"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 | 16 | 24 |
| 2000 | 9 | 14 | 23 |
| 2001 | 9 | 9 | 18 |
| 2002 | 3 | 10 | 13 |
| 2003 | 8 | 14 | 22 |
| 2004 | 5 | 4 | 9 |
| 2005 | 9 | 10 | 19 |
| 2006 | 9 | 10 | 19 |
| 2007 | 7 | 12 | 19 |
| 2008 | 6 | 5 | 11 |
| 2009 | 2 | 6 | 8 |
| 2010 | 4 | 5 | 9 |
| 2011 | 2 | 4 | 6 |
| 2012 | 3 | 1 | 4 |
| 2013 | 0 | 3 | 3 |
| 2014 | 1 | 3 | 4 |
| 2015 | 4 | 3 | 7 |
| 2016 | 0 | 2 | 2 |
| 2017 | 1 | 2 | 3 |
| 2018 | 0 | 4 | 4 |
| 2019 | 1 | 2 | 3 |
| 2021 | 1 | 1 | 2 |
| 2022 | 0 | 2 | 2 |
| 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 architecture reconciles linkage and association studies of complex traits. Nat Genet. 2024 Nov; 56(11):2352-2360.
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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 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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Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data. Hum Genet. 2019 Feb; 138(2):199-210.
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Confirmation of the Role of DHX38 in the Etiology of Early-Onset Retinitis Pigmentosa. Invest Ophthalmol Vis Sci. 2018 09 04; 59(11):4552-4557.
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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.