 Genetic Linkage
"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
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| MeSH Number(s) |
G05.540
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| Concept/Terms |
Genetic Linkage Analysis- Genetic Linkage Analysis
- Analyses, Genetic Linkage
- Analysis, Genetic Linkage
- Genetic Linkage Analyses
- Linkage Analyses, Genetic
- Linkage Analysis, Genetic
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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 |
|---|
| 1985 | 0 | 2 | 2 | | 1990 | 1 | 0 | 1 | | 1997 | 0 | 1 | 1 | | 2000 | 1 | 0 | 1 | | 2001 | 1 | 0 | 1 | | 2002 | 0 | 1 | 1 | | 2003 | 0 | 1 | 1 | | 2005 | 0 | 2 | 2 | | 2008 | 2 | 0 | 2 | | 2009 | 0 | 2 | 2 | | 2010 | 0 | 2 | 2 | | 2011 | 1 | 0 | 1 | | 2012 | 1 | 0 | 1 | | 2016 | 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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Meisel RP, Davey T, Son JH, Gerry AC, Shono T, Scott JG. Is Multifactorial Sex Determination in the House Fly, Musca domestica (L.), Stable Over Time? J Hered. 2016; 107(7):615-625.
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Meisel RP, Malone JH, Clark AG. Disentangling the relationship between sex-biased gene expression and X-linkage. Genome Res. 2012 Jul; 22(7):1255-65.
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Skiba T, Landi N, Wagner R, Grigorenko EL. In search of the perfect phenotype: an analysis of linkage and association studies of reading and reading-related processes. Behav Genet. 2011 Jan; 41(1):6-30.
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Smith SD, Grigorenko E, Willcutt E, Pennington BF, Olson RK, DeFries JC. Etiologies and molecular mechanisms of communication disorders. J Dev Behav Pediatr. 2010 Sep; 31(7):555-63.
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O'Byrne MR, Au KS, Morrison AC, Lin JI, Fletcher JM, Ostermaier KK, Tyerman GH, Doebel S, Northrup H. Association of folate receptor (FOLR1, FOLR2, FOLR3) and reduced folate carrier (SLC19A1) genes with meningomyelocele. Birth Defects Res A Clin Mol Teratol. 2010 Aug; 88(8):689-94.
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Boname JM, Thomas M, Stagg HR, Xu P, Peng J, Lehner PJ. Efficient internalization of MHC I requires lysine-11 and lysine-63 mixed linkage polyubiquitin chains. Traffic. 2010 Feb; 11(2):210-20.
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Qiu HT, Meng HQ, Song C, Xiu MH, Chen DC, Zhu FY, Wu GY, Kosten TA, Kosten TR, Zhang XY. Association between monoamine oxidase (MAO)-A gene variants and schizophrenia in a Chinese population. Brain Res. 2009 Sep 01; 1287:67-73.
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Grigorenko EL, Han SS, Yrigollen CM, Leng L, Mizue Y, Anderson GM, Mulder EJ, de Bildt A, Minderaa RB, Volkmar FR, Chang JT, Bucala R. Macrophage migration inhibitory factor and autism spectrum disorders. Pediatrics. 2008 Aug; 122(2):e438-45.
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Yrigollen CM, Han SS, Kochetkova A, Babitz T, Chang JT, Volkmar FR, Leckman JF, Grigorenko EL. Genes controlling affiliative behavior as candidate genes for autism. Biol Psychiatry. 2008 May 15; 63(10):911-6.
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Otteson DC, Tsujikawa M, Gunatilaka T, Malicki J, Zack DJ. Genomic organization of zebrafish cone-rod homeobox gene and exclusion as a candidate gene for retinal degeneration in niezerka and mikre oko. Mol Vis. 2005 Nov 17; 11:986-95.
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