"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 | 5 | 4 | 9 |
| 1995 | 6 | 5 | 11 |
| 1996 | 6 | 5 | 11 |
| 1997 | 6 | 7 | 13 |
| 1998 | 4 | 13 | 17 |
| 1999 | 6 | 7 | 13 |
| 2000 | 12 | 11 | 23 |
| 2001 | 5 | 15 | 20 |
| 2002 | 12 | 13 | 25 |
| 2003 | 10 | 19 | 29 |
| 2004 | 20 | 18 | 38 |
| 2005 | 8 | 19 | 27 |
| 2006 | 22 | 22 | 44 |
| 2007 | 20 | 21 | 41 |
| 2008 | 26 | 36 | 62 |
| 2009 | 30 | 30 | 60 |
| 2010 | 27 | 32 | 59 |
| 2011 | 26 | 25 | 51 |
| 2012 | 31 | 23 | 54 |
| 2013 | 30 | 32 | 62 |
| 2014 | 30 | 28 | 58 |
| 2015 | 32 | 28 | 60 |
| 2016 | 37 | 42 | 79 |
| 2017 | 36 | 23 | 59 |
| 2018 | 34 | 35 | 69 |
| 2019 | 38 | 38 | 76 |
| 2020 | 22 | 28 | 50 |
| 2021 | 19 | 25 | 44 |
| 2022 | 9 | 11 | 20 |
| 2023 | 3 | 8 | 11 |
| 2024 | 6 | 18 | 24 |
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Below are the most recent publications written about "Genetic Variation" by people in Profiles.
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Using multiplexed functional data to reduce variant classification inequities in underrepresented populations. Genome Med. 2024 Dec 03; 16(1):143.
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High-coverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalog of human genetic variation. Genome Res. 2024 Nov 20; 34(11):2061-2073.
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Genetic variants in canonical Wnt signaling pathway associated with pediatric immune thrombocytopenia. Blood Adv. 2024 11 12; 8(21):5529-5538.
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Association of common and rare variants with Alzheimer's disease in more than 13,000 diverse individuals with whole-genome sequencing from the Alzheimer's Disease Sequencing Project. Alzheimers Dement. 2024 Dec; 20(12):8470-8483.
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StratoMod: predicting sequencing and variant calling errors with interpretable machine learning. Commun Biol. 2024 Oct 13; 7(1):1316.
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Rare variant contribution to the heritability of coronary artery disease. Nat Commun. 2024 Oct 09; 15(1):8741.
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Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height. Nat Commun. 2024 Oct 03; 15(1):8549.
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Large-scale application of ClinGen-InSiGHT APC-specific ACMG/AMP variant classification criteria leads to substantial reduction in VUS. Am J Hum Genet. 2024 Nov 07; 111(11):2427-2443.
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Mitochondrial genome analysis across different populations reveals the intraspecific variation and phylogeography of the Caucasian soft tick relapsing fever vector, Ornithodoros (Pavlovskyella) verrucosus (Ixodida: Argasidae). Infect Genet Evol. 2024 Nov; 125:105673.
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Evaluation of Bayesian point-based system on the variant classification of hereditary cancer predisposition genes. Genet Med. 2024 Dec; 26(12):101276.