"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 |
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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 | 31 | 32 |
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 | 34 | 38 |
2013 | 3 | 43 | 46 |
2014 | 5 | 29 | 34 |
2015 | 7 | 34 | 41 |
2016 | 5 | 47 | 52 |
2017 | 6 | 40 | 46 |
2018 | 6 | 34 | 40 |
2019 | 7 | 52 | 59 |
2020 | 4 | 23 | 27 |
2021 | 1 | 36 | 37 |
2022 | 1 | 21 | 22 |
2023 | 0 | 12 | 12 |
2024 | 4 | 10 | 14 |
2025 | 3 | 7 | 10 |
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Below are the most recent publications written about "Alleles" by people in Profiles.
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Alzheimer's disease protective allele of Clusterin modulates neuronal excitability through lipid-droplet-mediated neuron-glia communication. Mol Neurodegener. 2025 May 03; 20(1):51.
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Bi-allelic UGGT1 variants cause a congenital disorder of glycosylation. Am J Hum Genet. 2025 May 01; 112(5):1139-1157.
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Bi-allelic pathogenic variants in TRMT1 disrupt tRNA modification and induce a neurodevelopmental disorder. Am J Hum Genet. 2025 May 01; 112(5):1117-1138.
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Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele. Nat Commun. 2025 Apr 11; 16(1):3470.
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K-mer analysis of long-read alignment pileups for structural variant genotyping. Nat Commun. 2025 Apr 04; 16(1):3218.
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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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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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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.