"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 | 2 | 0 | 2 |
| 1996 | 2 | 3 | 5 |
| 1997 | 0 | 3 | 3 |
| 1998 | 2 | 3 | 5 |
| 1999 | 2 | 5 | 7 |
| 2000 | 3 | 4 | 7 |
| 2001 | 4 | 6 | 10 |
| 2002 | 8 | 12 | 20 |
| 2003 | 6 | 6 | 12 |
| 2004 | 4 | 14 | 18 |
| 2005 | 7 | 19 | 26 |
| 2006 | 11 | 17 | 28 |
| 2007 | 3 | 24 | 27 |
| 2008 | 3 | 18 | 21 |
| 2009 | 0 | 20 | 20 |
| 2010 | 2 | 17 | 19 |
| 2011 | 2 | 17 | 19 |
| 2012 | 1 | 10 | 11 |
| 2013 | 1 | 17 | 18 |
| 2014 | 0 | 9 | 9 |
| 2015 | 1 | 3 | 4 |
| 2016 | 0 | 7 | 7 |
| 2017 | 0 | 8 | 8 |
| 2018 | 1 | 1 | 2 |
| 2019 | 0 | 4 | 4 |
| 2020 | 0 | 8 | 8 |
| 2021 | 0 | 5 | 5 |
| 2022 | 0 | 4 | 4 |
| 2023 | 0 | 2 | 2 |
| 2024 | 2 | 0 | 2 |
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Below are the most recent publications written about "Linkage Disequilibrium" by people in Profiles.
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Rare variant contribution to the heritability of coronary artery disease. Nat Commun. 2024 10 09; 15(1):8741.
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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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Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study. Lancet Neurol. 2023 11; 22(11):1015-1025.
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Multivariate adaptive shrinkage improves cross-population transcriptome prediction and association studies in underrepresented populations. HGG Adv. 2023 Oct 12; 4(4):100216.
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Fine-mapping from summary data with the "Sum of Single Effects" model. PLoS Genet. 2022 07; 18(7):e1010299.
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Properties of 2-locus genealogies and linkage disequilibrium in temporally structured samples. Genetics. 2022 05 05; 221(1).
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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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Polygenic risk prediction based on singular value decomposition with applications to alcohol use disorder. BMC Bioinformatics. 2022 Jan 10; 23(1):28.
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A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response. Nat Genet. 2021 Oct; 53(10):1504-1516.
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Fate or coincidence: do COPD and major depression share genetic risk factors? Hum Mol Genet. 2021 05 12; 30(7):619-628.