"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 | 2 | 7 | 9 |
| 1995 | 0 | 16 | 16 |
| 1996 | 4 | 20 | 24 |
| 1997 | 3 | 15 | 18 |
| 1998 | 4 | 11 | 15 |
| 1999 | 1 | 21 | 22 |
| 2000 | 2 | 20 | 22 |
| 2001 | 5 | 24 | 29 |
| 2002 | 3 | 25 | 28 |
| 2003 | 4 | 10 | 14 |
| 2004 | 9 | 23 | 32 |
| 2005 | 6 | 33 | 39 |
| 2006 | 2 | 28 | 30 |
| 2007 | 0 | 17 | 17 |
| 2008 | 4 | 25 | 29 |
| 2009 | 3 | 25 | 28 |
| 2010 | 2 | 33 | 35 |
| 2011 | 3 | 34 | 37 |
| 2012 | 7 | 25 | 32 |
| 2013 | 4 | 27 | 31 |
| 2014 | 6 | 38 | 44 |
| 2015 | 2 | 20 | 22 |
| 2016 | 5 | 25 | 30 |
| 2017 | 0 | 25 | 25 |
| 2018 | 3 | 21 | 24 |
| 2019 | 1 | 21 | 22 |
| 2020 | 4 | 12 | 16 |
| 2021 | 2 | 12 | 14 |
| 2022 | 1 | 16 | 17 |
| 2023 | 1 | 8 | 9 |
| 2024 | 1 | 11 | 12 |
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Below are the most recent publications written about "Alleles" by people in Profiles.
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Sequence variants influencing the regulation of serum IgG subclass levels. Nat Commun. 2024 Sep 14; 15(1):8054.
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Causal interpretations of family GWAS in the presence of heterogeneous effects. Proc Natl Acad Sci U S A. 2024 Sep 17; 121(38):e2401379121.
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Scaled and efficient derivation of loss-of-function alleles in risk genes for neurodevelopmental and psychiatric disorders in human iPSCs. Stem Cell Reports. 2024 Oct 08; 19(10):1489-1504.
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Selection with two alleles of X-linkage and its application to the fitness component analysis of OdsH in Drosophila. G3 (Bethesda). 2024 Sep 04; 14(9).
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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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Genome-wide association analyses of breast cancer in women of African ancestry identify new susceptibility loci and improve risk prediction. Nat Genet. 2024 May; 56(5):819-826.
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Investigation of inherited noncoding genetic variation impacting the pharmacogenomics of childhood acute lymphoblastic leukemia treatment. Nat Commun. 2024 May 01; 15(1):3681.
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Interpreting population- and family-based genome-wide association studies in the presence of confounding. PLoS Biol. 2024 Apr; 22(4):e3002511.
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Polygenic response of sex chromosomes to sexual antagonism. Evolution. 2024 Feb 29; 78(3):539-554.
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Next-generation sequencing identifies two novel HLA-DPB1 alleles: HLA-DPB1*1069:01 and DPB1*1072:01. HLA. 2024 02; 103(2):e15368.