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 | 9 | 17 |
| 2005 | 24 | 19 | 43 |
| 2006 | 17 | 25 | 42 |
| 2007 | 24 | 29 | 53 |
| 2008 | 38 | 38 | 76 |
| 2009 | 44 | 49 | 93 |
| 2010 | 48 | 68 | 116 |
| 2011 | 51 | 71 | 122 |
| 2012 | 63 | 100 | 163 |
| 2013 | 57 | 73 | 130 |
| 2014 | 40 | 71 | 111 |
| 2015 | 34 | 78 | 112 |
| 2016 | 39 | 89 | 128 |
| 2017 | 45 | 64 | 109 |
| 2018 | 32 | 65 | 97 |
| 2019 | 32 | 66 | 98 |
| 2020 | 21 | 52 | 73 |
| 2021 | 15 | 57 | 72 |
| 2022 | 5 | 38 | 43 |
| 2023 | 2 | 19 | 21 |
| 2024 | 19 | 30 | 49 |
| 2025 | 7 | 35 | 42 |
| 2026 | 0 | 7 | 7 |
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Below are the most recent publications written about "Polymorphism, Single Nucleotide" by people in Profiles.
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Rare heterozygous missense variants in VSX2 are associated with retinal detachment. PLoS Genet. 2026 Feb; 22(2):e1012027.
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Genetic Predictors of Response to Oral Insulin for Type 1 Diabetes Prevention. Diabetes Care. 2026 Feb 01; 49(2):344-351.
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Genetic Architecture of N-Terminal Pro-B-Type Natriuretic Peptide in a Multiancestry Study Population. Circ Genom Precis Med. 2026 Feb; 19(1):e005130.
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Unravelling the molecular mechanisms causal to type 2 diabetes across global populations and disease-relevant tissues. Nat Metab. 2026 Feb; 8(2):506-520.
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Cross-ancestry comparison of aptamer and antibody protein measures. Nat Commun. 2026 Jan 22; 17(1):1054.
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Genetic Risk and Transition Through Preclinical Stages of Type 1 Diabetes. J Clin Endocrinol Metab. 2026 Jan 21; 111(2):e493-e499.
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The biomedical landscape of genomic structural variation in the qatari population. Nat Commun. 2026 Jan 13; 17(1):1019.
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An integrated platform for concurrent structural and single-nucleotide variants improves copy-number detection and reveals pathogenic alleles in undiagnosed Mendelian families. Genome Med. 2025 Dec 31; 18(1):16.
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Evaluating the Genetic Overlap Between Congenital Heart Disease and Neuroblastoma Risk. Pediatr Blood Cancer. 2026 Feb; 73(2):e70055.
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Clair3-RNA: a deep learning-based small variant caller for long-read RNA sequencing data. Nat Commun. 2025 Dec 22; 16(1):11553.