"Alleles" 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.
Variant forms of the same gene, occupying the same locus on homologous CHROMOSOMES, and governing the variants in production of the same gene product.
| Descriptor ID |
D000483
|
| MeSH Number(s) |
G05.360.340.024.340.030
|
| Concept/Terms |
Alleles- Alleles
- Allele
- Allelomorphs
- Allelomorph
|
Below are MeSH descriptors whose meaning is more general than "Alleles".
Below are MeSH descriptors whose meaning is more specific than "Alleles".
This graph shows the total number of publications written about "Alleles" by people in this website by year, and whether "Alleles" 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 |
|---|
| 1995 | 2 | 19 | 21 |
| 1996 | 1 | 16 | 17 |
| 1997 | 1 | 14 | 15 |
| 1998 | 1 | 14 | 15 |
| 1999 | 0 | 21 | 21 |
| 2000 | 4 | 31 | 35 |
| 2001 | 4 | 29 | 33 |
| 2002 | 1 | 30 | 31 |
| 2003 | 2 | 36 | 38 |
| 2004 | 3 | 29 | 32 |
| 2005 | 2 | 27 | 29 |
| 2006 | 5 | 28 | 33 |
| 2007 | 11 | 27 | 38 |
| 2008 | 3 | 29 | 32 |
| 2009 | 3 | 26 | 29 |
| 2010 | 6 | 29 | 35 |
| 2011 | 4 | 37 | 41 |
| 2012 | 4 | 32 | 36 |
| 2013 | 3 | 42 | 45 |
| 2014 | 5 | 30 | 35 |
| 2015 | 7 | 34 | 41 |
| 2016 | 5 | 46 | 51 |
| 2017 | 6 | 40 | 46 |
| 2018 | 6 | 33 | 39 |
| 2019 | 7 | 49 | 56 |
| 2020 | 3 | 24 | 27 |
| 2021 | 1 | 36 | 37 |
| 2022 | 1 | 20 | 21 |
| 2023 | 0 | 12 | 12 |
| 2024 | 4 | 11 | 15 |
| 2025 | 3 | 4 | 7 |
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Below are the most recent publications written about "Alleles" by people in Profiles.
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The common HAQ STING allele prevents clinical penetrance of COPA syndrome. J Exp Med. 2025 Apr 07; 222(4).
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Genome-wide prediction of dominant and recessive neurodevelopmental disorder-associated genes. Am J Hum Genet. 2025 Mar 06; 112(3):693-708.
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Cerebrotendinous Xanthomatosis occurs at high frequency in Ashkenazi Jews. Mol Genet Metab. 2025 Mar; 144(3):109041.
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Bi-allelic KICS2 mutations impair KICSTOR complex-mediated mTORC1 regulation, causing intellectual disability and epilepsy. Am J Hum Genet. 2025 Feb 06; 112(2):374-393.
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Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood. Am J Hum Genet. 2025 Feb 06; 112(2):276-290.
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Monoallelic expression can govern penetrance of inborn errors of immunity. Nature. 2025 Jan; 637(8048):1186-1197.
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Refinement of a Published Gene-Physical Activity Interaction Impacting HDL-Cholesterol: Role of Sex and Lipoprotein Subfractions. Genet Epidemiol. 2025 Jan; 49(1):e22607.
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Structural variant allelic heterogeneity in MECP2 duplication syndrome provides insight into clinical severity and variability of disease expression. Genome Med. 2024 Dec 18; 16(1):146.
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Identification of allele-specific KIV-2 repeats and impact on Lp(a) measurements for cardiovascular disease risk. BMC Med Genomics. 2024 10 24; 17(1):255.
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The origin and maintenance of supergenes contributing to ecological adaptation in Atlantic herring. Nat Commun. 2024 Oct 23; 15(1):9136.