"Genetic Linkage" 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.
The co-inheritance of two or more non-allelic GENES due to their being located more or less closely on the same CHROMOSOME.
| Descriptor ID |
D008040
|
| MeSH Number(s) |
G05.348
|
| Concept/Terms |
Genetic Linkage Analysis- Genetic Linkage Analysis
- Analyses, Genetic Linkage
- Analysis, Genetic Linkage
- Genetic Linkage Analyses
- Linkage Analyses, Genetic
- Linkage Analysis, Genetic
|
Below are MeSH descriptors whose meaning is more general than "Genetic Linkage".
Below are MeSH descriptors whose meaning is more specific than "Genetic Linkage".
This graph shows the total number of publications written about "Genetic Linkage" by people in this website by year, and whether "Genetic Linkage" 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 | 0 | 3 | 3 |
| 1996 | 0 | 2 | 2 |
| 1997 | 0 | 2 | 2 |
| 1998 | 3 | 2 | 5 |
| 1999 | 0 | 1 | 1 |
| 2000 | 1 | 1 | 2 |
| 2001 | 0 | 2 | 2 |
| 2002 | 3 | 6 | 9 |
| 2003 | 1 | 0 | 1 |
| 2004 | 3 | 3 | 6 |
| 2005 | 4 | 0 | 4 |
| 2006 | 3 | 2 | 5 |
| 2007 | 3 | 1 | 4 |
| 2008 | 3 | 0 | 3 |
| 2009 | 1 | 1 | 2 |
| 2010 | 1 | 0 | 1 |
| 2011 | 4 | 0 | 4 |
| 2012 | 1 | 0 | 1 |
| 2013 | 1 | 0 | 1 |
| 2017 | 0 | 1 | 1 |
| 2018 | 0 | 1 | 1 |
| 2019 | 0 | 1 | 1 |
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Below are the most recent publications written about "Genetic Linkage" by people in Profiles.
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Genetic analysis of hsCRP in American Indians: The Strong Heart Family Study. PLoS One. 2019; 14(10):e0223574.
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Trans-Ethnic Mapping of BANK1 Identifies Two Independent SLE-Risk Linkage Groups Enriched for Co-Transcriptional Splicing Marks. Int J Mol Sci. 2018 Aug 08; 19(8).
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Reduced penetrance in a large Caucasian pedigree with Stickler syndrome. Ophthalmic Genet. 2017 Jan-Feb; 38(1):43-50.
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Genome-wide linkage analysis of carotid artery lumen diameter: the strong heart family study. Int J Cardiol. 2013 Oct 09; 168(4):3902-8.
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Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele. J Med Genet. 2012 Apr; 49(4):270-6.
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Analysis of autosomal genes reveals gene-sex interactions and higher total genetic risk in men with systemic lupus erythematosus. Ann Rheum Dis. 2012 May; 71(5):694-9.
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Refinement of the X-linked nonsyndromic high-grade myopia locus MYP1 on Xq28 and exclusion of 13 known positional candidate genes by direct sequencing. Invest Ophthalmol Vis Sci. 2011 Aug 29; 52(9):6814-9.
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Identification of novel suggestive loci for high-grade myopia in Polish families. Mol Vis. 2011; 17:2028-39.
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Genome-wide linkage scan to identify loci associated with type 2 diabetes and blood lipid phenotypes in the Sikh Diabetes Study. PLoS One. 2011; 6(6):e21188.
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The lupus family registry and repository. Rheumatology (Oxford). 2011 Jan; 50(1):47-59.