"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 |
|---|
| 1994 | 1 | 1 | 2 |
| 1995 | 2 | 2 | 4 |
| 1996 | 2 | 3 | 5 |
| 1997 | 4 | 1 | 5 |
| 1998 | 3 | 5 | 8 |
| 1999 | 3 | 4 | 7 |
| 2000 | 1 | 1 | 2 |
| 2001 | 1 | 4 | 5 |
| 2002 | 4 | 5 | 9 |
| 2003 | 2 | 2 | 4 |
| 2004 | 4 | 2 | 6 |
| 2005 | 1 | 1 | 2 |
| 2006 | 3 | 3 | 6 |
| 2007 | 2 | 2 | 4 |
| 2008 | 0 | 2 | 2 |
| 2009 | 2 | 3 | 5 |
| 2010 | 1 | 3 | 4 |
| 2011 | 3 | 4 | 7 |
| 2012 | 0 | 3 | 3 |
| 2013 | 2 | 1 | 3 |
| 2014 | 0 | 4 | 4 |
| 2015 | 5 | 1 | 6 |
| 2016 | 1 | 3 | 4 |
| 2017 | 1 | 2 | 3 |
| 2018 | 2 | 2 | 4 |
| 2019 | 1 | 1 | 2 |
| 2020 | 1 | 1 | 2 |
| 2021 | 0 | 1 | 1 |
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Below are the most recent publications written about "Polymorphism, Genetic" by people in Profiles.
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Identification of a Metabolic, Transcriptomic, and Molecular Signature of Patatin-Like Phospholipase Domain Containing 3-Mediated Acceleration of Steatohepatitis. Hepatology. 2021 04; 73(4):1290-1306.
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Physiologic Consequences of Caveolin-1 Ablation in Conventional Outflow Endothelia. Invest Ophthalmol Vis Sci. 2020 09 01; 61(11):32.
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Unraveling the Effect of a Potentiating Anti-Factor H Antibody on Atypical Hemolytic Uremic Syndrome-Associated Factor H Variants. J Immunol. 2020 10 01; 205(7):1778-1786.
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Working memory reflects vulnerability to early life adversity as a risk factor for substance use disorder in the FKBP5 cortisol cochaperone polymorphism, rs9296158. PLoS One. 2019; 14(6):e0218212.
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Obesity genetics and cardiometabolic health: Potential for risk prediction. Diabetes Obes Metab. 2019 05; 21(5):1088-1100.
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A plausibly causal functional lupus-associated risk variant in the STAT1-STAT4 locus. Hum Mol Genet. 2018 07 01; 27(13):2392-2404.
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Assessing the Incremental Contribution of Common Genomic Variants to Melanoma Risk Prediction in Two Population-Based Studies. J Invest Dermatol. 2018 12; 138(12):2617-2624.
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Genetic variants at the 16p13 locus confer risk for eosinophilic esophagitis. Genes Immun. 2019 04; 20(4):281-292.
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Genomic, Pathway Network, and Immunologic Features Distinguishing Squamous Carcinomas. Cell Rep. 2018 04 03; 23(1):194-212.e6.
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The methylenetetrahydrofolate reductase c.c.677 C>T and c.c.1298 A>C polymorphisms in reproductive failures: Experience from an RSA and RIF study on a Polish population. PLoS One. 2017; 12(10):e0186022.