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 | 24 | 19 | 43 |
| 2006 | 17 | 26 | 43 |
| 2007 | 25 | 32 | 57 |
| 2008 | 38 | 38 | 76 |
| 2009 | 45 | 49 | 94 |
| 2010 | 48 | 68 | 116 |
| 2011 | 52 | 72 | 124 |
| 2012 | 64 | 100 | 164 |
| 2013 | 57 | 73 | 130 |
| 2014 | 41 | 75 | 116 |
| 2015 | 37 | 83 | 120 |
| 2016 | 40 | 91 | 131 |
| 2017 | 46 | 65 | 111 |
| 2018 | 32 | 66 | 98 |
| 2019 | 33 | 69 | 102 |
| 2020 | 21 | 52 | 73 |
| 2021 | 15 | 57 | 72 |
| 2022 | 5 | 40 | 45 |
| 2023 | 3 | 23 | 26 |
| 2024 | 20 | 37 | 57 |
| 2025 | 7 | 53 | 60 |
| 2026 | 2 | 17 | 19 |
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Below are the most recent publications written about "Polymorphism, Single Nucleotide" by people in Profiles.
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Tractor workflow: a scalable Nextflow framework for local ancestry-aware genome-wide association studies. Bioinformatics. 2026 May 03; 42(5).
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Genomic and patient epidemiology of Streptococcus dysgalactiae subspecies equisimilis in Houston, Texas. Microbiol Spectr. 2026 Apr 07; 14(4):e0368325.
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Mapping epigenetic gene variant dynamics: comparative analysis of frequency, functional impact and trait associations in African and European populations. Sci Rep. 2026 Mar 06; 16(1).
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Comparison of variant callers using 60?532 multi-ancestry whole genome sequences. Brief Bioinform. 2026 Mar 01; 27(2).
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Phenome-wide analysis of copy number variants in 470,727 UK Biobank genomes. Nature. 2026 04; 652(8110):675-685.
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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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Morning Larks and Night Owls: Considering Chronotype in Evaluation of Patients with Pulmonary Hypertension. Ann Am Thorac Soc. 2026 Feb 01; 23(2):261-271.
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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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Barrett's esophagus-associated genetic loci in African Americans: a case-control study using the All of Us Research Program. Eur J Gastroenterol Hepatol. 2026 Jun 01; 38(6):684-690.
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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.