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 |
|---|
| 2001 | 0 | 1 | 1 |
| 2002 | 1 | 0 | 1 |
| 2003 | 0 | 3 | 3 |
| 2004 | 6 | 3 | 9 |
| 2005 | 3 | 7 | 10 |
| 2006 | 6 | 11 | 17 |
| 2007 | 4 | 6 | 10 |
| 2008 | 13 | 12 | 25 |
| 2009 | 15 | 17 | 32 |
| 2010 | 17 | 26 | 43 |
| 2011 | 17 | 32 | 49 |
| 2012 | 11 | 31 | 42 |
| 2013 | 13 | 33 | 46 |
| 2014 | 11 | 20 | 31 |
| 2015 | 13 | 16 | 29 |
| 2016 | 5 | 18 | 23 |
| 2017 | 10 | 14 | 24 |
| 2018 | 6 | 11 | 17 |
| 2019 | 8 | 12 | 20 |
| 2020 | 2 | 7 | 9 |
| 2021 | 2 | 12 | 14 |
| 2022 | 0 | 5 | 5 |
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Below are the most recent publications written about "Polymorphism, Single Nucleotide" by people in Profiles.
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Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries. Nat Genet. 2023 01; 55(1):89-99.
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Rare copy number variation in posttraumatic stress disorder. Mol Psychiatry. 2022 12; 27(12):5062-5069.
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A systematic review of genetic variation within nicotinic acetylcholine receptor genes and cigarette smoking cessation. Drug Alcohol Depend. 2022 Oct 01; 239:109596.
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Polymorphism rs3742330 in microRNA Biogenesis Gene DICER1 Is Associated with Pseudoexfoliation Glaucoma in Saudi Cohort. Genes (Basel). 2022 03 10; 13(3).
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GPA-Tree: statistical approach for functional-annotation-tree-guided prioritization of GWAS results. Bioinformatics. 2022 01 27; 38(4):1067-1074.
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Enhancing Discovery of Genetic Variants for Posttraumatic Stress Disorder Through Integration of Quantitative Phenotypes and Trauma Exposure Information. Biol Psychiatry. 2022 04 01; 91(7):626-636.
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Human SLE variant NCF1-R90H promotes kidney damage and murine lupus through enhanced Tfh2 responses induced by defective efferocytosis of macrophages. Ann Rheum Dis. 2022 02; 81(2):255-267.
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Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors. Biol Psychiatry. 2022 02 01; 91(3):313-327.
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Genome-Wide Association Meta-Analysis Supports Genes Involved in Valve and Cardiac Development to Associate With Mitral Valve Prolapse. Circ Genom Precis Med. 2021 10; 14(5):e003148.
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Average semivariance yields accurate estimates of the fraction of marker-associated genetic variance and heritability in complex trait analyses. PLoS Genet. 2021 08; 17(8):e1009762.