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 | 32 | 69 | 101 |
| 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 | 3 | 18 | 21 |
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Below are the most recent publications written about "Polymorphism, Single Nucleotide" by people in Profiles.
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Ethnic Differences in the Association Between SOD2 rs4880 and Hepatotoxicity in Pediatric Acute Lymphoblastic Leukemia: A Report From the REDIAL Consortium. Pediatr Blood Cancer. 2026 Jul; 73(7):e70387.
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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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Whole genome sequencing analysis of over 3500 individuals dementia-free over 85 years old. J Alzheimers Dis. 2026 Jun; 111(4):1772-1782.
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Genomic Characterization of a Locally Transmitted Leishmania mexicana Isolate from Texas. Am J Trop Med Hyg. 2026 Jun 03; 114(6):1104-1108.
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Exome sequencing identifies additional pathogenic variants in neurodevelopmental genes in 3.6% of individuals with tuberous sclerosis complex. Genet Med. 2026 Jun; 28(6):102582.
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Ultra-rare functional variants reveal early-onset breast cancer risk genes and pathways in the UK Biobank and All of Us Research Program. Am J Hum Genet. 2026 May 07; 113(5):1049-1066.
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Insights into inherited genetic variations and genetic ancestry of patients with high-risk melanoma. Melanoma Res. 2026 Jun 01; 36(3):189-196.
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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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Genomic and patient epidemiology of Streptococcus dysgalactiae subspecies equisimilis in Houston, Texas. Microbiol Spectr. 2026 Apr 07; 14(4):e0368325.
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Assessing the readiness of Oxford Nanopore sequencing for clinical genomics applications. Genome Res. 2026 Mar 02; 36(3):460-471.