"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 |
|---|
| 1996 | 8 | 12 | 20 |
| 1997 | 2 | 14 | 16 |
| 1998 | 4 | 13 | 17 |
| 1999 | 1 | 15 | 16 |
| 2000 | 0 | 9 | 9 |
| 2001 | 5 | 10 | 15 |
| 2002 | 0 | 7 | 7 |
| 2003 | 3 | 18 | 21 |
| 2004 | 3 | 14 | 17 |
| 2005 | 4 | 18 | 22 |
| 2006 | 2 | 8 | 10 |
| 2007 | 1 | 13 | 14 |
| 2008 | 3 | 12 | 15 |
| 2009 | 2 | 11 | 13 |
| 2010 | 0 | 8 | 8 |
| 2011 | 5 | 9 | 14 |
| 2012 | 0 | 8 | 8 |
| 2013 | 0 | 5 | 5 |
| 2014 | 3 | 10 | 13 |
| 2015 | 7 | 7 | 14 |
| 2016 | 4 | 9 | 13 |
| 2017 | 1 | 11 | 12 |
| 2018 | 5 | 9 | 14 |
| 2019 | 3 | 4 | 7 |
| 2020 | 1 | 3 | 4 |
| 2021 | 0 | 2 | 2 |
| 2023 | 0 | 1 | 1 |
| 2025 | 0 | 2 | 2 |
| 2026 | 0 | 2 | 2 |
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Below are the most recent publications written about "Genetic Markers" by people in Profiles.
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Clinical and genetic markers of vascular toxicity in glioblastoma patients: Insights from NRG Oncology RTOG-0825. Neuro Oncol. 2025 Mar 07; 27(3):767-778.
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Maternal Lactase Polymorphism (rs4988235) Is Associated with Neural Tube Defects in Offspring in the National Birth Defects Prevention Study. J Nutr. 2019 02 01; 149(2):295-303.
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Genetic epidemiology of neural tube defects. J Pediatr Rehabil Med. 2017 12 11; 10(3-4):189-194.
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Serum Sclerostin Levels in Adults With Osteogenesis Imperfecta: Comparison With Normal Individuals and Response to Teriparatide Therapy. J Bone Miner Res. 2018 02; 33(2):307-315.
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New statistical methods for estimation of recombination fractions in F2 population. BMC Bioinformatics. 2017 Oct 03; 18(Suppl 11):404.
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Disease-related gene module detection based on a multi-label propagation clustering algorithm. PLoS One. 2017; 12(5):e0178006.
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Linking newborn severe combined immunodeficiency screening with targeted exome sequencing: A case report. J Allergy Clin Immunol Pract. 2017 Sep - Oct; 5(5):1442-1444.
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Interpreting Incidentally Identified Variants in Genes Associated With Catecholaminergic Polymorphic Ventricular Tachycardia in a Large Cohort of Clinical Whole-Exome Genetic Test Referrals. Circ Arrhythm Electrophysiol. 2017 Apr; 10(4).
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Newborn screening: a review of history, recent advancements, and future perspectives in the era of next generation sequencing. Curr Opin Pediatr. 2016 12; 28(6):694-699.
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Association of RNA Biosignatures With Bacterial Infections in Febrile Infants Aged 60 Days or Younger. JAMA. 2016 Aug 23-30; 316(8):846-57.