"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 |
|---|
| 1996 | 1 | 15 | 16 |
| 1997 | 1 | 14 | 15 |
| 1998 | 1 | 15 | 16 |
| 1999 | 0 | 20 | 20 |
| 2000 | 4 | 30 | 34 |
| 2001 | 3 | 28 | 31 |
| 2002 | 1 | 28 | 29 |
| 2003 | 2 | 38 | 40 |
| 2004 | 2 | 27 | 29 |
| 2005 | 2 | 27 | 29 |
| 2006 | 3 | 25 | 28 |
| 2007 | 9 | 21 | 30 |
| 2008 | 3 | 30 | 33 |
| 2009 | 3 | 27 | 30 |
| 2010 | 6 | 29 | 35 |
| 2011 | 4 | 36 | 40 |
| 2012 | 3 | 29 | 32 |
| 2013 | 4 | 40 | 44 |
| 2014 | 7 | 30 | 37 |
| 2015 | 7 | 34 | 41 |
| 2016 | 5 | 51 | 56 |
| 2017 | 4 | 45 | 49 |
| 2018 | 8 | 31 | 39 |
| 2019 | 7 | 51 | 58 |
| 2020 | 5 | 26 | 31 |
| 2021 | 1 | 40 | 41 |
| 2022 | 1 | 22 | 23 |
| 2023 | 0 | 14 | 14 |
| 2024 | 4 | 10 | 14 |
| 2025 | 6 | 26 | 32 |
| 2026 | 1 | 11 | 12 |
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Below are the most recent publications written about "Alleles" by people in Profiles.
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High KIR diversity in Uganda and Botswana children living with HIV. Hum Immunol. 2026 Aug; 87(8):111787.
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Genetics of Cerebrotendinous Xanthomatosis. Mol Diagn Ther. 2026 Jul; 30(4):681-687.
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Bi-allelic loss-of-function variants in TMEM63B cause syndromic surfactant dysfunction disorder. Am J Hum Genet. 2026 Jul 02; 113(7):1558-1569.
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Monoallelic PSMB8 variants cause PRAAS with immunodeficiency through impaired immunoproteasome assembly. Am J Hum Genet. 2026 Jun 04; 113(6):1214-1232.
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An integrated cardiometabolic genetic testing program in a predominantly Hispanic population within a community setting. Genet Med. 2026 Jul; 28(7):102595.
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Influence of feature encoding and machine learning algorithms on ancestry inference using autosomal STR profiles: A simulation approach using Asian populations. Leg Med (Tokyo). 2026 May; 83:102851.
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Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes. Nat Genet. 2026 Apr; 58(4):761-773.
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Biallelic Novel SKOR2 Variants in Individuals With Cerebellar Hypoplasia and Intellectual Disability, Expanding the Phenotypic Spectrum of Valence-Farazi Cerebellar Ataxia Syndrome. Am J Med Genet A. 2026 Jul; 200(7):1725-1739.
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Bi-allelic variants in NRDC cause a neurodevelopmental disorder characterized by neonatal lethality, microcephaly, and brain abnormalities. Am J Hum Genet. 2026 Mar 05; 113(3):548-561.
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Rare heterozygous de novo variants in RAPGEF2 are associated with a neurodevelopmental disorder. Genet Med. 2026 Apr; 28(4):101685.