 Alleles
"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 | 5 | 6 | | 1997 | 1 | 5 | 6 | | 1998 | 0 | 7 | 7 | | 1999 | 2 | 7 | 9 | | 2000 | 2 | 7 | 9 | | 2001 | 1 | 15 | 16 | | 2002 | 0 | 12 | 12 | | 2003 | 3 | 11 | 14 | | 2004 | 0 | 20 | 20 | | 2005 | 0 | 16 | 16 | | 2006 | 4 | 17 | 21 | | 2007 | 2 | 24 | 26 | | 2008 | 6 | 20 | 26 | | 2009 | 3 | 27 | 30 | | 2010 | 5 | 22 | 27 | | 2011 | 3 | 26 | 29 | | 2012 | 2 | 22 | 24 | | 2013 | 1 | 30 | 31 | | 2014 | 5 | 28 | 33 | | 2015 | 5 | 32 | 37 | | 2016 | 1 | 28 | 29 | | 2017 | 9 | 35 | 44 | | 2018 | 7 | 26 | 33 | | 2019 | 4 | 32 | 36 | | 2020 | 2 | 18 | 20 | | 2021 | 4 | 27 | 31 | | 2022 | 1 | 13 | 14 | | 2023 | 0 | 10 | 10 | | 2024 | 6 | 13 | 19 | | 2025 | 3 | 15 | 18 | | 2026 | 0 | 2 | 2 |
To return to the timeline, click here.
Below are the most recent publications written about "Alleles" by people in Profiles.
-
Font-Porterias N, Nemat-Gorgani N, Kichula KM, Al-Hindi DR, Harrison GF, Tao S, Zhu F, Montero-Martin G, Fernández-Viña MA, Guethlein LA, Parham P, Oppenheimer SJ, Ioannidis AG, Moreno-Estrada A, Pomat W, Mentzer AJ, Henn BM, Norman PJ. Signatures of pathogen-driven selection and Austronesian gene flow of Papua New Guinea HLA alleles. Am J Hum Genet. 2026 Jun 04; 113(6):1175-1193.
-
Starosta RT, He M, Gracie S, Kierstein J, Thiel C, Himmelreich N, Liu Y, Zhang W, Edmondson AC, Meeks N, Larson A, Van Hove JLK, Kochhar A. L-fucose supplementation in a patient with global hypofucosylation and a mono-allelic variant in SLC35C1: Clinical improvement and assessment of biomarkers. Mol Genet Metab. 2026 Mar; 147(3):109727.
-
Doss RM, Wirth SA, Pitsch JW, Dias CM, Gropman AL, Breuss MW. Exon-skipping due to bi-allelic splice site mutations in the neurodevelopmental disease gene LNPK. HGG Adv. 2026 Jan 15; 7(1):100543.
-
Liao SY, Fingerlin TE, Jacobson S, Mroz MM, Rosenman KD, Rossman MD, Virji M, McCanlies EC, Schuler CR, Yucesoy B, Glessner J, Duke JL, Hakonarson H, Monos DS, Maier LA. Genome-wide association study and HLA genotyping for beryllium disease susceptibility in a European descent population. Gene. 2025 Nov 05; 971:149820.
-
Daines CL, Polineni D, Tullis E, Costa S, Linnemann RW, Mall MA, McKone EF, Quon BS, Ringshausen FC, Selvadurai H, Taylor-Cousar JL, Withers NJ, Sawicki GS, Lee T, Ahluwalia N, Morlando Geiger J, Jennings M, Tan YV, Waltz D, Ramsey B, Griese M. Long-Term Safety and Efficacy of Elexacaftor/Tezacaftor/Ivacaftor in Adults and Adolescents with Cystic Fibrosis and at Least One F508del Allele: A Phase 3 Open-Label Extension Study. Am J Respir Crit Care Med. 2025 10; 211(10):1901-1914.
-
Wainwright C, McColley SA, McNally P, Powers M, Ratjen F, Rayment JH, Retsch-Bogart G, Roesch E, Ramsey B, McKone EF, Tullis E, Mall MA, Taylor-Cousar JL, Waltz D, Ahluwalia N, Chu C, Scirica CV, Davies JC. Long-Term Safety and Efficacy of Elexacaftor/Tezacaftor/Ivacaftor in Children =6 Years with Cystic Fibrosis and at Least One F508del Allele: A 192-Week, Phase 3, Open-Label Extension Study. Am J Respir Crit Care Med. 2025 10; 211(10):1915-1925.
-
Mumme-Monheit A, Gustafson GE, Hopkins CA, Bailon-Zambrano R, Sucharov J, Lippincott MJ, Way GP, Colborn KL, Nichols JT. A quadratic paradigm describes the relationship between phenotype severity and variation. Nat Commun. 2025 Sep 01; 16(1):8154.
-
Ramadan DJ, Kichula KM, Tao S, Porfilio T, Lande A, Fluge Ø, Mella O, Strand EB, Saugstad OD, Norman PJ, Lie BA, Viken MK. Killer cell immunoglobulin-like receptor (KIR) alleles suggested to be associated with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). Brain Behav Immun. 2025 Nov; 130:106098.
-
Rai M, Okah P, Shefali SA, Fitt AJ, Shen MZ, Molomjamts M, Pepin R, Nemkov T, D'Alessandro A, Tennessen JM. New alleles of D-2-hydroxyglutarate dehydrogenase enable studies of oncometabolite function in Drosophila melanogaster. G3 (Bethesda). 2025 08 06; 15(8).
-
Antonicka H, Weraarpachai W, Szigety KM, Kopajtich R, Gibson JB, Van Hove JLK, Friederich MW, Lopriore P, Neuhofer C, Van Hove RA, Cole MA, Reisdorph R, Peterson JT, Dempsey KJ, Ganetzky RD, Mancuso M, Prokisch H, Shoubridge EA. Bi-allelic mutations in FASTKD5 are associated with cytochrome c oxidase deficiency and early- to late-onset Leigh syndrome. Am J Hum Genet. 2025 07 03; 112(7):1699-1710.
|
People  People who have written about this concept. _
Similar Concepts
People who have written about this concept.
_
Top Journals
Top journals in which articles about this concept have been published.
|