"Polymorphism, Genetic" 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.
The regular and simultaneous occurrence in a single interbreeding population of two or more discontinuous genotypes. The concept includes differences in genotypes ranging in size from a single nucleotide site (POLYMORPHISM, SINGLE NUCLEOTIDE) to large nucleotide sequences visible at a chromosomal level.
| Descriptor ID |
D011110
|
| MeSH Number(s) |
G05.365.795
|
| Concept/Terms |
Polymorphism, Genetic- Polymorphism, Genetic
- Polymorphisms, Genetic
- Genetic Polymorphisms
- Genetic Polymorphism
- Polymorphism (Genetics)
- Polymorphisms (Genetics)
|
Below are MeSH descriptors whose meaning is more general than "Polymorphism, Genetic".
Below are MeSH descriptors whose meaning is more specific than "Polymorphism, Genetic".
This graph shows the total number of publications written about "Polymorphism, Genetic" by people in this website by year, and whether "Polymorphism, Genetic" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1998 | 1 | 0 | 1 |
| 2000 | 1 | 1 | 2 |
| 2001 | 1 | 1 | 2 |
| 2002 | 0 | 1 | 1 |
| 2004 | 1 | 1 | 2 |
| 2006 | 2 | 2 | 4 |
| 2007 | 4 | 1 | 5 |
| 2008 | 1 | 4 | 5 |
| 2009 | 0 | 3 | 3 |
| 2011 | 2 | 4 | 6 |
| 2012 | 3 | 1 | 4 |
| 2013 | 0 | 2 | 2 |
| 2014 | 1 | 1 | 2 |
| 2015 | 1 | 3 | 4 |
| 2016 | 1 | 1 | 2 |
| 2017 | 1 | 1 | 2 |
| 2018 | 2 | 0 | 2 |
| 2019 | 1 | 4 | 5 |
| 2021 | 1 | 0 | 1 |
| 2022 | 0 | 1 | 1 |
| 2023 | 0 | 1 | 1 |
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click here.
Below are the most recent publications written about "Polymorphism, Genetic" by people in Profiles.
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Functional damaging germline variants in ETV6, IKZF1, PAX5 and RUNX1 predisposing to B-cell precursor acute lymphoblastic leukemia. Eur J Med Genet. 2023 Apr; 66(4):104725.
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Detailed stratified GWAS analysis for severe COVID-19 in four European populations. Hum Mol Genet. 2022 11 28; 31(23):3945-3966.
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Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality. J Clin Invest. 2021 12 01; 131(23).
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Protein-coding variants contribute to the risk of atopic dermatitis and skin-specific gene expression. J Allergy Clin Immunol. 2020 04; 145(4):1208-1218.
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Genetic Variants in the Promoter Region of the Macrophage Migration Inhibitory Factor are Associated with the Severity of Hepatitis C Virus-Induced Liver Fibrosis. Int J Mol Sci. 2019 Jul 31; 20(15).
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Presence of centromeric but absence of telomeric group B KIR haplotypes in stem cell donors improve leukaemia control after HSCT for childhood ALL. Bone Marrow Transplant. 2019 11; 54(11):1847-1858.
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Development of ten microsatellite markers for Alibertia edulis (Rubiaceae), a Brazilian savanna tree species. Mol Biol Rep. 2019 Aug; 46(4):4593-4597.
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Development and characterization of eleven microsatellite loci for the tropical understory tree Paypayrola blanchetiana Tul. (Violaceae). Mol Biol Rep. 2019 Apr; 46(2):2529-2532.
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Meta-analysis of genome-wide association studies of aggressive and chronic periodontitis identifies two novel risk loci. Eur J Hum Genet. 2019 01; 27(1):102-113.
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Search for cis-acting factors and maternal effect variants in Silver-Russell patients with ICR1 hypomethylation and their mothers. Eur J Hum Genet. 2019 01; 27(1):42-48.
MeSH information
