"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 |
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1995 | 0 | 1 | 1 |
2002 | 1 | 1 | 2 |
2003 | 0 | 1 | 1 |
2005 | 0 | 1 | 1 |
2007 | 0 | 1 | 1 |
2008 | 2 | 0 | 2 |
2009 | 1 | 2 | 3 |
2010 | 2 | 1 | 3 |
2011 | 0 | 3 | 3 |
2012 | 0 | 5 | 5 |
2013 | 1 | 2 | 3 |
2014 | 0 | 2 | 2 |
2015 | 0 | 2 | 2 |
2016 | 0 | 3 | 3 |
2017 | 0 | 2 | 2 |
2018 | 0 | 3 | 3 |
2019 | 1 | 2 | 3 |
2021 | 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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A Homozygous AKNA Frameshift Variant Is Associated with Microcephaly in a Pakistani Family. Genes (Basel). 2021 09 24; 12(10).
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Autosomal-dominant hypotrichosis with woolly hair: Novel gene locus on chromosome 4q35.1-q35.2. PLoS One. 2019; 14(12):e0225943.
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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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SSBP1 mutations in dominant optic atrophy with variable retinal degeneration. Ann Neurol. 2019 09; 86(3):368-383.
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Genetic correlation between multiple myeloma and chronic lymphocytic leukaemia provides evidence for shared aetiology. Blood Cancer J. 2018 12 21; 9(1):1.
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Identification of ADHD risk genes in extended pedigrees by combining linkage analysis and whole-exome sequencing. Mol Psychiatry. 2020 09; 25(9):2047-2057.
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Influence of obesity-related risk factors in the aetiology of glioma. Br J Cancer. 2018 04; 118(7):1020-1027.
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A deep intronic CLRN1 (USH3A) founder mutation generates an aberrant exon and underlies severe Usher syndrome on the Arabian Peninsula. Sci Rep. 2017 05 03; 7(1):1411.
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Identification of shared risk loci and pathways for bipolar disorder and schizophrenia. PLoS One. 2017; 12(2):e0171595.
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CDK5RAP2 interaction with components of the Hippo signaling pathway may play a role in primary microcephaly. Mol Genet Genomics. 2017 Apr; 292(2):365-383.