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 |
| 2005 | 2 | 2 | 4 |
| 2006 | 4 | 2 | 6 |
| 2007 | 12 | 5 | 17 |
| 2008 | 12 | 9 | 21 |
| 2009 | 10 | 9 | 19 |
| 2010 | 11 | 8 | 19 |
| 2011 | 8 | 12 | 20 |
| 2012 | 5 | 8 | 13 |
| 2013 | 10 | 12 | 22 |
| 2014 | 12 | 7 | 19 |
| 2015 | 11 | 16 | 27 |
| 2016 | 4 | 14 | 18 |
| 2017 | 6 | 10 | 16 |
| 2018 | 2 | 8 | 10 |
| 2019 | 1 | 9 | 10 |
| 2020 | 3 | 18 | 21 |
| 2021 | 2 | 5 | 7 |
| 2022 | 0 | 7 | 7 |
| 2023 | 0 | 5 | 5 |
| 2024 | 1 | 5 | 6 |
| 2025 | 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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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.
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Unraveling the genetic landscape of susceptibility to multiple primary cancers. HGG Adv. 2025 Apr 10; 6(2):100413.
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Reduced circulating sphingolipids and CERS2 activity are linked to T2D risk and impaired insulin secretion. Sci Adv. 2025 Jan 10; 11(2):eadr1725.
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Genome-wide association analyses identify distinct genetic architectures for age-related macular degeneration across ancestries. Nat Genet. 2024 Dec; 56(12):2659-2671.
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Structural framework to address variant-gene relationship in primary open-angle glaucoma. Vision Res. 2025 Jan; 226:108505.
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Commonly used genomic arrays may lose information due to imperfect coverage of discovered variants for autism spectrum disorder. J Neurodev Disord. 2024 Sep 12; 16(1):54.
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Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science. 2024 07 19; 385(6706):eadj1182.
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Mammographic density mediates the protective effect of early-life body size on breast cancer risk. Nat Commun. 2024 May 13; 15(1):4021.
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Multi-ancestry genome-wide meta-analysis identifies novel basal cell carcinoma loci and shared genetic effects with squamous cell carcinoma. Commun Biol. 2024 01 05; 7(1):33.