 Genetic Markers
"Genetic Markers" 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.
A phenotypically recognizable genetic trait which can be used to identify a genetic locus, a linkage group, or a recombination event.
| Descriptor ID |
D005819
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| MeSH Number(s) |
D23.101.387 G05.695.450
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| Concept/Terms |
Genetic Markers- Genetic Markers
- Markers, Genetic
- Genetic Marker
- Marker, Genetic
Chromosome Markers- Chromosome Markers
- Chromosome Marker
- Marker, Chromosome
- Markers, Chromosome
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Below are MeSH descriptors whose meaning is more general than "Genetic Markers".
Below are MeSH descriptors whose meaning is more specific than "Genetic Markers".
This graph shows the total number of publications written about "Genetic Markers" by people in this website by year, and whether "Genetic Markers" 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 |
|---|
| 1980 | 1 | 0 | 1 | | 1981 | 0 | 1 | 1 | | 1982 | 1 | 3 | 4 | | 1983 | 1 | 1 | 2 | | 1984 | 1 | 3 | 4 | | 1985 | 2 | 4 | 6 | | 1986 | 4 | 2 | 6 | | 1987 | 2 | 7 | 9 | | 1988 | 3 | 3 | 6 | | 1989 | 0 | 10 | 10 | | 1990 | 0 | 2 | 2 | | 1991 | 1 | 6 | 7 | | 1992 | 1 | 16 | 17 | | 1993 | 4 | 11 | 15 | | 1994 | 2 | 15 | 17 | | 1995 | 1 | 11 | 12 | | 1996 | 1 | 15 | 16 | | 1997 | 5 | 10 | 15 | | 1998 | 1 | 13 | 14 | | 1999 | 2 | 7 | 9 | | 2000 | 0 | 8 | 8 | | 2001 | 1 | 13 | 14 | | 2002 | 0 | 6 | 6 | | 2003 | 1 | 8 | 9 | | 2004 | 1 | 7 | 8 | | 2005 | 0 | 19 | 19 | | 2006 | 0 | 19 | 19 | | 2007 | 2 | 10 | 12 | | 2008 | 0 | 8 | 8 | | 2009 | 1 | 9 | 10 | | 2010 | 1 | 6 | 7 | | 2011 | 1 | 7 | 8 | | 2012 | 3 | 9 | 12 | | 2013 | 0 | 7 | 7 | | 2014 | 4 | 12 | 16 | | 2015 | 1 | 5 | 6 | | 2016 | 3 | 6 | 9 | | 2017 | 2 | 8 | 10 | | 2018 | 0 | 4 | 4 |
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Below are the most recent publications written about "Genetic Markers" by people in Profiles.
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Couser NL, Keelean-Fuller D, Davenport ML, Haverfield E, Masood MM, Henin M, Aylsworth AS. Cleft palate and hypopituitarism in a patient with Noonan-like syndrome with loose anagen hair-1. Am J Med Genet A. 2018 09; 176(9):2024-2027.
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Harris AG, Letourneau LR, Greeley SAW. Monogenic diabetes: the impact of making the right diagnosis. Curr Opin Pediatr. 2018 08; 30(4):558-567.
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Pande M, Joon A, Brewster AM, Chen WV, Hopper JL, Eng C, Shete S, Casey G, Schumacher F, Lin Y, Harrison TA, White E, Ahsan H, Andrulis IL, Whittemore AS, John EM, Ko Win A, Makalic E, Schmidt DF, Kapuscinski MK, Ochs-Balcom HM, Gallinger S, Jenkins MA, Newcomb PA, Lindor NM, Peters U, Amos CI, Lynch PM. Genetic susceptibility markers for a breast-colorectal cancer phenotype: Exploratory results from genome-wide association studies. PLoS One. 2018; 13(4):e0196245.
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Kalinina O, Louzoun Y, Wang Y, Utset T, Weigert M. Origins and specificity of auto-antibodies in Sm+ SLE patients. J Autoimmun. 2018 06; 90:94-104.
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Lu TX, Rothenberg ME. MicroRNA. J Allergy Clin Immunol. 2018 04; 141(4):1202-1207.
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Lanktree MB, Chapman AB. New treatment paradigms for ADPKD: moving towards precision medicine. Nat Rev Nephrol. 2017 Dec; 13(12):750-768.
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Kistler L, Johnson SM, Irwin MT, Louis EE, Ratan A, Perry GH. A massively parallel strategy for STR marker development, capture, and genotyping. Nucleic Acids Res. 2017 Sep 06; 45(15):e142.
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Bankoff RJ, Jerjos M, Hohman B, Lauterbur ME, Kistler L, Perry GH. Testing Convergent Evolution in Auditory Processing Genes between Echolocating Mammals and the Aye-Aye, a Percussive-Foraging Primate. Genome Biol Evol. 2017 07 01; 9(7):1978-1989.
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Talamonti M, Galluzzo M, van den Reek JM, de Jong EM, Lambert JLW, Malagoli P, Bianchi L, Costanzo A. Role of the HLA-C*06 allele in clinical response to ustekinumab: evidence from real life in a large cohort of European patients. Br J Dermatol. 2017 Aug; 177(2):489-496.
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Bidwell LC, Gray JC, Weafer J, Palmer AA, de Wit H, MacKillop J. Genetic influences on ADHD symptom dimensions: Examination of a priori candidates, gene-based tests, genome-wide variation, and SNP heritability. Am J Med Genet B Neuropsychiatr Genet. 2017 Jun; 174(4):458-466.
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