"Polymorphism, Genetic" 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 regular and simultaneous occurrence in a single interbreeding population of two or more discontinuous genotypes. The concept includes differences in genotypes ranging in size from a single nucleotide site (POLYMORPHISM, SINGLE NUCLEOTIDE) to large nucleotide sequences visible at a chromosomal level.
Descriptor ID |
D011110
|
MeSH Number(s) |
G05.365.795
|
Concept/Terms |
Polymorphism, Genetic- Polymorphism, Genetic
- Polymorphisms, Genetic
- Genetic Polymorphisms
- Genetic Polymorphism
- Polymorphism (Genetics)
- Polymorphisms (Genetics)
|
Below are MeSH descriptors whose meaning is more general than "Polymorphism, Genetic".
Below are MeSH descriptors whose meaning is more specific than "Polymorphism, Genetic".
This graph shows the total number of publications written about "Polymorphism, Genetic" by people in this website by year, and whether "Polymorphism, Genetic" 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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1994 | 7 | 13 | 20 |
1995 | 9 | 8 | 17 |
1996 | 5 | 17 | 22 |
1997 | 10 | 10 | 20 |
1998 | 6 | 12 | 18 |
1999 | 9 | 13 | 22 |
2000 | 23 | 22 | 45 |
2001 | 23 | 23 | 46 |
2002 | 28 | 26 | 54 |
2003 | 35 | 17 | 52 |
2004 | 33 | 31 | 64 |
2005 | 45 | 31 | 76 |
2006 | 36 | 20 | 56 |
2007 | 35 | 28 | 63 |
2008 | 36 | 19 | 55 |
2009 | 19 | 24 | 43 |
2010 | 17 | 17 | 34 |
2011 | 14 | 15 | 29 |
2012 | 15 | 6 | 21 |
2013 | 12 | 13 | 25 |
2014 | 10 | 18 | 28 |
2015 | 7 | 15 | 22 |
2016 | 4 | 8 | 12 |
2017 | 7 | 5 | 12 |
2018 | 4 | 9 | 13 |
2019 | 7 | 6 | 13 |
2020 | 1 | 5 | 6 |
2021 | 0 | 2 | 2 |
2022 | 0 | 6 | 6 |
2023 | 1 | 1 | 2 |
2024 | 0 | 2 | 2 |
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Below are the most recent publications written about "Polymorphism, Genetic" by people in Profiles.
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Insights into the genetic landscape of systemic sclerosis. Best Pract Res Clin Rheumatol. 2024 Dec; 38(4):101981.
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Sequencing of Kaposi's Sarcoma Herpesvirus (KSHV) genomes from persons of diverse ethnicities and provenances with KSHV-associated diseases demonstrate multiple infections, novel polymorphisms, and low intra-host variance. PLoS Pathog. 2024 Jul; 20(7):e1012338.
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Fentanyl Toxicity Related to Concomitant Use of Ciprofloxacin and its Effects as a CYP3A4 Inhibitor. J Pain Symptom Manage. 2023 08; 66(2):e307-e309.
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SVhound: detection of regions that harbor yet undetected structural variation. BMC Bioinformatics. 2023 Jan 20; 24(1):23.
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Detailed stratified GWAS analysis for severe COVID-19 in four European populations. Hum Mol Genet. 2022 11 28; 31(23):3945-3966.
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Gene Sequencing Identifies Perturbation in Nitric Oxide Signaling as a Nonlipid Molecular Subtype of Coronary Artery Disease. Circ Genom Precis Med. 2022 12; 15(6):e003598.
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A Novel SPTA1 Mutation in a Patient with Hereditary Spherocytosis without a Family History and Coexisting Gilbert's Syndrome. Intern Med. 2023 Jan 01; 62(1):107-111.
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Emotional self-regulation, impulsivity, 5-HTTLPR and tobacco use behavior among psychiatric inpatients. J Affect Disord. 2022 08 15; 311:631-636.
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Autophagopathies: from autophagy gene polymorphisms to precision medicine for human diseases. Autophagy. 2022 11; 18(11):2519-2536.
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Arterial thrombosis in a newborn with homozygous plasminogen activator inhibitor-1 4G/4G polymorphism. Pediatr Blood Cancer. 2022 08; 69(8):e29586.