 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) |
G05.348
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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 |
|---|
| 1994 | 1 | 5 | 6 | | 1995 | 3 | 6 | 9 | | 1996 | 2 | 4 | 6 | | 1997 | 0 | 5 | 5 | | 1998 | 2 | 5 | 7 | | 1999 | 6 | 8 | 14 | | 2000 | 1 | 7 | 8 | | 2001 | 3 | 3 | 6 | | 2002 | 0 | 4 | 4 | | 2003 | 8 | 4 | 12 | | 2004 | 5 | 7 | 12 | | 2005 | 8 | 11 | 19 | | 2006 | 9 | 11 | 20 | | 2007 | 2 | 10 | 12 | | 2008 | 5 | 6 | 11 | | 2009 | 5 | 2 | 7 | | 2010 | 3 | 5 | 8 | | 2011 | 4 | 9 | 13 | | 2012 | 0 | 8 | 8 | | 2013 | 1 | 4 | 5 | | 2014 | 2 | 7 | 9 | | 2015 | 0 | 5 | 5 | | 2016 | 1 | 2 | 3 | | 2018 | 0 | 2 | 2 | | 2019 | 1 | 0 | 1 | | 2020 | 0 | 3 | 3 | | 2021 | 0 | 1 | 1 | | 2022 | 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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He KY, Kelly TN, Wang H, Liang J, Zhu L, Cade BE, Assimes TL, Becker LC, Beitelshees AL, Bielak LF, Bress AP, Brody JA, Chang YC, Chang YC, de Vries PS, Duggirala R, Fox ER, Franceschini N, Furniss AL, Gao Y, Guo X, Haessler J, Hung YJ, Hwang SJ, Irvin MR, Kalyani RR, Liu CT, Liu C, Martin LW, Montasser ME, Muntner PM, Mwasongwe S, Naseri T, Palmas W, Reupena MS, Rice KM, Sheu WH, Shimbo D, Smith JA, Snively BM, Yanek LR, Zhao W, Blangero J, Boerwinkle E, Chen YI, Correa A, Cupples LA, Curran JE, Fornage M, He J, Hou L, Kaplan RC, Kardia SLR, Kenny EE, Kooperberg C, Lloyd-Jones D, Loos RJF, Mathias RA, McGarvey ST, Mitchell BD, North KE, Peyser PA, Psaty BM, Raffield LM, Rao DC, Redline S, Reiner AP, Rich SS, Rotter JI, Taylor KD, Tracy R, Vasan RS, Morrison AC, Levy D, Chakravarti A, Arnett DK, Zhu X. Rare coding variants in RCN3 are associated with blood pressure. BMC Genomics. 2022 Feb 19; 23(1):148.
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Tang NLS, Dobbs MB, Gurnett CA, Qiu Y, Lam TP, Cheng JCY, Hadley-Miller N. A Decade in Review after Idiopathic Scoliosis Was First Called a Complex Trait-A Tribute to the Late Dr. Yves Cotrel for His Support in Studies of Etiology of Scoliosis. Genes (Basel). 2021 07 01; 12(7).
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Veller C, Edelman NB, Muralidhar P, Nowak MA. Variation in Genetic Relatedness Is Determined by the Aggregate Recombination Process. Genetics. 2020 12; 216(4):985-994.
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Bragg J, Tomasi P, Zhang L, Williams T, Wood D, Lovell JT, Healey A, Schmutz J, Bonnette JE, Cheng P, Chanbusarakum L, Juenger T, Tobias CM. Environmentally responsive QTL controlling surface wax load in switchgrass. Theor Appl Genet. 2020 Nov; 133(11):3119-3137.
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Spritz RA, Santorico SA. The Genetic Basis of Vitiligo. J Invest Dermatol. 2021 02; 141(2):265-273.
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He KY, Li X, Kelly TN, Liang J, Cade BE, Assimes TL, Becker LC, Beitelshees AL, Bress AP, Chang YC, Chen YI, de Vries PS, Fox ER, Franceschini N, Furniss A, Gao Y, Guo X, Haessler J, Hwang SJ, Irvin MR, Kalyani RR, Liu CT, Liu C, Martin LW, Montasser ME, Muntner PM, Mwasongwe S, Palmas W, Reiner AP, Shimbo D, Smith JA, Snively BM, Yanek LR, Boerwinkle E, Correa A, Cupples LA, He J, Kardia SLR, Kooperberg C, Mathias RA, Mitchell BD, Psaty BM, Vasan RS, Rao DC, Rich SS, Rotter JI, Wilson JG, Chakravarti A, Morrison AC, Levy D, Arnett DK, Redline S, Zhu X. 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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Lea MV, Syring J, Jennings T, Cronn R, Bruederle LP, Neale JR, Tomback DF. Development of nuclear microsatellite loci for Pinus albicaulis Engelm. (Pinaceae), a conifer of conservation concern. PLoS One. 2018; 13(10):e0205423.
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Latif Z, Chakchouk I, Schrauwen I, Lee K, Santos-Cortez RLP, Abbe I, Acharya A, Jarral A, Ali I, Ullah E, Khan MN, Ali G, Tahir TH, Bamshad MJ, Nickerson DA, Ahmad W, Ansar M, Leal SM. 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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Rao AR, Yourshaw M, Christensen B, Nelson SF, Kerner B. Rare deleterious mutations are associated with disease in bipolar disorder families. Mol Psychiatry. 2017 07; 22(7):1009-1014.
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Hellwege JN, Palmer ND, Dimitrov L, Keaton JM, Tabb KL, Sajuthi S, Taylor KD, Ng MC, Speliotes EK, Hawkins GA, Long J, Ida Chen YD, Lorenzo C, Norris JM, Rotter JI, Langefeld CD, Wagenknecht LE, Bowden DW. Genome-wide linkage and association analysis of cardiometabolic phenotypes in Hispanic Americans. J Hum Genet. 2017 Feb; 62(2):175-184.
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