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 |
|---|
| 1999 | 0 | 1 | 1 |
| 2000 | 1 | 5 | 6 |
| 2001 | 3 | 2 | 5 |
| 2002 | 14 | 8 | 22 |
| 2003 | 15 | 13 | 28 |
| 2004 | 13 | 22 | 35 |
| 2005 | 23 | 21 | 44 |
| 2006 | 23 | 28 | 51 |
| 2007 | 34 | 30 | 64 |
| 2008 | 40 | 45 | 85 |
| 2009 | 37 | 45 | 82 |
| 2010 | 51 | 62 | 113 |
| 2011 | 47 | 87 | 134 |
| 2012 | 50 | 90 | 140 |
| 2013 | 34 | 66 | 100 |
| 2014 | 27 | 76 | 103 |
| 2015 | 25 | 61 | 86 |
| 2016 | 21 | 48 | 69 |
| 2017 | 17 | 47 | 64 |
| 2018 | 27 | 48 | 75 |
| 2019 | 13 | 48 | 61 |
| 2020 | 13 | 36 | 49 |
| 2021 | 15 | 43 | 58 |
| 2022 | 5 | 27 | 32 |
| 2023 | 2 | 19 | 21 |
| 2024 | 14 | 32 | 46 |
| 2025 | 0 | 18 | 18 |
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Below are the most recent publications written about "Polymorphism, Single Nucleotide" by people in Profiles.
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Alzheimer's disease protective allele of Clusterin modulates neuronal excitability through lipid-droplet-mediated neuron-glia communication. Mol Neurodegener. 2025 May 03; 20(1):51.
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Integration of functional genomics and statistical fine-mapping systematically characterizes adult-onset and childhood-onset asthma genetic associations. Genome Med. 2025 Apr 10; 17(1):35.
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EndoPRS: Incorporating endophenotype information to improve polygenic risk scores for clinical endpoints-A study in asthma. Am J Hum Genet. 2025 May 01; 112(5):1199-1214.
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Pharmacogenomics of chemotherapy induced peripheral neuropathy using an electronic health record-derived definition: a genome-wide association study. Support Care Cancer. 2025 Apr 08; 33(5):362.
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PKCd Germline Variants and Genetic Deletion in Mice Augment Antitumor Immunity through Regulation of Myeloid Cells. Cancer Immunol Res. 2025 Apr 02; 13(4):547-559.
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Fecal Microbial Profiles and Short-Chain Fatty Acid/Bile Acid Metabolomics in Patients With Age-Related Macular Degeneration: A Pilot Study. Invest Ophthalmol Vis Sci. 2025 Apr 01; 66(4):21.
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Genetic Loci Influencing Cue-Reactivity in Heterogeneous Stock Rats. Genes Brain Behav. 2025 Apr; 24(2):e70018.
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RatXcan: A framework for cross-species integration of genome-wide association and gene expression data. PLoS Genet. 2025 Mar; 21(3):e1011583.
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Missense variants in FRS3 affect body mass index in populations of diverse ancestries. Nat Commun. 2025 Mar 25; 16(1):2694.
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Genome-wide association study of prostate-specific antigen levels in 392,522 men identifies new loci and improves prediction across ancestry groups. Nat Genet. 2025 Feb; 57(2):334-344.