 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 |
|---|
| 1991 | 4 | 4 | 8 | | 1992 | 3 | 8 | 11 | | 1993 | 2 | 4 | 6 | | 1994 | 1 | 7 | 8 | | 1995 | 5 | 8 | 13 | | 1996 | 3 | 3 | 6 | | 1997 | 2 | 5 | 7 | | 1998 | 3 | 7 | 10 | | 1999 | 8 | 7 | 15 | | 2000 | 1 | 7 | 8 | | 2001 | 3 | 7 | 10 | | 2002 | 2 | 13 | 15 | | 2003 | 8 | 6 | 14 | | 2004 | 5 | 5 | 10 | | 2005 | 9 | 11 | 20 | | 2006 | 10 | 14 | 24 | | 2007 | 3 | 10 | 13 | | 2008 | 6 | 5 | 11 | | 2009 | 5 | 5 | 10 | | 2010 | 2 | 5 | 7 | | 2011 | 5 | 11 | 16 | | 2012 | 0 | 7 | 7 | | 2013 | 1 | 5 | 6 | | 2014 | 1 | 7 | 8 | | 2015 | 0 | 3 | 3 | | 2016 | 0 | 1 | 1 | | 2018 | 0 | 2 | 2 | | 2019 | 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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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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Fletcher RS, Herrmann D, Mullen JL, Li Q, Schrider DR, Price N, Lin J, Grogan K, Kern A, McKay JK. Identification of Polymorphisms Associated with Drought Adaptation QTL in Brassica napus by Resequencing. G3 (Bethesda). 2016 04 07; 6(4):793-803.
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Shah K, Ali RH, Ansar M, Lee K, Chishti MS, Abbe I, Li B, Smith JD, Nickerson DA, Shendure J, Coucke PJ, Steyaert W, Bamshad MJ, Santos-Cortez RLP, Leal SM, Ahmad W. Mitral regurgitation as a phenotypic manifestation of nonphotosensitive trichothiodystrophy due to a splice variant in MPLKIP. BMC Med Genet. 2016 Feb 16; 17:13.
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Shellman YG, Lambert KA, Brauweiler A, Fain P, Spritz RA, Martini M, Janssen KP, Box NF, Terzian T, Rewers M, Horvath A, Stratakis CA, Robinson WA, Robinson SE, Norris DA, Artinger KB, Pacheco TR. SASH1 Is Involved in an Autosomal Dominant Lentiginous Phenotype. J Invest Dermatol. 2015 Dec; 135(12):3192-3194.
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Zampini É, Lepage É, Tremblay-Belzile S, Truche S, Brisson N. Organelle DNA rearrangement mapping reveals U-turn-like inversions as a major source of genomic instability in Arabidopsis and humans. Genome Res. 2015 May; 25(5):645-54.
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Whitney KD, Broman KW, Kane NC, Hovick SM, Randell RA, Rieseberg LH. Quantitative trait locus mapping identifies candidate alleles involved in adaptive introgression and range expansion in a wild sunflower. Mol Ecol. 2015 May; 24(9):2194-211.
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Qi LL, Ma GJ, Long YM, Hulke BS, Gong L, Markell SG. Relocation of a rust resistance gene R 2 and its marker-assisted gene pyramiding in confection sunflower (Helianthus annuus L.). Theor Appl Genet. 2015 Mar; 128(3):477-88.
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Guo DC, Gong L, Regalado ES, Santos-Cortez RL, Zhao R, Cai B, Veeraraghavan S, Prakash SK, Johnson RJ, Muilenburg A, Willing M, Jondeau G, Boileau C, Pannu H, Moran R, Debacker J, Bamshad MJ, Shendure J, Nickerson DA, Leal SM, Raman CS, Swindell EC, Milewicz DM. MAT2A mutations predispose individuals to thoracic aortic aneurysms. Am J Hum Genet. 2015 Jan 08; 96(1):170-7.
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