"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
|
MeSH Number(s) |
D23.101.387 G05.695.450
|
Concept/Terms |
Genetic Markers- Genetic Markers
- Markers, Genetic
- Genetic Marker
- Marker, Genetic
Chromosome Markers- Chromosome Markers
- Chromosome Marker
- Marker, Chromosome
- Markers, Chromosome
|
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 |
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1995 | 0 | 3 | 3 |
1996 | 0 | 2 | 2 |
1997 | 1 | 3 | 4 |
1998 | 0 | 2 | 2 |
1999 | 1 | 4 | 5 |
2001 | 1 | 0 | 1 |
2002 | 0 | 4 | 4 |
2003 | 1 | 1 | 2 |
2004 | 0 | 3 | 3 |
2005 | 0 | 5 | 5 |
2006 | 0 | 4 | 4 |
2007 | 0 | 1 | 1 |
2008 | 2 | 7 | 9 |
2009 | 0 | 5 | 5 |
2010 | 3 | 2 | 5 |
2011 | 1 | 3 | 4 |
2012 | 2 | 10 | 12 |
2013 | 0 | 5 | 5 |
2014 | 0 | 4 | 4 |
2015 | 0 | 3 | 3 |
2016 | 1 | 4 | 5 |
2017 | 0 | 1 | 1 |
2018 | 0 | 2 | 2 |
2019 | 1 | 2 | 3 |
2021 | 0 | 1 | 1 |
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Below are the most recent publications written about "Genetic Markers" by people in Profiles.
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Average semivariance yields accurate estimates of the fraction of marker-associated genetic variance and heritability in complex trait analyses. PLoS Genet. 2021 08; 17(8):e1009762.
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Glycogen Storage Disease Type IV Diagnosed at Fetal Autopsy. Pediatr Dev Pathol. 2020 Aug; 23(4):301-305.
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Novel Genetic Markers for Early Detection of Elevated Breast Cancer Risk in Women. Int J Mol Sci. 2019 Sep 28; 20(19).
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Integrative analysis of DNA methylation in discordant twins unveils distinct architectures of systemic sclerosis subsets. Clin Epigenetics. 2019 04 04; 11(1):58.
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Opportunities for microRNAs in the Crowded Field of Cardiovascular Biomarkers. Annu Rev Pathol. 2019 01 24; 14:211-238.
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Impact of bitter taste receptor phenotype upon clinical presentation in chronic rhinosinusitis. Int Forum Allergy Rhinol. 2018 09; 8(9):1013-1020.
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First Report of Prenatal Ascertainment of a Fetus With Homozygous Loss of the SOX10 Gene and Phenotypic Correlation by Autopsy Examination. Pediatr Dev Pathol. 2018 Nov-Dec; 21(6):561-567.
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Standardized Markerless Gene Integration for Pathway Engineering in Yarrowia lipolytica. ACS Synth Biol. 2017 03 17; 6(3):402-409.
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Characterization of primary osteocyte-like cells from rat mandibles. Oral Surg Oral Med Oral Pathol Oral Radiol. 2017 Jan; 123(1):37-43.
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Adult body mass index and risk of ovarian cancer by subtype: a Mendelian randomization study. Int J Epidemiol. 2016 06; 45(3):884-95.