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 | 1 | 1 | 2 |
| 2001 | 5 | 2 | 7 |
| 2002 | 2 | 6 | 8 |
| 2003 | 10 | 10 | 20 |
| 2004 | 10 | 17 | 27 |
| 2005 | 32 | 26 | 58 |
| 2006 | 30 | 35 | 65 |
| 2007 | 41 | 49 | 90 |
| 2008 | 63 | 66 | 129 |
| 2009 | 68 | 84 | 152 |
| 2010 | 88 | 110 | 198 |
| 2011 | 88 | 119 | 207 |
| 2012 | 92 | 142 | 234 |
| 2013 | 84 | 129 | 213 |
| 2014 | 56 | 91 | 147 |
| 2015 | 49 | 101 | 150 |
| 2016 | 48 | 105 | 153 |
| 2017 | 58 | 88 | 146 |
| 2018 | 39 | 90 | 129 |
| 2019 | 34 | 90 | 124 |
| 2020 | 26 | 51 | 77 |
| 2021 | 16 | 57 | 73 |
| 2022 | 5 | 45 | 50 |
| 2023 | 3 | 27 | 30 |
| 2024 | 0 | 4 | 4 |
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Below are the most recent publications written about "Polymorphism, Single Nucleotide" by people in Profiles.
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Extend the benchmarking indel set by manual review using the individual cell line sequencing data from the Sequencing Quality Control 2 (SEQC2) project. Sci Rep. 2024 03 25; 14(1):7028.
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TMEM106B coding variant is protective and deletion detrimental in a mouse model of tauopathy. Acta Neuropathol. 2024 Mar 25; 147(1):61.
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Association between circulating inflammatory markers and adult cancer risk: a Mendelian randomization analysis. EBioMedicine. 2024 Feb; 100:104991.
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Multi-omics and pathway analyses of genome-wide associations implicate regulation and immunity in verbal declarative memory performance. Alzheimers Res Ther. 2024 01 20; 16(1):14.
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Re-analysis and meta-analysis of summary statistics from gene-environment interaction studies. Bioinformatics. 2023 12 01; 39(12).
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Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants. Nat Genet. 2023 Dec; 55(12):2065-2074.
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Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study. Am J Hum Genet. 2023 10 05; 110(10):1704-1717.
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Heritable Traits and Lung Cancer Risk: A Two-Sample Mendelian Randomization Study. Cancer Epidemiol Biomarkers Prev. 2023 10 02; 32(10):1421-1435.
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Identification of novel genetic loci for risk of multiple myeloma by functional annotation. Leukemia. 2023 11; 37(11):2326-2329.
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Candidate pathway analysis of surfactant proteins identifies CTSH and SFTA2 that influences lung cancer risk. Hum Mol Genet. 2023 09 05; 32(18):2842-2855.