"Linkage Disequilibrium" 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.
Nonrandom association of linked genes. This is the tendency of the alleles of two separate but already linked loci to be found together more frequently than would be expected by chance alone.
| Descriptor ID |
D015810
|
| MeSH Number(s) |
G05.348.500
|
| Concept/Terms |
Linkage Disequilibrium- Linkage Disequilibrium
- Disequilibrium, Linkage
- Disequilibriums, Linkage
- Linkage Disequilibriums
|
Below are MeSH descriptors whose meaning is more general than "Linkage Disequilibrium".
Below are MeSH descriptors whose meaning is more specific than "Linkage Disequilibrium".
This graph shows the total number of publications written about "Linkage Disequilibrium" by people in this website by year, and whether "Linkage Disequilibrium" was a major or minor topic of these publications.
View timeline visualization
| Year | Major Topic | Minor Topic | Total |
|---|
| 1995 | 4 | 0 | 4 |
| 1996 | 4 | 2 | 6 |
| 1997 | 4 | 4 | 8 |
| 1998 | 6 | 7 | 13 |
| 1999 | 5 | 14 | 19 |
| 2000 | 5 | 14 | 19 |
| 2001 | 14 | 17 | 31 |
| 2002 | 16 | 24 | 40 |
| 2003 | 15 | 22 | 37 |
| 2004 | 10 | 27 | 37 |
| 2005 | 10 | 50 | 60 |
| 2006 | 10 | 50 | 60 |
| 2007 | 8 | 47 | 55 |
| 2008 | 10 | 67 | 77 |
| 2009 | 5 | 58 | 63 |
| 2010 | 2 | 55 | 57 |
| 2011 | 2 | 56 | 58 |
| 2012 | 3 | 53 | 56 |
| 2013 | 6 | 57 | 63 |
| 2014 | 1 | 39 | 40 |
| 2015 | 6 | 26 | 32 |
| 2016 | 6 | 45 | 51 |
| 2017 | 3 | 35 | 38 |
| 2018 | 3 | 35 | 38 |
| 2019 | 7 | 27 | 34 |
| 2020 | 2 | 21 | 23 |
| 2021 | 6 | 31 | 37 |
| 2022 | 1 | 11 | 12 |
| 2023 | 0 | 3 | 3 |
| 2024 | 5 | 5 | 10 |
| 2025 | 0 | 1 | 1 |
Below are the most recent publications written about "Linkage Disequilibrium" by people in Profiles.
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Characterizing features affecting local ancestry inference performance in admixed populations. Am J Hum Genet. 2025 Feb 06; 112(2):224-234.
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Population genetic dissection of HLA-DPB1 amino acid polymorphism to infer selection. Hum Immunol. 2024 Nov; 85(6):111151.
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Rare variant contribution to the heritability of coronary artery disease. Nat Commun. 2024 Oct 09; 15(1):8741.
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Unraveling the shared genetics of common epilepsies and general cognitive ability. Seizure. 2024 Nov; 122:105-112.
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Finemap-MiXeR: A variational Bayesian approach for genetic finemapping. PLoS Genet. 2024 Aug; 20(8):e1011372.
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An Atlas Characterizing the Shared Genetic Architecture of Inflammatory Bowel Disease with Clinical and Behavioral Traits. Inflamm Bowel Dis. 2024 Jun 03; 30(6):884-893.
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Improved functional mapping of complex trait heritability with GSA-MiXeR implicates biologically specific gene sets. Nat Genet. 2024 Jun; 56(6):1310-1318.
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MagicalRsq-X: A cross-cohort transferable genotype imputation quality metric. Am J Hum Genet. 2024 05 02; 111(5):990-995.
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Attention-deficit/hyperactivity disorder and dopamine receptor D4 (DRD4) exon 3 variable number of tandem repeats (VNTR) 2-repeat allele. Ann Hum Genet. 2024 Sep; 88(5):382-391.
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Hierarchical joint analysis of marginal summary statistics-Part I: Multipopulation fine mapping and credible set construction. Genet Epidemiol. 2024 Sep; 48(6):241-257.