"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 |
|---|
| 1995 | 3 | 12 | 15 |
| 1996 | 3 | 10 | 13 |
| 1997 | 5 | 12 | 17 |
| 1998 | 8 | 9 | 17 |
| 1999 | 8 | 17 | 25 |
| 2000 | 9 | 14 | 23 |
| 2001 | 9 | 7 | 16 |
| 2002 | 2 | 9 | 11 |
| 2003 | 8 | 12 | 20 |
| 2004 | 2 | 5 | 7 |
| 2005 | 8 | 9 | 17 |
| 2006 | 9 | 9 | 18 |
| 2007 | 7 | 10 | 17 |
| 2008 | 6 | 5 | 11 |
| 2009 | 2 | 6 | 8 |
| 2010 | 3 | 5 | 8 |
| 2011 | 2 | 4 | 6 |
| 2012 | 3 | 1 | 4 |
| 2013 | 0 | 2 | 2 |
| 2014 | 1 | 2 | 3 |
| 2015 | 4 | 2 | 6 |
| 2016 | 0 | 2 | 2 |
| 2017 | 1 | 2 | 3 |
| 2018 | 0 | 4 | 4 |
| 2019 | 1 | 2 | 3 |
| 2021 | 1 | 1 | 2 |
| 2022 | 0 | 2 | 2 |
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Below are the most recent publications written about "Genetic Linkage" by people in Profiles.
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Chromosome-length genome assembly and linkage map of a critically endangered Australian bird: the helmeted honeyeater. Gigascience. 2022 03 29; 11.
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Rare coding variants in RCN3 are associated with blood pressure. BMC Genomics. 2022 Feb 19; 23(1):148.
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Toward an Improved Classification of Type 2 Diabetes: Lessons From Research into the Heterogeneity of a Complex Disease. J Clin Endocrinol Metab. 2021 11 19; 106(12):e4822-e4833.
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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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A quantitative trait rare variant nonparametric linkage method with application to age-at-onset of Alzheimer's disease. Eur J Hum Genet. 2020 12; 28(12):1734-1742.
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A diagnostic ceiling for exome sequencing in cerebellar ataxia and related neurological disorders. Hum Mutat. 2020 02; 41(2):487-501.
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Sequencing Analysis at 8p23 Identifies Multiple Rare Variants in DLC1 Associated with Sleep-Related Oxyhemoglobin Saturation Level. Am J Hum Genet. 2019 11 07; 105(5):1057-1068.
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A Rare Variant Nonparametric Linkage Method for Nuclear and Extended Pedigrees with Application to Late-Onset Alzheimer Disease via WGS Data. Am J Hum Genet. 2019 10 03; 105(4):822-835.
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OSBPL2-disrupted pigs recapitulate dual features of human hearing loss and hypercholesterolaemia. J Genet Genomics. 2019 08 20; 46(8):379-387.
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Multiple Differentially Methylated Regions Specific to Keratoconus Explain Known Keratoconus Linkage Loci. Invest Ophthalmol Vis Sci. 2019 04 01; 60(5):1501-1509.