"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 |
|---|
| 2004 | 2 | 3 | 5 |
| 2005 | 1 | 1 | 2 |
| 2006 | 3 | 1 | 4 |
| 2007 | 10 | 3 | 13 |
| 2008 | 7 | 12 | 19 |
| 2009 | 9 | 16 | 25 |
| 2010 | 16 | 18 | 34 |
| 2011 | 12 | 24 | 36 |
| 2012 | 11 | 32 | 43 |
| 2013 | 15 | 29 | 44 |
| 2014 | 11 | 28 | 39 |
| 2015 | 15 | 25 | 40 |
| 2016 | 7 | 16 | 23 |
| 2017 | 9 | 26 | 35 |
| 2018 | 8 | 19 | 27 |
| 2019 | 3 | 19 | 22 |
| 2020 | 6 | 13 | 19 |
| 2021 | 4 | 19 | 23 |
| 2022 | 2 | 12 | 14 |
| 2023 | 1 | 3 | 4 |
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Below are the most recent publications written about "Polymorphism, Single Nucleotide" by people in Profiles.
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Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Nat Immunol. 2023 09; 24(9):1540-1551.
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Reliable genotyping of recombinant genomes using a robust hidden Markov model. Plant Physiol. 2023 05 31; 192(2):821-836.
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Development and evaluations of the ancestry informative markers of the VISAGE Enhanced Tool for Appearance and Ancestry. Forensic Sci Int Genet. 2023 05; 64:102853.
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Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry. Genome Med. 2023 01 26; 15(1):7.
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Intronic enhancers of the human SNCA gene predominantly regulate its expression in brain in vivo. Sci Adv. 2022 11 25; 8(47):eabq6324.
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Novel genes and sex differences in COVID-19 severity. Hum Mol Genet. 2022 11 10; 31(22):3789-3806.
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Long-Lived Individuals Show a Lower Burden of Variants Predisposing to Age-Related Diseases and a Higher Polygenic Longevity Score. Int J Mol Sci. 2022 Sep 19; 23(18).
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Physical activity, sedentary time and breast cancer risk: a Mendelian randomisation study. Br J Sports Med. 2022 Oct; 56(20):1157-1170.
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Identification of Two Genetic Loci Associated with Leukopenia after Chemotherapy in Patients with Breast Cancer. Clin Cancer Res. 2022 08 02; 28(15):3342-3355.
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Benchmarking of univariate pleiotropy detection methods applied to epilepsy. Hum Mutat. 2022 09; 43(9):1314-1332.
MeSH information
