"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 | 15 | 16 |
| 1998 | 1 | 14 | 15 |
| 1999 | 0 | 21 | 21 |
| 2000 | 4 | 31 | 35 |
| 2001 | 4 | 30 | 34 |
| 2002 | 1 | 32 | 33 |
| 2003 | 2 | 38 | 40 |
| 2004 | 3 | 30 | 33 |
| 2005 | 2 | 29 | 31 |
| 2006 | 4 | 28 | 32 |
| 2007 | 11 | 26 | 37 |
| 2008 | 3 | 30 | 33 |
| 2009 | 3 | 27 | 30 |
| 2010 | 6 | 31 | 37 |
| 2011 | 4 | 40 | 44 |
| 2012 | 4 | 35 | 39 |
| 2013 | 4 | 45 | 49 |
| 2014 | 7 | 31 | 38 |
| 2015 | 7 | 35 | 42 |
| 2016 | 5 | 52 | 57 |
| 2017 | 6 | 43 | 49 |
| 2018 | 7 | 35 | 42 |
| 2019 | 8 | 55 | 63 |
| 2020 | 5 | 28 | 33 |
| 2021 | 1 | 41 | 42 |
| 2022 | 1 | 24 | 25 |
| 2023 | 0 | 13 | 13 |
| 2024 | 4 | 11 | 15 |
| 2025 | 4 | 20 | 24 |
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Below are the most recent publications written about "Alleles" by people in Profiles.
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A clinical and genotype-phenotype analysis of MACF1 variants. Am J Hum Genet. 2025 Oct 02; 112(10):2363-2380.
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HLA loci heterozygosity modulates genetic risk in idiopathic inflammatory myopathies. Ann Rheum Dis. 2025 Oct; 84(10):1696-1705.
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Cell type-specific purifying selection of synonymous mitochondrial DNA variation. Proc Natl Acad Sci U S A. 2025 Jul 29; 122(30):e2505704122.
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Mouse metastable epialleles are extremely rare. Nucleic Acids Res. 2025 Jul 19; 53(14).
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Identification of functional non-coding variants associated with orofacial cleft. Nat Commun. 2025 Jul 16; 16(1):6545.
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MICBG406A polymorphism reduces risk of mechanical ventilation and death during viral acute lung injury. JCI Insight. 2025 Aug 08; 10(15).
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Distinguishing PEX2 and PEX16 gene variant severity for mild, severe and atypical peroxisome biogenesis disorders. Dis Model Mech. 2025 Jul 01; 18(7).
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Recombinase polymerase amplification for single nucleotide polymorphism-specific detection of ?C variant in sickle cell disease. Anal Biochem. 2025 Oct; 705:115919.
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Biallelic Loss-of-Function Variant in MINPP1 Causes Pontocerebellar Hypoplasia with Characteristic Severe Neurodevelopmental Disorder. Int J Mol Sci. 2025 May 29; 26(11).
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High-affinity CD16A polymorphism associated with reduced risk ofsevere COVID-19. JCI Insight. 2025 Jul 08; 10(13).