"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.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1995 | 0 | 1 | 1 |
| 1996 | 0 | 4 | 4 |
| 1997 | 1 | 1 | 2 |
| 1998 | 0 | 2 | 2 |
| 1999 | 2 | 2 | 4 |
| 2000 | 4 | 4 | 8 |
| 2001 | 3 | 4 | 7 |
| 2002 | 2 | 4 | 6 |
| 2003 | 2 | 8 | 10 |
| 2004 | 4 | 9 | 13 |
| 2005 | 3 | 10 | 13 |
| 2006 | 0 | 11 | 11 |
| 2007 | 3 | 8 | 11 |
| 2008 | 0 | 10 | 10 |
| 2009 | 1 | 18 | 19 |
| 2010 | 0 | 9 | 9 |
| 2011 | 0 | 14 | 14 |
| 2012 | 1 | 13 | 14 |
| 2013 | 1 | 15 | 16 |
| 2014 | 0 | 7 | 7 |
| 2015 | 0 | 3 | 3 |
| 2016 | 0 | 10 | 10 |
| 2017 | 0 | 6 | 6 |
| 2018 | 1 | 6 | 7 |
| 2019 | 0 | 7 | 7 |
| 2020 | 0 | 2 | 2 |
| 2021 | 1 | 4 | 5 |
| 2022 | 1 | 4 | 5 |
| 2023 | 0 | 1 | 1 |
| 2024 | 1 | 2 | 3 |
| 2025 | 0 | 1 | 1 |
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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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Rare variant contribution to the heritability of coronary artery disease. Nat Commun. 2024 Oct 09; 15(1):8741.
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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.
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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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Single-nucleotide variant calling in single-cell sequencing data with Monopogen. Nat Biotechnol. 2024 May; 42(5):803-812.
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A saturated map of common genetic variants associated with human height. Nature. 2022 10; 610(7933):704-712.
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TOP-LD: A tool to explore linkage disequilibrium with TOPMed whole-genome sequence data. Am J Hum Genet. 2022 06 02; 109(6):1175-1181.
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Genome-Wide Causation Studies of Complex Diseases. J Comput Biol. 2022 08; 29(8):908-931.
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Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data. Nat Genet. 2022 Mar; 54(3):263-273.
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Shared genomic architecture between COVID-19 severity and numerous clinical and physiologic parameters revealed by LD score regression analysis. Sci Rep. 2022 02 03; 12(1):1891.