"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 |
|---|
| 1999 | 0 | 1 | 1 |
| 2003 | 2 | 0 | 2 |
| 2004 | 1 | 1 | 2 |
| 2005 | 0 | 3 | 3 |
| 2006 | 3 | 1 | 4 |
| 2007 | 3 | 2 | 5 |
| 2008 | 4 | 1 | 5 |
| 2009 | 2 | 2 | 4 |
| 2010 | 2 | 1 | 3 |
| 2011 | 3 | 1 | 4 |
| 2012 | 2 | 0 | 2 |
| 2013 | 0 | 3 | 3 |
| 2014 | 4 | 2 | 6 |
| 2015 | 2 | 1 | 3 |
| 2016 | 4 | 0 | 4 |
| 2017 | 3 | 2 | 5 |
| 2018 | 1 | 0 | 1 |
| 2019 | 2 | 3 | 5 |
| 2020 | 0 | 1 | 1 |
| 2021 | 1 | 1 | 2 |
| 2022 | 1 | 0 | 1 |
| 2023 | 1 | 0 | 1 |
| 2024 | 0 | 1 | 1 |
| 2026 | 3 | 0 | 3 |
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Below are the most recent publications written about "Genetic Variation" by people in Profiles.
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Influenza household transmission and genomic diversity in the United States: A prospective cohort study, 2022-2024. J Infect. 2026 May; 92(5):106748.
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Deleterious coding variation associated with autism is shared across ancestries. Nat Med. 2026 Apr; 32(4):1519-1529.
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Repeated Independent Formation of Triploid Lineages Contributes to Clonal Diversity in Heteronotia binoei Parthenogens. Mol Ecol. 2026 Jan; 35(2):e70240.
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Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science. 2024 07 19; 385(6706):eadj1182.
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Compendium of Clinical Variant Classification for 2,246 Unique ABCA4 Variants to Clarify Variant Pathogenicity in Stargardt Disease Using a Modified ACMG/AMP Framework. Hum Mutat. 2023; 2023:6815504.
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Genetic diversity fuels gene discovery for tobacco and alcohol use. Nature. 2022 12; 612(7941):720-724.
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Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing loss. Am J Hum Genet. 2021 10 07; 108(10):2006-2016.
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Genetic and Epigenetic Variations of HPV52 in Cervical Precancer. Int J Mol Sci. 2021 Jun 16; 22(12).
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Fine-mapping, trans-ancestral and genomic analyses identify causal variants, cells, genes and drug targets for type 1 diabetes. Nat Genet. 2021 07; 53(7):962-971.
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Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program. Am J Hum Genet. 2021 05 06; 108(5):874-893.