"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 | 4 | 3 | 7 |
| 1995 | 6 | 5 | 11 |
| 1996 | 5 | 5 | 10 |
| 1997 | 6 | 7 | 13 |
| 1998 | 4 | 13 | 17 |
| 1999 | 5 | 6 | 11 |
| 2000 | 11 | 11 | 22 |
| 2001 | 5 | 15 | 20 |
| 2002 | 12 | 13 | 25 |
| 2003 | 10 | 19 | 29 |
| 2004 | 19 | 18 | 37 |
| 2005 | 7 | 19 | 26 |
| 2006 | 22 | 22 | 44 |
| 2007 | 20 | 21 | 41 |
| 2008 | 26 | 35 | 61 |
| 2009 | 29 | 30 | 59 |
| 2010 | 27 | 31 | 58 |
| 2011 | 25 | 24 | 49 |
| 2012 | 31 | 23 | 54 |
| 2013 | 30 | 32 | 62 |
| 2014 | 30 | 28 | 58 |
| 2015 | 32 | 25 | 57 |
| 2016 | 31 | 41 | 72 |
| 2017 | 33 | 23 | 56 |
| 2018 | 34 | 35 | 69 |
| 2019 | 37 | 38 | 75 |
| 2020 | 22 | 28 | 50 |
| 2021 | 17 | 25 | 42 |
| 2022 | 9 | 11 | 20 |
| 2023 | 3 | 7 | 10 |
| 2024 | 4 | 17 | 21 |
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Below are the most recent publications written about "Genetic Variation" by people in Profiles.
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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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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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Parkinson's disease variant detection and disclosure: PD GENEration, a North American study. Brain. 2024 Aug 01; 147(8):2668-2679.
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Secondary ACMG and non-ACMG genetic findings in a multiethnic cohort of 16,713 pediatric participants. Genet Med. 2024 Nov; 26(11):101225.
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Systemic interindividual DNA methylation variants in cattle share major hallmarks with those in humans. Genome Biol. 2024 Jul 15; 25(1):185.
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Unveiling novel genetic variants in 370 challenging medically relevant genes using the long read sequencing data of 41 samples from 19 global populations. Mol Genet Genomics. 2024 Jul 07; 299(1):65.