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 |
|---|
| 2002 | 1 | 0 | 1 |
| 2003 | 0 | 1 | 1 |
| 2004 | 0 | 1 | 1 |
| 2005 | 0 | 1 | 1 |
| 2006 | 1 | 3 | 4 |
| 2007 | 3 | 0 | 3 |
| 2008 | 1 | 1 | 2 |
| 2009 | 1 | 2 | 3 |
| 2010 | 2 | 1 | 3 |
| 2011 | 1 | 2 | 3 |
| 2012 | 0 | 1 | 1 |
| 2013 | 2 | 6 | 8 |
| 2014 | 2 | 3 | 5 |
| 2015 | 2 | 3 | 5 |
| 2016 | 2 | 3 | 5 |
| 2017 | 1 | 6 | 7 |
| 2018 | 2 | 3 | 5 |
| 2019 | 5 | 5 | 10 |
| 2020 | 4 | 5 | 9 |
| 2021 | 4 | 4 | 8 |
| 2022 | 2 | 7 | 9 |
| 2023 | 0 | 6 | 6 |
| 2024 | 2 | 8 | 10 |
| 2025 | 0 | 1 | 1 |
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Below are the most recent publications written about "Polymorphism, Single Nucleotide" by people in Profiles.
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Strength of Genetic Associations with Thyrotropin Values Differs Between Populations with Similarity to African and European Reference Populations. Thyroid. 2025 Feb; 35(2):131-142.
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The vitamin D receptor TaqI TT genotype is associated with type 1 diabetes in the Black South African population. J Nutr Sci. 2024; 13:e73.
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High-coverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalog of human genetic variation. Genome Res. 2024 Nov 20; 34(11):2061-2073.
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Accounting for heterogeneity due to environmental sources in meta-analysis of genome-wide association studies. Commun Biol. 2024 Nov 14; 7(1):1512.
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Heterogeneous genetic architectures of prostate cancer susceptibility in sub-Saharan Africa. Nat Genet. 2024 Oct; 56(10):2093-2103.
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Ancestry-aligned polygenic scores combined with conventional risk factors improve prediction of cardiometabolic outcomes in African populations. Genome Med. 2024 Aug 26; 16(1):106.
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The variation landscape of CYP2D6 in a multi-ethnic Asian population. Sci Rep. 2024 07 20; 14(1):16725.
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Variability of polygenic prediction for body mass index in Africa. Genome Med. 2024 05 30; 16(1):74.
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Impact of donor CYP3A5 genotype on pharmacokinetics of tacrolimus in South African paediatric liver transplant patients. S Afr Med J. 2024 Apr 24; 114(3b):e1367.
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Determinants of early change in serum creatinine after initiation of dolutegravir-based antiretroviral therapy in South Africa. Br J Clin Pharmacol. 2024 May; 90(5):1247-1257.