"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 |
|---|
| 1996 | 3 | 10 | 13 |
| 1997 | 5 | 11 | 16 |
| 1998 | 8 | 9 | 17 |
| 1999 | 8 | 17 | 25 |
| 2000 | 8 | 14 | 22 |
| 2001 | 8 | 9 | 17 |
| 2002 | 3 | 10 | 13 |
| 2003 | 8 | 15 | 23 |
| 2004 | 5 | 4 | 9 |
| 2005 | 9 | 10 | 19 |
| 2006 | 9 | 8 | 17 |
| 2007 | 7 | 12 | 19 |
| 2008 | 7 | 5 | 12 |
| 2009 | 2 | 6 | 8 |
| 2010 | 4 | 5 | 9 |
| 2011 | 2 | 3 | 5 |
| 2012 | 3 | 1 | 4 |
| 2013 | 0 | 2 | 2 |
| 2014 | 1 | 2 | 3 |
| 2015 | 4 | 4 | 8 |
| 2016 | 0 | 2 | 2 |
| 2017 | 1 | 3 | 4 |
| 2018 | 0 | 4 | 4 |
| 2019 | 1 | 2 | 3 |
| 2021 | 1 | 1 | 2 |
| 2022 | 0 | 1 | 1 |
| 2024 | 1 | 0 | 1 |
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Below are the most recent publications written about "Genetic Linkage" by people in Profiles.
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Genetic Variation and Recurrent Haplotypes on Chromosome 6q23-25 Risk Locus in Familial Lung Cancer. Cancer Res. 2021 06 15; 81(12):3162-3173.
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Genetic epidemiology and risk factors for brain tumors. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2018 Apr 28; 43(4):345-353.
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New statistical methods for estimation of recombination fractions in F2 population. BMC Bioinformatics. 2017 Oct 03; 18(Suppl 11):404.
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Variants in angiopoietin-2 (ANGPT2) contribute to variation in nocturnal oxyhaemoglobin saturation level. Hum Mol Genet. 2016 12 01; 25(23):5244-5253.
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Targeted sequencing in chromosome 17q linkage region identifies familial glioma candidates in the Gliogene Consortium. Sci Rep. 2015 Feb 05; 5:8278.
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A missense mutation in HK1 leads to autosomal dominant retinitis pigmentosa. Invest Ophthalmol Vis Sci. 2014 Oct 14; 55(11):7159-64.
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A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data. Nat Biotechnol. 2014 Jul; 32(7):663-9.
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Relationship estimation from whole-genome sequence data. PLoS Genet. 2014 Jan; 10(1):e1004144.
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Common variation neighbouring micro-RNA 22 is associated with increased left ventricular mass. PLoS One. 2013; 8(1):e55061.
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A variable age of onset segregation model for linkage analysis, with correction for ascertainment, applied to glioma. Cancer Epidemiol Biomarkers Prev. 2012 Dec; 21(12):2242-51.