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 | 26 | 74 | 100 |
| 2015 | 25 | 61 | 86 |
| 2016 | 21 | 48 | 69 |
| 2017 | 17 | 47 | 64 |
| 2018 | 27 | 47 | 74 |
| 2019 | 12 | 48 | 60 |
| 2020 | 13 | 36 | 49 |
| 2021 | 14 | 43 | 57 |
| 2022 | 5 | 27 | 32 |
| 2023 | 2 | 19 | 21 |
| 2024 | 13 | 30 | 43 |
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Below are the most recent publications written about "Polymorphism, Single Nucleotide" by people in Profiles.
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Genome-wide meta-analysis associates donor-recipient non-HLA genetic mismatch with acute cellular rejection post-liver transplantation. Hepatol Commun. 2025 Jan 01; 9(1).
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A comprehensive framework for trans-ancestry pathway analysis using GWAS summary data from diverse populations. PLoS Genet. 2024 Oct; 20(10):e1011322.
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Rare variant contribution to the heritability of coronary artery disease. Nat Commun. 2024 Oct 09; 15(1):8741.
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Cross-ancestry analysis of brain QTLs enhances interpretation of schizophrenia genome-wide association studies. Am J Hum Genet. 2024 Nov 07; 111(11):2444-2457.
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Comprehensive investigation of long non-coding RNA HOTAIR polymorphisms and cancer risk: a current meta-analysis encompassing 96,458 participants. Sci Rep. 2024 09 30; 14(1):22670.
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Genetic variations in Interferon-Induced with Helicase C Domain 1: Impact on COVID-19 risk and severity in the Moroccan population. Hum Immunol. 2024 Nov; 85(6):111149.
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Sequence variants influencing the regulation of serum IgG subclass levels. Nat Commun. 2024 Sep 14; 15(1):8054.
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Causal interpretations of family GWAS in the presence of heterogeneous effects. Proc Natl Acad Sci U S A. 2024 Sep 17; 121(38):e2401379121.
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Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiency. Nat Genet. 2024 Sep; 56(9):1804-1810.
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Divergent ecological selection maintains species boundaries despite gene flow in a rare endemic tree, Quercus acerifolia (maple-leaf oak). J Hered. 2024 Aug 20; 115(5):575-587.