"Genetic Variation" 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.
Genotypic differences observed among individuals in a population.
| Descriptor ID |
D014644
|
| MeSH Number(s) |
G05.365
|
| Concept/Terms |
Genetic Variation- Genetic Variation
- Genetic Variations
- Variations, Genetic
- Variation, Genetic
- Diversity, Genetic
- Diversities, Genetic
- Genetic Diversities
- Genetic Diversity
|
Below are MeSH descriptors whose meaning is more general than "Genetic Variation".
Below are MeSH descriptors whose meaning is more specific than "Genetic Variation".
This graph shows the total number of publications written about "Genetic Variation" by people in this website by year, and whether "Genetic Variation" 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 | 0 | 1 | 1 |
| 1996 | 0 | 1 | 1 |
| 1997 | 2 | 0 | 2 |
| 1998 | 2 | 2 | 4 |
| 1999 | 2 | 2 | 4 |
| 2000 | 2 | 2 | 4 |
| 2001 | 1 | 4 | 5 |
| 2002 | 3 | 1 | 4 |
| 2003 | 2 | 1 | 3 |
| 2004 | 0 | 4 | 4 |
| 2005 | 6 | 1 | 7 |
| 2006 | 3 | 1 | 4 |
| 2007 | 7 | 2 | 9 |
| 2008 | 8 | 6 | 14 |
| 2009 | 5 | 5 | 10 |
| 2010 | 5 | 2 | 7 |
| 2011 | 2 | 7 | 9 |
| 2012 | 6 | 0 | 6 |
| 2013 | 1 | 6 | 7 |
| 2014 | 5 | 9 | 14 |
| 2015 | 2 | 10 | 12 |
| 2016 | 5 | 6 | 11 |
| 2017 | 1 | 1 | 2 |
| 2018 | 0 | 5 | 5 |
| 2019 | 4 | 8 | 12 |
| 2020 | 2 | 5 | 7 |
| 2021 | 2 | 3 | 5 |
| 2022 | 0 | 2 | 2 |
| 2023 | 1 | 0 | 1 |
| 2024 | 0 | 2 | 2 |
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Below are the most recent publications written about "Genetic Variation" by people in Profiles.
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Genetic and phenotypic diversification in a widespread fish, the Sailfin Molly (Poecilia latipinna). BMC Ecol Evol. 2024 Jul 01; 24(1):87.
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Genetic variant rs1205 is associated with COVID-19 outcomes: The Strong Heart Study and Strong Heart Family Study. PLoS One. 2024; 19(4):e0302464.
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Polygenic architecture of rare coding variation across 394,783 exomes. Nature. 2023 Feb; 614(7948):492-499.
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Pan-genomic, transcriptomic, and miRNA analyses to decipher genetic diversity and anthocyanin pathway genes among the traditional rice landraces. Genomics. 2022 09; 114(5):110436.
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Stone Age Yersinia pestis genomes shed light on the early evolution, diversity, and ecology of plague. Proc Natl Acad Sci U S A. 2022 04 26; 119(17):e2116722119.
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Patients with repaired tetralogy of Fallot and the HIF1A1744C/T variant have increased imaging markers of diffuse myocardial fibrosis. Int J Cardiol. 2022 Mar 01; 350:33-35.
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Variants on the UBE2L3/YDJC Autoimmune Disease Risk Haplotype Increase UBE2L3 Expression by Modulating CCCTC-Binding Factor and YY1 Binding. Arthritis Rheumatol. 2022 01; 74(1):163-173.
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Ten millennia of hepatitis B virus evolution. Science. 2021 Oct 08; 374(6564):182-188.
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APOC3 genetic variation, serum triglycerides, and risk of coronary artery disease in Asian Indians, Europeans, and other ethnic groups. Lipids Health Dis. 2021 Sep 21; 20(1):113.
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A multiple ion-uptake phenotyping platform reveals shared mechanisms affecting nutrient uptake by roots. Plant Physiol. 2021 04 02; 185(3):781-795.