"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 | 4 | 4 |
2006 | 3 | 2 | 5 |
2007 | 4 | 2 | 6 |
2008 | 5 | 1 | 6 |
2009 | 3 | 5 | 8 |
2010 | 4 | 1 | 5 |
2011 | 3 | 1 | 4 |
2012 | 2 | 0 | 2 |
2013 | 0 | 3 | 3 |
2014 | 4 | 2 | 6 |
2015 | 2 | 1 | 3 |
2016 | 5 | 0 | 5 |
2017 | 3 | 2 | 5 |
2018 | 1 | 0 | 1 |
2019 | 2 | 3 | 5 |
2020 | 0 | 1 | 1 |
2021 | 1 | 1 | 2 |
2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Genetic Variation" by people in Profiles.
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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.
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Phenotype and Genotype Correlations in Inherited Retinal Diseases: Population-Guided Variant Interpretation, Variable Expressivity and Incomplete Penetrance. Genes (Basel). 2020 10 29; 11(11).
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Association of blood pressure with cognitive function at midlife: a Mendelian randomization study. BMC Med Genomics. 2020 08 26; 13(1):121.
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Association of HPV35 with cervical carcinogenesis among women of African ancestry: Evidence of viral-host interaction with implications for disease intervention. Int J Cancer. 2020 11 15; 147(10):2677-2686.
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Deep-intronic variants in CNGB3 cause achromatopsia by pseudoexon activation. Hum Mutat. 2020 01; 41(1):255-264.
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Disruptive variants of CSDE1 associate with autism and interfere with neuronal development and synaptic transmission. Sci Adv. 2019 09; 5(9):eaax2166.