"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 |
|---|
| 1994 | 5 | 18 | 23 |
| 1995 | 6 | 30 | 36 |
| 1996 | 4 | 28 | 32 |
| 1997 | 3 | 20 | 23 |
| 1998 | 7 | 25 | 32 |
| 1999 | 4 | 29 | 33 |
| 2000 | 10 | 45 | 55 |
| 2001 | 8 | 46 | 54 |
| 2002 | 4 | 44 | 48 |
| 2003 | 3 | 49 | 52 |
| 2004 | 7 | 40 | 47 |
| 2005 | 4 | 45 | 49 |
| 2006 | 8 | 45 | 53 |
| 2007 | 15 | 45 | 60 |
| 2008 | 6 | 49 | 55 |
| 2009 | 5 | 36 | 41 |
| 2010 | 7 | 47 | 54 |
| 2011 | 7 | 49 | 56 |
| 2012 | 5 | 41 | 46 |
| 2013 | 8 | 57 | 65 |
| 2014 | 10 | 48 | 58 |
| 2015 | 10 | 40 | 50 |
| 2016 | 8 | 65 | 73 |
| 2017 | 5 | 58 | 63 |
| 2018 | 7 | 44 | 51 |
| 2019 | 12 | 65 | 77 |
| 2020 | 3 | 31 | 34 |
| 2021 | 1 | 41 | 42 |
| 2022 | 1 | 23 | 24 |
| 2023 | 0 | 15 | 15 |
| 2024 | 8 | 12 | 20 |
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Below are the most recent publications written about "Alleles" by people in Profiles.
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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 Oct 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.
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Influence of TP53 gene mutations and their allelic status in myelodysplastic syndromes with isolated 5q deletion. Blood. 2024 10 17; 144(16):1722-1731.
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ASXL1/TET2 genotype-based risk stratification outperforms ASXL1 mutational impact and is independent of mutant variant allele fractions in chronic myelomonocytic leukemia. Haematologica. 2024 Oct 01; 109(10):3419-3425.
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Impact of essential genes on the success of genome editing experiments generating 3313 new genetically engineered mouse lines. Sci Rep. 2024 09 30; 14(1):22626.
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Extended haplotype with rs41524547-G defines the ancestral origin of SCA10. Hum Mol Genet. 2024 09 03; 33(18):1567-1574.
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A multiplexed, allele-specific recombinase polymerase amplification assay with lateral flow readout for sickle cell disease detection. Lab Chip. 2024 08 20; 24(17):4115-4127.
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De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome. Nature. 2024 Aug; 632(8026):832-840.
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Monoallelic de novo AJAP1 loss-of-function variants disrupt trans-synaptic control of neurotransmitter release. Sci Adv. 2024 Jul 12; 10(28):eadk5462.
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High-throughput characterization of functional variants highlights heterogeneity and polygenicity underlying lung cancer susceptibility. Am J Hum Genet. 2024 07 11; 111(7):1405-1419.