-415.
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Shared genetic architecture and therapeutic targets across paediatric immune-mediated diseases. Ann Rheum Dis. 2026 Sep; 85(9):1866-1878.
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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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Exploratory identification of candidate SNP markers associated with recurrent clinical mastitis in Holstein cattle. PLoS One. 2026; 21(7):e0355230.
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Extending genome-wide association studies to admixed cohorts with high degrees of relatedness. Nat Genet. 2026 Aug; 58(8):1822-1830.
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Multi-ancestry genome-wide association meta-analysis of hepatocellular carcinoma identifies 15 risk loci including MAP3K9, DHRS1, MTTP, and 8q24.21. HGG Adv. 2026 Oct 08; 7(4):100639.